Organophosphorus poisoning and anaesthesia

被引:102
作者
Karalliedde, L
机构
[1] Guys Hosp, Med Toxicol Unit, London SE14 5ER, England
[2] St Thomas Hosp, Med Toxicol Unit, London SE14 5ER, England
关键词
chemicals; organophosphorus compounds complications; poisoning;
D O I
10.1046/j.1365-2044.1999.01061.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Organophosphorus compounds, used as insecticides and agents of chemical warfare, are a major global cause of health problems. These irreversible inhibitors of cholinesterase produce three well-recognised clinical entities: the initial cholinergic phase, which is a medical emergency often requiring management in an intensive care unit the intermediate syndrome, during which prolonged ventilatory care is necessary and delayed polyneuropathy. In addition, disturbances of body temperature and endocrine function, electrolyte imbalances, immunological dysfunction and disorders of reproduction have been reported in animals and man. Vocal cord paralysis, pancreatitis, cardiac arrhythmias and a wide range of neuropsychiatric disorders are known to follow acute and chronic exposure to organophosphorus compounds. As a result of the inhibition of plasma cholinesterase, there can be increased sensitivity to drugs hydrolysed by this enzyme, e.g. suxamethonium and mivacurium. The inhibition of acetylcholinesterase causes dysfunction at the neuromuscular junction which can produce altered responses to nondepolarising neuromuscular blockers. Anaesthetists may encounter patients exposed to organophosphorus compounds either following acute poisoning, trauma (warfare) or as patients with a wide range of nonspecific disorders presenting for surgery. The traditional use of oximes and atropine in treatment has failed to reduce the morbidity and mortality associated with poisoning. The roles of agents that have reduced the toxicity of organophosphorus compounds in animal experiments are discussed as potential therapeutic agents. There is an urgent need for accurate information on the problems associated with exposure to organophosphorus compounds. This would best be achieved by collaborative research between technologically advanced countries and developing countries, where organophosphorus compounds are a leading cause of ill health.
引用
收藏
页码:1073 / 1088
页数:16
相关论文
共 162 条
[21]   Organophosphate myotoxicity [J].
Cavaliere, MJ ;
Calore, EE ;
Perez, NM ;
Puga, FR .
REVISTA DE SAUDE PUBLICA, 1996, 30 (03) :267-272
[22]   Lesson of the week - A foodborne outbreak of organophosphate poisoning [J].
Chaudhry, R ;
Lall, SB ;
Mishra, B ;
Dhawan, B .
BMJ-BRITISH MEDICAL JOURNAL, 1998, 317 (7153) :268-269
[23]   The use of glycopyrrolate in a case of intermediate syndrome following acute organophosphate poisoning [J].
Choi, PTL ;
Quinonez, LG ;
Cook, DJ ;
Baxter, F ;
Whitehead, L .
CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE, 1998, 45 (04) :337-340
[24]   QT(c) prolongation indicates a poor prognosis in patients with organophosphate poisoning [J].
Chuang, FR ;
Jang, SW ;
Lin, JL ;
Chern, MS ;
Chen, JB ;
Hsu, KT .
AMERICAN JOURNAL OF EMERGENCY MEDICINE, 1996, 14 (05) :451-453
[25]   EFFECTS OF LOW-LEVEL ADMINISTRATION OF DICHLORVOS ON ADRENOCORTICOTROPIC HORMONE-SECRETION, ADRENAL CHOLESTERYL ESTER AND STEROID-METABOLISM [J].
CIVEN, M ;
LEEB, JE ;
WISHNOW, RM ;
WOLFSEN, A ;
MORIN, RJ .
BIOCHEMICAL PHARMACOLOGY, 1980, 29 (04) :635-641
[26]   ANTIDOTE EFFECT OF SODIUM-FLUORIDE AGAINST ORGANO-PHOSPHATE POISONING IN MICE [J].
CLEMENT, JG ;
FILBERT, M .
LIFE SCIENCES, 1983, 32 (16) :1803-1810
[27]  
COOK DR, 1989, ANESTH ANALG, V68, P452
[28]  
Cunha J, 1995, Acta Med Port, V8, P469
[29]  
DAGLI AJ, 1983, BRIT J CLIN PRACT, V37, P270
[30]  
Davies JE, 1997, ANN NY ACAD SCI, V837, P257