Exercise testing in cystic fibrosis: Who and why?

被引：18
|
作者：
Urquhart, D. S. [1 ,2 ]
Saynor, Z. L. [3 ,4 ,5 ]
机构：
[1] Royal Hosp Sick Children, Dept Paediat Resp & Sleep Med, Edinburgh, Midlothian, Scotland
[2] Univ Edinburgh, Dept Child Life & Hlth, Edinburgh, Midlothian, Scotland
[3] Univ Portsmouth, Dept Sport & Exercise Sci, Portsmouth, Hants, England
[4] Univ Hosp Southampton, Paediat Dept, Southampton, Hants, England
[5] Univ Hosp Southampton, Adult Resp Outpatient Dept, Southampton, Hants, England
来源：
PAEDIATRIC RESPIRATORY REVIEWS | 2018年 / 27卷
关键词：
Cystic fibrosis; Exercise; Exercise physiology; Cardiopulmonary exercise testing [CPET; CHILDREN; TRIAL; PROGRAM; LUNG;
D O I：
10.1016/j.prrv.2018.01.004
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Annual review exercise testing is recommended by the Cystic Fibrosis (CF) Trust. Testing to date has focused on evaluating aerobic fitness, a key prognostic indicator. Tests available range from simple field tests, to comprehensive evaluations of aerobic exercise (dys)function - cardiopulmonary exercise testing (CPET). 'Field tests', although easy to perform are limited in the information they provide,whereas CPET, the 'gold standard' measure of aerobic fitness, is recommended as the first-choice exercise test by the European CF Society Exercise Working Group. CPET offers a precise cardiovascular, respiratory and metabolic evaluation of exercise capacity, including assessment of mechanism(s) of exercise limitation. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码：28 / 32
页数：5
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