预测精神分裂症或分裂情感性障碍患者的症状和功能预后

I. Lipkovich , W. Deberdt , P.F. Buckley , J.G. Csernansky , J. Peuskens , S. Kollack-Walker , J.P. Houston , M. Rotelli
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引用次数: 2

摘要

目的:早期对6项随机、主动对照研究的数据进行分析,涉及1449名患者,确定了5个不同的集群,其特征是精神病学和功能结局的不同组合。我们探讨了基线人口统计学、疾病特征、早期症状反应、治疗和不良事件作为代表最佳和最差临床结果的群集的可能预测因子。方法在联合治疗组的6个月终点中,良好的结局(A组)与良好的功能和有限的精神病理相关。不良预后与功能不良和中度(D类)或重度(E类)精神病理相关。采用逐步逻辑回归对基线预测因子和治疗2/4/8周的聚类隶属度(N = 1260)构建预测模型。根据研究效果调整优势比。结果A类基线预测因子包括女性性别和较高水平的职业和社会心理功能。在早期治疗期间,PANSS因素的改善也预示着良好的结果。D类基线预测因子包括发病早、年龄大、假性帕金森病、职业和社会心理功能差;随后PANSS抑郁、积极因素评分和功能评分的恶化预测了d类的不良预后。E类的预测因子包括发病早、非奥氮平治疗、PANSS抑郁、敌意和积极因素评分较高;PANSS紊乱、阴性和阳性因子评分的随后恶化可预测e类患者预后不良。结论早期症状改善/恶化可预测预后。对精神症状和功能的早期监测可能会根据个体特征做出更好的治疗决定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prediction of Combined Symptomatic and Functional Outcome in Patients with Schizophrenia or Schizoaffective Disorder

Purpose

An earlier analysis of data from six randomized, active-control studies involving 1449 patients identified five distinct clusters characterized by different combinations of psychiatric and functional outcomes. We explored baseline demographics, disease characteristics, early symptom response, treatment, and adverse events as possible predictors of clusters representing best and worst clinical outcomes.

Methods

At 6-month endpoint in combined treatment groups, good outcome (Cluster A) was associated with good functioning and limited psychopathology. Poor outcome was associated with poor functioning and moderate (Cluster D) or severe (Cluster E) psychopathology. Stepwise logistic regression was used to construct predictive models of cluster membership (N = 1260) for baseline predictors and with 2/4/8 weeks of treatment. Odds ratios were adjusted for study effects.

Results

Cluster A baseline predictors included female gender and higher levels of occupational and psychosocial functioning. Greater improvement across PANSS factors during early treatment also predicted good outcome. Cluster D baseline predictors included earlier onset of illness, older age, pseudoparkinsonism, and worse occupational and psychosocial functioning; subsequent worsening in PANSS depression and positive factor scores and in functioning predicted poor outcome for Cluster D. Predictors of Cluster E included earlier onset of illness, non-olanzapine treatment, and higher scores on the PANSS depression, hostility, and positive factors; subsequent worsening in PANSS disorganization, negative, and positive factor scores was predictive of poor outcome for Cluster E.

Conclusion

Early symptom improvement/worsening was predictive of outcome. Early monitoring of psychiatric symptoms and functioning may lead to better therapeutic decisions based on individual characteristics.

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