Department of Internal Medicine Ditmanson Medical Foundation Chia-yi Christian Hospital Chiayi Taiwan.
Department of Applied Life Science and Health Chia-Nan University of Pharmacy and Science Tainan Taiwan.
J Am Heart Assoc. 2021 Jul 20;10(14):e019529. doi: 10.1161/JAHA.120.019529. Epub 2021 Jun 26.
Background Targeting higher hemoglobin levels with erythropoietin to treat anemia in patients with chronic kidney disease is associated with increased cardiovascular risk, including that of stroke. The risks of the subtypes of stroke, ischemic, hemorrhagic, and unspecified, following the administration of erythropoietin in patients with end-stage renal disease receiving hemodialysis remain unclear. Methods and results Overall, 12 948 adult patients with end-stage renal disease treated during 1999 to 2010 who had undergone hemodialysis were included. The study end points were the incidences of stroke and its subtypes. We used Cox proportional hazards regression models to estimate hazard ratios (HRs) of stroke and its subtypes in erythropoietin recipients compared with nonrecipients. Patients in the erythropoietin cohort did not have an increased risk of stroke compared with those in the nonerythropoietin cohort (adjusted HR, 1.03; 95% CI, 0.92-1.15). Compared with patients in the nonerythropoietin cohort, the risks of ischemic, hemorrhagic, or unspecified stroke were not higher in patients in the erythropoietin cohort (adjusted HRs, 1.08 [95% CI, 0.93-1.26], 0.96 [95% CI, 0.78-1.18], and 1.03 [95% CI, 0.80-1.32], respectively). Increased risks of stroke and its subtypes were not observed with even large annual defined daily doses of erythropoietin (>201). Conclusions Erythropoietin in patients receiving hemodialysis is not associated with increased risk of stroke or any of its subtypes.
用促红细胞生成素治疗慢性肾脏病患者的贫血以提高血红蛋白水平与心血管风险增加有关,包括中风风险。接受血液透析的终末期肾病患者使用促红细胞生成素后,缺血性、出血性和未特指型中风的亚组风险仍不清楚。
共有 12948 名 1999 年至 2010 年期间接受血液透析的终末期肾病成年患者纳入研究。研究终点为中风及其亚型的发生率。我们使用 Cox 比例风险回归模型来估计促红细胞生成素组与非促红细胞生成素组中风及其亚型的风险比(HR)。与非促红细胞生成素组相比,促红细胞生成素组的中风风险没有增加(校正 HR,1.03;95%CI,0.92-1.15)。与非促红细胞生成素组相比,促红细胞生成素组的缺血性、出血性或未特指型中风风险并不更高(校正 HRs,1.08[95%CI,0.93-1.26]、0.96[95%CI,0.78-1.18]和 1.03[95%CI,0.80-1.32])。即使使用较大的年度定义日剂量(>201)的促红细胞生成素,也未观察到中风及其亚型风险增加。
接受血液透析的患者使用促红细胞生成素与中风或其任何亚型的风险增加无关。