Intravenous Versus Oral Iron Supplementation for the Treatment of Anemia in CKD: An Updated Systematic Review and Meta-analysis

医学 荟萃分析 转铁蛋白饱和度 肾脏疾病 内科学 贫血 不利影响 透析 肾病科 科克伦图书馆 随机对照试验 人口 阿尔法 铁蛋白 缺铁 重症监护医学 环境卫生
作者
Daniel Shepshelovich,Benaya Rozen‐Zvi,Tomer Avni,Uzi Gafter,Anat Gafter‐Gvili
出处
期刊:American Journal of Kidney Diseases [Elsevier BV]
卷期号:68 (5): 677-690 被引量:304
标识
DOI:10.1053/j.ajkd.2016.04.018
摘要

Background Iron supplementation is crucial for the treatment of anemia of chronic kidney disease (CKD). Although intravenous (IV) iron is preferred for patients with CKD receiving dialysis (CKD stage 5D), the method of iron replacement for patients with CKD stages 3 to 5 is controversial. Study Design Systematic review and meta-analysis. A search was performed until October 2015 of MEDLINE, Cochrane Library, conference proceedings in nephrology, and reference lists of included trials. Setting & Population Patients with CKD stages 3 to 5 or 5D. Selection Criteria for Studies All randomized controlled trials, regardless of publication status or language. Intervention IV versus oral iron supplementation. Outcomes The primary outcome was defined as percentage of patients reaching an elevation in hemoglobin (Hb) concentration > 1 g/dL. Secondary end points included percentage of patients who reached Hb levels > 11 g/dL, absolute Hb concentration, change in Hb concentration, transferrin saturation, ferritin levels, erythropoiesis-stimulating agents and blood transfusion requirement, and quality of life. Safety analysis included all-cause mortality and serious and all adverse events. Results 24 trials were identified, 13 including 2,369 patients with CKD stages 3 to 5 and 11 including 818 patients with CKD stage 5D. Patients treated with IV iron were more likely to reach an Hb response > 1 g/dL (risk ratios [RRs] of 1.61 [95% CI, 1.39-1.87] for CKD stages 3-5 and 2.14 [95% CI, 1.68-2.72] for CKD stage 5D). Safety analysis showed similar rates of mortality and serious and any adverse effects. IV iron replacement was associated with higher risk for hypotension (RR, 3.71; 95% CI, 1.74-7.94) and fewer gastrointestinal adverse events (RR, 0.43; 95% CI, 0.28-0.67). Limitations Significant heterogeneity between trials; follow-up was usually limited to 3 months. Conclusions Our results agree with current recommendations for IV iron replacement for patients with CKD stage 5D and support increased use of IV iron for patients with CKD stages 3 to 5. Iron supplementation is crucial for the treatment of anemia of chronic kidney disease (CKD). Although intravenous (IV) iron is preferred for patients with CKD receiving dialysis (CKD stage 5D), the method of iron replacement for patients with CKD stages 3 to 5 is controversial. Systematic review and meta-analysis. A search was performed until October 2015 of MEDLINE, Cochrane Library, conference proceedings in nephrology, and reference lists of included trials. Patients with CKD stages 3 to 5 or 5D. All randomized controlled trials, regardless of publication status or language. IV versus oral iron supplementation. The primary outcome was defined as percentage of patients reaching an elevation in hemoglobin (Hb) concentration > 1 g/dL. Secondary end points included percentage of patients who reached Hb levels > 11 g/dL, absolute Hb concentration, change in Hb concentration, transferrin saturation, ferritin levels, erythropoiesis-stimulating agents and blood transfusion requirement, and quality of life. Safety analysis included all-cause mortality and serious and all adverse events. 24 trials were identified, 13 including 2,369 patients with CKD stages 3 to 5 and 11 including 818 patients with CKD stage 5D. Patients treated with IV iron were more likely to reach an Hb response > 1 g/dL (risk ratios [RRs] of 1.61 [95% CI, 1.39-1.87] for CKD stages 3-5 and 2.14 [95% CI, 1.68-2.72] for CKD stage 5D). Safety analysis showed similar rates of mortality and serious and any adverse effects. IV iron replacement was associated with higher risk for hypotension (RR, 3.71; 95% CI, 1.74-7.94) and fewer gastrointestinal adverse events (RR, 0.43; 95% CI, 0.28-0.67). Significant heterogeneity between trials; follow-up was usually limited to 3 months. Our results agree with current recommendations for IV iron replacement for patients with CKD stage 5D and support increased use of IV iron for patients with CKD stages 3 to 5.
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