Halothane
Anesthetics, Inhalation
Anesthesia, Inhalation
Isoflurane
Enflurane
Anesthetics
Nitrous Oxide
Malignant Hyperthermia
Trifluoroacetic Acid
Thiopental
Ethers
Dogs
Anesthesia
Depression, Chemical
Ether
Methoxyflurane
Ethyl Ethers
Anesthesia, General
Chlorofluorocarbons
Hydrocarbons, Halogenated
Anesthetics, General
Pentobarbital
Dose-Response Relationship, Drug
Drug-Induced Liver Injury
Succinylcholine
Respiration
Hypotension, Controlled
Fluoroacetates
Thiamylal
Mutation screening of the RYR1 gene and identification of two novel mutations in Italian malignant hyperthermia families. (1/1763)
Point mutations in the ryanodine receptor (RYR1) gene are associated with malignant hyperthermia, an autosomal dominant disorder triggered in susceptible people (MHS) by volatile anaesthetics and depolarising skeletal muscle relaxants. To date, 17 missense point mutations have been identified in the human RYR1 gene by screening of the cDNA obtained from muscle biopsies. Here we report single strand conformation polymorphism (SSCP) screening for nine of the most frequent RYR1 mutations using genomic DNA isolated from MHS patients. In addition, the Argl63Cys mutation was analysed by restriction enzyme digestion. We analysed 57 unrelated patients and detected seven of the known RYR1 point mutations. Furthermore, we found a new mutation, Arg2454His, segregating with the MHS phenotype in a large pedigree and a novel amino acid substitution at position 2436 in another patient, indicating a 15.8% frequency of these mutations in Italian patients. A new polymorphic site in intron 16 that causes the substitution of a G at position -7 with a C residue was identified. (+info)A neomorphic syntaxin mutation blocks volatile-anesthetic action in Caenorhabditis elegans. (2/1763)
The molecular mechanisms underlying general anesthesia are unknown. For volatile general anesthetics (VAs), indirect evidence for both lipid and protein targets has been found. However, no in vivo data have implicated clearly any particular lipid or protein in the control of sensitivity to clinical concentrations of VAs. Genetics provides one approach toward identifying these mechanisms, but genes strongly regulating sensitivity to clinical concentrations of VAs have not been identified. By screening existing mutants of the nematode Caenorhabditis elegans, we found that a mutation in the neuronal syntaxin gene dominantly conferred resistance to the VAs isoflurane and halothane. By contrast, other mutations in syntaxin and in the syntaxin-binding proteins synaptobrevin and SNAP-25 produced VA hypersensitivity. The syntaxin allelic variation was striking, particularly for isoflurane, where a 33-fold range of sensitivities was seen. Both the resistant and hypersensitive mutations decrease synaptic transmission; thus, the indirect effect of reducing neurotransmission does not explain the VA resistance. As assessed by pharmacological criteria, halothane and isoflurane themselves reduced cholinergic transmission, and the presynaptic anesthetic effect was blocked by the resistant syntaxin mutation. A single gene mutation conferring high-level resistance to VAs is inconsistent with nonspecific membrane-perturbation theories of anesthesia. The genetic and pharmacological data suggest that the resistant syntaxin mutant directly blocks VA binding to or efficacy against presynaptic targets that mediate anesthetic behavioral effects. Syntaxin and syntaxin-binding proteins are candidate anesthetic targets. (+info)Functional brain imaging during anesthesia in humans: effects of halothane on global and regional cerebral glucose metabolism. (3/1763)
BACKGROUND: Propofol and isoflurane anesthesia were studied previously with functional brain imaging in humans to begin identifying key brain areas involved with mediating anesthetic-induced unconsciousness. The authors describe an additional positron emission tomography study of halothane's in vivo cerebral metabolic effects. METHODS: Five male volunteers each underwent two positron emission tomography scans. One scan assessed awake-baseline metabolism, and the other scan assessed metabolism during halothane anesthesia titrated to the point of unresponsiveness (mean +/- SD, expired = 0.7+/-0.2%). Scans were obtained using a GE2048 scanner and the F-18 fluorodeoxyglucose technique. Regions of interest were analyzed for changes in both absolute and relative glucose metabolism. In addition, relative changes in metabolism were evaluated using statistical parametric mapping. RESULTS: Awake whole-brain metabolism averaged 6.3+/-1.2 mg x 100 g(-1) x min(-1) (mean +/- SD). Halothane reduced metabolism 40+/-9% to 3.7+/-0.6 mg x 100 g(-1) x min(-1) (P< or =0.005). Regional metabolism did not increase in any brain areas for any volunteer. The statistical parametric mapping analysis revealed significantly less relative metabolism in the basal forebrain, thalamus, limbic system, cerebellum, and occiput during halothane anesthesia. CONCLUSIONS: Halothane caused a global whole-brain metabolic reduction with significant shifts in regional metabolism. Comparisons with previous studies reveal similar absolute and relative metabolic effects for halothane and isoflurane. Propofol, however, was associated with larger absolute metabolic reductions, suppression of relative cortical metabolism more than either inhalational agent, and significantly less suppression of relative basal ganglia and midbrain metabolism. (+info)Primary and secondary hyperalgesia in a rat model for human postoperative pain. (4/1763)
BACKGROUND: Previously, the authors developed and characterized a rat model for postoperative pain to learn more about pain produced by incisions. In this study, the responses to heat and mechanical stimuli were evaluated directly on or adjacent to the incision and at varying distances from the incision. METHODS: Rats were anesthetized with halothane and incisions were made at different locations in the plantar aspect of the foot. The response frequency to a blunt mechanical stimulus, the withdrawal threshold to von Frey filaments (15-522 mN), and the withdrawal latency to radiant heat were measured. Rats were tested before surgery, 2 h later, and then daily through postoperative day 9. RESULTS: After plantar incision, persistent hyperalgesia was observed immediately adjacent to or directly on the incision to punctate and blunt mechanical stimuli, respectively. The withdrawal threshold to punctate stimuli applied 1 cm from the incision was decreased through postoperative day 1. In a transitional area, between the distant and adjacent sites, the withdrawal threshold was intermediate and the duration of hyperalgesia was transient. Heat hyperalgesia was persistent but present when the stimulus was applied to the site of injury but not to a distant site. CONCLUSION: Robust primary hyperalgesia to punctate and blunt mechanical stimuli was present. Hyperalgesia distant to the wound, or secondary hyperalgesia, occurred in response to punctate mechanical stimuli, was short-lived, and required greater forces. These results suggest that the most persistent pain behaviors in this model are largely primary hyperalgesia. (+info)Halothane, an inhalational anesthetic agent, increases folding stability of serum albumin. (5/1763)
Inhalational anesthetic agents are known to alter protein function, but the nature of the interactions underlying these effects remains poorly understood. We have used differential scanning calorimetry to study the effects of the anesthetic agent halothane on the thermally induced unfolding transition of bovine serum albumin. We find that halothane (0.6-10 mM) stabilizes the folded state of this protein, increasing its transition midpoint temperature from 62 to 71 degrees C. Binding of halothane to the native state of serum albumin thus outweighs any non-specific interactions between the thermally unfolded state of serum albumin and halothane in this concentration range. Based on the average enthalpy change DeltaH for unfolding of 170 kcal/mol, the increase from 62 to 71 degrees C corresponds to an additional Gibbs energy of stabilization (DeltaDeltaG) due to halothane of more than 4 kcal/mol. Analysis of the dependence of DeltaDeltaG on halothane concentration shows that thermal unfolding of a bovine serum albumin molecule is linked to the dissociation of about one halothane molecule at lower halothane concentrations and about six at higher halothane concentrations. Serum albumin is the first protein that has been shown to be stabilized by an inhalational anesthetic. (+info)A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease. (6/1763)
Central core disease is a rare, nonprogressive myopathy that is characterized by hypotonia and proximal muscle weakness. In a large Mexican kindred with an unusually severe and highly penetrant form of the disorder, DNA sequencing identified an I4898T mutation in the C-terminal transmembrane/luminal region of the RyR1 protein that constitutes the skeletal muscle ryanodine receptor. All previously reported RYR1 mutations are located either in the cytoplasmic N terminus or in a central cytoplasmic region of the 5,038-aa protein. The I4898T mutation was introduced into a rabbit RYR1 cDNA and expressed in HEK-293 cells. The response of the mutant RyR1 Ca2+ channel to the agonists halothane and caffeine in a Ca2+ photometry assay was completely abolished. Coexpression of normal and mutant RYR1 cDNAs in a 1:1 ratio, however, produced RyR1 channels with normal halothane and caffeine sensitivities, but maximal levels of Ca2+ release were reduced by 67%. [3H]Ryanodine binding indicated that the heterozygous channel is activated by Ca2+ concentrations 4-fold lower than normal. Single-cell analysis of cotransfected cells showed a significantly increased resting cytoplasmic Ca2+ level and a significantly reduced luminal Ca2+ level. These data are indicative of a leaky channel, possibly caused by a reduction in the Ca2+ concentration required for channel activation. Comparison with two other coexpressed mutant/normal channels suggests that the I4898T mutation produces one of the most abnormal RyR1 channels yet investigated, and this level of abnormality is reflected in the severe and penetrant phenotype of affected central core disease individuals. (+info)Effects of the halothane genotype and slaughter weight on texture of pork. (7/1763)
The objective of this study was to investigate the effects of the halothane (HAL) genotype, slaughter weight (SW), and the HAL x SW interaction on compositional and textural traits of raw and cooked pork. Pigs were bred to exhibit one of the three HAL genotypes (NN, Nn, and nn) with otherwise equivalent genomes. The nn halothane reactors are known to typically produce PSE pork, whereas NN pigs do not typically produce PSE pork. Pietrain x Large White gilts and boars, all with verified Nn genotype (by DNA test), were mated to obtain F2 littermates of the three HAL genotypes. These pigs were slaughtered at either 101 +/- 3 ("light") or 127 +/- 3 ("heavy") kg BW and were evaluated for longissimus muscle traits. The pH at .5 h after death (pH1) was 6.35, 6.13, and 5.68 in NN, Nn, and nn pigs, respectively. Sarcomere length was greater in nn than in NN and Nn pigs (1.94 vs 1.83 and 1.85 microm, respectively). Mechanical resistance was higher in nn than in NN pigs for both raw and cooked meat. Meat from nn pigs was judged by a trained panel to be less rough, more cohesive, harder, more fibrous, less granular, more elastic, and less easy to swallow than meat from NN pigs. For most traits under study, the heterozygotes were intermediate between the homozygotes but closer to NN than to nn pigs. Muscle from heavy pigs had longer sarcomeres and less moisture than muscle from light pigs. The n allele of the HAL gene unfavorably affects pork texture, and this effect is maintained throughout the range of 101 to 127 kg BW. (+info)Halothane effect on formalin-induced paw edema and flinching in rat. (8/1763)
The formalin test is a model of injury-produced inflammatory pain. Anesthetics, in clinically relevant concentrations, affect neutrophils and immune suppression. This study was to determine whether halothane reliably inhibits inflammatory reaction and formalin induced pain behavior or does not. Rats were exposed to 100% oxygen (control) or halothane, respectively for 30 min and then 24 hr later five percent formalin test was assessed. The base values of the paw's diameter were obtained earlier, and then formalin induced edema was assessed by measuring diameters of the injected paws at 5 min, 1 hr, 4 hr and 24 hr after the injection. Nociceptive behavior was quantified by counting the number of times with the paw flinched at 5 min intervals for 60 min. The diameters of edema in the halothane group lessened more than those in the oxygen group at 1 and 24 hr in each following of the injection (p<0.05). The rats pre-administered with oxygen or halothane were similar appearances in nociceptive behaviors. It suggests that halothane anesthesia might inhibit slightly the inflammatory reaction with the formalin-induced edema but might not inhibit the formalin-induced pain behavior in the event of pre-administration halothane 24 hr earlier before the formalin test of rat. (+info)Halothane is a general anesthetic agent, which is a volatile liquid that evaporates easily and can be inhaled. It is used to produce and maintain general anesthesia (a state of unconsciousness) during surgical procedures. Halothane is known for its rapid onset and offset of action, making it useful for both induction and maintenance of anesthesia.
The medical definition of Halothane is:
Halothane (2-bromo-2-chloro-1,1,1-trifluoroethane) is a volatile liquid general anesthetic agent with a mild, sweet odor. It is primarily used for the induction and maintenance of general anesthesia in surgical procedures due to its rapid onset and offset of action. Halothane is administered via inhalation and acts by depressing the central nervous system, leading to a reversible loss of consciousness and analgesia.
It's important to note that Halothane has been associated with rare cases of severe liver injury (hepatotoxicity) and anaphylaxis (a severe, life-threatening allergic reaction). These risks have led to the development and use of alternative general anesthetic agents with better safety profiles.
Inhalational anesthetics are a type of general anesthetic that is administered through the person's respiratory system. They are typically delivered in the form of vapor or gas, which is inhaled through a mask or breathing tube. Commonly used inhalational anesthetics include sevoflurane, desflurane, isoflurane, and nitrous oxide. These agents work by depressing the central nervous system, leading to a loss of consciousness and an inability to feel pain. They are often used for their rapid onset and offset of action, making them useful for both induction and maintenance of anesthesia during surgical procedures.
Inhalational anesthesia is a type of general anesthesia that is induced by the inhalation of gases or vapors. It is administered through a breathing system, which delivers the anesthetic agents to the patient via a face mask, laryngeal mask airway, or endotracheal tube.
The most commonly used inhalational anesthetics include nitrous oxide, sevoflurane, isoflurane, and desflurane. These agents work by depressing the central nervous system, causing a reversible loss of consciousness, amnesia, analgesia, and muscle relaxation.
The depth of anesthesia can be easily adjusted during the procedure by changing the concentration of the anesthetic agent. Once the procedure is complete, the anesthetic agents are eliminated from the body through exhalation, allowing for a rapid recovery.
Inhalational anesthesia is commonly used in a wide range of surgical procedures due to its ease of administration, quick onset and offset of action, and ability to rapidly adjust the depth of anesthesia. However, it requires careful monitoring and management by trained anesthesia providers to ensure patient safety and optimize outcomes.
Isoflurane is a volatile halogenated ether used for induction and maintenance of general anesthesia. It is a colorless liquid with a pungent, sweet odor. Isoflurane is an agonist at the gamma-aminobutyric acid type A (GABAA) receptor and inhibits excitatory neurotransmission in the brain, leading to unconsciousness and immobility. It has a rapid onset and offset of action due to its low blood solubility, allowing for quick adjustments in anesthetic depth during surgery. Isoflurane is also known for its bronchodilator effects, making it useful in patients with reactive airway disease. However, it can cause dose-dependent decreases in heart rate and blood pressure, so careful hemodynamic monitoring is required during its use.
Enflurane is a volatile halogenated ether that was commonly used as an inhalational general anesthetic agent. Its chemical formula is C3H2ClF5O. It has been largely replaced by newer and safer anesthetics, but it is still occasionally used in certain clinical situations due to its favorable properties such as rapid onset and offset of action, stable hemodynamics, and low blood solubility. However, it can cause adverse effects such as respiratory depression, arrhythmias, and neurotoxicity, particularly with prolonged use or high doses. Therefore, its use requires careful monitoring and management by anesthesia professionals.
Methyl ethers are a type of organic compound where a methyl group (CH3-) is attached to an oxygen atom, which in turn is connected to another carbon atom. They are formed by the process of methylation, where a methyl group replaces a hydrogen atom in another molecule.
Methyl ethers can be found in various natural and synthetic substances. For example, dimethyl ether (CH3-O-CH3) is a common fuel used in refrigeration systems and as a propellant in aerosol sprays. Anisole (CH3-O-C6H5), another methyl ether, is found in anise oil and is used as a flavoring agent and solvent.
It's worth noting that some methyl ethers have been associated with potential health risks, particularly when they are volatile and can be inhaled or ingested. For example, exposure to high levels of dimethyl ether can cause respiratory irritation, headaches, and dizziness. Therefore, it's important to handle these substances with care and follow appropriate safety guidelines.
Anesthetics are medications that are used to block or reduce feelings of pain and sensation, either locally in a specific area of the body or generally throughout the body. They work by depressing the nervous system, interrupting the communication between nerves and the brain. Anesthetics can be administered through various routes such as injection, inhalation, or topical application, depending on the type and the desired effect. There are several classes of anesthetics, including:
1. Local anesthetics: These numb a specific area of the body and are commonly used during minor surgical procedures, dental work, or to relieve pain from injuries. Examples include lidocaine, prilocaine, and bupivacaine.
2. Regional anesthetics: These block nerve impulses in a larger area of the body, such as an arm or leg, and can be used for more extensive surgical procedures. They are often administered through a catheter to provide continuous pain relief over a longer period. Examples include spinal anesthesia, epidural anesthesia, and peripheral nerve blocks.
3. General anesthetics: These cause a state of unconsciousness and are used for major surgical procedures or when the patient needs to be completely immobile during a procedure. They can be administered through inhalation or injection and affect the entire body. Examples include propofol, sevoflurane, and isoflurane.
Anesthetics are typically safe when used appropriately and under medical supervision. However, they can have side effects such as drowsiness, nausea, and respiratory depression. Proper dosing and monitoring by a healthcare professional are essential to minimize the risks associated with anesthesia.
Nitrous oxide, also known as laughing gas, is a colorless and non-flammable gas with a slightly sweet odor and taste. In medicine, it's commonly used for its anesthetic and pain reducing effects. It is often used in dental procedures, surgery, and childbirth to help reduce anxiety and provide mild sedation. Nitrous oxide works by binding to the hemoglobin in red blood cells, which reduces the oxygen-carrying capacity of the blood, but this effect is usually not significant at the low concentrations used for analgesia and anxiolysis. It's also considered relatively safe when administered by a trained medical professional because it does not cause depression of the respiratory system or cardiovascular function.
Malignant hyperthermia (MH) is a rare, but potentially life-threatening genetic disorder that can occur in susceptible individuals as a reaction to certain anesthetic drugs or other triggers. The condition is characterized by a rapid and uncontrolled increase in body temperature (hyperthermia), muscle rigidity, and metabolic rate due to abnormal skeletal muscle calcium regulation.
MH can develop quickly during or after surgery, usually within the first hour of exposure to triggering anesthetics such as succinylcholine or volatile inhalational agents (e.g., halothane, sevoflurane, desflurane). The increased metabolic rate and muscle activity lead to excessive production of heat, carbon dioxide, lactic acid, and potassium, which can cause severe complications such as heart rhythm abnormalities, kidney failure, or multi-organ dysfunction if not promptly recognized and treated.
The primary treatment for MH involves discontinuing triggering anesthetics, providing supportive care (e.g., oxygen, fluid replacement), and administering medications to reduce body temperature, muscle rigidity, and metabolic rate. Dantrolene sodium is the specific antidote for MH, which works by inhibiting calcium release from the sarcoplasmic reticulum in skeletal muscle cells, thereby reducing muscle contractility and metabolism.
Individuals with a family history of MH or who have experienced an episode should undergo genetic testing and counseling to determine their susceptibility and take appropriate precautions when receiving anesthesia.
Trifluoroacetic acid (TFA) is not typically considered a medical term, but rather a chemical one. However, it does have relevance to the medical field in certain contexts, such as in laboratory settings or pharmaceutical manufacturing. Here's a definition of TFA:
Trifluoroacetic acid (C2HF3O2) is an inorganic compound that is a colorless liquid at room temperature. It has a strong, pungent odor and is highly corrosive. In the chemical industry, it is commonly used as a reagent or solvent due to its ability to dissolve a wide range of organic compounds.
In the medical field, TFA may be encountered in laboratory settings where it can be used for various purposes such as peptide synthesis, chromatography, and other chemical reactions. It is also sometimes used as an ingredient in certain pharmaceutical formulations, although its use is generally limited due to its potential toxicity.
It's worth noting that TFA is not a medication or drug, but rather a chemical compound with various industrial and laboratory applications.
Thiopental, also known as Thiopentone, is a rapid-onset, ultrashort-acting barbiturate derivative. It is primarily used for the induction of anesthesia due to its ability to cause unconsciousness quickly and its short duration of action. Thiopental can also be used for sedation in critically ill patients, though this use has become less common due to the development of safer alternatives.
The drug works by enhancing the inhibitory effects of gamma-aminobutyric acid (GABA), a neurotransmitter in the brain that produces a calming effect. This results in the depression of the central nervous system, leading to sedation, hypnosis, and ultimately, anesthesia.
It is worth noting that Thiopental has been largely replaced by newer drugs in many clinical settings due to its potential for serious adverse effects, such as cardiovascular and respiratory depression, as well as the risk of anaphylaxis. Additionally, it has been used in controversial procedures like capital punishment in some jurisdictions.
In medical or clinical terms, "ethers" do not have a specific relevance as a single medical condition or diagnosis. However, in a broader chemical context, ethers are a class of organic compounds characterized by an oxygen atom connected to two alkyl or aryl groups. Ethers are not typically used as therapeutic agents but can be found in certain medications as solvents or as part of the drug's chemical structure.
An example of a medication with an ether group is the antihistamine diphenhydramine (Benadryl), which has a phenyl ether moiety in its chemical structure. Another example is the anesthetic sevoflurane, which is a fluorinated methyl isopropyl ether used for inducing and maintaining general anesthesia during surgeries.
It's important to note that 'ethers' as a term primarily belongs to the field of chemistry rather than medicine.
I believe there might be a misunderstanding in your question. "Dogs" is not a medical term or condition. It is the common name for a domesticated carnivore of the family Canidae, specifically the genus Canis, which includes wolves, foxes, and other extant and extinct species of mammals. Dogs are often kept as pets and companions, and they have been bred in a wide variety of forms and sizes for different purposes, such as hunting, herding, guarding, assisting police and military forces, and providing companionship and emotional support.
If you meant to ask about a specific medical condition or term related to dogs, please provide more context so I can give you an accurate answer.
Anesthesia is a medical term that refers to the loss of sensation or awareness, usually induced by the administration of various drugs. It is commonly used during surgical procedures to prevent pain and discomfort. There are several types of anesthesia, including:
1. General anesthesia: This type of anesthesia causes a complete loss of consciousness and is typically used for major surgeries.
2. Regional anesthesia: This type of anesthesia numbs a specific area of the body, such as an arm or leg, while the patient remains conscious.
3. Local anesthesia: This type of anesthesia numbs a small area of the body, such as a cut or wound, and is typically used for minor procedures.
Anesthesia can be administered through various routes, including injection, inhalation, or topical application. The choice of anesthesia depends on several factors, including the type and duration of the procedure, the patient's medical history, and their overall health. Anesthesiologists are medical professionals who specialize in administering anesthesia and monitoring patients during surgical procedures to ensure their safety and comfort.
I couldn't find a medical definition for "Depression, Chemical" as it is not a recognized medical term. However, I can provide you with information about chemical imbalances in the brain that are associated with depression.
Major depressive disorder (MDD), commonly referred to as depression, is believed to be caused by a combination of genetic, environmental, and physiological factors. While there is no definitive evidence that depression is solely caused by a "chemical imbalance," neurotransmitter irregularities in the brain are associated with depressive symptoms. Neurotransmitters are chemical messengers that transmit signals in the brain and other parts of the body. Some of the primary neurotransmitters involved in mood regulation include serotonin, norepinephrine, and dopamine.
In depression, it is thought that there may be alterations in the functioning of these neurotransmitter systems, leading to an imbalance. For example:
1. Serotonin: Low levels of serotonin are associated with depressive symptoms. Selective serotonin reuptake inhibitors (SSRIs), a common class of antidepressants, work by increasing the availability of serotonin in the synapse (the space between neurons) to improve communication between brain cells.
2. Norepinephrine: Imbalances in norepinephrine levels can contribute to depressive symptoms and anxiety. Norepinephrine reuptake inhibitors (NRIs), tricyclic antidepressants (TCAs), and monoamine oxidase inhibitors (MAOIs) are medications that target norepinephrine to help alleviate depression.
3. Dopamine: Deficiencies in dopamine can lead to depressive symptoms, anhedonia (the inability to feel pleasure), and motivation loss. Some antidepressants, like bupropion, work by increasing dopamine levels in the brain.
In summary, while "Chemical Depression" is not a recognized medical term, chemical imbalances in neurotransmitter systems are associated with depressive symptoms. However, depression is a complex disorder that cannot be solely attributed to a single cause or a simple chemical imbalance. It is essential to consider multiple factors when diagnosing and treating depression.
In medical terms, "ether" is an outdated term that was used to refer to a group of compounds known as diethyl ethers. The most common member of this group, and the one most frequently referred to as "ether," is diethyl ether, also known as sulfuric ether or simply ether.
Diethyl ether is a highly volatile, flammable liquid that was once widely used as an anesthetic agent in surgical procedures. It has a characteristic odor and produces a state of unconsciousness when inhaled, allowing patients to undergo surgery without experiencing pain. However, due to its numerous side effects, such as nausea, vomiting, and respiratory depression, as well as the risk of explosion or fire during use, it has largely been replaced by safer and more effective anesthetic agents.
It's worth noting that "ether" also has other meanings in different contexts, including a term used to describe a substance that produces a feeling of detachment from reality or a sense of unreality, as well as a class of organic compounds characterized by the presence of an ether group (-O-, a functional group consisting of an oxygen atom bonded to two alkyl or aryl groups).
Methoxyflurane is a sweet-smelling, volatile liquid that is used as an inhalational general anesthetic agent. It is chemically described as 2,2-dichloro-1,1-difluoro-1-methoxyethane. Methoxyflurane is a fluorinated hydrocarbon with low blood/gas solubility, which allows for rapid induction and emergence from anesthesia. It has been used for the induction and maintenance of anesthesia in both adults and children. However, its use has been limited due to concerns about nephrotoxicity associated with high concentrations or prolonged exposure.
Ethyl ether, also known as diethyl ether or simply ether, is a type of organic compound that is classified as a simple ether. It is a colorless and highly volatile liquid with a characteristic odor that is often described as sweet or fruity. In medical contexts, ethyl ether has been historically used as an anesthetic agent due to its ability to produce unconsciousness and insensitivity to pain when inhaled. However, its use as an anesthetic has largely been replaced by safer and more effective alternatives due to its flammability, explosiveness, and potential for causing serious adverse effects such as heart problems and liver damage.
Ethyl ether is a simple ether consisting of two ethyl groups (-C2H5) linked to an oxygen atom (O), with the molecular formula C4H10O. It is produced by the reaction of ethanol with sulfuric acid, followed by distillation to separate the resulting ethyl ether from other products.
In addition to its historical use as an anesthetic, ethyl ether has been used in various industrial and laboratory applications, such as a solvent for fats, oils, resins, and waxes, and as a starting material for the synthesis of other chemicals. However, due to its flammability and potential for causing harm, it is important to handle ethyl ether with care and follow appropriate safety precautions when using it.
General anesthesia is a state of controlled unconsciousness, induced by administering various medications, that eliminates awareness, movement, and pain sensation during medical procedures. It involves the use of a combination of intravenous and inhaled drugs to produce a reversible loss of consciousness, allowing patients to undergo surgical or diagnostic interventions safely and comfortably. The depth and duration of anesthesia are carefully monitored and adjusted throughout the procedure by an anesthesiologist or certified registered nurse anesthetist (CRNA) to ensure patient safety and optimize recovery. General anesthesia is typically used for more extensive surgical procedures, such as open-heart surgery, major orthopedic surgeries, and neurosurgery.
Chlorofluorocarbons (CFCs) are synthetic, volatile organic compounds that consist of carbon atoms, chlorine atoms, and fluorine atoms. They were widely used in various applications such as refrigerants, aerosol propellants, solvents, and fire extinguishing agents due to their non-toxicity, non-flammability, and chemical stability.
However, CFCs have been found to contribute significantly to the depletion of the Earth's ozone layer when released into the atmosphere. This is because they are stable enough to reach the upper atmosphere, where they react with ultraviolet radiation to release chlorine atoms that can destroy ozone molecules. As a result, the production and use of CFCs have been phased out under the Montreal Protocol, an international treaty aimed at protecting the ozone layer.
Halogenated hydrocarbons are organic compounds containing carbon (C), hydrogen (H), and one or more halogens, such as fluorine (F), chlorine (Cl), bromine (Br), or iodine (I). These compounds are formed when halogens replace one or more hydrogen atoms in a hydrocarbon molecule.
Halogenated hydrocarbons can be further categorized into two groups:
1. Halogenated aliphatic hydrocarbons: These include alkanes, alkenes, and alkynes with halogen atoms replacing hydrogen atoms. Examples include chloroform (trichloromethane, CHCl3), methylene chloride (dichloromethane, CH2Cl2), and trichloroethylene (C2HCl3).
2. Halogenated aromatic hydrocarbons: These consist of aromatic rings, such as benzene, with halogen atoms attached. Examples include chlorobenzene (C6H5Cl), bromobenzene (C6H5Br), and polyhalogenated biphenyls like polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs).
Halogenated hydrocarbons have various industrial applications, including use as solvents, refrigerants, fire extinguishing agents, and intermediates in chemical synthesis. However, some of these compounds can be toxic, environmentally persistent, and bioaccumulative, posing potential health and environmental risks.
General anesthetics are a type of medication used to render a person unconscious and insensible to pain during surgical procedures. They work by depressing the central nervous system, affecting the brain's ability to process information and transmit signals, including those related to pain and muscle movement. General anesthesia involves a combination of intravenous (IV) drugs and inhaled gases that produce a state of controlled unconsciousness, amnesia, analgesia, and immobility.
General anesthetics can be classified into several categories based on their chemical structure and mechanism of action, including:
1. Inhalation anesthetics: These are volatile liquids or gases that are vaporized and inhaled through a breathing circuit. Examples include sevoflurane, desflurane, isoflurane, and nitrous oxide.
2. Intravenous anesthetics: These are drugs that are administered directly into the bloodstream through an IV line. Examples include propofol, etomidate, and ketamine.
3. Dissociative anesthetics: These are drugs that produce a state of dissociation between the thalamus and the cerebral cortex, resulting in altered consciousness, analgesia, and amnesia. Ketamine is a commonly used example.
4. Neurodegenerative anesthetics: These are drugs that cause degeneration of neurons in specific areas of the brain, leading to loss of consciousness. Examples include barbiturates such as thiopental and methohexital.
The choice of general anesthetic depends on several factors, including the patient's medical history, the type and duration of surgery, and the anesthesiologist's preference. The administration of general anesthetics requires careful monitoring and management by a trained anesthesia provider to ensure the patient's safety and comfort throughout the procedure.
Pentobarbital is a barbiturate medication that is primarily used for its sedative and hypnotic effects in the treatment of insomnia, seizure disorders, and occasionally to treat severe agitation or delirium. It works by decreasing the activity of nerves in the brain, which produces a calming effect.
In addition to its medical uses, pentobarbital has been used for non-therapeutic purposes such as euthanasia and capital punishment due to its ability to cause respiratory depression and death when given in high doses. It is important to note that the use of pentobarbital for these purposes is highly regulated and restricted to licensed medical professionals in specific circumstances.
Like all barbiturates, pentobarbital has a high potential for abuse and addiction, and its use should be closely monitored by a healthcare provider. It can also cause serious side effects such as respiratory depression, decreased heart rate, and low blood pressure, especially when used in large doses or combined with other central nervous system depressants.
A dose-response relationship in the context of drugs refers to the changes in the effects or symptoms that occur as the dose of a drug is increased or decreased. Generally, as the dose of a drug is increased, the severity or intensity of its effects also increases. Conversely, as the dose is decreased, the effects of the drug become less severe or may disappear altogether.
The dose-response relationship is an important concept in pharmacology and toxicology because it helps to establish the safe and effective dosage range for a drug. By understanding how changes in the dose of a drug affect its therapeutic and adverse effects, healthcare providers can optimize treatment plans for their patients while minimizing the risk of harm.
The dose-response relationship is typically depicted as a curve that shows the relationship between the dose of a drug and its effect. The shape of the curve may vary depending on the drug and the specific effect being measured. Some drugs may have a steep dose-response curve, meaning that small changes in the dose can result in large differences in the effect. Other drugs may have a more gradual dose-response curve, where larger changes in the dose are needed to produce significant effects.
In addition to helping establish safe and effective dosages, the dose-response relationship is also used to evaluate the potential therapeutic benefits and risks of new drugs during clinical trials. By systematically testing different doses of a drug in controlled studies, researchers can identify the optimal dosage range for the drug and assess its safety and efficacy.
Drug-Induced Liver Injury (DILI) is a medical term that refers to liver damage or injury caused by the use of medications or drugs. This condition can vary in severity, from mild abnormalities in liver function tests to severe liver failure, which may require a liver transplant.
The exact mechanism of DILI can differ depending on the drug involved, but it generally occurs when the liver metabolizes the drug into toxic compounds that damage liver cells. This can happen through various pathways, including direct toxicity to liver cells, immune-mediated reactions, or metabolic idiosyncrasies.
Symptoms of DILI may include jaundice (yellowing of the skin and eyes), fatigue, abdominal pain, nausea, vomiting, loss of appetite, and dark urine. In severe cases, it can lead to complications such as ascites, encephalopathy, and bleeding disorders.
The diagnosis of DILI is often challenging because it requires the exclusion of other potential causes of liver injury. Liver function tests, imaging studies, and sometimes liver biopsies may be necessary to confirm the diagnosis. Treatment typically involves discontinuing the offending drug and providing supportive care until the liver recovers. In some cases, medications that protect the liver or promote its healing may be used.
Succinylcholine is a neuromuscular blocking agent, a type of muscle relaxant used in anesthesia during surgical procedures. It works by inhibiting the transmission of nerve impulses at the neuromuscular junction, leading to temporary paralysis of skeletal muscles. This facilitates endotracheal intubation and mechanical ventilation during surgery. Succinylcholine has a rapid onset of action and is metabolized quickly, making it useful for short surgical procedures. However, its use may be associated with certain adverse effects, such as increased heart rate, muscle fasciculations, and potentially life-threatening hyperkalemia in susceptible individuals.
Medical Definition of Respiration:
Respiration, in physiology, is the process by which an organism takes in oxygen and gives out carbon dioxide. It's also known as breathing. This process is essential for most forms of life because it provides the necessary oxygen for cellular respiration, where the cells convert biochemical energy from nutrients into adenosine triphosphate (ATP), and releases waste products, primarily carbon dioxide.
In humans and other mammals, respiration is a two-stage process:
1. Breathing (or external respiration): This involves the exchange of gases with the environment. Air enters the lungs through the mouth or nose, then passes through the pharynx, larynx, trachea, and bronchi, finally reaching the alveoli where the actual gas exchange occurs. Oxygen from the inhaled air diffuses into the blood, while carbon dioxide, a waste product of metabolism, diffuses from the blood into the alveoli to be exhaled.
2. Cellular respiration (or internal respiration): This is the process by which cells convert glucose and other nutrients into ATP, water, and carbon dioxide in the presence of oxygen. The carbon dioxide produced during this process then diffuses out of the cells and into the bloodstream to be exhaled during breathing.
In summary, respiration is a vital physiological function that enables organisms to obtain the necessary oxygen for cellular metabolism while eliminating waste products like carbon dioxide.
Controlled hypotension is a medical procedure in which the healthcare provider intentionally lowers the patient's blood pressure during surgery. This is done to reduce bleeding and improve surgical conditions. The goal is to maintain the patient's blood pressure at a level that is lower than their normal resting blood pressure, but high enough to ensure adequate blood flow to vital organs such as the heart and brain. Controlled hypotension is closely monitored and managed throughout the surgery to minimize risks and ensure the best possible outcomes for the patient.
Fluoroacetates are organic compounds that contain a fluorine atom and an acetic acid group. The most well-known and notorious compound in this family is sodium fluoroacetate, also known as 1080 or compound 1080, which is a potent metabolic poison. It works by interfering with the citric acid cycle, a critical process that generates energy in cells. Specifically, fluoroacetates are converted into fluorocitrate, which inhibits an enzyme called aconitase, leading to disruption of cellular metabolism and ultimately cell death.
Fluoroacetates have been used as rodenticides and pesticides, but their use is highly regulated due to their high toxicity to non-target species, including humans. Exposure to fluoroacetates can cause a range of symptoms, including nausea, vomiting, seizures, and cardiac arrest, and can be fatal if not treated promptly.
Thiamylal is a fast-acting, ultra-short-acting barbiturate drug that is primarily used for the induction of anesthesia before surgical procedures. It works by depressing the central nervous system, producing sedation, relaxation, and hypnosis. Thiamylal has a rapid onset of action and its effects last only a short time, making it useful for quickly achieving a desired level of anesthesia while minimizing the risk of prolonged sedation or respiratory depression.
It is important to note that thiamylal should be administered under the close supervision of trained medical personnel, as its use carries certain risks and potential complications, such as cardiovascular and respiratory depression. Additionally, patients with a history of drug allergies, liver or kidney disease, or other medical conditions may require special precautions before receiving thiamylal.
Intratracheal anesthesia refers to the administration of anesthetic agents directly into the trachea. This type of anesthesia is typically used in specific medical procedures, such as bronchoscopy or airway surgery, where it is necessary to achieve adequate anesthesia and analgesia of the airways while avoiding systemic effects.
Intratracheal anesthesia is usually delivered through a specialized device called a laryngoscope, which is used to visualize the vocal cords and introduce a narrow tube (endotracheal tube) into the trachea. Once the endotracheal tube is in place, anesthetic gases or liquids can be administered directly into the airways, providing rapid onset of action and minimal systemic absorption.
It's important to note that intratracheal anesthesia should only be performed by trained medical professionals, as there are potential risks associated with this procedure, including damage to the airway, respiratory compromise, and other complications.
Halothane
CYP2E1
Bill Inman
NMDA receptor antagonist
Liquid breathing
Azeotrope
Orchestrated objective reduction
Theories of general anaesthetic action
2-Chloro-1,1-difluoroethylene
Trifluoroacetic acid
Malignant hyperthermia
TRPC5
Widnes Laboratory
PSE meat
Charles Suckling
General anaesthetic
Trichloroethylene
History of general anesthesia
Methoxyflurane
Atracurium besilate
Chlorobutanol
Sevoflurane
Minimum alveolar concentration
Trifluoroacetyl chloride
Fluorine
North West England
Balanced anesthesia
Cisatracurium besilate
Curare
IUPAC nomenclature of organic chemistry
Halothane - Wikipedia
Halothane
Halothane Hepatotoxicity: Practice Essentials, Pathophysiology, Etiology
Halothane - Fluothane Summary Report | CureHunter
Medical Science Monitor | Emergence agitation in children after propofol versus halothane anesthesia - Article abstract #869679
A344 HALOTHANE, ISOFLURANE AND Ca2+ TRANSIENTS IN CULTURED VASCULAR SMOOTH MUSCLE CELLS | Anesthesiology | American Society of...
Selective bond breaking of halothane induced by electron transfer in potassium collisions<...
DATEX OHMEDA TEC-5 HALOTHANE - Med Equip
"Halothane Hepatitis" | Anesthesiology | American Society of...
The Metabolic Effects of Halothane on Mammalian Hepatoma Cells in Vitro | Anesthesiology | American Society of Anesthesiologists
Anaesthesia Products - Goldmans Halothane Vaporizer Manufacturer from Kolkata
"How Safe is Halothane?" by Peter J. Cohen
Halothane | 英国离科中国公司
Comparison between halothane and sevoflurane for adult vital capacity induction -ORCA
physical chemistry - How to calculate what mass of halothane is inspired in one minute given the partial pressure and...
CDC - NIOSH Pocket Guide to Chemical Hazards - Index of Chemical Names : H
Elevation of serum xanthine oxidase following halothane anesthesia in the rat<...
Direct and neurally mediated effects of halothane on pulmonary resistance in vivo<...
Effects of halothane sensitivity on growth and body composition traits in pigs | Animal Research
Comparison Of Halothane, Enflurane And Isoflurane Kidney Effects Through Alanine Aminopeptidase Urine Creatinine Values
FDA Warns on Anesthetic, Sedative Use in Pregnant Women, Kids (Transcript)
The Effect of Occupational Exposure to Wasted Halothane on Liver Functions of Operating Room Personnel
Myocardial Effects of Halothane and Isoflurane in Hamsters with Hypertrophic Cardiomyopathy | Anesthesiology | American...
Use of halothane as a model for investigating chemical-induced autoimmune hepatotoxicity - Fingerprint - University of...
Ritalin-SR Advanced Patient Information - Drugs.com
Gabapentin Enacarbil (Oral Route) Before Using - Mayo Clinic
Duo-Vil 2-25 Advanced Patient Information - Drugs.com
Inhalational anesthetics
Isoflurane13
- Concern for hepatitis resulted in a dramatic reduction in the use of halothane for adults and it was replaced in the 1980s by enflurane and isoflurane. (wikipedia.org)
- The kidney effects of halothane, enflurane and isoflurane were evaluated by using the ratio of urinary excretion of alanine aminopeptidase (AAP) to urine creatinine. (hacettepe.edu.tr)
- Groups 1, 2 and 3 received halothane, enflurane and isoflurane respectively, Creatinine and AAP activities in urine spot tests, serum creatinine and BUN levels were determined preoperatively and on the first and second postoperative days. (hacettepe.edu.tr)
- The present study did not reveal any significant difference in the kidney effects of halothane, enflurane and isoflurane through AAP/creatinine in spot urine values. (hacettepe.edu.tr)
- The effects of halothane and isoflurane on myocardial contraction and relaxation in diseased myocardium are not completely understood. (silverchair.com)
- However, the negative inotropic effects of halothane and isoflurane were not different for cardiomyopathic or healthy hamsters when their concentrations were corrected for minimum alveolar concentration (MAC) values in each strain. (silverchair.com)
- Halothane and isoflurane induced no significant lusitropic effect under high load. (silverchair.com)
- Halothane and isoflurane had greater negative inotropic effects in cardiomyopathic than in healthy hamsters. (silverchair.com)
- 2. Inhalant anesthetics (e.g., halothane, isoflurane) can be used for euthanasia of rodents. (theodora.com)
- We have examined the short-term effects of three volatile anaesthetics, halothane, isoflurane and desflurane, on mucociliary activity in the rabbit maxillary sinus in vivo. (lu.se)
- Administration of 1.0 MAC of halothane, isoflurane or desflurane caused a temporary increase in mucociliary activity, with mean peak responses of 47.8 (SEM 13.0)%, 44.0 (9.6)% and 45.1 (23.7)% (n = 6), respectively. (lu.se)
- The second peak at 3-5 min was less pronounced for halothane than for isoflurane or desflurane. (lu.se)
- the inhalational anesthetic is most often halothane, but other anesthetics (eg, isoflurane , sevoflurane , desflurane ) may also be involved. (msdmanuals.com)
Sevoflurane10
- Currently, halothane is rarely used in economically developed nations due to the availability of newer and safer volatile anesthetics, such as enflurane and sevoflurane . (medscape.com)
- We have examined the differences in ventilatory characteristics between halothane and sevoflurane when used for adult vital capacity induction of anaesthesia. (cardiff.ac.uk)
- Differential effects of halothane and sevoflurane on hypoxia-induced intracellular calcium transients of neonatal rat carotid body type I cells. (ox.ac.uk)
- BACKGROUND: The purpose of this study was to investigate the effects of halothane and sevoflurane on the magnitude of the increase in intracellular calcium with hypoxia in carotid body type I (glomus) cells. (ox.ac.uk)
- We wished to ascertain if the effects of these agents in single cells paralleled their known effects on the human hypoxic ventilatory response, where halothane depresses this response more than does sevoflurane. (ox.ac.uk)
- Halothane and sevoflurane were administered in concentrations ranging from 0.18 to 1.45 and 0.1 to 2 minimum alveolar concentration (MAC), respectively (rat values). (ox.ac.uk)
- RESULTS: Halothane depressed the increase in intracellular calcium with hypoxia more than did sevoflurane (P=0.036). (ox.ac.uk)
- Although halothane was depressive at all concentrations tested, sevoflurane depressed the calcium response only at 2 MAC. (ox.ac.uk)
- Both agents also depressed the calcium response to elevated extracellular potassium-halothane more so than sevoflurane (P=0.004). (ox.ac.uk)
- For single breath induction, what percentage Halothane or Sevoflurane? (studystack.com)
Anesthesia7
- Since the risk of halothane hepatitis in children was substantially lower than in adults, halothane continued to be used in pediatrics in the 1990s as it was especially useful for inhalation induction of anesthesia. (wikipedia.org)
- The aim of this study was to compare the incidence of emergence agitation in children receiving either propofol or halothane anesthesia for a variety of surgical treatments using the Pediatric Anesthesia Emergence Delirium (PAED) scale. (medscimonit.com)
- The subjects were 83 premedicated children aged 1 to 6 years who underwent surgical procedures with propofol (group P, n=41) or with halothane (group H, n=42) anesthesia. (medscimonit.com)
- The mean dose during maintenance of anesthesia with propofol was 9.0 mg/kg/h or halothane 1.5-2% and fentanyl at a total dose of 5 microg/kg administered during surgery. (medscimonit.com)
- In children, the administration of propofol maintenance anesthesia is associated with a significantly higher incidence of emergence agitation than halothane maintenance anesthesia. (medscimonit.com)
- The GE Datex Ohmeda TEC 5 Halothane anesthesia vaporizers are temperature, flow, and pressure compensated so that its output remains relatively constant despite cooling due to evaporation.Designed for out of circuit use in continuous flow techniques of inhalation anesthesia,The TEC 5 is designed to be used on Selectatec Series Mounted Manifolds.Our All Units Are Refurbished , Ready to Use and all units are checked with our Biomedical Engineer team. (med-equip.ca)
- Halothane anesthesia was found to be hepatotoxic in the rat, as demonstrated by a significant elevation of serum xanthine oxidase (SXO) level. (tau.ac.il)
Anesthetics1
- Chemically, halothane is an alkyl halide (not an ether like many other anesthetics). (wikipedia.org)
Fluothane1
- Halothane, sold under the brand name Fluothane among others, is a general anaesthetic. (wikipedia.org)
Metabolism of halothane1
- The resulting syndrome was referred to as halothane hepatitis, immunoallergic in origin, and is thought to result from the metabolism of halothane to trifluoroacetic acid via oxidative reactions in the liver. (wikipedia.org)
Concentrations4
- To examine possible mechanisms of action of halothane at clinically relevant concentrations the authors studied the effect of halothane on increases in pulmonary resistance (R(L)) produced by either vagus nerve stimulation (VNS, which caused neurally mediated constriction) or the inhalation of nebulized acetylcholine (ACh, which directly stimulated the smooth muscle cell) in nine mongrel dogs. (elsevierpure.com)
- At halothane concentrations greater than or equal to 0.4 MAC, the VNS response was significantly less than the ACh response. (elsevierpure.com)
- The authors conclude that in addition to neurally mediated effects, halothane at clinically used concentrations has significant direct effects on airway smooth muscle stimulated by ACh. (elsevierpure.com)
- The aims of our study were to determine concentrations of wasted halothane in operating rooms and to investigate the effect of halothane pollution on liver functions of exposed personnel. (pjoes.com)
Hepatitis6
- In rare cases, cirrhosis may develop following halothane hepatitis. (medscape.com)
- However, the findings in halothane hepatitis are indistinguishable from those of fulminant viral hepatitis . (medscape.com)
- Because halothane hepatitis is a diagnosis of exclusion, ruling out other causes is essential. (medscape.com)
- We evaluated various dimensions of this replacement through a literature review to assess the incidence of halothane-induced hepatitis and costs of anaesthetics in the country. (who.int)
- The results indicate that the incidence of halothane hepatitis in the Islamic Republic of Iran is very low and could mostly be avoided by strict adherence to guidelines. (who.int)
- Anaesthesia has been influential in dif- Iran in 2006 when a number of experts thane-induced hepatitis, some profes- ferent fields of medical practice, espe- claimed that halothane should be sionals have insisted on the necessity cially in surgical procedures and efforts considered a major health threat [10]. (who.int)
Vaporizer3
- Our product range includes a wide range of goldmans halothane vaporizer. (ipsmedicalproducts.com)
- We are prime manufacturers of Goldman halothane vaporizer which is primarily used in hospitals due to their critical and very important requirement and performance. (ipsmedicalproducts.com)
- Halothane vaporizer. (theodoregray.com)
Exposure4
- In rare cases, repeated exposure to halothane in adults was noted to result in severe liver injury. (wikipedia.org)
- Type I (mild) halothane hepatotoxicity occurs within hours of halothane exposure. (medscape.com)
- Type II (fulminant) halothane hepatotoxicity usually occurs 5-7 days following exposure, although it can be delayed by up to 4 weeks. (medscape.com)
- The results suggest that exposure to wasted halothane may be harmful to the livers of operating room personnel. (pjoes.com)
Anesthetic4
- Halothane given with succinylcholine for induction anesthetic is associated with masseter spasm. (medscape.com)
- Halothane (2-bromo-2-chloro-1, 1, 1-trifluoro-ethane) is the most popular inhalation agent in today's anesthetic practice. (vcu.edu)
- Inhalation anesthetic molecules such as halothane cause these lipid regions to mix, potentially affecting the function of ion channel proteins found imbedded in the membrane. (nist.gov)
- Halothane is the most effective inhalant anesthetic for euthanasia. (theodora.com)
Contraction1
- It has been suggested that halothane inhibits contraction of airway smooth muscle in vivo mainly by reducing reflex activity in nerves innervating the muscle with only minimal direct effects on the muscle itself. (elsevierpure.com)
Incidence1
- The National Halothane Study, a retrospective analysis, reviewed the incidence and mortality rates of postoperative hepatic necrosis from 1959-1962. (medscape.com)
1516771
- Worker exposures to nitrous - oxide (10024972), halothane (151677), and ethrane (13838169) were surveyed on August 6 to 8, 1980 and February 9 to 12, 1981 at the Lincoln Medical and Mental Health Center (SIC-8062) in the Bronx, New York. (cdc.gov)
Ethrane1
- Exposures to nitrous - oxide , halothane, and ethrane ranged from 16 to 850, up to 14.4, and up to 2.4 parts per million (ppm), respectively. (cdc.gov)
Propofol1
- Halothane and propofol appear to cause much less emergence agitation. (medscimonit.com)
Liver dysfunction1
- Although these investigations disclosed no evidence of adverse effects, reports of liver dysfunction after halothane administration have appeared constantly in the literature. (vcu.edu)
Inhalation1
- of complete replacement of halothane have been ongoing over the years to Consequently, under supervision of with other inhalation agents such as find the most suitable anaesthetic agent. (who.int)
Cardiac1
- Halothane sensitises the heart to catecholamines, so it is liable to cause cardiac arrhythmia, occasionally fatal, particularly if hypercapnia has been allowed to develop. (wikipedia.org)
HBrClF1
- Halothane is C 2 HBrClF 3 , basically a chlorofluorocarbon of the ozone-depleting variety. (theodoregray.com)
Analgesia1
- Torske KE, Dyson DH, Pettifer G. End tidal halothane concentration and postoperative analgesia requirements in dogs: a comparison between intravenous oxymorphone and epidural bupivacaine alone and in combination with oxymorphone. (scielo.br)
Serum1
- Serum autoantibodies may be present in 30-44% of patients with type II halothane hepatotoxicity. (medscape.com)
Bromine1
- This is then reacted with bromine at 450 °C to produce halothane. (wikipedia.org)
Hepatotoxicity7
- Based on this study, the risk of fatal halothane hepatotoxicity was estimated to be 1 in 35,000. (medscape.com)
- Halothane hepatotoxicity is more likely to occur in lower resource settings where halothane continues to be used. (medscape.com)
- Halothane hepatotoxicity is a diagnosis of exclusion. (medscape.com)
- Physical findings in type II halothane hepatotoxicity include delayed pyrexia (up to 75% of patients). (medscape.com)
- Eosinophilia occurs in 8-32% of patients with type II halothane hepatotoxicity. (medscape.com)
- No specific therapy is available for either fulminant hepatic necrosis or mild hepatotoxicity due to halothane. (medscape.com)
- Two major types of hepatotoxicity are associated with halothane administration. (medscape.com)
Adverse1
- After the randomization code was revealed, the adverse events were found to be in the halothane group. (cardiff.ac.uk)
Lipid1
- Halothane changes the domain structure of a binary lipid membrane. (nist.gov)
Adults1
- Given this risk, halothane is not recommended for use in adults. (medscape.com)
Concentration1
- Surgeons were exposed to an average concentration of 29.41 mg/m 3 , anesthesiologists to 34.60 mg/m 3 , instrumenting nurses to 28.62 mg/m 3 and anesthetists to 30.09 mg/m 3 of halothane. (pjoes.com)
Potassium1
- We present novel experimental results of negative ion formation of halothane (C2HBrClF3) upon electron transfer from hyperthermal neutral potassium atoms (K°) in the collision energy range of 8-1000 eV. (unl.pt)
Muscle relaxation1
- Because halothane may not produce sufficient muscle relaxation, supplemental neuromuscular blocking agents may be required. (curehunter.com)
Anaesthetics1
- Comprehensive cost-effectiveness studies are needed before a decision is made on complete replacement of halothane with other anaesthetics. (who.int)
Citation1
- citation needed] The commercial synthesis of halothane starts from trichloroethylene, which is reacted with hydrogen fluoride in the presence of antimony trichloride at 130 °C to form 2-chloro-1,1,1-trifluoroethane. (wikipedia.org)
Effect1
- Halothane induced a negative lusitropic effect under low load, which was more important in cardiomyopathic hamsters, suggesting a greater impairment in calcium uptake by the sarcoplasmic reticulum. (silverchair.com)
Response3
- The frequency of bilateral VNS and the dose of nebulized ACh were adjusted to produce approximately equal increases in R(L). Halothane reduced the response to both types of stimulation in a dose-dependent fashion. (elsevierpure.com)
- The second response was not significant for halothane. (lu.se)
- A combination of atropine and CP-99 pretreatment abolished the mucociliary response to halothane. (lu.se)
Products1
- About 20% of inhaled halothane is metabolized by the liver and these products are excreted in the urine. (wikipedia.org)