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促红细胞生成素剂量选择中的争议。问题与解答。

Controversies in selection of epoetin dosages. Issues and answers.

作者信息

Zachée P

机构信息

Division of Haematology, University of Leuven, Belgium.

出版信息

Drugs. 1995 Apr;49(4):536-47. doi: 10.2165/00003495-199549040-00004.

DOI:10.2165/00003495-199549040-00004
PMID:7789287
Abstract

Epoetin (recombinant human erythropoietin) is now a widely available though expensive treatment for the anaemia of chronic renal failure, and is effective in more than 95% of patients. Complications of epoetin in this context include hypertension in a third of cases, including hypertensive encephalopathy in a few, and thrombosis of shunts or vascular access devices. Fears that epoetin would cause progression of renal failure have not generally been confirmed, but hyperkalaemia may be a problem in the initial phase of treatment. Epoetin is up to twice as effective when administered subcutaneously rather than intravenously. Responding patients will normally do so within 3 months of starting epoetin. Failures to respond are usually due to iron deficiency or intercurrent disease. Other diseases associated with anaemia and an inappropriately low serum epoetin level include prematurity, the anaemia of cancer and rheumatoid arthritis. The baseline serum endogenous erythropoietin may provide a guide to response in some of these cases. Some encouraging results are being published. Situations where the serum erythropoietin levels are normal or elevated where epoetin has been employed include boosting of haematocrit presurgery as an adjunct to autologous blood donation, treatment of anaemic patients with myelodysplastic syndromes, and improvement of athletic performances.

摘要

促红细胞生成素(重组人促红细胞生成素)目前是一种广泛应用但价格昂贵的治疗慢性肾衰竭贫血的药物,对超过95%的患者有效。在此情况下,促红细胞生成素的并发症包括三分之一的患者出现高血压,少数患者出现高血压脑病,以及分流器或血管通路装置血栓形成。关于促红细胞生成素会导致肾衰竭进展的担忧通常未得到证实,但高钾血症可能是治疗初期的一个问题。皮下注射促红细胞生成素的效果是静脉注射的两倍。有反应的患者通常在开始使用促红细胞生成素后的3个月内出现反应。无反应通常是由于缺铁或并发疾病。与贫血和血清促红细胞生成素水平异常降低相关的其他疾病包括早产、癌症贫血和类风湿关节炎。在某些情况下,基线血清内源性促红细胞生成素水平可能为反应提供指导。一些令人鼓舞的结果正在发表。使用促红细胞生成素时血清促红细胞生成素水平正常或升高的情况包括术前提高血细胞比容作为自体献血的辅助手段、治疗骨髓增生异常综合征的贫血患者以及提高运动成绩。

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本文引用的文献

1
Serial changes in endogenous erythropoietin levels in patients with myelodysplastic syndromes and aplastic anemia undergoing erythropoietin treatment.接受促红细胞生成素治疗的骨髓增生异常综合征和再生障碍性贫血患者内源性促红细胞生成素水平的系列变化。
Ann Hematol. 1993 Apr;66(4):175-80. doi: 10.1007/BF01703232.
2
Erythropoietin treatment for chronic anemia of selected hematological malignancies and solid tumors.促红细胞生成素治疗特定血液系统恶性肿瘤和实体瘤所致的慢性贫血。
Ann Oncol. 1993 Feb;4(2):161-7. doi: 10.1093/oxfordjournals.annonc.a058423.
3
Red blood cell regeneration induced by subcutaneous recombinant erythropoietin: iron-deficient erythropoiesis in iron-replete subjects.
β-促红细胞生成素:癌症患者贫血治疗中临床应用的综述
Drugs. 2004;64(3):323-46. doi: 10.2165/00003495-200464030-00006.
4
Epoetin beta. A review of its pharmacological properties and clinical use in the management of anaemia associated with chronic renal failure.β-促红细胞生成素。其药理学特性及在治疗慢性肾衰竭相关性贫血中的临床应用综述。
Drugs. 1996 Feb;51(2):299-318. doi: 10.2165/00003495-199651020-00008.
Blood. 1993 Feb 15;81(4):956-64.
4
Use of erythropoietin to increase the volume of autologous blood donated by orthopedic patients.
Transfusion. 1993 Jan;33(1):55-60. doi: 10.1046/j.1537-2995.1993.33193142311.x.
5
Effect of serum parathyroid hormone and bone marrow fibrosis on the response to erythropoietin in uremia.血清甲状旁腺激素和骨髓纤维化对尿毒症患者促红细胞生成素反应的影响。
N Engl J Med. 1993 Jan 21;328(3):171-5. doi: 10.1056/NEJM199301213280304.
6
Recombinant human erythropoietin dosage requirements over the years.多年来重组人促红细胞生成素的剂量需求。
Nephrol Dial Transplant. 1993;8(4):374-5.
7
National Cooperative rHu Erythropoietin Study in patients with chronic renal failure--an interim report. The National Cooperative rHu Erythropoietin Study Group.慢性肾衰竭患者的国家合作重组人促红细胞生成素研究——中期报告。国家合作重组人促红细胞生成素研究组
Am J Kidney Dis. 1993 Aug;22(2 Suppl 1):3-12. doi: 10.1016/0272-6386(93)70176-y.
8
Optimizing epoetin therapy in end-stage renal disease: the case for subcutaneous administration.
Am J Kidney Dis. 1993 Aug;22(2 Suppl 1):13-22. doi: 10.1016/0272-6386(93)70177-z.
9
A phase III trial of recombinant human erythropoietin therapy in nonanemic orthopedic patients subjected to aggressive removal of blood for autologous use: dose, response, toxicity, and efficacy.一项针对接受大量采血以供自体使用的非贫血骨科患者进行重组人促红细胞生成素治疗的III期试验:剂量、反应、毒性及疗效。
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The efficacy of subcutaneous recombinant human erythropoietin in the correction of phlebotomy-induced anemia in autologous blood donors.
Transfusion. 1993 Oct;33(10):825-9. doi: 10.1046/j.1537-2995.1993.331094054619.x.