Institute of General Practice and Primary Care, Chair of General Practice II and Patient-Centredness in Primary Care, Faculty of Health, Witten/Herdecke University, Witten, Germany.
Institute of General Practice, Medical Faculty, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
JAMA Netw Open. 2023 Mar 1;6(3):e234723. doi: 10.1001/jamanetworkopen.2023.4723.
For older adults with frailty syndrome, reducing polypharmacy may have utility as a safety-promoting treatment option.
To investigate the effects of family conferences on medication and clinical outcomes in community-dwelling older adults with frailty receiving polypharmacy.
DESIGN, SETTING, AND PARTICIPANTS: This cluster randomized clinical trial was conducted from April 30, 2019, to June 30, 221, at 110 primary care practices in Germany. The study included community-dwelling adults aged 70 years or older with frailty syndrome, daily use of at least 5 different medications, a life expectancy of at least 6 months, and no moderate or severe dementia.
General practitioners (GPs) in the intervention group received 3 training sessions on family conferences, a deprescribing guideline, and a toolkit with relevant nonpharmacologic interventions. Three GP-led family conferences for shared decision-making involving the participants and family caregivers and/or nursing services were subsequently held per patient at home over a period of 9 months. Patients in the control group received care as usual.
The primary outcome was the number of hospitalizations within 12 months, as assessed by nurses during home visits or telephone interviews. Secondary outcomes included the number of medications, the number of European Union list of the number of potentially inappropriate medication (EU[7]-PIM) for older people, and geriatric assessment parameters. Both per-protocol and intention-to-treat analyses were conducted.
The baseline assessment included 521 individuals (356 women [68.3%]; mean [SD] age, 83.5 [6.17] years). The intention-to-treat analysis with 510 patients showed no significant difference in the adjusted mean (SD) number of hospitalizations between the intervention group (0.98 [1.72]) and the control group (0.99 [1.53]). In the per-protocol analysis including 385 individuals, the mean (SD) number of medications decreased from 8.98 (3.56) to 8.11 (3.21) at 6 months and to 8.49 (3.63) at 12 months in the intervention group and from 9.24 (3.44) to 9.32 (3.59) at 6 months and to 9.16 (3.42) at 12 months in the control group, with a statistically significant difference at 6 months in the mixed-effect Poisson regression model (P = .001). After 6 months, the mean (SD) number of EU(7)-PIMs was significantly lower in the intervention group (1.30 [1.05]) than in the control group (1.71 [1.25]; P = .04). There was no significant difference in the mean number of EU(7)-PIMs after 12 months.
In this cluster randomized clinical trial with older adults taking 5 or more medications, the intervention consisting of GP-led family conferences did not achieve sustainable effects in reducing the number of hospitalizations or the number of medications and EU(7)-PIMs after 12 months.
German Clinical Trials Register: DRKS00015055.
重要性:对于患有衰弱综合征的老年人来说,减少多药治疗可能是一种促进安全的治疗选择。
目的:调查家庭会议对接受多药治疗的社区居住的衰弱老年人的药物治疗和临床结局的影响。
设计、地点和参与者:这是一项于 2019 年 4 月 30 日至 2021 年 6 月 30 日在德国 110 个初级保健机构进行的集群随机临床试验。研究纳入了年龄在 70 岁及以上、患有衰弱综合征、每天使用至少 5 种不同药物、预期寿命至少 6 个月且无中度或重度痴呆的社区居住成年人。
干预措施:干预组的全科医生(GP)接受了 3 次关于家庭会议、处方减少指南和包含相关非药物干预措施的工具包的培训课程。随后,每位患者在家中进行了 3 次由 GP 主导的家庭会议,以便共同决策,涉及参与者及其家庭护理人员和/或护理服务。
主要结果和措施:主要结局是在 12 个月内的住院次数,由护士在家庭访视或电话访谈中评估。次要结局包括药物数量、欧洲老年人潜在不适当药物清单(EU[7]-PIM)的药物数量以及老年评估参数。均进行了意向治疗和按方案分析。
结果:基线评估包括 521 人(356 名女性[68.3%];平均[SD]年龄,83.5 [6.17]岁)。意向治疗分析纳入 510 名患者,干预组(0.98 [1.72])和对照组(0.99 [1.53])的调整后平均(SD)住院次数无显著差异。在包括 385 名个体的方案分析中,干预组的平均(SD)药物数量从 6 个月时的 8.98(3.56)降至 8.11(3.21),12 个月时降至 8.49(3.63),对照组从 9.24(3.44)降至 9.32(3.59),6 个月时混合效应泊松回归模型有统计学意义(P=0.001)。6 个月后,干预组的平均(SD)EU[7]-PIM 数量(1.30 [1.05])明显低于对照组(1.71 [1.25];P=0.04)。12 个月后,EU[7]-PIM 数量的平均差异无统计学意义。
结论:在这项针对服用 5 种或更多药物的老年人的集群随机临床试验中,由 GP 主导的家庭会议干预在 12 个月后并未实现减少住院次数或药物和 EU[7]-PIM 数量的可持续效果。