Literature DB >> 11722033

Aortic root replacement in patients with Marfan's syndrome: the Southampton experience.

C Alexiou1, S M Langley, P Charlesworth, M P Haw, S A Livesey, J L Monro.   

Abstract

BACKGROUND: The purpose of this study was to evaluate the early and late clinical outcome after aortic root replacement (ARR) in patients with Marfan's syndrome.
METHODS: A total of 65 consecutive patients with Marfan's syndrome (mean age 41.7 +/- 10.7 years, range 15 to 76 years) undergoing ARR between 1972 and 1998 in Southampton were studied. Of the patients, 45 had a chronic aneurysm of the ascending aorta and 20 had a type A dissection (16 acute and 4 chronic). The operations were elective in 38 and nonelective in 27 cases (emergency in 22 and urgent in 5). Mean size of the ascending aorta was 6.3 +/- 1.4 cm (3.8 to 12 cm). A Bentall procedure was performed in 62 and a homograft root replacement in 3 patients. Mean follow-up was 8 +/- 4.1 years (0 to 22.9 years).
RESULTS: Operative mortality was 6.1% (4 deaths) (for the elective vs nonelective procedures it was 2.6% vs 11%, p = 0.2). The 10-year freedom from thromboembolism, hemorrhage, and endocarditis was 88%, 89.8%, and 98.4% (0.9%, 0.9%, and 0.2% per patient-year) and from late aortic events it was 86.3% (1.3% per patient-year). Aortic root replacement for dissection was an independent predictor of occurrence of late aortic events (p = 0.01). Five patients had a reoperation with one early death. The 10-year freedom from reoperation was 89.2% (1.1% per patient year) (for elective and nonelective procedures, 90.8% vs 84.6%, p = 0.6). The 10-year survival, including operative mortality, was 72.7% (for elective and nonelective procedures, 78% vs 66.5%, p = 0.6). Late aortic events was an independent adverse predictor of survival (p = 0.02).
CONCLUSIONS: In patients with Marfan's syndrome, elective ARR, usually for chronic aneurysm, is associated with a low mortality, low rate of aortic complications, and good late survival. Nonelective ARR, mostly for dissection, has a greater operative risk and a significantly higher incidence of late catastrophic aortic events. Early prophylactic surgery in these patients is therefore recommended. Long-term clinical and radiologic follow-up to prevent or to treat late aortic events is highly desirable.

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Year:  2001        PMID: 11722033     DOI: 10.1016/s0003-4975(01)02993-9

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  3 in total

1.  Comparison of clinical characteristics and frequency of adverse outcomes in patients with Marfan syndrome diagnosed in adulthood versus childhood.

Authors:  Lisa Willis; Genie E Roosevelt; Anji T Yetman
Journal:  Pediatr Cardiol       Date:  2009-01-30       Impact factor: 1.655

Review 2.  Systematic review and meta-analysis of surgical outcomes in Marfan patients undergoing aortic root surgery by composite-valve graft or valve sparing root replacement.

Authors:  Campbell D Flynn; David H Tian; Ashley Wilson-Smith; Tirone David; George Matalanis; Martin Misfeld; Stefano Mastrobuoni; Gebrine El Khoury; Tristan D Yan
Journal:  Ann Cardiothorac Surg       Date:  2017-11

Review 3.  Current role of endovascular therapy in Marfan patients with previous aortic surgery.

Authors:  Ibrahim Akin; Stephan Kische; Tim C Rehders; Tushar Chatterjee; Henrik Schneider; Thomas Körber; Christoph A Nienaber; Hüseyin Ince
Journal:  Vasc Health Risk Manag       Date:  2008
  3 in total

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