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The impact of pregnancy on urinary ketorolac metabolites after single intravenous bolus

  • Aida Kulo
  • , Sarah Hendrickx
  • , Jan De Hoon
  • , Nedzad Mulabegovic
  • , Kristel Van Calsteren
  • , Rene Verbesselt
  • , Karel Allegaert*
  • *Corresponding author for this work
  • University Hospitals Leuven
  • University of Sarajevo
  • KU Leuven

Research output: Contribution to journalArticleAcademicpeer-review

4 Citations (Scopus)

Abstract

Compared to female volunteers or postpartum, ketorolac clearance is higher at delivery. To explore the alterations that explain this higher clearance, urinary ketorolac metabolites collected at delivery (n = 40) were compared to female volunteers (unpaired, n = 8) or postpartum (paired, n = 8) following intravenous administration of 30 mg ketorolac tromethamine. A mean 38 (SD 9) % of the ketorolac dose was retrieved in 8-h urine collections. This was based on mean portions of 56 (20), 10 (14) and 33 (12) % for free ketorolac, ketorolac-glucuronide and p-hydroxy-ketorolac, respectively. The mean ketorolac-glucuronide portion at delivery (5 %) was lower compared to female volunteers (21 %) or postpartum (21 %) (p = 0.003 and p = 0.002, respectively). Similarly, there was a difference in mean portion of free urinary ketorolac at delivery when compared to healthy female volunteers (60-45 %, p = 0.046). Using paired statistics, the mean portion of total urinary ketorolac was lower (62-73 %, p = 0.015) while the portion retrieved as p-hydroxy-ketorolac was significantly higher at delivery compared to postpartum (38-28 %, p = 0.031). The differences in urine metabolites suggest that the increased ketorolac clearance at delivery is in part explained by increased metabolic clearance to p-hydroxy-ketorolac, reflecting increased oxidation activity.

Original languageEnglish
Pages (from-to)1-4
Number of pages4
JournalEuropean Journal of Drug Metabolism and Pharmacokinetics
Volume38
Issue number1
DOIs
Publication statusPublished - Mar 2013
Externally publishedYes

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