Chen Ho-Ching, Chen Kuan-Hsing, Lin Yu-Jr, Chang Chee-Jen, Tian Ya-Chung, Yang Chih-Wei, Hung Cheng-Chieh
Department of Nephrology, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyun, Taiwan.
Chang Gung Med J. 2012 Jan-Feb;35(1):79-87. doi: 10.4103/2319-4170.106163.
Hemoglobin variability in hemodialysis patients treated with erythropoiesis-stimulating agents has been used to evaluate mortality and comorbidity. Different outcomes have been reported in American and European hemodialysis patients. There are, however, few studies of the effects of hemoglobin variability in peritoneal dialysis patients.
We investigated hemoglobin variability in 363 peritoneal dialysis patients over 2 years to evaluate mortality and the association with comorbidity, peritonitis, and hospitalization. The hemoglobin of all patients selected for the study had been monitored for at least 6 months (April 2008 to September 2008). We assessed hemoglobin variability as fluctuations from the target hemoglobin level (11-12.5 g/dL). We defined the following 6 patient groups on the basis of hemoglobin patterns: consistently low (< 11 g/dL), consistently target range (11-12.5 g/dL), consistently high (> 12.5 g/dL), low-amplitude fluctuation with low hemoglobin levels, low-amplitude fluctuation with high hemoglobin levels, and high amplitude fluctuation.
Only 2% of patients maintained a stable hemoglobin level within the target range and 46.8% of patients exhibited consistently low hemoglobin levels. After 2 years of observation, there was no difference in mortality as assessed by Kaplan-Meier analysis. There were also no differences in peritonitis and hospitalization between the 6 groups. However, the length of hospital stay was longer in the high amplitude fluctuation group (p = 0.008).
Hemoglobin variability does not predict mortality in peritoneal dialysis patients.
接受促红细胞生成素治疗的血液透析患者的血红蛋白变异性已被用于评估死亡率和合并症。在美国和欧洲的血液透析患者中报告了不同的结果。然而,关于血红蛋白变异性对腹膜透析患者影响的研究很少。
我们对363例腹膜透析患者进行了为期2年的血红蛋白变异性调查,以评估死亡率以及与合并症、腹膜炎和住院治疗的相关性。入选研究的所有患者的血红蛋白均已监测至少6个月(2008年4月至2008年9月)。我们将血红蛋白变异性评估为相对于目标血红蛋白水平(11 - 12.5 g/dL)的波动。我们根据血红蛋白模式定义了以下6组患者:持续低水平(< 11 g/dL)、持续处于目标范围(11 - 12.5 g/dL)、持续高水平(> 12.5 g/dL)、低血红蛋白水平的低幅度波动、高血红蛋白水平的低幅度波动以及高幅度波动。
只有2%的患者在目标范围内维持稳定的血红蛋白水平,46.8%的患者血红蛋白水平持续较低。经过2年的观察,通过Kaplan - Meier分析评估的死亡率没有差异。6组之间在腹膜炎和住院治疗方面也没有差异。然而,高幅度波动组的住院时间更长(p = 0.008)。
血红蛋白变异性不能预测腹膜透析患者的死亡率。