Literature DB >> 19769881

Long-term results of aortic valve-sparing operations in patients with Marfan syndrome.

Tirone E David1, Sue Armstrong, Manjula Maganti, Jack Colman, Timothy J Bradley.   

Abstract

OBJECTIVE: The appropriateness of aortic valve-sparing operations in patients with Marfan syndrome has been questioned. This study examines the long-term results of these operations in patients with Marfan syndrome.
METHODS: From 1988 to 2006, 103 consecutive patients with Marfan syndrome (mean age, 37 +/- 12 years) and aortic root aneurysm had aortic valve-sparing operations. Emergency surgery was performed in 11 patients: 8 for acute type A aortic dissection and 3 for unexplained persistent chest pain. Fourteen patients also had mitral valve surgery. The technique of aortic valve reimplantation was used in 77 patients, and aortic root remodeling was used in 26 patients. Patients were followed prospectively and underwent annual echocardiographic studies. The mean follow-up was 7.3 +/- 4.2 years and 100% complete.
RESULTS: There was 1 operative death and 5 late deaths. Four of the 6 deaths were due to complications of aortic dissections. The patients' survival at 15 years was 87.2% compared with 95.6% for the general population of Ontario matched for age and sex. Seven patients had important aortic insufficiency: 4 mild to moderate, 2 moderate, and 1 moderate to severe. Freedom from greater than mild aortic insufficiency at 15 years was 79.2%. Three patients, all after aortic root remodeling, had aortic valve replacement, 2 for aortic insufficiency and 1 for endocarditis. At the most recent follow-up, 97 patients were alive: 86 were in functional class I, and 11 were in functional class II.
CONCLUSIONS: Aortic valve-sparing operations provided excellent clinical outcomes in this series of patients with Marfan syndrome. Postoperatively, complications of aortic dissections were the leading cause of death.

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Year:  2009        PMID: 19769881     DOI: 10.1016/j.jtcvs.2009.06.014

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  17 in total

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Review 2.  Marfan syndrome. Part 2: treatment and management of patients.

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Authors:  Masato Tochii; Koji Hattori; Hiroshi Ishikawa; Michiko Ishida; Yoshiro Higuchi; Kentaro Amano; Yusuke Sakurai; Mika Noda; Takashi Watanabe; Yasushi Takagi
Journal:  Gen Thorac Cardiovasc Surg       Date:  2014-12-19

6.  Valve-sparing aortic root replacement in patients with Marfan syndrome enrolled in the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions.

Authors:  Howard K Song; Liliana R Preiss; Cheryl L Maslen; Barbara Kroner; Richard B Devereux; Mary J Roman; Kathryn W Holmes; H Eser Tolunay; Patrice Desvigne-Nickens; Federico M Asch; Rita K Milewski; Joseph Bavaria; Scott A LeMaire
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7.  Simultaneous individually controlled upper and lower body perfusion for valve-sparing root and total aortic arch replacement: a case study.

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8.  Aortic valve sparing operations: a review.

Authors:  Tirone E David
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Review 9.  Surgical treatment of aortic valve disease.

Authors:  Tirone E David
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