Douglas A P, Hamlyn A N, James O
Lancet. 1976 Jan 17;1(7951):111-5. doi: 10.1016/s0140-6736(76)93154-8.
A randomised controlled trial of the use of intravenous cysteamine in the treatment of severe paracetamol poisoning has been performed. Thirty-eight patients presenting 3-17 h after ingestion were admitted to the trial; of these eighteen received cysteamine. Two patients died from hepatic failure, one in each treatment group. Analysis of the series as a whole showed no advantage of cysteamine in preventing biochemical abnormalities of liver function except for aspartate aminotranferase and serum ferritin levels, which were significantly less after cysteamine therapy. Separate analysis of the patients treated within 9 h of paractamol ingestion and of those treated 9-17 h after paracetamol ingesion similarly showed no definite advantage of cysteamine. Histological evidence of liver damage showed a possible beneficial effect of cysteamine. Cysteamine therapy did not prevent renal or pancreatic damage.
已开展一项关于静脉注射半胱胺治疗对乙酰氨基酚严重中毒的随机对照试验。38例摄入对乙酰氨基酚3 - 17小时后就诊的患者纳入该试验;其中18例接受了半胱胺治疗。两名患者死于肝衰竭,各治疗组有一名。对整个系列病例的分析表明,除天冬氨酸转氨酶和血清铁蛋白水平外,半胱胺在预防肝功能生化异常方面并无优势,半胱胺治疗后这两项指标显著降低。对在摄入对乙酰氨基酚9小时内接受治疗的患者以及在摄入对乙酰氨基酚9 - 17小时后接受治疗的患者分别进行分析,同样显示半胱胺无明确优势。肝损伤的组织学证据表明半胱胺可能具有有益作用。半胱胺治疗未能预防肾或胰腺损伤。