[Cystic fibrosis: how to use pulmonary function tests].

Abstract:

INTRODUCTION:Neonatal screening for cystic fibrosis (CF) leads to early dedicated specialist care for all patients. BACKGROUND:Pulmonary function tests (PFT) are mandatory for routine monitoring of CF patients. The aim of this article is to review the current guidelines for PFTs in CF, particularly the type of test, the age and the clinical status of the patient. VIEWPOINT:The regular use of spirometry is generally accepted. Many other tests are used but their clinical value in the routine follow-up of CF patients remains to be established. CONCLUSION:Further efforts should be made to evaluate the value of PFTs in CF, particularly in very young children.

journal_name

Rev Mal Respir

authors

Counil FP,Karila C,Le Bourgeois M,Matecki S,Lebras MN,Couderc L,Fajac I,Reynaud-Gaubert M,Bellet M,Gauthier R,Denjean A,Groupe de travail Explorations Fonctionnelles Respiratoires de la Société Française de la Mucoviscidose.

doi

10.1016/s0761-8425(07)91145-6

subject

Has Abstract

pub_date

2007-06-01 00:00:00

pages

691-701

issue

6

eissn

0761-8425

issn

1776-2588

pii

MDOI-RMR-06-2007-24-6-0761-8425-101019-200720064

journal_volume

24

pub_type

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