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Eur J Cardiothorac Surg 2005;28:607-610
© 2005 Elsevier Science NL
Original articles |
a Department of Paediatric Surgery, Birmingham Children's Hospital NHS Trust, Steelhouse Lane, Birmingham B4 6NH, UK
b Department of Paediatric Surgery, Box 267, Addenbrookes NHS Trust, Cambridge CB22QQ, UK
Received 23 February 2005; received in revised form 6 May 2005; accepted 29 June 2005.
* Corresponding author. Tel.: +44 1223 274455; fax: +44 1223 216015. (Email: dakshesh.parikh{at}bch.nhs.uk; madan.samuel{at}addenbrookes.nhs.uk).
Abstract
Objective: Congenital cystic lung lesions associated with fetal hydrops and polyhydramnios are rare, and reported to have greater than 50% mortality, can this be reversed? To propose a period of pulmonary stabilisation and delayed surgery for neonates with congenital cystic lung lesions and pulmonary hypertension. Results: Four neonates with antenatal diagnosed congenital cystic lung lesions with associated fetal hydrops and maternal polyhydramnios, presented with pulmonary hypertension due to lung hypoplasia. Contrast spiral computerised tomography scan was diagnostic. Three had congenital cystic adenomatoid malformation and one extra-lobar pulmonary sequestration with anomalous blood supply from the abdominal aorta. All four were pre-operatively ventilated for 9.8±0.9 days on conventional mechanical ventilators. Definitive surgery was performed at 10.8±0.8 days following stabilisation of lung function (preductal PO2 of greater than 60torr with a SaO2 of 90100%) and resolution of pulmonary hypertension with absence of persistent fetal circulation on echocardiography. Optimal timing of delayed surgery was in the range of 216360h. All four are thriving with absent respiratory complications. Conclusion: Delayed surgery following pulmonary stabilisation results in favourable outcome.
Key Words: Congenital cystic adenomatoid malformation Pulmonary intralobar sequestration Pulmonary hypoplasia Pulmonary hypertension Congenital diaphragmatic hernia
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