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High-Throughput Screening for Prescribing Cascades Among Real-World Angiotensin-II Receptor Blockers (ARBs)
Asinamai M Ndai1,2,3, Kayla Smith1,2,3, Shailina Keshwani1,2,3
1Department of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, Gainesville, Florida, USA.
This study identified potential prescribing cascades linked to Angiotensin-II Receptor Blockers (ARBs). Three drug classes, including benzodiazepines, showed significant signals for adverse events in Medicare beneficiaries.
Area of Science:
- Pharmacovigilance
- Drug Safety
- Health Services Research
Background:
- Angiotensin-II Receptor Blockers (ARBs) are widely prescribed medications.
- Adverse events associated with ARBs can lead to a prescribing cascade (PC), where new drugs are prescribed to manage side effects of the initial drug.
Purpose of the Study:
- To identify potential ARB-induced prescribing cascades using high-throughput sequence symmetry analysis.
- To evaluate the association between ARB initiation and subsequent prescription of other drug classes.
Main Methods:
- Utilized Medicare claims data from 2011-2020 for beneficiaries aged 66 years and older.
- Analyzed 446 non-antihypertensive drug classes initiated within ±90 days of ARB initiation.
- Calculated sequence ratios (SRs) and adjusted SRs (aSRs), with number needed to harm (NNTH) for significant signals.
Main Results:
- Identified 320,663 ARB initiators; 17 significant signals were detected among 446 marker classes.
- Three potential PCs were confirmed by clinical experts: benzodiazepine derivatives, adrenergics with anticholinergics (including triple combinations), and other antianemic preparations.
- Benzodiazepine derivatives showed the lowest NNTH (2130) and a significant aSR (1.18).
Conclusions:
- The study identified potential prescribing cascades associated with ARBs, reflecting known and possibly under-recognized adverse events.
- These findings highlight the need for further research into the impact of ARB-induced PCs on patient outcomes.
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