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缺铁性贫血患者使用静脉注射羧麦芽糖铁的经验。

Experience with intravenous ferric carboxymaltose in patients with iron deficiency anemia.

作者信息

Bregman David B, Goodnough Lawrence T

机构信息

Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

Departments of Pathology and Medicine, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Ther Adv Hematol. 2014 Apr;5(2):48-60. doi: 10.1177/2040620714521127.

Abstract

Erythropoiesis may be limited by absolute or functional iron deficiency or when chronic inflammatory conditions lead to iron sequestration. Intravenous iron may be indicated when oral iron cannot address the deficiency. Ferric carboxymaltose (FCM) is a nondextran iron preparation recently approved in the United States for intravenous treatment of iron deficiency anemia (IDA) in adult patients with intolerance or unsatisfactory response to oral iron or with nondialysis-dependent chronic kidney disease. The full dose is two administrations of up to 750 mg separated by at least 7 days (up to 1500 mg total). FCM can be injected in 7-8 min or diluted in saline for slower infusion. The efficacy and safety of this dose was established in two prospective trials that randomized over 3500 subjects, 1775 of whom received FCM. One trial showed similar efficacy of FCM to an approved intravenous iron regimen (1000 mg of iron sucrose) in 2500 subjects with chronic kidney disease and additional cardiovascular risk factors. The other trial showed superior efficacy of FCM to oral iron in subjects with IDA due to various etiologies (e.g. gastrointestinal or uterine bleeding). In these trials, there was no significant difference between FCM and comparator with respect to an independently adjudicated composite safety endpoint, including death, myocardial infarction, or stroke. A database of 5799 subjects exposed to FCM provided a safety profile acceptable for regulatory approval. Mechanistic studies demonstrated that the transient, asymptomatic reduction in serum phosphate observed following FCM administration results from induction of fibroblast growth factor 23, which in turn induces renal phosphate excretion. An elevated hepcidin level may identify patients with IDA who will not respond to oral iron but will respond to FCM. The ability to administer FCM in two rapid injections or infusions will likely be viewed favorably by patients and healthcare providers.

摘要

红细胞生成可能会受到绝对或功能性缺铁的限制,或者在慢性炎症状态导致铁隔离时受到限制。当口服铁剂无法纠正缺铁时,可能需要静脉补铁。羧基麦芽糖铁(FCM)是一种非右旋糖酐铁制剂,最近在美国被批准用于静脉治疗成年缺铁性贫血(IDA)患者,这些患者对口服铁剂不耐受或反应不佳,或患有非透析依赖性慢性肾脏病。全剂量为分两次给药,每次最多750mg,间隔至少7天(总量最多1500mg)。FCM可在7 - 8分钟内注射,或用生理盐水稀释后缓慢输注。该剂量的疗效和安全性在两项前瞻性试验中得到证实,这两项试验将超过3500名受试者随机分组,其中1775人接受FCM治疗。一项试验表明,在2500名患有慢性肾脏病和其他心血管危险因素的受试者中,FCM与已批准的静脉铁剂方案(1000mg蔗糖铁)疗效相似。另一项试验表明,在因各种病因(如胃肠道或子宫出血)导致IDA的受试者中,FCM比口服铁剂疗效更佳。在这些试验中,就包括死亡、心肌梗死或中风在内的独立判定的综合安全终点而言,FCM与对照药物之间没有显著差异。一个包含5799名接受FCM治疗受试者的数据库提供了可接受的安全性资料,足以获批。机制研究表明,FCM给药后血清磷酸盐短暂、无症状的降低是由成纤维细胞生长因子23的诱导所致,而成纤维细胞生长因子23继而诱导肾脏磷酸盐排泄。铁调素水平升高可能有助于识别对口服铁剂无反应但对FCM有反应的IDA患者。能够分两次快速注射或输注FCM,可能会受到患者和医护人员的青睐。

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