4.5 Article

The Impact of Chronic Depression on Acute and Long-Term Outcomes in a Randomized Trial Comparing Selective Serotonin Reuptake Inhibitor Monotherapy Versus Each of 2 Different Antidepressant Medication Combinations

期刊

JOURNAL OF CLINICAL PSYCHIATRY
卷 73, 期 7, 页码 967-976

出版社

PHYSICIANS POSTGRADUATE PRESS
DOI: 10.4088/JCP.11m07043

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资金

  1. Abbott
  2. lkermes
  3. Aspect Medical Systems
  4. AstraZeneca
  5. BioResearch
  6. BrainCells
  7. Bristol-Myers Squibb
  8. Cephalon
  9. CeNeRx BioPharma
  10. Clinical Trials Solutions
  11. Clintara
  12. Covidien
  13. Eli Lilly
  14. EnVivo
  15. Euthymics Bioscience
  16. Forest
  17. Ganeden
  18. GlaxoSmithKline
  19. Icon Clinical Research
  20. i3 Innovus/Ingenix
  21. Johnson Johnson PRD
  22. Lichtwer
  23. Lorex
  24. NARSAD
  25. National Center for Complementary and Alternative Medicine
  26. National Institute on Drug Abuse (NIDA)
  27. National Institute of Mental Health (NIMH)
  28. Novartis
  29. Organon
  30. PamLab
  31. Pfizer
  32. Pharmavite
  33. Photothera
  34. Roche
  35. RCT Logic
  36. Sanofi-Aventis US
  37. Shire
  38. Solvay
  39. Synthelabo
  40. Wyeth-Ayerst
  41. MGH from NIMH
  42. PamLabs
  43. Agency for Healthcare Research and Quality
  44. Corcept
  45. Cyberonics
  46. Merck
  47. NIMH [N01MH90003]
  48. NIDA
  49. Pharmacia Upjohn
  50. Predix (EPIX)
  51. Targacept
  52. Abdi Ibrahim
  53. Akzo (Organon)
  54. Axon
  55. CME Institute of Physicians Postgraduate Press
  56. Evotec
  57. Fabre-Kramer
  58. Janssen
  59. Lundbeck
  60. Mead Johnson
  61. MedAvante
  62. Medtronic
  63. Neuronetics
  64. Otsuka
  65. Parke-Davis
  66. PGx Health
  67. Rexahn
  68. Sepracor
  69. Shire Development
  70. Takeda
  71. VantagePoint
  72. University of Michigan
  73. Brain Resource

向作者/读者索取更多资源

Objective: To compare sociodemographic and clinical features, acute and continuation treatment outcomes, and adverse events/side effect burden between outpatients with chronic (current episode > 2 years) versus nonchronic major depressive disorder (MDD) who were treated with combination antidepressant therapy or selective serotonin reuptake inhibitor (SSRI) monotherapy. Method: 663 outpatients with chronic (n = 368) or nonchronic (n = 295) moderate to severe DSM-IV-TR MDD (17-item Hamilton Depression Rating Scale score >= 16) were enrolled from March 2008 through September 2009 in a single-blind 7-month prospective randomized trial conducted at 6 primary and 9 psychiatric care sites across the United States. Participants were treated with escitalopram monotherapy plus placebo or 1 of 2 combination treatments (bupropion sustained-release [SR] + escitalopram or venlafaxine extended-release [XR] + mirtazapine). Analyses compared baseline sociodemographic and clinical characteristics, rates of remission (at least 1 of the last 2 consecutive scores on the 16-item Quick Inventory of Depressive Symptomatology Self-Report [QIDS-SR16] < 6, with the other < 8), and adverse events/side effect burden (Frequency, Intensity, and Burden of Side Effects Ratings) obtained at 12 and 28 weeks. Results: Participants with chronic MDD were at greater socioeconomic disadvantage and had greater medical and psychiatric disease burden. The chronic and nonchronic groups did not differ in rates of remission at 12 weeks (35.9% vs 42.0%, respectively; odds ratio [OR] = 0.778, P = .1500; adjusted OR [AGR] = 0.956, P = .8130) or at 28 weeks (41.0% vs 49.8%, respectively; OR = 0.706, P = .0416; AOR = 0.837, P = .3448). Participants with chronic MDD had higher final QIDS-SR16 scores and smaller overall percent changes in QIDS-SR16 from baseline to exit, but these differences did not remain after adjusting for covariates. There were no significant differences in adverse events or side effect burden. No significant interactions were found between chronicity and type of treatment at 12 or 28 weeks. Conclusion: Chronicity of illness does not appear to differentially impact acute or longer-term outcomes with SSRI monotherapy or combination antidepressant medication treatment in patients with moderate to severe nonpsychotic MDD.

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