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Do antipsychotic medications reduce or increase mortality in schizophrenia? A critical appraisal of the FIN-11 study

机译:抗精神病药会降低或增加精神分裂症的死亡率吗?对FIN-11研究的批判性评价

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Compared to the general population, people with schizophrenia are at risk of dying prematurely due to suicide and due to different somatic illnesses. The potential role of antipsychotic treatment in affecting suicide rates and in explaining the increased mortality due to somatic disorders is highly debated.A recent study of death registers in Finland compared the cause-specific mortality in 66,881 patients versus the total population (5.2 million) between 1996 and 2006, suggesting that antipsychotic use decreased all-cause mortality compared to no antipsychotic use in patients with schizophrenia, and that clozapine had the most beneficial profile in this regard (Tiihonen et al., 2009). The benefits of clozapine were conferred by significant protective effects for suicide compared to perphenazine, whereas, a mixed group of 'other' antipsychotics, haloperidol, quetiapine and risperidone were reported to be associated with significantly higher all-cause mortality than perphenazine. By contrast, despite known differences in effects on cardiovascular risk factors, there were no significant differences between any of the examined antipsychotics regarding death due to ischemic heart disease. A number of methodological and conceptual issues make the interpretation of these findings problematic, including incomplete reporting of data, questionable selection of drug groups and comparisons, important unmeasured risk factors, inadequate control for potentially confounding variables, exclusion of deaths occurring during hospitalization leading to exclusion of 64% of deaths on current antipsychotics from the analysis, and survivorship bias due to strong and systematic differences in illness duration across the treatment groups.Well designed, prospective mortality studies, with direct measurement of and adjustment for all known relevant risk factors for premature mortality, are needed to identify risk and protective medication and patient factors and to, ultimately, inform clinical practice.
机译:与普通人群相比,精神分裂症患者由于自杀和不同的躯体疾病而有过早死亡的风险。抗精神病药物治疗对自杀率的影响以及解释由于躯体疾病导致死亡率增加的潜在作用备受争议。最近一项关于芬兰死亡登记的研究比较了66,881名患者与总人口(520万)之间因特定原因造成的死亡率1996年和2006年,表明与精神分裂症患者不使用抗精神病药相比,抗精神病药物的使用降低了全因死亡率,并且氯氮平在这方面具有最有益的作用(Tiihonen等,2009)。与奋乃静相比,氯氮平对自杀的保护作用具有明显的益处,而据报道,“其他”抗精神病药,氟哌啶醇,喹硫平和利培酮的混合组比奋乃静具有更高的全因死亡率。相比之下,尽管已知对心血管危险因素的作用存在差异,但是在任何一种抗精神病药物之间,由于缺血性心脏病导致的死亡均无显着差异。许多方法和概念上的问题使对这些发现的解释变得困难,包括数据报告不完整,药物组和比较的选择有问题,重要的无法衡量的危险因素,对可能造成混淆的变量的控制不足,住院期间导致死亡的死亡被排除在外分析显示,目前有64%的死亡是由目前使用的抗精神病药造成的,并且由于各治疗组之间疾病持续时间的强烈和系统性差异而导致生存率存在偏差。需要确定死亡率,风险和保护性用药以及患者因素,并最终告知临床实践。

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