Hypertension pulmonary medicine. Medical search

Pulmonary Medicine: A subspecialty of internal medicine concerned with the study of the RESPIRATORY SYSTEM. It is especially concerned with diagnosis and treatment of diseases and defects of the lungs and bronchial tree.Lung Diseases: Pathological processes involving any part of the LUNG.Hypertension: Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more.Hypertension, Pulmonary: Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES.Hypertension, Renal: Persistent high BLOOD PRESSURE due to KIDNEY DISEASES, such as those involving the renal parenchyma, the renal vasculature, or tumors that secrete RENIN.Hypertension, Portal: Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN.Blood Pressure: PRESSURE of the BLOOD on the ARTERIES and other BLOOD VESSELS.Hypertension, Renovascular: Hypertension due to RENAL ARTERY OBSTRUCTION or compression.Antihypertensive Agents: Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS.Pulmonary Artery: The short wide vessel arising from the conus arteriosus of the right ventricle and conveying unaerated blood to the lungs.Bone Morphogenetic Protein Receptors, Type II: A subtype of bone morphogenetic protein receptors with low affinity for BONE MORPHOGENETIC PROTEINS. They are constitutively active PROTEIN-SERINE-THREONINE KINASES that can interact with and phosphorylate TYPE I BONE MORPHOGENETIC PROTEIN RECEPTORS.Chicago Monocrotaline: A pyrrolizidine alkaloid and a toxic plant constituent that poisons livestock and humans through the ingestion of contaminated grains and other foods. The alkaloid causes pulmonary artery hypertension, right ventricular hypertrophy, and pathological changes in the pulmonary vasculature. Significant attenuation of the cardiopulmonary changes are noted after oral magnesium treatment.Dendrobium: A plant genus of the family ORCHIDACEAE that contains dihydroayapin (COUMARINS) and phenanthraquinones.Newspapers: Publications printed and distributed daily, weekly, or at some other regular and usually short interval, containing news, articles of opinion (as editorials and letters), features, advertising, and announcements of current interest. (Webster's 3d ed)Heart Murmurs: Heart sounds caused by vibrations resulting from the flow of blood through the heart. Heart murmurs can be examined by HEART AUSCULTATION, and analyzed by their intensity (6 grades), duration, timing (systolic, diastolic, or continuous), location, transmission, and quality (musical, vibratory, blowing, etc).Vectorcardiography: Recording of the moment-to-moment electromotive forces of the heart on a plane of the body surface delineated as a vector function of time.Heart Sounds: The sounds heard over the cardiac region produced by the functioning of the heart. There are four distinct sounds: the first occurs at the beginning of SYSTOLE and is heard as a "lubb" sound; the second is produced by the closing of the AORTIC VALVE and PULMONARY VALVE and is heard as a "dupp" sound; the third is produced by vibrations of the ventricular walls when suddenly distended by the rush of blood from the HEART ATRIA; and the fourth is produced by atrial contraction and ventricular filling.Heart Auscultation: Act of listening for sounds within the heart.Phonocardiography: Graphic registration of the heart sounds picked up as vibrations and transformed by a piezoelectric crystal microphone into a varying electrical output according to the stresses imposed by the sound waves. The electrical output is amplified by a stethograph amplifier and recorded by a device incorporated into the electrocardiograph or by a multichannel recording machine.Radiography, Thoracic: X-ray visualization of the chest and organs of the thoracic cavity. It is not restricted to visualization of the lungs.Marketing: Activity involved in transfer of goods from producer to consumer or in the exchange of services.Research Report: Detailed account or statement or formal record of data resulting from empirical inquiry.Accreditation: Certification as complying with a standard set by non-governmental organizations, applied for by institutions, programs, and facilities on a voluntary basis.Joint Commission on Accreditation of Healthcare Organizations: A private, voluntary, not-for-profit organization which establishes standards for the operation of health facilities and services, conducts surveys, and awards accreditation.Illinois Software: Sequential operating programs and data which instruct the functioning of a digital computer.Kidney Transplantation: The transference of a kidney from one human or animal to another.Emergency Shelter: Temporary shelter provided in response to a major disaster or emergency.Nitric Oxide: A free radical gas produced endogenously by a variety of mammalian cells, synthesized from ARGININE by NITRIC OXIDE SYNTHASE. Nitric oxide is one of the ENDOTHELIUM-DEPENDENT RELAXING FACTORS released by the vascular endothelium and mediates VASODILATION. It also inhibits platelet aggregation, induces disaggregation of aggregated platelets, and inhibits platelet adhesion to the vascular endothelium. Nitric oxide activates cytosolic GUANYLATE CYCLASE and thus elevates intracellular levels of CYCLIC GMP.Kidney Failure, Chronic: The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION.Endothelium, Vascular: Single pavement layer of cells which line the luminal surface of the entire vascular system and regulate the transport of macromolecules and blood components.Still's Disease, Adult-Onset: Systemic-onset rheumatoid arthritis in adults. It differs from classical rheumatoid arthritis in that it is more often marked by acute febrile onset, and generalized lymphadenopathy and hepatosplenomegaly are more prominent.HLA-B39 Antigen: A specific HLA-B surface antigen subtype. Members of this subtype contain alpha chains that are encoded by the HLA-B*39 allele family.Arthritis, Juvenile: Arthritis of children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent.Interleukin-18: A cytokine which resembles IL-1 structurally and IL-12 functionally. It enhances the cytotoxic activity of NK CELLS and CYTOTOXIC T-LYMPHOCYTES, and appears to play a role both as neuroimmunomodulator and in the induction of mucosal immunity.Prostaglandins I: A class of cyclic prostaglandins that contain the 6,9-epoxy bond. Endogenous members of this family are biosynthesized enzymatically from PROSTAGLANDIN ENDOPEROXIDES.Hypertrophy, Right Ventricular: Enlargement of the RIGHT VENTRICLE of the heart. This increase in ventricular mass is often attributed to PULMONARY HYPERTENSION and is a contributor to cardiovascular morbidity and mortality.Bronchopulmonary Dysplasia: A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS.Surface-Active Agents: Agents that modify interfacial tension of water; usually substances that have one lipophilic and one hydrophilic group in the molecule; includes soaps, detergents, emulsifiers, dispersing and wetting agents, and several groups of antiseptics.Phosphodiesterase 5 Inhibitors: Compounds that specifically inhibit PHOSPHODIESTERASE 5.Pyrazoles: Azoles of two nitrogens at the 1,2 positions, next to each other, in contrast with IMIDAZOLES in which they are at the 1,3 positions.Pyrimidines: A family of 6-membered heterocyclic compounds occurring in nature in a wide variety of forms. They include several nucleic acid constituents (CYTOSINE; THYMINE; and URACIL) and form the basic structure of the barbiturates.Guanylate Cyclase: An enzyme that catalyzes the conversion of GTP to 3',5'-cyclic GMP and pyrophosphate. It also acts on ITP and dGTP. (From Enzyme Nomenclature, 1992) EC 4.6.1.2.Archives Awareness: The act of "taking account" of an object or state of affairs. It does not imply assessment of, nor attention to the qualities or nature of the object.Fees, Pharmaceutical: Amounts charged to the patient or third-party payer for medication. It includes the pharmacist's professional fee and cost of ingredients, containers, etc.Copyright: It is a form of protection provided by law. In the United States this protection is granted to authors of original works of authorship, including literary, dramatic, musical, artistic, and certain other intellectual works. This protection is available to both published and unpublished works. (from Circular of the United States Copyright Office, 6/30/2008)BooksComplement C3d: A 302-amino-acid fragment in the alpha chain (672-1663) of C3b. It is generated when C3b is inactivated (iC3b) and its alpha chain is cleaved by COMPLEMENT FACTOR I into C3c, and C3dg (955-1303) in the presence COMPLEMENT FACTOR H. Serum proteases further degrade C3dg into C3d (1002-1303) and C3g (955-1001).Epoprostenol: A prostaglandin that is a powerful vasodilator and inhibits platelet aggregation. It is biosynthesized enzymatically from PROSTAGLANDIN ENDOPEROXIDES in human vascular tissue. The sodium salt has been also used to treat primary pulmonary hypertension (HYPERTENSION, PULMONARY).Heart Failure: A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION.Iloprost: An eicosanoid, derived from the cyclooxygenase pathway of arachidonic acid metabolism. It is a stable and synthetic analog of EPOPROSTENOL, but with a longer half-life than the parent compound. Its actions are similar to prostacyclin. Iloprost produces vasodilation and inhibits platelet aggregation.Treatment Outcome: Evaluation undertaken to assess the results or consequences of management and procedures used in combating disease in order to determine the efficacy, effectiveness, safety, and practicability of these interventions in individual cases or series.Stroke Volume: The amount of BLOOD pumped out of the HEART per beat, not to be confused with cardiac output (volume/time). It is calculated as the difference between the end-diastolic volume and the end-systolic volume.

Anorectic

"Appetite-Suppressant Drugs and the Risk of Primary Pulmonary Hypertension". New England Journal of Medicine. 335 (9): 609-16. ... Epidemics of fatal pulmonary hypertension and heart valve damage associated with pharmaceutical anorectic agents have led to ... "Journal of Natural Science, Biology and Medicine. 5 (2): 340-4. doi:10.4103/0976-9668.136180. PMC 4121911. PMID 25097411.. ... Many amphetamines produce side effects, including addiction, tachycardia and hypertension,[4] making prolonged unsupervised use ...

Exercise intolerance

Fowler, Robin (2012). "Exercise Intolerance in Pulmonary Arterial Hypertension". Pulmonary Medicine. June: 359204. doi:10.1155/ ... Cardiac arrhythmia Aortic valve insufficiency Pulmonary artery hypertension: PAH has the following symptoms; dyspnea and ... 110 mm Hg Severe pulmonary hypertension Severe chronic fatigue syndrome Suspected or known dissecting aortic aneurysm Recent ... Dysfunctions involving the pulmonary, cardiovascular or neuromuscular systems have been frequently found to be associated with ...

Rapeseed

"Risk factors for pulmonary arterial hypertension". Clinics in chest medicine. 22 (3): 459-475. doi:10.1016/S0272-5231(05)70284- ... Symptoms appeared as a typical pneumonia with interstitial infiltrates on chest X-ray, complicated by pulmonary hypertension in ...

5-HT2B receptor

"Function of the serotonin 5-hydroxytryptamine 2B receptor in pulmonary hypertension". Nature Medicine. 8 (10): 1129-35. doi: ... This article incorporates text from the United States National Library of Medicine, which is in the public domain.. ... Roth BL (Jan 2007). "Drugs and valvular heart disease". The New England Journal of Medicine. 356 (1): 6-9. doi:10.1056/ ... The 5-HT2B receptor subtype is involved in: CNS: presynaptic inhibition, behavioural effects Vascular: pulmonary ...

Iloprost

"Inhaled Iloprost for Severe Pulmonary Hypertension". New England Journal of Medicine. 347 (5): 322-329. doi:10.1056/ ... This may be a sign of pulmonary venous hypertension. Pulmonary arterial hypertension (PAH) Raynaud's phenomenon Scleroderma " ... Should signs of pulmonary edema occur when inhaled iloprost is administered in patients with pulmonary hypertension, the ... Iloprost should be stopped immediately if signs of pulmonary edema occur. This may be a sign of pulmonary venous hypertension. ...

Nifedipine

... is also used in high-altitude medicine to treat high altitude pulmonary edema. Other uses include painful spasms of ... It is also used for the small subset of people with pulmonary hypertension. Nifedipine rapidly lowers blood pressure, and ... Hypertension: management of hypertension in adults in primary care. Clinical guideline CG34. National Institute for Health and ... It is on the World Health Organization's List of Essential Medicines, the most effective and safe medicines needed in a health ...

Haemodynamic response

"Treatment of Pulmonary Arterial Hypertension". The New England Journal of Medicine. 351: 1425-1436. doi:10.1056/NEJMra040291. " ... Pulmonary hypertension (PAH) is disease of small pulmonary arteries that is usually caused by more than one mechanism. This ... Complications in this response arise in acute coronary syndromes and pulmonary arterial hypertension. These complications lead ... there are no current cures for pulmonary arterial hypertension, but there are treatment options for patients with the disease ...

Riociguat

"Adempas not for use in patients with pulmonary hypertension caused by idiopathic interstitial pneumonia". European Medicines ... chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertension (PAH). Riociguat constitutes the ... "Riociguat for the Treatment of Chronic Thromboembolic Pulmonary Hypertension". New England Journal of Medicine. 369 (4): 319- ... The Pulmonary Arterial Hypertension sGC-Stimulator Trial (PATENT) was a randomized, placebo-controlled trial that investigated ...

Sildenafil

"Efficacy and Safety of Sildenafil Treatment in Pulmonary Arterial Hypertension: a Systematic Review". Respiratory Medicine. 108 ... Pulmonary hypertension. While sildenafil improves some markers of disease in people with pulmonary arterial hypertension, it ... Sildenafil is available as a generic drug in the United States, labelled for pulmonary arterial hypertension.[77] As of 2016[ ... In Canada, Pfizer's patent 2,324,324 for Revatio (sildenafil used to treat pulmonary hypertension) was found invalid by the ...

Lutembacher's syndrome

Patients with coronary artery disease or pulmonary hypertension will take additional medicines described by their physician. ... Pulmonary artery enlargement: the test will help to determine if there is a large volume of blood in the pulmonary veins and ... Loud mitral S1 and wide fixed split of pulmonary S2: The loud sound of the mitral S1 and the wide fixed split of pulmonary S2 ... pulmonary vascular congestion, marked left atrial enlargement: the test will help to determine if there is a sign of MS and ...

Prostacyclin receptor

"Comparative Efficacy and Safety of Prostacyclin Analogs for Pulmonary Arterial Hypertension: A Network Meta-Analysis". Medicine ... IP receptor agonists are front-line drugs to treat pulmonary hypertension. Major drugs in this category include PGI2 itself (i. ... Sitbon O, Vonk Noordegraaf A (January 2017). "Epoprostenol and pulmonary arterial hypertension: 20 years of clinical experience ... This article incorporates text from the United States National Library of Medicine, which is in the public domain. ...

Ambrisentan

... and European Medicines Agency, and designated an orphan drug, for the treatment of pulmonary hypertension. Ambrisentan is ... "Initial Use of Ambrisentan plus Tadalafil in Pulmonary Arterial Hypertension". New England Journal of Medicine. 373 (9): 834-44 ... "FDA Approves New Orphan Drug for Treatment of Pulmonary Arterial Hypertension" (Press release). Food and Drug Administration. ... "U.S. Food and Drug Administration Approves Gilead's Letairis Treatment of Pulmonary Arterial Hypertension" (Press release). ...

Harrison Farber

Harrison "Hap" Farber is Professor of Medicine and Director of the Pulmonary Hypertension Center at Boston University. He ... Farber is a Professor in the Department of Medicine and attends in the Medical Intensive Care Unit and on the Pulmonary ... He completed a fellowship in pulmonary and critical care medicine at Boston University and Boston City Hospital Program. Dr. ... He also oversees the care of all patients with Pulmonary Hypertension at Boston Medical Center. Dr. Farber's research focuses ...

United Therapeutics

The marketed medicines are Remodulin, Tyvaso, Orenitram and Adcirca for pulmonary arterial hypertension, and Unituxin for ... Clinical trials of new medicines related to pulmonary hypertension include INCREASE for interstitial lung disease, SOUTHPAW for ... "United Therapeutics and DEKA Sign Agreement for New PAH Remodulin Delivery System". Pulmonary Hypertension News. January 2, ... In 1994, Rothblatt's young daughter was diagnosed with a fatal orphan disease, pulmonary arterial hypertension (PAH). Rothblatt ...

Saul Brandman

... and endowed the Chair in Pulmonary Arterial Hypertension at the David Geffen School of Medicine at UCLA. In 2008, Brandman ...

Eisenmenger's syndrome

Various medicines and therapies for pulmonary hypertension are under investigation for treatment of the symptoms. Eisenmenger ... After pulmonary hypertension is sufficient to reverse the blood flow through the defect, however, the maladaptation is ... Wood, P (1958). "Pulmonary hypertension with special reference to the vasoconstrictive factor". British heart journal. 20 (4): ... If the inciting defect in the heart is identified before it causes significant pulmonary hypertension, it can normally be ...

Sildenafil

"Efficacy and Safety of Sildenafil Treatment in Pulmonary Arterial Hypertension: a Systematic Review". Respiratory Medicine. 108 ... While sildenafil improves some markers of disease in people with pulmonary arterial hypertension, it does not appear to affect ... Sildenafil is available as a generic drug in the United States, labelled for pulmonary arterial hypertension. As of 2016[update ... In Canada, Pfizer's patent 2,324,324 for Revatio (sildenafil used to treat pulmonary hypertension) was found invalid by the ...

Prostacyclin receptor

"Comparative Efficacy and Safety of Prostacyclin Analogs for Pulmonary Arterial Hypertension: A Network Meta-Analysis". Medicine ... IP receptor agonists are front-line drugs to treat pulmonary hypertension. Major drugs in this category include PGI2 itself (i. ... Sitbon O, Vonk Noordegraaf A (January 2017). "Epoprostenol and pulmonary arterial hypertension: 20 years of clinical experience ... "A Comparison of Inhaled Nitric Oxide Versus Inhaled Epoprostenol for Acute Pulmonary Hypertension Following Cardiac Surgery". ...

Right-to-left shunt

"Pulmonary arterial hypertension associated with congenital heart disease". Clinics in chest medicine. 34 (4): 707-17. doi: ... This switch in blood flow direction is precipitated by pulmonary hypertension due to increased pulmonary blood flow in a left- ... The right ventricle hypertrophies to compensate for this pulmonary hypertension, so the right ventricular pressure becomes ... Pulmonary stenosis (narrowing of the pulmonary valve and outflow tract, obstructing blood flow from the right ventricle to the ...

Lung transplantation

The New England Journal of Medicine. 306 (10): 557-64. doi:10.1056/NEJM198203113061001. PMID 6799824. Pulmonary Hypertension: A ... Pulmonary Hypertension: A Patient's Survival Guide 3rd ed. p.134. Pulmonary Hypertension: A Patient's Survival Guide 3rd ed. p ... idiopathic pulmonary fibrosis; 14% cystic fibrosis; 12% idiopathic (formerly known as "primary") pulmonary hypertension; 5% ... Bruce Reitz of Stanford University in 1981 on a woman who had idiopathic pulmonary hypertension. 1983: First successful long- ...

Sitaxentan

2004). "Sitaxsentan therapy for pulmonary arterial hypertension". American Journal of Respiratory and Critical Care Medicine. ... Sitaxentan sodium (TBC-11251) is a medication for the treatment of pulmonary arterial hypertension (PAH). It was marketed as ... "Encysive Pharmaceuticals to Conduct Phase III Study With Thelin (Sitaxsentan Sodium) in Pulmonary Arterial Hypertension". ... 2007). "Selective endothelinA receptor antagonism with sitaxsentan for pulmonary arterial hypertension associated with ...

Sildenafil, den frie encyklopædi

Richalet, Jean-Paul (2005): Sildenafil Inhibits Altitude-induced Hypoxemia and Pulmonary Hypertension. I: American Journal of ... Respiratory and Critical Care Medicine, 171 (3): 275-281. *^ European Medicines Agency. Science Medicines Health: Bilag 1 - ... Pulmonal arteriel hypertension og lungefibrose[redigér , redigér wikikode]. Pulmonal arteriel hypertension er for højt blodtryk ... Ghofrani, Hossein Ardeschir (2002): Sildenafil for treatment of lung fibrosis and pulmonary hypertension: a randomised ...

Persistent fetal circulation

It can be associated with pulmonary hypertension. Because of this, the condition is also widely known as Persistent Pulmonary ... In many countries patients must bring their own supplies, even acquire their own medicines, before treatment can be given." The ... Persistent fetal circulation (also called Persistent Pulmonary Hypertension of the Newborn, PPHN) is a condition caused by a ... Graves ED, Redmond CR, Arensman RM (March 1988). "Persistent pulmonary hypertension in the neonate". Chest. 93 (3): 638-41. doi ...

TOPBP1

Mutations in TOPBP1 cause Idiopathic pulmonary arterial hypertension . GRCh38: Ensembl release 89: ENSG00000163781 - Ensembl, ... American Journal of Respiratory and Critical Care Medicine. 189 (10): 1260-72. doi:10.1164/rccm.201310-1749OC. PMID 24702692. ... "Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension". ...

Jason X.-J. Yuan

Advances in the Management of Pulmonary Arterial Hypertension (Future Medicine, London, UK. 2013); and Lung Stem Cells in the ... for Scholarly Activities of the Department of Medicine at the College of Medicine and Director of the Program in Pulmonary ... Yuan began his academic career as a Research Assistant Professor of Medicine at the University of Maryland School of Medicine ( ... an American physician scientist whose research interests center on pulmonary vascular pathobiology and pulmonary hypertension. ...

Nosebleed

a b MedlinePlus Medical Encyclopedia: Nosebleed U.S. National Library of Medicine Medline Plus service. Retrieved 2010-03-15. ... due to general hypertension) tends to increase the duration of spontaneous epistaxis.[7] Anticoagulant medication and disorders ... British journal of hospital medicine (London, England : 2005). 75 (3): 143-7. doi:10.12968/hmed.2014.75.3.143. PMID 24621629.. ... "Is epistaxis evidence of end-organ damage in patients with hypertension?". Laryngoscope. 109 (7): 1111-1115. doi:10.1097/ ...

Pulmonary arterial hypertension in adult onset Still's disease: a case report of a severe complication | BMC Pulmonary Medicine...

Pulmonary arterial hypertension (PAH) occurring in AOSD is rarely described in literature. We present the case of a young ... From: Pulmonary arterial hypertension in adult onset Stills disease: a case report of a severe complication ...

bmcpulmmed.biomedcentral.com

Primary Pulmonary Hypertension | Johns Hopkins Medicine

Its a rare lung disorder in which the blood vessels in the lungs narrow and the pressure in the pulmonary artery rises far ... Primary pulmonary hypertension (PPH) is high blood pressure in the lungs. ... Pulmonary Lung and Respiratory System What is primary pulmonary hypertension?. Primary pulmonary hypertension (PPH) is high ... Key points about pulmonary hypertension. *Primary pulmonary hypertension (PPH) is a rare lung disorder that causes high blood ...

hopkinsmedicine.org

Persistent Pulmonary Hypertension | Johns Hopkins Medicine Health Library

What is persistent pulmonary hypertension?. In persistent pulmonary hypertension, also known as persistent fetal circulation, a ... Blood Test Shows Promise In Gauging Severity Of Pulmonary Arterial Hypertension. *Drug Now In Clinical Trials For Parkinsons ...

hopkinsmedicine.org

Researchers revisit pulmonary arterial hypertension survival - UChicago Medicine

Setting out to determine the survival of patients with pulmonary arterial hypertension (PAH), researchers at the University of ... Associate Professor of Medicine and Director of Pulmonary Hypertension at the University of Chicago Medical Center. Our ... Researchers revisit pulmonary arterial hypertension survival. Survival improves but prognostication tool sorely outdated. ... Setting out to determine the survival of patients with pulmonary arterial hypertension (PAH), researchers at the University of ...

uchospitals.edu

Past Symposiums | From Precision Biology to Precision Medicine in Pulmonary Hypertension | Stanford Medicine

Professor of Medicine. Pulmonary and Critical Care Medicine. Director, Pulmonary Hypertension Program. Johns Hopkins Medicine ... Associate Professor of Medicine. Pulmonary and Critical Care Medicine. Director, Adult Pulmonary Hypertension Program. Stanford ... Associate Professor of Medicine. Pulmonary and Critical Care Medicine. Director, Adult Pulmonary Hypertension Program. Stanford ... Ford Investigator of Pulmonary Medicine. Director of Pulmonary Research. Co-director, Pulmonary Hypertension Program. Indiana ...

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Pulmonary hypertension | BMJ Evidence-Based Medicine

BMJ Evidence-Based Medicine Jun 2013, 18 (3) e26; DOI: 10.1136/eb-2012-100971 ... BMJ Evidence-Based Medicine Feb 2013, 18 (1) 37-38; DOI: 10.1136/ebmed-2012-100651 ... BMJ Evidence-Based Medicine Oct 2008, 13 (5) 154; DOI: 10.1136/ebm.13.5.154 ... BMJ Evidence-Based Medicine Aug 2007, 12 (4) 125; DOI: 10.1136/ebm.12.4.125 ...

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Global Pulmonary Arterial Hypertension (PAH) Medicine Market Professional Survey Report 2016

Medicine Market Professional Survey Report 2016 to their offerings. ... ReportBazzar has included a new report titled Global Pulmonary Arterial Hypertension (PAH) ... Global Pulmonary Arterial Hypertension (PAH) Medicine Market Professional Survey Report 2016. Thursday, August 25, 2016 General ...

medindia.net

Blocking molecular pathway reverses pulmonary hypertension in rats, study finds | News Center | Stanford Medicine

NHLBI grants will fund use of iPS cells to study insulin resistance and pulmonary hypertension Two School of Medicine research ... Pulmonary hypertension, a deadly form of high blood pressure that develops in the lungs, may be caused by an inflammation- ... Pulmonary hypertension, while rare, usually strikes young and middle-aged women, leaving them short of breath and often unable ... About 100,000 people in the United States and Europe have been diagnosed with pulmonary hypertension, but many others are ...

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Phentolamine for Primary Pulmonary Hypertension | Annals of Internal Medicine | American College of Physicians

Phentolamine for Primary Pulmonary Hypertension SE DO CHA, M.D.; MICHAEL KIRSCHBAUM, D.O.; VLADIR MARANHAO, M.D.; EMMONS PAINE ... To the editor: In the May issue, Ruskin and Hutter (1) reported a case of primary pulmonary hypertension in a patient who ... Phentolamine for Primary Pulmonary Hypertension. Ann Intern Med. 1979;91:927-928. doi: 10.7326/0003-4819-91-6-927_2 ...

annals.org

PPARγ Activation: A Potential Treatment For Pulmonary Hypertension | Science Translational Medicine

PPARγ Activation: A Potential Treatment For Pulmonary Hypertension Message Subject. (Your Name) has forwarded a page to you ... Citation: G. Hansmann, R. T. Zamanian, PPARγ activation: A potential treatment for pulmonary hypertension. Sci. Transl. Med. 1 ... The pathobiology of pulmonary arterial hypertension (PAH) involves multiple molecular pathways and environmental modifiers and ... 3Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, USA. ...

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Primary Pulmonary Hypertension Treated with Oral Phentolamine | Annals of Internal Medicine | American College of Physicians

Vasodilator-Responsive Idiopathic Pulmonary Arterial Hypertension: Evidence for a New Disease? Annals of Internal Medicine; 162 ... Primary Pulmonary Hypertension and Oral Phentolamine Annals of Internal Medicine; 91 (3): 495-496 ... Adverse Hemodynamic Effects of Phentolamine in Primary Pulmonary Hypertension Annals of Internal Medicine; 95 (5): 591-592 ... Primary Pulmonary Hypertension Treated with Oral Phentolamine JEREMY N. RUSKIN, M.D.; ADOLPH M. HUTTER Jr., M.D. ...

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Pulmonary hypertension | Complementary and Alternative Medicine | St. Luke's Hospital

Pulmonary hypertension. Pulmonary hypertension is high blood pressure in the arteries of your lungs. It happens when the lungs ... Pulmonary hypertension in advanced chronic obstructive pulmonary disease. Curr Opin Pulm Med . 2012;18(2):138-43. ... Pulmonary hypertension and right ventricular failure. Part VI. Classification and pathomorphology of primary pulmonary arterial ... Bech-Hanssen O, Karason K, Rundqvist B, Bollano E, Lindgren F, Selimovic N. Can pulmonary hypertension and increased pulmonary ...

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Global Pulmonary Arterial Hypertension (PAH) Medicine Market Research Report 2016

Medicine Revenue, means the sales value of Pulmonary Arterial Hypertension (PAH) Medicine This report studies Pulmonary ... Arterial Hypertension (PAH) Medicine in Global market, especially in North America, Europe, China, Japan, Southeast Asia and ... means the output of Pulmonary Arterial Hypertension (PAH) ... 1.2 Pulmonary Arterial Hypertension (PAH) Medicine Segment by ... 1.3 Pulmonary Arterial Hypertension (PAH) Medicine Segment by Application. 1.3.1 Pulmonary Arterial Hypertension (PAH) Medicine ...

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Pulmonary Hypertension | Circulation: Genomic and Precision Medicine

Chloroquine in Pulmonary Arterial HypertensionA New Role for an Old Drug? John J. Ryan ... BMPR2 Mutations Influence Phenotype More Obviously in Male Patients With Pulmonary Arterial HypertensionClinical Perspective ... Osteoprotegerin Disruption Attenuates HySu-Induced Pulmonary Hypertension Through Integrin αvβ3/FAK/AKT Pathway Suppression ... α1-A680T Variant in GUCY1A3 as a Candidate Conferring Protection From Pulmonary Hypertension Among Kyrgyz HighlandersCLINICAL ...

circgenetics.ahajournals.org

Inhibition of pyruvate dehydrogenase kinase improves pulmonary arterial hypertension in genetically susceptible patients |...

2Department of Medicine, Imperial College London, London W12 0NN, UK.. *. 3National Pulmonary Hypertension Service, Imperial ... Research ArticlePulmonary Arterial Hypertension. Inhibition of pyruvate dehydrogenase kinase improves pulmonary arterial ... National Pulmonary Hypertension Service, Imperial College Healthcare National Health Service Trust, Hammersmith Hospital, Du ... National Pulmonary Hypertension Service, Imperial College Healthcare National Health Service Trust, Hammersmith Hospital, Du ...

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UChicago Medicine earns pulmonary hypertension accreditation - UChicago Medicine

... is the first Comprehensive Pulmonary Hypertension Care Center in Illinois to be recognized by the Pulmonary Hypertension ... nursing manager for the Pulmonary Hypertension Center. Accreditation as a Comprehensive Pulmonary Hypertension Care Center ... The University of Chicago Medicine is the first Comprehensive Pulmonary Hypertension Care Center in Illinois to be recognized ... associate professor of medicine, director of Pulmonary Hypertension Center and medical director of the lung transplant program ...

uchicagomedicine.org

Pulmonary Hypertension - UChicago Medicine

... our Advanced Heart Failure and Pulmonary Hypertension Program. ... The University of Chicago Medicine is now home to the Midwests ... Why Choose UChicago Medicine for Pulmonary Hypertension. Evaluating and treating pulmonary hypertension (PH) can be very ... Diagnosing & Treating Pulmonary Hypertension. Detecting Pulmonary Hypertension Your doctor may suspect that you have PH based ... Idiopathic and familial pulmonary arterial hypertension, formerly known as primary pulmonary hypertension, which is a rare ...

uchicagomedicine.org

RePub, Erasmus University Repository: Therapeutic targets in neonatal pulmonary hypertension: Linking pathophysiology to...

Therapeutic targets in neonatal pulmonary hypertension: Linking pathophysiology to clinical medicine. Publication. Publication ... Therapeutic targets in neonatal pulmonary hypertension: Linking pathophysiology to clinical medicine. Expert Review of ... Endothelin, Neonates, Nitric oxide, Pharmacotherapy, Phosphodiesterase, Prostaglandin, Pulmonary hypertension Persistent URL. ... Treatment of pulmonary hypertension in neonates is a major challenge on the intensive care unit and involves high morbidity and ...

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European Medicines Agency - Clinical efficacy and safety - Clinical investigation of medicinal products for the treatment of...

... responsible for the protection of public and animal health through the scientific evaluation and supervision of medicines. ... Pulmonary arterial hypertension (PAH), revised WHO classification on pulmonary hypertension. Description. This document ... Clinical investigation of medicinal products for the treatment of pulmonary arterial hypertension. * Email ... Data on medicines (ISO IDMP standards)*SPOR master data*Referentials and organisations ...

ema.europa.eu

Respiratory Medicine - Pulmonary Hypertension - Controversial and Emerging Topics - H. James Ford - 9783030527860 - Schweitzer...

... exercise pulmonary hypertension, sickle cell disease and pulmonary hypertension, and sarcoid pulmonary hypertension, among many ... This book provides a deep dive into the diagnosis and therapeutics of pulmonary hypertension supported by the literature and ... and other specialty practitioners caring for patients with pulmonary hypertension. ... review of recent guidelines and their applicability to the multiple different nuanced presentations of pulmonary hypertension. ...

schweitzer-online.de

Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease | Genome Medicine |...

... is a rare disease characterized by distinctive changes in pulmonary arterioles that lead to progressive pulmonary arterial ... many of which are highly expressed in developing heart and pulmonary vasculature. In the cohort of PAH without CHD, rare ... Pulmonary arterial hypertension (PAH) is a rare disease characterized by distinctive changes in pulmonary arterioles that lead ... Pulmonary arterial hypertension (PAH[MIM:178600]) is a rare disease characterized by distinctive changes in pulmonary ...

genomemedicine.biomedcentral.com

Pulmonary hypertension - Oxford Medicine

Pulmonary hypertension is heterogeneous from a pathophysiological point of view, and the diversity is reflected in the ... The different haemodynamic forms of pulmonary hypertension can be found in multiple clinical conditions which have been ... In fact, while transthoracic echocardiography may provide clues on the presence of pulmonary hypertension, the haemodynamic ... The presence of pulmonary hypertension, as defined above, is always an ominous prognostic sign, even if the severity may differ ...

oxfordmedicine.com

Meet the Downtown Chicago Pulmonary Hypertension Team | Northwestern Medicine

Northwestern Medicine Bluhm Cardiovascular Institute is a nationally recognized destination for those who require highly ... Meet the Downtown Chicago Pulmonary Hypertension Team. Northwestern Medicine Bluhm Cardiovascular Institute is a nationally ... 2019 by Northwestern Medicine® and Northwestern Memorial HealthCare.. Northwestern Medicine® is a trademark of Northwestern ... Choose dates and times from several of our Family Medicine, Internal Medicine and Pediatric doctors. ...

nm.org

Academic Position for Pulmonary Physician specializing in Lung Transplantation and Pulmonary Hypertension in the Division of...

... for Pulmonary Physician specializing in Lung Transplantation and Pulmonary Hypertension in the Division of Pulmonary Medicine. ... The University of Alberta, Faculty of Medicine & Dentistry, Department of Medicine, Division of Pulmonary Medicine in ... Pulmonary Hypertension and Interventional Pulmonary Medicine.. Division members also care for the second largest Lung ... www.ualberta.ca/department-of-medicine/divisions/pulmonary-medicine/publications).. The successful candidate will be an MD (or ...

careers.ualberta.ca

Osteoprotegerin Disruption Attenuates HySu-Induced Pulmonary Hypertension Through Integrin αvβ3/FAK/AKT Pathway...

From the Department of Cardiology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China. ... 7 idiopathic pulmonary hypertension and 2 congenital heart disease) or bosentan (5/14, 4 idiopathic pulmonary hypertension and ... Alteration of pulmonary artery integrin levels in chronic hypoxia and monocrotaline-induced pulmonary hypertension. J Vasc Res ... Predicting survival in pulmonary arterial hypertension: insights from the Registry to Evaluate Early and Long-Term Pulmonary ...

circgenetics.ahajournals.org

Primary pulmonary hypertension (PPH) is high blood pressure in the lungs. (hopkinsmedicine.org)
The cause of primary pulmonary hypertension (PPH) is unknown. (hopkinsmedicine.org)
What are the symptoms of primary pulmonary hypertension? (hopkinsmedicine.org)
The following are the most common symptoms for primary pulmonary hypertension (PPH). (hopkinsmedicine.org)
How is primary pulmonary hypertension diagnosed? (hopkinsmedicine.org)
Primary pulmonary hypertension (PPH) is rarely discovered in a routine medical exam. (hopkinsmedicine.org)
How is primary pulmonary hypertension treated? (hopkinsmedicine.org)
There is no cure for primary pulmonary hypertension (PPH). (hopkinsmedicine.org)
To the editor: In the May issue, Ruskin and Hutter (1) reported a case of primary pulmonary hypertension in a patient who showed impressive symptomatic and hemodynamic improvement after a trial of phentolamine. (annals.org)
RUSKIN JN, HUTTER AM. Primary Pulmonary Hypertension Treated with Oral Phentolamine. (annals.org)
Idiopathic and familial pulmonary arterial hypertension , formerly known as primary pulmonary hypertension, which is a rare condition that may be caused by a genetic defect. (uchicagomedicine.org)
SUN X.-G., HANSEN J. E., OUDIZ R. J., WASSERMAN K.. Exercise Pathophysiology in Patients With Primary Pulmonary Hypertension. (explainmedicine.com)
We believe that the monoclonal cell expansion in primary pulmonary hypertension is the result of autonomous growth of stem cell-like endothelial cells, whereas the polyclonal proliferation in secondary pulmonary hypertension occurs as a response of endothelial cells to exogenous stimuli (like vital infection or high shear stress). (elsevier.com)
Tuder, R. M. / Primary pulmonary hypertension between inflammation and cancer . (elsevier.com)
Diagnostic Confirmation: Are you sure your patient has Primary Pulmonary Hypertension? (oncologynurseadvisor.com)
C. History Part 3: Competing diagnoses that can mimic Primary Pulmonary Hypertension. (oncologynurseadvisor.com)
Another name is primary pulmonary hypertension (PPH). (upmc.com)

Department of Pediatrics and Vera Moulton Wall Center for Pulmonary Vascular Disease, Stanford University School of Medicine, Stanford, California (M.R. (asahq.org)
Led by Stuart Rich, MD , a pioneer in the treatment of pulmonary hypertension, the Pulmonary Vascular Disease Program is part of Northwestern Medicine's Bluhm Cardiovascular Institute . (nm.org)
Pulmonary vascular disease is defined as a condition of blood flow to the lung's artery is blocked suddenly due to a blood clot somewhere in the body, including pulmonary embolism, chronic thromboembolic disease, pulmonary arterial hypertension, pulmonary veno-occlusive disease, pulmonary arteriovenous malformations, pulmonary edema, etc. (healthblogs.org)
All physicians are board-certified pulmonologists with special interest and expertise in pulmonary vascular disease and hemodynamic evaluation. (iupui.edu)
We have some of the most extensive experience in using immunosuppressive drugs, such as cyclosporine and rapamycin, for the treatment of pulmonary vascular disease. (umn.edu)
We have many 15-year survivors with collagen vascular-associated pulmonary hypertension, thanks to our use of poly-drug treatments to attack the redundancy of molecular mechanisms inherent in pulmonary vascular disease. (umn.edu)
We are looking at myoglobin iron and oxygen saturation in peripheral muscle with a magnet to attempt to explain the exercise limitations in pulmonary vascular disease. (umn.edu)
We are designing a clinical trial to biologically or genetically engineer outgrowth endothelial cells for human use in pulmonary vascular disease. (umn.edu)
We have begun studies in the proteonomics of pulmonary vascular disease. (umn.edu)
Pulmonary hypertension , an abnormal elevation in pulmonary artery pressure, may be the result of left heart failure, pulmonary parenchymal or vascular disease, thromboembolism, or a combination of these factors. (mhmedical.com)
Whether the pulmonary hypertension arises from cardiac, pulmonary, or intrinsic vascular disease, it generally is a feature of advanced disease. (mhmedical.com)
In subjects with moderate to severe pulmonary vascular disease, as the resting PVR increases, there will be a corresponding increase in mean PAP until the cardiac output (CO) is compromised and starts to fall. (mhmedical.com)
This workshop was timely to leverage the anticipated scientific output from the recently launched "Redefining Pulmonary Hypertension through Pulmonary Vascular Disease Phenomics" (PVDOMICS) program with the Precision Medicine Initiative. (nih.gov)
PVDOMICS is supporting collaborative, protocol driven, comprehensive, deep phenotyping across all groups of PH patient populations in order to define novel pulmonary vascular disease (PVD) phenotypes. (nih.gov)

Some forms of pulmonary hypertension are linked to a gene defect that can run in families. (hopkinsmedicine.org)
The different haemodynamic forms of pulmonary hypertension can be found in multiple clinical conditions which have been classified into six main groups and at least twenty-six subgroups. (oxfordmedicine.com)

Treatment of pulmonary hypertension in neonates is a major challenge on the intensive care unit and involves high morbidity and mortality. (eur.nl)
This review provides an overview of currently available drugs and promising new targets in the treatment of pulmonary hypertension in neonates. (eur.nl)
This study will provide long-term, open-label data regarding the effect of continued long-term oral treprostinil therapy for the treatment of pulmonary hypertension (PH) associated with heart failure with preserved ejection fraction (HFpEF). (mayoclinic.org)
Our data from the use of sildenafil provided Pfizer with the basis for beginning trials on the use of PDE-V inhibitors (SUPER) for the treatment of pulmonary hypertension. (umn.edu)
Two graduate engineering students at the university founded ARIA Cardiovascular using the first implanted mechanical device for the treatment of pulmonary hypertension. (umn.edu)
BIDMC's Pulmonary Hypertension Center provides a state-of-the-art multidisciplinary approach to the evaluation and treatment of pulmonary hypertension. (bidmc.org)
He aims to establish a diagnostic test that allows clinicians to make treatment recommendations on a personalized basis and tailor the therapeutic approach to treatment of pulmonary hypertension. (akcchf.org)

Because the causes of pulmonary hypertension are so diverse, it is essential that the etiology underlying the pulmonary hypertension be clearly determined before beginning treatment. (mhmedical.com)
Pulmonary arterial hypertension (PAH) is a rare disease characterized by a sustained increase in pulmonary artery pressure (PAP), without common causes of pulmonary hypertension such as heart, lung, and other chronic diseases [ 1 ]. (clinmedjournals.org)

Pulmonary veno-occlusive disease and pulmonary capillary hemangiomatosis. (schweitzer-online.de)
EIF2AK4 has been identified as the major gene linked to pulmonary veno-occlusive disease. (clinmedjournals.org)

The new research could also lead to a better understanding of other diseases involving inflammation of blood vessels, such as coronary artery disease, said Mark Nicolls , MD, senior author of the study and division chief of pulmonary and critical care medicine at Stanford, as well as a staff physician at the Veterans Affairs Palo Alto Health Care System . (stanford.edu)
Associated pulmonary arterial hypertension , which includes cases linked to connective tissue diseases (lupus and scleroderma), congenital heart disease, diet pills, HIV and liver disease. (uchicagomedicine.org)
The Division is affiliated with the Alberta Respiratory Centre and has PhD and MD members involved in various areas of research in lung and airway diseases (https://www.ualberta.ca/department-of-medicine/divisions/pulmonary-medicine/publications). (ualberta.ca)
Pulmonary hypertension (PH) is a serious disorder that worsens the course of chronic heart, lung or systemic diseases. (biomedcentral.com)
Lung diseases like chronic obstructive pulmonary disease and diseases that cause venous occlusion or obstruction. (myupchar.com)
Group 3 pulmonary hypertension (PH) encompasses PH owing to lung diseases and/or hypoxia. (biomedcentral.com)
Pulmonary hypertension (PH) is a spectrum of diseases involving the pulmonary vasculature, and defined as an elevation in pulmonary arterial pressures (mean pulmonary artery pressure [PAP] >22 mmHg or an estimated systolic PAP >36 mmHg). (mhmedical.com)
These diseases include neuromuscular diseases, including amyotrophic lateral sclerosis and end-stage COPD or pulmonary fibrosis. (iu.edu)
Chronic Pulmonary Heart Diseases (incl. (healthgrades.com)
Diseases that affect the lungs or cause low oxygen levels can also result in secondary pulmonary hypertension, WHO Group 3. (kentucky.com)
Hypertrophic growth accompanies many heart diseases such as hypertension, ischemia, and valvular diseases. (biomedcentral.com)
According to this system, Group 1 PAH is divided into disease subgroups including heritable (HPAH, formerly familial PAH), idiopathic (IPAH), and PAH associated with drug/toxin exposures or a variety of other medical conditions including connective tissue diseases, human immunodeficiency virus (HIV) infection, congenital heart disease, and portal hypertension [ 7 , 8 ]. (clinmedjournals.org)
The Division of Pulmonary and Critical Care Medicine at Massachusetts General Hospital provides comprehensive care for the full range of respiratory conditions and diseases. (massgeneral.org)
The Division of Pulmonary and Critical Care Medicine at Mayo Clinic specializes in the prevention, diagnosis and treatment of diseases of the lung and chest and of sleep and critical care issues. (mayo.edu)
Patient care is provided by teams of physicians and other health care staff with broad expertise in all forms of pulmonary and critical care diseases. (mayo.edu)
Pulmonary hypertension can happen in association with many other diseases, such as lung disease and heart disease. (cdc.gov)

Pulmonary hypertension, defined as a resting mean pulmonary artery pressure greater than or equal to 25 mmHg, results from a myriad of conditions. (asahq.org)
2 Hemodynamically, pulmonary arterial hypertension can be defined as a mean pulmonary artery pressure greater than 25 mmHg, a pulmonary capillary wedge pressure less than 15 mmHg, and a pulmonary vascular resistance (PVR) greater than 3 Wood units in the absence of a more common cause such as left heart disease, chronic venothromboembolic disease, or lung disease. (asahq.org)
PAH is defined by a resting mean pulmonary artery pressure (mPAP) of greater than 25mmHg, pulmonary vascular resistance (PVR) greater than 3 Wood units and pulmonary capillary wedge pressure (PCWP) of less than 15mmHg - in the absence of other causes of PH. (oncologynurseadvisor.com)
Pulmonary hypertension (PH) is defined by a mean pulmonary artery pressure ≥25 mm Hg at rest, measured during right heart catheterization. (oncologynurseadvisor.com)

Pulmonary hypertension is a serious, chronic disease that can lead to heart failure if it's not treated. (hopkinsmedicine.org)

This contributes to abnormal smooth muscle growth into arterioles, with luminal narrowing, increased pulmonary vascular resistance and pressure, decreased pulmonary autoregulation and ultimately, resultant increase in larger arterial and RV pressures, finally leading to RV failure. (oncologynurseadvisor.com)
As a consequence of underdevelopment of the lung parenchyma, due to herniated abdominal contents in thorax, abnormal pulmonary vasculature growth may occur resulting in increased pulmonary vascular resistance and pulmonary hypertension (PAH). (anesthpain.com)

Our staff members are leading authorities in all types of pulmonary hypertension. (uchicagomedicine.org)
Effective treatment is available for all types of pulmonary hypertension. (kentucky.com)
What Are the Types of Pulmonary Hypertension? (upmc.com)

Expert Review of Respiratory Medicine (Vol. 2, pp. 85-96). (eur.nl)

Dilated RA/RV and she had HRCT and opinion is severe thoracic scoliosis with secondary lumber curve, pulmonary artery hypertension with bilateral perihilar interstitial edema cardiomegaly and current medicine used is Clopidogrel and Asprin, Digoxin, Bosentan, Ramipril ACE, Furosemide, Budesonide, Salbutamol, etc., but her recovery is nil. (icliniq.com)

For best patient outcomes, we emphasize a multidisciplinary approach with collaboration of related specialties such as pulmonary, cardiology, rheumatology, critical care and transplantation within the institution" Dr. Bag said. (uchicagomedicine.org)
The success of Temple's program relies on a team of experts - including cardiology specialists in pulmonary hypertension, interventional cardiology, thoracic imaging and cardiovascular surgery - for optimal preoperative assessment, surgical care, and postoperative patient management. (temple.edu)
Written by internationally recognized experts, Pulmonary Hypertension bridges the gap between pulmonology and cardiology to provide clinicians in both disciplines with knowledge of the signs, symptoms, diagnosis, and pharmacologic and surgical treatments for pulmonary hypertension (PH). (routledge.com)
She is, along with Dr. Ronald Zolty (Cardiology), assembling a Montefiore multi-disciplinary Pulmonary Hypertension Center. (montefiore.org)

According to various combinations of values of pulmonary capillary wedge pressure (PCWP), pulmonary vascular resistance (PVR) and cardiac output, different hemodynamic types of PH can be identified. (biomedcentral.com)
Can a cardiac MRI show anything in regards to pulmonary hypertension? (icliniq.com)
The right ventricle responds to an increase in pulmonary vascular resistance by increasing right ventricular (RV) systolic pressure to preserve cardiac output. (mhmedical.com)
Inhibition of the MIF inflammatory active site, during hypoxic exposure, significantly reduced pulmonary vascular remodeling, cardiac hypertrophy and right ventricular systolic pressure. (beds.ac.uk)
Reduced oxygen tension provokes pulmonary vessel constriction and if persistent induces pulmonary vascular remodeling resulting in increased vessel wall thickness and pulmonary vascular resistance which in turn lead to right ventricular failure, decreased left ventricular preload and reduced cardiac output ( 2 , 3 ). (beds.ac.uk)
This program is part of a series of outreach meetings for Primary Care, Family Medicine, Cardiologists, Hematologists, Cardiac Surgeons, Pulmonologists and their midlevel providers. (mmheadlines.org)
PH may either be primary or secondary to cardiac disease, pulmonary disease, thrombotic causes, or primary arterial hypertension. (oncologynurseadvisor.com)
Pulmonary Hypertension in sickle cell disease: cardiac catheterization results and survival. (ijmedicine.com)
A noninvasive test called an echocardiogram can suggest the diagnosis, and it is confirmed by a cardiac catheterization procedure called right heart catheterization, in which the pulmonary artery pressure is directly measured. (kentucky.com)
For example, a combination of essential ("regular") hypertension and obesity can lead to malfunction of the left ventricle in diastole, the filling half of the cardiac cycle, leading to secondary pulmonary hypertension. (kentucky.com)
Initial appointments for the Pulmonary Hypertension Clinic are scheduled through the Cardiac and Vascular Center at the University of Colorado Hospital. (ucdenver.edu)

Michael G. Risbano, MD, MA is Assistant Professor of Medicine in the Division of Pulmonary, Allergy and Critical Care Medicine at the University of Pittsburgh Medical Center. (schweitzer-online.de)
Dr. Auger was most recently Director of the CTEPH Program at UCSD Healthcare in San Diego - the nation's number one CTEPH/Pulmonary Thromboendarterectomy (PTE) program by volume and Professor of Clinical Medicine in the Division of Pulmonary and Critical Care Medicine at UCSD School of Medicine. (temple.edu)
80 studies in Pulmonary and Critical Care Medicine (open studies only). (mayoclinic.org)
Dr. Rajesh Harrykissoon, MD is a pulmonary critical care medicine doctor who practices in College Station, TX. (healthgrades.com)
Looking for a Pulmonary Critical Care Medicine Specialist? (healthgrades.com)
Principal Investigator of the project is Kim Kerr, MD , professor of clinical medicine in the Division of Pulmonary and Critical Care Medicine . (ucsd.edu)
The Division of Pulmonary and Critical Care Medicine has comprehensive diagnostic and therapeutic capabilities, offering a number of special tests and procedures. (massgeneral.org)
For information on the Pulmonary and Critical Care Medicine Fellowship Program, click here . (montefiore.org)
This research appears in the first issue for November 2006 of the American Journal of Respiratory and Critical Care Medicine, published by the American Thoracic Society. (innovations-report.com)
You have direct access to the pulmonary and critical care faculty at Mayo Clinic throughout your training in the Pulmonary and Critical Care Medicine Fellowship. (mayo.edu)

If another medical condition is causing the problem, it is called secondary pulmonary hypertension. (stlukes-stl.com)
Other pulmonary hypertension categories (formerly termed secondary), which include cases related to heart disease, blood clots, intrinsic lung disease and sleep disorders. (uchicagomedicine.org)
Clinically the diagnosis of pulmonary arterial hypertension (primary PH) is made when these secondary causes have been clinically excluded. (beds.ac.uk)
In group 2 WHO, raised left atrial pressures result in secondary elevation of pulmonary pressure. (oncologynurseadvisor.com)
Since the left ventricle is downstream of the lungs, any disease significantly affecting left ventricular filling pressure has the potential to lead to secondary pulmonary hypertension. (kentucky.com)
When another health problem is the cause, it is called secondary pulmonary hypertension. (upmc.com)

Pulmonary hypertension (PH) and pulmonary arterial hypertension (PAH) include different cardiopulmonary disorders in which the interaction of multiple genes with environmental and behavioural factors modulates the onset and the progression of these severe conditions. (ersjournals.com)
PPH is the former collective name of a group of pulmonary arterial hypertension (PAH) disorders including idiopathic PAH (IPAH), heritable PAH (HPAH) and anorexigen-induced PAH. (oncologynurseadvisor.com)
At the College Station Center for Pulmonary and Sleep Disorders we strive to provide optimal quality of life to you through the diagnosis and management of many types of lung and sleep disorders. (healthgrades.com)
Describing key concepts of precision medicine and relating these to pulmonary, critical care and sleep disorders is essential to educate relevant stakeholders and increase the impact of pulmonary precision medicine. (springer.com)
Pulmonary hypertension is a common, complex group of disorders that result from different pathophysiologic mechanisms but are all defined by a mean pulmonary arterial pressure of 25 mm Hg or greater. (aafp.org)
Pulmonary hypertension is a heterogeneous group of disorders characterized by a mean pulmonary arterial pressure of 25 mm Hg or greater at rest during right heart catheterization. (aafp.org)
Additionally, we collaborate in a multidisciplinary fashion, regularly interacting with other services, particularly internal medicine and subspecialties, thoracic surgery , medical and radiation oncology , transplant medicine, and the respective neurology-based sleep disorders centers , in order to maximize each patient's care and tailor treatment plans accordingly. (montefiore.org)

Right Heart Catheterization - Or pulmonary artery catheterization is a test used to see how well your heart is pumping (how much it pumps per minute) and to measure the blood pressure in your heart and the main blood vessels in your lungs. (bch.org)

UChicago Medicine and Ingalls Memorial offer a broad range of challenging clinical and non-clinical career opportunities doing work that really matters. (uchicagomedicine.org)
This book is a clinical guide to controversial and emerging topics in pulmonary hypertension. (schweitzer-online.de)
This book provides a deep dive into the diagnosis and therapeutics of pulmonary hypertension supported by the literature and balanced with personal clinical experience. (schweitzer-online.de)
Chapters address the diagnostic and treatment dilemmas posed by these various clinical entities through literature review, sharing of expert opinion, and review of recent guidelines and their applicability to the multiple different nuanced presentations of pulmonary hypertension. (schweitzer-online.de)
There he is Director of the Invasive Cardiopulmonary Exercise Program and Head of Clinical Operations for Pulmonary Hypertension. (schweitzer-online.de)
Pulmonary Hypertension in Sickle Cell Disease: Current Controversies and Clinical Practices. (schweitzer-online.de)
The presence of pulmonary hypertension, as defined above, is always an ominous prognostic sign, even if the severity may differ according to the haemodynamic changes and underlying clinical condition. (oxfordmedicine.com)
The Division provides a wide range of clinical programs in Pulmonary Medicine and Allergy. (ualberta.ca)
Since the second world symposium on PH held in Evian in 1998, a clinical classification was established using a precision medicine approach in order to individualise and gather together different categories of PH sharing similar haemodynamic criteria, types of pulmonary vascular lesions and similar management [ 1 , 2 ]. (ersjournals.com)
William R. Auger, MD , has joined Temple University Hospital as a pulmonologist in the Pulmonary Hypertension, Right Heart Failure and Chronic Thromboembolic Pulmonary Hypertension (CTEPH) Program in the Temple Heart and Vascular Institute, and Clinical Professor of Medicine at the Lewis Katz School of Medicine at Temple University. (temple.edu)
Dr Robin Condliffe and the Royal Hallamshire Clinical Research Facility are starting a trial of Riociguat, a drug for people with Pulmonary Arterial Hypertension (PAH). (lungsheffield.org)
Epidemiologic studies of this condition are hampered by the fact that no diagnostic code exists to differentiate hypertensive emergency from less serious clinical presentations associated with hypertension, despite the need for such a code. (mhmedical.com)
The Department of Internal Medicine is one of 16 clinical departments in the USF Morsani College of Medicine. (usf.edu)
The Department's research activities are numerous and involve both basic and clinical research activities in all subspecialties of Internal Medicine. (usf.edu)
PAH is a clinical diagnosis that cannot be made accurately without hemodynamic measurements taken from pulmonary artery catheterization. (clinmedjournals.org)
Services are provided Monday through Friday in the Pulmonary Ambulatory Center located in the Shapiro Clinical Center, East Campus. (bidmc.org)
Services are provided in the Pulmonary Hypertension Center located in the Shapiro Clinical Center, East Campus. (bidmc.org)
Like asthma, pulmonary arterial hypertension is a clinical syndrome, encompassing a host of causative factors. (medscape.com)
Stakeholders in PVD need to be brought together (scientists, clinicians, patient advocacy organizations, regulatory agency representatives, and pharmaceutical industries) to discuss the current needs, challenges, and new opportunities in applying precision medicine to PVD clinical research and treatments. (nih.gov)
The workshop addressed multiple topics that are central to the development of true personalized medicine in PVD, including inputs from all the stakeholders, from basic science, to drug development to clinical trials to master protocol. (nih.gov)
Current gaps and needs in applying precision medicine for PVD: clinical trials issues. (nih.gov)
The biostatistical challenges facing a precision medicine approach in PVD clinical trials. (nih.gov)
A taskforce of stakeholders to develop a master clinical trials protocol for PVD that will apply precision medicine principles to future interventional clinical trials should be created with development of a template for phase II and phase III clinical trials as the goal. (nih.gov)
Clinical, translational and basic research endeavors are incorporated into the very essence of Montefiore's Division of Pulmonary Medicine, with the goal of implementing new and innovative treatment therapies. (montefiore.org)
Research directed at practical clinical, translational, and fundamental questions is incorporated into the very essence of the Montefiore-Einstein Pulmonary Medicine Division. (montefiore.org)
Fulltime members of the Pulmonary Medicine Division are actively engaged in basic, translational, and clinical research endeavors, ranging from studies of functional and population genetics and epigenetics, to respiratory and vascular physiology to clinical investigations on pathophysiology and treatment. (montefiore.org)
Dr. Josanna Rodriguez-Lopez's main clinical research interest is in pulmonary hypertension, and associated clinical trials. (montefiore.org)
Clinical features and outcome in 25 dogs with respiratory-associated pulmonary hypertension treated with sildenafil. (akcchf.org)

Pharmacological activation of the transcription factor PPARγ affects the expression of key genes involved in the development of pulmonary hypertension (PH), subsequently has a variety of beneficial effects in the vasculature, and hence might be a powerful treatment of PH. (sciencemag.org)
The ability of the RV to adapt to increased vascular resistance is influenced by several factors, including age and the rapidity of the development of pulmonary hypertension. (mhmedical.com)
Scientists at the Max Planck Institute for Heart and Lung Research in Bad Nauheim and Giessen University have discovered that transcription factor FoxO1 regulates the division of cells and plays a key role in the development of pulmonary hypertension. (eurekalert.org)
Reduced FoxO1 activity is therefore an important factor in the development of pulmonary hypertension. (eurekalert.org)

About 100,000 people in the United States and Europe have been diagnosed with pulmonary hypertension, but many others are believed to go undiagnosed because the main symptom, shortness of breath, is nonspecific. (stanford.edu)
The most common symptom of pulmonary hypertension is shortness of breath, first when you exercise and later while at rest. (stlukes-stl.com)

The results, published Aug. 28 in Science Translational Medicine , suggest that using medications to block this pathway could lead to the first-known cure for the disease, apart from lung transplantation. (stanford.edu)
We believe that targeting inflammation is an exciting approach to augment current treatments for pulmonary hypertension because it may reverse the underlying cause of the disease,' said Nicolls, who is also director of the Lung Immunology Program and an associate professor of medicine. (stanford.edu)
In experiments in live rats with induced pulmonary hypertension, the disease was reversed when researchers blocked the inflammation-producing pathway. (stanford.edu)
Vasodilator-Responsive Idiopathic Pulmonary Arterial Hypertension: Evidence for a New Disease? (annals.org)
These topics include: exercise pulmonary hypertension, sickle cell disease and pulmonary hypertension, and sarcoid pulmonary hypertension, among many others. (schweitzer-online.de)
Controversies in the Management of Pulmonary Hypertension in the Setting of Lung Disease. (schweitzer-online.de)
Pulmonary Hypertension in Chronic Kidney Disease and End Stage Renal Disease. (schweitzer-online.de)
Pulmonary arterial hypertension (PAH) is a rare disease characterized by distinctive changes in pulmonary arterioles that lead to progressive pulmonary arterial pressures, right-sided heart failure, and a high mortality rate. (biomedcentral.com)
Background- Pulmonary arterial remodeling characterized by increased vascular smooth muscle proliferation is commonly seen in life-threatening disease, pulmonary arterial hypertension (PAH). (ahajournals.org)
Conclusions- Osteoprotegerin facilitates PAH pathogenesis by regulating pulmonary arterial smooth muscle cell proliferation, suggesting that it may be a potential biomarker and therapeutic target in this disease. (ahajournals.org)
Pulmonary arterial hypertension (PAH) is a progressive cardiopulmonary disease characterized by pulmonary artery remodeling. (ahajournals.org)
1 , 2 Despite an improved understanding of the disease development and treatment in recent decades, the mechanisms associated with pulmonary arterial hypertension (PAH) pathogenesis remain poorly understood. (ahajournals.org)
1 This review focuses on pulmonary arterial hypertension (Group 1 pulmonary hypertension), a disease in which progressive pulmonary vascular obstruction, remodeling, and destruction lead to increased right ventricular afterload and hypertrophy, right heart failure, and death. (asahq.org)
In this review, our focus will be on pulmonary arterial hypertension specifically (World Health Organization Group 1), predominantly comprising idiopathic and heritable pulmonary arterial hypertension, as well as pulmonary arterial hypertension associated with connective tissue disease, congenital heart disease, or other systemic conditions. (asahq.org)
For example, a large acute pulmonary thromboembolism can result in RV failure and shock, whereas chronic thromboembolic disease of equal severity may result in only mild exercise intolerance. (mhmedical.com)
Pulmonary function tests are helpful in documenting underlying obstructive airways disease, whereas high-resolution chest computed tomography (CT) is preferred to diagnose restrictive lung disease. (mhmedical.com)
As the disease advances, intimal proliferation and pathologic remodeling progress resulting in decreased compliance of the pulmonary vasculature. (mhmedical.com)
Pulmonary hypertension is a very treatable disease. (massgeneral.org)
Pulmonary hypertension (PH) is a devastating disease leading to progressive hypoxemia, right ventricular failure, and death. (beds.ac.uk)
Pulmonary hypertension (PH) is a devastating disease associated with progressive hypoxemia and right ventricular failure. (beds.ac.uk)
As a result of its commitment to patient care and ability to provide disease-focused programs, this division was recognized by U.S. News and World Report as the 14th best pulmonary and critical care program in the United States. (iu.edu)
You will hear an overview of Chronic Thromboembolic Pulmonary Hypertension as well as a discussion regarding surgical and noninvasive approaches for this disease. (mmheadlines.org)
Echocardiography estimates pulmonary artery pressure as well as assessing for shunt, valvular disease, and ventricular function. (oncologynurseadvisor.com)
Pulmonary function test (PFT) to identify obstructive and restrictive lung disease. (oncologynurseadvisor.com)
Powars D, Weidman J, Odom-Maryon T, Niland J, Johnson C. Sickle cell chronic lung disease: Prior morbidity and the risk of pulmonary failure. (ijmedicine.com)
Pulmonary Hypertension in sickle cell disease. (ijmedicine.com)
Abubakr SE, Girgis R, Swerdlow P. Pulmonary Hypertension in sickle cell disease. (ijmedicine.com)
Precision medicine is focused on the integration of individual variability with disease prevention and treatment principles derived from population studies. (springer.com)
Pulmonary arterial hypertension (PAH) is a devastating disease with significantly reduced survival. (clinmedjournals.org)
Persistent pulmonary hypertension of the newborn (PPHN) is a potentially fatal disease. (bvsalud.org)
Although much debate continues on the topic of the primary insult that leads to pulmonary arterial hypertension, it is clear that the disease is characterized by smoldering inflammation. (medscape.com)
Our better understanding of pulmonary arterial hypertension as an immunologic disease will certainly usher in a new era of targeted therapies for this fatal condition and shift management away from vasodilation toward immunomodulation. (medscape.com)
The European Medicines Agency (EMA) has started a review of the medicine Zinbryta (daclizumab) used to treat adults with relapsing forms of multiple sclerosis (a disease in which inflammation damages the protective sheath around the nerve cells in the brain and spinal cord). (bda.bg)
A multi-center, randomized, bouble-blinded, placebo-controlled trial to evaluate the safety and efficacy on inhaled Trepostinil in subjects with pulmonary hypertension due to parenchymal lung disease. (scleroderma.org)
Longtime members of our faculty have published extensively on topics such as: hypoxia, cough, environmental lung disease and sleep medicine, with many of the projects ongoing. (montefiore.org)
Pulmonary hypertension, however, is still incurable, not least of all due to insufficient knowledge of what causes the disease at the molecular level. (eurekalert.org)
The unique DNA signature of an individual is now recognized as a pivotal influence on disease outcome during treatment and has become the central concept propelling the study of pharmacogenomics and individualized medicine. (akcchf.org)
Dr. Stern will apply this cutting-edge knowledge to pulmonary hypertension in dogs, a common disease with serious consequences including exercise intolerance, respiratory distress, and sudden death. (akcchf.org)
Our Pulmonary Hypertension Clinics are located in the Advanced Heart and Lung Disease Center at IU Health Methodist Hospital and at the Roudebush VA Medical Center. (iupui.edu)
The symptoms of pulmonary hypertension during the initial stage of the disease are common to many other medical conditions (e.g., difficulty breathing, fatigue). (cdc.gov)
While not all pulmonary hypertension can be prevented, you can take steps to prevent it by making healthy lifestyle changes and managing high blood pressure, coronary heart disease, chronic liver disease, and chronic lung disease from tobacco use. (cdc.gov)

Congenital heart defects can result in left-to-right (systemic-to-pulmonary) shunts leading to increased pulmonary blood flow and risk of PAH. (biomedcentral.com)
Carol Mazur, 61, of suburban Chicago, has pulmonary hypertension from a congenital heart defect that went undetected until she was 23 years old. (nm.org)
Das B P, Singh A P, Singh R B. Emergency Corrective Surgery of Congenital Diaphragmatic Hernia With Pulmonary Hypertension: Prolonged Use of Dexmedetomidine as a Pharmacologic Adjunct, Anesth Pain Med. (anesthpain.com)

We have a general pulmonary practice (Pulmonary Associates), 11 subspecialty clinics, an interventional pulmonology program and a critical care program. (massgeneral.org)
Continuing our longstanding tradition of delivering exceptional patient care, we have recently added staff in emerging fields such as interventional pulmonary medicine, sleep medicine, early lung cancer detection, and other areas. (montefiore.org)

Current approved therapies for pulmonary hypertension have focused on dilating blood vessels without special attention being paid to the inflammation that is frequently seen around blood vessels,' Nicolls said. (stanford.edu)
DO NOT use complementary and alternative therapies (CAM) by themselves to treat pulmonary hypertension, unless directed to do so by your doctor. (stlukes-stl.com)
SEFERIAN A., SIMONNEAU G.. Therapies for pulmonary arterial hypertension: where are we today, where do we go tomorrow? (explainmedicine.com)
All available therapies for pulmonary hypertension are offered by our program. (massgeneral.org)

State-of-the-art treatment for this uncommon, but potentially fatal condition is available at only a few centers in the nation, including UChicago Medicine. (uchicagomedicine.org)

Have you or anyone of you family been diagnosed with deep vein thrombosis (DVT) or pulmonary embolism? (oncologynurseadvisor.com)

The device is based on the concepts of adding compliance to the pulmonary circulation as well as slowing the augmented reflectance wave in the diseased pulmonary circulation. (umn.edu)
The signaling mechanisms that underlie the structural and functional abnormalities in the pulmonary circulation of these infants are not yet clear. (elsevier.com)
Pulmonary Circulation , 3 (3), 454-466. (elsevier.com)
Fike, CD & Aschner, JL 2013, ' Looking beyond PPHN: The unmet challenge of chronic progressive pulmonary hypertension in the newborn ', Pulmonary Circulation , vol. 3, no. 3, pp. 454-466. (elsevier.com)
Although difficult, such search for metabolic patterns that might lead to replacing the term biomarker by metabolic fingerprinting in the area of pulmonary circulation has already begun. (cdc.gov)

The University of Alberta, Faculty of Medicine & Dentistry, Department of Medicine, Division of Pulmonary Medicine in partnership with Alberta Health Services invites applications for an academic Pulmonary Physician specializing in Lung Transplantation and Pulmonary Hypertension to be based at the University of Alberta Hospital. (ualberta.ca)
The Division of Pulmonary Medicine at Montefiore Medical Center takes pride in providing comprehensive care for inpatients and outpatients with all types of lung and respiratory conditions. (montefiore.org)

Like pulmonary hypertension in general, pulmonary arterial hypertension can result from multiple causes, including infectious and autoimmune pathologies. (asahq.org)
Faculty physicians in this specialty area provide general pulmonary and critical care services across the Indianapolis campus in primarily closed ICU settings, including 24/7 in-house critical care services at IU Health University and Methodist hospitals. (iu.edu)
The Division provides general pulmonary and critical care services across campus in primarily closed ICU settings. (iupui.edu)

A patient with symptomatic primary pulmonary artery hypertension underwent therapeutic trials with parenteral and oral phentolamine. (annals.org)
Which medicine will be helpful in pulmonary artery hypertension patient? (icliniq.com)
Q. Kindly suggest medicines to manage pulmonary artery hypertension patient. (icliniq.com)
Her lung functions are not good, similarly, pulmonary artery hypertension is also bad. (icliniq.com)
She can take Tadalafil along with Bosentan for better control of PAH (pulmonary artery hypertension). (icliniq.com)

The Fifth World Symposium on Pulmonary Hypertension proposed a classification system that organizes pulmonary hypertension into five groups based on common hemodynamic, pathophysiologic, and therapeutic parameters. (asahq.org)
This is part of the Group I in the revised WHO Pulmonary Hypertension (PH) classification based on the most recent concensus. (oncologynurseadvisor.com)
For a classification of pulmonary hypertension, see Figure 1 . (oncologynurseadvisor.com)

Thank you for your interest in spreading the word about Science Translational Medicine. (sciencemag.org)
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Hence, this form is known as idiopathic pulmonary arterial hypertension, or iPAH. (kentucky.com)

All approved medical and surgical treatments for pulmonary hypertension are available to you. (massgeneral.org)

5 Pulmonary hypertension is categorized on the basis of pathophysiology, hemodynamics, and therapeutic options. (aafp.org)
None experienced rebound pulmonary hypertension, a common therapeutic complication. (innovations-report.com)
Inhaled nitric oxide was first introduced in the early 1990s as a therapeutic agent to widen pulmonary blood vessels in ventilated lung regions by relaxing pulmonary vascular smooth muscle. (innovations-report.com)

Global "Pulmonary Arterial Hypertension (Pah) Medicine Market" report provides an elaborated overview of market with respect to the important drivers influencing the revenue graph of this business domain. (clinicalhearts.com)

As such, it is likely that a variety of treatments will be required to address the various causes of pulmonary arterial hypertension. (medscape.com)
To support a transition towards a precision medicine approach to treatments, the NHLBI in partnership with the Cardiovascular Medical Research and Education Fund (CMREF) organized a workshop to address the barriers, gaps and opportunities to applying precision medicine to PVD including pulmonary hypertension. (nih.gov)

However, we have gained considerable insights into the pathophysiology of pulmonary hypertension leading to an increasing number of possible treatment targets. (eur.nl)

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