抗精神病药物延迟治疗与青少年首发精神病5年预后的关系

Tomi Bergström, Tapio Gauffin
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摘要

背景与假设基于需求适应方法,延迟抗精神病药物可以帮助识别可能不需要它们的首发精神病青少年。然而,有些人可能需要抗精神病药物,推迟服用可能会损害他们的预后。这项基于全国登记的随访旨在检验这两个假设。研究设计从2003-2013年芬兰国家登记册中确定了所有13-20岁患有精神障碍(ICD-10代码:F20-F29)的青少年(n= 6354)。对于每个病例,从精神病发作到死亡,确定了1825天的固定随访期。如果青少年在随访的最后一年没有死亡,没有接受精神治疗和/或残疾津贴,则结果被认为是“良好的”。对第一种假设的检验涉及所有抗精神病药物treatment-naïve首发精神病青少年(n=3714)。第二个假设是在随访期间接受抗精神病药物治疗的亚样本中进行检验的(n=3258)。为了考虑基线混杂因素,通过具有logit链接函数的稳定逆概率处理加权广义线性模型来检验假设。研究结果:精神病发作后立即接受抗精神病药物治疗与5年预后不良相关(校正优势比[aOR]: 1.8, 95% CI: 1.6-2.1)。在最终接受抗精神病药物治疗的患者中,抗精神病药物延迟治疗与治疗结果之间无统计学意义的关联(aOR: 1.02, 95%CI: 0.7-1.2, p: 0.8),因此不支持第二种假设。结论青少年精神病患者中有一个重要的亚组不需要立即抗精神病药物治疗。需要一个更稳健的设计来评估观察到的关联的因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The association of antipsychotic postponement with 5-year outcomes of adolescent first-episode psychosis
Abstract Background and Hypothesis Based on the need-adapted approach, delaying antipsychotics could help identify first-episode psychosis adolescents who might not require them. However, some individuals might need antipsychotics, and postponing could harm their prognosis. This nationwide register-based follow-up aimed to test these two hypotheses. Study Design All adolescents aged 13-20 with a psychotic disorder (ICD-10 codes: F20-F29) in Finland between 2003-2013 were identified (n=6,354) from national registers. For each case, a fixed 1825-day follow-up period was established from the onset of psychosis or until death. The outcome was considered "good" if adolescents did not die and had not received psychiatric treatment and/or disability allowances during the final year of follow-up. Testing the first hypothesis involved all antipsychotic treatment-naïve adolescents with first-episode psychosis (n=3714). The second hypothesis was tested with a sub-sample of only those who had received antipsychotics during follow-up (n=3258). To account for baseline confounders, hypotheses were tested via a stabilized inverse probability of treatment weighted generalized linear models with logit link function. Study Results Immediate antipsychotic treatment after the onset of psychosis was associated with poor five-year outcome (adjusted odds ratio [aOR]: 1.8, 95% CI: 1.6-2.1). There was no statistically significant association between antipsychotic postponement and treatment outcome in those who eventually received antipsychotic treatment (aOR: 1.02, 95%CI: 0.7-1.2, p: 0.8), thus not providing support for second hypothesis. Conclusions There is a significant subgroup of adolescent with psychosis who do not require immediate antipsychotic treatment. A more robust design is needed to evaluate the causality of the observed association.
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