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肥厚型梗阻性心肌病相关获得性血管性血友病综合征患者行间隔减少治疗后复发性胃肠道出血的缓解。

Remission of recurrent gastrointestinal bleeding after septal reduction therapy in patients with hypertrophic obstructive cardiomyopathy-associated acquired von Willebrand syndrome.

机构信息

Division of Cardiovascular Diseases, Mayo Clinic Florida, Jacksonville, FL, USA.

出版信息

J Thromb Haemost. 2015 Feb;13(2):191-6. doi: 10.1111/jth.12780. Epub 2014 Dec 12.

Abstract

BACKGROUND

Gastrointestinal hemorrhage is considered to be a severe complication of von Willebrand disease. The optimal therapy for acquired von Willebrand syndrome and severe gastrointestinal bleeding with hypertrophic cardiomyopathy is undefined.

PATIENTS/METHODS: Seventy-seven patients (median age, 67 years; interquartile range [IQR], 56-75 years; 49% women) with hypertrophic cardiomyopathy underwent von Willebrand factor multimer testing and acquisition of bleeding history. Bleeding was detected in 27 (36%) (median age, 74 years; IQR 66-76 years; 74% women), 20 with gastrointestinal bleeding, including 11 women with transfusion dependence. In these 11 women, the median duration of transfusion dependency was 36 months (IQR 18-44 months), and the median number of transfusions required was 25 (IQR 20-38). Two patients had undergone bowel resection for bleeding, one of them twice. Seven patients showed angiodysplasia, and the remainder had no endoscopic lesion. Bleeding recurred after bowel surgery or endoscopic intervention and medical therapy for hypertrophic cardiomyopathy in 10 of 11 patients. Two patients had septal myectomy, and six patients underwent alcohol septal ablation. With the exception of one patient in whom a significant gradient persisted after septal ablation, after the periprocedural period, patients after septal reduction therapy remained free of recurrent bleeding and need for transfusions.

CONCLUSION

Acquired von Willebrand syndrome is common in hypertrophic cardiomyopathy. Gastrointestinal bleeding often recurs after endoscopic therapy, but may be relieved by structural cardiac repair.

摘要

背景

胃肠道出血被认为是 von Willebrand 病的严重并发症。获得性 von Willebrand 综合征和伴有肥厚型心肌病的严重胃肠道出血的最佳治疗方法尚未确定。

患者/方法:77 例(中位年龄 67 岁;四分位距 [IQR],56-75 岁;49%为女性)肥厚型心肌病患者进行 von Willebrand 因子多聚体检测和出血史采集。27 例(36%)(中位年龄 74 岁;IQR 66-76 岁;74%为女性)检测到出血,其中 20 例有胃肠道出血,包括 11 例依赖输血。在这 11 例女性中,依赖输血的中位持续时间为 36 个月(IQR 18-44 个月),需要输注的中位数为 25(IQR 20-38)。2 例患者因出血而行肠切除术,其中 1 例患者行过 2 次肠切除术。7 例患者有血管扩张症,其余患者无内镜下病变。11 例患者中,10 例在肠手术后或内镜干预及肥厚型心肌病药物治疗后出现再出血,其中 2 例患者行室间隔心肌切除术,6 例患者行酒精室间隔消融术。除 1 例患者在室间隔消融术后仍存在明显梯度外,在围手术期后,接受室间隔减少治疗的患者未再出现复发性出血和输血需求。

结论

获得性 von Willebrand 综合征在肥厚型心肌病中很常见。胃肠道出血经内镜治疗后常复发,但结构性心脏修复可缓解出血。

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