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重度甲型血友病患者心脏外科手术围术期凝血管理:一例报告

Peri-cardiac surgery coagulation management in a severe hemophilia A patient: A case report.

作者信息

Xu Hongfei, Henry Davies, Li Chengcheng, Zhao Haige, Yang Yanyan

机构信息

Department of Cardiothoracic Surgery.

Department of pharmacy, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Medicine (Baltimore). 2019 Jun;98(24):e15897. doi: 10.1097/MD.0000000000015897.

Abstract

RATIONALE

Hemophilia A (HA) is an X-linked recessive disorder caused by clotting factor VIII (FVIII) deficiency. There is limited data on the use of replacement therapy in cardiac surgery. Since no international guideline for anticoagulation in such patient exists, careful thought should be taken to design an individualized anticoagulation strategy.

PATIENT CONCERNS

We report a 54-year-old male with severe HA with FVIII activity of 0.8% when he was first diagnosed, who underwent successful mitral valve repair and coronary artery bypass graft with FVIII replacement perioperatively.

DIAGNOSES

Transthoracic echocardiography and coronary angiography confirmed the HA patient with the diagnosis of severe mitral valve regurgitation and left anterior descending artery stenosis.

INTERVENTIONS

Before surgery, a bolus of 1000 IU FVIII was injected, which obtained an FVIII of 80%. After induction, a 3750 IU bolus of FVIII was injected and subsequent FVIII level reached 135%. Mitral valve repair and coronary artery bypass graft with FVIII replacement were performed. After the surgery, a repeat FVIII activity level was 50.6%. The 400 mL of autologous blood and 700 mL of cardiopulmonary bypass (CPB) machine blood was returned to the patient as well as 4 units of fresh frozen plasma with an additional bolus of 1000 IU FVIII. 100 mg aspirin per day alone was given after surgery.

OUTCOMES

The patient recovered uneventfully and 1-year follow-up showed no complications.

LESSONS

The anticoagulant or antiplatelet regimen of HA patient following surgery should be individualized based on the evaluation of the risk factors for bleeding and thrombosis and the lowest FVIII activity ever recorded after FVIII replacement therapy.

摘要

理论依据

甲型血友病(HA)是一种由凝血因子VIII(FVIII)缺乏引起的X连锁隐性疾病。关于心脏手术中替代疗法的应用数据有限。由于目前尚无针对此类患者抗凝的国际指南,因此在设计个体化抗凝策略时应慎重考虑。

患者情况

我们报告一例54岁男性重度HA患者,初诊时FVIII活性为0.8%,该患者在围手术期接受FVIII替代治疗,成功进行了二尖瓣修复术和冠状动脉旁路移植术。

诊断

经胸超声心动图和冠状动脉造影确诊该HA患者患有重度二尖瓣反流和左前降支动脉狭窄。

干预措施

手术前,注射1000 IU FVIII推注剂量,使FVIII水平达到80%。诱导后,注射3750 IU FVIII推注剂量,随后FVIII水平达到135%。进行了二尖瓣修复术和冠状动脉旁路移植术并给予FVIII替代治疗。手术后,重复检测FVIII活性水平为50.6%。将400 mL自体血和700 mL体外循环(CPB)机血回输给患者,并输注4单位新鲜冰冻血浆以及额外1000 IU FVIII推注剂量。术后仅给予每天100 mg阿司匹林。

结果

患者恢复顺利,1年随访未出现并发症。

经验教训

HA患者术后的抗凝或抗血小板方案应根据出血和血栓形成的危险因素评估以及FVIII替代治疗后记录到的最低FVIII活性进行个体化制定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/651c/6587658/527c793aac8a/medi-98-e15897-g001.jpg

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