Aortic dissection and pregnancy

被引：0

作者：

Roos-Hesselink, J. W. ^{[1
]}

Ruys, P. T. E. ^{[1
]}

Cuyper, J. A. A. E. ^{[1
]}

机构：

[1] Erasmus MC, Rotterdam, Netherlands

来源：

FIRST INTERNATIONAL CONGRESS ON CARDIAC PROBLEMS IN PREGNANCY (CPP) | 2010年

关键词：

CONGENITAL HEART-DISEASE; MARFAN-SYNDROME; VALVE; DILATATION; MANAGEMENT; ANEURYSMS;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Pregnancy is a high-risk period for women with aorta pathology, with dissection occurring most often in the last trimester of pregnancy or the early postpartum period. A patient of childbearing age with a family history of Marfan syndrome or other familial aorta pathology, should have a complete evaluation including imaging of the entire aorta before pregnancy. Prepregnancy repair of the dilated aorta should be performed patients with a diameter > 45 mm, especially in those with progressive aortic dilatation or a family history of aortic dissection.

引用

收藏

页码：53 / 58

页数：6

相关论文

共 19 条

[1]

[Anonymous], 2003, EUR HEART J, V24, P761

[2] EXTRACORPOREAL-CIRCULATION IN THE ISOLATED INSITU LAMB PLACENTA - HEMODYNAMIC CHARACTERISTICS [J].

ASSAD, RS ;

LEE, FY ;

BERGNER, K ;

HANLEY, FL .

JOURNAL OF APPLIED PHYSIOLOGY, 1992, 72 (06) :2176-2180

[3] Mechanisms underlying aortic dilatation in congenital aortic valve malformation [J].

Bonderman, D ;

Gharehbaghi-Schnell, E ;

Wollenek, G ;

Maurer, G ;

Baumgartner, H ;

Lang, IM .

CIRCULATION, 1999, 99 (16) :2138-2143

[4] Discussion: Session 4 - Descending/thoracoabdominal aorta [J].

Coselli, JS ;

Jacobs, M ;

Dion, R ;

Karck, M ;

Done, C ;

Elefteriades, JA ;

Kouchoukos, NT ;

Gill, IS .

ANNALS OF THORACIC SURGERY, 2002, 74 (05) :S1892-S1898

[5] Natural history of thoracic aortic aneurysms: Indications for surgery, and surgical versus nonsurgical risks [J].

Elefteriades, JA .

ANNALS OF THORACIC SURGERY, 2002, 74 (05) :S1877-S1880

[6] Vascular matrix remodeling in patients with bicuspid aortic valve malformations: Implications for aortic dilatation [J].

Fedak, PWM ;

de Sa, MP ;

Verma, S ;

Nili, N ;

Kazemian, P ;

Butany, J ;

Strauss, BH ;

Weisel, RD ;

David, TE .

JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2003, 126 (03) :797-806

[7] Aortic root replacement in 271 Marfan patients: A 24-year experience [J].

Gott, VL ;

Cameron, DE ;

Alejo, DE ;

Greene, PS ;

Shake, JG ;

Caparrelli, DJ ;

Dietz, HC .

ANNALS OF THORACIC SURGERY, 2002, 73 (02) :438-443

[8] Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome [J].

Habashi, JP ;

Judge, DP ;

Holm, TM ;

Cohn, RD ;

Loeys, BL ;

Cooper, TK ;

Myers, L ;

Klein, EC ;

Liu, GS ;

Calvi, C ;

Podowski, M ;

Neptune, ER ;

Halushka, MK ;

Bedja, D ;

Gabrielson, K ;

Rifkin, DB ;

Carta, L ;

Ramirez, F ;

Huso, DL ;

Dietz, HC .

SCIENCE, 2006, 312 (5770) :117-121

[9] Thoracic and abdominal aortic aneurysms [J].

Isselbacher, EM .

CIRCULATION, 2005, 111 (06) :816-828

[10] Outcome of pregnancy in women with Marfan's syndrome [J].

Lipscomb, KJ ;

Smith, JC ;

Clarke, B ;

Donnai, P ;

Harris, R .

BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1997, 104 (02) :201-206