Division of Nephrology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Am J Nephrol. 2024;55(4):450-462. doi: 10.1159/000538253. Epub 2024 Mar 29.
Case reports have suggested a causative role between sevelamer use and subsequent gastrointestinal bleeding (GIB), but no large observational studies have evaluated this association.
Using the United States Renal Data System database from 2015 to 2019, we examined the association between initiation of sevelamer (vs. non-sevelamer containing phosphate binders) and GIB hospitalization as well as all-cause mortality among individuals on hemodialysis. We emulated a target trial using Cox regression models and inverse probability of treatment weights to estimate the adjusted hazard ratios (HR) across outcomes and subgroups.
Among 21,354 new users of phosphate binders (11,276 sevelamer and 10,078 non-sevelamer) with baseline lab data (calcium, phosphorus, hemoglobin, and albumin), there were 2,811 GIB hospitalizations and 5,920 deaths after a median follow-up of 1.3 years. Compared with the initiation of non-sevelamer binders, sevelamer was not associated with an increased risk of GIB hospitalization (89 vs. 90 events per 1,000 person-years; IPTW-HR: 0.98, 95% CI: 0.91-1.06) or all-cause mortality (220 vs. 224 events per 1,000 person-years; IPTW-HR: 0.98, 95% CI: 0.93-1.03). Subgroup analyses (such as diabetes and anti-coagulation use) were generally consistent, and there was no association between sevelamer dose and GIB hospitalization.
Among patients requiring hemodialysis, sevelamer (vs. non-sevelamer) containing phosphate binders was not associated with increased risk of GIB hospitalization.
病例报告表明,司维拉姆的使用与随后的胃肠道出血(GIB)之间存在因果关系,但没有大型观察性研究评估这种关联。
我们使用 2015 年至 2019 年期间美国肾脏数据系统数据库,研究了在接受血液透析的患者中,开始使用司维拉姆(与不含司维拉姆的磷结合剂相比)与 GIB 住院以及全因死亡率之间的关联。我们使用 Cox 回归模型和治疗反概率加权来模拟目标试验,以估算各个结局和亚组的调整后的危险比(HR)。
在有基线实验室数据(钙、磷、血红蛋白和白蛋白)的 21354 名新使用磷结合剂(11276 名司维拉姆和 10078 名非司维拉姆)的患者中,中位随访 1.3 年后有 2811 例 GIB 住院和 5920 例死亡。与开始使用非司维拉姆结合剂相比,司维拉姆与 GIB 住院风险增加无关(每 1000 人年发生 89 例 vs. 90 例事件;IPTW-HR:0.98,95%CI:0.91-1.06)或全因死亡率增加(每 1000 人年发生 220 例 vs. 224 例事件;IPTW-HR:0.98,95%CI:0.93-1.03)。亚组分析(如糖尿病和抗凝治疗的使用)通常一致,并且司维拉姆剂量与 GIB 住院之间没有关联。
在需要血液透析的患者中,含司维拉姆(与不含司维拉姆)的磷结合剂与 GIB 住院风险增加无关。