Campbell Noll L, Holden Richard J, Gao Sujuan, Unverzagt Frederick W, Lane Kathleen A, Carter Allie, Harrington Addison B, Manoharan Sneha, Manoharan Neha, Rosenthal Danielle L, Pitts Christopher, Pelkey Kathryn, Papineau Emily, Lauck David A, Keshk Noha, Alamer Khalid, Khalil Hussein, Boustani Malaz A
Purdue University College of Pharmacy Nursing and Health Sciences: Purdue University.
Indiana University Bloomington.
Res Sq. 2024 Oct 28:rs.3.rs-4682599. doi: 10.21203/rs.3.rs-4682599/v1.
Older adults commonly experience chronic medical conditions and are at risk of cognitive impairment as a result of age, chronic comorbidity, and medications prescribed to manage multiple chronic conditions. Anticholinergic medications are common treatments for chronic conditions, and have been repeatedly associated with poor cognitive outcomes, including delirium and dementia, in epidemiologic studies. However, no study has definitively evaluated the causal relationship between anticholinergics and cognition in a randomized controlled trial design. Utilizing our prior experience in deprescribing anticholinergic medications in various clinical environments, we designed an outpatient deprescribing intervention to prospectively test the potential causal relationship between anticholinergics and cognition in primary care older adults.
This cluster randomized clinical trial will be conducted to evaluate the impact of an anticholinergic deprescribing intervention compared to usual care on outcomes of cognition and safety in primary care older adults. Participants will include those aged 65 years and over, receiving primary care in the greater Indianapolis area, using a strong anticholinergic within the last two weeks or with evidence of high-risk exposure in the past year. Those excluded will have a diagnosis of Alzheimer's disease or related dementia, or serious mental illness. The trial plans to enroll 344 participants who will be cluster-randomized at the level of primary care physician to avoid contamination. Participants will complete outcome assessments every six months up to 2 years by blinded outcome assessors. The primary outcome of the study is a composite measure of cognition that includes domains assessing executive cognitive function, language, and memory. Secondary outcomes include patient-reported measures of pain intensity, depression, anxiety, sleep disturbance, and health-related quality of life.
The R2D2 trial will be the largest and longest prospective randomized trial testing the impact of an anticholinergic-specific deprescribing intervention on cognition in primary care older adults. Results could influence deprescribing methodology and provide new insight on the relationship between anticholinergics and cognition.
老年人常患有慢性疾病,由于年龄、慢性合并症以及用于治疗多种慢性疾病的药物,他们面临认知障碍的风险。抗胆碱能药物是慢性疾病的常见治疗方法,在流行病学研究中,其与包括谵妄和痴呆在内的不良认知结果反复相关。然而,尚无研究在随机对照试验设计中明确评估抗胆碱能药物与认知之间的因果关系。利用我们此前在各种临床环境中停用抗胆碱能药物的经验,我们设计了一项门诊停药干预措施,以前瞻性地测试抗胆碱能药物与初级保健老年患者认知之间的潜在因果关系。
将开展这项整群随机临床试验,以评估抗胆碱能药物停药干预与常规护理相比,对初级保健老年患者认知和安全性结果的影响。参与者将包括65岁及以上、在大印第安纳波利斯地区接受初级保健、在过去两周内使用强效抗胆碱能药物或在过去一年中有高风险暴露证据的患者。排除标准为患有阿尔茨海默病或相关痴呆症,或患有严重精神疾病。该试验计划招募344名参与者,他们将在初级保健医生层面进行整群随机分组,以避免交叉污染。参与者将由盲法结果评估人员每六个月进行一次长达两年的结果评估。该研究的主要结果是一项认知综合指标,包括评估执行认知功能、语言和记忆的领域。次要结果包括患者报告的疼痛强度、抑郁、焦虑、睡眠障碍和健康相关生活质量的指标。
R2D2试验将是规模最大、历时最长的前瞻性随机试验,测试抗胆碱能药物特异性停药干预对初级保健老年患者认知的影响。研究结果可能会影响停药方法,并为抗胆碱能药物与认知之间的关系提供新的见解。