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

页码：28 / 32

页数：5

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