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:抗坏血酸在血液透析患者贫血管理中的作用:系统评价和荟萃分析。

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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:抗坏血酸被认为可改善终末期肾脏疾病患者的贫血,但尚不清楚其总体有效性。研究设计:系统评价和荟萃分析。地点和人口:成人血液透析患者。研究选择标准:除标准贫血管理外,还使用抗坏血酸的随机临床试验。干预:抗坏血酸。结果:血红蛋白水平,重组人促红细胞生成素(rHuEPO)剂量,转铁蛋白饱和度和铁蛋白水平以及不良事件的变化的加权平均差异(WMD)。结果:在157项潜在相关研究中,有6项研究(n = 326例患者)符合纳入标准。结合基线血红蛋白水平<11 g / dL患者的3项随机临床试验,抗坏血酸的使用与标准治疗相比,血红蛋白水平变化更大(WMD,0.9 g / dL; 95%CI,0.5-1.2 g / dL )。与标准护理相比,抗坏血酸的使用还与rHuEPO剂量的统计学显着降低(WMD,-17.1 U / kg / wk; 95%CI,-26.0至-8.2 U / kg / wk)和转铁蛋白饱和度改善有关(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的使用有关,令人怀疑。没有研究报告草酸盐水平或草酸沉着的发生。局限性:研究数量少,研究人群之间的异质性和研究持续时间短。不良事件报道很少。结论:尽管研究受限于受试者人数少,随访时间短和质量参差不齐,但这些结果表明,与标准护理相比,抗坏血酸的使用可能导致血红蛋白浓度和转铁蛋白饱和度增加,并降低血红蛋白浓度。 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可以改善患者的预后和成本效益。

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