Javier Santandreu, Francisco Félix Caballero, Elena González-Burgos
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引用次数: 0
Abstract
Introduction: Dementia is the most prevalent neurodegenerative disorder. Several studies have demonstrated an association between anticholinergic drug use and an increased risk of cognitive and physical impairment. However, anticholinergic drugs are commonly prescribed for various clinical conditions, and their cumulative effects, referred to as anticholinergic burden, can contribute to cognitive decline and dementia. Although the causal relationship remains inconclusive, a higher anticholinergic burden is linked to a greater risk of cognitive deterioration.
Objective: This study aims to assess the compliance of patients aged ≥ 65 years with the STOPP-START and Beers criteria concerning the concurrent use of medications with high anticholinergic potency in situations where their use is not clinically justified.
Methods: This observational descriptive study was conducted using data from the Spanish Database for Pharmacoepidemiological Research (BIFAP). The study population comprised male and female patients aged ≥ 65 years.
Results: Of the 81,405 patients who developed dementia during the study period, 46.7% had been exposed to multiple anticholinergic drugs. Among them, 81.1% used these drugs sequentially, while 18.9% used two or more simultaneously. The absolute risk of developing dementia was 6.5% in patients who met the STOPP-START and BEERS criteria, compared to 13.4% in those who did not.
Conclusion: Although a high anticholinergic burden is a risk factor for cognitive decline, the unjustified concurrent use of multiple anticholinergic drugs remains uncommon among the elderly population in Spain.
期刊介绍:
Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes:
Overviews of contentious or emerging issues.
Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes.
In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area.
Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement.
Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics.
Editorials and commentaries on topical issues.
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