The evolution of exercise capacity and its limiting factors in Cystic Fibrosis

被引：43

作者：

Almajed, Athari ^{[1
]}

Lands, Larry C. ^{[1
]}

机构：

[1] McGill Univ, Montreal Childrens Hosp, Div Pediat Resp Med, Dept Pdiatr,Hlth Ctr, Montreal, PQ H3H 1P3, Canada

来源：

PAEDIATRIC RESPIRATORY REVIEWS | 2012年 / 13卷 / 04期

关键词：

CF prognosis; CF outcome; Skeletal muscle; Nutrition; Deadspace; Pulmonary function; Cardiac function; Habitual physical activity; HABITUAL PHYSICAL-ACTIVITY; PULMONARY-FUNCTION; MUSCLE FUNCTION; LUNG-FUNCTION; CHILDREN; PERFORMANCE; VENTILATION; CF; TOLERANCE; STANDARD;

D O I：

10.1016/j.prrv.2012.01.001

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

The ability to perform exercise is an important determinant of both longevity and quality of life for patients with Cystic Fibrosis. There are a variety of physical and behavioural factors that contribute to exercise limitation. These, such as lung function or habitual physical activity, change over time. However, these factors can also be modified by treatments and interventions. This review discusses the various factors that contribute to exercise limitation in Cystic Fibrosis, and how these change with age. (C) 2012 Elsevier Ltd. All rights reserved,

引用

页码：195 / 199

页数：5

共 46 条

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