TY - JOUR KW - Antidepressive Agents/therapeutic use KW - Antipsychotic Agents/therapeutic use KW - Central Nervous System Agents/therapeutic use KW - Cocaine/adverse effects KW - Cocaine-Related Disorders/drug therapy/epidemiology/psychology KW - Drug Therapy KW - Humans KW - cocaine KW - pharmacotherapy KW - substance use KW - Systematic Review AU - B. Chan AU - K. Kondo AU - M. Freeman AU - C. Ayers AU - J. Montgomery AU - D. Kansagara A1 - AB - BACKGROUND: Currently, there are no accepted FDA-approved pharmacotherapies for cocaine use disorder, though numerous medications have been tested in clinical trials. We conducted a systematic review and meta-analysis to better understand the effectiveness of pharmacotherapy for cocaine use disorder. METHODS: We searched multiple data sources (MEDLINE, PsycINFO, and Cochrane Library) through November 2017 for systematic reviews and randomized controlled trials (RCTs) of pharmacological interventions in adults with cocaine use disorder. When possible, we combined the findings of trials with comparable interventions and outcome measures in random-effects meta-analyses. We assessed the risk of bias of individual trials and the strength of evidence for each outcome using standardized criteria. Outcomes included continuous abstinence (3+ consecutive weeks); cocaine use; harms; and study retention. For relapse prevention studies (participants abstinent at baseline), we examined lapse (first cocaine positive or missing UDS) and relapse (two consecutive cocaine positive or missed UDS'). RESULTS: Sixty-six different drugs or drug combinations were studied in seven systematic reviews and 48 RCTs that met inclusion criteria. Antidepressants were the most widely studied drug class (38 RCTs) but appear to have no effect on cocaine use or treatment retention. Increased abstinence was found with bupropion (2 RCTs: RR 1.63, 95% CI 1.02 to 2.59), topiramate (2 RCTs: RR 2.56, 95% CI 1.39 to 4.73), and psychostimulants (14 RCTs: RR 1.36, 95% CI 1.05 to 1.77), though the strength of evidence for these findings was low. We found moderate strength of evidence that antipsychotics improved treatment retention (8 RCTs: RR 1.33, 95% CI 1.03 to 1.75). DISCUSSION: Most of the pharmacotherapies studied were not effective for treating cocaine use disorder. Bupropion, psychostimulants, and topiramate may improve abstinence, and antipsychotics may improve retention. Contingency management and behavioral interventions along with pharmacotherapy should continue to be explored. SR REGISTRATION: Prospero CRD42018085667. AD - Division of General Internal Medicine and Geriatrics, Oregon Health & Science University, 3181 SW Sam Jackson Park Road L475, Portland, OR, 97239-3098, USA. chanbri@ohsu.edu.; Central City Concern, Portland, OR, USA. chanbri@ohsu.edu.; Evidence Synthesis Program Center, VA Portland Health Care System, Portland, OR, USA.; Research Integrity Office, Oregon Health & Science University, Portland, OR, USA.; Evidence Synthesis Program Center, VA Portland Health Care System, Portland, OR, USA.; Evidence Synthesis Program Center, VA Portland Health Care System, Portland, OR, USA.; Evidence Synthesis Program Center, VA Portland Health Care System, Portland, OR, USA.; Division of General Internal Medicine and Geriatrics, Oregon Health & Science University, 3181 SW Sam Jackson Park Road L475, Portland, OR, 97239-3098, USA.; Evidence Synthesis Program Center, VA Portland Health Care System, Portland, OR, USA.; Department of Medicine, VA Portland Health Care System, Portland, OR, USA. BT - Journal of general internal medicine C5 - Opioids & Substance Use CP - 12 DO - 10.1007/s11606-019-05074-8 IS - 12 JF - Journal of general internal medicine LA - eng M1 - Journal Article N2 - BACKGROUND: Currently, there are no accepted FDA-approved pharmacotherapies for cocaine use disorder, though numerous medications have been tested in clinical trials. We conducted a systematic review and meta-analysis to better understand the effectiveness of pharmacotherapy for cocaine use disorder. METHODS: We searched multiple data sources (MEDLINE, PsycINFO, and Cochrane Library) through November 2017 for systematic reviews and randomized controlled trials (RCTs) of pharmacological interventions in adults with cocaine use disorder. When possible, we combined the findings of trials with comparable interventions and outcome measures in random-effects meta-analyses. We assessed the risk of bias of individual trials and the strength of evidence for each outcome using standardized criteria. Outcomes included continuous abstinence (3+ consecutive weeks); cocaine use; harms; and study retention. For relapse prevention studies (participants abstinent at baseline), we examined lapse (first cocaine positive or missing UDS) and relapse (two consecutive cocaine positive or missed UDS'). RESULTS: Sixty-six different drugs or drug combinations were studied in seven systematic reviews and 48 RCTs that met inclusion criteria. Antidepressants were the most widely studied drug class (38 RCTs) but appear to have no effect on cocaine use or treatment retention. Increased abstinence was found with bupropion (2 RCTs: RR 1.63, 95% CI 1.02 to 2.59), topiramate (2 RCTs: RR 2.56, 95% CI 1.39 to 4.73), and psychostimulants (14 RCTs: RR 1.36, 95% CI 1.05 to 1.77), though the strength of evidence for these findings was low. We found moderate strength of evidence that antipsychotics improved treatment retention (8 RCTs: RR 1.33, 95% CI 1.03 to 1.75). DISCUSSION: Most of the pharmacotherapies studied were not effective for treating cocaine use disorder. Bupropion, psychostimulants, and topiramate may improve abstinence, and antipsychotics may improve retention. Contingency management and behavioral interventions along with pharmacotherapy should continue to be explored. SR REGISTRATION: Prospero CRD42018085667. PY - 2019 SN - 1525-1497; 0884-8734; 0884-8734 SP - 2858 EP - 2873 EP - T1 - Pharmacotherapy for Cocaine Use Disorder-a Systematic Review and Meta-analysis T2 - Journal of general internal medicine TI - Pharmacotherapy for Cocaine Use Disorder-a Systematic Review and Meta-analysis U1 - Opioids & Substance Use U2 - 31183685 U3 - 10.1007/s11606-019-05074-8 VL - 34 VO - 1525-1497; 0884-8734; 0884-8734 Y1 - 2019 Y2 - Dec ER -