Effect of Mobile Device-Assisted N-of-1 Trial Participation on Analgesic Prescribing for Chronic Pain: Randomized Controlled Trial

被引:15
|
作者
Odineal, David D. [1 ,2 ]
Marois, Maria T. [3 ]
Ward, Deborah [4 ]
Schmid, Christopher H. [5 ,6 ]
Cabrera, Rima [3 ]
Sim, Ida [7 ,8 ]
Wang, Youdan [5 ]
Wilsey, Barth [9 ,10 ]
Duan, Naihua [11 ]
Henry, Stephen G. [12 ]
Kravitz, Richard L. [12 ]
机构
[1] Madigan Army Med Ctr, Dept Med, Joint Base Lewis McChord, Tacoma, WA 98431 USA
[2] Univ Calif Davis, Sch Med, Sacramento, CA 95817 USA
[3] Univ Calif Davis, Ctr Hlth Care Policy & Res, Sacramento, CA 95817 USA
[4] Univ Calif Davis, Betty Irene Moore Sch Nursing, Sacramento, CA 95817 USA
[5] Brown Univ, Sch Publ Hlth, Dept Biostat, Providence, RI 02912 USA
[6] Brown Univ, Sch Publ Hlth, Ctr Evidence Synth Hlth, Providence, RI 02912 USA
[7] Univ Calif San Francisco, Div Gen Internal Med, San Francisco, CA 94143 USA
[8] Open mHlth, New York, NY USA
[9] Vet Affairs Northern Calif Hlth Care Syst, Sacramento Med Ctr, Mather, CA USA
[10] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[11] Columbia Coll Phys & Surg, Dept Psychiat, New York, NY USA
[12] Univ Calif Davis, Dept Internal Med, Div Gen Med, Sacramento, CA 95817 USA
基金
美国国家卫生研究院;
关键词
N-of-1; trials; chronic pain; non-steroidal anti-inflammatory agent; opioid; analgesic; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; TERM OPIOID THERAPY; OF-HEALTH PATHWAYS; NONOPIOID ANALGESICS; KNEE OSTEOARTHRITIS; CDC GUIDELINE; UNITED-STATES; RISK; IBUPROFEN; EFFICACY;
D O I
10.1007/s11606-019-05303-0
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
Objectives Opioids and non-steroidal anti-inflammatory drugs (NSAIDs) are frequently prescribed for chronic musculoskeletal pain, despite limited evidence of effectiveness and well-documented adverse effects. We assessed the effects of participating in a structured, personalized self-experiment ("N-of-1 trial") on analgesic prescribing in patients with chronic musculoskeletal pain. Methods We randomized 215 patients with chronic pain to participate in an N-of-1 trial facilitated by a mobile health app or to receive usual care. Medical records of participating patients were reviewed at enrollment and 6 months later to assess analgesic prescribing. We established thresholds of >= 50, >= 20, and > 0 morphine milligram equivalents (MMEs) per day to capture patients taking relatively high doses only, patients taking low-moderate as well as relatively high doses, and patients taking any dose of opioids, respectively. Results There was no significant difference between the N-of-1 and control groups in the percentage of patients prescribed any opioids (relative odds ratio (ROR) = 1.05; 95% confidence interval [CI] = 0.61 to 1.80, p = 0.87). There was a clinically substantial but statistically not significant reduction of the percentage of patients receiving >= 20 MME (ROR = 0.58; 95% CI = 0.33 to 1.04, p = 0.07) and also in the percentage receiving >= 50 MME (ROR = 0.50; 95% CI = 0.19 to 1.34, p = 0.17). There was a significant reduction in the proportion of patients in the N-of-1 group prescribed NSAIDs compared with control (relative odds ratio = 0.53; 95% CI = 0.29 to 0.96, p = 0.04), with no concomitant increase in average pain intensity. There was no significant change in use of adjunctive medications (acetaminophen, gabapentenoids, or topicals). Discussion These exploratory results suggest that participation in N-of-1 trials may reduce long-term use of NSAIDs; there is also a weak signal for an effect on use of opioids. Additional research is needed to confirm these results and elucidate possible mechanisms.
引用
收藏
页码:102 / 111
页数:10
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