PMID- 38318261 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240207 IS - 8755-1225 (Print) IS - 1549-4810 (Electronic) IS - 1549-4810 (Linking) VI - 40 IP - 1 DP - 2024 Feb TI - Evaluation of Gabapentin and Pregabalin Use in Hospitalized Patients With Decreased Kidney Function. PG - 30-36 LID - 10.1177/87551225231217906 [doi] AB - Background: Gabapentin and pregabalin are well-tolerated medications primarily cleared by the kidney. Patients receiving higher gabapentinoid doses with decreased kidney function may be at an increased risk of adverse effects (AEs), but limited evidence exists evaluating gabapentinoid dosing and AEs in this population. Objective: To determine whether patients with decreased creatinine clearance (CrCl) experienced increased frequency of AEs related to gabapentinoid dose at hospital admission. Methods: Single-center retrospective cohort study in adults with a gabapentinoid prescription and serum creatinine measurement documented on hospital admission. The primary outcome was the appropriateness of gabapentinoid prescription based on CrCl (stratified by CrCl >/=60 mL/min, <60 mL/min, 15-29 mL/min, and <15 mL/min) at admission. Secondary outcomes included the incidence of AEs related to gabapentinoids and concomitant opioid and psychiatric prescriptions. Results: A total of 286 patients were included in this study (gabapentin n = 234, pregabalin n = 52). Patients with a CrCl <60 mL/min and doses above the manufacturer's recommendation were prescribed gabapentin (34%) and pregabalin (22.7%). For patients with a CrCl of 15 to 29 mL/min and <15 mL/min groups, inappropriately high doses were prescribed for gabapentin (48.8%) and pregabalin (45%). A significant increase in recorded falls (P = 0.029) was identified in patients with a CrCl <60 mL/min. Concomitant opioid and psychiatric medications contributed to a higher prevalence of AEs regardless of CrCl. Conclusions: Patients with a CrCl <60 mL/min were frequently prescribed inappropriately high doses of gabapentinoids. The relationship between gabapentinoid dosing, kidney function, and the incidence of gabapentinoid-related AEs at hospital admission requires larger, multicentre studies. CI - (c) The Author(s) 2023. FAU - Knowles, Gwendolyn M AU - Knowles GM AD - Department of Pharmacy Practice and Administration, University of Maryland Eastern Shore School of Pharmacy, Princess Anne, MD, USA. FAU - LaFleur, Grace E AU - LaFleur GE AUID- ORCID: 0000-0001-7216-1354 AD - Department of Pharmacotherapy, College of Pharmacy, University of Utah, Salt Lake City, UT, USA. FAU - Churchwell, Mariann D AU - Churchwell MD AUID- ORCID: 0000-0001-5866-0456 AD - Department of Pharmacy Practice, College of Pharmacy and Pharmaceutical Sciences, The University of Toledo, Toledo, OH, USA. LA - eng PT - Journal Article DEP - 20231218 PL - United States TA - J Pharm Technol JT - The Journal of pharmacy technology : jPT : official publication of the Association of Pharmacy Technicians JID - 8504643 PMC - PMC10838538 OTO - NOTNLM OT - adverse effects OT - gabapentin OT - gabapentinoid OT - kidney function OT - pregabalin COIS- The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. EDAT- 2024/02/06 06:42 MHDA- 2024/02/06 06:43 PMCR- 2024/12/18 CRDT- 2024/02/06 03:56 PHST- 2024/12/18 00:00 [pmc-release] PHST- 2024/02/06 06:43 [medline] PHST- 2024/02/06 06:42 [pubmed] PHST- 2024/02/06 03:56 [entrez] AID - 10.1177_87551225231217906 [pii] AID - 10.1177/87551225231217906 [doi] PST - ppublish SO - J Pharm Technol. 2024 Feb;40(1):30-36. doi: 10.1177/87551225231217906. Epub 2023 Dec 18.