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治疗性血浆置换似乎对骨髓移植后血栓性血小板减少性紫癜/溶血性尿毒症综合征的治疗无效。

Therapeutic plasma exchange does not appear to be effective in the management of thrombotic thrombocytopenic purpura/hemolytic uremic syndrome following bone marrow transplantation.

作者信息

Sarode R, McFarland J G, Flomenberg N, Casper J T, Cohen E P, Drobyski W R, Ash R C, Horowitz M M, Camitta B, Lawton C

机构信息

Blood Center of Southeastern Wisconsin, Milwaukee 53233-2194, USA.

出版信息

Bone Marrow Transplant. 1995 Aug;16(2):271-5.

PMID:7581147
Abstract

Recognition of thrombotic thrombocytopenic purpura (TTP)/hemolytic uremic syndrome (HUS) following BMT has increased in recent years. The pathogenesis and etiology may be related to endothelial cell damage secondary to irradiation and/or CsA. Optimal management of this condition remains unclear. Due to similarity between this syndrome and classical TTP, patients with TTP/HUS following BMT are commonly treated with therapeutic plasma exchange (TPE). We describe our experience with 9 such patients who were treated with TPE (8 cases) and immunoadsorption with a Staphylococcal Protein A column (1 case). The exchanges were done with fresh frozen plasma and/or cryoprecipitate-depleted frozen plasma. Out of 8 patients treated with TPE, 6 died within 2 months of TPE due to secondary infections, metabolic disturbances and progression of TTP/HUS. Of these 6 patients, 5 had no hematological response, while 1 had hematological improvement. Two patients are alive 4 and 3 years later, however, they had shown only minimal hematological response at the end of 28 and 20 TPE, respectively. Their renal function remains stable but severely reduced. The ninth patient who received Staphylococcal Protein A column treatment died within 5 days of treatment without hematological improvement. Thus, in contrast to its effectiveness in classical TTP, TPE does not appear to be as effective in the management of well established TTP/HUS following BMT.

摘要

近年来,骨髓移植(BMT)后血栓性血小板减少性紫癜(TTP)/溶血尿毒症综合征(HUS)的诊断率有所上升。其发病机制和病因可能与放疗和/或环孢素A(CsA)继发的内皮细胞损伤有关。目前,针对这种情况的最佳治疗方案仍不明确。由于该综合征与经典TTP相似,BMT后发生TTP/HUS的患者通常接受治疗性血浆置换(TPE)。我们描述了9例此类患者的治疗经验,其中8例接受了TPE治疗,1例接受了葡萄球菌蛋白A柱免疫吸附治疗。置换液采用新鲜冰冻血浆和/或去除冷沉淀的冰冻血浆。在接受TPE治疗的8例患者中,6例在TPE治疗后2个月内死亡,原因是继发感染、代谢紊乱以及TTP/HUS病情进展。这6例患者中,5例无血液学反应,1例有血液学改善。2例患者分别在4年和3年后存活,但在28次和20次TPE治疗结束时,仅表现出轻微的血液学反应。他们的肾功能保持稳定,但严重受损。接受葡萄球菌蛋白A柱治疗的第9例患者在治疗后5天内死亡,且无血液学改善。因此,与TPE在经典TTP中的有效性相反,TPE在治疗BMT后确诊较久的TTP/HUS时似乎效果不佳。

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