Patient registry analyses: seize the data, but caveat lector

Editorial

Michael S Schechter. J Pediatr. 2008 Dec.

. 2008 Dec;153(6):733-5.

doi: 10.1016/j.jpeds.2008.09.011.

No abstract available

Comment on

Improvements in lung function outcomes in children with cystic fibrosis are associated with better nutrition, fewer chronic pseudomonas aeruginosa infections, and dornase alfa use.
McPhail GL, Acton JD, Fenchel MC, Amin RS, Seid M. McPhail GL, et al. J Pediatr. 2008 Dec;153(6):752-7. doi: 10.1016/j.jpeds.2008.07.011. Epub 2008 Aug 29. J Pediatr. 2008. PMID: 18760423
Relationship between inhaled corticosteroid therapy and rate of lung function decline in children with cystic fibrosis.
Ren CL, Pasta DJ, Rasouliyan L, Wagener JS, Konstan MW, Morgan WJ; Scientific Advisory Group and the Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Ren CL, et al. J Pediatr. 2008 Dec;153(6):746-51. doi: 10.1016/j.jpeds.2008.07.010. Epub 2008 Aug 30. J Pediatr. 2008. PMID: 18760805