• Data on 16 sibling pairs with cystic fibrosis were analyzed to test the hypothesis that early treatment of this condition improves prognosis. Younger siblings' conditions were diagnosed before 1 year of age, usually before the onset of pulmonary disease. Older siblings' conditions were diagnosed after 1 year of age and after the onset of pulmonary disease. Although the sibling pairs received similar treatment, comparison at 7 years of age showed that the younger siblings had significantly better chest roentgenogram scores, total clinical scores, residual lung volumes, and ratios of residual volume to total lung volume. Younger siblings also required fewer hospital admissions to control their lung disease. The results suggest that, in general, early initiation of therapy is beneficial for patients with cystic fibrosis.
(Am J Dis Child 131:973-975, 1977)
Orenstein DM, Boat TF, Stern RC, et al. The Effect of Early Diagnosis and Treatment in Cystic Fibrosis: A Seven-Year Study of 16 Sibling Pairs. Am J Dis Child. 1977;131(9):973–975. doi:10.1001/archpedi.1977.02120220039005
Customize your JAMA Network experience by selecting one or more topics from the list below.
Create a personal account or sign in to: