一种首发精神病非缓解风险预测模型的建立和验证:两项纵向研究的分析。

Samuel P Leighton, Rajeev Krishnadas, Rachel Upthegrove, Steven Marwaha, Ewout W Steyerberg, Georgios V Gkoutos, Matthew R Broome, Peter F Liddle, Linda Everard, Swaran P Singh, Nicholas Freemantle, David Fowler, Peter B Jones, Vimal Sharma, Robin Murray, Til Wykes, Richard J Drake, Iain Buchan, Simon Rogers, Jonathan Cavanagh, Shon W Lewis, Max Birchwood, Pavan K Mallikarjun
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引用次数: 4

摘要

精神病是一种主要的精神疾病,在年轻人中首发。大约一半的患者预后很差,而且很难预测。目前仅有的几种预测预后的工具存在很大的缺陷,这限制了它们在临床实践中的应用。我们的目的是建立并验证首发精神病症状不缓解的风险预测模型。我们的发展队列包括1027名首发精神病患者,这些患者于2005年至2010年间从英国国家卫生服务体系的14个早期干预服务机构招募。我们的验证队列包括2006年至2009年间从另外11个英国早期干预服务机构招募的399名首发精神病患者。开发组和验证组的1年非缓解率分别为52%和54%。采用多变量logistic回归建立非缓解风险预测模型,并进行外部验证。预测模型的判别c统计量为0.73(0.71,0.75),校正充分,截距α为0.12(0.02,0.22),斜率β为0.98(0.85,1.11)。与治疗所有患者的策略相比,我们的模型在风险阈值为50%的情况下将净收益提高了15%,相当于每100例未确诊的首发精神病患者中增加了15例,而不会对确诊病例进行错误分类。一旦前瞻性验证,我们的首次发作精神病预测模型可以帮助识别在初次临床接触时不缓解风险增加的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development and Validation of a Nonremission Risk Prediction Model in First-Episode Psychosis: An Analysis of 2 Longitudinal Studies.

Development and Validation of a Nonremission Risk Prediction Model in First-Episode Psychosis: An Analysis of 2 Longitudinal Studies.

Development and Validation of a Nonremission Risk Prediction Model in First-Episode Psychosis: An Analysis of 2 Longitudinal Studies.

Development and Validation of a Nonremission Risk Prediction Model in First-Episode Psychosis: An Analysis of 2 Longitudinal Studies.

Psychosis is a major mental illness with first onset in young adults. The prognosis is poor in around half of the people affected, and difficult to predict. The few tools available to predict prognosis have major weaknesses which limit their use in clinical practice. We aimed to develop and validate a risk prediction model of symptom nonremission in first-episode psychosis. Our development cohort consisted of 1027 patients with first-episode psychosis recruited between 2005 and 2010 from 14 early intervention services across the National Health Service in England. Our validation cohort consisted of 399 patients with first-episode psychosis recruited between 2006 and 2009 from a further 11 English early intervention services. The one-year nonremission rate was 52% and 54% in the development and validation cohorts, respectively. Multivariable logistic regression was used to develop a risk prediction model for nonremission, which was externally validated. The prediction model showed good discrimination C-statistic of 0.73 (0.71, 0.75) and adequate calibration with intercept alpha of 0.12 (0.02, 0.22) and slope beta of 0.98 (0.85, 1.11). Our model improved the net-benefit by 15% at a risk threshold of 50% compared to the strategy of treating all, equivalent to 15 more detected nonremitted first-episode psychosis individuals per 100 without incorrectly classifying remitted cases. Once prospectively validated, our first episode psychosis prediction model could help identify patients at increased risk of nonremission at initial clinical contact.

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