Identification of Adverse Drug Withdrawal Events after Older Adults Discontinue Statins
Jonathan Norton, Glenn Goodrich, Jennifer Barrow, Valerie Paolino, Ariel Green, Orla Sheehan, Elizabeth Bayliss, Cynthia Boyd

TL;DR
This paper explores methods to identify adverse effects in older adults after they stop taking statins, using health records and clinical review.
Contribution
The study introduces new methods to identify adverse drug withdrawal events using ICD-10 and procedure codes in electronic health records.
Findings
48% of potential adverse drug withdrawal events were classified as doubtful.
48% were classified as possible, with no events classified as definite.
The methods require clinical review but offer a scalable approach for future deprescribing studies.
Abstract
Assessing the safety of deprescribing interventions is difficult due to inadequate methods of accurately identifying adverse drug withdrawal events (ADWE) at scale. We explored methods to identify ADWEs after a medication discontinuation using electronic health record (EHR) data, and report on the relationship between statin discontinuations and potential ADWEs. The study population was older adults (65+), taking a statin, and had a confirmed statin discontinuation by chart review. Potential ADWEs were identified by ICD-10 and procedure codes (e.g. stroke, carotid artery disease, ischemic heart disease, coronary artery bypass graft, or percutaneous coronary intervention) within a 12-month time frame following the discontinuation. Two clinicians adjudicated each record to determine if the identified events were related to discontinuations and could constitute ADWEs. Outcome categories…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsPharmacovigilance and Adverse Drug Reactions · Lipoproteins and Cardiovascular Health · Pharmaceutical Practices and Patient Outcomes
