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Intravenous Versus Oral Iron Supplementation for the Treatment of Anemia in CKD: An Updated Systematic Review and Meta-analysis.静脉补铁与口服补铁治疗 CKD 贫血的疗效比较:一项更新的系统评价和荟萃分析。
Am J Kidney Dis. 2016 Nov;68(5):677-690. doi: 10.1053/j.ajkd.2016.04.018. Epub 2016 Jun 16.
2
An Overview of Regular Dialysis Treatment in Japan (As of 31 December 2013).日本常规透析治疗概述(截至2013年12月31日)
Ther Apher Dial. 2015 Dec;19(6):540-74. doi: 10.1111/1744-9987.12378.
3
A randomized trial of intravenous and oral iron in chronic kidney disease.慢性肾脏病静脉和口服铁剂的随机试验
Kidney Int. 2015 Oct;88(4):905-14. doi: 10.1038/ki.2015.163. Epub 2015 Jun 17.
4
A randomized trial of JTT-751 versus sevelamer hydrochloride in patients on hemodialysis.JTT-751 与盐酸司维拉姆在血液透析患者中随机对照试验。
Nephrol Dial Transplant. 2014 May;29(5):1053-60. doi: 10.1093/ndt/gft483. Epub 2013 Dec 26.
5
Protein apoferritin and ferritin in iron feeding and absorption.铁摄入与吸收过程中的脱铁铁蛋白和铁蛋白
Science. 1946 Jan 25;103(2665):107.
6
Determinants of hepcidin in patients on maintenance hemodialysis: role of inflammation.维持性血液透析患者铁调素的决定因素:炎症的作用。
Am J Nephrol. 2010;31(6):534-40. doi: 10.1159/000312381. Epub 2010 May 14.
7
Hypophosphatemia induced by intravenous administration of saccharated ferric oxide: another form of FGF23-related hypophosphatemia.静脉注射含糖氧化铁诱导的低磷血症:FGF23相关低磷血症的另一种形式。
Bone. 2009 Oct;45(4):814-6. doi: 10.1016/j.bone.2009.06.017. Epub 2009 Jun 23.
8
FGF23 elevation and hypophosphatemia after intravenous iron polymaltose: a prospective study.静脉注射聚麦芽糖铁后FGF23升高与低磷血症:一项前瞻性研究。
J Clin Endocrinol Metab. 2009 Jul;94(7):2332-7. doi: 10.1210/jc.2008-2396. Epub 2009 Apr 14.
9
Effect of saccharated ferric oxide and iron dextran on the metabolism of phosphorus in rats.
J Lab Clin Med. 2005 Jul;146(1):25-9. doi: 10.1016/j.lab.2005.02.015.
10
Definition and classification of chronic kidney disease: a position statement from Kidney Disease: Improving Global Outcomes (KDIGO).慢性肾脏病的定义与分类:来自改善全球肾脏病预后组织(KDIGO)的立场声明
Kidney Int. 2005 Jun;67(6):2089-100. doi: 10.1111/j.1523-1755.2005.00365.x.

口服铁剂对日本血液透析患者的有益作用。

Beneficial Effects of Oral Iron in Japanese Patients on Hemodialysis.

作者信息

Sanai Toru, Ono Takashi, Fukumitsu Toma

机构信息

The Division of Nephrology, Department of Internal Medicine, Fukumitsu Hospital, Japan.

Department of Surgery, Fukumitsu Hospital, Japan.

出版信息

Intern Med. 2017 Sep 15;56(18):2395-2399. doi: 10.2169/internalmedicine.8520-16. Epub 2017 Aug 21.

DOI:10.2169/internalmedicine.8520-16
PMID:28824065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5643164/
Abstract

Objective Iron deficiency anemia (IDA) has become important with regard to mortality in hemodialysis (HD) patients. Therefore, it is necessary to optimize the treatment of these patients. Methods IDA in end-stage renal disease patients on HD was observed in 42 (33.6%) of 125 patients. We examined the influence of daily orally iron [sodium ferrous citrate (SFC) iron/tablet 50 mg, 1-2 tablets] on the renal function markers, anemia and iron data for about 6 months. Results The hematocrit and hemoglobin levels were significantly increased in the patients treated with SFC [hematocrit: before 28.5%±2.1% (mean ± standard deviation), 1st month 30.0%±2.3%, p<0.05; 3rd month 32.4%±2.9%, p<0.05; 6th month 31.3%±3.4%, p<0.05; and hemoglobin: before 9.25±0.70, 1st month 9.72±0.71, p<0.05; 3rd month 10.54±0.96, p<0.05; 6th month 10.25±1.21 g/dL, p<0.05]. The transferrin saturation (TSAT) and serum ferritin levels were significantly increased in the patients treated with SFC (TSAT: before 21.5%±10.0%, 1st-3rd month, 34.1%±15.1%, p<0.05; 6-8th month 34.7%±11.9%, p<0.05; and ferritin: before 38.2±37.1, 6-8th month 67.5±44.0 ng/mL, p<0.05). The present findings clearly indicate that oral iron is an effective route of iron supplementation in HD patients, and no adverse effects associated with SFC occurred during the treatment and follow-up period. Conclusion Our results clearly indicate that oral iron delivered via SFC is a well-tolerated and effective form of iron supplementation in long-term HD and IDA patients in Japan.

摘要

目的 缺铁性贫血(IDA)在血液透析(HD)患者的死亡率方面已变得至关重要。因此,有必要优化这些患者的治疗。方法 在125例患者中,观察到42例(33.6%)终末期肾病HD患者存在IDA。我们研究了每日口服铁剂[枸橼酸铁钠(SFC),每片含铁50mg,1 - 2片]对肾功能指标、贫血及铁相关数据的影响,为期约6个月。结果 接受SFC治疗的患者血细胞比容和血红蛋白水平显著升高[血细胞比容:治疗前28.5%±2.1%(均值±标准差),第1个月30.0%±2.3%,p<0.05;第3个月32.4%±2.9%,p<0.05;第6个月31.3%±3.4%,p<0.05;血红蛋白:治疗前9.25±0.70,第1个月9.72±0.71,p<0.05;第3个月10.54±0.96,p<0.05;第6个月10.25±1.21g/dL,p<0.05]。接受SFC治疗的患者转铁蛋白饱和度(TSAT)和血清铁蛋白水平显著升高(TSAT:治疗前21.5%±10.0%,第1 - 3个月34.1%±15.1%,p<0.05;第6 - 8个月34.7%±11.9%,p<0.05;铁蛋白:治疗前38.2±37.1,第6 - 8个月67.5±44.0ng/mL,p<0.05)。目前的研究结果清楚地表明,口服铁剂是HD患者补充铁的有效途径,且在治疗和随访期间未出现与SFC相关的不良反应。结论 我们的结果清楚地表明,在日本,通过SFC口服补铁是长期HD和IDA患者耐受性良好且有效的补铁方式。