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Expert Consensus on the Nephrotoxic Potential of 195 Medications in the Non-intensive Care Setting: A Modified Delphi
Britney A Stottlemyer1, Kaleab Z Abebe2, Paul M Palevsky3,4
1University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA.
A consensus was reached on the nephrotoxic potential (NxP) of 195 medications for non-critical care patients, establishing a standardized list for identifying drugs that may cause acute kidney injury (AKI). This NxP index aids future clinical evaluations and research.
Area of Science:
- Pharmacology
- Nephrology
- Clinical Pharmacy
Background:
- Nephrotoxin exposure is a significant risk factor for acute kidney injury (AKI).
- A standardized list and perceived nephrotoxic potential (NxP) of medications for non-critically ill patients are currently lacking.
- This gap hinders effective surveillance and management of drug-induced kidney damage in general hospital settings.
Purpose of the Study:
- To generate expert consensus on the nephrotoxic potential (NxP) of 195 commonly used medications in non-intensive care settings.
- To establish a standardized rating scale for perceived nephrotoxicity.
- To provide a foundation for improved clinical monitoring and research into nephrotoxic medications.
Main Methods:
- A comprehensive literature search identified potentially nephrotoxic medications.
- 29 experts in nephrology and pharmacy rated the NxP of 195 medications on a 0-3 scale.
- Consensus was defined as ≥75% of participants providing a single rating or two consecutive ratings.
Main Results:
- Consensus was achieved for 152 medications, with 39 removed from consideration.
- The majority of rated medications were classified as unlikely to possibly nephrotoxic (rating 0.5) or possibly to probably nephrotoxic (rating 1.5).
- No medications were rated as definitely nephrotoxic (rating 3) by consensus.
Conclusions:
- The NxP index provides valuable clinical consensus on the perceived nephrotoxicity of medications in non-critical care.
- This standardized rating facilitates consistent clinical evaluations and future research endeavors.
- The findings support the development of targeted strategies to mitigate nephrotoxic medication risks in non-critically ill patients.
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