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患有马凡综合征的孕妇急性A型主动脉夹层的手术治疗。

Surgery for acute type A aortic dissection in pregnant patients with Marfan syndrome.

作者信息

Sakaguchi Masayuki, Kitahara Hiroto, Seto Tatsuichiro, Furusawa Takehiko, Fukui Daisuike, Yanagiya Nobuyuki, Nishimura Kazunori, Amano Jun

机构信息

Department of Cardiovascular Surgery, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.

出版信息

Eur J Cardiothorac Surg. 2005 Aug;28(2):280-3; discussion 283-5. doi: 10.1016/j.ejcts.2005.02.047.

Abstract

OBJECTIVE

Acute type A aortic dissection during pregnancy can be fatal to both the mother and the fetus. The goal of the present study was to characterize the prevalence, treatment and outcomes of this dangerous condition in an effort to determine optimal management.

METHODS

A retrospective study was conducted using data from four Marfan patients with acute type A aortic dissection during pregnancy at our institution between 1991 and 2003.

RESULTS

The mean gestational period at the time of operative repair was 31 weeks, with a range of 26-34 weeks, and the aortic root diameter ranged from 35 to 85 mm. Two of the four patients underwent a combined operation with cesarean section followed by aortic repair. One patient underwent operative aortic repair following spontaneous delivery. The final patient underwent aortic repair with the fetus remaining in situ. Median sternotomy and cardiopulmonary bypass were established via the femoral artery with direct right atria drainage and left atrial venting in all patients. Composite graft replacement combined with re-implantation of the coronary artery and aortic valve replacement were performed in three patients, and aortic valve replacement with coronary artery bypass grafting of the right coronary artery was performed in one patient. Three of four patients underwent aortic arch repair utilizing antegrade cerebral perfusion and deep hypothermia with total circulatory arrest. The patient that underwent operative correction with the fetus remaining in situ experienced fetal demise with miscarriage just after cardiac surgery, and the patient died 4 days later secondary to disseminated intravascular coagulation and multi-organ failure. The remaining three cases recovered uneventfully, and the mothers and babies were discharged in good condition.

CONCLUSIONS

Based on these data, we advocate cesarean section with concomitant aortic repair for patients with Marfan syndrome and acute type A aortic dissection during pregnancy. Minimization of deep hypothermic circulatory arrest time is also recommended for cases in which the fetus remains in situ.

摘要

目的

妊娠期间发生的急性A型主动脉夹层对母亲和胎儿均可能致命。本研究的目的是描述这种危险情况的患病率、治疗方法及预后,以确定最佳治疗方案。

方法

采用回顾性研究方法,分析了1991年至2003年间在我院就诊的4例患有急性A型主动脉夹层的马凡综合征患者的资料。

结果

手术修复时的平均孕周为31周,范围为26 - 34周,主动脉根部直径为35至85毫米。4例患者中有2例接受了剖宫产联合主动脉修复手术。1例患者在自然分娩后接受了主动脉修复手术。最后1例患者在胎儿原位的情况下进行了主动脉修复。所有患者均通过股动脉建立正中胸骨切开术和体外循环,采用直接右心房引流和左心房排气。3例患者进行了复合移植物置换联合冠状动脉再植入及主动脉瓣置换,1例患者进行了主动脉瓣置换及右冠状动脉冠状动脉搭桥术。4例患者中有3例采用顺行脑灌注和深度低温并完全循环停止进行主动脉弓修复。在胎儿原位情况下接受手术矫正的患者在心脏手术后不久出现胎儿死亡并流产,该患者4天后因弥散性血管内凝血和多器官衰竭死亡。其余3例恢复顺利,母婴均健康出院。

结论

基于这些数据,我们主张对妊娠期间患有马凡综合征和急性A型主动脉夹层的患者进行剖宫产并同时进行主动脉修复。对于胎儿原位的病例,也建议尽量缩短深度低温循环停止时间。

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