Literature DB >> 21817813

Pregnancy-associated aortic dilatation or dissection in Japanese women with Marfan syndrome.

Shinji Katsuragi1, Keiko Ueda, Kaoru Yamanaka, Reiko Neki, Chizuko Kamiya, Yoshihito Sasaki, Kazuhiro Osato, Koichiro Niwa, Tomoaki Ikeda.   

Abstract

BACKGROUND: Aortic dilatation and dissection are severe complications of pregnancy that may cause maternal death. The purpose of the present study was to investigate risk factors for aortic dilatation or dissection in pregnant Japanese women with Marfan syndrome. METHODS AND
RESULTS: A total of 28 patients with Marfan syndrome were investigated retrospectively during pregnancy and after delivery at 1 institution. These patients were divided into 2 groups: those who experienced aortic dilatation or dissection (group D, n=11) and those who did not (group ND, n = 17). In group D, aortic dilatation or dissection occurred in 7 cases during pregnancy (2 in the 2(nd) trimester, 5 in the 3(rd) trimester) and 4 cases after birth. The 2 cases in the 2nd trimester involved aortic dilatation > 60mm and those patients underwent hemiarch replacement and a David operation, respectively. Delivery by cesarean section (64% vs. 18%, P < 0.05), sinus of Valsalva ≥ 40mm (86% vs. 21%, P < 0.05), aortic size index (size of sinus of Valsalva/body surface area) ≥ 25 mm/m² (7/7, 100% vs. 0/14, 0%, P < 0.0001), and faster growth of the sinus of the Valsalva (median, [interquartile range]: 0.41 mm/month [0.23-0.66 mm/month] vs. 0.05 mm/month [-0.13 to 0.22 mm/month]; P < 0.05) were significantly higher in group D than in group ND.
CONCLUSIONS: A large sinus of Valsalva, increased aortic size index, and rapid growth of the sinus of Valsalva are risk factors for aortic dilatation or dissection in pregnant Japanese women with Marfan syndrome.

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Year:  2011        PMID: 21817813     DOI: 10.1253/circj.cj-11-0465

Source DB:  PubMed          Journal:  Circ J        ISSN: 1346-9843            Impact factor:   2.993


  8 in total

Review 1.  Aortic dilatation in complex congenital heart disease.

Authors:  Koichiro Niwa
Journal:  Cardiovasc Diagn Ther       Date:  2018-12

2.  Pregnancy and Marfan syndrome.

Authors:  Sorel Goland; Uri Elkayam
Journal:  Ann Cardiothorac Surg       Date:  2017-11

Review 3.  Preconception Counseling for Patients With Thoracic Aortic Aneurysms.

Authors:  Prashant Rao; Eric M Isselbacher
Journal:  Curr Treat Options Cardiovasc Med       Date:  2018-05-10

4.  Marfan syndrome and pregnancy: maternal and neonatal outcomes.

Authors:  R A Curry; E Gelson; L Swan; D Dob; S V Babu-Narayan; M A Gatzoulis; P J Steer; M R Johnson
Journal:  BJOG       Date:  2014-01-13       Impact factor: 6.531

Review 5.  Adult Congenital Heart Disease with Pregnancy.

Authors:  Koichiro Niwa
Journal:  Korean Circ J       Date:  2018-04       Impact factor: 3.243

6.  Rupture of a Type B Aortic Dissection in a Postpartum Patient with Marfan Syndrome.

Authors:  Elizabeth Patberg; Jennifer Duffy; Afshan B Hameed
Journal:  AJP Rep       Date:  2019-08-20

7.  Acute Type A Dissection during Pregnancy with Marfan's Syndrome.

Authors:  Christian Heim; Philipp P Müller; Michael Weyand; Frank Harig
Journal:  Thorac Cardiovasc Surg Rep       Date:  2021-03-11

8.  Preimplantation genetic diagnosis in marfan syndrome.

Authors:  N F Vlahos; O Triantafyllidou; N Vitoratos; C Grigoriadis; G Creatsas
Journal:  Case Rep Obstet Gynecol       Date:  2013-05-27
  8 in total

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