Naloxone Co-Dispensing with Opioids: a Cluster Randomized Pragmatic Trial

被引:11
作者
Binswanger, Ingrid A. [1 ,2 ,3 ,4 ]
Rinehart, Deborah [3 ,5 ]
Mueller, Shane R. [1 ]
Narwaney, Komal J. [1 ]
Stowell, Melanie [5 ]
Wagner, Nicole [1 ,3 ]
Xu, Stan [6 ]
Hanratty, Rebecca [3 ,7 ]
Blum, Josh [3 ,7 ]
McVaney, Kevin [7 ]
Glanz, Jason M. [1 ,8 ]
机构
[1] Kaiser Permanente Colorado, Inst Hlth Res, Aurora, CO 80012 USA
[2] Colorado Permanente Med Grp, Aurora, CO USA
[3] Univ Colorado, Sch Med, Div Gen Internal Med, Aurora, CO USA
[4] Kaiser Permanente Bernard J Tyson Sch Med, Pasadena, CA USA
[5] Denver Hlth, Denver Hlth & Hosp Author, Off Res, Ctr Hlth Syst Res, Denver, CO USA
[6] Kaiser Permanente Southern Calif, Dept Res & Evaluat, Pasadena, CA USA
[7] Denver Hlth, Dept Med, Denver, CO USA
[8] Colorado Sch Publ Hlth, Aurora, CO USA
基金
美国国家卫生研究院;
关键词
naloxone; prescription opioids; risk compensation; overdose; substance use; SCREENING-TEST ASSIST; UNITED-STATES; PRIMARY-CARE; OVERDOSE DEATHS; CLINICAL-TRIAL; AUDIT-C; DRUG; ALCOHOL; SMOKING; RISK;
D O I
10.1007/s11606-021-07356-6
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: Although naloxone prevents opioid overdose deaths, few patients prescribed opioids receive naloxone, limiting its effectiveness in real-world settings. Barriers to naloxone prescribing include concerns that naloxone could increase risk behavior and limited time to provide necessary patient education. OBJECTIVE: To determine whether pharmacy-based naloxone co-dispensing affected opioid risk behavior. Secondary objectives were to assess if co-dispensing increased naloxone acquisition, increased patient knowledge about naloxone administration, and affected opioid dose and other substance use. DESIGN: Cluster randomized pragmatic trial of naloxone co-dispensing. SETTING: Safety-net health system in Denver, Colorado, between 2017 and 2020. PARTICIPANTS: Seven pharmacies were randomized. Pharmacy patients (N=768) receiving opioids were followed using automated data for 10 months. Pharmacy patients were also invited to complete surveys at baseline, 4 months, and 8 months; 325 survey participants were enrolled from November 15, 2017, to January 8, 2019. INTERVENTION: Intervention pharmacies implemented workflows to co-dispense naloxone while usual care pharmacies provided usual services. MAIN MEASURES: Survey instruments assessed opioid risk behavior; hazardous drinking; tobacco, cannabis, and other drug use; and knowledge. Naloxone dispensings and opioid dose were evaluated using pharmacy data among pharmacy patients and survey participants. Intention-to-treat analyses were conducted using generalized linear mixed models accounting for clustering at the pharmacy level. KEY RESULTS: Opioid risk behavior did not differ by trial group (P=0.52; 8-month vs. baseline adjusted risk ratio [ARR] 1.07; 95% CI 0.78, 1.47). Compared with usual care pharmacies, naloxone dispensings were higher in intervention pharmacies (ARR 3.38; 95% CI 2.21, 5.15) and participant knowledge increased (P=0.02; 8-month vs. baseline adjusted mean difference 1.05; 95% CI 0.06, 2.04). There was no difference in other substance use by the trial group. CONCLUSION: Co-dispensing naloxone with opioids effectively increased naloxone receipt and knowledge but did not increase self-reported risk behavior.
引用
收藏
页码:2624 / 2633
页数:10
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