Ekman Joelsson B M, Sunnegårdh J, Hanseus K, Berggren H, Jonzon A, Jögi P, Lundell B
Central Hospital, Skövde, Sweden.
Scand Cardiovasc J. 2001 Jul;35(3):192-8. doi: 10.1080/140174301750305072.
To study the outcome of all children born with pulmonary atresia and intact ventricular septum in Sweden between 1980 and 1999.
Retrospective study of medical records with review of the initial, preoperative angiocardiographic and echocardiographic examinations.
A total of 84 children were born with pulmonary atresia and intact ventricular septum, giving an incidence of 4.2 per 100,000 live births. In all, 77 were operated on with a 1-year survival rate of 75%. Thirty-six children had ventriculocoronary communications, with a 1-year survival rate of 50%. At the end of the study period, 52 children were alive, 32 with biventricular repair, and 19 with univentricular repair. Follow-up time was 14 days-20 years (median, 6 years). Statistical analysis of incremental risk factors for death showed statistical significance for low birth weight, male sex, muscular pulmonary atresia, and having a systemic-to-pulmonary shunt as the sole initial intervention.
Complete national data of all patients born with pulmonary atresia and intact ventricular septum during 1980-1999 in Sweden revealed a total mortality in accordance with previous reports for results for surgery. Further improvements demand a thorough preoperative investigation of the cardiac anatomy, particularly of the ventriculocoronary communications, to enable right ventricular decompression whenever possible.
