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非甾体抗炎药所致急性中毒。临床特征与处理

Acute poisoning due to non-steroidal anti-inflammatory drugs. Clinical features and management.

作者信息

Vale J A, Meredith T J

出版信息

Med Toxicol. 1986 Jan-Feb;1(1):12-31. doi: 10.1007/BF03259825.

Abstract

Despite the widespread use of non-steroidal anti-inflammatory drugs (NSAIDs), the current number of reported cases of poisoning is small. However, with the introduction of 'over-the-counter' preparations of NSAIDs in some countries (e.g. ibuprofen in the UK and USA) an increased incidence of acute poisoning from this group of drugs can be expected. Conventionally, NSAIDs are divided into the following groups based on their chemical structure: arylpropionic acids, indole and indene acetic acids, heteroarylacetic acids, fenamates, phenylacetic acids, pyrazolones and oxicams. Unless NSAIDs are ingested in substantial overdose, acute poisoning with these agents does not usually result in significant morbidity or mortality. In most cases the clinical features are mild and confined to the gastrointestinal and central nervous systems, though acute renal failure, hepatic dysfunction, respiratory depression, coma, convulsions, cardiovascular collapse and cardiac arrest may complicate severe poisoning. Arylpropionic acid derivatives were thought initially to have a low order of toxicity in overdose but, in addition to anticipated gastrointestinal symptoms, headache, tinnitus, hyperventilation, sinus tachycardia, hypoprothrombinaemia, haematuria, proteinuria and acute renal failure have been described. In addition, drowsiness, coma, nystagmus, diplopia, hypothermia, hypotension, respiratory depression and cardiac arrest have been reported in severe cases of poisoning. Oxyphenbutazone and phenylbutazone are considerably more toxic in overdose. Complications of severe poisoning include coma, convulsions, hepatic dysfunction, acute renal failure, sodium and water retention, haematuria, cardiovascular collapse, respiratory alkalosis, metabolic acidosis, hypoprothrombinaemia and thrombocytopenia. In contrast, indomethacin appears to be much less toxic. In addition to gastrointestinal symptoms, indomethacin taken in overdose induces headache, tinnitus, dizziness, lethargy, drowsiness, confusion, disorientation and restlessness. Only 1 case of acute sulindac poisoning has been reported in the literature. A 16-year-old boy was admitted with hypokalaemia (2.2 mmol/L), transient granulocytosis and 'scanty' haematemesis after ingesting 12 g sulindac. No case of acute tolmetin poisoning have been reported. The fenamates (flufenamic acid, meclofenamic acid, mefenamic acid, tolfenamic acid) are, with the exception of mefenamic acid, not as widely prescribed as other groups of NSAIDs. In overdose, mefenamic acid may result in nausea, vomiting, diarrhoea, muscle twitching, convulsions and coma.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

尽管非甾体抗炎药(NSAIDs)被广泛使用,但目前报告的中毒病例数量较少。然而,随着一些国家引入非处方NSAIDs制剂(如英国和美国的布洛芬),预计这类药物引起的急性中毒发生率将会增加。按照传统分类,NSAIDs根据其化学结构可分为以下几类:芳基丙酸类、吲哚和茚乙酸类、杂芳基乙酸类、灭酸类、苯乙酸类、吡唑酮类和昔康类。除非大量过量服用NSAIDs,否则这些药物引起的急性中毒通常不会导致严重的发病或死亡。在大多数情况下,临床症状较轻,局限于胃肠道和中枢神经系统,不过严重中毒可能会并发急性肾衰竭、肝功能障碍、呼吸抑制、昏迷、抽搐、心血管衰竭和心脏骤停。芳基丙酸衍生物最初被认为过量服用时毒性较低,但除了预期的胃肠道症状外,还出现了头痛、耳鸣、换气过度、窦性心动过速、凝血酶原血症降低、血尿、蛋白尿和急性肾衰竭的报道。此外,严重中毒病例还出现了嗜睡、昏迷、眼球震颤、复视、体温过低、低血压、呼吸抑制和心脏骤停的情况。羟基保泰松和保泰松过量服用时毒性要大得多。严重中毒的并发症包括昏迷、抽搐、肝功能障碍、急性肾衰竭、钠和水潴留、血尿、心血管衰竭、呼吸性碱中毒、代谢性酸中毒、凝血酶原血症降低和血小板减少。相比之下,吲哚美辛的毒性似乎要小得多。过量服用吲哚美辛除了引起胃肠道症状外,还会导致头痛、耳鸣、头晕、乏力、嗜睡、意识模糊、定向障碍和烦躁不安。文献中仅报道了1例舒林酸急性中毒病例。一名16岁男孩在服用12克舒林酸后因低钾血症(2.2毫摩尔/升)、短暂性粒细胞增多症和“少量”呕血入院。尚未有托美汀急性中毒的病例报道。除甲芬那酸外,灭酸类(氟芬那酸、甲氯芬那酸、甲芬那酸、托芬那酸)的处方量不如其他NSAIDs类药物广泛。过量服用甲芬那酸可能会导致恶心、呕吐、腹泻、肌肉抽搐、抽搐和昏迷。(摘要截选至400字)

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