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首页> 外文期刊>The American Journal of Psychiatry >Difference in Treatment Outcome in Outpatients With Anxious Versus Nonanxious Depression: A STAR*D Report
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Difference in Treatment Outcome in Outpatients With Anxious Versus Nonanxious Depression: A STAR*D Report

机译:焦虑与非焦虑抑郁症患者的治疗结果差异:STAR * D报告

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摘要

About half of outpatients with major depressive disorder also have clinically meaningful levels of anxiety. The authors conducted a secondary data analysis to compare antidepressant treatment outcomes for patients with anxious and nonanxious major depression in Levels 1 and 2 of the STAR*D study. A total of 2,876 adult outpatients with major depressive disorder, enrolled from 18 primary and 23 psychiatric care sites, received citalopram in Level 1 of STAR*D. In Level 2, a total of 1,292 patients who did not remit with or tolerate citalopram were randomly assigned either to switch to sustained-release bupropion (N=239), sertraline (N=238), or extended-release venlafaxine (N=250) or to continue taking citalopram and receive augmentation with sustained-release bupropion (N=279) or buspirone (N=286). Treatment could last up to 14 weeks in each level. Patients were designated as having anxious depression if their anxiety/somatization factor score from the 17-item Hamilton Depression Rating Scale (HAM-D) was 7 or higher at baseline. Rates of remission and response as well as times to remission and response were compared between patients with anxious depression and those with nonanxious depression.In Level 1 of STAR*D, 53.2% of patients had anxious depression. Remission was significantly less likely and took longer to occur in these patients than in those with nonanxious depression. Ratings of side effect frequency, intensity, and burden, as well as the number of serious adverse events, were significantly greater in the anxious depression group. Similarly, in Level 2, patients with anxious depression fared significantly worse in both the switching and augmentation options. Anxious depression is associated with poorer acute outcomes than nonanxious depression following antidepressant treatment.
机译:重度抑郁症的门诊患者中约有一半还具有临床上有意义的焦虑水平。作者进行了二次数据分析,以比较STAR * D研究的1级和2级焦虑和非焦虑重度抑郁症患者的抗抑郁治疗结果。从STAR * D的1级患者中,总共从18个初级和23个精神科护理点入组的2876名重度抑郁症成年门诊患者接受了西酞普兰治疗。在2级患者中,共有1,292例未接受西酞普兰缓解或不耐受的患者被随机分配为转用缓释安非他酮(N = 239),舍曲林(N = 238)或缓释文拉法辛(N = 250) )或继续服用西酞普兰并接受持续释放的安非他酮(N = 279)或丁螺环酮(N = 286)增强。每个级别的治疗可能持续长达14周。如果来自17个项的汉密尔顿抑郁量表(HAM-D)的焦虑/躯体化因子评分在基线时为7或更高,则将患者指定为焦虑抑郁症。比较焦虑抑郁患者和非焦虑抑郁患者的缓解和缓解率以及缓解和缓解时间。在STAR * D级别1中,有53.2%的患者患有焦虑抑郁。与无焦虑抑郁症的患者相比,缓解的可能性明显更低,并且花费的时间更长。焦虑抑郁组的副作用发生频率,强度和负担以及严重不良事件的发生率明显更高。同样,在第2级中,焦虑抑郁症患者在转换和增强选择方面的表现均显着恶化。与抗抑郁药治疗后的非焦虑抑郁症相比,焦虑抑郁症的急性预后较差。

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  • 来源
    《The American Journal of Psychiatry》 |2008年第3期|p.342-351|共10页
  • 作者单位

    Maurizio Fava, M.D.A. John Rush, M.D.Jonathan E. Alpert, M.D., Ph.D.G.K. Balasubramani, Ph.D.Stephen R. Wisniewski, Ph.D.Cheryl N. Carmin, Ph.D.Melanie M. Biggs, Ph.D.Sidney Zisook, M.D.Andrew Leuchter, M.D.Robert Howland, M.D.Diane Warden, Ph.D.Madhukar H. Trivedi, M.D.Received Nov. 16, 2006, revisions received March 20, June 18, and Aug. 20, 2007, accepted Aug. 27, 2007 (doi: 10.1176/ appi.ajp.2007.06111868). From the Depression Clinical and Research Program, Massachusetts General Hospital, Boston, Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Epidemiology Data Center, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, University of Illinois at Chicago, Department of Psychiatry, University of California, San Diego, and San Diego VA Medical Center, Semel Institute for Neuroscience and Human Behavior, UCLA, Los Angeles, and the Department of Psychiatry, University of Pittsburgh Medical Center, Pittsburgh. Address correspondence and reprint requests to Dr. Fava, Depression Clinical and Research Program, Massachusetts General Hospital, 55 Fruit St., Bulfinch 351, Boston, MA 02114, mfava@partners.org (e-mail).Supported by NIMH under contract N01MH90003 to University of Texas Southwestern Medical Center at Dallas (principal investigator, Dr. Rush). Medications for this trial were provided at no cost by Bristol-Myers Squibb, Forest Laboratories, GlaxoSmithKline, King Pharmaceuticals, Organon, Pfizer, and Wyeth. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U-S. Government.Dr. Fava has received research support from or served as an adviser, consultant, or speaker for Abbott Laboratories, Alkermes, Aspect Medical Systems, Astra-Zeneca, Auspex Pharmaceuticals, Bayer AG, Best Practice Project Management, Biovail Pharmaceuticals, Boehringer-lngelheim, BrainCells. Bristol-Myers Squibb, Cephalon, CNS Response. Compellis, Cypress Pharmaceuticals, Dov Pharmaceuticals, EPIX Pharmaceuticals, Fabre-Kramer Pharmaceuticals, Forest Pharmaceuticals, GlaxoSmithKline, Grunenthal GmbH, Janssen Pharmaceutica, Jazz Pharmaceuticals. Johnson & Johnson Pharmaceuticals, Knoll Pharmaceutical Company, Lichtwer Pharma GmbH, Eli Lilly, Lorex Pharmaceuticals, Lundbeck, MedAvante, Merck, Neuronetics, Novartis, Nutrition 21, Organon, PamLab, Pfizer, PharmaStar, Pharmavite, Pfizer, Precision Human Biolaboratory, Roche, Sanofi/Synthelabo. Sepracor, Solvay, Somaxon, Somerset Pharmaceuticals, Takeda. TetraGenex, Transcept Pharmaceuticals, and WyethAyerst, he also holds equity in Compellis and MedAvante. Dr. Rush has received research support from or served as an adviser, consultant, or speaker for Advanced Neuromodulation Systems, Best Practice Project Management, Bristol-Myers Squibb, Cyberonics, Eli Lilly, Forest Pharmaceuticals. Gerson Lehman Group, GlaxoSmithKline, Healthcare Technology Systems, Jazz Pharmaceuticals. Merck, Neuronetics, NIMH, Ono Pharmaceuticals, Organon, Personality Disorder Research Corp.. Robert Wood Johnson Foundation, Stanley Medical Research Institute. Urban Institute, and Wyeth-Ayerst, he also receives royalties from Guilford Publications and Healthcare Technology Systems and holds stock in Pfizer, Dr. Alpert has received research support from or served as an adviser, consultant, or speaker for Abbott Laboratories, Alkermes. Lichtwer Pharma GmbH, Lorex Pharmaceuticals Aspect Medical Systems. Astra-Zeneca, Bristol-Myers Squibb. Cephalon. Cyberonics, Eli Lilly. Forest Pharmaceuticals, GlaxoSmithKline, Johnson & Johnson Pharmaceuticals. Novartis, Organon. PamLab. Pfizer, Pharmavite. Roche. Sanofi/Synthelabo, Solvay, and Wyeth-Ayerst. Dr. Wisniewski has consulted for Cyberonics. ImaRx Therapeutics, Bristol-Myers Squibb, and Organon. Dr. Biggs has consulted for Bristol-Myers Squibb. GlaxoSmithKline, Eli Lilly, Merck, and Pfizer. Dr. Zisook has received research support from or served as an adviser, consultant, or speaker for Aspect Medical Systems, Forest Laboratories. GlaxoSmithKline, PamLab. NIMH, and Veterans Administrative Health Care. Dr. Leuchter has received research support from or served as an adviser, consultant, or speaker for Aspect Medical Systems, Bristol-Myers Squibb, Eli Lilly, GlaxoSmithKline, MEDACorp, MedAvante, Merck. Novartis, Pfizer, Shire. Vivometrics, and Wyeth, and he holds equity in Aspect Medical Systems. Dr. Howland has received research support from or served as a speaker for Aspect Medical Systems. AstraZeneca, Eli Lilly. Organon. Bristol-Myers Squibb, Cyberonics, National Center for Complementary and Alternative Medicine. NIH, and Wyeth. Dr. Warden has received research support from NIMH and holds equity in Bristol-Myers Squibb and Pfizer. Dr. Trivedi has received research support from or served as an adviser, consultant, or speaker for Abbott Laboratories. Abdi Brahim, Akzo (Organon), AstraZeneca. Bayer. Bristol-Myers Squibb. Cephalon, Corcept Therapeutics. Cyberonics, Fabre-Kramer, Forest Pharmaceuticals, GlaxoSmithKline, Janssen Pharmaceutica. Johnson & Johnson PRD, Eli Lilly, Meade Johnson, Merck. National Alliance for Research in Schizophrenia and Depression, NIMH, Neuronetics, Novartis, Organon. Parke-Davis, Pfizer, Pharmacia & Upjohn. Predix Pharmaceuticals, Sepracor. Solvay. VantagePoint. and Wyeth-Ayerst. Drs. Balasubramani and Carmin report no competing interests.,;

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