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通过同伴实施围产期抑郁症的“健康思维计划”:印度一项个体随机对照试验

Delivering the Thinking Healthy Programme for perinatal depression through peers: an individually randomised controlled trial in India.

作者信息

Fuhr Daniela C, Weobong Benedict, Lazarus Anisha, Vanobberghen Fiona, Weiss Helen A, Singla Daisy Radha, Tabana Hanani, Afonso Ejma, De Sa Aveena, D'Souza Ethel, Joshi Akankasha, Korgaonkar Priya, Krishna Revathi, Price LeShawndra N, Rahman Atif, Patel Vikram

机构信息

Department of Health Services Research and Policy, Faculty of Public Health and Policy, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK.

Department of Population Health, Faculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, UK; School of Public Health, Department of Social and Behavioural Sciences, College of Health Sciences, University of Ghana, Accra, Ghana; Sangath Centre, Socorro, Bardez, Goa, India.

出版信息

Lancet Psychiatry. 2019 Feb;6(2):115-127. doi: 10.1016/S2215-0366(18)30466-8.

Abstract

BACKGROUND

The Thinking Healthy Programme (THP) is a psychological intervention recommended for the treatment of perinatal depression. However, efforts to integrate the intervention at scale into the routines of community health workers who delivered the THP when it was first evaluated were compromised by the competing responsibilities of community health workers. We aimed to assess the effectiveness and cost-effectiveness of THP peer-delivered (THPP) in Goa, India.

METHODS

In this single-blind, individually randomised controlled trial, we recruited pregnant women aged 18 years or older who scored at least 10 on the Patient Health Questionnaire-9 (PHQ-9) from antenatal clinics in Goa. Participants were randomly allocated (1:1) to receive enhanced usual care (EUC; so-called because, in India, perinatal depression is not typically treated) only (control group) or THPP in addition to EUC (intervention group) in randomly sized blocks that were stratified by area of residence (urban or rural). Group allocations were concealed from participants and researchers before assignments were made by use of sequentially numbered opaque envelopes. The primary outcomes were the severity of depressive symptoms (assessed by PHQ-9 score) and the prevalence of remission (defined as a PHQ-9 score of less than 5) in participants with available data 6 months after childbirth, which was assessed by researchers who were masked to treatment allocations. We analysed outcomes by intention to treat, adjusting for covariates that were defined a priori or that showed imbalance at baseline. The trial is registered with ClinicalTrials.gov, number NCT02104232.

FINDINGS

Between Oct 24, 2014, and June 24, 2016, we assessed 118 260 women for their eligibility for screening, of whom 111 851 (94·6%) women were ineligible. 6409 (5·4%) women were eligible for screening and 6369 (99·4%) of these women consented to be screened with the PHQ-9 (40 women did not consent), of whom 333 (5·2%) screened positive for depression (defined as a PHQ-9 score of at least 10). We enrolled 280 (84·1%) women with perinatal depression; 140 women were assigned to the THPP and EUC group and 140 women to the EUC only group. The final treatment was given on May 27, 2017. The final 6-month outcome assessment was completed on June 9, 2017. At 6 months after birth, 122 (87%) women in the THPP and EUC group and 129 (92%) women in the EUC only group were assessed for the primary outcome. There was a higher prevalence of remission at 6 months after birth in the THPP and EUC group compared with the EUC only group (89 [73%] women in the intervention group vs 77 [60%] women in the control group; prevalence ratio 1·21, 95% CI 1·01 to 1·45; p=0·04), but there was no evidence of a difference in symptom severity between the groups (mean PHQ-9 score 3·47 [SD 4·49] in the intervention group vs 4·48 [5·11] in the control group; standardised mean difference -0·18, 95% CI -0·43 to 0·07; p=0·16). There was no evidence of significant differences in serious adverse events between the groups.

INTERPRETATION

THPP had a moderate effect on remission from perinatal depression over the 6-month postnatal period. THPP is relatively cheap to deliver and is cost-saving through reduced health-care, time and productivity costs.

FUNDING

National Institute of Mental Health (USA).

摘要

背景

“思维健康计划”(THP)是一项推荐用于治疗围产期抑郁症的心理干预措施。然而,在该计划首次评估时,将其大规模纳入社区卫生工作者日常工作的努力因社区卫生工作者的多项职责相互冲突而受到影响。我们旨在评估在印度果阿邦由同伴提供的THP(THPP)的有效性和成本效益。

方法

在这项单盲、个体随机对照试验中,我们从果阿邦的产前诊所招募了年龄在18岁及以上、在患者健康问卷-9(PHQ-9)上得分至少为10分的孕妇。参与者被随机分配(1:1),以随机大小的区组按居住地区(城市或农村)分层,仅接受强化常规护理(EUC;之所以称为强化常规护理,是因为在印度,围产期抑郁症通常未得到治疗)(对照组)或除EUC外还接受THPP(干预组)。在使用顺序编号的不透明信封进行分配之前,参与者和研究人员对组分配情况均不知情。主要结局是产后6个月有可用数据的参与者的抑郁症状严重程度(通过PHQ-9评分评估)和缓解率(定义为PHQ-9评分小于5),由对治疗分配不知情的研究人员进行评估。我们按意向性分析对结局进行分析,并对预先定义或在基线时显示不平衡的协变量进行调整。该试验已在ClinicalTrials.gov注册,注册号为NCT02104232。

结果

在2014年10月24日至2016年6月24日期间,我们评估了118260名妇女的筛查资格,其中111851名(94.6%)妇女不符合资格。6409名(5.4%)妇女符合筛查资格,其中6369名(99.4%)妇女同意接受PHQ-9筛查(40名妇女不同意),其中333名(5.2%)妇女抑郁筛查呈阳性(定义为PHQ-9评分至少为10)。我们招募了280名(84.1%)患有围产期抑郁症的妇女;140名妇女被分配到THPP和EUC组,140名妇女被分配到仅EUC组。最后一次治疗于2017年5月27日进行。最终的6个月结局评估于2017年6月9日完成。产后6个月时,对THPP和EUC组的122名(87%)妇女和仅EUC组的129名(92%)妇女进行了主要结局评估。与仅EUC组相比,THPP和EUC组产后6个月的缓解率更高(干预组89名[73%]妇女,对照组77名[60%]妇女;患病率比1.21,95%CI 1.01至1.45;p=0.04),但两组之间症状严重程度没有差异的证据(干预组平均PHQ-9评分为3.47[标准差4.49],对照组为4.48[5.11];标准化平均差-0.18,95%CI -0.43至0.07;p=0.16)。两组之间严重不良事件没有显著差异的证据。

解读

THPP在产后6个月对围产期抑郁症的缓解有中度效果。THPP的实施成本相对较低,通过降低医疗保健、时间和生产力成本实现了成本节约。

资助

美国国立精神卫生研究所。

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