Thoracic sequelae after surgical closure of the patent ductus arteriosus in premature infants

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Abstract
Thirty‐six children (median chronological age 6 years 1 month) who had undergone surgical closure of a patent ductus arteriosus through a left posterolateral thoracotomy in the neonatal period (median gestational age 32 weeks) were investigated prospectively with respect to anatomical and functional changes of the chest. At follow‐up examination, residual or recurrent patent ductus arteriosus was not observed. Three patients had chronic bronchial obstruction. Two patients showed pathological musculoskeletal thoracic sequelae that did not require any treatment at the time of follow‐up: persistence of immediate postoperative left phrenic palsy (n= 1) and thoracic scoliosis (n= 1). Twenty of the 27 patients in whom chest X‐ray was performed had minor radiological skeletal anomalies in the form of rib deformation or fusion related to die thoracotomy, lesions which have a potential to induce thoracic scoliosis. Left shoulder elevation at chest X‐ray and isolated left arm dysfunction at clinical examination were not observed. Despite the low incidence of scoliosis and the absence of left arm dysfunction observed at mid‐term follow‐up in our series, the incidence of minor rib deformations with a potential to induce severe anomalies such as scoliosis should motivate late follow‐up examination at adolescence to definitively assess the prevalence of thoracic sequelae after surgical closure of the patent ductus arteriosus in premature infants.