Early Results of the Ross Procedure in Simple and Complex Left Heart Disease
- 9 November 1999
- journal article
- Published by Wolters Kluwer Health in Circulation
- Vol. 100 (Supplement) , II-162-162
- https://doi.org/10.1161/01.cir.100.suppl_2.ii-162
Abstract
Background—The Ross procedure has been used increasingly to treat aortic valve disease in children and young adults. Benefits include the lack of anticoagulation after surgery and the potential growth and durability of the autograft. The purpose of this study was to review our institutional experience with the Ross procedure and to compare early outcome in simple aortic valve disease and complex left heart disease. Methods and Results—Between January 1995 and October 1998, 66 patients (median age, 10.8 years; range, 6 days to 34.8 years) underwent the Ross procedure. The primary indication for surgery was isolated valvular disease in 41 patients: aortic stenosis (AS; n=3), aortic insufficiency (AI; n=11), and AS/AI (n=27). The remaining 25 patients had multiple levels of left ventricular outflow tract obstruction, 12 of whom had at least moderate AI. Additional left heart disease in the complex group included subaortic stenosis (n=20), arch obstruction (n=7), mitral valve disease (n=5), apical aortic conduit stenosis or insufficiency (n=3), and supravalvar AS (n=2). There were 123 prior interventions performed in 51 patients, including aortic valvotomy/valvuloplasty (n=56), coarctation repair (n=21), subaortic stenosis resection/Konno procedure (n=10), ventricular septal defect closure (n=8), apical aortic conduit placement (n=3), aortic valve replacement (n=3), and other (n=22). An isolated Ross procedure was performed in 41 patients, 10 of whom required concurrent aortic annulus enlargement procedure to accommodate the larger pulmonary autograft. In the remaining 25 patients, 49 concurrent procedures were performed, including the Konno procedure (n=17), aortic annulus enlargement (n=2), subaortic membrane resection (n=9), arch augmentation (n=5), mitral valvuloplasty (n=5), ventricular septal defect closure (n=4), apicoaortic conduit division (n=3), and other (n=4). One patient (1.5%) died 3 days after a Ross-Konno procedure, which included arch reconstruction, from presumed arrhythmia. There were no other early deaths. One patient required ECMO (extracorporeal membrane oxygenation) for 3 days after a ventricular tachycardia (VT)–related cardiac arrest. Transient complete heart block was seen in 4 patients; the duration was Conclusions—The Ross procedure can be performed in isolation or in combination with other complex procedures with low mortality (1.5%) and acceptable short-term results, even in patients with complex left heart disease and multiple prior interventions. Postoperative VT is common. Anatomic abnormalities of the pulmonary valve preclude its use as an autograft.Keywords
This publication has 8 references indexed in Scilit:
- Perioperative conduction and rhythm disturbances after the Ross procedure in young patientsThe Annals of Thoracic Surgery, 1998
- Clinical Outcome and Left Ventricular Function After Pulmonary Autograft Implantation in ChildrenThe Annals of Thoracic Surgery, 1997
- Aortoventriculoplasty with the pulmonary autograft: The "Ross-Konno" procedureThe Journal of Thoracic and Cardiovascular Surgery, 1996
- Relief of complex left ventricular outflow tract obstruction with pulmonary autograftsThe Journal of Thoracic and Cardiovascular Surgery, 1995
- Pulmonary autograft in children: Realized growth potentialThe Annals of Thoracic Surgery, 1994
- Replacement of the Aortic Root with a Pulmonary Autograft in Children and Young Adults with Aortic-Valve DiseaseNew England Journal of Medicine, 1994
- Replacement of the aortic valve or root with a pulmonary autograft in childrenThe Annals of Thoracic Surgery, 1991
- Aortic Valve and Left Ventricular Outflow Tract Replacement Using Allograft and Autograft Valves: A Preliminary ReportThe Annals of Thoracic Surgery, 1989