Abstract: SA-PO043
Benzodiazepines and Opioid Co-Prescriptions: Outcome Implications in Kidney Transplant Recipients
Session Information
- Transplantation: Clinical Outcomes
October 27, 2018 | Location: Exhibit Hall, San Diego Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Transplantation
- 1802 Transplantation: Clinical
Authors
- Lam, Ngan, University of Alberta, Edmonton, Alberta, Canada
- Schnitzler, Mark, Saint Louis Univ, St Louis, Missouri, United States
- Axelrod, David A., Lahey Hospital and Clinic, Burlington, Massachusetts, United States
- Dharnidharka, Vikas R., Washington University School of Medicine, St Louis, Missouri, United States
- Segev, Dorry L., Johns Hopkins University, Baltimore, Maryland, United States
- Naik, Abhijit S., University of Michigan, St. Louis, Michigan, United States
- Xiao, Huiling, St. Louis University, St. Louis, Missouri, United States
- Hess, Gregory P., LDI University of Pennsylvania/Symphony Health, Conshohocken, Pennsylvania, United States
- Kasiske, Bertram L., Hennepin County Medical Center, Minneapolis, Minnesota, United States
- Alhamad, Tarek, Washington University in St. Louis, St. Louis, Missouri, United States
- Lentine, Krista L., Saint Louis University, St. Louis, Missouri, United States
Background
Recent studies identify coprescription of benzodiazepines and opioids as a risk factor for adverse outcomes in the general population. We previously described associations of opioid use before kidney transplantation (KTx) with mortality after KTx, but the implications of benzodiazepine use in the KTx population have not been described.
Methods
We examined a novel linkages of SRTR registry data with records from a pharmaceutical claims warehouse (2008-2015) to characterize benzodiazepine and opioid use in the year before KTx and associations (adjusted hazard ratio, 95% LCLaHR95% UCL) with death over 1yr post-KTx.
Results
Among 75,430 KTx recipients with available medication data in the year prior to KTx, 7.3% & 43.1% filled a prescription for a benzodiazepine or opioid in the pre-KTx year. Use of both medications was more common among recipients who were white, unemployed, and received prior KTx. Benzodiazepine use rose with higher opioid use, from 3.2% among opioid non-uses to 10.2% among those with highest level opioid use (Fig 1).
Compared to non-users, high-level pre-KTx benzodiazepine use was associated with a 51% (aHR 1.141.511.99) increased risk of death in the year after transplant. Opioid use bore a strong graded relationship with post-KTx survival, and prognostic impact high pre-KTx benzodiazepines was preserved after adjustment for opioids, although an interaction was not present (aHR 1.041.371.83) (Fig 2).
Conclusion
Benzodiazepines use is correlated with opioid fills before KTx, and these agents have additive associations with post-KTx mortality. Future research is needed to examine mechanisms of these associations and impact of reducing coprescription on improving outcomes after KTx.