Newborn screening for cystic fibrosis.

Tanja Gonska, Felix Ratjen

Journal: Expert review of respiratory medicine 2016;9(5):619-31

PMID: 26366807

Abstract

Newborn screening for cystic fibrosis (CF NBS) has been introduced in almost all of the Western countries, and most of the children with CF are now being identified via CF NBS before disease-related symptoms develop. This review summarizes the evidence that has been generated to date to support the benefit of CF NBS and the various screening algorithms that are used in different jurisdictions. A special focus is directed towards the challenges arising from false-negative and -positive screening results. Finally, we review the emerging data reporting on positively-screened newborns, in whom confirmatory sweat testing resulted in an inconclusive diagnosis for CF.

Address: a 1 Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, University of Toronto, Toronto, ON, Canada.; b 2 Program of Physiology and Experimental Medicine, Research Institute, the Hospital for Sick Children, Toronto, ON, Canada.; c 3 Department of Pediatrics, Division of Respirology, University of Toronto, Toronto, ON, Canada.
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.