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初级和二级医疗保健之间开展针对性强化联络以识别首次发生精神病性疾病风险个体的临床有效性和成本效益(LEG研究):一项整群随机对照试验

Clinical effectiveness and cost-effectiveness of tailored intensive liaison between primary and secondary care to identify individuals at risk of a first psychotic illness (the LEGs study): a cluster-randomised controlled trial.

作者信息

Perez Jesus, Jin Huajie, Russo Debra A, Stochl Jan, Painter Michelle, Shelley Gill, Jackson Erica, Crane Carolyn, Graffy Jonathan P, Croudace Tim J, Byford Sarah, Jones Peter B

机构信息

CAMEO Early Intervention Services, Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK; Department of Psychiatry, University of Cambridge, Cambridge, UK; National Institute of Health Research Collaboration for Leadership in Applied Health Research and Care East of England (CLAHRC-EoE), Cambridge, UK.

Centre for the Economics of Mental and Physical Health, King's College London, London, UK.

出版信息

Lancet Psychiatry. 2015 Nov;2(11):984-93. doi: 10.1016/S2215-0366(15)00157-1. Epub 2015 Aug 19.

Abstract

BACKGROUND

General practitioners are usually the first health professionals to be contacted by people with early signs of psychosis. We aimed to assess whether increased liaison between primary and secondary care improves the clinical effectiveness and cost-effectiveness of detection of people with, or at high risk of developing, a first psychotic illness.

METHODS

Our Liaison and Education in General Practices (LEGs) study was a cluster-randomised controlled trial of primary care practices (clusters) in Cambridgeshire and Peterborough, UK. Consenting practices were randomly allocated (1:1) to a 2 year low-intensity intervention (a postal campaign, consisting of biannual guidelines to help identify and refer individuals with early signs of psychosis) or a high-intensity intervention, which additionally included a specialist mental health professional who liaised with every practice and a theory-based educational package. Practices were not masked to group allocation. Practices that did not consent to be randomly assigned comprised a practice-as-usual (PAU) group. The primary outcome was number of referrals of patients at high risk of developing psychosis to the early intervention service per practice site. New referrals were assessed clinically and stratified into those who met criteria for high risk or first-episode psychotic illness (FEP; together: psychosis true positives), and those who did not fulfil such criteria for psychosis (false positives). Referrals from PAU practices were also analysed. We assessed cost-effectiveness with decision analytic modelling in terms of the incremental cost per additional true positive identified. The trial is registered at the ISRCTN registry, number ISRCTN70185866.

FINDINGS

Between Dec 22, 2009, and Sept 7, 2010, 54 of 104 eligible practices provided consent and between Feb 16, 2010, and Feb 11, 2011, these practices were randomly allocated to interventions (28 to low intensity and 26 to high intensity); the remaining 50 practices comprised the PAU group. Two high-intensity practices were excluded from the analysis. In the 2 year intervention period, high-intensity practices referred more FEP cases than did low-intensity practices (mean 1.25 [SD 1.2] for high intensity vs 0.7 [0.9] for low intensity; incidence rate ratio [IRR] 1.9, 95% CI 1.05-3.4, p=0.04), although the difference was not statistically significant for individuals at high risk of psychosis (0.9 [1.0] vs 0.5 [1.0]; 2.2, 0.9-5.1, p=0.08). For high risk and FEP combined, high-intensity practices referred both more true-positive (2.2 [1.7] vs 1.1 [1.7]; 2.0, 1.1-3.6, p=0.02) and false-positive (2.3 [2.4] vs 0.9 [1.2]; 2.6, 1.3-5.0, p=0.005) cases. Referral patterns did not differ between low-intensity and PAU practices. Total cost per true-positive referral in the 2 year follow-up was £26,785 in high-intensity practices, £27,840 in low-intensity practices, and £30,007 in PAU practices.

INTERPRETATION

This intensive intervention to improve liaison between primary and secondary care for people with early signs of psychosis was clinically and cost effective.

FUNDING

UK National Institute for Health Research.

摘要

背景

全科医生通常是出现精神病早期症状的患者首先联系的医疗专业人员。我们旨在评估加强初级保健与二级保健之间的联络是否能提高首次发生精神病性疾病或有发生此类疾病高风险者的检测的临床效果和成本效益。

方法

我们的全科医疗联络与教育(LEGs)研究是一项针对英国剑桥郡和彼得伯勒的初级保健机构(群组)的整群随机对照试验。同意参与的机构被随机分配(1:1)至为期2年的低强度干预组(一项邮政宣传活动,包括每半年发布一次帮助识别和转诊有精神病早期症状个体的指南)或高强度干预组,后者还包括一名与每个机构联络的专科心理健康专业人员以及一套基于理论的教育包。机构不设分配分组盲法。不同意随机分配的机构组成常规治疗(PAU)组。主要结局是每个实践地点转诊至早期干预服务的有发生精神病高风险患者的数量。新转诊患者接受临床评估,并分层为符合高风险或首次发作精神病性疾病(FEP;合称:精神病真阳性)标准的患者,以及不符合此类精神病标准的患者(假阳性)。还分析了PAU机构的转诊情况。我们通过决策分析模型根据每识别出一例额外真阳性的增量成本评估成本效益。该试验已在国际标准随机对照试验编号注册库注册,编号为ISRCTN70185866。

结果

在2009年12月22日至2010年9月7日期间,104家符合条件的机构中有54家表示同意,在2010年2月16日至2011年2月11日期间,这些机构被随机分配至干预组(28家至低强度组,26家至高强度组);其余50家机构组成PAU组。两家高强度机构被排除在分析之外。在2年的干预期内,高强度机构转诊的FEP病例多于低强度机构(高强度组均值为1.25[标准差1.2],低强度组为0.7[0.9];发病率比[IRR]为1.9,95%置信区间为1.05 - 3.4,p = 0.04),尽管对于有精神病高风险的个体差异无统计学意义(0.9[1.0]对0.5[1.0];2.2,0.9 - 5.1,p = 0.08)。对于高风险和FEP合并情况,高强度机构转诊的真阳性(2.2[1.7]对1.1[1.7];2.0,1.1 - 3.6,p = 0.02)和假阳性(2.3[2.4]对0.9[1.2];2.6,1.3 - 5.0,p = 0.005)病例均更多。低强度机构和PAU机构的转诊模式无差异。在2年随访中,高强度机构每例真阳性转诊的总成本为26,785英镑,低强度机构为27,840英镑,PAU机构为30,007英镑。

解读

这种旨在改善有精神病早期症状患者的初级保健与二级保健之间联络的强化干预在临床和成本效益方面均有效。

资金来源

英国国家卫生研究院。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9830/4641188/00498a2d0dfa/gr1.jpg

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