Barer D, Ogilvie A, Henry D, Dronfield M, Coggon D, French S, Ellis S, Atkinson M, Langman M
N Engl J Med. 1983 Jun 30;308(26):1571-5. doi: 10.1056/NEJM198306303082606.
We studied the effects of tranexamic acid (an antifibrinolytic agent) and cimetidine on acute upper-gastrointestinal-tract bleeding in a double-blind randomized placebo-controlled trial in 775 patients with hematemesis or melena or both. Mortality was significantly reduced in patients receiving either tranexamic acid (mortality, 6.3 per cent) or cimetidine (7.7 per cent), as compared with patients receiving placebo (13.5 per cent) (P = 0.0092 for tranexamic acid vs. placebo, P = 0.045 for cimetidine vs. placebo). Ninety-nine patients were withdrawn before the code was broken, mainly because their primary illness was considered not to be due to acute upper-gastrointestinal-tract bleeding. Mortality among those withdrawn was high (22 per cent), and their exclusion reduced death rates to 4 per cent in those given tranexamic acid, 8 per cent in those given cimetidine, and 11 per cent in those given placebo (P = 0.0072 for tranexamic acid vs. placebo, P greater than 0.50 for cimetidine vs. placebo). The reduced mortality associated with tranexamic acid was detectable at both participating hospitals and in most of the main subgroups of patients classified according to site of bleeding. However, treatment with this agent was not associated with any decrease in the rate of rebleeding or the need for operation.
我们在一项双盲随机安慰剂对照试验中,研究了氨甲环酸(一种抗纤溶药物)和西咪替丁对775例有呕血或黑便或两者皆有的患者急性上消化道出血的影响。与接受安慰剂的患者(死亡率13.5%)相比,接受氨甲环酸(死亡率6.3%)或西咪替丁(7.7%)的患者死亡率显著降低(氨甲环酸与安慰剂相比,P = 0.0092;西咪替丁与安慰剂相比,P = 0.045)。99例患者在揭盲前退出,主要是因为他们的原发性疾病被认为并非由急性上消化道出血所致。退出患者的死亡率很高(22%),将他们排除后,接受氨甲环酸的患者死亡率降至4%,接受西咪替丁的患者为8%,接受安慰剂的患者为11%(氨甲环酸与安慰剂相比,P = 0.0072;西咪替丁与安慰剂相比,P>0.50)。在两家参与研究的医院以及根据出血部位分类的大多数主要患者亚组中,均可检测到氨甲环酸相关的死亡率降低。然而,使用该药物治疗并未使再出血率或手术需求有所降低。