ANN. THORAC. SURG. 62/4 (1996) 981-989


Anterior pericardial tracheoplasty for congenital tracheal stenosis: Intermediate to long-term outcomes

Bando K., Turrentine M.W., Sun K., Sharp T.G., Matt B., Karmazyn B., Heifetz S.A. , Stevens J., Kesler K.A., Brown J.W.

Sections of Cardiothorac. Surg., P., James W. Riley Hospital for Children, Indiana University Medical Center, Indianapolis, IN, USA

Abstract
Background. Although several techniques for the treatment of long-segment stenosis of the trachea have been reported, including slide tracheoplasty, rib grafting, and use of a pericardial patch, the optimal repair remains controversial because of a lack of midterm to long-term follow-up data. Methods. To assess the intermediate and long-term outcomes of patients having repair with anterior pericardial tracheoplasty, we reviewed case histories of 12 patients (1984 to present). The median age was 6.7 months (range, 1 to 98 months), and the median weight was 6.0 kg (range, 0.97 to 42 kg). All patients underwent anterior pericardial tracheoplasty through a median sternotomy during partial normothermic cardiopulmonary bypass. An average of 13 tracheal rings (range, five to 23) were divided anteriorly, and a patch of fresh autologous pericardium was used to enlarge the trachea by 1.5 times the predicted diameter for patient age and weight. Results. There was one hospital death, and all but 2 patients are long-term survivors. All but 1 current survivor remain asymptomatic, with no bronchoscopic evidence of airway obstruction or granulation on the pericardial patch. All survivors examined have normal tracheal growth and development, with a median follow-up of 5.5 years (range, 1 to 11 years). Conclusions. Anterior pericardial tracheoplasty for congenital tracheal stenosis provides excellent results at intermediate to long-term follow-up.


 

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