Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA.
Division of Nephrology and Hypertension, Kaiser Permanente Los Angeles Medical Center. Los Angeles, CA.
Am J Kidney Dis. 2021 May;77(5):704-712. doi: 10.1053/j.ajkd.2020.07.023. Epub 2020 Nov 15.
RATIONAL & OBJECTIVE: Beta-blockers are recommended for patients with heart failure (HF) but their benefit in the dialysis population is uncertain. Beta-blockers are heterogeneous, including with respect to their removal by hemodialysis. We sought to evaluate whether β-blocker use and their dialyzability characteristics were associated with early mortality among patients with chronic kidney disease with HF who transitioned to dialysis.
Retrospective cohort study.
SETTING & PARTICIPANTS: Adults patients with chronic kidney disease (aged≥18 years) and HF who initiated either hemodialysis or peritoneal dialysis during January 1, 2007, to June 30, 2016, within an integrated health system were included.
Patients were considered treated with β-blockers if they had a quantity of drug dispensed covering the dialysis transition date.
All-cause mortality within 6 months and 1 year or hospitalization within 6 months after transition to maintenance dialysis.
Inverse probability of treatment weights using propensity scores was used to balance covariates between treatment groups. Cox proportional hazard analysis and logistic regression were used to investigate the association between β-blocker use and study outcomes.
3,503 patients were included in the study. There were 2,115 (60.4%) patients using β-blockers at transition. Compared with nonusers, the HR for all-cause mortality within 6 months was 0.79 (95% CI, 0.65-0.94) among users of any β-blocker and 0.68 (95% CI, 0.53-0.88) among users of metoprolol at transition. There were no observed differences in all-cause or cardiovascular-related hospitalization.
The observational nature of our study could not fully account for residual confounding.
Beta-blockers were associated with a lower rate of mortality among incident hemodialysis patients with HF. Similar associations were not observed for hospitalizations within the first 6 months following transition to dialysis.
β受体阻滞剂推荐用于心力衰竭(HF)患者,但在透析人群中的获益尚不确定。β受体阻滞剂具有异质性,包括其通过血液透析清除的情况。我们旨在评估慢性肾脏病伴 HF 患者过渡到透析时β受体阻滞剂的使用及其可透析性特征是否与早期死亡率相关。
回顾性队列研究。
纳入 2007 年 1 月 1 日至 2016 年 6 月 30 日期间在一个综合卫生系统内开始血液透析或腹膜透析的年龄≥18 岁的慢性肾脏病(CKD)合并 HF 成年患者。
如果患者在药物分配量中覆盖了透析过渡日期,则认为其接受了β受体阻滞剂治疗。
透析过渡后 6 个月和 1 年内的全因死亡率或住院率;透析过渡后 6 个月内的全因死亡率或住院率。
使用倾向评分的逆概率治疗权重来平衡治疗组之间的协变量。使用 Cox 比例风险分析和逻辑回归来研究β受体阻滞剂使用与研究结局之间的关联。
共纳入 3503 例患者。在过渡时,有 2115 例(60.4%)患者使用β受体阻滞剂。与未使用者相比,任何β受体阻滞剂使用者在透析过渡后 6 个月内的全因死亡率 HR 为 0.79(95%CI,0.65-0.94),美托洛尔使用者的 HR 为 0.68(95%CI,0.53-0.88)。在全因或心血管相关住院方面,未观察到差异。
我们研究的观察性质不能完全解释残留的混杂因素。
β受体阻滞剂与 HF 并发的新血液透析患者死亡率降低相关。在透析过渡后 6 个月内,住院率无类似关联。