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J Thorac Cardiovasc Surg 2006;132:656-664
© 2006 The American Association for Thoracic Surgery
Surgery for Congenital Heart Disease |
a Clinic for Cardiovascular Surgery, University Hospital of Geneva, Geneva, Switzerland
c Department of Radiology, University Hospital of Geneva, Geneva, Switzerland
b Unit of Pediatric Cardiology, University Children's Hospital of Geneva, Geneva, Switzerland.
Received for publication February 8, 2006; revisions received March 27, 2006; accepted for publication April 18, 2006. * Address for reprints: Afksendiyos Kalangos, MD, PhD, DSc, FECTS, Department of Cardiovascular Surgery, University Hospital of Geneva, 1211 Geneva, Switzerland. (Email: afksendyios.kalangos{at}hcuge.ch).
OBJECTIVE: There is little information available on the results of reconstructive arterial surgery for Takayasu's arteritis in children. This study evaluates midterm to long-term outcome after surgical, as well as interventional, procedures.
METHODS: From 1984 through 2004, 10 children (5 boys and 5 girls; age, 12.7 ± 2.6 years) with Takayasu's arteritis were referred to our center. Baseline cardiovascular assessment included contrast angiography (n = 4), magnetic resonance imagingangiography (n = 3), and combined contrast angiography plus magnetic resonance imagingangiography (n = 3). Two patients had disease confined to the thoracic aorta, 4 had disease confined to the abdominal aorta, and 4 had combined thoracoabdominal aortic disease. Steno-occlusive lesions were predominant in 92% of cases. Seven patients were maintained on steroid therapy throughout the follow-up period. Eight children underwent complex surgical procedures, 1 patient had balloon dilatation of the renal and mesenteric arteries, and 1 patient had combined vascular surgery with percutaneous transluminal angioplasty. Overall, 24 grafts (polytetrafluoroethylene, Dacron grafts, and cryopreserved homografts) were implanted in various locations.
RESULTS: There were no perioperative deaths. Arterial hypertension regressed in all patients, and cardiac function normalized in all 4 patients with dilative cardiomyopathy. Over a 20-year period, 1 patient presented with sudden death and 2 showed nonfatal disease progression, one of whom required surgical reintervention. The occlusion rate was higher in Dacron grafts.
CONCLUSIONS: Our study shows that despite the extent and severity of vascular lesions, children with Takayasu's arteritis could benefit from reconstructive surgery, with low mortality, morbidity, and satisfactory long-term results.
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