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Eur J Cardiothorac Surg 2006;29:1061-1063
© 2006 Elsevier Science NL
Case report |
a Department of Cardio-Vascular Surgery, National CardioVascular Center, Suita, Osaka, 5-7-1 Fujishirodai, Suita, Osaka 565-8565, Japan
b Department of Obstetrics, National CardioVascular Center, Suita, Osaka, Japan
Received 12 November 2005; received in revised form 2 March 2006; accepted 13 March 2006.
* Corresponding author. Tel.: +81 6 6833 5012; fax: +81 6 6872 7486. (Email: hitmat{at}hsp.ncvc.go.jp).
A 20-year-old woman with Marfan syndrome in the 19 weeks of pregnancy was admitted for a dissecting aneurysm of the ascending aorta to the proximal arch. She wanted to continue with pregnancy. A cardiotocography and a trans-esophageal echo probe which allowed visualization of the fetal heart contraction were attached on the abdomen. A cardio-pulmonary bypass was established via the right axillar and femoral arteries with bicaval drainage. The aortic isthmus and arch branches were clamped. After opening the ascending aorta, selective cerebral perfusion was initiated by quick cannulation into the left carotid and left subclavian arteries. Peripheral pressure was maintained above 80 mmHg with the flow of the selective cerebral perfusion at 1.0 L/min and flow from the femoral artery at 3.5 L/min. Hemi-arch replacement was performed using a Dacron graft. The body temperature passively descended to 35 °C. She normally delivered a healthy female baby after 37 weeks of gestation.
Key Words: Dissecting aortic aneurysm Pregnancy Cerebral perfusion
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