Washing liquid obtained from irrigation of the lung, including the BRONCHI and the PULMONARY ALVEOLI. It is generally used to assess biochemical, inflammatory, or infection status of the lung.
Washing out of the lungs with saline or mucolytic agents for diagnostic or therapeutic purposes. It is very useful in the diagnosis of diffuse pulmonary infiltrates in immunosuppressed patients.
Either of the pair of organs occupying the cavity of the thorax that effect the aeration of the blood.
Endoscopic examination, therapy or surgery of the bronchi.
The washing of a body cavity or surface by flowing water or solution for therapy or diagnosis.
Round, granular, mononuclear phagocytes found in the alveoli of the lungs. They ingest small inhaled particles resulting in degradation and presentation of the antigen to immunocompetent cells.
Sarcoidosis affecting predominantly the lungs, the site most frequently involved and most commonly causing morbidity and mortality in sarcoidosis. Pulmonary sarcoidosis is characterized by sharply circumscribed granulomas in the alveolar, bronchial, and vascular walls, composed of tightly packed cells derived from the mononuclear phagocyte system. The clinical symptoms when present are dyspnea upon exertion, nonproductive cough, and wheezing. (Cecil Textbook of Medicine, 19th ed, p431)
Infection of the lung often accompanied by inflammation.
A process in which normal lung tissues are progressively replaced by FIBROBLASTS and COLLAGEN causing an irreversible loss of the ability to transfer oxygen into the bloodstream via PULMONARY ALVEOLI. Patients show progressive DYSPNEA finally resulting in death.
Small polyhedral outpouchings along the walls of the alveolar sacs, alveolar ducts and terminal bronchioles through the walls of which gas exchange between alveolar air and pulmonary capillary blood takes place.
Pathological processes involving any part of the LUNG.
An idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands.
Medical procedure involving the emptying of contents in the stomach through the use of a tube inserted through the nose or mouth. It is performed to remove poisons or relieve pressure due to intestinal blockages or during surgery.
A common interstitial lung disease caused by hypersensitivity reactions of PULMONARY ALVEOLI after inhalation of and sensitization to environmental antigens of microbial, animal, or chemical sources. The disease is characterized by lymphocytic alveolitis and granulomatous pneumonitis.
A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents.
Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory.
Granular leukocytes with a nucleus that usually has two lobes connected by a slender thread of chromatin, and cytoplasm containing coarse, round granules that are uniform in size and stainable by eosin.
Granular leukocytes having a nucleus with three to five lobes connected by slender threads of chromatin, and cytoplasm containing fine inconspicuous granules and stainable by neutral dyes.
An albumin obtained from the white of eggs. It is a member of the serpin superfamily.
A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis.
The larger air passages of the lungs arising from the terminal bifurcation of the TRACHEA. They include the largest two primary bronchi which branch out into secondary bronchi, and tertiary bronchi which extend into BRONCHIOLES and PULMONARY ALVEOLI.
A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL).
A cyclin B subtype that colocalizes with MICROTUBULES during INTERPHASE and is transported into the CELL NUCLEUS at the end of the G2 PHASE.
The number of WHITE BLOOD CELLS per unit volume in venous BLOOD. A differential leukocyte count measures the relative numbers of the different types of white cells.
Washing out of the peritoneal cavity. The procedure is a diagnostic as well as a therapeutic technique following abdominal trauma or inflammation.
A form of hypersensitivity affecting the respiratory tract. It includes ASTHMA and RHINITIS, ALLERGIC, SEASONAL.
Damage to any compartment of the lung caused by physical, chemical, or biological agents which characteristically elicit inflammatory reaction. These inflammatory reactions can either be acute and dominated by NEUTROPHILS, or chronic and dominated by LYMPHOCYTES and MACROPHAGES.
A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features.
Antigen-type substances that produce immediate hypersensitivity (HYPERSENSITIVITY, IMMEDIATE).
Fluid obtained by THERAPEUTIC IRRIGATION or washout of the nasal cavity and NASAL MUCOSA. The resulting fluid is used in cytologic and immunologic assays of the nasal mucosa such as with the NASAL PROVOCATION TEST in the diagnosis of nasal hypersensitivity.
A condition of lung damage that is characterized by bilateral pulmonary infiltrates (PULMONARY EDEMA) rich in NEUTROPHILS, and in the absence of clinical HEART FAILURE. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological).
A PULMONARY ALVEOLI-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and DYSPNEA. This disease is often related to, congenital or acquired, impaired processing of PULMONARY SURFACTANTS by alveolar macrophages, a process dependent on GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR.
A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA.
Non-antibody proteins secreted by inflammatory leukocytes and some non-leukocytic cells, that act as intercellular mediators. They differ from classical hormones in that they are produced by a number of tissue or cell types rather than by specialized glands. They generally act locally in a paracrine or autocrine rather than endocrine manner.
Naturally occurring or experimentally induced animal diseases with pathological processes sufficiently similar to those of human diseases. They are used as study models for human diseases.
A genus of ascomycetous FUNGI, family Pneumocystidaceae, order Pneumocystidales. It includes various host-specific species causing PNEUMOCYSTIS PNEUMONIA in humans and other MAMMALS.
Inflammation of the lung parenchyma that is caused by bacterial infections.
A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function.
Substances and drugs that lower the SURFACE TENSION of the mucoid layer lining the PULMONARY ALVEOLI.
An abundant pulmonary surfactant-associated protein that binds to a variety of lung pathogens and enhances their opsinization and killing by phagocytic cells. Surfactant protein D contains a N-terminal collagen-like domain and a C-terminal lectin domain that are characteristic of members of the collectin family of proteins.
Material coughed up from the lungs and expectorated via the mouth. It contains MUCUS, cellular debris, and microorganisms. It may also contain blood or pus.
An abundant pulmonary surfactant-associated protein that binds to a variety of lung pathogens, resulting in their opsinization. It also stimulates MACROPHAGES to undergo PHAGOCYTOSIS of microorganisms. Surfactant protein A contains a N-terminal collagen-like domain and a C-terminal lectin domain that are characteristic of members of the collectin family of proteins.
The mucous membrane lining the RESPIRATORY TRACT, including the NASAL CAVITY; the LARYNX; the TRACHEA; and the BRONCHI tree. The respiratory mucosa consists of various types of epithelial cells ranging from ciliated columnar to simple squamous, mucous GOBLET CELLS, and glands containing both mucous and serous cells.
The administration of drugs by the respiratory route. It includes insufflation into the respiratory tract.
Measurement of the various processes involved in the act of respiration: inspiration, expiration, oxygen and carbon dioxide exchange, lung volume and compliance, etc.
Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening.
An enzyme that catalyzes the hydrolysis of proteins, including elastin. It cleaves preferentially bonds at the carboxyl side of Ala and Val, with greater specificity for Ala. EC 3.4.21.37.
An immunoglobulin associated with MAST CELLS. Overexpression has been associated with allergic hypersensitivity (HYPERSENSITIVITY, IMMEDIATE).
Colloids with a gaseous dispersing phase and either liquid (fog) or solid (smoke) dispersed phase; used in fumigation or in inhalation therapy; may contain propellant agents.
Tests involving inhalation of allergens (nebulized or in dust form), nebulized pharmacologically active solutions (e.g., histamine, methacholine), or control solutions, followed by assessment of respiratory function. These tests are used in the diagnosis of asthma.
Ratio of T-LYMPHOCYTES that express the CD4 ANTIGEN to those that express the CD8 ANTIGEN. This value is commonly assessed in the diagnosis and staging of diseases affecting the IMMUNE SYSTEM including HIV INFECTIONS.
The transference of either one or both of the lungs from one human or animal to another.
The production of adhesions between the parietal and visceral pleura. The procedure is used in the treatment of bronchopleural fistulas, malignant pleural effusions, and pneumothorax and often involves instillation of chemicals or other agents into the pleural space causing, in effect, a pleuritis that seals the air leak. (From Fishman, Pulmonary Diseases, 2d ed, p2233 & Dorland, 27th ed)
The unstable triatomic form of oxygen, O3. It is a powerful oxidant that is produced for various chemical and industrial uses. Its production is also catalyzed in the ATMOSPHERE by ULTRAVIOLET RAY irradiation of oxygen or other ozone precursors such as VOLATILE ORGANIC COMPOUNDS and NITROGEN OXIDES. About 90% of the ozone in the atmosphere exists in the stratosphere (STRATOSPHERIC OZONE).
Inflammation of the lung parenchyma that is caused by a viral infection.
The diffusion or accumulation of neutrophils in tissues or cells in response to a wide variety of substances released at the sites of inflammatory reactions.
Quartz (SiO2). A glassy or crystalline form of silicon dioxide. Many colored varieties are semiprecious stones. (From Grant & Hackh's Chemical Dictionary, 5th ed)
A cytokine that promotes differentiation and activation of EOSINOPHILS. It also triggers activated B-LYMPHOCYTES to differentiate into IMMUNOGLOBULIN-secreting cells.
Pulmonary diseases caused by fungal infections, usually through hematogenous spread.
A quaternary ammonium parasympathomimetic agent with the muscarinic actions of ACETYLCHOLINE. It is hydrolyzed by ACETYLCHOLINESTERASE at a considerably slower rate than ACETYLCHOLINE and is more resistant to hydrolysis by nonspecific CHOLINESTERASES so that its actions are more prolonged. It is used as a parasympathomimetic bronchoconstrictor agent and as a diagnostic aid for bronchial asthma. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1116)
The tubular and cavernous organs and structures, by means of which pulmonary ventilation and gas exchange between ambient air and the blood are brought about.
Any method of artificial breathing that employs mechanical or non-mechanical means to force the air into and out of the lungs. Artificial respiration or ventilation is used in individuals who have stopped breathing or have RESPIRATORY INSUFFICIENCY to increase their intake of oxygen (O2) and excretion of carbon dioxide (CO2).
A complex of related glycopeptide antibiotics from Streptomyces verticillus consisting of bleomycin A2 and B2. It inhibits DNA metabolism and is used as an antineoplastic, especially for solid tumors.
A CXC chemokine that is synthesized by activated MONOCYTES and NEUTROPHILS. It has specificity for CXCR2 RECEPTORS.
The exposure to potentially harmful chemical, physical, or biological agents by inhaling them.
Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen.
Compounds that accept electrons in an oxidation-reduction reaction. The reaction is induced by or accelerated by exposure to electromagnetic radiation in the spectrum of visible or ultraviolet light.
Water-soluble proteins found in egg whites, blood, lymph, and other tissues and fluids. They coagulate upon heating.
Proteins found in the LUNG that act as PULMONARY SURFACTANTS.
Lipid-containing polysaccharides which are endotoxins and important group-specific antigens. They are often derived from the cell wall of gram-negative bacteria and induce immunoglobulin secretion. The lipopolysaccharide molecule consists of three parts: LIPID A, core polysaccharide, and O-specific chains (O ANTIGENS). When derived from Escherichia coli, lipopolysaccharides serve as polyclonal B-cell mitogens commonly used in laboratory immunology. (From Dorland, 28th ed)
Endoscopes for the visualization of the interior of the bronchi.
Abnormal increase of EOSINOPHILS in the blood, tissues or organs.
Pneumonia due to aspiration or inhalation of various oily or fatty substances.
A human or animal whose immunologic mechanism is deficient because of an immunodeficiency disorder or other disease or as the result of the administration of immunosuppressive drugs or radiation.
Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI.
The relatively long-lived phagocytic cell of mammalian tissues that are derived from blood MONOCYTES. Main types are PERITONEAL MACROPHAGES; ALVEOLAR MACROPHAGES; HISTIOCYTES; KUPFFER CELLS of the liver; and OSTEOCLASTS. They may further differentiate within chronic inflammatory lesions to EPITHELIOID CELLS or may fuse to form FOREIGN BODY GIANT CELLS or LANGHANS GIANT CELLS. (from The Dictionary of Cell Biology, Lackie and Dow, 3rd ed.)
A member of the CXC chemokine family that plays a role in the regulation of the acute inflammatory response. It is secreted by variety of cell types and induces CHEMOTAXIS of NEUTROPHILS and other inflammatory cells.
A form of pneumoconiosis caused by inhalation of asbestos fibers which elicit potent inflammatory responses in the parenchyma of the lung. The disease is characterized by interstitial fibrosis of the lung, varying from scattered sites to extensive scarring of the alveolar interstitium.
Delivery of medications through the nasal mucosa.
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)
Class of pro-inflammatory cytokines that have the ability to attract and activate leukocytes. They can be divided into at least three structural branches: C; (CHEMOKINES, C); CC; (CHEMOKINES, CC); and CXC; (CHEMOKINES, CXC); according to variations in a shared cysteine motif.
The administration of therapeutic agents drop by drop, as eye drops, ear drops, or nose drops. It is also administered into a body space or cavity through a catheter. It differs from THERAPEUTIC IRRIGATION in that the irrigate is removed within minutes, but the instillate is left in place.
The small airways branching off the TERTIARY BRONCHI. Terminal bronchioles lead into several orders of respiratory bronchioles which in turn lead into alveolar ducts and then into PULMONARY ALVEOLI.
Serious INFLAMMATION of the LUNG in patients who required the use of PULMONARY VENTILATOR. It is usually caused by cross bacterial infections in hospitals (NOSOCOMIAL INFECTIONS).
A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT.
An immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed.
A hemeprotein from leukocytes. Deficiency of this enzyme leads to a hereditary disorder coupled with disseminated moniliasis. It catalyzes the conversion of a donor and peroxide to an oxidized donor and water. EC 1.11.1.7.
Infections of the lungs with parasites, most commonly by parasitic worms (HELMINTHS).
White blood cells formed in the body's lymphoid tissue. The nucleus is round or ovoid with coarse, irregularly clumped chromatin while the cytoplasm is typically pale blue with azurophilic (if any) granules. Most lymphocytes can be classified as either T or B (with subpopulations of each), or NATURAL KILLER CELLS.
The cartilaginous and membranous tube descending from the larynx and branching into the right and left main bronchi.
Serum glycoprotein produced by activated MACROPHAGES and other mammalian MONONUCLEAR LEUKOCYTES. It has necrotizing activity against tumor cell lines and increases ability to reject tumor transplants. Also known as TNF-alpha, it is only 30% homologous to TNF-beta (LYMPHOTOXIN), but they share TNF RECEPTORS.
The viscous secretion of mucous membranes. It contains mucin, white blood cells, water, inorganic salts, and exfoliated cells.
Inflammation of the BRONCHIOLES leading to an obstructive lung disease. Bronchioles are characterized by fibrous granulation tissue with bronchial exudates in the lumens. Clinical features include a nonproductive cough and DYSPNEA.
A species of PNEUMOCYSTIS infecting humans and causing PNEUMOCYSTIS PNEUMONIA. It also occasionally causes extrapulmonary disease in immunocompromised patients. Its former name was Pneumocystis carinii f. sp. hominis.
A form of alveolitis or pneumonitis due to an acquired hypersensitivity to inhaled antigens associated with farm environment. Antigens in the farm dust are commonly from bacteria actinomycetes (SACCHAROPOLYSPORA and THERMOACTINOMYCES), fungi, and animal proteins in the soil, straw, crops, pelts, serum, and excreta.
Inflammation of the lung parenchyma that is associated with BRONCHITIS, usually involving lobular areas from TERMINAL BRONCHIOLES to the PULMONARY ALVEOLI. The affected areas become filled with exudate that forms consolidated patches.
Narrowing of the caliber of the BRONCHI, physiologically or as a result of pharmacological intervention.
The endogenous compounds that mediate inflammation (AUTACOIDS) and related exogenous compounds including the synthetic prostaglandins (PROSTAGLANDINS, SYNTHETIC).
Earth or other matter in fine, dry particles. (Random House Unabridged Dictionary, 2d ed)
An interstitial lung disease of unknown etiology, occurring between 21-80 years of age. It is characterized by a dramatic onset of a "pneumonia-like" illness with cough, fever, malaise, fatigue, and weight loss. Pathological features include prominent interstitial inflammation without collagen fibrosis, diffuse fibroblastic foci, and no microscopic honeycomb change. There is excessive proliferation of granulation tissue within small airways and alveolar ducts.
Lung damage that is caused by the adverse effects of PULMONARY VENTILATOR usage. The high frequency and tidal volumes produced by a mechanical ventilator can cause alveolar disruption and PULMONARY EDEMA.
Measurable and quantifiable biological parameters (e.g., specific enzyme concentration, specific hormone concentration, specific gene phenotype distribution in a population, presence of biological substances) which serve as indices for health- and physiology-related assessments, such as disease risk, psychiatric disorders, environmental exposure and its effects, disease diagnosis, metabolic processes, substance abuse, pregnancy, cell line development, epidemiologic studies, etc.
A glandular epithelial cell or a unicellular gland. Goblet cells secrete MUCUS. They are scattered in the epithelial linings of many organs, especially the SMALL INTESTINE and the RESPIRATORY TRACT.
Elements of limited time intervals, contributing to particular results or situations.
Strains of mice in which certain GENES of their GENOMES have been disrupted, or "knocked-out". To produce knockouts, using RECOMBINANT DNA technology, the normal DNA sequence of the gene being studied is altered to prevent synthesis of a normal gene product. Cloned cells in which this DNA alteration is successful are then injected into mouse EMBRYOS to produce chimeric mice. The chimeric mice are then bred to yield a strain in which all the cells of the mouse contain the disrupted gene. Knockout mice are used as EXPERIMENTAL ANIMAL MODELS for diseases (DISEASE MODELS, ANIMAL) and to clarify the functions of the genes.
A steroid-inducible protein that was originally identified in uterine fluid. It is a secreted homodimeric protein with identical 70-amino acid subunits that are joined in an antiparallel orientation by two disulfide bridges. A variety of activities are associated with uteroglobin including the sequestering of hydrophobic ligands and the inhibition of SECRETORY PHOSPHOLIPASE A2.
The structural changes in the number, mass, size and/or composition of the airway tissues.
Protein-lipid combinations abundant in brain tissue, but also present in a wide variety of animal and plant tissues. In contrast to lipoproteins, they are insoluble in water, but soluble in a chloroform-methanol mixture. The protein moiety has a high content of hydrophobic amino acids. The associated lipids consist of a mixture of GLYCEROPHOSPHATES; CEREBROSIDES; and SULFOGLYCOSPHINGOLIPIDS; while lipoproteins contain PHOSPHOLIPIDS; CHOLESTEROL; and TRIGLYCERIDES.
Subset of helper-inducer T-lymphocytes which synthesize and secrete the interleukins IL-4, IL-5, IL-6, and IL-10. These cytokines influence B-cell development and antibody production as well as augmenting humoral responses.
Enlargement of air spaces distal to the TERMINAL BRONCHIOLES where gas-exchange normally takes place. This is usually due to destruction of the alveolar wall. Pulmonary emphysema can be classified by the location and distribution of the lesions.
In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
Mechanical devices used to produce or assist pulmonary ventilation.
A secreted matrix metalloproteinase which is highly expressed by MACROPHAGES where it may play a role in INFLAMMATION and WOUND HEALING.
Infections with fungi of the genus ASPERGILLUS.
Inhaling liquid or solids, such as stomach contents, into the RESPIRATORY TRACT. When this causes severe lung damage, it is called ASPIRATION PNEUMONIA.
A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.
The barrier between capillary blood and alveolar air comprising the alveolar EPITHELIUM and capillary ENDOTHELIUM with their adherent BASEMENT MEMBRANE and EPITHELIAL CELL cytoplasm. PULMONARY GAS EXCHANGE occurs across this membrane.
A cytokine synthesized by T-LYMPHOCYTES that produces proliferation, immunoglobulin isotype switching, and immunoglobulin production by immature B-LYMPHOCYTES. It appears to play a role in regulating inflammatory and immune responses.
X-ray visualization of the chest and organs of the thoracic cavity. It is not restricted to visualization of the lungs.
An abnormal increase in the amount of oxygen in the tissues and organs.
Liquid components of living organisms.
A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock.
Physiologically, the opposition to flow of air caused by the forces of friction. As a part of pulmonary function testing, it is the ratio of driving pressure to the rate of air flow.
Inhaling and exhaling the smoke of burning TOBACCO.
Removal and pathologic examination of specimens in the form of small pieces of tissue from the living body.
Polysaccharides consisting of mannose units.
The capability of the LUNGS to distend under pressure as measured by pulmonary volume change per unit pressure change. While not a complete description of the pressure-volume properties of the lung, it is nevertheless useful in practice as a measure of the comparative stiffness of the lung. (From Best & Taylor's Physiological Basis of Medical Practice, 12th ed, p562)
Substances that reduce or suppress INFLAMMATION.
White blood cells. These include granular leukocytes (BASOPHILS; EOSINOPHILS; and NEUTROPHILS) as well as non-granular leukocytes (LYMPHOCYTES and MONOCYTES).
A class of statistical methods applicable to a large set of probability distributions used to test for correlation, location, independence, etc. In most nonparametric statistical tests, the original scores or observations are replaced by another variable containing less information. An important class of nonparametric tests employs the ordinal properties of the data. Another class of tests uses information about whether an observation is above or below some fixed value such as the median, and a third class is based on the frequency of the occurrence of runs in the data. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1284; Corsini, Concise Encyclopedia of Psychology, 1987, p764-5)
The technology of transmitting light over long distances through strands of glass or other transparent material.
The property of blood capillary ENDOTHELIUM that allows for the selective exchange of substances between the blood and surrounding tissues and through membranous barriers such as the BLOOD-AIR BARRIER; BLOOD-AQUEOUS BARRIER; BLOOD-BRAIN BARRIER; BLOOD-NERVE BARRIER; BLOOD-RETINAL BARRIER; and BLOOD-TESTIS BARRIER. Small lipid-soluble molecules such as carbon dioxide and oxygen move freely by diffusion. Water and water-soluble molecules cannot pass through the endothelial walls and are dependent on microscopic pores. These pores show narrow areas (TIGHT JUNCTIONS) which may limit large molecule movement.
Pulmonary injury following the breathing in of toxic smoke from burning materials such as plastics, synthetics, building materials, etc. This injury is the most frequent cause of death in burn patients.
A genus of mitosporic fungi containing about 100 species and eleven different teleomorphs in the family Trichocomaceae.
Infections with bacteria of the genus PSEUDOMONAS.
Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
Agents causing the narrowing of the lumen of a bronchus or bronchiole.
A form of alveolitis or pneumonitis due to an acquired hypersensitivity to inhaled avian antigens, usually proteins in the dust of bird feathers and droppings.
An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression.
A 66-kDa peroxidase found in EOSINOPHIL granules. Eosinophil peroxidase is a cationic protein with a pI of 10.8 and is comprised of a heavy chain subunit and a light chain subunit. It possesses cytotoxic activity towards BACTERIA and other organisms, which is attributed to its peroxidase activity.
A mixture of liquid hydrocarbons obtained from petroleum. It is used as laxative, lubricant, ointment base, and emollient.
Water content outside of the lung vasculature. About 80% of a normal lung is made up of water, including intracellular, interstitial, and blood water. Failure to maintain the normal homeostatic fluid exchange between the vascular space and the interstitium of the lungs can result in PULMONARY EDEMA and flooding of the alveolar space.
A commonly used prosthesis that results in a strong, permanent restoration. It consists of an electrolytically etched cast-metal retainer that is cemented (bonded), using resins, to adjacent teeth whose enamel was previously acid-treated (acid-etched). This type of bridgework is sometimes referred to as a Maryland bridge.
Proteins found in EOSINOPHIL granules. They are primarily basic proteins that play a role in host defense and the proinflammatory actions of activated eosinophils.
RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm.
An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
Animals or humans raised in the absence of a particular disease-causing virus or other microorganism. Less frequently plants are cultivated pathogen-free.
A procedure involving placement of a tube into the trachea through the mouth or nose in order to provide a patient with oxygen and anesthesia.
MYCOBACTERIUM infections of the lung.
A highly toxic gas that has been used as a chemical warfare agent. It is an insidious poison as it is not irritating immediately, even when fatal concentrations are inhaled. (From The Merck Index, 11th ed, p7304)
The major immunoglobulin isotype class in normal human serum. There are several isotype subclasses of IgG, for example, IgG1, IgG2A, and IgG2B.
A cytokine that stimulates the growth and differentiation of B-LYMPHOCYTES and is also a growth factor for HYBRIDOMAS and plasmacytomas. It is produced by many different cells including T-LYMPHOCYTES; MONOCYTES; and FIBROBLASTS.
Diseases of domestic and wild horses of the species Equus caballus.
A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
Infections of the respiratory tract with fungi of the genus ASPERGILLUS. Infections may result in allergic reaction (ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS), colonization in pulmonary cavities as fungus balls (MYCETOMA), or lead to invasion of the lung parenchyma (INVASIVE PULMONARY ASPERGILLOSIS).
A form of pneumoconiosis resulting from inhalation of dust containing crystalline form of SILICON DIOXIDE, usually in the form of quartz. Amorphous silica is relatively nontoxic.
A metabolite of BROMHEXINE that stimulates mucociliary action and clears the air passages in the respiratory tract. It is usually administered as the hydrochloride.
Excess of normal lymphocytes in the blood or in any effusion.
Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases.
The major metabolite in neutrophil polymorphonuclear leukocytes. It stimulates polymorphonuclear cell function (degranulation, formation of oxygen-centered free radicals, arachidonic acid release, and metabolism). (From Dictionary of Prostaglandins and Related Compounds, 1990)
A pulmonary surfactant associated-protein that plays an essential role in alveolar stability by lowering the surface tension at the air-liquid interface. Inherited deficiency of pulmonary surfactant-associated protein B is one cause of RESPIRATORY DISTRESS SYNDROME, NEWBORN.
A CC-type chemokine that is specific for CCR3 RECEPTORS. It is a potent chemoattractant for EOSINOPHILS.
A soluble factor produced by activated T-LYMPHOCYTES that induces the expression of MHC CLASS II GENES and FC RECEPTORS on B-LYMPHOCYTES and causes their proliferation and differentiation. It also acts on T-lymphocytes, MAST CELLS, and several other hematopoietic lineage cells.
A form of pneumoconiosis caused by inhaled rare metal BERYLLIUM or its soluble salts which are used in a wide variety of industry including alloys, ceramics, radiographic equipment, and vacuum tubes. Berylliosis is characterized by an acute inflammatory reaction in the upper airway leading to BRONCHIOLITIS; PULMONARY EDEMA; and pneumonia.
Disease having a short and relatively severe course.
Technique using an instrument system for making, processing, and displaying one or more measurements on individual cells obtained from a cell suspension. Cells are usually stained with one or more fluorescent dyes specific to cell components of interest, e.g., DNA, and fluorescence of each cell is measured as it rapidly transverses the excitation beam (laser or mercury arc lamp). Fluorescence provides a quantitative measure of various biochemical and biophysical properties of the cell, as well as a basis for cell sorting. Other measurable optical parameters include light absorption and light scattering, the latter being applicable to the measurement of cell size, shape, density, granularity, and stain uptake.
Genomes of temperate BACTERIOPHAGES integrated into the DNA of their bacterial host cell. The prophages can be duplicated for many cell generations until some stimulus induces its activation and virulence.
The major interferon produced by mitogenically or antigenically stimulated LYMPHOCYTES. It is structurally different from TYPE I INTERFERON and its major activity is immunoregulation. It has been implicated in the expression of CLASS II HISTOCOMPATIBILITY ANTIGENS in cells that do not normally produce them, leading to AUTOIMMUNE DISEASES.
The study of the structure, growth, function, genetics, and reproduction of fungi, and MYCOSES.
A strain of albino rat used widely for experimental purposes because of its calmness and ease of handling. It was developed by the Sprague-Dawley Animal Company.
Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent.
A class of cell surface receptors that prefer ADENOSINE to other endogenous PURINES. Purinergic P1 receptors are widespread in the body including the cardiovascular, respiratory, immune, and nervous systems. There are at least two pharmacologically distinguishable types (A1 and A2, or Ri and Ra).
Long, pliable, cohesive natural or manufactured filaments of various lengths. They form the structure of some minerals. The medical significance lies in their potential ability to cause various types of PNEUMOCONIOSIS (e.g., ASBESTOSIS) after occupational or environmental exposure. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p708)
Toxins closely associated with the living cytoplasm or cell wall of certain microorganisms, which do not readily diffuse into the culture medium, but are released upon lysis of the cells.
Family of house dust mites, in the superfamily Analgoidea, order Astigmata. They include the genera Dermatophagoides and Euroglyphus.
An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
Interstitial pneumonia caused by extensive infection of the lungs (LUNG) and BRONCHI, particularly the lower lobes of the lungs, by MYCOPLASMA PNEUMONIAE in humans. In SHEEP, it is caused by MYCOPLASMA OVIPNEUMONIAE. In CATTLE, it may be caused by MYCOPLASMA DISPAR.
Measure of the maximum amount of air that can be expelled in a given number of seconds during a FORCED VITAL CAPACITY determination . It is usually given as FEV followed by a subscript indicating the number of seconds over which the measurement is made, although it is sometimes given as a percentage of forced vital capacity.
Soluble mediators of the immune response that are neither antibodies nor complement. They are produced largely, but not exclusively, by monocytes and macrophages.
Plasma glycoprotein member of the serpin superfamily which inhibits TRYPSIN; NEUTROPHIL ELASTASE; and other PROTEOLYTIC ENZYMES.
The reaction product of bisphenol A and glycidyl methacrylate that undergoes polymerization when exposed to ultraviolet light or mixed with a catalyst. It is used as a bond implant material and as the resin component of dental sealants and composite restorative materials.
A common name used for the genus Cavia. The most common species is Cavia porcellus which is the domesticated guinea pig used for pets and biomedical research.
A member of the MATRIX METALLOPROTEINASES that cleaves triple-helical COLLAGEN types I, II, and III.
Hypersensitivity reaction (ALLERGIC REACTION) to fungus ASPERGILLUS in an individual with long-standing BRONCHIAL ASTHMA. It is characterized by pulmonary infiltrates, EOSINOPHILIA, elevated serum IMMUNOGLOBULIN E, and skin reactivity to Aspergillus antigen.
Granulated cells that are found in almost all tissues, most abundantly in the skin and the gastrointestinal tract. Like the BASOPHILS, mast cells contain large amounts of HISTAMINE and HEPARIN. Unlike basophils, mast cells normally remain in the tissues and do not circulate in the blood. Mast cells, derived from the bone marrow stem cells, are regulated by the STEM CELL FACTOR.
Hypersensitivity reactions which occur within minutes of exposure to challenging antigen due to the release of histamine which follows the antigen-antibody reaction and causes smooth muscle contraction and increased vascular permeability.
Forceful administration into the peritoneal cavity of liquid medication, nutrient, or other fluid through a hollow needle piercing the abdominal wall.
A CXC chemokine with specificity for CXCR2 RECEPTORS. It has growth factor activities and is implicated as a oncogenic factor in several tumor types.
Relating to the size of solids.
The process in which the neutrophil is stimulated by diverse substances, resulting in degranulation and/or generation of reactive oxygen products, and culminating in the destruction of invading pathogens. The stimulatory substances, including opsonized particles, immune complexes, and chemotactic factors, bind to specific cell-surface receptors on the neutrophil.
The engulfing and degradation of microorganisms; other cells that are dead, dying, or pathogenic; and foreign particles by phagocytic cells (PHAGOCYTES).
A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA.
Group of chemokines with paired cysteines separated by a different amino acid. CXC chemokines are chemoattractants for neutrophils but not monocytes.
The range or frequency distribution of a measurement in a population (of organisms, organs or things) that has not been selected for the presence of disease or abnormality.
A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA.
Cells that line the inner and outer surfaces of the body by forming cellular layers (EPITHELIUM) or masses. Epithelial cells lining the SKIN; the MOUTH; the NOSE; and the ANAL CANAL derive from ectoderm; those lining the RESPIRATORY SYSTEM and the DIGESTIVE SYSTEM derive from endoderm; others (CARDIOVASCULAR SYSTEM and LYMPHATIC SYSTEM) derive from mesoderm. Epithelial cells can be classified mainly by cell shape and function into squamous, glandular and transitional epithelial cells.
Short filamentous organism of the genus Mycoplasma, which binds firmly to the cells of the respiratory epithelium. It is one of the etiologic agents of non-viral primary atypical pneumonia in man.

GM-CSF-deficient mice are susceptible to pulmonary group B streptococcal infection. (1/5496)

Granulocyte-macrophage colony-stimulating factor (GM-CSF) gene-targeted mice (GM-/-) cleared group B streptococcus (GBS) from the lungs more slowly than wild-type mice. Expression of GM-CSF in the respiratory epithelium of GM-/- mice improved bacterial clearance to levels greater than that in wild-type GM+/+ mice. Acute aerosolization of GM-CSF to GM+/+ mice significantly enhanced clearance of GBS at 24 hours. GBS infection was associated with increased neutrophilic infiltration in lungs of GM-/- mice, while macrophage infiltrates predominated in wild-type mice, suggesting an abnormality in macrophage clearance of bacteria in the absence of GM-CSF. While phagocytosis of GBS was unaltered, production of superoxide radicals and hydrogen peroxide was markedly deficient in macrophages from GM-/- mice. Lipid peroxidation, assessed by measuring the isoprostane 8-iso-PGF2alpha, was decreased in the lungs of GM-/- mice. GM-CSF plays an important role in GBS clearance in vivo, mediated in part by its role in enhancing superoxide and hydrogen peroxide production and bacterial killing by alveolar macrophages.  (+info)

Molecular detection of tumor cells in bronchoalveolar lavage fluid from patients with early stage lung cancer. (2/5496)

BACKGROUND: Conventional cytologic analysis of sputum is an insensitive test for the diagnosis of non-small-cell lung cancer (NSCLC). We have recently demonstrated that polymerase chain reaction (PCR)-based molecular methods are more sensitive than cytologic analysis in diagnosing bladder cancer. In this study, we examined whether molecular assays could identify cancer cells in bronchoalveolar lavage (BAL) fluid. METHODS: Tumor-specific oncogene mutations, CpG-island methylation status, and microsatellite alterations in the DNA of cells in BAL fluid from 50 consecutive patients with resectable (stages I through IIIa) NSCLC were assessed by use of four PCR-based techniques. RESULTS: Of 50 tumors, 28 contained a p53 mutation, and the identical mutation was detected with a plaque hybridization assay in the BAL fluid of 39% (11 of 28) of the corresponding patients. Eight of 19 adenocarcinomas contained a K-ras mutation, and the identical mutation was detected with a mutation ligation assay in the BAL fluid of 50% (four of eight) of the corresponding patients. The p16 gene was methylated in 19 of 50 tumors, and methylated p16 alleles were detected in the BAL fluid of 63% (12 of 19) of the corresponding patients. Microsatellite instability in at least one marker was detected with a panel of 15 markers frequently altered in NSCLC in 23 of 50 tumors; the identical alteration was detected in the BAL fluid of 14% (three of 22) of the corresponding patients. When all four techniques were used, mutations or microsatellite instability was detected in the paired BAL fluid of 23 (53%) of the 43 patients with tumors carrying a genetic alteration. CONCLUSION: Although still limited by sensitivity, molecular diagnostic strategies can detect the presence of neoplastic cells in the proximal airway of patients with surgically resectable NSCLC.  (+info)

Localization of a candidate surfactant convertase to type II cells, macrophages, and surfactant subfractions. (3/5496)

Pulmonary surfactant exists in the alveolus in several distinct subtypes that differ in their morphology, composition, and surface activity. Experiments by others have implicated a serine hydrolase in the production of the inactive small vesicular subtype of surfactant (N. J. Gross and R. M. Schultz. Biochim. Biophys. Acta 1044: 222-230, 1990). Our laboratory recently identified this enzyme in the rat as the serine carboxylesterase ES-2 [F. Barr, H. Clark, and S. Hawgood. Am. J. Physiol. 274 (Lung Cell. Mol. Physiol. 18): L404-L410, 1998]. In the present study, we determined the cellular sites of expression of ES-2 in rat lung using a digoxygenin-labeled ES-2 riboprobe. ES-2 mRNA was localized to type II cells and alveolar macrophages but not to Clara cells. Using a specific ES-2 antibody, we determined the protein distribution of ES-2 in the lung by immunohistochemistry, and it was found to be consistent with the sites of mRNA expression. Most of the ES-2 in rat bronchoalveolar lavage is in the surfactant-depleted supernatant, but ES-2 was also consistently localized to the small vesicular surfactant subfraction presumed to form as a consequence of conversion activity. These results are consistent with a role for endogenous lung ES-2 in surfactant metabolism.  (+info)

Expression of heat shock protein 72 by alveolar macrophages in hypersensitivity pneumonitis. (4/5496)

The current study was done to look at a possible role of heat shock proteins (HSPs) in hypersensitivity pneumonitis (HP). The specific aims were to determine whether there was a difference in the expression of HSP72 in alveolar macrophages (AMs) between mice challenged with HP antigen and saline-treated control mice and between AMs obtained by bronchoalveolar lavage from 18 patients with HP and 11 normal subjects. The expression of HSP72 was studied under basal conditions and under a mild heat shock. HSP72 expression by AMs in response to in vitro stimulation with Saccharopolyspora rectivirgula was lower in AMs of control mice than in those of HP animals. HSP72 was constitutively expressed in AMs of both normal and HP subjects. Densitometric ratios showed that AMs from normal subjects responded to heat shock with a 39 degrees C-to-37 degrees C ratio of 1.72 +/- 0.18 (mean +/- SE), and AMs from HP patients responded with a ratio of 1.16 +/- 0.16 (P = 0.0377). This decreased induction by additional stress of AMs could lead to an altered immunoregulatory activity and account for the inflammation seen in HP.  (+info)

A rapid polymerase chain reaction technique for detecting M tuberculosis in a variety of clinical specimens. (5/5496)

A rapid in-house polymerase chain reaction (PCR) assay is described for the direct detection of Mycobacterium tuberculosis complex in clinical material. Its performance is compared with two kit based systems. The results of the in-house assay were comparable with the commercial assays, detecting M tuberculosis in 100% of smear positive, culture positive samples. The in-house assay proved to be rapid, easy, and inexpensive to perform, and the inclusion of an internal inhibitor control permitted validation of the PCR results.  (+info)

Cigarette smoking decreases interleukin-8 secretion by human alveolar macrophages. (6/5496)

Cigarette smoking can impair pulmonary immune function, and hence influences the development of lung diseases. Interleukin-8 (IL-8) is a proinflammatory peptide and a potent chemotactic factor for neutrophils, and is produced by both immune and non-immune cells including monocytes and alveolar macrophages (AM). We investigated the effect of cigarette smoking on the secretion of IL-8 by human AM. The IL-8 concentration in bronchoalveolar lavage fluid (BALF) was much higher in smokers than in non-smokers (18.4 +/- 3.9 vs 4.1 +/- 1.0 pg ml-1; P < 0.005). However, spontaneous IL-8 secretion by cultured AM was lower in smokers than in non-smokers (46.8 +/- 12.7 vs 124.1 +/- 24.0 ng ml-1; P < 0.01). When stimulated with lipopolysaccharide (LPS), AM from smokers secreted significantly less IL-8 than those from non-smokers at all tested concentrations of LPS. In contrast, the amount of IL-8 secreted by peripheral blood monocytes with or without LPS stimulation was comparable in smokers and non-smokers. These observations indicate that smoking decreases IL-8 secretion by AM, which may modify or decrease the inflammatory response in the lung.  (+info)

Effect of hyperoxia on human macrophage cytokine response. (7/5496)

In the development of lung damage induced by oxidative stress, it has been proposed that changes in alveolar macrophages (AM) function with modifications in cytokine production may contribute to altered repair processes. To characterize the changes in profiles of cytokine production by macrophages exposed to oxidants, the effects of hyperoxia (95% O2) on interleukin (IL)-1 beta, IL-6, IL-8, and tumour necrosis factor-alpha (TNF-alpha) expression were studied. Experiments were first performed using AM obtained from control subjects and children with interstitial lung disease. Results showed that a 48 h O2 exposure was associated with two distinct patterns of response: a decrease in TNF-alpha, IL-1 beta and IL-6 expression, and an increase in IL-8. To complete these observations we used U937 cells that were exposed for various durations to hyperoxia. We confirmed that a 48 h O2 exposure led to similar changes with a decrease in TNF-alpha, IL-1 beta and IL-6 production and an increase in IL-8. Interestingly, this cytokine response was preceded during the first hours of O2 treatment by induction of TNF-alpha, IL-1 beta and IL-6. These data indicate that hyperoxia induces changes in the expression of macrophages inflammatory cytokines, and that these modifications appear to be influenced by the duration of O2 exposure.  (+info)

Pneumonia in febrile neutropenic patients and in bone marrow and blood stem-cell transplant recipients: use of high-resolution computed tomography. (8/5496)

PURPOSE: To obtain statistical data on the use of high-resolution computed tomography (HRCT) for early detection of pneumonia in febrile neutropenic patients with unknown focus of infection. MATERIALS AND METHODS: One hundred eighty-eight HRCT studies were performed prospectively in 112 neutropenic patients with fever of unknown origin persisting for more than 48 hours despite empiric antibiotic treatment. Fifty-four of these studies were performed in transplant recipients. All patients had normal chest roentgenograms. If pneumonia was detected by HRCT, guided bronchoalveolar lavage was recommended. Evidence of pneumonia on chest roentgenograms during follow-up and micro-organisms detected during follow-up were regarded as documentation of pneumonia. RESULTS: Of the 188 HRCT studies, 112 (60%) showed pneumonia and 76 were normal. Documentation of pneumonia was possible in 61 cases by chest roentgenography or micro-organism detection (54%) (P < 10(-6)). Sensitivity of HRCT was 87% (88% in transplant recipients), specificity was 57% (67%), and the negative predictive value was 88% (97%). A time gain of 5 days was achieved by the additional use of HRCT compared to an exclusive use of chest roentgenography. CONCLUSION: The high frequency of inflammatory pulmonary disease after a suspicious HRCT scan (> 50%) proves that pneumonia is not excluded by a normal chest roentgenogram. Given the significantly longer duration of febrile episodes in transplant recipients, HRCT findings are particularly relevant in this subgroup. Patients with normal HRCT scans, particularly transplant recipients, have a low risk of pneumonia during follow-up. All neutropenic patients with fever of unknown origin and normal chest roentgenograms should undergo HRCT.  (+info)

The symptoms of pulmonary sarcoidosis can vary depending on the severity of the condition, but may include:

* Shortness of breath (dyspnea)
* Chest pain or discomfort (granulomas)
* Coughing up blood or mucus
* Fatigue
* Fevers
* Weight loss

Pulmonary sarcoidosis can be difficult to diagnose, as the symptoms are similar to other conditions such as tuberculosis or cancer. A diagnosis is typically made based on a combination of the following tests:

* Chest X-rays: To look for abnormalities in the lungs
* Computed tomography (CT) scans: To provide detailed images of the lungs
* Pulmonary function tests: To assess lung function and identify any damage to the lungs
* Biopsy: To collect a sample of tissue from the lungs for examination under a microscope

There is no cure for pulmonary sarcoidosis, but treatment can help manage symptoms and prevent complications. Treatment options may include:

* Corticosteroids: To reduce inflammation and suppress the immune system
* Immunosuppressive medications: To prevent further damage to the lungs
* Oxygen therapy: To help improve oxygen levels in the blood
* Antibiotics: To treat any accompanying bacterial infections

The prognosis for pulmonary sarcoidosis varies depending on the severity of the condition and the response to treatment. In general, most people with pulmonary sarcoidosis experience a good prognosis, but some may experience persistent inflammation and scarring. With proper treatment and follow-up care, many people with pulmonary sarcoidosis are able to lead active lives with minimal symptoms.

Symptoms of pneumonia may include cough, fever, chills, difficulty breathing, and chest pain. In severe cases, pneumonia can lead to respiratory failure, sepsis, and even death.

There are several types of pneumonia, including:

1. Community-acquired pneumonia (CAP): This type of pneumonia is caused by bacteria or viruses and typically affects healthy people outside of hospitals.
2. Hospital-acquired pneumonia (HAP): This type of pneumonia is caused by bacteria or fungi and typically affects people who are hospitalized for other illnesses or injuries.
3. Aspiration pneumonia: This type of pneumonia is caused by food, liquids, or other foreign matter being inhaled into the lungs.
4. Pneumocystis pneumonia (PCP): This type of pneumonia is caused by a fungus and typically affects people with weakened immune systems, such as those with HIV/AIDS.
5. Viral pneumonia: This type of pneumonia is caused by viruses and can be more common in children and young adults.

Pneumonia is typically diagnosed through a combination of physical examination, medical history, and diagnostic tests such as chest X-rays or blood tests. Treatment may involve antibiotics, oxygen therapy, and supportive care to manage symptoms and help the patient recover. In severe cases, hospitalization may be necessary to provide more intensive care and monitoring.

Prevention of pneumonia includes vaccination against certain types of bacteria and viruses, good hygiene practices such as frequent handwashing, and avoiding close contact with people who are sick. Early detection and treatment can help reduce the risk of complications and improve outcomes for those affected by pneumonia.

There are several types of pulmonary fibrosis, including:

1. Idiopathic pulmonary fibrosis (IPF): This is the most common and severe form of the disease, with no known cause or risk factors. It is characterized by a rapid decline in lung function and poor prognosis.
2. Connective tissue disease-associated pulmonary fibrosis: This type is associated with conditions such as rheumatoid arthritis, systemic lupus erythematosus, and scleroderma.
3. Drug-induced pulmonary fibrosis: Certain medications, such as amiodarone and nitrofurantoin, can cause lung damage and scarring.
4. Radiation-induced pulmonary fibrosis: Exposure to high doses of radiation, especially in childhood, can increase the risk of developing pulmonary fibrosis later in life.
5. Environmental exposures: Exposure to pollutants such as silica, asbestos, and coal dust can increase the risk of developing pulmonary fibrosis.

Symptoms of pulmonary fibrosis include shortness of breath, coughing, and fatigue. The disease can be diagnosed through a combination of imaging tests such as chest X-rays, computed tomography (CT) scans, and magnetic resonance imaging (MRI), as well as lung biopsy.

Treatment options for pulmonary fibrosis are limited and vary depending on the underlying cause of the disease. Medications such as pirfenidone and nintedanib can help slow the progression of the disease, while lung transplantation may be an option for advanced cases.

Some common types of lung diseases include:

1. Asthma: A chronic condition characterized by inflammation and narrowing of the airways, leading to wheezing, coughing, and shortness of breath.
2. Chronic Obstructive Pulmonary Disease (COPD): A progressive condition that causes chronic inflammation and damage to the airways and lungs, making it difficult to breathe.
3. Pneumonia: An infection of the lungs that can be caused by bacteria, viruses, or fungi, leading to fever, chills, coughing, and difficulty breathing.
4. Bronchiectasis: A condition where the airways are damaged and widened, leading to chronic infections and inflammation.
5. Pulmonary Fibrosis: A condition where the lungs become scarred and stiff, making it difficult to breathe.
6. Lung Cancer: A malignant tumor that develops in the lungs, often caused by smoking or exposure to carcinogens.
7. Cystic Fibrosis: A genetic disorder that affects the respiratory and digestive systems, leading to chronic infections and inflammation in the lungs.
8. Tuberculosis (TB): An infectious disease caused by Mycobacterium Tuberculosis, which primarily affects the lungs but can also affect other parts of the body.
9. Pulmonary Embolism: A blockage in one of the arteries in the lungs, often caused by a blood clot that has traveled from another part of the body.
10. Sarcoidosis: An inflammatory disease that affects various organs in the body, including the lungs, leading to the formation of granulomas and scarring.

These are just a few examples of conditions that can affect the lungs and respiratory system. It's important to note that many of these conditions can be treated with medication, therapy, or surgery, but early detection is key to successful treatment outcomes.

Sarcoidosis is characterized by an abnormal immune response, which leads to the formation of granulomas. These granulomas are made up of a mix of immune cells, including macrophages, lymphocytes, and epithelioid cells. The exact cause of sarcoidosis is not known, but it is believed that a combination of genetic and environmental factors may contribute to its development.

There are several types of sarcoidosis, each with different symptoms and characteristics:

* Cutaneous sarcoidosis affects the skin and can cause red or purple patches on the face, arms, or legs.
* Lung sarcoidosis is the most common form of the disease and can cause shortness of breath, coughing, and chest pain.
* Ocular sarcoidosis can affect the eyes and cause blurred vision, sensitivity to light, and eye pain.
* Cardiac sarcoidosis can affect the heart and cause arrhythmias, heart failure, or cardiac arrest.

There is no cure for sarcoidosis, but treatment options are available to manage symptoms and prevent complications. Treatment options may include medications such as corticosteroids, immunosuppressive drugs, and biologics, as well as lifestyle changes such as exercise and stress management. In severe cases, surgery or other procedures may be necessary to remove affected tissue or organs.

Overall, sarcoidosis is a complex and debilitating disease that can affect various parts of the body. While there is no cure, with proper treatment and self-care, many people with sarcoidosis are able to manage their symptoms and lead active lives.

alveolitis /al?veo?lit?s/ (noun) A type of inflammation affecting the air sacs (alveoli) caused by an allergic reaction to substances inhaled into the lungs.

Synonyms: allergic alveolitis, extrinsic allergic alveolitis

Medicine dictionary

Scientific definition of alveolitis, extrinsic allergic:
Alveolitis, also known as allergic alveolitis, is a type of inflammatory disease that affects the air sacs (alveoli) in the lungs. It occurs when an individual's immune system overreacts to certain substances inhaled into the lungs, causing an allergic reaction that leads to inflammation and damage to the alveolar tissue.

The term "extrinsic" refers to the fact that the allergen is coming from outside the body, as opposed to "intrinsic" allergies where the allergen is produced within the body.

This condition can be caused by a variety of substances including dust mites, mold, pollen, and animal dander. People with a history of asthma or atopic dermatitis are more likely to develop allergic alveolitis. Symptoms include coughing, wheezing, chest tightness, and shortness of breath.

Treatment for allergic alveolitis typically involves avoidance of the allergen, medications such as corticosteroids, and immunotherapy. In severe cases, hospitalization may be necessary to manage symptoms and prevent complications.

The diagnosis of pulmonary eosinophilia is based on a combination of clinical symptoms, physical examination findings, and laboratory tests such as chest X-rays, blood tests, and bronchoalveolar lavage (BAL) fluid analysis.

Treatment of pulmonary eosinophilia depends on the underlying cause and may include medications such as corticosteroids, antihistamines, or antibiotics, as well as lifestyle modifications such as avoiding allergens and managing stress. In severe cases, hospitalization may be necessary to monitor and treat the condition.

Some common symptoms of pulmonary eosinophilia include:

* Coughing
* Shortness of breath (dyspnea)
* Chest tightness or discomfort
* Fatigue
* Wheezing
* Recurrent respiratory infections

Complications of pulmonary eosinophilia can include:

* Respiratory failure
* Asthma exacerbation
* Chronic obstructive pulmonary disease (COPD)
* Pneumonia or other respiratory infections
* Airway obstruction

It is important to seek medical attention if you experience any of these symptoms, as early diagnosis and treatment can help prevent complications and improve outcomes.

The diagnosis of BHR is based on a combination of clinical, physiological, and imaging tests. The most common method used to assess BHR is the methacholine or histamine challenge test, which involves inhaling progressively increasing concentrations of these substances to measure airway reactivity. Other tests include exercise testing, hyperventilation, and mannitol challenge.

BHR is characterized by an increased responsiveness of the airways to various stimuli, such as allergens, cold or exercise, leading to inflammation and bronchoconstriction. This can cause symptoms such as wheezing, coughing, shortness of breath, and chest tightness.

There are several risk factors for BHR, including:

* Allergies
* Respiratory infections
* Exposure to environmental pollutants
* Genetic predisposition
* Obesity
* Smoking

Treatment of BHR typically involves the use of bronchodilators, corticosteroids, and other medications to reduce inflammation and airway constriction. In severe cases, surgical procedures such as lung volume reduction or bronchial thermoplasty may be necessary. Environmental modifications, such as avoiding triggers and using HEPA filters, can also help manage symptoms.

In summary, bronchial hyperreactivity is a condition characterized by an exaggerated response of the airways to various stimuli, leading to increased smooth muscle contraction and narrowing of the bronchi. It is commonly seen in asthma and other respiratory diseases, and can cause symptoms such as wheezing, coughing, shortness of breath, and chest tightness. Treatment typically involves medications and environmental modifications to reduce inflammation and airway constriction.

This type of pneumonia can cause severe respiratory symptoms, including cough, fever, chest pain, and difficulty breathing. It can also lead to respiratory failure and other complications if left untreated.

Pneumocystis pneumonia is diagnosed through a combination of physical examination, medical history, and diagnostic tests such as chest X-rays or CT scans, and blood tests. Treatment typically involves antifungal medications, and hospitalization may be necessary for severe cases.

Prevention measures include avoiding exposure to people with weakened immune systems, avoiding smoking, and maintaining good hygiene practices. Vaccines are also available for some populations at high risk of developing Pneumocystis pneumonia.

Asthma can cause recurring episodes of wheezing, coughing, chest tightness, and shortness of breath. These symptoms occur when the muscles surrounding the airways contract, causing the airways to narrow and swell. This can be triggered by exposure to environmental allergens or irritants such as pollen, dust mites, pet dander, or respiratory infections.

There is no cure for asthma, but it can be managed with medication and lifestyle changes. Treatment typically includes inhaled corticosteroids to reduce inflammation, bronchodilators to open up the airways, and rescue medications to relieve symptoms during an asthma attack.

Asthma is a common condition that affects people of all ages, but it is most commonly diagnosed in children. According to the American Lung Association, more than 25 million Americans have asthma, and it is the third leading cause of hospitalization for children under the age of 18.

While there is no cure for asthma, early diagnosis and proper treatment can help manage symptoms and improve quality of life for those affected by the condition.

Respiratory hypersensitivity can be diagnosed through medical history, physical examination, and allergy testing. Treatment options include avoidance of allergens, medication, such as antihistamines or corticosteroids, and immunotherapy, which involves exposing the person to small amounts of the allergen over time to build up their tolerance.

Some people with respiratory hypersensitivity may experience more severe symptoms, such as asthma, which can be life-threatening if left untreated. It is important for individuals with respiratory hypersensitivity to work closely with their healthcare provider to manage their condition and prevent complications.

1. Acute respiratory distress syndrome (ARDS): This is a severe and life-threatening condition that occurs when the lungs become inflamed and fill with fluid, making it difficult to breathe.
2. Pneumonia: This is an infection of the lungs that can cause inflammation and damage to the air sacs and lung tissue.
3. Aspiration pneumonitis: This occurs when food, liquid, or other foreign substances are inhaled into the lungs, causing inflammation and damage.
4. Chemical pneumonitis: This is caused by exposure to harmful chemicals or toxins that can damage the lungs and cause inflammation.
5. Radiation pneumonitis: This occurs when the lungs are exposed to high levels of radiation, causing damage and inflammation.
6. Lung fibrosis: This is a chronic condition in which the lungs become scarred and stiff, making it difficult to breathe.
7. Pulmonary embolism: This occurs when a blood clot forms in the lungs, blocking the flow of blood and oxygen to the heart and other organs.

Symptoms of lung injury can include:

* Shortness of breath
* Chest pain or tightness
* Coughing up blood or pus
* Fever
* Confusion or disorientation

Treatment for lung injury depends on the underlying cause and severity of the condition, and may include oxygen therapy, medications to reduce inflammation, antibiotics for infections, and mechanical ventilation in severe cases. In some cases, lung injury can be a life-threatening condition and may require hospitalization and intensive care.

Examples of lung diseases, interstitial include:

1. Idiopathic pulmonary fibrosis (IPF): A chronic and progressive disease characterized by inflammation and scarring of the lungs without a known cause.
2. Sarcoidosis: A systemic disease characterized by inflammation and granulomas in various organs, including the lungs.
3. Hypersensitivity pneumonitis (HP): An immune-mediated reaction to inhaled antigens that can lead to inflammation and scarring of the lungs.
4. Pneumoconiosis: A group of lung diseases caused by inhaling dust, including asbestos, silica, and coal dust.
5. Desquamative interstitial pneumonitis (DIP): A rare disease characterized by progressive inflammation and scarring of the lungs.
6. Respiratory bronchiolitis-associated interstitial lung disease (RB-ILD): A rare disease caused by inflammation and scarring of the small airways and surrounding tissue.
7. Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF): A sudden worsening of IPF symptoms, often accompanied by inflammation and scarring of the lungs.

Symptoms of lung diseases, interstitial can include:

1. Shortness of breath (dyspnea)
2. Cough
3. Fatigue
4. Chest tightness or pain
5. Dry cough
6. Weight loss
7. Fever

Diagnosis is typically made through a combination of physical examination, medical history, laboratory tests (such as blood tests and lung function tests), and imaging studies (such as chest X-rays and computed tomography (CT) scans).

Treatment options for interstitial lung disease depend on the specific diagnosis and severity of the condition. These may include:

1. Medications to reduce inflammation and prevent further scarring, such as corticosteroids or immunosuppressants.
2. Oxygen therapy to help improve oxygen levels in the blood.
3. Pulmonary rehabilitation to improve lung function and overall health.
4. Surgical procedures, such as lung transplantation, in severe cases where other treatments have failed.
5. Lifestyle changes, such as quitting smoking and avoiding exposure to dust and pollutants.

The symptoms of ALI can vary depending on the severity of the condition, but may include:

* Shortness of breath (dyspnea)
* Chest pain or tightness (pleurisy)
* Cough, which may produce mucus or pus
* Fatigue, confusion, or disorientation
* Low oxygen levels in the blood (hypoxia)

If left untreated, ALI can progress to a more severe condition called acute respiratory distress syndrome (ARDS), which can be fatal. Treatment for ALI typically involves supportive care, such as mechanical ventilation, medications to manage inflammation and fluid buildup in the lungs, and management of underlying causes. In severe cases, extracorporeal membrane oxygenation (ECMO) or lung transplantation may be necessary.

It's important to note that ALI can occur in people of all ages and can be caused by a variety of factors, so it's important to seek medical attention right away if you or someone you know is experiencing symptoms of the condition.

The primary symptom of PAP is shortness of breath (dyspnea), which can range from mild to severe and may be accompanied by coughing, wheezing, and chest tightness. PAP can also lead to respiratory failure, which can be life-threatening if left untreated.

The diagnosis of PAP is based on a combination of clinical symptoms, physical examination findings, and diagnostic tests such as chest radiographs (X-rays), computed tomography (CT) scans, and lung biopsy. A lung biopsy is the most definitive test for PAP, allowing for the identification of characteristic pathological features such as the accumulation of lipoproteinaceous material within the air spaces of the lungs.

Treatment options for PAP include surgical lung biopsy to obtain a definitive diagnosis and monitor disease progression, chest radiation therapy to reduce symptoms and slow disease progression, and medications such as corticosteroids to modulate the immune system and reduce inflammation. In severe cases, lung transplantation may be necessary.

The prognosis for PAP varies depending on the severity of the disease and response to treatment. With appropriate therapy, many patients with PAP can achieve stabilization of their symptoms and improved lung function. However, some patients may experience recurrent episodes of disease exacerbation and may require long-term management and monitoring.

In adults, RDS is less common than in newborns but can still occur in certain situations. These include:

* Sepsis (a severe infection that can cause inflammation throughout the body)
* Pneumonia or other respiratory infections
* Injury to the lung tissue, such as from a car accident or smoke inhalation
* Burns that cover a large portion of the body
* Certain medications, such as those used to treat cancer or autoimmune disorders.

Symptoms of RDS in adults can include:

* Shortness of breath
* Rapid breathing
* Chest tightness or pain
* Low oxygen levels in the blood
* Blue-tinged skin (cyanosis)
* Confusion or disorientation

Diagnosis of RDS in adults is typically made based on a combination of physical examination, medical history, and diagnostic tests such as chest X-rays or blood gas analysis. Treatment may involve oxygen therapy, mechanical ventilation (a machine that helps the patient breathe), and medications to help increase surfactant production or reduce inflammation in the lungs. In severe cases, a lung transplant may be necessary.

Prevention of RDS in adults includes avoiding exposure to risk factors such as smoking and other pollutants, maintaining good overall health, and seeking prompt medical attention if any respiratory symptoms develop.

1) They share similarities with humans: Many animal species share similar biological and physiological characteristics with humans, making them useful for studying human diseases. For example, mice and rats are often used to study diseases such as diabetes, heart disease, and cancer because they have similar metabolic and cardiovascular systems to humans.

2) They can be genetically manipulated: Animal disease models can be genetically engineered to develop specific diseases or to model human genetic disorders. This allows researchers to study the progression of the disease and test potential treatments in a controlled environment.

3) They can be used to test drugs and therapies: Before new drugs or therapies are tested in humans, they are often first tested in animal models of disease. This allows researchers to assess the safety and efficacy of the treatment before moving on to human clinical trials.

4) They can provide insights into disease mechanisms: Studying disease models in animals can provide valuable insights into the underlying mechanisms of a particular disease. This information can then be used to develop new treatments or improve existing ones.

5) Reduces the need for human testing: Using animal disease models reduces the need for human testing, which can be time-consuming, expensive, and ethically challenging. However, it is important to note that animal models are not perfect substitutes for human subjects, and results obtained from animal studies may not always translate to humans.

6) They can be used to study infectious diseases: Animal disease models can be used to study infectious diseases such as HIV, TB, and malaria. These models allow researchers to understand how the disease is transmitted, how it progresses, and how it responds to treatment.

7) They can be used to study complex diseases: Animal disease models can be used to study complex diseases such as cancer, diabetes, and heart disease. These models allow researchers to understand the underlying mechanisms of the disease and test potential treatments.

8) They are cost-effective: Animal disease models are often less expensive than human clinical trials, making them a cost-effective way to conduct research.

9) They can be used to study drug delivery: Animal disease models can be used to study drug delivery and pharmacokinetics, which is important for developing new drugs and drug delivery systems.

10) They can be used to study aging: Animal disease models can be used to study the aging process and age-related diseases such as Alzheimer's and Parkinson's. This allows researchers to understand how aging contributes to disease and develop potential treatments.

The most common bacteria that cause pneumonia are Streptococcus pneumoniae (also known as pneumococcus), Haemophilus influenzae, and Staphylococcus aureus. These bacteria can infect the lungs through various routes, including respiratory droplets, contaminated food or water, or direct contact with an infected person.

Symptoms of pneumonia may include cough, fever, chills, shortness of breath, and chest pain. In severe cases, pneumonia can lead to serious complications such as respiratory failure, sepsis, and death.

Diagnosis of pneumonia typically involves a physical examination, medical history, and diagnostic tests such as chest X-rays or blood cultures. Treatment typically involves antibiotics to eliminate the infection, as well as supportive care to manage symptoms and prevent complications. Vaccines are also available to protect against certain types of bacterial pneumonia, particularly in children and older adults.

Preventative measures for bacterial pneumonia include:

* Getting vaccinated against Streptococcus pneumoniae and Haemophilus influenzae type b (Hib)
* Practicing good hygiene, such as washing hands regularly and covering the mouth and nose when coughing or sneezing
* Avoiding close contact with people who are sick
* Staying hydrated and getting enough rest
* Quitting smoking, if applicable
* Managing underlying medical conditions, such as diabetes or heart disease

It is important to seek medical attention promptly if symptoms of pneumonia develop, particularly in high-risk populations. Early diagnosis and treatment can help prevent serious complications and improve outcomes for patients with bacterial pneumonia.

There are several key features of inflammation:

1. Increased blood flow: Blood vessels in the affected area dilate, allowing more blood to flow into the tissue and bringing with it immune cells, nutrients, and other signaling molecules.
2. Leukocyte migration: White blood cells, such as neutrophils and monocytes, migrate towards the site of inflammation in response to chemical signals.
3. Release of mediators: Inflammatory mediators, such as cytokines and chemokines, are released by immune cells and other cells in the affected tissue. These molecules help to coordinate the immune response and attract more immune cells to the site of inflammation.
4. Activation of immune cells: Immune cells, such as macrophages and T cells, become activated and start to phagocytose (engulf) pathogens or damaged tissue.
5. Increased heat production: Inflammation can cause an increase in metabolic activity in the affected tissue, leading to increased heat production.
6. Redness and swelling: Increased blood flow and leakiness of blood vessels can cause redness and swelling in the affected area.
7. Pain: Inflammation can cause pain through the activation of nociceptors (pain-sensing neurons) and the release of pro-inflammatory mediators.

Inflammation can be acute or chronic. Acute inflammation is a short-term response to injury or infection, which helps to resolve the issue quickly. Chronic inflammation is a long-term response that can cause ongoing damage and diseases such as arthritis, asthma, and cancer.

There are several types of inflammation, including:

1. Acute inflammation: A short-term response to injury or infection.
2. Chronic inflammation: A long-term response that can cause ongoing damage and diseases.
3. Autoimmune inflammation: An inappropriate immune response against the body's own tissues.
4. Allergic inflammation: An immune response to a harmless substance, such as pollen or dust mites.
5. Parasitic inflammation: An immune response to parasites, such as worms or fungi.
6. Bacterial inflammation: An immune response to bacteria.
7. Viral inflammation: An immune response to viruses.
8. Fungal inflammation: An immune response to fungi.

There are several ways to reduce inflammation, including:

1. Medications such as nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and disease-modifying anti-rheumatic drugs (DMARDs).
2. Lifestyle changes, such as a healthy diet, regular exercise, stress management, and getting enough sleep.
3. Alternative therapies, such as acupuncture, herbal supplements, and mind-body practices.
4. Addressing underlying conditions, such as hormonal imbalances, gut health issues, and chronic infections.
5. Using anti-inflammatory compounds found in certain foods, such as omega-3 fatty acids, turmeric, and ginger.

It's important to note that chronic inflammation can lead to a range of health problems, including:

1. Arthritis
2. Diabetes
3. Heart disease
4. Cancer
5. Alzheimer's disease
6. Parkinson's disease
7. Autoimmune disorders, such as lupus and rheumatoid arthritis.

Therefore, it's important to manage inflammation effectively to prevent these complications and improve overall health and well-being.

Symptoms of pulmonary edema may include:

* Shortness of breath (dyspnea)
* Coughing up frothy sputum
* Chest pain or tightness
* Fatigue
* Confusion or disorientation

Pulmonary edema can be diagnosed through physical examination, chest x-rays, electrocardiogram (ECG), and blood tests. Treatment options include oxygen therapy, diuretics, and medications to manage underlying conditions such as heart failure or sepsis. In severe cases, hospitalization may be necessary to provide mechanical ventilation.

Prevention measures for pulmonary edema include managing underlying medical conditions, avoiding exposure to pollutants and allergens, and seeking prompt medical attention if symptoms persist or worsen over time.

In summary, pulmonary edema is a serious condition that can impair lung function and lead to shortness of breath, chest pain, and other respiratory symptoms. Prompt diagnosis and treatment are essential to prevent complications and improve outcomes for patients with this condition.

A type of pneumonia caused by a viral infection. The most common viruses that cause pneumonia are the respiratory syncytial virus (RSV), influenza virus, and adenovirus.

Symptoms include fever, cough, chest pain, difficulty breathing, and loss of appetite.

Treatment typically involves antiviral medications and supportive care to manage symptoms and improve lung function. In severe cases, hospitalization may be necessary.

Prevention measures include vaccination against the flu and RSV, good hygiene practices such as frequent handwashing, and avoiding close contact with people who are sick.

Types of fungal lung diseases include:

1. Aspergillosis: This is an infection caused by the fungus Aspergillus, which is commonly found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with cancer, HIV/AIDS, or taking immunosuppressive drugs.
2. Cryptococcosis: This is an infection caused by the fungus Cryptococcus neoformans, which is found in soil and decaying wood. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.
3. Histoplasmosis: This is an infection caused by the fungus Histoplasma capsulatum, which is found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.
4. Pneumocystis pneumonia (PCP): This is an infection caused by the fungus Pneumocystis jirovecii, which is found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.
5. Sporotrichosis: This is an infection caused by the fungus Sporothrix schenckii, which is found in soil and decaying organic matter. It can affect people with weakened immune systems, such as those with HIV/AIDS or taking immunosuppressive drugs.

Symptoms of fungal lung diseases can include:

* Cough
* Fever
* Chest pain
* Shortness of breath
* Fatigue

Diagnosis of fungal lung diseases is typically made through a combination of physical examination, medical history, and laboratory tests such as chest X-rays, CT scans, and fungal cultures. Treatment usually involves antifungal medications and may also include supportive care to manage symptoms.

Prevention of fungal lung diseases includes:

1. Avoiding exposure to fungal spores by wearing protective clothing and gear when working with soil or decaying organic matter.
2. Maintaining good indoor air quality by using ventilation systems and reducing humidity.
3. Reducing the risk of infection by avoiding close contact with people who are at high risk of developing fungal lung diseases, such as those with weakened immune systems.
4. Avoiding smoking and other tobacco products, which can increase the risk of developing fungal lung diseases.
5. Managing underlying medical conditions, such as HIV/AIDS or taking immunosuppressive drugs, to reduce the risk of developing fungal lung diseases.

There are several types of hypersensitivity reactions, including:

1. Type I hypersensitivity: This is also known as immediate hypersensitivity and occurs within minutes to hours after exposure to the allergen. It is characterized by the release of histamine and other chemical mediators from immune cells, leading to symptoms such as hives, itching, swelling, and difficulty breathing. Examples of Type I hypersensitivity reactions include allergies to pollen, dust mites, or certain foods.
2. Type II hypersensitivity: This is also known as cytotoxic hypersensitivity and occurs within days to weeks after exposure to the allergen. It is characterized by the immune system producing antibodies against specific proteins on the surface of cells, leading to their destruction. Examples of Type II hypersensitivity reactions include blood transfusion reactions and serum sickness.
3. Type III hypersensitivity: This is also known as immune complex hypersensitivity and occurs when antigens bind to immune complexes, leading to the formation of deposits in tissues. Examples of Type III hypersensitivity reactions include rheumatoid arthritis and systemic lupus erythematosus.
4. Type IV hypersensitivity: This is also known as delayed-type hypersensitivity and occurs within weeks to months after exposure to the allergen. It is characterized by the activation of T cells, leading to inflammation and tissue damage. Examples of Type IV hypersensitivity reactions include contact dermatitis and toxic epidermal necrolysis.

The diagnosis of hypersensitivity often involves a combination of medical history, physical examination, laboratory tests, and elimination diets or challenges. Treatment depends on the specific type of hypersensitivity reaction and may include avoidance of the allergen, medications such as antihistamines or corticosteroids, and immunomodulatory therapy.

Causes:

There are many possible causes of eosinophilia, including:

* Allergies
* Parasitic infections
* Autoimmune disorders
* Cancer
* Medications

Symptoms:

The symptoms of eosinophilia can vary depending on the underlying cause, but may include:

* Swelling of the skin, lips, and eyes
* Hives or itchy skin
* Shortness of breath or wheezing
* Abdominal pain
* Diarrhea

Diagnosis:

Eosinophilia is typically diagnosed through a blood test that measures the number of eosinophils in the blood. Other tests such as imaging studies, skin scrapings, and biopsies may also be used to confirm the diagnosis and identify the underlying cause.

Treatment:

The treatment of eosinophilia depends on the underlying cause, but may include medications such as antihistamines, corticosteroids, and chemotherapy. In some cases, removal of the causative agent or immunomodulatory therapy may be necessary.

Complications:

Eosinophilia can lead to a number of complications, including:

* Anaphylaxis (a severe allergic reaction)
* Asthma
* Eosinophilic granulomas (collections of eosinophils that can cause organ damage)
* Eosinophilic gastrointestinal disorders (conditions where eosinophils invade the digestive tract)

Prognosis:

The prognosis for eosinophilia depends on the underlying cause, but in general, the condition is not life-threatening. However, if left untreated, complications can arise and the condition can have a significant impact on quality of life.

In conclusion, eosinophilia is a condition characterized by an abnormal increase in eosinophils in the body. While it can be caused by a variety of factors, including allergies, infections, and autoimmune disorders, the underlying cause must be identified and treated in order to effectively manage the condition and prevent complications.

The symptoms of lipid pneumonia can be similar to those of other types of pneumonia, such as cough, fever, chills, and difficulty breathing. However, lipid pneumonia may also cause a distinctive "fatty" or "oily" appearance on chest X-rays.

There are several possible causes of lipid pneumonia, including inhalation of lipids from the environment or from certain medical procedures (such as intratracheal lipid injections), and certain underlying medical conditions (such as cystic fibrosis). The diagnosis of lipid pneumonia is typically made through a combination of clinical evaluation, chest X-rays, and laboratory tests.

Treatment of lipid pneumonia usually involves supportive care measures such as oxygen therapy, hydration, and pain management, as well as antibiotics to prevent or treat any underlying bacterial infections. In severe cases, hospitalization may be necessary to monitor and treat the condition.

Prognosis for lipid pneumonia is generally good if treated promptly and effectively, but the condition can be serious and potentially life-threatening if left untreated or if there are underlying medical conditions that complicate treatment.

Acute bronchitis is a short-term infection that is usually caused by a virus or bacteria, and can be treated with antibiotics and supportive care such as rest, hydration, and over-the-counter pain relievers. Chronic bronchitis, on the other hand, is a long-term condition that is often associated with smoking and can lead to chronic obstructive pulmonary disease (COPD).

Bronchitis can cause a range of symptoms including:

* Persistent cough, which may be dry or produce mucus
* Chest tightness or discomfort
* Shortness of breath or wheezing
* Fatigue and fever
* Headache and body aches

The diagnosis of bronchitis is usually made based on a physical examination, medical history, and results of diagnostic tests such as chest X-rays and pulmonary function tests. Treatment for bronchitis typically focuses on relieving symptoms and managing the underlying cause, such as a bacterial infection or smoking cessation.

Bronchitis can be caused by a variety of factors, including:

* Viral infections, such as the common cold or flu
* Bacterial infections, such as pneumonia
* Smoking and exposure to environmental pollutants
* Asthma and other allergic conditions
* Chronic lung diseases, such as COPD

Preventive measures for bronchitis include:

* Quitting smoking and avoiding exposure to secondhand smoke
* Getting vaccinated against flu and pneumonia
* Practicing good hygiene, such as washing hands frequently
* Avoiding exposure to environmental pollutants
* Managing underlying conditions such as asthma and allergies.

There are several types of asbestos, including chrysotile, amianthus, and crocidolite, each of which has different levels of toxicity. Prolonged exposure to any type of asbestos can cause asbestosis, but some types are more dangerous than others.

Symptoms of asbestosis may not appear until many years after exposure to asbestos, and they can vary in severity. Common symptoms include:

* Shortness of breath
* Coughing
* Permanent lung damage
* Scarring of the lungs
* Decreased lung function

Treatment for asbestosis usually involves managing symptoms and improving lung function. This can include medications to relieve coughing and shortness of breath, pulmonary rehabilitation to improve lung function, and oxygen therapy to help increase oxygen levels in the blood. In severe cases, lung transplantation may be necessary.

Prevention is key in avoiding asbestosis. If you suspect that you have been exposed to asbestos, it is important to speak with a healthcare professional as soon as possible. Proper safety measures and precautions can help minimize the risk of developing asbestosis.

VAP is a serious complication of mechanical ventilation and can lead to severe illness, organ failure, and death. The risk of developing VAP is increased in patients who are ventilated for longer periods of time, have underlying medical conditions such as chronic obstructive pulmonary disease (COPD) or sepsis, or have invasive medical devices such as central lines or urinary catheters.

The diagnosis of VAP is based on a combination of clinical and laboratory findings, including fever, purulent respiratory secretions, and evidence of lung infection on chest radiographs or computed tomography (CT) scans. Treatment typically involves administration of broad-spectrum antibiotics and supportive care, such as mechanical ventilation and fluid management.

Prevention of VAP is an important goal in critical care medicine, and strategies to reduce the risk of developing VAP include:

1. Early recognition and treatment of respiratory tract infections
2. Proper hand hygiene and use of personal protective equipment (PPE) by healthcare workers
3. Regular cleaning and disinfection of medical devices and equipment
4. Use of selective digestive decontamination (SDD) with antibiotics and probiotics to reduce the risk of colonization of the respiratory tract by pathogenic bacteria
5. Avoiding invasive medical procedures whenever possible, and using alternative methods when feasible.

The incidence of VAP has been declining in recent years due to improved infection control practices and the use of evidence-based guidelines for prevention and treatment. However, VAP remains a significant challenge in critical care medicine, and ongoing research is needed to develop more effective strategies for prevention and treatment.

The symptoms of aspiration pneumonia may include cough, fever, chills, difficulty breathing, and chest pain. The infection can be mild, moderate, or severe and can affect people of all ages, but it is more common in older adults or those with underlying medical conditions.

The diagnosis of aspiration pneumonia is usually made based on a combination of physical examination findings, medical history, and diagnostic tests such as chest x-rays or CT scans. Treatment typically involves antibiotics and supportive care such as oxygen therapy and mechanical ventilation in severe cases. In some cases, hospitalization may be required to monitor and treat the infection.

Prevention of aspiration pneumonia includes avoiding eating or drinking before lying down, taking small bites and chewing food thoroughly, and avoiding alcohol and sedatives. It is also important to maintain good oral hygiene and to avoid smoking and other forms of tobacco use. Vaccination against certain types of pneumonia may also be recommended for some individuals at high risk.

Some common types of lung diseases, parasitic include:

1. Aspergillosis: This is a fungal infection that can affect the lungs and other parts of the body. It is caused by the Aspergillus fungus and can lead to chronic inflammation and scarring in the lungs.
2. Pneumocystis pneumonia (PCP): This is a type of pneumonia that is caused by the Pneumocystis jirovecii fungus and is more common in people with weakened immune systems, such as those with HIV/AIDS or cancer.
3. Cryptococcosis: This is a fungal infection that can affect the lungs and central nervous system. It is caused by the Cryptococcus neoformans fungus and can lead to chronic inflammation and scarring in the lungs.
4. Histoplasmosis: This is a fungal infection that can affect the lungs and other parts of the body. It is caused by the Histoplasma capsulatum fungus and can lead to chronic inflammation and scarring in the lungs.
5. Chagas disease: This is a parasitic infection that is caused by the Trypanosoma cruzi parasite and can affect the heart and lungs, among other organs. It is more common in Latin America and can lead to chronic inflammation and scarring in the lungs.
6. Leishmaniasis: This is a parasitic infection that can affect various parts of the body, including the lungs. It is caused by the Leishmania parasite and can lead to chronic inflammation and scarring in the lungs.
7. Strongyloidiasis: This is a parasitic infection that is caused by the Strongyloides stercoralis parasite and can affect the lungs and other parts of the body. It can lead to chronic inflammation and scarring in the lungs.
8. Schistosomiasis: This is a parasitic infection that is caused by the Schistosoma parasite and can affect various parts of the body, including the lungs. It can lead to chronic inflammation and scarring in the lungs.
9. Lymphatic filariasis: This is a parasitic infection that is caused by the Wuchereria bancrofti or Brugia malayi parasites and can affect the lymph nodes and other parts of the body, including the lungs. It can lead to chronic inflammation and scarring in the lungs.
10. Tuberculosis: This is a bacterial infection that primarily affects the lungs and can lead to chronic inflammation and scarring in the lungs. It is caused by Mycobacterium tuberculosis and can be spread through the air when an infected person coughs or sneezes.

It is important to note that these conditions are not mutually exclusive, and individuals may have more than one condition affecting their lungs at the same time. It is also important to note that other factors such as smoking, exposure to environmental pollutants, and underlying medical conditions can increase the risk of developing chronic lung disease.

A healthcare professional should be consulted for an accurate diagnosis and appropriate treatment of any suspected lung conditions.

The exact cause of Bronchiolitis Obliterans is not fully understood, but it is believed to be due to a combination of genetic and environmental factors. The condition is often associated with allergies and asthma, and viral infections such as respiratory syncytial virus (RSV) can trigger the onset of symptoms.

Symptoms of Bronchiolitis Obliterans include:

* Persistent coughing, which may be worse at night
* Shortness of breath or wheezing
* Chest tightness or discomfort
* Fatigue and poor appetite
* Recurrent respiratory infections

BO is typically diagnosed through a combination of physical examination, medical history, and diagnostic tests such as chest X-rays or pulmonary function tests. There is no cure for Bronchiolitis Obliterans, but treatment options are available to manage symptoms and slow the progression of the disease. These may include:

* Medications such as bronchodilators and corticosteroids to reduce inflammation and improve lung function
* Pulmonary rehabilitation programs to improve breathing and overall health
* Oxygen therapy to help increase oxygen levels in the blood
* In severe cases, lung transplantation may be considered.

While Bronchiolitis Obliterans can significantly impact quality of life, with proper management and care, many individuals with the condition are able to lead active and productive lives.

A type of hypersensitivity pneumonitis caused by inhalation of fungal spores or dust from moldy hay, straw, or grain, commonly seen in farmers and others who work with agricultural products. Symptoms include fever, cough, chest tightness, and shortness of breath, which may be severe and even life-threatening if left untreated. Also called agricultural lung disease or moldy hay fever.

Source: Dorland's Medical Dictionary for Health Professionals.

Bronchopneumonia is a serious condition that can lead to respiratory failure and other complications if left untreated. It is important for individuals with bronchopneumonia to seek medical attention promptly if they experience any worsening symptoms or signs of infection, such as increased fever or difficulty breathing.

Bronchopneumonia can be caused by a variety of factors, including bacterial and viral infections, and can affect individuals of all ages. It is most common in young children and the elderly, as well as those with pre-existing respiratory conditions such as asthma or chronic obstructive pulmonary disease (COPD).

Treatment for bronchopneumonia typically involves antibiotics to treat any bacterial infections, as well as supportive care to help manage symptoms and improve lung function. In severe cases, hospitalization may be necessary to provide more intensive treatment and monitoring.

In addition to antibiotics and supportive care, other treatments for bronchopneumonia may include:

* Oxygen therapy to help increase oxygen levels in the blood
* Pain management medications to relieve chest pain and fever
* Breathing exercises and pulmonary rehabilitation to improve lung function
* Rest and relaxation to help the body recover

Prevention is key in avoiding bronchopneumonia, and this can be achieved through:

* Good hand hygiene and respiratory etiquette
* Avoiding close contact with individuals who are sick
* Getting vaccinated against pneumococcal disease and the flu
* Practicing good hygiene during travel to avoid exposure to respiratory infections.

In conclusion, bronchopneumonia is a serious condition that can be caused by a variety of factors and can affect individuals of all ages. Treatment typically involves antibiotics and supportive care, and prevention strategies include good hygiene practices and vaccination. With proper treatment and care, individuals with bronchopneumonia can recover and lead active lives.

COP typically affects middle-aged adults and is more common in women than men. Symptoms include cough, shortness of breath, fever, and fatigue. The condition can be acute or chronic, and it can lead to respiratory failure if left untreated.

The exact cause of COP is not known, but it is believed to be related to an abnormal immune response to environmental triggers, such as cigarette smoke or other inhaled substances. The disease is often associated with other autoimmune disorders, such as rheumatoid arthritis or lupus.

Diagnosis of COP is based on a combination of clinical findings, radiologic imaging (such as chest x-rays and CT scans), and lung biopsy. Treatment typically involves corticosteroids to reduce inflammation and improve lung function. In severe cases, respiratory support may be necessary.

The prognosis for COP varies depending on the severity of the disease and the response to treatment. In general, the condition can be managed with appropriate therapy, but it can be challenging to diagnose and treat effectively.

There are several factors that can contribute to the development of VILI, including:

1. High inspiratory pressures: Ventilators that set peak inspiratory pressures too high can cause damage to the lungs.
2. Volume-targeted ventilation: This type of ventilation can lead to over-inflation of the lungs, particularly in patients with poor compliance (i.e., those who do not easily expand their lungs).
3. Positive end-expiratory pressure (PEEP): PEEP is a mode of ventilation that keeps the airways open during expiration, but can cause over-inflation of the lungs if set too high.
4. Frequent or deep tidal volumes: Tidal volume is the amount of air exchanged with each breath. Frequent or deep tidal volumes can cause over-inflation of the lungs and lead to VILI.
5. Duration of mechanical ventilation: Prolonged use of mechanical ventilation can increase the risk of VILI, particularly if the patient requires high levels of support.

To diagnose VILI, a physician may perform a physical examination, take a medical history, and order diagnostic tests such as chest X-rays or CT scans to assess lung function and look for signs of inflammation or scarring. Treatment for VILI typically involves adjusting the ventilator settings to reduce the risk of further injury, providing supportive care to manage symptoms, and addressing any underlying conditions that may be contributing to the injury. In severe cases, patients with VILI may require extracorporeal membrane oxygenation (ECMO) or other forms of respiratory support to help restore lung function.

Airway remodeling is a complex process that involves changes in the structure and function of the airways, as well as an immune response. It is characterized by the following features:

* Airway wall thickening and inflammation
* Increased mucus production
* Narrowing of the airway lumina due to smooth muscle hypertrophy and fibrosis
* Increased airway resistance and decreased lung function.

Airway remodeling is a hallmark of asthma and COPD, and it can lead to exacerbations and poor disease control if left untreated. The exact mechanisms driving airway remodeling are not fully understood, but it is believed that a combination of genetic and environmental factors contribute to its development.

There are several techniques used to assess airway remodeling in patients with respiratory diseases, including:

* Quantitative computed tomography (QCT) - This technique allows for the measurement of airway wall thickness and luminal area.
* Magnetic resonance imaging (MRI) - MRI can provide information on airway size and shape, as well as tissue composition.
* Bronchoscopy with biopsy - This procedure allows for the examination of airway tissue and the assessment of inflammation and fibrosis.

There are several treatments available for airway remodeling in patients with respiratory diseases, including:

* Medications such as bronchodilators, corticosteroids, and anti-inflammatory drugs
* Pulmonary rehabilitation - This includes exercises and education to help improve lung function and overall health.
* Lung transplantation - In severe cases of airway remodeling that do not respond to other treatments, lung transplantation may be considered.

It is important for patients with respiratory diseases to work closely with their healthcare provider to monitor their condition and adjust their treatment plan as needed. With appropriate management, many patients with airway remodeling can experience improved lung function and quality of life.

There are several types of pulmonary emphysema, including:

1. Centriacinar emphysema: This type of emphysema affects the central airways and is caused by the destruction of the walls of the air sacs, leading to their enlargement.
2. Paraseptal emphysema: This type of emphysema affects the spaces between the air sacs and is caused by the destruction of the connective tissue that supports the air sacs.
3. Panacinar emphysema: This type of emphysema affects all parts of the lungs and is caused by the destruction of the walls of the air sacs, leading to their enlargement.

Pulmonary emphysema can be caused by a variety of factors, including smoking, exposure to air pollutants, and genetic predisposition. The symptoms of pulmonary emphysema can vary in severity and may include shortness of breath, fatigue, wheezing, and chest tightness.

Diagnosis of pulmonary emphysema typically involves a physical examination, medical history, and lung function tests such as spirometry and bronchodilator testing. Imaging tests such as chest X-rays and computed tomography (CT) scans may also be used to evaluate the extent of the disease.

Treatment for pulmonary emphysema typically involves a combination of medications, including bronchodilators, corticosteroids, and antibiotics, as well as lifestyle modifications such as quitting smoking, avoiding exposure to air pollutants, and exercising regularly. In severe cases, lung transplantation may be necessary.

Prevention of pulmonary emphysema includes avoiding smoking and other environmental risk factors, maintaining a healthy diet and exercise regimen, and managing any underlying medical conditions that may contribute to the development of the disease. Early detection and treatment can help to slow the progression of the disease and improve quality of life for those affected.

In conclusion, pulmonary emphysema is a chronic respiratory disease characterized by the destruction of the walls of the air sacs in the lungs, leading to enlargement of the sacs and difficulty breathing. While there is no cure for pulmonary emphysema, treatment can help to manage symptoms and slow the progression of the disease. Prevention includes avoiding smoking and other environmental risk factors, maintaining a healthy lifestyle, and managing any underlying medical conditions. Early detection and treatment can improve quality of life for those affected by this condition.

The symptoms of aspergillosis depend on the location and severity of the infection. In the lungs, it may cause coughing, fever, chest pain, and difficulty breathing. In the sinuses, it can cause headaches, facial pain, and nasal congestion. In the brain, it can cause seizures, confusion, and weakness.

Aspergillosis is typically diagnosed through a combination of imaging tests such as chest X-rays, CT scans, and MRI scans, along with a biopsy to confirm the presence of Aspergillus fungi.

Treatment of aspergillosis depends on the severity and location of the infection. In mild cases, treatment may involve antifungal medications and supportive care such as oxygen therapy and pain management. In severe cases, treatment may require hospitalization and intravenous antifungal medications.

Preventive measures for aspergillosis include avoiding exposure to dusty or damp environments, managing chronic conditions such as asthma and COPD, and taking antifungal medications as prescribed.

Aspergillosis can be a serious condition, especially in people with weakened immune systems, such as those with cancer, HIV/AIDS, or taking immunosuppressive drugs. In severe cases, aspergillosis can lead to life-threatening complications such as respiratory failure, sepsis, and organ damage.

In conclusion, aspergillosis is a common fungal infection that can affect various parts of the body, and it can be serious and potentially life-threatening, especially in people with weakened immune systems. Early diagnosis and appropriate treatment are essential to prevent complications and improve outcomes.

Respiratory aspiration can lead to a range of complications, including pneumonia, bronchitis, and lung abscesses. It can also cause respiratory failure, which can be life-threatening.

Symptoms of respiratory aspiration may include coughing, wheezing, difficulty breathing, and fever. Diagnosis is typically made through a combination of physical examination, medical history, and diagnostic tests such as chest X-rays or endoscopy. Treatment may involve antibiotics for any infections that have developed, as well as supportive care to help the individual breathe more easily. In severe cases, respiratory aspiration may require hospitalization and mechanical ventilation.

Preventing respiratory aspiration is important, especially for individuals who are at high risk. This can involve modifications to their diet, such as thickening liquids or pureeing foods, as well as using specialized feeding tubes or devices that help to prevent the entry of foreign substances into the respiratory tract.

The term "idiopathic" means that the cause of the disease is unknown, and "pulmonary fibrosis" refers to the scarring and thickening of the lung tissue that occurs in the disease. The scarring can lead to loss of lung function, shortness of breath, and coughing, making it difficult for patients to perform everyday activities.

IPF typically affects older adults, and men are more likely to be affected than women. The symptoms of IPF can vary from person to person but may include:

* Shortness of breath
* Coughing
* Fatigue
* Loss of appetite
* Weight loss
* Chest tightness or pain

There is no cure for IPF, and treatment options are limited. However, there are medications available that can help manage symptoms and slow the progression of the disease. It is important for patients with suspected IPF to seek medical attention as soon as possible to receive an accurate diagnosis and appropriate treatment.

Hyperoxia can cause damage to the body's tissues and organs, particularly the lungs and brain. In severe cases, hyperoxia can lead to respiratory failure, seizures, and even death.

There are several ways to diagnose hyperoxia, including:

1. Blood tests: These can measure the levels of oxygen in the blood.
2. Arterial blood gas (ABG) analysis: This is a test that measures the amounts of oxygen and carbon dioxide in the blood.
3. Pulse oximetry: This is a non-invasive test that measures the amount of oxygen in the blood by shining a light through the skin.

Treatment for hyperoxia depends on the underlying cause, but may include:

1. Oxygen therapy: This involves administering oxygen to the patient through a mask or nasal tubes.
2. Medications: These may be used to treat any underlying conditions that are causing hyperoxia.
3. Mechanical ventilation: In severe cases, this may be necessary to support the patient's breathing.

In summary, hyperoxia is a condition where there is too much oxygen in the body, and it can cause damage to the body's tissues and organs. Diagnosis is typically made through blood tests or other tests, and treatment may involve oxygen therapy, medications, or mechanical ventilation.

The severity of smoke inhalation injury can vary depending on factors such as the amount and type of smoke inhaled, the duration of exposure, and the individual's overall health. In mild cases, symptoms may include coughing, sneezing, and shortness of breath, while more severe cases can lead to respiratory failure, burns, and even death.

Treatment for smoke inhalation injury typically involves supportive care such as oxygen therapy, hydration, and pain management, as well as medications to help reduce inflammation and open up airways. In severe cases, hospitalization and mechanical ventilation may be necessary.

Long-term effects of smoke inhalation injury can include chronic obstructive pulmonary disease (COPD), bronchiectasis, and pulmonary fibrosis, among others. These conditions can significantly impact an individual's quality of life and may require ongoing medical care and monitoring.

Prevention of smoke inhalation injury involves taking steps to avoid exposure to smoke, such as evacuating a building during a fire or wearing protective equipment when working with flammable materials. In cases where exposure has already occurred, prompt medical attention can help reduce the risk of long-term health effects and improve outcomes for those affected.

Pseudomonas infections are challenging to treat due to the bacteria's ability to develop resistance against antibiotics. The treatment typically involves a combination of antibiotics and other supportive therapies, such as oxygen therapy or mechanical ventilation, to manage symptoms and prevent complications. In some cases, surgical intervention may be necessary to remove infected tissue or repair damaged organs.

Bird fancier's lung primarily affects men who work with or have contact with birds, such as veterinarians, bird breeders, and pigeon fanciers. The disease is also seen in people who live in areas where the fungus is common, such as rural farmers and construction workers.

The symptoms of bird fancier's lung can be non-specific and may resemble those of other respiratory conditions, such as tuberculosis or pneumonia. They include:

* Coughing up blood or mucus
* Chest pain
* Fatigue
* Weight loss
* Fever
* Night sweats
* Loss of appetite

If left untreated, bird fancier's lung can lead to serious complications, such as respiratory failure, heart problems, and cancer. Treatment typically involves antifungal medications, which may need to be taken for several months or even years. In severe cases, surgery may be required to remove infected tissue.

Preventive measures include wearing protective clothing and masks when handling birds, avoiding contact with bird droppings, and using proper ventilation in areas where birds are kept. Early diagnosis and treatment are essential to prevent long-term lung damage and improve the chances of a successful outcome.

Examples of OIs include:

1. Pneumocystis pneumonia (PCP): A type of pneumonia caused by the fungus Pneumocystis jirovecii, which is commonly found in the lungs of individuals with HIV/AIDS.
2. Cryptococcosis: A fungal infection caused by Cryptococcus neoformans, which can affect various parts of the body, including the lungs, central nervous system, and skin.
3. Aspergillosis: A fungal infection caused by Aspergillus fungi, which can affect various parts of the body, including the lungs, sinuses, and brain.
4. Histoplasmosis: A fungal infection caused by Histoplasma capsulatum, which is commonly found in the soil and can cause respiratory and digestive problems.
5. Candidiasis: A fungal infection caused by Candida albicans, which can affect various parts of the body, including the skin, mouth, throat, and vagina.
6. Toxoplasmosis: A parasitic infection caused by Toxoplasma gondii, which can affect various parts of the body, including the brain, eyes, and lymph nodes.
7. Tuberculosis (TB): A bacterial infection caused by Mycobacterium tuberculosis, which primarily affects the lungs but can also affect other parts of the body.
8. Kaposi's sarcoma-associated herpesvirus (KSHV): A viral infection that can cause various types of cancer, including Kaposi's sarcoma, which is more common in individuals with compromised immunity.

The diagnosis and treatment of OIs depend on the specific type of infection and its severity. Treatment may involve antibiotics, antifungals, or other medications, as well as supportive care to manage symptoms and prevent complications. It is important for individuals with HIV/AIDS to receive prompt and appropriate treatment for OIs to help prevent the progression of their disease and improve their quality of life.

Symptoms of cystic fibrosis can vary from person to person, but may include:

* Persistent coughing and wheezing
* Thick, sticky mucus that clogs airways and can lead to respiratory infections
* Difficulty gaining weight or growing at the expected rate
* Intestinal blockages or digestive problems
* Fatty stools
* Nausea and vomiting
* Diarrhea
* Rectal prolapse
* Increased risk of liver disease and respiratory failure

Cystic fibrosis is usually diagnosed in infancy, and treatment typically includes a combination of medications, respiratory therapy, and other supportive care. Management of the disease focuses on controlling symptoms, preventing complications, and improving quality of life. With proper treatment and care, many people with cystic fibrosis can lead long, fulfilling lives.

In summary, cystic fibrosis is a genetic disorder that affects the respiratory, digestive, and reproductive systems, causing thick and sticky mucus to build up in these organs, leading to serious health problems. It can be diagnosed in infancy and managed with a combination of medications, respiratory therapy, and other supportive care.

Pulmonary tuberculosis typically affects the lungs but can also spread to other parts of the body, such as the brain, kidneys, or spine. The symptoms of pulmonary TB include coughing for more than three weeks, chest pain, fatigue, fever, night sweats, and weight loss.

Pulmonary tuberculosis is diagnosed by a combination of physical examination, medical history, laboratory tests, and radiologic imaging, such as chest X-rays or computed tomography (CT) scans. Treatment for pulmonary TB usually involves a combination of antibiotics and medications to manage symptoms.

Preventive measures for pulmonary tuberculosis include screening for latent TB infection in high-risk populations, such as healthcare workers and individuals with HIV/AIDS, and vaccination with the bacillus Calmette-Guérin (BCG) vaccine in countries where it is available.

Overall, pulmonary tuberculosis is a serious and potentially life-threatening disease that requires prompt diagnosis and treatment to prevent complications and death.

Some common horse diseases include:

1. Equine Influenza (EI): A highly contagious respiratory disease caused by the equine influenza virus. It can cause fever, coughing, and nasal discharge.
2. Strangles: A bacterial infection of the lymph nodes, which can cause swelling of the neck and difficulty breathing.
3. West Nile Virus (WNV): A viral infection that can cause fever, weakness, and loss of coordination. It is transmitted by mosquitoes and can be fatal in some cases.
4. Tetanus: A bacterial infection caused by Clostridium tetani, which can cause muscle stiffness, spasms, and rigidity.
5. Rabies: A viral infection that affects the central nervous system and can be fatal if left untreated. It is transmitted through the saliva of infected animals, usually through a bite.
6. Cushing's Disease: A hormonal disorder caused by an overproduction of cortisol, which can cause weight gain, muscle wasting, and other health issues.
7. Laminitis: An inflammation of the laminae, the tissues that connect the hoof to the bone. It can be caused by obesity, overeating, or excessive exercise.
8. Navicular Syndrome: A condition that affects the navicular bone and surrounding tissue, causing pain and lameness in the foot.
9. Pneumonia: An inflammation of the lungs, which can be caused by bacteria, viruses, or fungi.
10. Colic: A general term for abdominal pain, which can be caused by a variety of factors, including gas, impaction, or twisting of the intestines.

These are just a few examples of the many potential health issues that can affect horses. Regular veterinary care and proper management can help prevent many of these conditions, and early diagnosis and treatment can improve the chances of a successful outcome.

Pulmonary aspergillosis is a type of fungal infection that affects the lungs and is caused by the fungus Aspergillus. It can occur in people with weakened immune systems, such as those with cancer, HIV/AIDS, or taking immunosuppressive drugs following an organ transplant.

The symptoms of pulmonary aspergillosis can vary depending on the severity of the infection and may include:

* Coughing up blood or mucus
* Chest pain or tightness
* Fever
* Shortness of breath
* Chills
* Weight loss

In severe cases, pulmonary aspergillosis can lead to respiratory failure, which can be life-threatening.

Pulmonary aspergillosis is diagnosed through a combination of imaging tests such as chest X-rays, CT scans, and fungal cultures. Treatment typically involves antifungal medications and supportive care to manage symptoms and prevent complications. In severe cases, hospitalization may be necessary to provide oxygen therapy and other respiratory support.

Prevention is key in avoiding pulmonary aspergillosis, especially for individuals with weakened immune systems. This includes avoiding exposure to fungal spores, managing underlying health conditions, and taking antifungal medications as prescribed. Early diagnosis and treatment can significantly improve outcomes for those affected by this condition.

There are three main types of silicosis:

1. Acute silicosis: This type of silicosis occurs shortly after exposure to high levels of silica dust and is often seen in workers who have been exposed to very high concentrations of silica for a short period of time, such as in a mines or quarries. Symptoms include coughing, fever, and difficulty breathing.
2. Chronic silicosis: This type of silicosis occurs after long-term exposure to lower levels of silica dust and is the most common form of the disease. Symptoms may not appear until years after exposure and can include shortness of breath, coughing, and fatigue.
3. Accelerated silicosis: This type of silicosis is a combination of acute and chronic silicosis and is typically seen in workers who have been exposed to high levels of silica dust for an extended period of time. Symptoms can include all of those listed for acute and chronic silicosis, as well as weight loss and night sweats.

Silicosis is diagnosed through a combination of physical examination, medical history, and lung function tests. Chest X-rays and CT scans may also be used to confirm the presence of silicosis and assess its severity. There is no cure for silicosis, but treatment can help manage symptoms and slow the progression of the disease. This may include medications to reduce inflammation and improve lung function, as well as respiratory therapy and oxygen therapy. In severe cases, lung transplantation may be necessary.

Prevention is key in reducing the risk of developing silicosis. This includes using proper ventilation and protection equipment when working with silica-containing materials, implementing strict safety protocols, and providing adequate training and education to workers. Regular monitoring of worker exposure levels can also help identify and address any potential risks before they become serious.

In conclusion, silicosis is a debilitating and potentially fatal respiratory disease caused by the inhalation of silica dust. While there is no cure for silicosis, early diagnosis and appropriate treatment can help manage symptoms and slow the progression of the disease. Prevention through proper safety protocols and monitoring of worker exposure levels is crucial in reducing the risk of developing silicosis.

There are several possible causes of lymphocytosis, including:

1. Infection: Lymphocytosis can be caused by a variety of infections, such as viral or bacterial infections.
2. Autoimmune disorders: Conditions such as rheumatoid arthritis, lupus, and multiple sclerosis can cause an abnormal increase in lymphocytes.
3. Cancer: Lymphocytosis can be a symptom of certain types of cancer, such as Hodgkin's disease and non-Hodgkin's lymphoma.
4. Reaction to medication: Certain medications, such as antibiotics and chemotherapy drugs, can cause lymphocytosis.
5. Genetic disorders: Certain genetic disorders, such as X-linked agammaglobulinemia, can cause lymphocytosis.

Symptoms of lymphocytosis may include swollen lymph nodes, fatigue, fever, and weight loss. Treatment depends on the underlying cause of the condition, and may involve antibiotics, chemotherapy, or other medications. In some cases, no treatment is necessary, as the condition may resolve on its own over time.

The common types of RTIs include:

1. Common cold: A viral infection that affects the upper respiratory tract, causing symptoms such as runny nose, sneezing, coughing, and mild fever.
2. Influenza (flu): A viral infection that can affect both the upper and lower respiratory tract, causing symptoms such as fever, cough, sore throat, and body aches.
3. Bronchitis: An inflammation of the bronchial tubes, which can be caused by viruses or bacteria, resulting in symptoms such as coughing, wheezing, and shortness of breath.
4. Pneumonia: An infection of the lungs that can be caused by bacteria, viruses, or fungi, leading to symptoms such as fever, chills, coughing, and difficulty breathing.
5. Tonsillitis: An inflammation of the tonsils, which can be caused by bacteria or viruses, resulting in symptoms such as sore throat, difficulty swallowing, and bad breath.
6. Sinusitis: An inflammation of the sinuses, which can be caused by viruses, bacteria, or fungi, leading to symptoms such as headache, facial pain, and nasal congestion.
7. Laryngitis: An inflammation of the larynx (voice box), which can be caused by viruses or bacteria, resulting in symptoms such as hoarseness, loss of voice, and difficulty speaking.

RTIs can be diagnosed through physical examination, medical history, and diagnostic tests such as chest X-rays, blood tests, and nasal swab cultures. Treatment for RTIs depends on the underlying cause and may include antibiotics, antiviral medications, and supportive care to manage symptoms.

It's important to note that RTIs can be contagious and can spread through contact with an infected person or by touching contaminated surfaces. Therefore, it's essential to practice good hygiene, such as washing hands frequently, covering the mouth and nose when coughing or sneezing, and avoiding close contact with people who are sick.

Berylliosis is characterized by inflammation and scarring in the lungs, which can lead to shortness of breath, coughing, and fatigue. It can also cause lung collapse and respiratory failure. In severe cases, berylliosis can be fatal.

The symptoms of berylliosis can vary depending on the extent of exposure to beryllium, the duration of exposure, and individual susceptibility. Some people may experience mild symptoms, while others may develop more severe disease.

Berylliosis is diagnosed through a combination of medical history, physical examination, lung function tests, and imaging studies such as chest X-rays or CT scans. There is no cure for berylliosis, but treatment options include medications to manage symptoms and slow the progression of the disease, as well as pulmonary rehabilitation.

Prevention is key in avoiding berylliosis, and this includes minimizing exposure to beryllium in workplaces and ensuring proper ventilation and safety measures. Workers handling beryllium should wear protective gear such as masks and gloves, and employers must adhere to strict safety protocols to prevent exposure.

In summary, berylliosis is a serious lung disease caused by exposure to beryllium, with symptoms ranging from mild to severe. Diagnosis is based on a combination of medical history, physical examination, and imaging studies, and treatment involves managing symptoms and slowing the progression of the disease. Prevention is crucial in avoiding berylliosis, which includes minimizing exposure to beryllium in workplaces and ensuring proper ventilation and safety measures.

Examples of acute diseases include:

1. Common cold and flu
2. Pneumonia and bronchitis
3. Appendicitis and other abdominal emergencies
4. Heart attacks and strokes
5. Asthma attacks and allergic reactions
6. Skin infections and cellulitis
7. Urinary tract infections
8. Sinusitis and meningitis
9. Gastroenteritis and food poisoning
10. Sprains, strains, and fractures.

Acute diseases can be treated effectively with antibiotics, medications, or other therapies. However, if left untreated, they can lead to chronic conditions or complications that may require long-term care. Therefore, it is important to seek medical attention promptly if symptoms persist or worsen over time.

There are several types of lung diseases that are classified as obstructive, including:

1. Chronic obstructive pulmonary disease (COPD): This is a progressive condition that makes it hard to breathe and can cause long-term disability and even death. COPD is caused by damage to the lungs, usually from smoking or exposure to other forms of pollution.
2. Emphysema: This is a condition where the air sacs in the lungs are damaged and cannot properly expand and contract. This can cause shortness of breath and can lead to respiratory failure.
3. Chronic bronchitis: This is a condition where the airways in the lungs become inflamed and narrowed, making it harder to breathe.
4. Asthma: This is a condition where the airways in the lungs become inflamed and narrowed, causing wheezing, coughing, and shortness of breath.
5. Bronchiectasis: This is a condition where the airways in the lungs become damaged and widened, leading to thickening of the walls of the airways and chronic infection.
6. Pulmonary fibrosis: This is a condition where the lung tissue becomes scarred and stiff, making it harder to breathe.
7. Lung cancer: This is a malignant tumor that can occur in the lungs and can cause breathing difficulties and other symptoms.

These diseases can be caused by a variety of factors, including smoking, exposure to air pollution, genetics, and certain occupations or environments. Treatment for obstructive lung diseases may include medications, such as bronchodilators and corticosteroids, and lifestyle changes, such as quitting smoking and avoiding exposure to pollutants. In severe cases, surgery or lung transplantation may be necessary.

It's important to note that these diseases can have similar symptoms, so it's important to see a doctor if you experience any persistent breathing difficulties or other symptoms. A proper diagnosis and treatment plan can help manage the condition and improve quality of life.

Symptoms:

* Fever
* Cough
* Chest pain or tightness
* Shortness of breath
* Headache
* Muscle aches
* Fatigue

Diagnosis:

* Physical examination
* Complete blood count (CBC)
* Blood cultures
* Chest X-ray
* Polymerase chain reaction (PCR)

Treatment:

* Antibiotics (macrolides, fluoroquinolones, and aminoglycosides)
* Supportive care (fluids, oxygen therapy, pain management)

Prevention:

* Vaccination (not available in the US)
* Good hand hygiene
* Avoiding close contact with people who are sick

Prognosis:

* Most cases of Mycoplasma pneumoniae pneumonia are mild and resolve quickly with antibiotic treatment.
* In severe cases, the infection can spread to other parts of the body and cause serious complications such as respiratory failure, sepsis, and meningitis.

Epidemiology:

* Mycoplasma pneumoniae is a common cause of community-acquired pneumonia (CAP) worldwide.
* It is more common in children than adults.
* The incidence of Mycoplasma pneumoniae infection varies by age, with the highest incidence in children under 5 years old.

The main cause of ABPA is exposure to airborne spores of the fungus Aspergillus, which are commonly found in soil and decaying organic matter. Individuals with a pre-existing allergic condition may be more susceptible to developing an allergic reaction to these spores, leading to inflammation and damage to the airways.

Diagnosis of ABPA typically involves a combination of physical examination, medical history, and diagnostic tests such as chest X-rays, CT scans, and bronchoscopy with biopsy. Treatment for ABPA typically involves corticosteroids to reduce inflammation and antifungal medications to treat any underlying infection. In severe cases, hospitalization may be necessary to provide oxygen therapy and other supportive care.

Prevention of ABPA includes avoiding exposure to known allergens and maintaining good respiratory hygiene. This can involve regularly cleaning and disinfecting surfaces and objects, using HEPA filters in air purifiers, and wearing a mask when working with or around potentially contaminated materials.

Prognosis for ABPA is generally good if treated promptly and effectively, but untreated cases can lead to serious complications such as respiratory failure and other organ damage. With proper management and prevention strategies in place, individuals with ABPA can lead active and fulfilling lives.

Some of the key features of immediate hypersensitivity include:

1. Rapid onset of symptoms: Symptoms typically occur within minutes to hours of exposure to the allergen.
2. IgE antibodies: Immediate hypersensitivity is caused by the binding of IgE antibodies to surface receptors on mast cells and basophils.
3. Mast cell and basophil activation: The activation of mast cells and basophils leads to the release of histamine and other chemical mediators that cause symptoms.
4. Anaphylaxis: Immediate hypersensitivity can progress to anaphylaxis, a life-threatening allergic reaction that requires immediate medical attention.
5. Specificity: Immediate hypersensitivity is specific to a particular allergen and does not occur with other allergens.
6. Cross-reactivity: There may be cross-reactivity between different allergens, leading to similar symptoms.
7. Prevention: Avoidance of the allergen is the primary prevention strategy for immediate hypersensitivity. Medications such as antihistamines and epinephrine can also be used to treat symptoms.

There are two main types of systemic scleroderma: diffuse cutaneous systemic sclerosis (DCSS) and limited cutaneous systemic sclerosis (LCSS). DCSS is characterized by skin thickening and scar formation over the trunk, arms, and legs, while LCSS is characterized by skin tightening and patches of scaly skin on the hands and face.

The symptoms of systemic scleroderma can include:

* Skin hardening and tightening
* Fatigue
* Joint pain and stiffness
* Muscle weakness
* Swallowing difficulties
* Heartburn and acid reflux
* Shortness of breath
* Raynaud's phenomenon (pale or blue-colored fingers and toes in response to cold temperatures or stress)

The exact cause of systemic scleroderma is not known, but it is believed to involve a combination of genetic and environmental factors. Treatment options for systemic scleroderma include medications to manage symptoms such as pain, stiffness, and swallowing difficulties, as well as physical therapy and lifestyle modifications to improve quality of life.

In summary, systemic scleroderma is a chronic autoimmune disease that affects multiple systems in the body, causing skin hardening and thickening, fatigue, joint pain, and other symptoms. While there is no cure for systemic scleroderma, treatment options are available to manage symptoms and improve quality of life.

1. Chronic bronchitis: This condition causes inflammation of the bronchial tubes (the airways that lead to the lungs), which can cause coughing and excessive mucus production.
2. Emphysema: This condition damages the air sacs in the lungs, making it difficult for the body to take in oxygen and release carbon dioxide.

The main causes of COPD are smoking and long-term exposure to air pollution, although genetics can also play a role. Symptoms of COPD can include shortness of breath, wheezing, and coughing, particularly during exercise or exertion. The disease can be diagnosed through pulmonary function tests, chest X-rays, and blood tests.

There is no cure for COPD, but there are several treatment options available to manage the symptoms and slow the progression of the disease. These include medications such as bronchodilators and corticosteroids, pulmonary rehabilitation programs, and lifestyle changes such as quitting smoking and increasing physical activity. In severe cases, oxygen therapy may be necessary to help the patient breathe.

Prevention is key in avoiding the development of COPD, and this includes not smoking and avoiding exposure to air pollution. Early detection and treatment can also help manage the symptoms and slow the progression of the disease. With proper management, many people with COPD are able to lead active and productive lives.

Orthomyxoviridae infections are a group of viral infections caused by the Orthomyxoviridae family of viruses, which includes influenza A and B viruses, as well as other related viruses. These infections can affect both humans and animals and can cause a range of symptoms, from mild to severe.

The most common type of Orthomyxoviridae infection is seasonal influenza, which occurs when the virus is transmitted from person to person through the air or by contact with infected surfaces. Other types of Orthomyxoviridae infections include:

1. Pandemic influenza: This occurs when a new strain of the virus emerges and spreads quickly around the world, causing widespread illness and death. Examples of pandemic influenza include the Spanish flu of 1918 and the Asian flu of 1957.
2. Avian influenza: This occurs when birds are infected with the virus and can be transmitted to humans through close contact with infected birds or their droppings.
3. Swine influenza: This occurs when pigs are infected with the virus and can be transmitted to humans through close contact with infected pigs or their droppings.
4. H5N1 and H7N9: These are two specific types of bird flu viruses that have caused serious outbreaks in humans in recent years.

Symptoms of Orthomyxoviridae infections can include fever, cough, sore throat, runny nose, muscle aches, and fatigue. In severe cases, these infections can lead to pneumonia, bronchitis, and other respiratory complications, as well as hospitalization and even death.

Diagnosis of Orthomyxoviridae infections is typically made through a combination of physical examination, medical history, and laboratory tests, such as PCR (polymerase chain reaction) or viral culture. Treatment is generally focused on relieving symptoms and supporting the immune system, with antiviral medications may be used in severe cases.

Prevention of Orthomyxoviridae infections can include avoiding close contact with infected birds or pigs, wearing protective clothing and gear when handling animals, and practicing good hygiene such as washing hands frequently. Vaccines are also available for some species of birds and pigs to protect against these viruses.

Overall, Orthomyxoviridae is a family of viruses that can cause serious illness in humans and other animals, and it's important to take precautions to prevent exposure and spread of these viruses.

The symptoms of legionellosis typically develop within two to 14 days after exposure to the bacteria and can include fever, chills, cough, shortness of breath, muscle aches, and headaches. In severe cases, the infection can cause respiratory failure, septic shock, and even death.

Diagnosis of legionellosis is based on a combination of clinical findings, laboratory tests, and environmental investigations to identify potential sources of Legionella exposure. Treatment typically involves antibiotics and supportive care, such as mechanical ventilation and fluid replacement. Prevention strategies include maintaining water systems at temperatures that inhibit bacterial growth, cleaning and disinfecting cooling towers and other water systems regularly, and monitoring water quality regularly.

Legionellosis is a significant public health concern, as it can be difficult to diagnose and treat and can have severe consequences for older adults and those with underlying medical conditions. In the United States, an estimated 20,000 cases of legionellosis occur each year, and the infection is responsible for approximately 10% of all pneumonia cases in hospitalized patients.

RSV infections can cause a range of symptoms, including:

* Runny nose
* Decreased appetite
* Coughing
* Sneezing
* Wheezing
* Apnea (pauses in breathing)
* Blue-tinged skin and lips (cyanosis)
* Fever
* Inflammation of the lower respiratory tract (bronchiolitis)
* Pneumonia

In severe cases, RSV infections can lead to hospitalization and may require oxygen therapy or mechanical ventilation. In rare cases, RSV infections can be life-threatening, particularly in premature babies and infants with underlying medical conditions.

There is no specific treatment for RSV infections, but antiviral medications may be prescribed in severe cases. Treatment focuses on relieving symptoms and managing the infection, such as providing hydration and nutrition, administering oxygen therapy, and monitoring vital signs.

Prevention measures for RSV infections include:

* Frequent handwashing, especially after contact with an infected person or their secretions
* Avoiding close contact with anyone who has RSV infection
* Keeping children home from school or daycare if they are showing symptoms of RSV infection
* Practicing good hygiene, such as avoiding sharing utensils or personal items with anyone who is infected

There is currently no vaccine available to protect against RSV infections, but researchers are working on developing one.

The VLM is characterized by the presence of migrating larvae in the tissues, which can cause inflammation and damage to the affected organs. The symptoms of VLM can vary depending on the severity of the infection and the location of the parasites. Some common symptoms include abdominal pain, diarrhea, nausea, and fever.

The diagnosis of VLM is based on a combination of clinical findings, laboratory tests, and imaging studies such as ultrasound or CT scans. Treatment usually involves the use of anthelmintic drugs to eliminate the parasites from the body. In severe cases, surgery may be necessary to remove affected tissues or organs.

Preventive measures for VLM include avoiding contact with contaminated soil or feces, wearing protective clothing and footwear when working or traveling in areas where the parasite is common, and using safe water and sanitation practices.

In medical field, larva migrans visceral is a type of parasitic infection that affects the viscera (organs within the thoracic and abdominal cavities) and is caused by the larvae of Strongyloides stercoralis.

The term "larva migrans" refers to the migratory movement of the parasite's larvae through the tissues of the host organism. The term "visceral" refers to the location of the infection within the viscera.

CMV infections are more common in people with weakened immune systems, such as those with HIV/AIDS, cancer, or taking immunosuppressive drugs after an organ transplant. In these individuals, CMV can cause severe and life-threatening complications, such as pneumonia, retinitis (inflammation of the retina), and gastrointestinal disease.

In healthy individuals, CMV infections are usually mild and may not cause any symptoms at all. However, in some cases, CMV can cause a mononucleosis-like illness with fever, fatigue, and swollen lymph nodes.

CMV infections are diagnosed through a combination of physical examination, blood tests, and imaging studies such as CT scans or MRI. Treatment is generally not necessary for mild cases, but may include antiviral medications for more severe infections. Prevention strategies include avoiding close contact with individuals who have CMV, practicing good hygiene, and considering immunoprophylaxis (prevention of infection through the use of immune globulin) for high-risk individuals.

Overall, while CMV infections can be serious and life-threatening, they are relatively rare in healthy individuals and can often be treated effectively with supportive care and antiviral medications.

Examples of AROIs include:

1. Pneumocystis pneumonia (PCP): a type of pneumonia caused by the fungus Pneumocystis jirovecii.
2. Tuberculosis (TB): a bacterial infection that can affect the lungs, brain, or other organs.
3. Toxoplasmosis: an infection caused by the parasite Toxoplasma gondii that can affect the brain, eyes, and other organs.
4. Cryptococcosis: a fungal infection that can affect the lungs, brain, or skin.
5. Histoplasmosis: a fungal infection caused by Histoplasma capsulatum that can affect the lungs, skin, and other organs.
6. Aspergillosis: a fungal infection caused by Aspergillus species that can affect the lungs, sinuses, and other organs.
7. Candidiasis: a fungal infection caused by Candida species that can affect the mouth, throat, vagina, or skin.
8. Kaposi's sarcoma: a type of cancer that is caused by the human herpesvirus 8 (HHV-8) and can affect the skin and lymph nodes.
9. Wasting syndrome: a condition characterized by weight loss, fatigue, and diarrhea.
10. Opportunistic infections that can affect the gastrointestinal tract, such as cryptosporidiosis and isosporiasis.

AROIs are a major cause of morbidity and mortality in individuals with HIV/AIDS, and they can be prevented or treated with antimicrobial therapy, supportive care, and other interventions.

There are many different types of collagen diseases, each with its own set of symptoms and characteristics. Some common examples include:

* Osteogenesis imperfecta (OI): A genetic disorder that affects the development of bones and connective tissue, leading to fragile bones, joint deformities, and other complications.
* Ehlers-Danlos syndrome (EDS): A group of genetic disorders that affect the production and structure of collagen, leading to loose joints, bruising, and other symptoms.
* Marfan syndrome: A genetic disorder that affects the body's connective tissue, particularly the heart, blood vessels, and joints. It can cause tall stature, long limbs, and cardiovascular problems.
* Cutis laxa: A rare genetic disorder that affects the production of collagen in the skin, leading to loose, wrinkled skin and other complications.
* Pseudoxanthoma elasticum (PXE): A genetic disorder that affects the elastic tissue in the skin, leading to mineral deposits and changes in the skin's texture and color.

Collagen diseases can be caused by a variety of factors, including genetics, environmental exposures, and autoimmune disorders. Treatment for these conditions can vary depending on the specific type and severity of the disease, but may include medication, physical therapy, and surgery.

There are several forms of pneumoconiosis, including:

* Coal workers' pneumoconiosis (CWP): caused by inhalation of coal dust in coal miners.
* Silicosis: caused by inhalation of silica dust in workers such as quarry workers, miners, and others who work with silica-containing materials.
* Asbestosis: caused by inhalation of asbestos fibers, which can lead to inflammation and scarring of the lungs.
* Hypersensitivity pneumonitis: caused by exposure to specific organic dusts, such as those found in agricultural or woodworking settings.

The symptoms of pneumoconiosis can vary depending on the type and severity of the disease, but may include coughing, shortness of breath, fatigue, and fever. In severe cases, pneumoconiosis can lead to respiratory failure and other complications.

Diagnosis of pneumoconiosis typically involves a combination of physical examination, medical history, and diagnostic tests such as chest X-rays, CT scans, and lung function tests. Treatment for pneumoconiosis may include medications to manage symptoms, pulmonary rehabilitation, and measures to reduce exposure to the offending particles. In severe cases, lung transplantation may be necessary.

Prevention of pneumoconiosis is critical, and this involves implementing appropriate safety measures in workplaces where workers are exposed to dusts or other particles. This can include using respiratory protection equipment, improving ventilation, and reducing exposure to hazardous materials. Early detection and treatment of pneumoconiosis can help to slow the progression of the disease and improve outcomes for affected individuals.

The burden of chronic diseases is significant, with over 70% of deaths worldwide attributed to them, according to the World Health Organization (WHO). In addition to the physical and emotional toll they take on individuals and their families, chronic diseases also pose a significant economic burden, accounting for a large proportion of healthcare expenditure.

In this article, we will explore the definition and impact of chronic diseases, as well as strategies for managing and living with them. We will also discuss the importance of early detection and prevention, as well as the role of healthcare providers in addressing the needs of individuals with chronic diseases.

What is a Chronic Disease?

A chronic disease is a condition that lasts for an extended period of time, often affecting daily life and activities. Unlike acute diseases, which have a specific beginning and end, chronic diseases are long-term and persistent. Examples of chronic diseases include:

1. Diabetes
2. Heart disease
3. Arthritis
4. Asthma
5. Cancer
6. Chronic obstructive pulmonary disease (COPD)
7. Chronic kidney disease (CKD)
8. Hypertension
9. Osteoporosis
10. Stroke

Impact of Chronic Diseases

The burden of chronic diseases is significant, with over 70% of deaths worldwide attributed to them, according to the WHO. In addition to the physical and emotional toll they take on individuals and their families, chronic diseases also pose a significant economic burden, accounting for a large proportion of healthcare expenditure.

Chronic diseases can also have a significant impact on an individual's quality of life, limiting their ability to participate in activities they enjoy and affecting their relationships with family and friends. Moreover, the financial burden of chronic diseases can lead to poverty and reduce economic productivity, thus having a broader societal impact.

Addressing Chronic Diseases

Given the significant burden of chronic diseases, it is essential that we address them effectively. This requires a multi-faceted approach that includes:

1. Lifestyle modifications: Encouraging healthy behaviors such as regular physical activity, a balanced diet, and smoking cessation can help prevent and manage chronic diseases.
2. Early detection and diagnosis: Identifying risk factors and detecting diseases early can help prevent or delay their progression.
3. Medication management: Effective medication management is crucial for controlling symptoms and slowing disease progression.
4. Multi-disciplinary care: Collaboration between healthcare providers, patients, and families is essential for managing chronic diseases.
5. Health promotion and disease prevention: Educating individuals about the risks of chronic diseases and promoting healthy behaviors can help prevent their onset.
6. Addressing social determinants of health: Social determinants such as poverty, education, and employment can have a significant impact on health outcomes. Addressing these factors is essential for reducing health disparities and improving overall health.
7. Investing in healthcare infrastructure: Investing in healthcare infrastructure, technology, and research is necessary to improve disease detection, diagnosis, and treatment.
8. Encouraging policy change: Policy changes can help create supportive environments for healthy behaviors and reduce the burden of chronic diseases.
9. Increasing public awareness: Raising public awareness about the risks and consequences of chronic diseases can help individuals make informed decisions about their health.
10. Providing support for caregivers: Chronic diseases can have a significant impact on family members and caregivers, so providing them with support is essential for improving overall health outcomes.

Conclusion

Chronic diseases are a major public health burden that affect millions of people worldwide. Addressing these diseases requires a multi-faceted approach that includes lifestyle changes, addressing social determinants of health, investing in healthcare infrastructure, encouraging policy change, increasing public awareness, and providing support for caregivers. By taking a comprehensive approach to chronic disease prevention and management, we can improve the health and well-being of individuals and communities worldwide.

The main symptoms of hemosiderosis include:

1. Yellowish discoloration of the skin and eyes (jaundice)
2. Fatigue, weakness, and shortness of breath
3. Abdominal pain, nausea, and vomiting
4. Pale or clay-colored stools
5. Dark urine
6. Liver enlargement and tenderness
7. Heart failure
8. Arrhythmias (irregular heart rhythms)
9. Anemia
10. Weight loss and loss of appetite

Hemosiderosis is diagnosed through a combination of physical examination, medical history, laboratory tests, and imaging studies such as ultrasound, CT scan, or MRI. Treatment options for hemosiderosis depend on the underlying cause of the condition and may include:

1. Iron chelation therapy to remove excess iron from the body
2. Blood transfusions to reduce iron levels
3. Dietary modifications to limit iron intake
4. Medications to manage symptoms such as anemia, liver failure, or heart problems
5. Surgery to remove affected tissues or organs in severe cases

It is important to seek medical attention if you experience any of the symptoms of hemosiderosis, especially if you have a history of excessive iron intake or chronic blood transfusions. Early diagnosis and treatment can help prevent complications and improve outcomes for this condition.

RDS is a common condition in premature babies, but it can also occur in full-term babies if they have certain medical conditions or are exposed to substances during pregnancy that can affect lung development. Symptoms of RDS include rapid breathing, grunting, and flared nostrils. The condition can be diagnosed through chest X-rays or blood tests.

Treatment for RDS typically involves providing oxygen therapy and other supportive care to help the baby breathe more easily. In severe cases, a ventilator may be used to assist with breathing. Surfactant replacement therapy may also be given to help the baby's lungs function properly. With appropriate treatment, most babies with RDS can recover and go on to lead healthy lives. However, in some cases, the condition can be fatal if left untreated or if there are complications such as infection or bleeding in the lungs.

There are several types of emphysema, including:

1. Centriacinar emphysema: This type of emphysema affects the central airways and is often caused by smoking or other forms of respiratory irritation.
2. Paraseptal emphysema: This type of emphysema affects the septal veins and is often caused by smoking or other forms of respiratory irritation.
3. Panacinar emphysema: This type of emphysema affects the entire airway and is often caused by smoking or other forms of respiratory irritation.
4. Cystic fibrosis-related emphysema: This type of emphysema is associated with cystic fibrosis, a genetic disorder that affects the respiratory and digestive systems.

The main symptoms of emphysema are shortness of breath, wheezing, and coughing. The condition can also cause fatigue, chest pain, and difficulty sleeping. Emphysema is often diagnosed through a combination of physical examination, medical history, and diagnostic tests such as chest X-rays or CT scans.

Treatment for emphysema typically involves lifestyle changes such as quitting smoking and avoiding exposure to air pollution, as well as medications such as bronchodilators and corticosteroids. In severe cases, surgery may be necessary to remove damaged lung tissue or to repair damaged blood vessels.

The prognosis for emphysema varies depending on the severity of the condition and the individual's overall health. However, with proper treatment and lifestyle changes, many people with emphysema are able to manage their symptoms and improve their quality of life.

Legionnaires' disease is typically acquired by inhaling aerosolized water droplets contaminated with Legionella bacteria. The most common sources of exposure are cooling towers, hot tubs, and plumbing systems in large buildings. The risk of infection increases with age, and people with weakened immune systems, such as those with cancer, HIV/AIDS, or chronic lung disease, are at greater risk for severe illness and death.

The symptoms of Legionnaires' disease can resemble those of pneumonia and include fever, chills, cough, muscle aches, and shortness of breath. In severe cases, the disease can lead to respiratory failure, septic shock, and even death.

Legionnaires' disease is diagnosed through a combination of physical examination, medical history, and laboratory tests, including blood cultures and urinary antigen tests. Treatment typically involves antibiotics, which can be effective if started early in the course of the illness. In severe cases, hospitalization may be required to provide supportive care, such as mechanical ventilation.

Prevention is key to avoiding Legionnaires' disease, and this includes regularly cleaning and disinfecting cooling towers and plumbing systems, maintaining proper water temperatures, and ensuring that the system is properly designed and maintained. Testing for Legionella bacteria can also be performed to ensure that the system is free of contamination.

In summary, Legionnaires' disease is a severe form of pneumonia caused by the bacterium Legionella pneumophila, typically acquired through inhalation of contaminated aerosolized water droplets. Early diagnosis and treatment are critical to preventing severe illness and death, and prevention measures include regular cleaning and maintenance of cooling towers and plumbing systems, as well as testing for Legionella bacteria.

Tracheomalacia can be caused by a variety of factors, including:

1. Prematurity: Premature babies are at risk for tracheomalacia due to the underdevelopment of their respiratory system.
2. Respiratory infections: Infections such as bronchiolitis or pneumonia can cause inflammation and damage to the trachea, leading to tracheomalacia.
3. Neuromuscular disorders: Conditions such as cerebral palsy or muscular dystrophy can affect the muscles and nerves that control breathing, leading to tracheomalacia.
4. Trauma: Injuries to the neck or throat can cause tracheomalacia by damaging the trachea.
5. Anatomical abnormalities: Abnormalities such as a narrow trachea or a condition called subglottic stenosis can increase the risk of tracheomalacia.

Symptoms of tracheomalacia may include:

1. Stridor: A high-pitched sound when breathing in.
2. Wheezing: A whistling sound when breathing out.
3. Difficulty breathing.
4. Coughing or gasping for air.
5. Chest retractions (the chest sinks in with each breath).
6. Blue tinge to the skin (cyanosis).

Diagnosis of tracheomalacia is typically made based on a physical examination and medical history, as well as imaging tests such as X-rays or endoscopy. Treatment for tracheomalacia may include:

1. Oxygen therapy: Providing extra oxygen to help the baby breathe easier.
2. Nasal continuous positive airway pressure (nCPAP): A machine that delivers a steady stream of air into the nose to help keep the airways open.
3. Endotracheal tube: In severe cases, a tube may be inserted through the mouth or nose and into the trachea to help the baby breathe.
4. Surgery: In some cases, surgery may be necessary to repair any underlying anatomical abnormalities or to remove any blockages in the airway.
5. Medications: May be used to help manage symptoms such as stridor or wheezing.

It is important to note that tracheomalacia is a serious condition and requires prompt medical attention to prevent complications and ensure proper treatment. With appropriate treatment, most babies with tracheomalacia can recover and lead normal, healthy lives.

Some common examples of respiratory tract diseases include:

1. Pneumonia: An infection of the lungs that can be caused by bacteria, viruses, or fungi.
2. Bronchitis: Inflammation of the airways (bronchi) that can cause coughing, wheezing, and difficulty breathing.
3. Asthma: A chronic condition that causes inflammation and narrowing of the airways, leading to symptoms such as wheezing, coughing, and shortness of breath.
4. Chronic obstructive pulmonary disease (COPD): A progressive condition that makes it difficult to breathe due to damage to the lungs over time.
5. Tuberculosis: An infectious disease caused by the bacteria Mycobacterium tuberculosis that primarily affects the lungs.
6. Laryngitis: Inflammation of the voice box (larynx) that can cause hoarseness and difficulty speaking.
7. Tracheitis: Inflammation of the trachea, or windpipe, that can cause coughing, fever, and difficulty breathing.
8. Croup: An infection of the throat and lungs that can cause a barky cough and difficulty breathing.
9. Pleurisy: Inflammation of the lining around the lungs (pleura) that can cause chest pain, fever, and difficulty breathing.
10. Pertussis (whooping cough): An infectious disease caused by the bacteria Bordetella pertussis that can cause coughing fits and difficulty breathing.

These are just a few examples of the many different types of respiratory tract diseases that exist. Each one has its own unique symptoms, causes, and treatment options.

The risk factors for developing bronchogenic carcinoma include smoking, exposure to secondhand smoke, exposure to radon gas, asbestos, and certain industrial chemicals, as well as a family history of lung cancer. Symptoms of bronchogenic carcinoma can include coughing, chest pain, difficulty breathing, fatigue, weight loss, and coughing up blood.

Bronchogenic carcinoma is diagnosed through a combination of imaging tests such as chest x-rays, computed tomography (CT) scans, and positron emission tomography (PET) scans, as well as biopsy. Treatment options for bronchogenic carcinoma can include surgery, radiation therapy, chemotherapy, or a combination of these. The prognosis for bronchogenic carcinoma is generally poor, with a five-year survival rate of about 18%.

Prevention is the best approach to managing bronchogenic carcinoma, and this includes quitting smoking, avoiding exposure to secondhand smoke and other risk factors, and getting regular screenings if you are at high risk. Early detection and treatment can improve survival rates for patients with bronchogenic carcinoma, so it is important to seek medical attention if symptoms persist or worsen over time.

There are several possible causes of airway obstruction, including:

1. Asthma: Inflammation of the airways can cause them to narrow and become obstructed.
2. Chronic obstructive pulmonary disease (COPD): This is a progressive condition that damages the lungs and can lead to airway obstruction.
3. Bronchitis: Inflammation of the bronchial tubes (the airways that lead to the lungs) can cause them to narrow and become obstructed.
4. Pneumonia: Infection of the lungs can cause inflammation and narrowing of the airways.
5. Tumors: Cancerous tumors in the chest or throat can grow and block the airways.
6. Foreign objects: Objects such as food or toys can become lodged in the airways and cause obstruction.
7. Anaphylaxis: A severe allergic reaction can cause swelling of the airways and obstruct breathing.
8. Other conditions such as sleep apnea, cystic fibrosis, and vocal cord paralysis can also cause airway obstruction.

Symptoms of airway obstruction may include:

1. Difficulty breathing
2. Wheezing or stridor (a high-pitched sound when breathing in)
3. Chest tightness or pain
4. Coughing up mucus or phlegm
5. Shortness of breath
6. Blue lips or fingernail beds (in severe cases)

Treatment of airway obstruction depends on the underlying cause and may include medications such as bronchodilators, inhalers, and steroids, as well as surgery to remove blockages or repair damaged tissue. In severe cases, a tracheostomy (a tube inserted into the windpipe to help with breathing) may be necessary.

The primary symptoms of silo filler's disease are:

1. Coughing and shortness of breath
2. Chest tightness and pain
3. Fatigue and fever
4. Weight loss and night sweats
5. In extreme cases, respiratory failure can occur.

The disease is diagnosed through a combination of physical examination, chest X-rays, and lung function tests. Treatment typically involves antibiotics to control infection and medication to reduce inflammation. In severe cases, hospitalization may be required.

Prevention of silo filler's disease includes:

1. Improving ventilation in confined spaces where grain is stored
2. Using protective equipment such as respirators and gloves
3. Regularly cleaning and disinfecting equipment and facilities
4. Providing education and training on safe working practices to workers.

Silo filler's disease is an occupational lung disease that can have serious consequences for those who work with grain in confined spaces. It is important for employers and workers to be aware of the risks and take appropriate measures to prevent exposure and reduce the risk of developing this condition.

Altraja A, Nigol K, Altraja S, Viitak A (2012-03-12). "Increased bronchoalveolar lavage fluid tin content in stannosis". Chest ... In comparison to health, non-tinning workers, the patient had significantly higher bronchoalveolar lavage fluid (BLAF) ...
"Vitamin E Acetate in Bronchoalveolar-Lavage Fluid Associated with EVALI". New England Journal of Medicine. 382 (8): 697-705. ... "The Chemical Components of Electronic Cigarette Cartridges and Refill Fluids: Review of Analytical Methods". Nicotine & Tobacco ...
Samples from bronchoalveolar lavage fluid specimens returned the highest sensitivity. The authors argued that CT scans showed ...
... diagnosis using routinely processed smears of bronchoalveolar lavage fluid". Journal of Clinical Pathology. 50 (12): 981-4. doi ... and ultrastructural findings in bronchoalveolar lavage fluid". Diagnostic Cytopathology. 24 (6): 389-95. doi:10.1002/dc.1086. ... The reported treatment of PAP using therapeutic bronchoalveolar lavage was in 1960 by Dr. Jose Ramirez-Rivera at the Veterans' ... Lung washings or tissue for histopathologic analysis are most commonly obtained using bronchoalveolar lavage and/or lung biopsy ...
Assessment of alveolar crystal burden in bronchoalveolar lavage fluid may aid diagnosis. For uncomplicated silicosis, chest x- ... fluid in the lungs), pneumonia, or tuberculosis. Using workplace controls, silicosis is almost always a preventable disease. ...
Inhaled pentamidine is mainly deposited into the bronchoalveolar lavage fluid of the lungs. Metabolism: Pentamidine is ... When inhaled through a nebulizer, pentamidine accumulates in the bronchoalveolar fluid of the lungs at a higher concentration ... Ample fluids or intravenous hydration may prevent some nephrotoxicity. Liver: Elevated liver enzymes are associated with ... Additionally, pentamidine does not reach curative levels in the cerebrospinal fluid. It has a volume of distribution of 286- ...
... it is present in bronchoalveolar lavage fluid from cats undergoing experimentally induced asthma; it stimulates the local ...
"Osteopontin is increased in the bronchoalveolar lavage fluid and bronchial tissue of smoking asthmatics". Cytokine. 61 (3): 713 ... PD patients serum and cerebrospinal fluid (CSF) concentrations of OPN were studied, it shows that OPN levels in the body fluid ...
2001). "Human bronchoalveolar lavage fluid protein two-dimensional database: study of interstitial lung diseases". ...
The sample types were bronchoalveolar lavage (BAL) fluid samples (fluid samples collected from the lungs). The chemical was ... In May 2019, a 21-year-old was hospitalized for more than two weeks due to fluid in his lungs and was in a medically induced ... necessitating a medically induced coma and removal of fluid from the lungs. Vomiting, coughing up blood, and lipid pneumonia ... My Lungs Were Full of Fluid'". People. Bojórquez, Kim (6 August 2019). "What Utah doctors are saying about vaping". Deseret ...
Allergen inhalation challenge of humans produces rises in the PGD2 levels in their Bronchoalveolar lavage fluids. Furthermore, ...
Wattiez R, Hermans C, Bernard A, Lesur O, Falmagne P (June 1999). "Human bronchoalveolar lavage fluid: two-dimensional gel ...
2015). "High-throughput sequencing of 16S rDNA amplicons characterizes bacterial composition in bronchoalveolar lavage fluid in ... Bronchoalveolar lavage (BAL) (also known as bronchoalveolar washing) is a diagnostic method of the lower respiratory system in ... "Therapeutic limited bronchoalveolar lavage with fiberoptic bronchoscopy as a bridging procedure prior to total lung lavage in a ... Bronchoalveolar lavage can be a more sensitive method of detection than nasal swabs in respiratory molecular diagnostics, as ...
Typical inclusions called "Leventhal-Cole-Lillie bodies" can be seen within macrophages in BAL (bronchoalveolar lavage) fluid. ...
"De Novo Assembly of the Pneumocystis jirovecii Genome from a Single Bronchoalveolar Lavage Fluid Specimen from a Patient". mBio ... The genome of P. jirovecii has been sequenced from a bronchoalveolar lavage sample. The genome is small, low in G+C content, ... Fluid leaks into alveoli, producing an exudate seen as honeycomb/cotton candy appearance on hematoxylin and eosin-stained ... and those that have been detected in many mammals are only known from molecular sample detection from lung tissue or fluids, ...
"Novel Neutrophil-derived Proteins in Bronchoalveolar Lavage Fluid Indicate and Exaggerated Inflammatory Response in Pediatric ... "Costs of Bronchoalveolar Lavage-Directed Therapy in the First 5 Years of Life for Children with Cystic Fibrosis". Journal of ... "Effect of Bronchoalveolar Lavage-directed Therapy on Pseudomonas Aeruginosa Infection and Structural Lung Injury in Children ... "Safety of Bronchoalveolar Lavage in Young Children with Cystic Fibrosis". Pediatric Pulmonology. 43 (10): 965-72. doi:10.1002/ ...
Bronchoalveolar Lavage Fluid". PLOS ONE. 10 (5): e0124194. doi:10.1371/journal.pone.0124194. ISSN 1932-6203. Galvão, Klibs N.; ...
Mizuki M, Komatsu H, Akiyama Y, Iwane S, Tsuda T (1999). "Inhibition of eosinophil activation in bronchoalveolar lavage fluid ...
... bronchoalveolar lavage fluids, and conjunctival smears. Definitive diagnosis can also be achieved through fluorescein-tagged ...
Eosinophilic bronchitis is characterized by eosinophils in sputum and in bronchoalveolar lavage fluid without airway ... A cough is a sudden expulsion of air through the large breathing passages that can help clear them of fluids, irritants, ...
The bronchoalveolar lavage (BAL) fluid of patients with idiopathic pulmonary fibrosis contains a higher concentration of ATP ... Following tissue injury in patients with Graft-versus-host disease (GVHD), ATP is released into the peritoneal fluid. It binds ...
If this is unavailable, a bronchoalveolar lavage can be done, and the bronchial wash fluid can be examined for eosinophils. The ... is also significantly increased in the bronchial wash fluid of eosinophilic bronchitis patients compared to asthmatic patients ...
IL-13 expression has demonstrated to be increased in bronchoalveolar lavage (BAL) fluid and cells in patients with atopic mild ...
... in broncho-alveolar lavage fluids of ARDS, it can be observed trichomonads, which are unicellular flagellated parasites of the ... Fewer cases of ARDS are linked to large volumes of fluid used during post-trauma resuscitation. ARDS is a form of fluid ... Generally, radiographic findings of fluid accumulation (pulmonary edema) affecting both lungs and unrelated to increased ... ISBN 978-0-7817-3548-3. Cherkas, David (Nov 2011). "Traumatic Hemorrhagic Shock: Advances In Fluid Management". Emergency ...
... bronchoalveolar lavage fluids (BAL), nasal lavage fluids (NLF), sputum, among others. The identification and quantification of ...
Neutrophils, beta-defensins, leukotrienes, and chemokines can also be detected in bronchoalveolar lavage fluid injected then ... has a normal neutrophil count detected in BAL fluid, and blood gas (an arterial blood test that measures the amount of oxygen ...
Similarly, increased levels of 5-oxo-ETE have been detected in the bronchoalveolar lavage fluid following the inhalation of ...
... can be measured in a number of biological fluids including bronchoalveolar lavage fluid (BALF) from asthmatic patients. " ... and limit markers of inflammation such as eosinophil counts in the peripheral blood and bronchoalveolar lavage fluid. This ...
... or when increased eosinophils are found in fluid obtained by a bronchoscopy (bronchoalveolar lavage fluid). Association with ... of white blood cells in fluid obtained by bronchoalveolar lavage. Other typical laboratory abnormalities include an elevated ... changes in multiple areas and fluid in the area surrounding the lungs on a chest X-ray, and eosinophils comprising more than 25 ...
... bronchoalveolar lavage, lung biopsy, cerebrospinal fluid or brain biopsy specimens on selective agar allows differentiation ... Cryptococcal antigen testing from serum or cerebrospinal fluid is a useful preliminary test for cryptococcal infection, and has ...
Flexible bronchoscopy is often used to gather samples of bronchoalveolar lavage for quantitative bacteriological tests as well ... If there is a large accumulation of fluid within the lungs, drainage of the fluid may also aid in the healing process. ... They make up the majority of normal oral flora and the presence of putrid fluid in the lungs is highly suggestive of aspiration ... Chemical pneumonitis is caused by damage to the inner layer of lung tissue, which triggers an influx of fluid. The inflammation ...
... to the overall abnormal airway epithelial damage and there is a significant correlation between RL and bronchoalveolar lavage ... Moreover, the injury to epithelial cells handicaps the lung's ability to pump fluid out of airspaces. Fluid filled airspaces, ... Song W, Wei S, Zhou Y, Lazrak A, Liu G, Londino JD, Squadrito GL, Matalon S. (2010) Inhibition of lung fluid clearance and ... In the acute phase of ALI, there is increased permeability of this barrier and protein rich fluid leaks out of the capillaries ...
Trough insulin levels in bronchoalveolar lavage following inhaled human insulin (Exubera®) in patients with diabetes mellitus. ... Metabolic hormones, apolipoproteins, adipokines, and cytokines in the alveolar lining fluid of healthy adults: ...
Some lacritin was reported in lung bronchoalveolar lavage and plasma. In lacrimal gland, polarized lacrimal acinar cells appear ... protein in the tear fluid is a potential biomarker of dry eye syndrome". PLOS ONE. 7 (12): e51979. Bibcode:2012PLoSO...751979A ... Lacritin is a glycoprotein of the human tear film, and to a lesser extent of saliva, lung lavage and plasma. It is mainly ... "Quantitative Analysis of N-linked Glycoproteins in Tear Fluid of Climatic Droplet Keratopathy by Glycopeptide Capture and iTRAQ ...
In 2018, a bronchoalveolar lavage technique was proposed for tuberculosis diagnosis in elephants. This technique is safer to ... The European Association of Zoos and Aquaria's (EAZA) treatment guidelines recommend administering fluid therapy, fresh plasma ... "Bronchoalveolar lavage for diagnosis of tuberculosis infection in elephants". Epidemiology and Infection. 146 (4): 481-488. doi ...
Bronchoalveolar lavage (BAL) is a procedure whereby a small volume of fluid is put into the airways in order sample the cells ... Cytopathology (examination under a microscope) of either a tracheal wash or a bronchoalveolar lavage sample can determine ... McKane, SA; Rose, RJ (10 June 2010). "Effects of exercise intensity and training on bronchoalveolar lavage cytology". Equine ... Doucet, Michele Y.; Viel, Laurent (May 2002). "Alveolar Macrophage Graded Hemosiderin Score from Bronchoalveolar Lavage in ...
To view abnormalities of the airway To obtain tissue specimens of the inside the lungs by biopsy, bronchoalveolar lavage, or ... is a medical emergency and should be addressed with initiation of intravenous fluids and examination with rigid bronchoscopy. ...
A bronchoalveolar lavage can show an elevated (of at least 3.5) CD4/CD8 T cell ratio, which is indicative (but not proof) of ... In at least one study the induced sputum ratio of CD4/CD8 and level of TNF was correlated to those in the lavage fluid. A ... Cardiac sarcoidosis can cause fibrosis, granuloma formation, or the accumulation of fluid in the interstitium of the heart, or ...
... can be definitively confirmed by histological identification of the causative organism in sputum or bronchoalveolar lavage ( ... Notably, simple molecular detection of P. jirovecii in lung fluids does not mean that a person has PCP or infection by HIV. The ...
Subsequent studies of bronchoalveolar lavage fluid from pediatric patients with asthma and also other severe chronic ... Webley WC, Salva PS, Andrzejewski C, Cirino F, West CA, Tilahun Y, Stuart ES (May 2005). "The bronchial lavage of pediatric ... Chlamydia pneumoniae has also been found in the cerebrospinal fluid of patients diagnosed with multiple sclerosis. Chlamydia ...
These other tests may include basic blood work, blood cultures, and bronchoalveolar lavage.[citation needed] The clinical ... An X-ray that shows ARDS is necessary for diagnosis (fluid in the small air sacs (alveoli) in both lungs). In addition, a ... The presence of fluid means the person experiences a feeling similar to 'drowning'. Difficulties breathing can quickly progress ...
... bronchoalveolar lavage fluid of BAL) and human eosinophils, which are implicated in contributing to human asthma, metabolize ... "Lipidomic Profiling of Serum and Pancreatic Fluid in Chronic Pancreatitis". Pancreas. 41 (4): 518-22. doi:10.1097/MPA. ...
... can be measured in a number of biological fluids including bronchoalveolar lavage fluid (BALF) from asthmatic patients. ...
In suspected ventilator-associated pneumonia it has been suggested that bronchoscopy or bronchoalveolar lavage is necessary ... In case of pleural effusion, thoracentesis is performed for examination of pleural fluid. ...
... for bronchoalveolar lavage. The likelihood of detecting the virus depends on collection method and how much time has passed ... RDTs may process blood samples, saliva samples, or nasal swab fluids. RDTs produce colored lines to indicate positive or ...
... a bronchoalveolar lavage might be taken by an experienced pneumologist. If no bacteria or fungi grow, the culture is negative. ... Sputum is a thick fluid produced in the lungs and in the adjacent airways. Normally, fresh morning sample is preferred for the ...
Bronchoscopy and bronchoalveolar lavage can be part of the clinical and diagnostic workup of e-cigarette, or vaping, product ... Bronchoscopy and bronchoalveolar lavage can be part of the clinical and diagnostic workup of e-cigarette, or vaping, product ... Evaluation of Bronchoalveolar Lavage Fluid from Patients in an Outbreak of E-cigarette, or Vaping, Product Use-Associated Lung ... Evaluation of Bronchoalveolar Lavage Fluid from Patients in an Outbreak of E-cigarette, or Vaping, Product Use-Associated Lung ...
Smith LJ, Houston M, Anderson J. Increased levels of glutathione in bronchoalveolar lavage fluid from patients with asthma. ... Increased levels of glutathione in bronchoalveolar lavage fluid from patients with asthma. / Smith, L. J.; Houston, M.; ... Smith, L. J. ; Houston, M. ; Anderson, J. / Increased levels of glutathione in bronchoalveolar lavage fluid from patients with ... Smith, L. J., Houston, M., & Anderson, J. (1993). Increased levels of glutathione in bronchoalveolar lavage fluid from patients ...
... bronchoalveolar lavage (BAL), and endotracheal aspirates (EA) was prospectively evaluated in a series of 28 mechanically ... Bronchoalveolar Lavage Fluid / microbiology * Evaluation Studies as Topic * Female * Humans * Lung / microbiology ... The diagnostic accuracy of protected-specimen brush (PSB), bronchoalveolar lavage (BAL), and endotracheal aspirates (EA) was ... Values of 10(3) cfu/ml of Ringers solution, 10(4) cfu/ml of retrieved fluid, and 10(6) cfu/ml of respiratory secretions were ...
BAL, bronchoalveolar lavage; BALF, BAL fluid; BL, bronchial lavage; BMI, body mass index; CAPA, COVID-19-associated pulmonary ...
nov., a novel anaerobic bacterium isolated from human bronchoalveolar lavage fluid.. Sun, Yifan; Wang, Likun; Han, Dexing; Li, ... Two related anaerobic strains, designated as SWB101512T and SWB19611, were isolated from the bronchoalveolar lavage fluid of ...
We examined cell-free human bronchoalveolar lavage fluid (BALF) for enzymes of the 5-lipoxygenase pathway. BALF was obtained ... Most conjecture about fluid transport is based on measurements of Na+ and Cl- transport performed under short circuit ... Therefore, we measured fluid transport and mucosal electrolyte composition in primary cultures of CF airway epithelia without ... But in striking contrast to predictions based on Ussing chamber studies, CF epithelia absorbed fluid at a rate no greater than ...
Bronchoalveolar lavage (BAL) fluid for bacterial, viral, fungal, [99, 122] and AFB stains and cultures; direct fluorescent ... it is not a fixed phenomenon but represents a fluid process. [26] ...
Bronchoalveolar Lavage Fluid. 2. 2020. 841. 1.280. Why? Placenta Diseases. 3. 2022. 188. 1.040. Why? ...
estimated the proportion of CD163+ macrophages in bronchoalveolar lavage fluids by immunocytochemistry [32]. The proportion of ...
Abbreviations: CXCL10, C-X-C motif chemokine ligand 10; BALF, cell-free bronchoalveolar lavage fluid; HNS, healthy non-smokers ... Abbreviations: IL-36α, interleukin-36α; BALF, cell-free bronchoalveolar lavage fluid; FEV1, forced expiratory volume in 1 ... Abbreviations: BALF, cell-free bronchoalveolar lavage fluid; HNS, healthy non-smokers; LTS, long-term smokers without COPD; LTS ... Abbreviations: IL-8, interleukin-8; BALF, cell-free bronchoalveolar lavage fluid; HNS, healthy non-smokers; LTS, long-term ...
Plasma and bronchoalveolar lavage fluid oxylipin levels in experimental porcine lung injury ... Multi-platform metabolomics assays for human lung lavage fluids in an air pollution exposure study ... Mass spectrometry profiling of oxylipins, endocannabinoids, and N-acylethanolamines in human lung lavage fluids reveals ... Oxylipins in cerebrospinal fluid in clinically isolated syndrome and relapsing remitting multiple sclerosis ...
Evaluation of centrifugation cultures of bronchoalveolar lavage fluid for the diagnosis of cytomegalovirus pneumonitis. 2854035 ... associations between viral load in bronchoalveolar lavage samples, viral RNA detection in serum samples, and clinical outcomes ... Recovery of human immunodeficiency virus type 1 from supernatant fluid of routine viral cultures. 2768453 J Clin Microbiol, ... Haemophilus influenzae and Streptococcus pneumoniae infections in children with cerebrospinal fluid shunts. 19609096 Pediatr ...
Vitamin E Acetate in Bronchoalveolar-Lavage Fluid Associated with EVALI. N Eng J Med [Internet]. 2019 Dec 20 [cited 2019 Dec 23 ...
Bronchoalveolar lavage fluid (BALF), tracheas and lungs were collected. HDE stimulated a 2-4 fold increase in lung and tracheal ... elevated lavage fluid cytokines/chemokines including interleukin-6 (IL-6), and the development of significant lung pathology. ... Similarly, alcohol-fed mice demonstrated significantly less IL-6 in lung lavage in response to dust than that observed in ...
Objective-To determine cytologic and microbiologic findings in bronchoalveolar lavage (BAL) fluid and SpO 2 values obtained ... Results of cytologic and microbiologic analysis of bronchoalveolar lavage fluid in New Zealand White rabbits ... Percentage fluid recovered, total leukocyte counts, and differential cell counts were determined. Aerobic and anaerobic ... Results-Mean ± SD percentage fluid volumes recovered from LB2 and RB4 were 53 ± 13% and 63 ± 13%, respectively. Mean ± SD total ...
Evaluation of PCR in bronchoalveolar lavage fluid for diagnosis of Pneumocystis jirovecii pneumonia: a bivariate meta-analysis ... Hohenadel IA, Kiworr M, Genitsariotis R, Zeidler D, Lorenz J. Role of bronchoalveolar lavage in immunocompromised patients with ... allows collection of diagnostic samples by bronchoalveolar lavage (BAL), fibrobronchial aspirate (FBAS), and protected specimen ... CT of AML patient with a fungal pneumonia in the right upper lobe characterized by a cavitary lesion without air fluid levels. ...
Eosinophil (left panel) and lymphocyte (right panel) counts were determined in bronchoalveolar lavage fluid (BALF) 24h after ...
2016). Characterization of microbiome in bronchoalveolar lavage fluid of patients with lung cancer comparing with benign mass ...
Lymphadenopathy-associated virus isolated from bronchoalveolar lavage fluids in AIDS-related complex with lymphoid interstitial ... fluid Body fluids and procedures for which hand-washing is sufficient for preventing transmission of blood-borne pathogens ( ... alveolar fluid (6), saliva (7-9), tears (10), throat swabs (11) and cerebrospinal fluid (12). HIV nucleic acid sequences have ... Body fluids to which universal precautions apply - Blood - Any body fluid containing visible blood - Semen and vaginal ...
Altered microRNA profiles in bronchoalveolar lavage fluid exosomes in asthmatic patients. J Allergy Clin Immunol. 2013 Mar; 131 ...
The agency said that the chemical was found in the bronchoalveolar lavage fluid of 48 of 51 EVALI patients who were tested. The ...
... an endotracheal aspirate or bronchoalveolar lavage fluid) collected, if possible.. For severely ill persons, multiple ... disposable fluid-resistant coveralls, and disposable head cover or hair cover. PPE should be worn when in direct or close ...
... bronchoalveolar lavage fluid. American Review of Respiratory Disease, 1991, 143:1121-1129. ... isolation of pathogenic bacteria from endotracheal aspiration/blood/pleural fluid; and increasing oxygen requirements; and ...
Microscopic examination of intracellular organisms in protected bronchoalveolar mini-lavage fluid for the diagnosis of ...
Elevated levels of IL-8 have been found in the bronchoalveolar lavage fluid of smokers and COPD patients that correlated ... it has been demonstrated that increased amounts of MMPs and especially MMP-9 are found in bronchoalveolar lavage fluid from ... 12 have been found in bronchoalveolar lavage samples of COPD patients [9]. ... Increased levels of interleukin-8 in BAL fluid from smokers susceptible to pulmonary emphysema. Thorax 57:405-411 ...
Monocyte depletion resulted in reductions in lung wet:dry ratios, bronchoalveolar lavage fluid protein, and perfusate levels of ... METHODS: Longitudinal samples of perfusate, bronchoalveolar lavage, and tissue from 42 human donor lungs undergoing clinical ...
If they arent going by total bronchoalveolar lavage fluid particle or mass load, in which even heaviest pot smokers have an ...
  • The neutrophil-related cytokines IL-36α, -β and -γ were quantified (ELISA) along with IL-6, IL-8, INF-γ and CXCL10 (U-Plex ® ) in plasma and cell-free BAL fluid (BALF). (dovepress.com)
  • Bronchoalveolar lavage fluid (BALF), tracheas and lungs were collected. (cdc.gov)
  • The quality of case-associated BAL specimens was assessed by measuring dipalmitoylphosphatidylcholine (DPPC), the principal phospholipid in naturally-occurring lung surfactant: the presence of acceptable levels of DPPC confirms that the lavage procedure recovered adequate pulmonary epithelial fluid. (cdc.gov)
  • Two related anaerobic strains , designated as SWB101512T and SWB19611, were isolated from the bronchoalveolar lavage fluid of two lung cancer patients . (bvsalud.org)
  • The diagnostic accuracy of protected-specimen brush (PSB), bronchoalveolar lavage (BAL), and endotracheal aspirates (EA) was prospectively evaluated in a series of 28 mechanically ventilated patients (MV patients) who died within 3 d of the bronchoscopic procedure, using postmortem lung examination as the gold standard for establishing the diagnosis of pneumonia. (nih.gov)
  • Previously, we have shown in a mouse model that exposure to hog dust extract (HDE) collected from a CAFO results in the activation of protein kinase C (PKC), elevated lavage fluid cytokines/chemokines including interleukin-6 (IL-6), and the development of significant lung pathology. (cdc.gov)
  • Similarly, alcohol-fed mice demonstrated significantly less IL-6 in lung lavage in response to dust than that observed in control mice instilled with HDE. (cdc.gov)
  • The fluids recovered from the first 20-ml aliquot and that from the next four aliquots were labeled bronchial and alveolar fluid, respectively. (northwestern.edu)
  • During August-October 2019, BAL fluid specimens were collected by clinical teams caring for hospitalized EVALI patients. (cdc.gov)
  • Among the 27 BAL fluid specimens with sufficient volume for testing, all had measurable levels of DPPC. (cdc.gov)
  • HIV has been isolated from blood (2), semen (2), vaginal and cervical secretions (3), amniotic fluid (4), breast milk (5), alveolar fluid (6), saliva (7-9), tears (10), throat swabs (11) and cerebrospinal fluid (12). (cdc.gov)
  • Free HIV, not associated with cells, has also been isolated from plasma and cerebrospinal fluid but its contribution to transmission is not well-documented (5,12,14). (cdc.gov)
  • To expedite and automate raw sample processing for clinical diagnostics, we introduce an on-chip sample preparation and immunosubtraction diagnostic for emergency room screening of cerebrospinal fluid (CSF) rhinorrhea. (berkeley.edu)
  • We have examined the production of MIP-1 alpha using sera, synovial fluid (SF), and synovial tissue (ST) from 63 arthritic patients. (jci.org)
  • sputum, bronchoalveolar lavage (BAL), sinus discharge, urine and synovial fluid collected from HAI suspected patients with clinical symptoms after hospitalization. (who.int)
  • a similar trend was seen in the alveolar fluid (36.5 ± 9.4 vs 23.3 ± 3.0 μM/mg protein). (northwestern.edu)
  • The efficacy of TGA was determined through the measurement of airway inflammation, bronchoconstriction, serum IgE levels, and bronchoalveolar lavage fluid cytokine and eicosanoid levels. (uncg.edu)
  • Bronchoscopy and bronchoalveolar lavage † (BAL) can be part of the clinical and diagnostic workup of EVALI patients. (cdc.gov)
  • To better characterize exposure among EVALI patients, CDC developed and validated isotope dilution mass spectrometry methods to analyze specific toxicants of concern and active compounds in case-associated BAL fluid. (cdc.gov)
  • Patients with asthma generate increased amounts of reactive oxygen species (ROS) from peripheral blood cells and cells recovered by bronchoalveolar lavage (BAL). (northwestern.edu)
  • The present study was designed to begin to explore these defenses by measuring superoxide dismutase (SOD) and catalase activities and total glutathione (GSH) levels in BAL fluid from normal subjects and patients with mild asthma. (northwestern.edu)
  • The agency said that the chemical was found in the bronchoalveolar lavage fluid of 48 of 51 EVALI patients who were tested. (wtkr.com)
  • Values of 10(3) cfu/ml of Ringer's solution, 10(4) cfu/ml of retrieved fluid, and 10(6) cfu/ml of respiratory secretions were used as cutoff points for quantitative PSB, BAL, and EA cultures, respectively. (nih.gov)
  • nov., a novel anaerobic bacterium isolated from human bronchoalveolar lavage fluid. (bvsalud.org)
  • To provide guidance for implementing such practices, this article reviews how HIV is transmitted, including the presence of HIV in various body fluids and the risk of transmission after various exposures, and provides specific guidelines for preventing the transmission of HIV in settings where children are cared for. (cdc.gov)
  • The serious nature of HIV infection, the presence of HIV in a variety of body fluids and the close contact that children often enjoy with their playmates and caretakers have combined to generate considerable concern about HIV transmission in homes, schools, day-care centers and playgrounds. (cdc.gov)
  • Presence of HIV in body fluids. (cdc.gov)
  • Neutrophils were quantified in blood and bronchoalveolar lavage samples (BAL). (dovepress.com)
  • This 2019 image depicted a Centers for Disease Control and Prevention (CDC) laboratory technician, dressed in personal protective equipment (PPE), in the process of pipetting samples of bronchoalveolar lavage (BAL) fluid, which would undergo analysis, here, in this laboratory environment. (cdc.gov)
  • however, these fluids theoretically may contain HIV if they are contaminated with blood. (cdc.gov)
  • These CDC analytic methods can identify vitamin E acetate, MCT oil (medium chain triglycerides), plant oils (long chain triglycerides), petroleum distillates (including mineral oil), diluent terpenes, cannabinoids, and nicotine in BAL fluid. (cdc.gov)
  • If they aren't going by total bronchoalveolar lavage fluid particle or mass load, in which even heaviest pot smokers have an advantage over filter cigarette smokers, I don't want to know about it. (jwz.org)
  • Control of fluid streams is useful in biological processing, chemical reaction engineering, and creating structured materials. (berkeley.edu)
  • However, general strategies to engineer the cross-sectional form and motion of fluid streams have been limited. (berkeley.edu)
  • Strategies to mix fluid and control particles using engineered systems exist, often relying on chaotic fluid transformations to disrupt sustained regions of order in the flow. (berkeley.edu)
  • Comparative analysis of inhaled particles contained in human bronchoalveolar lavage fluids, lung parenchyma and lymph nodes. (nih.gov)
  • 16. Intracellular detection of interleukin 17 and other cytokines in human bronchoalveolar lavage fluid: a first assessment. (nih.gov)
  • Using the BAL fluid, we performed isotope dilution mass spectrometry to measure several priority toxicants: vitamin E acetate, plant oils, medium-chain triglyceride oil, coconut oil, petroleum distillates, and diluent terpenes. (nih.gov)
  • Recent CDC laboratory testing of bronchoalveolar lavage (BAL) fluid samples from 29 patients with EVALI submitted to CDC from 10 states found vitamin E acetate in all of the samples. (cdc.gov)
  • CDC a nalytic methods can identify vitamin E acetate, MCT oil (medium chain triglycerides), plant oils (long chain triglycerides), petroleum distillates (including mineral oil), diluent terpenes, cannabinoids, and nicotine in BAL fluid. (cdc.gov)
  • Animals were euthanized 6, 24, 48h or 7days post-exposure and bronchoalveolar lavage fluid (BAL) and lung tissue collected. (nih.gov)
  • Gemifloxacin penetrates well into lung tissue and fluids. (nih.gov)
  • In ILD assessment, bronchoalveolar lavage (BAL) fluid examination is a minimally invasive and routinely performed step. (medscape.com)
  • Cytological examination of cells from bronchoalveolar lavage (BAL) is commonly used for the diagnosis of lung cancer. (nih.gov)
  • 2. Evaluation of cytokines in the tumor microenvironment of lung cancer using bronchoalveolar lavage fluid analysis. (nih.gov)
  • 17. Evaluation of CD30 as a marker for th2 lymphocytes in bronchoalveolar lavage in interstitial lung diseases. (nih.gov)
  • Glycoproteomic analysis of bronchoalveolar lavage (BAL) fluid identifies tumor-associated glycoproteins from lung adenocarcinoma. (nih.gov)
  • 11. Variability of cytokine concentration in whole blood serum and bronchoalveolar lavage over time. (nih.gov)
  • Our study demonstrates that potential protein biomarkers in BAL fluid can be detected and quantified. (nih.gov)