Comparison of different decision support software programs in perspective of potential drug-drug interactions in the

Muhammed Yunus Bektay1,2, Zehra Seker3, Hatice Kubra Eke4

  • 1Department of Clinical Pharmacy, Faculty of Pharmacy, Bezmialem Vakif University, Istanbul, Turkey.

Abstract

Insights

Cancer patients face significant risks from drug-drug interactions (DDIs). This study found major differences in how cancer decision support software (CDSS) identifies potential DDIs, highlighting a need for improved validation.

Area of Science:

  • Oncology
  • Clinical Pharmacy
  • Health Informatics

Background:

  • Drug-drug interactions (DDIs) contribute to 20-30% of adverse events.
  • Cancer patients are at higher risk for DDIs due to polypharmacy with chemotherapeutic agents.
  • Identifying and managing potential DDIs is crucial for patient safety in cancer care.

Purpose of the Study:

  • To compare the performance of different clinical decision support software (CDSS) programs in identifying potential drug-drug interactions (pDDIs) in cancer patients.
  • To evaluate the discrepancies in pDDI detection and severity assessment among various CDSS.

Main Methods:

  • A cross-sectional study involving 231 cancer patients.
  • Clinical pharmacists assessed patient treatment regimens.
  • Potential DDIs were evaluated using three distinct CDSS: Lexicomp®, Medscape®, and Micromedex®.

Main Results:

  • Lexicomp® identified the highest pDDI ratio (19.50%), followed by Micromedex® (11.15%) and Medscape® (7.09%).
  • Significant variations in the number and severity of pDDIs were observed across the evaluated CDSS.
  • Common pDDIs included diclofenac/dexamethasone and escitalopram/granisetron, with differing recommendations from each CDSS.

Conclusions:

  • Substantial disparities exist in the detection and reporting of pDDIs among different CDSS.
  • The findings underscore the issue of suboptimal prescribing in cancer care.
  • Regulatory bodies should implement and verify robust validation and reporting mechanisms for CDSS.

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