Early and Long-Term Results of a Valve-Sparing Operation for Marfan Syndrome
- 9 November 1999
- journal article
- Published by Wolters Kluwer Health in Circulation
- Vol. 100 (Supplement) , II-29-29
- https://doi.org/10.1161/01.cir.100.suppl_2.ii-29
Abstract
Background—We have previously described the experience, rationale, and development of a valve preserving technique, but its role in patients with Marfan syndrome has not previously been defined. Here, we attempt to determine the early and long-term results, timing, and determinants of outcome of this operation in patients with Marfan syndrome. Methods and Results—Since 1979, 82 patients (73.2% of all patients with Marfan syndrome undergoing resection of aneurysm of the ascending aorta) were operated on using this technique. Ages ranged from 2 to 69 years (mean, 33.9 years). In all, there were 4 early deaths (4.9%), 2 with acute dissection and 2 with chronic aneurysm operated on as emergencies. There were no early deaths in 67 patients operated on electively. Actuarial survival for patients operated for chronic aneurysm was 94.2%, 94.2%, and 94.2% at 1, 5, and 10 years, respectively; that for acute dissection was 72.7%, 63.6%, and 63.6%; and that for chronic dissection was 100%, 85.7%, and 75.0%. The probability of needing reoperation was 5.7%, 17.3%, and 17.3% at 1, 5, and 10 years. There were no instances of infective endocarditis or thromboembolic complications except in 2 patients operated on early in the series who had cusp extension. At the end of the follow-up, trivial or no aortic regurgitation was demonstrated in 33.3%, mild in 45.6%, moderate in 21.1%, and severe in 0. Conclusions—Valve-sparing operations are feasible in most patients with Marfan syndrome; they are applicable to patients with both dissection and chronic aneurysm. The early and long-term results are encouraging. Results are better in the absence of dissection, and prophylactic operation is warranted in some cases.Keywords
This publication has 9 references indexed in Scilit:
- Replacement of the Aortic Root in Patients with Marfan's SyndromeNew England Journal of Medicine, 1999
- Late results of a valve-preserving operation in patients with aneurysms of the ascending aorta and rootThe Journal of Thoracic and Cardiovascular Surgery, 1998
- Marfan syndrome.Journal of Medical Genetics, 1996
- Aortic root replacement with a composite graft*Factors influencing immediate and long-term resultsEuropean Journal of Cardio-Thoracic Surgery, 1996
- The Marfan syndrome and the cardiovascular surgeonEuropean Journal of Cardio-Thoracic Surgery, 1996
- Progression of Aortic Dilatation and the Benefit of Long-Term β-Adrenergic Blockade in Marfan's SyndromeNew England Journal of Medicine, 1994
- Sixteen-year Experience With Aortic Root ReplacementAnnals of Surgery, 1991
- The Marfan Syndrome: Diagnosis and ManagementNew England Journal of Medicine, 1979
- A technique for complete replacement of the ascending aortaThorax, 1968