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在初级保健中对青少年抑郁症患者进行协作式护理:一项随机临床试验。

Collaborative care for adolescents with depression in primary care: a randomized clinical trial.

机构信息

Department of Pediatrics, University of Washington School of Medicine, Seattle2Seattle Children's Research Institute Center for Child Health, Behavior, and Development, Seattle.

Group Health Research Institute, Seattle, Washington.

出版信息

JAMA. 2014 Aug 27;312(8):809-16. doi: 10.1001/jama.2014.9259.

Abstract

IMPORTANCE

Up to 20% of adolescents experience an episode of major depression by age 18 years yet few receive evidence-based treatments for their depression.

OBJECTIVE

To determine whether a collaborative care intervention for adolescents with depression improves depressive outcomes compared with usual care.

DESIGN

Randomized trial with blinded outcome assessment conducted between April 2010 and April 2013.

SETTING

Nine primary care clinics in the Group Health system in Washington State.

PARTICIPANTS

Adolescents (aged 13-17 years) who screened positive for depression (Patient Health Questionnaire 9-item [PHQ-9] score ≥10) on 2 occasions or who screened positive and met criteria for major depression, spoke English, and had telephone access were recruited. Exclusions included alcohol/drug misuse, suicidal plan or recent attempt, bipolar disorder, developmental delay, and seeing a psychiatrist.

INTERVENTIONS

Twelve-month collaborative care intervention including an initial in-person engagement session and regular follow-up by master's-level clinicians. Usual care control youth received depression screening results and could access mental health services through Group Health.

MAIN OUTCOMES AND MEASURES

The primary outcome was change in depressive symptoms on a modified version of the Child Depression Rating Scale-Revised (CDRS-R; score range, 14-94) from baseline to 12 months. Secondary outcomes included change in Columbia Impairment Scale score (CIS), depression response (≥50% decrease on the CDRS-R), and remission (PHQ-9 score <5).

RESULTS

Intervention youth (n = 50), compared with those randomized to receive usual care (n = 51), had greater decreases in CDRS-R scores such that by 12 months intervention youth had a mean score of 27.5 (95% CI, 23.8-31.1) compared with 34.6 (95% CI, 30.6-38.6) in control youth (overall intervention effect: F2,747.3 = 7.24, P < .001). Both intervention and control youth experienced improvement on the CIS with no significant differences between groups. At 12 months, intervention youth were more likely than control youth to achieve depression response (67.6% vs 38.6%, OR = 3.3, 95% CI, 1.4-8.2; P = .009) and remission (50.4% vs 20.7%, OR = 3.9, 95% CI, 1.5-10.6; P = .007).

CONCLUSIONS AND RELEVANCE

Among adolescents with depression seen in primary care, a collaborative care intervention resulted in greater improvement in depressive symptoms at 12 months than usual care. These findings suggest that mental health services for adolescents with depression can be integrated into primary care.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT01140464.

摘要

重要性

多达 20%的青少年在 18 岁之前会经历一次重度抑郁症发作,但很少有接受过针对其抑郁症的循证治疗。

目的

确定针对青少年抑郁症的协作式护理干预是否比常规护理更能改善抑郁结局。

设计

2010 年 4 月至 2013 年 4 月进行的随机试验,结果评估为盲法。

地点

华盛顿州 Group Health 系统的 9 个初级保健诊所。

参与者

筛选出在两次就诊时出现抑郁(PHQ-9 量表得分为≥10 分)或筛选阳性且符合重度抑郁症标准、会讲英语且有电话访问的 13-17 岁青少年。排除标准包括酒精/药物滥用、自杀计划或最近尝试、双相情感障碍、发育迟缓以及看精神科医生。

干预措施

为期 12 个月的协作式护理干预,包括最初的面对面参与会议和由硕士级临床医生定期进行的随访。常规护理对照组的青少年会收到抑郁筛查结果,并可以通过 Group Health 获得心理健康服务。

主要结局和措施

主要结局是从基线到 12 个月时使用儿童抑郁评定量表修订版(CDRS-R;评分范围为 14-94)的抑郁症状变化。次要结局包括哥伦比亚损伤量表(CIS)评分变化、抑郁反应(CDRS-R 降低≥50%)和缓解(PHQ-9 评分<5)。

结果

与接受常规护理(n = 51)的青少年相比,干预组(n = 50)的 CDRS-R 评分下降幅度更大,干预组的青少年在 12 个月时的平均得分为 27.5(95%CI,23.8-31.1),而对照组的平均得分为 34.6(95%CI,30.6-38.6)(总体干预效果:F2,747.3 = 7.24,P < .001)。干预组和对照组的 CIS 均有所改善,但两组之间无显著差异。在 12 个月时,干预组青少年比对照组更有可能达到抑郁反应(67.6% vs 38.6%,OR = 3.3,95%CI,1.4-8.2;P = .009)和缓解(50.4% vs 20.7%,OR = 3.9,95%CI,1.5-10.6;P = .007)。

结论和相关性

在初级保健中接受治疗的青少年中,与常规护理相比,协作式护理干预在 12 个月时可更有效地改善抑郁症状。这些发现表明,青少年抑郁症的心理健康服务可以整合到初级保健中。

试验注册

clinicaltrials.gov 标识符:NCT01140464。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7988/4492537/4d44d5a114a2/nihms695226f1.jpg

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