补铁治疗围手术期贫血患者血液管理

M. Muñoz, S. Gómez‐Ramírez, A. Campos
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引用次数: 6

摘要

在接受重大外科手术的患者中,术前贫血和围手术期异基因输血(ABT)与术后发病率和死亡率增加以及住院时间延长有关。一种多学科、多模式、个性化的策略-统称为患者血液管理-用于减少或消除ABT,以改善结果。这一新的护理标准依赖于围手术期贫血的检测和治疗(支柱1)以及减少手术失血量和围手术期凝血功能障碍(支柱2),以利用和优化贫血的生理耐受性(支柱3),从而允许使用限制性输血标准。术前血红蛋白水平正常化是世界卫生组织的建议。如有需要,应常规补铁。在已发表的试验中,术前口服铁耗时且耐受性差,依从性低。术后口服铁已被证明是无效的,不再推荐。术前和围手术期静脉注射铁,无论是否使用促红细胞生成素,在降低ABT率和加速术后贫血恢复方面都是安全有效的。静脉注射铁似乎不会增加术后血栓栓塞、感染或死亡的风险。较新的静脉注射铁制剂显示出潜在的低得多的免疫原性活性,允许在15至60分钟内完全替代剂量,显着促进护理,并且在许多临床环境中可能具有成本效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Iron Supplementation for Perioperative Anaemia in Patient Blood Management
In patients undergoing major surgical procedures, preoperative anaemia and perioperative allogeneic blood transfusion (ABT) have been linked to increased postoperative morbidity and mortality, as well as longer hospital stays. A multidisciplinary, multimodal, individualised strategy – collectively termed patient blood management – used to minimise or eliminate ABT is indicated to improve outcomes. This new standard of care relies on detection and treatment of perioperative anaemia (Pillar 1) and reduction of surgical blood loss and perioperative coagulopathy (Pillar 2) to harness and optimise physiological tolerance of anaemia (Pillar 3), thus allowing the use of restrictive transfusion criteria. Normalisation of preoperative hemoglobin levels is a World Heath Organization recommendation. Iron repletion should be routinely ordered when indicated. Preoperative oral iron is time-consuming and poorly tolerated with low adherence in published trials. Postoperative oral iron has been proven to be inefficacious and is no longer recommended. Preoperative and perioperative intravenous iron, with or without erythropoiesis stimulating agents, is safe and effective at reducing ABT rate and hastening the recovery from postoperative anaemia. Intravenous iron does not seem to increase the risk for postoperative thromboembolism, infection, or mortality. Newer intravenous iron formulations demonstrate potentially much lower immunogenic activity, allow complete replacement dosing in 15 to 60 minutes, markedly facilitating care, and may be cost-effective in many clinical settings.
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