Collaborative Care for Chronic Pain in Primary Care A Cluster Randomized Trial

被引:245
|
作者
Dobscha, Steven K. [1 ,4 ]
Corson, Kathryn [1 ,4 ]
Perrin, Nancy A. [6 ]
Hanson, Ginger C. [6 ]
Leibowitz, Ruth Q. [1 ]
Doak, Melanie N. [2 ,5 ]
Dickinson, Kathryn C. [1 ]
Sullivan, Mark D. [7 ]
Gerrity, Martha S. [1 ,3 ,5 ]
机构
[1] Portland VA Med Ctr, Portland Ctr Study Chron Comorbid Mental & Phys D, Portland, OR 97239 USA
[2] Portland VA Med Ctr, Div Primary Care, Portland, OR 97239 USA
[3] Portland VA Med Ctr, Div Hosp & Specialty Med, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Dept Psychiat, Portland, OR 97201 USA
[5] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97201 USA
[6] Oregon Hlth & Sci Univ, Sch Nursing, Portland, OR 97201 USA
[7] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2009年 / 301卷 / 12期
关键词
CHRONIC NONCANCER PAIN; CLINICALLY IMPORTANT DIFFERENCE; IMPROVING PRIMARY-CARE; BACK-PAIN; DEPRESSION CARE; CHRONIC ILLNESS; SCREENING-TEST; HEALTH-STATUS; DISABILITY; MANAGEMENT;
D O I
10.1001/jama.2009.377
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Chronic pain is common in primary care patients and is associated with distress, disability, and increased health care use. Objective To assess whether a collaborative intervention can improve chronic pain related outcomes, including comorbid depression severity, in a Department of Veterans Affairs primary care setting. Design, Setting, and Participants Cluster randomized controlled trial of a collaborative care assistance with pain treatment intervention vs treatment as usual at 5 primary care clinics of 1 Department of Veterans Affairs Medical Center. Forty-two primary care clinicians were randomized to the assistance with pain treatment intervention group or the treatment as usual group. The 401 patients had musculoskeletal pain diagnoses, moderate or greater pain intensity, and disability lasting 12 weeks or longer and were assigned to the same treatment groups as their clinicians. Recruitment occurred from January 2006 to January 2007 and follow-up concluded in January 2008. Intervention Assistance with pain treatment included a 2-session clinician education program, patient assessment, education and activation, symptom monitoring, feedback and recommendations to clinicians, and facilitation of specialty care. Main Outcome Measures Changes over 12 months in pain-related disability (Roland-Morris Disability Questionnaire, range of 0-24), pain intensity (Chronic Pain Grade [CPG] Pain Intensity subscale, range of 0-100), and depression (Patient Health Questionnaire 9 [PHQ-9], range of 0-27), measured as beta coefficients (difference in slopes in points per month). Results Intervention patients had a mean (SD) of 10.6 (4.5) contacts with the assistance with pain treatment team. Compared with the patients receiving treatment as usual, intervention patients showed greater improvements in pain-related disability (Roland-Morris Disability Questionnaire beta, -0.101 [95% confidence interval {CI}, -0.163 to -0.040]; P=.004 and CPG Pain Intensity subscale beta, -0.270 [95% CI, -0.480 to -0.061]; P=.01). Among patients with baseline depression (PHQ-9 score >= 10), there was greater improvement in depression severity in patients receiving the intervention compared with patients receiving treatment as usual (PHQ-9 beta, -0.177 [95% CI, -0.295 to -0.060]; P=.003). The differences in scores between baseline and 12 months for the assistance with pain treatment intervention group and the treatment as usual group, respectively, were -1.4 vs -0.2 for the Roland-Morris Disability Questionnaire, -4.7 vs -0.6 for the CPG Pain Intensity subscale, and -3.7 vs -1.2 for PHQ-9. Conclusion The assistance with pain treatment collaborative intervention resulted in modest but statistically significant improvement in a variety of outcome measures. Trial Registration clinicaltrials.gov Identifier: NCT00129480
引用
收藏
页码:1242 / 1252
页数:11
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