Divisions of Nephrology and.
J Am Soc Nephrol. 2014 Apr;25(4):799-809. doi: 10.1681/ASN.2013060667. Epub 2014 Jan 2.
BP variability (BPV) is an important predictor of outcomes in the general population, but its association with clinical outcomes in hemodialysis patients is not clear. We identified 11,291 patients starting dialysis in 2003-2008 and followed them through December 31, 2008 (median=22 months). Predialysis systolic BPV was assessed over monthly intervals. Outcomes included factors associated with BPV, mortality (all-cause and cardiovascular), and first cardiovascular event (cardiovascular death or hospitalization). Patients' mean age was 62 years, 55% of patients were men, and 58% of patients were white. Modifiable factors associated with higher BPV included obesity, higher calcium-phosphate product levels, and lower hemoglobin concentration; factors associated with lower BPV included greater fluid removal, achievement of prescribed dry weight during dialysis, higher hemoglobin concentration, and antihypertensive regimens without β-blockers or renin-angiotensin system blocking agents. In total, 3200 deaths occurred, including 1592 cardiovascular deaths. After adjustment for demographics, comorbidities, and clinical factors, higher predialysis BPV was associated with increased risk of all-cause mortality (hazard ratio [HR], 1.18; 95% confidence interval [95% CI] per 1 SD increase in BPV, 1.13 to 1.22), cardiovascular mortality (HR, 1.18; 95% CI, 1.12 to 1.24), and first cardiovascular event (HR, 1.11; 95% CI, 1.07 to 1.15). Results were similar when BPV was categorized in tertiles and patients were stratified by baseline systolic BP. In summary, predialysis systolic BPV is an important, potentially modifiable risk factor for death and cardiovascular outcomes in incident hemodialysis patients. Studies of BP management in dialysis patients should focus on both absolute BP and BPV.
血压变异性(BPV)是一般人群预后的重要预测因素,但它与血液透析患者的临床结局的关系尚不清楚。我们确定了 2003-2008 年开始透析的 11291 例患者,并随访至 2008 年 12 月 31 日(中位数为 22 个月)。在每月间隔评估预透析收缩压变异性。结果包括与 BPV 相关的因素、死亡率(全因和心血管)以及首次心血管事件(心血管死亡或住院)。患者的平均年龄为 62 岁,55%的患者为男性,58%的患者为白人。与更高 BPV 相关的可改变因素包括肥胖、更高的钙磷乘积水平和更低的血红蛋白浓度;与更低 BPV 相关的因素包括更多的液体清除、在透析期间达到规定的干体重、更高的血红蛋白浓度以及不包含β受体阻滞剂或肾素血管紧张素系统阻滞剂的降压方案。共有 3200 例死亡,其中 1592 例为心血管死亡。在调整了人口统计学、合并症和临床因素后,更高的预透析收缩压变异性与全因死亡率(危险比[HR],1.18;每增加 1 个标准差的 BPV,风险增加 1.13 至 1.22)、心血管死亡率(HR,1.18;95%置信区间[95%CI],1.12 至 1.24)和首次心血管事件(HR,1.11;95%CI,1.07 至 1.15)风险增加相关。当按三分位法对 BPV 进行分类并按基线收缩压对患者进行分层时,结果相似。总之,预透析收缩压变异性是血液透析患者死亡和心血管结局的一个重要的、潜在可改变的危险因素。透析患者血压管理的研究应同时关注绝对血压和血压变异性。