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初级保健中抑郁症治疗的依从性:一项随机临床试验。

Adherence to Depression Treatment in Primary Care: A Randomized Clinical Trial.

作者信息

Sirey Jo Anne, Banerjee Samprit, Marino Patricia, Bruce Martha L, Halkett Ashley, Turnwald Molly, Chiang Claire, Liles Brian, Artis Amanda, Blow Fred, Kales Helen C

机构信息

Department of Psychiatry, Weill Cornell Medicine, White Plains, New York.

Department of Healthcare Policy & Research, Weill Cornell Medicine, White Plains, New York.

出版信息

JAMA Psychiatry. 2017 Nov 1;74(11):1129-1135. doi: 10.1001/jamapsychiatry.2017.3047.

Abstract

IMPORTANCE

Nonadherence to antidepressant medication is common and leads to poor outcomes. Early nonadherence is especially problematic.

OBJECTIVE

To test the effectiveness of a psychosocial intervention to improve early adherence among older patients whose primary care physician newly initiated an antidepressant for depression.

DESIGN, SETTING, AND PARTICIPANTS: The Treatment Initiation and Participation Program (TIP) was offered in a 2-site randomized clinical effectiveness study between January 2011 and December 2014 at primary care practices in New York, New York, and Ann Arbor, Michigan. Analyses began in February 2016. All participants were middle-aged and older adults (aged ≥55 years) who received newly initiated depression treatment by their primary care physician and recruited within 10 days of their prescription. Analyses were intention-to-treat.

INTERVENTIONS

Participants were randomly assigned to the intervention (TIP) or treatment as usual. Participants in the TIP group identified and addressed barriers to adherence, including stigma, misconceptions, and fears about treatment, before developing a personalized adherence strategy. The Treatment Initiation and Participation Program was delivered in three 30-minute contacts scheduled during a 6-week period just after the antidepressant was prescribed.

MAIN OUTCOMES AND MEASURES

The primary outcome was self-reported adherence on the Brief Medication Questionnaire, with adequate early adherence defined as taking 80% or more of the prescribed doses at 6 and 12 weeks. The secondary outcome was depression severity.

RESULTS

In total, 231 middle-aged and older adults (167 women [72.3%] and 64 men [27.7%]) without significant cognitive impairment were randomly assigned to the TIP intervention (n = 115) or treatment as usual (n = 116). Participants had a mean (SD) age of 67.3 (8.4) years. Participants in the TIP group were 5 times more likely to be adherent at 6 weeks (odds ratio, 5.54; 95% CI, 2.57 to 11.96; χ21 = 19.05; P < .001) and 3 times more likely to be adherent at both 6 and 12 weeks (odds ratio, 3.27; 95% CI, 1.73 to 6.17; χ21 = 13.34; P < .001). Participants in the TIP group showed a significant earlier reduction (24.9%) in depressive symptoms (95% CI, 13.9 to 35.9; t337 = 4.46; adjusted P < .001). In both groups, participants who were 80% adherent at weeks 6 and 12 had a 15% greater improvement in depressive symptoms from baseline over the course of treatment (95% CI, -0.2 to -30; t369 = 1.93; P = .051).

CONCLUSIONS AND RELEVANCE

The Treatment Initiation and Participation Program is an effective intervention to improve early adherence to pharmacotherapy. Improved adherence can promote improvement in depression.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT01301859.

摘要

重要性

不坚持服用抗抑郁药物的情况很常见,且会导致不良后果。早期不坚持服药尤其成问题。

目的

测试一种心理社会干预措施对提高老年患者早期服药依从性的有效性,这些老年患者的初级保健医生新开出了治疗抑郁症的抗抑郁药物。

设计、地点和参与者:2011年1月至2014年12月在纽约州纽约市和密歇根州安阿伯市的初级保健机构进行了一项双地点随机临床有效性研究,开展了治疗启动与参与项目(TIP)。2016年2月开始分析。所有参与者均为中老年成年人(年龄≥55岁),他们由初级保健医生开始接受新的抑郁症治疗,并在开处方后10天内被招募。分析采用意向性分析。

干预措施

参与者被随机分配到干预组(TIP)或常规治疗组。TIP组的参与者在制定个性化的服药依从策略之前,先识别并解决了妨碍服药的因素,包括耻辱感、误解以及对治疗的恐惧。治疗启动与参与项目在开出抗抑郁药物后的6周内分三次进行,每次30分钟。

主要结局和测量指标

主要结局是通过简易药物问卷自我报告的服药依从性,早期充分依从性定义为在6周和12周时服用规定剂量的80%或更多。次要结局是抑郁严重程度。

结果

共有231名无明显认知障碍的中老年成年人(167名女性[72.3%]和64名男性[27.7%])被随机分配到TIP干预组(n = 115)或常规治疗组(n = 116)。参与者的平均(标准差)年龄为67.3(8.4)岁。TIP组的参与者在6周时坚持服药的可能性高出5倍(优势比,5.54;95%置信区间,2.57至11.96;χ21 = 19.05;P <.001),在6周和12周时都坚持服药的可能性高出3倍(优势比,3.27;95%置信区间,1.73至6.17;χ21 = 13.34;P <.001)。TIP组的参与者抑郁症状显著更早减轻(24.9%)(95%置信区间,13.9至35.9;t337 = 4.46;校正P <.001)。在两组中,在6周和12周时服药依从性达到80%的参与者在治疗过程中抑郁症状较基线改善幅度高出15%(95%置信区间,-0.2至-30;t369 = 1.93;P = 0.051)。

结论与意义

治疗启动与参与项目是提高药物治疗早期依从性的有效干预措施。提高依从性可促进抑郁症的改善。

试验注册

clinicaltrials.gov标识符:NCT01301859。

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