Type A aortic dissection during late pregnancy in a patient with Marfan syndrome

被引:5
|
作者
Haas, Sebastian [1 ]
Trepte, Constantin [1 ]
Rybczynski, Maike [2 ]
Somville, Thierry [3 ]
Treede, Hendrik [4 ]
Reuter, Daniel A. [1 ]
机构
[1] Hamburg Eppendorf Univ, Dept Anesthesiol, Ctr Anesthesiol & Intens Care Med, Med Ctr, D-20246 Hamburg, Germany
[2] Hamburg Eppendorf Univ, Dept Gen & Intervent Cardiol, Med Ctr, D-20246 Hamburg, Germany
[3] Hamburg Eppendorf Univ, Dept Obstet & Fetal Med, Med Ctr, D-20246 Hamburg, Germany
[4] Hamburg Eppendorf Univ, Dept Cardiovasc Surg, Med Ctr, D-20246 Hamburg, Germany
关键词
ROOT REPLACEMENT;
D O I
10.1007/s12630-011-9569-4
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
To report the management of a 38-yr-old patient with known Marfan syndrome who presented with acute Stanford type A dissection of the aorta in the 34(th) week of pregnancy. A Cesarean delivery was performed under deep general anesthesia with high-dose opioid administration to avoid tachycardia and hypertension during tracheal intubation and obstetric surgery. Delivery took place less than five minutes after induction of anesthesia, and tracheal intubation of the newborn was required due to opioid-induced hypoventilation. Subsequently, aortic arch repair was performed in the mother after connection to extracorporal bypass. Despite extensive replacement of coagulation factors, severe vaginal bleeding persisted after weaning from extracorporal bypass, and the bleeding stopped only after a hysterectomy was performed. Postoperatively, after a short period in the intensive care unit, mother and child were discharged from hospital in excellent condition ten days after surgery. Deep general anesthesia for emergency Cesarean delivery while accepting the risk of respiratory depression in the newborn is a viable option for the anesthetic management of life-threatening events such as Stanford type A dissection.
引用
收藏
页码:1024 / 1028
页数:5
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