首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Ascorbic acid for anemia management in hemodialysis patients: a systematic review and meta-analysis.
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Ascorbic acid for anemia management in hemodialysis patients: a systematic review and meta-analysis.

机译:血液透析患者贫血管理抗坏血酸:系统审查和荟萃分析。

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BACKGROUND: Ascorbic acid is believed to improve anemia in patients with end-stage renal disease, but its overall effectiveness is unclear. STUDY DESIGN: Systematic review and meta-analysis. SETTING & POPULATION: Adult hemodialysis patients. SELECTION CRITERIA FOR STUDIES: Randomized clinical trials of ascorbic acid use in addition to standard anemia management. INTERVENTION: Ascorbic acid. OUTCOMES: Weighted mean difference (WMD) for change in hemoglobin level, recombinant human erythropoietin (rHuEPO) dose, transferrin saturation and ferritin level and adverse events. RESULTS: Of 157 potentially relevant studies, 6 studies (n = 326 patients) met the inclusion criteria. Combining the 3 randomized clinical trials involving patients with baseline hemoglobin levels <11 g/dL, change in hemoglobin level was greater for ascorbic acid use compared with standard care (WMD, 0.9 g/dL; 95% CI, 0.5-1.2 g/dL). Compared with standard care, ascorbic acid use also was associated with a statistically significant decrease in rHuEPO dose (WMD, -17.1 U/kg/wk; 95% CI, -26.0 to -8.2 U/kg/wk) and improvement in transferrin saturation (WMD, 7.9%; 95% CI, 5.2-10.5%), with no change in ferritin concentration. Adverse events had questionable relevance to ascorbic acid use; no study reported oxalate levels or occurrence of oxalosis. LIMITATIONS: Small number of studies, heterogeneity between study populations, and study durations were short. Adverse events were poorly reported. CONCLUSIONS: Although the studies are limited by small numbers of subjects, short durations of follow-up, and variable quality, these results suggest that compared with standard care, ascorbic acid use may result in an increase in hemoglobin concentration and transferrin saturation and decrease in rHuEPO requirements. Longer term studies are required to confirm these results, provide information about adverse events, and determine whether these changes translate into improved patient outcomes and cost-effectiveness.
机译:背景:抗坏血酸被认为改善患者患有肾病患者的贫血,但其整体有效性尚不清楚。研究设计:系统评论和荟萃分析。环境和人口:成人血液透析患者。研究选择标准:除标准贫血管理外,抗坏血酸的随机临床试验。干预:抗坏血酸。结果:加权平均差异(WMD)用于血红蛋白水平的变化,重组人促红细胞生成素(RHUEPO)剂量,转移素饱和和铁蛋白水平和不良事件。结果:157个潜在相关的研究,6项研究(n = 326名患者)达到了纳入标准。结合涉及基线血红蛋白水平<11g / dL患者的3种随机临床试验,血红蛋白水平的变化与标准护理(WMD,0.9g / dL; 95%CI,0.5-1.2g / d1相比,血红蛋白水平的变化更大。 )。与标准护理相比,抗坏血酸使用也与RHUEPO剂量(WMD,-17.1u / kg / WK; 95%CI,-26.0至-8.2U / kg / WK)的统计学上显着降低以及转化素饱和的改善(WMD,7.9%; 95%CI,5.2-10.5%),铁蛋白浓度没有变化。不良事件与抗坏血酸使用具有可疑的相关性;没有研究报告草酸水平或草药的发生。限制:少数研究,研究人群之间的异质性,以及研究持续时间短。不良事件报告不佳。结论:尽管研究受到少数科目的限制,但随访的短持续时间和可变质量,这些结果表明,与标准护理相比,抗坏血酸使用可能导致血红蛋白浓度增加和转化素饱和度和减少Rhuepo要求。需要长期研究以确认这些结果,提供有关不良事件的信息,并确定这些变化是否转化为改善的患者结果和成本效益。

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