Division of Internal Medicine, Stanford University, Stanford, CA 94305-5114, USA.
Am J Kidney Dis. 2010 Jan;55(1):148-51. doi: 10.1053/j.ajkd.2009.06.013. Epub 2009 Jul 23.
Intravenous immunoglobulin (IVIG), a product initially developed for patients with immunodeficiencies, now has multiple other indications and increasing off-label use. IVIG generally is well tolerated, with few adverse effects. Antibody-mediated (Coombs-positive) hemolysis is known to occur after IVIG infusion, but often is subclinical and previously has not been reported to lead to acute kidney injury (AKI). The predominantly known mechanism of AKI after IVIG infusion has been osmotic nephrosis, primarily associated with sucrose-containing formulations. We present a case of a bone marrow transplant recipient who was treated with a sucrose-free IVIG product and subsequently developed Coombs-positive hemolysis leading to AKI requiring hemodialysis, who ultimately died secondary to infectious complications. The severity of this case emphasizes the importance of identifying populations who may be at increased risk of pigment-mediated kidney injury before consideration of IVIG therapy.
静脉注射免疫球蛋白(IVIG)最初是为免疫缺陷患者开发的一种产品,现在有多种其他适应症和越来越多的非适应证使用。IVIG 通常耐受性良好,不良反应很少。已知在 IVIG 输注后会发生抗体介导的(抗球蛋白阳性)溶血,但通常是亚临床的,以前没有报道导致急性肾损伤(AKI)。IVIG 输注后 AKI 的主要已知机制是渗透压肾病,主要与含有蔗糖的制剂有关。我们报告了一例骨髓移植受者的病例,该患者接受了无蔗糖 IVIG 产品治疗,随后发生抗球蛋白阳性溶血导致 AKI,需要血液透析,最终因感染并发症死亡。该病例的严重程度强调了在考虑 IVIG 治疗之前,确定可能增加色素介导的肾脏损伤风险的人群的重要性。