Prescription cascades associated with acetylcholinesterase inhibitors use: a high-throughput sequence symmetry analysis.

Background Acetylcholinesterase inhibitors (AChEIs), are commonly prescribed for dementia and can cause adverse drug events that may lead to new prescriptions, known as prescription cascades. We aimed to identify potential AChEI-induced prescription cascades using high-throughput sequence symmetry a...

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Detalles Bibliográficos
Publicado en:Age & Ageing Vol. 55; no. 6; pp. 1 - 11
Autores principales: Newby, Danielle, Bobba, Sai Sumedha, Raventós, Berta, Rowlands, Elin J, Chen, Xihang, Molina-Porcel, Laura, Reyes, Carlen, Duarte-Salles, Talita, Delmestri, Antonella, Man, Wai Yi
Formato: Artículo
Publicado: Oxford University Press / USA Jun2026
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Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:Background Acetylcholinesterase inhibitors (AChEIs), are commonly prescribed for dementia and can cause adverse drug events that may lead to new prescriptions, known as prescription cascades. We aimed to identify potential AChEI-induced prescription cascades using high-throughput sequence symmetry analysis (SSA). Methods Patients aged ≥18 years with 365 days of prior observation initiating AChEIs (donepezil, rivastigmine, or galantamine) were identified from the Clinical Practice Research Datalink GOLD (2002–2022). We screened 510 drug classes and 1213 individual ingredients initiated within ±180 days of AChEI initiation (365 days in sensitivity analyses). Crude and adjusted sequence ratios (ASRs) were calculated, and positive signals were reviewed for clinical plausibility. Results We identified 66 155 AChEI initiators (median age 81 years [IQR 76–85]; 62.8% female). Among ATC classes and individual ingredients, 51 and 46 signals were positive with 28 (55%) and 22 (48%) classified as potential prescription cascades after review. Gastrointestinal drugs showed positive signals including antipropulsives (ASR 1.50 [99% CI 1.28–1.75]), loperamide (ASR 1.52 [1.30–1.77]) and cyclizine (ASR 2.10 [1.72–2.59]). Positive signals were also observed nervous system drugs such as benzodiazepine derivatives (ASR 1.83 [1.55–2.16]) and respiratory drugs including corticosteroids (ASR 1.66 [1.33–2.08]) and glucocorticoids (ASR 1.54 [1.30–1.83]). Most positive signals remained in sensitivity analysis. Conclusions These findings suggest potential AChEI-related prescription cascades consistent with gastrointestinal, neuropsychiatric, dermatological and respiratory adverse effects. While findings require further validation, this study demonstrates the utility of high-throughput signal detection to support pharmacovigilance in high-risk populations.