Storosum Jitschak G, van Zwieten Barbara J, Wohlfarth Tamar, de Haan Lieuwe, Khan Arif, van den Brink Wim
Medicines Evaluation Board of the Netherlands, Den Haag, the Netherlands.
Arch Gen Psychiatry. 2003 Apr;60(4):365-8. doi: 10.1001/archpsyc.60.4.365.
If there is an increased risk of suicide in the placebo arms of placebo-controlled studies in patients with schizophrenia, it would be a strong ethical argument against the conduct of placebo-controlled studies in this patient population. We tested whether the risk of suicide and attempted suicide in the placebo arms of placebo-controlled studies among patients with schizophrenia is higher than in the active treatment arms of such studies.
All placebo-controlled double-blind studies that were part of a registration dossier for the indication schizophrenia, and that were submitted to the regulatory authority of the Netherlands from January 1, 1992, through December 31, 2002, were reviewed for suicide and attempted suicide.
In 31 studies, 7152 patients were included: 1888 in placebo groups (398.2 person-years) and 5264 in active compound groups (981.3 person-years). One suicide occurred in the placebo groups (0.05%, or an incidence rate of 251 per 100,000 years of exposure) and 1 in the active compound groups (0.02%, or an incidence rate of 102 per 100,000 years of exposure). This difference was not statistically significant. Two attempted suicides occurred in the placebo groups (0.11%, or an incidence rate of 502 per 100,000 years of exposure) and 11 in the active compound groups (0.21%, or an incidence rate of 1121 per 100,000 years of exposure). This difference was also not statistically significant.
Concern about increased risk of suicide or attempted suicide in the placebo group should not be an argument against the conduct of placebo-controlled trials in schizophrenia, provided that appropriate precautions are taken.
如果在精神分裂症患者的安慰剂对照研究中,安慰剂组的自杀风险增加,那么这将成为反对在该患者群体中进行安慰剂对照研究的有力伦理依据。我们测试了精神分裂症患者安慰剂对照研究中,安慰剂组的自杀和自杀未遂风险是否高于此类研究的活性治疗组。
对1992年1月1日至2002年12月31日期间提交给荷兰监管机构的、作为精神分裂症适应症注册档案一部分的所有安慰剂对照双盲研究进行自杀和自杀未遂情况审查。
31项研究共纳入7152例患者:安慰剂组1888例(398.2人年),活性化合物组5264例(981.3人年)。安慰剂组发生1例自杀(0.05%,即每100,000人年暴露率为251例),活性化合物组发生1例自杀(0.02%,即每100,000人年暴露率为102例)。这种差异无统计学意义。安慰剂组发生2例自杀未遂(0.11%,即每100,000人年暴露率为502例),活性化合物组发生11例自杀未遂(0.21%,即每100,000人年暴露率为1121例)。这种差异也无统计学意义。
如果采取适当预防措施,对安慰剂组自杀或自杀未遂风险增加的担忧不应成为反对在精神分裂症中进行安慰剂对照试验的理由。