Mc. Seghaye et al., THORACIC SEQUELAE AFTER SURGICAL CLOSURE OF THE PATENT DUCTUS-ARTERIOSUS IN PREMATURE-INFANTS, Acta paediatrica, 86(2), 1997, pp. 213-216
Thirty-six children (median chronological age 6 years 1 month) who had
undergone surgical closure of a patent ductus arteriosus through a le
ft posterolateral thoracotomy in the neonatal period (median gestation
al age 32 weeks) were investigated prospectively with respect to anato
mical and functional changes of the chest. At follow-up examination, r
esidual or recurrent patent ductus arteriosus was not observed. Three
patients had chronic bronchial obstruction. Two patients showed pathol
ogical musculoskeletal thoracic sequelae that did not require any trea
tment 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 radiologic
al skeletal anomalies in the form of rib deformation or fusion related
to the thoracotomy, lesions which have a potential to induce thoracic
scoliosis. Left shoulder elevation at chest X-ray and isolated left a
rm dysfunction at clinical examination were not observed. Despite the
low incidence of scoliosis and the absence of left arm dysfunction obs
erved at mid-term follow-up in our series, the incidence of minor rib
deformations with a potential to induce severe anomalies such as scoli
osis should motivate late follow-up examination at adolescence to defi
nitively assess the prevalence of thoracic sequelae after surgical clo
sure of the patent ductus arteriosus in premature infants.