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Patient Engagement Programs for Recognition and Initial Treatment of Depression in Primary Care A Randomized Trial

机译:在初级保健中识别和初始治疗抑郁症的患者参与计划-一项随机试验

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RESULTS Of the 925 eligible patients, 867 were included in the primary analysis (depressed, 559; nondepressed, 308). Among depressed patients, rates of achieving the primary outcome were 17.5% for DEV, 26% for IMCP, and 16.3% for control (DEV vs control, 1.1 [95% Cl, -6.7 to 8.9], P = .79; IMCP vs control, 9.9 [95% Cl, 1.6 to 18.2], P = .02). There were no effects on PHQ-8 measured depression score at the 12-week follow-up: DEV vs control, -0.2 (95% Cl, -1.2 to 0.8); IMCP vs control, 0.9 (95% Cl, -0.1 to 1.9). Among nondepressed patients, clinician-reported antidepressant prescribing in the DEV and IMCP groups was noninferior to control (mean percentage point difference [PPD]: DEV vs control, -2.2 [90% Cl, -8.0 to 3.49], P = .0499 for noninferiority; IMCP vs control, -3.3 [90% Cl, -9.1 to 2.4], P = .02 for noninferiority); patient-reported antidepressant recommendation did not achieve noninferiority (mean PPD: DEV vs control, 0.9 [90% Cl, -4.9 to 6.7], P = .23 for noninferiority; IMCP vs control, 0.3 [90% Cl, -5.1 to 5.7], P = .16 for noninferiority).
机译:结果在925名符合条件的患者中,有867名患者被纳入了主要分析(抑郁者559名;非抑郁者308名)。在抑郁患者中,DEV达到主要结局的比率为17.5%,IMCP为26%,对照为16.3%(DEV vs对照,1.1 [95%Cl,-6.7至8.9],P = .79; IMCP vs对照,9.9 [95%Cl,1.6至18.2],P = .02)。在第12周的随访中,对PHQ-8测量的抑郁评分没有影响:DEV vs对照,-0.2(95%Cl,-1.2至0.8); IMCP vs.对照,为0.9(95%Cl,-0.1至1.9)。在非抑郁症患者中,DEV和IMCP组中临床医生报告的抗抑郁药处方不逊于对照(平均百分率[PPD]:DEV vs对照,-2.2 [90%Cl,-8.0至3.49],P = .0499非劣效性; IMCP vs对照,-3.3 [90%Cl,-9.1至2.4],非劣效性P = .02);患者报告的抗抑郁药推荐未达到非劣效性(平均PPD:DEV vs对照,0.9 [90%Cl,-4.9至6.7],非劣效性P = 0.23; IMCP vs对照,0.3 [90%Cl,-5.1至5.7 ],对于非自卑者,P = 0.16)。

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