False normal Lung Clearance Index in infants with cystic fibrosis due to software algorithms

Pediatric Pulmonology

Volumn 50, Issue 10, 2015, Pages 970-977

  Anagnostopoulou, Pinelopi ^a,b   Yammine, Sophie ^a   Schmidt, Anne ^a,c   Korten, Insa ^a   Kieninger, Elisabeth ^a,c   Mack, Ines ^a   Trachsel, Daniel ^c   Hafen, Gaudenz ^d   Moeller, Alexander ^e   Casaulta, Carmen ^a   Latzin, Philipp ^a,c  

^a UNIVERSITY OF BERN   (Switzerland)

^b ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

^c UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^d LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^e UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

Author keywords

cystic fibrosis; infant pulmonary function; multiple breath washout; ultrasonic flowmeter

Indexed keywords

ACCURACY; ALGORITHM; ARTICLE; AUTOMATION; CLINICAL ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE ASSOCIATION; DISEASE MARKER; FEMALE; HUMAN; INFANT; LUNG CLEARANCE INDEX; MALE; MULTIPLE BREATH WASHOUT; OUTCOME ASSESSMENT; PREDICTIVE VALUE; PRIORITY JOURNAL; RESPIRATORY TRACT DISEASE ASSESSMENT; SOFTWARE ALGORITHM; VALIDATION PROCESS; CASE CONTROL STUDY; COMPUTER PROGRAM; DEVICES; LUNG FUNCTION TEST; PATHOPHYSIOLOGY; PROCEDURES; REFERENCE VALUE;

ALGORITHMS; CASE-CONTROL STUDIES; CYSTIC FIBROSIS; FEMALE; HUMANS; INFANT; MALE; REFERENCE VALUES; RESPIRATORY FUNCTION TESTS; SOFTWARE;

EID: 84941735032     PISSN: 87556863     EISSN: 10990496     Source Type: Journal    
DOI: 10.1002/ppul.23256     Document Type: Article

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