Primary versus specialty care outcomes for depressed outpatients managed with measurement-based care: Results from STAR*D

被引:86
作者
Gaynes, Bradley N. [1 ]
Rush, A. John [2 ]
Trivedi, Madhukar H. [2 ]
Wisniewski, Stephen R. [3 ]
Balasubramani, G. K.
McGrath, Patrick J. [4 ,5 ]
Thase, Michael E. [9 ]
Klinkman, Michael [6 ]
Nierenberg, Andrew A. [7 ]
Yates, William R. [8 ]
Fava, Maurizio [7 ]
机构
[1] Univ N Carolina, Sch Med, Dept Psychiat, Chapel Hill, NC 27599 USA
[2] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
[3] Univ Pittsburgh, Dept Epidemiol, Pittsburgh, PA 15261 USA
[4] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[5] Columbia Univ, Coll Phys & Surg, New York, NY USA
[6] Univ Michigan, Ann Arbor, MI 48109 USA
[7] Massachusetts Gen Hosp, Boston, MA 02114 USA
[8] Univ Oklahoma, Coll Med, Tulsa, OK USA
[9] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
primary care; depression; clinical trial; outcomes;
D O I
10.1007/s11606-008-0522-3
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
BACKGROUND: Whether the acute outcomes of major depressive disorder (MDD) treated in primary (PC) or specialty care (SC) settings are different is unknown. OBJECTIVE: To compare the treatment and outcomes for depressed outpatients treated in primary versus specialty settings with citalopram in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study (www.star-d.org), a broadly inclusive effectiveness trial. DESIGN: Open clinical trial with citalopram for up to 14 weeks at 18 primary and 23 specialty sites. Participants received measurement-based care with 5 recommended treatment visits, manualized pharmacotherapy, ongoing support and guidance by a clinical research coordinator, the use of structured evaluation of depressive symptoms and side effects at each visit, and a centralized treatment monitoring and feedback system. PARTICIPANTS: A total of 2,876 previously established outpatients in primary (n=1091) or specialty (n=1785) with nonpsychotic depression who had at least 1 post-baseline measure. MEASUREMENTS AND MAIN RESULTS: Remission (Hamilton Depression Rating Scale for Depression [Hamilton] or 16-item Quick Inventory of Depressive Symptomatology-Self-Rated [QIDS-SR16]); response (QIDS-SR16); time to first remission (QIDS-SR16). Remission rates by Hamilton (26.6% PC vs 28.0% SC, p=.40) and by QIDS-SR16 (32.5% PC vs 33.1% SC, p=.78) and response rates by QIDS-SR16 (45.7% PC vs 47.6% SC, p=.33) were not different. For those who reached remission or response at exit, the time to remission (6.2 weeks PC vs 6.9 weeks SC, p=.12) and to response (5.5 weeks PC vs 5.4 weeks SC, p=.97) did not differ by setting. CONCLUSIONS: Identical remission and response rates can be achieved in primary and specialty settings when identical care is provided.
引用
收藏
页码:551 / 560
页数:10
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