Type A aortic dissection in Marfan syndrome: extent of initial surgery determines long-term outcome.
Publication/Presentation Date
4-1-2014
Abstract
BACKGROUND: Data on outcomes after Stanford type A aortic dissection in patients with Marfan syndrome are limited. We investigated the primary surgery and long-term results in patients with Marfan syndrome who suffered aortic dissection.
METHODS AND RESULTS: Among 1324 consecutive patients with aortic dissection type A, 74 with Marfan syndrome (58% men; median age, 37 years [first and third quartiles, 29 and 48 years]) underwent surgical repair (85% acute dissections; 68% DeBakey I; 55% composite valved graft, 30% supracoronary ascending replacement, 15% valve-sparing aortic root replacement; 12% total arch replacement; 3% in-hospital mortality) at 2 tertiary centers in the United States and Europe over the past 25 years. The rate of aortic reintervention with resternotomy was 24% (18 of 74) and of descending aorta (thoracic+abdominal) intervention was 30% (22 of 74) at a median follow-up of 8.4 years (first and third quartiles, 2.2 and 12.7 years). Freedom from need for aortic root reoperation in patients who underwent primarily a composite valved graft or valve-sparing aortic root replacement procedure was 95±3%, 88±5%, and 79±5% and in patients who underwent supracoronary ascending replacement was 83±9%, 60±13%, 20±16% at 5, 10, and 20 years. Secondary aortic arch surgery was necessary only in patients with initial hemi-arch replacement.
CONCLUSIONS: Emergency surgery for type A dissection in patients with Marfan syndrome is associated with low in-hospital mortality. Failure to extend the primary surgery to aortic root or arch repair leads to a highly complex clinical course. Aortic root replacement or repair is highly recommended because supracoronary ascending replacement is associated with a high need (>40%) for root reintervention.
Volume
129
Issue
13
First Page
1381
Last Page
1386
ISSN
1524-4539
Published In/Presented At
Rylski, B., Bavaria, J. E., Beyersdorf, F., Branchetti, E., Desai, N. D., Milewski, R. K., Szeto, W. Y., Vallabhajosyula, P., Siepe, M., & Kari, F. A. (2014). Type A aortic dissection in Marfan syndrome: extent of initial surgery determines long-term outcome. Circulation, 129(13), 1381–1386. https://doi.org/10.1161/CIRCULATIONAHA.113.005865
Disciplines
Medicine and Health Sciences
PubMedID
24594630
Department(s)
Department of Surgery
Document Type
Article