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Clinical Utility of Applying PGx and Deprescribing-Based Decision Support in Polypharmacy
DOAB Contributor

Clinical Utility of Applying PGx and Deprescribing-Based Decision Support in Polypharmacy

Author / Organization:
Open Access Books Published 2023 Verification Pending

Overview & Synopsis

Polypharmacy is a necessary and important aspect of drug treatment; however, it becomes a challenge when the medication risks outweigh the benefits for an individual patient. Drug–drug interactions and the introduction of prescribing cascades are common features of polypharmacy, which can lead to ineffectiveness and increased risk of adverse drug reactions (ADR). Genes encoding CYP450 isozymes and other drug-related biomarkers have attracted considerable attention as targets for pharmacogenetic (PGx) testing due to their impact on drug metabolism and response. This Special Issue is devoted to explore the status and initiatives taken to circumvent ineffectiveness and to improve medication safety for polypharmacy patients. Specific areas include drug–drug interactions and consequences thereof in therapeutic management, including PK- and PD-profiling; the application of PGx-based guidance and/or decision tools for drug–gene and drug–drug gene interactions; medication reviews; development and application of deprescribing tools; and drivers and barriers to overcome for successful implementation in the healthcare system.

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Indexed from repository: Directory of Open Access Books (www.doabooks.org)

Document Information

Document Title Clinical Utility of Applying PGx and Deprescribing-Based Decision Support in Polypharmacy
Author / Organization DOAB Contributor
Subject & Discipline acute kidney injury
Categories Open Access Books
Publication Year 2023
License / Rights Open Access / Creative Commons
Resource Verification Listed PDF (Verification Pending)
Original Host Website Directory of Open Access Books (www.doabooks.org)
File Format application/pdf (Portable Document Format)
Language EN
Catalog ID DOC-74780
Original Source Link Visit Source Page on www.doabooks.org »