Department of Pharmacy Systems, Outcomes and Policy, University of Illinois at Chicago, Chicago, IL, USA.
Division of Geriatric and Palliative Medicine, UTHealth McGovern Medical School, Houston, TX, USA.
J Gen Intern Med. 2019 Oct;34(10):2029-2037. doi: 10.1007/s11606-019-05152-x. Epub 2019 Jul 25.
The use of medications not relieving symptoms or maximizing quality of life should be minimized following hospice enrollment.
To evaluate the frequency of and predictive factors for continuation of medications with limited benefit after hospice admission among those admitted for cancer- and non-cancer-related causes.
Cohort study using the Surveillance, Epidemiology and End Results-Medicare linked database.
Medicare Part D-enrolled beneficiaries 66 years and older who were admitted to and died under hospice care between January 1, 2008, and December 31, 2013 (N = 70,035).
Patients were followed from hospice enrollment through death for Part D dispensing of limited benefit medications (LBMs) they had used in the 6 months prior to hospice admission, including anti-hyperlipidemics, anti-hypertensives, oral anti-diabetics, anti-platelets, anti-dementia medications, anti-osteoporotic medications, and proton pump inhibitors. The proportion of patients continuing an LBM after hospice admission was evaluated. Adjusted relative risks (RRs) were estimated for factors associated with LBM continuation.
Overall, 29.8% and 30.5% of patients admitted to hospice for a cancer- and non-cancer-related cause, respectively, continued at least one LBM after hospice admission. Anti-dementia medications were continued most frequently (29.3%) while anti-osteoporotic medications were continued least often (14.1%). Compared to home hospice, LBM continuation was greater in hospice patients residing in skilled nursing (RR 1.25, 95% CI 1.20-1.29), non-skilled nursing (RR 1.29, 95% CI 1.25-1.32), and assisted living facilities (RR 1.28, 95% CI 1.24-1.32). Patients with hospice stays ≥ 180 days were more likely to continue at least one LBM compared to those with stays of 1 week or less (RR 13.11, 95% CI 12.25-14.02).
A substantial proportion of Medicare hospice beneficiaries continued to receive LBMs following hospice enrollment. Providers should evaluate the necessity of continuing non-palliative medications at the end of life through a careful, patient-centric consideration of their potential risks and benefits.
在注册临终关怀后,应尽量减少使用不能缓解症状或最大限度提高生活质量的药物。
评估癌症和非癌症相关原因导致的临终关怀入院患者在入院后继续使用有限受益药物(LBM)的频率和预测因素。
使用监测、流行病学和最终结果-医疗保险关联数据库的队列研究。
2008 年 1 月 1 日至 2013 年 12 月 31 日期间,接受并在临终关怀下死亡的 66 岁及以上的 Medicare Part D 参保受益人均纳入本研究(N=70035)。
从临终关怀登记开始,对患者进行为期 6 个月的有限受益药物(LBM)的处方配药随访,这些药物是他们在临终关怀入院前 6 个月内使用的,包括降脂药、抗高血压药、口服抗糖尿病药、抗血小板药、抗痴呆药、抗骨质疏松药和质子泵抑制剂。评估患者在临终关怀入院后继续使用 LBM 的比例。对与 LBM 持续相关的因素进行调整相对风险(RR)估计。
总体而言,分别有 29.8%和 30.5%的癌症和非癌症相关原因导致的临终关怀入院患者在入院后继续至少一种 LBM。抗痴呆药的使用率最高(29.3%),而抗骨质疏松药的使用率最低(14.1%)。与家庭临终关怀相比,在疗养院(RR 1.25,95%CI 1.20-1.29)、非疗养院(RR 1.29,95%CI 1.25-1.32)和辅助生活设施(RR 1.28,95%CI 1.24-1.32)的临终关怀患者中,LBM 持续使用的可能性更大。与入住时间为 1 周或更短的患者相比,入住时间≥180 天的患者更有可能继续至少使用一种 LBM(RR 13.11,95%CI 12.25-14.02)。
相当一部分 Medicare 临终关怀受益人的临终关怀登记后继续接受 LBM。医生应通过仔细、以患者为中心的方式评估非姑息治疗药物在生命末期的必要性,充分考虑其潜在的风险和获益。