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Predictors of Spontaneous and Systematically Assessed Suicidal Adverse Events in the Treatment of SSRI-Resistant Depression in Adolescents (TORDIA) Study

机译:青少年自发性和系统性评估的自杀性不良事件的预测因子(青少年抗SSRI抵抗)(TORDIA)研究

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The authors sought to identify predictors of self-harm adverse events in treatment-resistant, depressed adolescents during the first 12 weeks of treatment. Depressed adolescents (N-334) who had not responded to a previous trial with an SSRI antidepressant were randomized to a switch to either another SSRI or venlafaxine, with or without cognitive behavior therapy. Self-harm events, i.e., suicidal and non-suicidal self-injury adverse events were assessed by spontaneous report for the first 181 participants, and by systematic weekly assessment for the last 153 participants. Higher rates of suicidal (20.8% vs. 8.8%) and nonsuicidal self-injury (17.6% vs. 2.2%), but not serious adverse events (8.4% vs. 7.3%) were detected with systematic monitoring. Median time to a suicidal event was 3 weeks, predicted by high baseline suicidal ideation, family conflict, and drug and alcohol use. Median time to nonsuicidal self-injury was 2 weeks, predicted by previous history of nonsuicidal self-injury. While there were no main effects of treatment, venlafaxine treatment was associated with a higher rate of self-harm adverse events in those with higher suicidal ideation. Adjunctive use of benzodiazepines, while in a small number of participants (N=10) was associated with higher rate of both suicidal and nonsuicidal self-injury adverse events. Since predictors of suicidal adverse events also predict poor response to treatment, and many of these events occurred early in treatment, improving the speed of response to depression, by targeting of family conflict, suicidal ideation, and drug use may help to reduce their incidence. The relationship of venlafaxine and of benzodiazepines to self-harm events requires further study and clinical caution.
机译:作者试图确定在治疗的前12周内抗药性抑郁青少年的自我伤害不良事件的预测因素。对先前对SSRI抗抑郁药没有反应的抑郁青少年(N-334)被随机分配至另一种SSRI或文拉法辛治疗,或不进行认知行为治疗。自我伤害事件(即自杀和非自杀性自残不良事件)是通过对前181位参与者的自发报告进行评估,并通过对最近153位参与者的每周系统评估来评估的。通过系统监测发现自杀率较高(20.8%对8.8%)和非自杀性自残率(17.6%对2.2%),但未发现严重的不良事件(8.4%对7.3%)。根据高基线自杀观念,家庭冲突以及吸毒和酗酒的预测,自杀事件的中位时间为3周。根据先前的非自杀性自我伤害史,非自杀性自我伤害的中位时间为2周。尽管没有治疗的主要作用,但在具有较高自杀观念的患者中,文拉法辛治疗与较高的自残不良事件发生率相关。辅助使用苯二氮卓类药物(少数参与者(N = 10))与自杀和非自杀性自残不良事件发生率较高相关。由于自杀性不良事件的预测因素也预示着对治疗的不良反应,而且许多此类事件都发生在治疗的早期,通过针对家庭冲突,自杀观念和吸毒,提高了对抑郁症的反应速度,可能有助于降低其发生率。文拉法辛和苯二氮卓类药物与自残事件的关系需要进一步研究和临床注意。

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    《The American Journal of Psychiatry》 |2009年第4期|p.418-426|共9页
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    David A. Brent, M. D.Graham J. Emslie, M. D.Greg N. Clarke, Ph.D.Joan Asarnow, Ph.D.Anthony Spirito, Ph.D.Louise Ritz, M.B.A.Benedetto Vitiello, M. D.Satish lyengar, Ph.D.Boris Birmaher, M. D.Neal D. Ryan, M. D.Jamie Zelazny, M. P.M., R.N.Matthew Onorato, L.C.S.W.Betsy Kennard, Psy.D.Taryn L Mayes, M.S.Lynn L DeBar, Ph.D.James T. McCracken, M. D.Michael Strober, Ph.D.Robert Suddath, M.D.Henrietta Leonard, M.D.Giovanna Porta, M.S.Martin B. Keller, M.D.Received July 1, 2008, revision received Oct. 3, 2008, accepted Nov. 6, 2008 (doi: 10.1176/appl.ajp.2008.08070976). From the University of Pittsburgh School of Medicine, Western Psychiatric Institute and Clinic. Address correspondence and reprint requests to Dr. Brent, University of Pittsburgh School of Medicine, Western University School of Medicine, Western Psychiatric Institute and Clinic, 3811 O'Hara St., Suite 112, Pittsburgh, PA, 15213-2593, brentda@upmc.edu (e-mail).Dr. Asarnow has consulted on cognitive behavior therapy and cognitive behavior therapy for depression on an unrestricted grant from Pfizer, has funding from Philip Morris, a family member has funding from Bristol-Myers Squibb and has consulted for Roche. Dr. Birmaher has participated in forums sponsored by Solvay Pharmaceuticals, Inc. and Abcomm, Inc. He presented on bipolar disorders in children at a meeting sponsored by Solvay. Dr. Birmaher also received royalties from Random House, Inc. Dr. Emslie receives research support from Biobehavioral Diagnostics Inc., Forest Laboratories, Shire, and Somerset, and is a consultant for Biobehavioral Diagnostics, Inc., Eli Lilly, Forest Laboratories, Inc., Shire, Validus Pharmaceuticals, and Wyeth Pharmaceuticals. Dr. Hughes is a consultant for Biobehavioral Diagnostics, Inc. Dr. Keller has reported research support from Pfizer. He is a consultant with CENEREX, Cephalon, Cypress Bioscience, Cyberonics, Forest Laboratories, Janssen, JDS, Organon, Novartis, Pfizer, and Wyeth. Or. Keller has served on advisory boards for Abbott Laboratories, Bristol-Myers Squibb, CENEREX, Cyberomcs, Cypress Bioscience, Forest Laboratories, Janssen, Novartis, Organon, and Pfizer. Dr. McCracken has received research support from Eli Lilly, McNeil, Bristol-Myers Squibb, and Shire. He is a consultant for Shire, Eli Lilly, McNeil, Pfizer, Janssen, Johnson & Johnson, Novartis and Wyeth. Dr. Wagner is a consultant or serves on the advisory board for Abbott Laboratories, AstraZeneca, Bristol-Myers Squibb, Eli Lilly, Forest Laboratories, Johnson & Johnson, Otsuka, Solvay, and Wyeth. All other authors report no competing interests.Dr. Leonard passed away in August 2007.,;

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