老年DLBCL患者多药及潜在不适当用药与预后的关系:一项人群研究。

IF 16.4
Inna Y Gong, Abi Vijenthira, Zharmaine Ante, Andrew Calzavara, Tammy T Hshieh, Clark DuMontier, Gregory A Abel, Jane A Driver, Shabbir M H Alibhai, Anca Prica, Matthew C Cheung, Lee Mozessohn
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引用次数: 0

摘要

背景:在接受弥漫性大b细胞淋巴瘤(DLBCL)治疗的老年患者中,多药和可能不适当的药物(pim)可能与生存和医疗保健利用有关。方法:这项基于人群的研究调查了2006年1月1日至2017年12月31日期间接受利妥昔单抗治疗的年龄≥66岁的DLBCL患者,并随访至2019年3月31日。多重用药定义为在开始治疗的90天内同时服用≥5或≥8种药物。采用抗胆碱能风险量表(ARS)和老年肿瘤学潜在不适当药物(GO-PIM)量表对pim进行评估。进行Cox回归和负二项模型,调整年龄、性别、虚弱和合并症负担(汇总诊断组[ADGs])。主要结局是全因死亡率,次要结局是医疗保健利用,通过计划外急诊就诊和住院来衡量。结果:共纳入5527例患者(中位年龄75岁;(48%为女性),其中69%和40%分别有≥5种和≥8种药物的多重用药。在PIM方面,27%的患者至少有一次基于ARS的PIM,而70%的患者有基于GO-PIM量表的高风险药物。在校正分析中,多种用药与全因死亡风险增加相关,校正风险比(aHR)为1.14 (95% CI, 1.05-1.23;服用≥5种药物的患者P= 0.0021), 1.18 (95% CI, 1.09-1.27;结论:在接受治疗的老年DLBCL患者中,多种药物和pim与死亡率和医疗保健使用率的相对风险增加有关,与虚弱和合并症无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Polypharmacy and Potentially Inappropriate Medications With Outcomes in Older Adults With DLBCL: A Population Study.

Background: Polypharmacy and potentially inappropriate medications (PIMs) may be associated with survival and health care utilization in older patients undergoing treatment for diffuse large B-cell lymphoma (DLBCL).

Methods: This population-based study examined patients with DLBCL aged ≥66 years receiving rituximab-based therapy from January 1, 2006, to December 31, 2017, and followed them until March 31, 2019. Polypharmacy was defined as taking ≥5 or ≥8 concurrent medications within 90 days of treatment initiation. PIMs were assessed using the Anticholinergic Risk Scale (ARS) and the Geriatric Oncology Potentially Inappropriate Medications (GO-PIM) scale. Cox regression and negative binomial models were conducted, adjusting for age, sex, frailty, and comorbidity burden (Aggregated Diagnosis Groups [ADGs]). The primary outcome was all-cause mortality, and the secondary outcome was health care utilization, measured by unplanned emergency department visits and hospitalizations.

Results: A total of 5,527 patients were included (median age, 75 years; 48% female), of whom 69% and 40% had polypharmacy defined as ≥5 and ≥8 medications, respectively. In terms of PIMs, 27% of patients had at least one PIM based on ARS, whereas 70% had a high-risk medication based on the GO-PIM scale. Polypharmacy was associated with increased risk of all-cause mortality in the adjusted analysis, with an adjusted hazard ratio (aHR) of 1.14 (95% CI, 1.05-1.23; P=.0021) for patients taking ≥5 medications, and 1.18 (95% CI, 1.09-1.27; P<.0001) for those taking ≥8 medications. Increasing number of PIMs was associated with increased mortality risk. Polypharmacy was associated with an increased relative risk of health care utilization, with an adjusted rate ratio (aRR) of 1.14 (95% CI, 1.06-1.22; P=.0004) for patients taking ≥5 medications, and 1.16 (95% CI, 1.08-1.24; P<.0001) for those taking ≥8 medications. For PIMs, a higher score on the GO-PIM scale was associated with greater risk of health care utilization (aRR for ≥3 medications, 1.20; 95% CI, 1.09-1.32; P=.0003), whereas ARS was not.

Conclusions: Polypharmacy and PIMs are associated with an increased relative risk of mortality and health care utilization among older adults with DLBCL undergoing treatment, independent of frailty and comorbidity.

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