Original article
Adult cardiac
Dilatation of the Remaining Aorta After Aortic Valve or Aortic Root Replacement in Patients With Bicuspid Aortic Valve: A 5-Year Follow-Up

https://doi.org/10.1016/j.athoracsur.2013.03.086Get rights and content

Background

The natural history and management of ascending aorta (AA) and arch dilatation in patients with bicuspid aortic valve (BAV) after aortic valve replacement (AVR) or aortic root replacement (ARR) remains controversial. Our aim is to identify dilatation of the remaining aorta after AVR or ARR in patients with BAV compared with patients with tricuspid aortic valve (TAV).

Methods

Three hundred ninety-five patients who underwent AVR or ARR between 2002 and 2009 were studied. Preoperative computed tomography (CT) and echocardiography were performed in 192 patients with BAV, and the results were compared with those of 203 patients with TAV. An AA diameter 4.5 cm or greater was regarded as aneurysmal. Postoperative echocardiograms, computed tomographic scans, and magnetic resonance images were compared with subsequent imaging at a median follow-up of 4.6 years (2.2–9.8 years).

Result

Median ages of patients with BAV and patients with TAV were 57 ± 14 and 65 ± 16 years, respectively (p < 0.05). Preoperative diameter of AA in the BAV group with no aneurysm (3.5 cm; range, 3.0–4.0 cm; n = 143) was significantly higher than in the TAV group (3.3 cm; range, 3.1–3.8 cm; n = 129) (p < 0.001). In both BAV and TAV groups with nonaneurysmal aortas who underwent AVR, there was no significant expansion of the AA and arch at 5 years' follow-up. In patients with aneurysmal aorta (BAV group, n = 49; TAV group, n = 74) who underwent ARR, there was also no significant difference in growth of the remaining aorta at 3 and 5 years' follow-up.

Conclusions

No significant dilatation of the AA or arch was observed after AVR or ARR, respectively, in patients when a cut-off diameter of 4.5 cm or greater was considered for replacement in patients with BAV compared with patients with TAV up to 5 years after operation. The need for aortic replacement at smaller diameters was not found.

Section snippets

Study Design

From January 2002 to December 2009, 395 consecutive patients who were operated on under the care of 1 surgeon and underwent AVR or ARR, or both, were studied. Patients with known connective tissue disorders, eg, Marfan's syndrome, were excluded from the study. Familial screening was not systematically performed when familial aortopathies existed; however, those patients were not excluded from the study. Younger patients with functionally normal BAVs underwent valve-preserving procedures and

Results

From a total of 395 patients, 203 had TAV and 192 had BAV. In the BAV group, 12 patients had AVR with supracoronary AA replacement and 37 patients had ARR. In the TAV group, 49 patients had AVR with supracoronary AA replacement and 25 had ARR (Fig 1). Concomitant coronary artery bypass grafting (CABG) was performed in 36 (25%) patients with BAV, 4 patients (8.2%) with BAV and aortic aneurysm (AA-BAV), 70 (54.2%) patients with TAV, and 10 (13.5%) patients with TAV and aortic aneurysm (AA-TAV).

Comment

In this study, patients with BAV and an AA absolute diameter of 4.5 cm or greater and a dilated root underwent ARR. This was a uniform policy. We have shown that there was no significant difference in morbidity and mortality comparing AVR with ARR in patients with BAV and that no patient with an aortic diameter of less than 4.5 cm required operation for dissection or resection of aneurysm during follow-up. Also, no patient required surgical intervention for the arch.

These findings concur with

References (20)

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