Brunelli Steven M, Lynch Katherine E, Ankers Elizabeth D, Joffe Marshall M, Yang Wei, Thadhani Ravi I, Feldman Harold I
Renal-Electrolyte and Hypertension Division, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Clin J Am Soc Nephrol. 2008 Nov;3(6):1733-40. doi: 10.2215/CJN.02390508. Epub 2008 Oct 15.
Evidence exists that variability in hemoglobin may be an independent risk factor for mortality among hemodialysis patients. These observations were based on a 1996 cohort, a time when anemia management differed greatly from present. Design, settings, participants and measurements: A retrospective cohort study of patients incident to Fresenius Medical Care units between 2004 and 2005 (n = 6644). Hemoglobin variability (Hgb-Var) was defined for each subject as the residual SD of a linear regression model of time on hemoglobin.
The mean (SD) of Hgb-Var was 1.13 (0.55) g/dl. In the primary analysis, each g/dl increase of Hgb-Var was associated with an adjusted hazard ratio (95% confidence interval) for all-cause mortality of 1.11 (0.92 to 1.33). No significant interaction with Hgb-Var and mortality was found on the basis of age (P = 0.22), arterial disease (P = 0.45), Hgb slope (P = 0.68), or mean Hgb (P = 0.78). When Hgb-Var was defined by a regression model that included a quadratic term for time (enabling descriptions of curvilinear hemoglobin trajectories), model fit was greatly improved (P for difference <0.001). The corresponding adjusted hazard ratio (95% confidence interval) for all-cause mortality was 1.17 (0.93 to 1.49).
Hgb-Var was not found to be associated with all-cause mortality when examined in a contemporary incident hemodialysis population. More research is needed to determine whether differences in these findings compared with prior analyses relate to temporal trends in anemia management or from differences in the relationship between Hgb-Var and outcomes among incident versus prevalent hemodialysis patients.
有证据表明,血红蛋白变异性可能是血液透析患者死亡的独立危险因素。这些观察结果基于1996年的队列研究,当时贫血管理与现在有很大不同。设计、设置、参与者与测量:对2004年至2005年期间在费森尤斯医疗护理单位就诊的患者进行回顾性队列研究(n = 6644)。将每个受试者的血红蛋白变异性(Hgb-Var)定义为血红蛋白随时间线性回归模型的残差标准差。
Hgb-Var的均值(标准差)为1.13(0.55)g/dl。在初步分析中,Hgb-Var每增加1 g/dl,全因死亡率的调整后风险比(95%置信区间)为1.11(0.92至1.33)。未发现Hgb-Var与死亡率在年龄(P = 0.22)、动脉疾病(P = 0.45)、Hgb斜率(P = 0.68)或平均Hgb(P = 0.78)方面存在显著交互作用。当通过包含时间二次项的回归模型定义Hgb-Var(能够描述曲线血红蛋白轨迹)时,模型拟合得到极大改善(差异P <0.001)。全因死亡率的相应调整后风险比(95%置信区间)为1.17(0.93至1.49)。
在当代新发病例血液透析人群中,未发现Hgb-Var与全因死亡率相关。需要更多研究来确定与先前分析相比,这些结果的差异是与贫血管理的时间趋势有关,还是与新发病例与现患血液透析患者中Hgb-Var与结局之间关系的差异有关。