Long-Term Outcomes of the Coarctation of the Aorta Stent Trials

Author:

Holzer Ralf J.1ORCID,Gauvreau Kimberlee2,McEnaney Kerry3ORCID,Watanabe Hanano4,Ringel Richard5ORCID

Affiliation:

1. NewYork-Presbyterian Hospital, Weill Cornell Medicine, NY (R.J.H.).

2. Department of Cardiology, Boston Children’s Hospital, MA. (K.G.)

3. Department of Cardiology, Boston Children’s Hospital, MA. (K.M.)

4. Maimonides Medical Center, Brooklyn, NY (H.W.).

5. John Hopkins School of Medicine, Baltimore, MD (R.R.).

Abstract

Background: Long-term outcome data of stent-implantation for coarctation of the aorta are limited. We report up to 5 years of postimplant follow-up in patients enrolled into the COAST (Coarctation of the Aorta Stent Trial) and the COAST II trial (Covered Cheatham-Platinum Stents for Prevention or Treatment of Aortic Wall Injury Associated With Coarctation of the Aorta), evaluating the bare and Covered Cheatham-Platinum Stents for the treatment of coarctation of the aorta and associated aortic wall injury. Methods: Data was prospectively collected during the 2 multi-center studies, enrolling 248 patients (COAST: n=121, COAST II: n=127). Late follow-up data (48–60 month) was compared with immediate (1 month) and early (12 months) follow-up. Results: There was a notable decrease in the use of antihypertensive medication, from 53% at immediate, to 42% at early, and 29% at late follow-up. The cumulative incidence of stent fractures was 0% immediately, 2.9% at early, and 24.4% at late follow-up. Independent predictors for stent fractures at late follow-up were age <18 years, male sex, minimum stent diameter ≥12 mm, and use of bare metal stent. The cumulative incidence of reintervention was 1.6% at immediate, 5.1% at early, and 21.3% at late follow-up. Independent predictors for reinterventions at late follow-up were age <18 years, post implantation systolic arm-leg blood pressure gradient ≥10 mm Hg, minimum stent diameter at implantation <12 mm, and initial coarctation minimum diameter <6 mm. There were 13 patients with aortic aneurysms, with a cumulative incidence of 6.3% at late follow-up. Conclusions: Coarctation stenting is effective at maintaining obstruction relief up to 60 months postimplant with reduction in the number of patients requiring antihypertensive medication. However, an increase in-stent fractures and reinterventions were observed between medium and long-term follow-up. Covered stents appear to confer some protection from the development of stent fractures but do not provide complete protection from late aneurysm formation. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifiers: NCT00552812 and NCT01278303.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference14 articles.

1. Stenting of coarctation of the aorta;Cheatham JP;Catheter Cardiovasc Interv.,2001

2. Intermediate outcomes in the prospective, multicenter coarctation of the Aorta Stent Trial (COAST);Meadows J;Circulation.,2015

3. Coarctation of the Aorta Stent Trial (COAST): study design and rationale;Ringel RE;Am Heart J.,2012

4. Acute outcome of stent therapy for coarctation of the aorta: results of the coarctation of the aorta stent trial;Ringel RE;Catheter Cardiovasc Interv.,2013

5. Immediate outcomes of covered stent placement for treatment or prevention of aortic wall injury associated with coarctation of the aorta (COAST II);Taggart NW;JACC Cardiovasc Interv.,2016

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