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Late outcomes in adults with coarctation of the aorta
  1. P Choudhary1,2,3,
  2. C Canniffe1,4,
  3. D J Jackson1,2,
  4. D Tanous1,3,
  5. K Walsh4,
  6. D S Celermajer1,2
  1. 1Department of Cardiology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia
  2. 2Discipline of Medicine, Central Clinical School, University of Sydney, Sydney, New South Wales, Australia
  3. 3Department of Cardiology, Westmead Hospital, Sydney, New South Wales, Australia
  4. 4Department of Cardiology, Mater Misericordiae Hospital, Dublin, Ireland
  1. Correspondence to Professor D S Celermajer, Department of Cardiology, Royal Prince Alfred Hospital, Camperdown, Sydney, NSW 2050, Australia; david.celermajer{at}email.cs.nsw.gov.au

Abstract

Aims Previous cohort studies of patients with coarctation of the aorta (CoA) demonstrate reduced long-term survival. Improved surgical outcomes in children and evolution of adult congenital heart disease (ACHD) services have resulted in improved survival in patients with other CHDs. We hypothesise that for young adult patients with CoA long-term outcomes have improved in the contemporary era.

Methods 151 patients (58% men) with simple CoA followed up at a tertiary ACHD service in Sydney, Australia, from 1993 to 2013 were included. We documented mortality and major morbidity such as the need for re-intervention for re-coarctation or aneurysms.

Results 140 patients (mean age 35±15 years) underwent CoA repair at median age of 5 (IQR 0–10) years. Initial surgical strategy included end-to-end repair in 43, subclavian flap aortoplasty in 28 and patch aortoplasty in 31 patients (and was not documented in 28 cases). 6 patients had endovascular repair, 4 had interposition tube grafts and 11 were unrepaired. There were a total of seven deaths at a median age of 60 years. Actuarial survival was 98% at 40, 98% at 50 and 89% at 60 years of age. Re-coarctation occurred in 34% and descending aortic aneurysms were noted in 18%. Patients with end-to-end repair had lower rates of significant re-coarctation or descending aortic aneurysms (p=0.026 and <0.001, respectively). 66% had bicuspid aortic valve and 44% were hypertensive.

Conclusions Patients with CoA who reach adolescence demonstrate very good long-term survival up to age 60 years. Long-term morbidity is common, however, related largely to aortic complications and late hypertension.

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