• Obstetrics and gynecology · Sep 2018

    Randomized Controlled Trial Comparative Study

    Individualized Compared With Standard Postdischarge Oxycodone Prescribing After Cesarean Birth: A Randomized Controlled Trial.

    • Sarah S Osmundson, Britany L Raymond, Bradley T Kook, LeAnn Lam, Elizabeth B Thompson, Leslie A Schornack, Catherine E Voorhees, and Michael G Richardson.
    • Departments of Obstetrics and Gynecology and Anesthesiology, Vanderbilt University Medical Center, Nashville, Tennessee; the University of Utah, Salt Lake City, Utah; and Vanderbilt University, Nashville, Tennessee.
    • Obstet Gynecol. 2018 Sep 1; 132 (3): 624-630.

    ObjectiveTo evaluate whether individualized postdischarge oxycodone prescribing guided by inpatient opioid use reduces the number of unused opioid tablets after cesarean birth.MethodsWe conducted a randomized, controlled trial of women aged 18 years or older undergoing cesarean birth. Participants were randomized at discharge in a 1:1 ratio to a standard (30 tablets of 5 mg oxycodone) or an individualized oxycodone prescription (predicted based on each patient's inpatient opioid use). All women were contacted starting 14 days after cesarean birth to assess number of oxycodone tablets used and adequacy of pain control. The Tennessee Controlled Substance Monitoring Database was accessed to confirm dispensed opioids. The primary outcome was number of unused oxycodone tablets prescribed for pain control after cesarean birth. A total sample size of 160 women was necessary to detect a 30% difference in leftover tablets between groups with 80% power and α of 0.05.ResultsBetween June 14, 2017, and August 26, 2017, we screened 323 women and randomized 172. Baseline characteristics and inpatient opioid use were similar between groups. Women in the individualized group were prescribed fewer tablets (14 [interquartile range 12-16] vs 30 [interquartile range 30-30], P<.001) and had 50% fewer unused tablets than women in the standard group (5 [interquartile range 1-8] vs 10 [interquartile range 0-22], P<.001). Overall, 13% (23/172) used no opioids after discharge and 26% (44/172) used all prescribed opioids. There were no differences between the standard and individualized groups in the proportion of women who used no opioids or all opioids and no difference in the proportion of dispensed opioids used (60% [interquartile range 23-100] vs 61% [29-89], P=.93). Women in the individualized group used only half the number of prescribed opioids as women in the standard group (8 [interquartile range 4-14] vs 15 [interquartile range 6-30], P<.001). Patient-reported pain outcomes did not differ significantly by group.ConclusionIndividualized opioid prescribing based on inpatient use reduces the number of unused oxycodone tablets compared with standard prescribing.Clinical Trials RegistrationClinicalTrials.gov, NCT03168425.

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