Literature DB >> 23493319

Acute aortic dissection determines the fate of initially untreated aortic segments in Marfan syndrome.

Florian S Schoenhoff1, Silvan Jungi, Martin Czerny, Eva Roost, David Reineke, Gabor Matyas, Beat Steinmann, Juerg Schmidli, Alexander Kadner, Thierry Carrel.   

Abstract

BACKGROUND: The aim of the current study was to investigate incidence and causes of surgical interventions in primarily nontreated aortic segments after previous aortic repair in patients with Marfan syndrome. METHODS AND
RESULTS: Retrospective analysis of 86 consecutive Marfan syndrome patients fulfilling Ghent criteria that underwent 136 aortic surgeries and were followed at this institution in the past 15 years. Mean follow-up was 8.8±6.8 y. Thirty-day, 6-month, 1-year, and overall mortality was 3.5%, 5.8%, 7.0%, and 12.8%, respectively. Ninety-two percent of patients initially presented with aortic root, ascending aortic or arch lesions, whereas 8% presented with descending aortic or thoraco-abdominal lesions. Primary presentation was acute aortic dissection (AAD) in 36% (77% type A, 23% type B) and aneurismal disease in 64%. Secondary complete arch replacement had to be performed in only 6% of patients without AAD, but in 36% with AAD (P=0.0005). In patients without AAD, 11% required surgery on primarily nontreated aortic segments (5 of 6 patients experienced type B dissection during follow-up), whereas in patients after AAD, 48% underwent surgery of initially nontreated aortic segments (42% of patients with type A and 86% of those with type B dissection; P=0.0002).
CONCLUSIONS: The need for surgery in primarily nontreated aortic segments is precipitated by an initial presentation with AAD. Early elective surgery is associated with low mortality and reintervention rates. Type B dissection in patients with Marfan syndrome is associated with a high need for extensive aortic repair, even if the dissection is being considered uncomplicated by conventional criteria.

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Year:  2013        PMID: 23493319     DOI: 10.1161/CIRCULATIONAHA.113.001457

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  20 in total

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2.  Recurrent aortic dissection: a challenging but rare dilemma.

Authors:  Joshua M Rosenblum; Edward P Chen
Journal:  J Thorac Dis       Date:  2017-03       Impact factor: 2.895

3.  Marfan syndrome is the main independent predictor of recurrent aortic dissection in patients enrolled in the International Registry of Aortic Dissection (IRAD).

Authors:  Florian S Schoenhoff; Thierry P Carrel
Journal:  J Thorac Dis       Date:  2016-12       Impact factor: 2.895

4.  Type B aortic dissection triggered by heart transplantation in a patient with Marfan syndrome.

Authors:  Tjorven Audenaert; Michel De Pauw; Katrien François; Julie De Backer
Journal:  BMJ Case Rep       Date:  2015-10-16

5.  Natural history of Type B aortic dissection: ten tips.

Authors:  Bulat A Ziganshin; Julia Dumfarth; John A Elefteriades
Journal:  Ann Cardiothorac Surg       Date:  2014-05

6.  Re-interventions on the thoracic and thoracoabdominal aorta in patients with Marfan syndrome.

Authors:  Florian S Schoenhoff; Thierry P Carrel
Journal:  Ann Cardiothorac Surg       Date:  2017-11

Review 7.  Fever of unknown origin in aortic dissection.

Authors:  S-M Yuan
Journal:  Z Rheumatol       Date:  2017-05       Impact factor: 1.372

8.  Mid-term outcomes of cardiovascular surgery for patients with Marfan syndrome.

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Journal:  Gen Thorac Cardiovasc Surg       Date:  2014-12-19

Review 9.  Overview of current surgical strategies for aortic disease in patients with Marfan syndrome.

Authors:  Shunsuke Miyahara; Yutaka Okita
Journal:  Surg Today       Date:  2015-11-19       Impact factor: 2.549

10.  Total arch replacement and frozen elephant trunk for type A aortic dissection after Bentall procedure in Marfan syndrome.

Authors:  Yu Chen; Wei-Guo Ma; Jun Zheng; Yong-Min Liu; Jun-Ming Zhu; Li-Zhong Sun
Journal:  J Thorac Dis       Date:  2018-04       Impact factor: 2.895

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