Derry S, Loke Y K
Department of Clinical Pharmacology, University of Oxford, Radcliffe Infirmary, Oxford OX2 6HE.
BMJ. 2000 Nov 11;321(7270):1183-7. doi: 10.1136/bmj.321.7270.1183.
To assess the incidence of gastrointestinal haemorrhage associated with long term aspirin therapy and to determine the effect of dose reduction and formulation on the incidence of such haemorrhage.
Meta-analysis of 24 randomised controlled trials (almost 66 000 participants).
Aspirin compared with placebo or no treatment, for a minimum of one year.
Incidence of gastrointestinal haemorrhage.
Gastrointestinal haemorrhage occurred in 2.47% of patients taking aspirin compared with 1.42% taking placebo (odds ratio 1.68; 95% confidence interval 1.51 to 1.88); the number needed to harm was 106 (82 to 140) based on an average of 28 months' therapy. At doses below 163 mg/day, gastrointestinal haemorrhage occurred in 2.30% of patients taking aspirin compared with 1.45% taking placebo (1.59; 1.40 to 1.81). Meta-regression showed no relation between gastrointestinal haemorrhage and dose. For modified release formulations of aspirin the odds ratio was 1.93 (1.15 to 3.23).
Long term therapy with aspirin is associated with a significant increase in the incidence of gastrointestinal haemorrhage. No evidence exists that reducing the dose or using modified release formulations would reduce the incidence of gastrointestinal haemorrhage.
评估长期服用阿司匹林治疗相关的胃肠道出血发生率,并确定剂量降低及剂型对该出血发生率的影响。
对24项随机对照试验(近66000名参与者)进行荟萃分析。
阿司匹林与安慰剂或不治疗相比,治疗至少一年。
胃肠道出血的发生率。
服用阿司匹林的患者中胃肠道出血发生率为2.47%,服用安慰剂的患者为1.42%(优势比1.68;95%置信区间1.51至1.88);基于平均28个月的治疗,伤害所需人数为106(82至140)。在每日剂量低于163毫克时,服用阿司匹林的患者中胃肠道出血发生率为2.30%,服用安慰剂的患者为1.45%(1.59;1.40至1.81)。荟萃回归显示胃肠道出血与剂量之间无关联。对于阿司匹林缓释剂型,优势比为1.93(1.15至3.23)。
长期服用阿司匹林治疗与胃肠道出血发生率显著增加相关。没有证据表明降低剂量或使用缓释剂型会降低胃肠道出血的发生率。