Université Paris-Saclay, UVSQ, Inserm, CESP, Echappement aux anti-infectieux et pharmaco-epidémiologie, 78180, Montigny-le-Bretonneux, France.
Département Hospitalier d'Epidémiologie et de Santé Publique, AP-HP. Université Paris-Saclay, Paris, France.
Drugs Aging. 2021 Jan;38(1):63-74. doi: 10.1007/s40266-020-00817-3. Epub 2021 Jan 7.
Because of insufficient data about their benefit-risk ratio in real life, drugs used for Alzheimer's disease (AD; cholinesterase inhibitors and memantine) were withdrawn from the list of reimbursable drugs in France on 1 August 2018.
In this context, this study aimed to investigate the effects of the removal of AD drugs from the list of reimbursed drugs among patients followed in memory centres in France, in terms of prevalence and factors associated with drug discontinuation and evolution of disease management and cognition after drug discontinuation.
This is an observational study based on data from the National Alzheimer Data Bank ('Banque Nationale Alzheimer' [BNA]), which centralizes information about patients consulting in memory centres. The drug discontinuation rate was estimated among patients receiving AD drugs at the last visit before the end of reimbursement. Factors associated with drug discontinuation were investigated among sociodemographic and disease characteristics, as well as among the use of healthcare resources before the end of reimbursement. We compared the evolution of disease management (psychotropic drugs and non-pharmacological interventions) and Mini-Mental State Examination (MMSE) score during the year following the end of reimbursement among patients with a diagnosis of AD.
Among the 19,380 patients of the study sample (62.5% females, mean age 81 years, 86.8% with a diagnosis of AD), 19.5% discontinued their treatment after the end of reimbursement. The main factors associated with drug discontinuation were the type of dementia and lower MMSE level. Compared with patients with a diagnosis of AD, those with vascular dementia were more likely to stop their treatment, whereas those with dementia with Lewy bodies were less likely to discontinue. Among patients with a diagnosis of AD, drug discontinuation was associated with increased use of psychotropic medications, especially antidepressants, and non-pharmacological interventions afterwards, but there was no difference regarding the evolution of MMSE score.
This study provides real-life information about the use of AD drugs after they were withdrawn from reimbursement in France and shows that drug discontinuation was limited among patients followed in memory centres and accompanied by increased use of other healthcare resources.
由于缺乏关于其在现实生活中的获益-风险比的数据,用于治疗阿尔茨海默病(AD;胆碱酯酶抑制剂和盐酸美金刚)的药物于 2018 年 8 月 1 日从法国的报销药物清单中删除。
在这种情况下,本研究旨在调查 AD 药物从法国记忆中心随访患者的报销药物清单中移除后,在药物停药率以及疾病管理和停药后认知的演变方面,与停药相关的因素。
这是一项基于国家阿尔茨海默病数据库('Banque Nationale Alzheimer' [BNA])数据的观察性研究,该数据库集中了在记忆中心就诊患者的信息。在最后一次报销前就诊时,估计接受 AD 药物治疗的患者的停药率。在停药前的社会人口学和疾病特征以及医疗保健资源使用情况中,调查了与药物停药相关的因素。我们比较了停药后一年中 AD 患者的疾病管理(精神药物和非药物干预)和简易精神状态检查(MMSE)评分的变化。
在研究样本的 19380 名患者中(62.5%为女性,平均年龄 81 岁,86.8%诊断为 AD),19.5%的患者在报销结束后停止治疗。与药物停药相关的主要因素是痴呆类型和较低的 MMSE 水平。与 AD 患者相比,血管性痴呆患者更有可能停止治疗,而路易体痴呆患者则不太可能停药。在 AD 患者中,药物停药与精神药物,尤其是抗抑郁药的使用增加以及随后的非药物干预有关,但 MMSE 评分的演变没有差异。
本研究提供了法国 AD 药物从报销清单中撤出后的实际使用情况信息,并表明在记忆中心随访的患者中,药物停药率有限,并且伴随着其他医疗保健资源的使用增加。