Gustafsson Maria, Altufaili Muna, Sjölander Maria
Department of Integrative Medical Biology, Umeå University, 901 87, Umeå, Sweden.
Drugs Real World Outcomes. 2023 Mar;10(1):61-68. doi: 10.1007/s40801-022-00341-3. Epub 2022 Nov 9.
People with major neurocognitive disorder might be susceptible to drug-induced QT interval prolongation due to the presence of a number of concomitant risk factors.
The aim of this study was to investigate the prevalence of QT-prolonging drugs and QT-prolonging drug-drug interactions and associated factors among older people with major neurocognitive disorder.
In this register-based study, we obtained information regarding QT-prolonging drug use in a large population of older people with major neurocognitive disorder, through record linkage between the Swedish registry for cognitive/dementia disorders, and the Swedish Prescribed Drug Register. QT-prolonging drugs were identified according to the CredibleMeds online database and interactions using the Janusmed interaction database. Drug use was defined as one or more filled prescriptions during a 6-month timeframe, July 01 to December 31, 2017. Associations between people with a QT-prolonging drug and the factors of age and gender were analysed through multiple logistic regression.
Of 35,212 people included in the study, 41.6% had one or more QT-prolonging drug prescribed. The most commonly prescribed drug was donepezil, with a prevalence of 25.0%, followed by citalopram and escitalopram, representing 14.5% and 3.9% of prescriptions in the study population, respectively. Significant associations were found between QT-prolonging drug use and the factors of younger age and female gender. The most prevalent interaction was between citalopram and donepezil (2.7%), followed by the combination of escitalopram and donepezil (0.7%).
In this population of older people with major neurocognitive disorder, QT-prolonging drugs and interactions that increase the risk of torsade de pointes were prevalent. Due to the presence of many risk factors in this population, it is important to continuously evaluate current QT-prolonging drugs and concomitant drug treatment in each individual.
由于存在多种伴随风险因素,患有重度神经认知障碍的人可能易受药物诱导的QT间期延长影响。
本研究旨在调查患有重度神经认知障碍的老年人中QT间期延长药物及QT间期延长药物-药物相互作用的患病率及相关因素。
在这项基于登记处的研究中,我们通过瑞典认知/痴呆症疾病登记处与瑞典处方药登记处之间的记录链接,获取了大量患有重度神经认知障碍的老年人使用QT间期延长药物的信息。根据CredibleMeds在线数据库识别QT间期延长药物,并使用Janusmed相互作用数据库识别相互作用。药物使用定义为在2017年7月1日至12月31日这6个月时间范围内有一张或多张已配药处方。通过多因素逻辑回归分析使用QT间期延长药物的人与年龄和性别因素之间的关联。
在纳入研究的35212人中,41.6%的人开具了一种或多种QT间期延长药物。最常开具的药物是多奈哌齐,患病率为25.0%,其次是西酞普兰和艾司西酞普兰,分别占研究人群处方的14.5%和3.9%。发现使用QT间期延长药物与年龄较小和女性性别因素之间存在显著关联。最常见的相互作用是西酞普兰与多奈哌齐之间的相互作用(2.7%),其次是艾司西酞普兰与多奈哌齐的组合(0.7%)。
在这群患有重度神经认知障碍的老年人中,QT间期延长药物及增加尖端扭转型室速风险的相互作用很普遍。由于该人群中存在许多风险因素,持续评估每个个体当前使用的QT间期延长药物及伴随的药物治疗非常重要。