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系统性 AL 淀粉样变性伴获得性因子 X 缺乏症:60 例患者围手术期出血风险和治疗结局研究。

Systemic AL amyloidosis with acquired factor X deficiency: A study of perioperative bleeding risk and treatment outcomes in 60 patients.

机构信息

Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

出版信息

Am J Hematol. 2010 Mar;85(3):171-3. doi: 10.1002/ajh.21603.

Abstract

Systemic light-chain (AL) amyloidosis may be associated with acquired factor X (FX) deficiency and optimal management of this coagulopathy is unknown. We reviewed our experience with 60 patients with isolated FX deficiency (< or =50%) due to AL amyloidosis that underwent an invasive procedure between 1975 and 2007. They were classified as having severe (<10%; n = 6), moderate (10-25%; n = 15), or mild (26-50%; n = 39) FX deficiency. The patients underwent a total of 112 procedures, 19 (17%) of which were managed with periprocedural treatment with one or more hemostatic agents. There were complications in 14 (13%) procedures (bleeding = 12, thrombosis = 1, death = 1). Baseline FX level was not predictive of bleeding risk; the only association with postintervention bleeding was central venous catheter placement. However, bleeding complications were relatively infrequent, particularly in patients with mild or moderate FX deficiency undergoing nonvascular procedures. Activated recombinant factor VII might be considered in patients undergoing major surgical procedures, but further experience is needed. Optimal management of AL patients with FX deficiency undergoing invasive procedures remains to be determined.

摘要

系统性轻链(AL)淀粉样变性可能与获得性因子 X(FX)缺乏有关,目前尚不清楚这种凝血异常的最佳治疗方法。我们回顾了 1975 年至 2007 年间 60 例因 AL 淀粉样变性导致孤立性 FX 缺乏症(<或=50%)的患者的治疗经验,这些患者接受了侵入性操作。根据 FX 缺乏症的严重程度,将他们分为 3 组:严重组(<10%,n=6)、中度组(10-25%,n=15)和轻度组(26-50%,n=39)。这些患者共接受了 112 次操作,其中 19 次(17%)在围手术期使用了一种或多种止血剂进行处理。14 次操作(13%)出现了并发症(出血=12 次,血栓形成=1 次,死亡=1 次)。FX 基础水平不能预测出血风险;与术后出血唯一相关的因素是中心静脉置管。然而,出血并发症相对较少,特别是在接受非血管操作的轻度或中度 FX 缺乏症患者中。对于接受重大手术的患者,可以考虑使用活化的重组因子 VII,但还需要更多的经验。对于接受侵入性操作的 FX 缺乏症的 AL 患者,最佳的管理方法仍有待确定。

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