Jun 17, 2015 · Question 2 of 75 1.0 Points What has kept paraldehyde from being widely used? A. danger to the CNS B. bad taste and odor C. danger to the respiratory system D. irritation to the gastric system Answer Key: B. Upload your study docs or become a. Course Hero member to access this document. Continue to access.
Sep 12, 2019 · View Quiz 2 HLTH.docx from PSYCH PHYSIOLOGI at Cornell University. Question 1 2 out of 2 points What has prevented paraldehyde from being widely used? Selected Answer: Bad taste and odor Question
Jul 13, 2019 · Question 2 2 out of 2 points What has prevented paraldehyde from being widely used? Selected Answer: Bad taste and odor. Selected Answer : Bad taste and odor ... Course Hero member to access this document. Continue to access. End of preview. Want to read all 8 pages? Upload your study docs or become a.
Question 5 2 out of 2 points What has prevented paraldehyde from being widely used? Selected Answer: Bad taste and odor. ... Course Hero, Inc. Course Hero is not sponsored or endorsed by any college or university. ...
Paraldehyde is also used in resin manufacture, as a preservative, and in other processes as a solvent. Paraldehyde overdose, produces symptoms similar to those of chloral hydrate overdose which may include coma, severe hypotension, respiratory depression, pulmonary edema, and cardiac failure.
Paraldehyde slowly oxidizes in air, turning brown , and producing an odor of acetic acid. It quickly reacts with most plastics and rubber. Paraldehyde is also used in resin manufacture, as a preservative, and in other processes as a solvent. Paraldehyde overdose, produces symptoms similar to those of chloral hydrate overdose which may include coma, severe hypotension, respiratory depression, pulmonary edema, and cardiac failure. Prolonged use of paraldehyde may produce tolerance and physical and/or psychological dependence. Paraldehyde may enter the environment via industrial effluents or hospital wastes. Acetaldehyde and acetic acid are two products of degradation of paraldehyde. This compound and its degradation products may be released into water, soil, or atmosphere and then they may be removed from the atmosphere by precipitation.
About 10–16% of paraldehyde in 5% dextrose or 0.9% sodium chloride is lost when it is delivered from PVC bags through standard intravenous administration sets and burettes over 6 hours [26 ].
Paraldehyde is metabolized in the liver to acetaldehyde [23 ], and the metabolism of aldehyde by aldehyde dehydrogenase is inhibited by disulfiram, causing aldehyde toxicity. The adverse effects of this have been shown in experimental animals [ 24] and there have been reports of confusional psychosis in patients given disulfiram and paraldehyde ...
Paraldehyde has some anticonvulsant activity and has been used for the emergency treatment of convulsions arising from various causes, e.g. tetanus, eclampsia, status epilepticus and poisoning with convulsant drugs. Sign in to download full-size image. Figure 11.7.
Paraldehyde. Paraldehyde is an alternative to phenytoin and phenobarbital for the treatment of early SE and also may be used for RSE. The primary advantages of paraldehyde are its wide spectrum of efficacy for different seizure types and relatively modest respiratory depressant effect.
Regions of the brain that appear to be the most sensitive to the effects of chronic alcohol include the neocortex, limbic system, and cerebellum. Subsequently, alcoholics exhibit a host of cognitive and behavioral abnormalities including deficits in executive functioning, learning and memory, as well as problems with emotion and personality (Licata and Renshaw, 2010; Figures 4 and 5 ). Withdrawal symptoms can be unpleasant and, in the case of alcohol, potentially fatal. Delirium tremens may be complicated by several severe or life-threatening conditions. When diagnosed and managed insufficiently, complications frequently occur such as status epilepticus, coma, or injuries (bed falls, seizures) with fractures, intracranial hemorrhage, hypokalemia, hypomagnesemia, respiratory arrest, and arrhythmias ( Ramos et al., 2013; Table 3 ).
Paraldehyde was introduced into clinical practice in the UK by the Italian physician Vincenzo Cervello (1854–1918) in 1882. It is a central nervous system depressant and was soon found to be an effective anticonvulsant, hypnotic and sedative.
Paraldehyde slowly oxidizes in air, turning brown and producing an odour of acetic acid. It quickly reacts with most plastics and rubber. Paraldehyde was first observed in 1835 by the German chemist Justus Liebig; its empirical formula was determined in 1838 by Liebig's student Hermann Fehling.
Unlike diazepam and other benzodiazepines, it does not suppress breathing at therapeutic doses and so is safer when no resuscitation facilities exist or when the patient's breathing is already compromised. This makes it a useful emergency medication for parents and other caretakers of children with epilepsy.
Paraldehyde is the cyclic trimer of acetaldehyde molecules. Formally, it is a derivative of 1,3,5-trioxane, with a methyl group substituted for a hydrogen atom at each carbon. The corresponding tetramer is metaldehyde. A colourless liquid, it is sparingly soluble in water and highly soluble in ethanol.
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If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.
Use this medicine only as directed by your doctor. Do not use more of it, do not use it more often, and do not use it for a longer time than your doctor ordered. If too much is used, the medicine may become habit-forming. Do not use if liquid turns brownish in color or if it has a strong vinegar-like odor, since this means ...