Cardiovascular medicine
Natural and unnatural history of pulmonary atresia
H Leonard, G Derrick, J O'Sullivan, C Wren
Department of
Paediatric Cardiology, Freeman Hospital, Newcastle upon Tyne NE7
7DN, UK
Correspondence to: Dr Leonard email: Christopher.Wren{at}tfh.nuth.northy.nhs.uk
Accepted 3 May 2000
OBJECTIVE
To investigate mortality,
cause of death, survival, and quality of life in all types of cardiac
malformation with congenital pulmonary atresia.
DESIGN
Retrospective analysis.
SETTING
The resident population of
one health region with a single tertiary referral centre.
PATIENTS
All babies with pulmonary
atresia live born in 1980 to 1995.
MAIN OUTCOME MEASURES
Anatomical
classification, total mortality, cause of death, duration of survival,
exercise ability. All cases were classified as pulmonary atresia with
intact septum (PA-IVS), pulmonary atresia with ventricular septal
defect (PA-VSD), or pulmonary atresia with complex cardiac malformation
(complex pulmonary atresia).
RESULTS
129 cardiac malformations
with congenital pulmonary atresia were identified from 601 635 live
births (21.4/100 000): 29 had PA-IVS, 60 had PA-VSD, and 40 had
complex pulmonary atresia. Total mortality was 72/129 (56%), with 15 deaths in the first week and 49 in the first year. There were 23 surgical deaths, 33 hospital deaths (not related to surgery), and 16 sudden deaths, 12 of which remained unexplained. The sudden death rate
was 29/1000 patient years of follow up. Of the 57 survivors, 39% have
exercise ability I or II and 61% III or IV. Definitive surgical repair
produced better exercise ability.
CONCLUSIONS
Early mortality is high
in all types of pulmonary atresia, although survival has improved in
recent years. Most children who have not undergone definitive repair
have significant exercise limitation.
Keywords: congenital heart disease; pulmonary atresia; sudden death; quality of life
© 2000 by Heart
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