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囊性纤维化心肺运动试验的临床解读及其对运动咨询的影响。

Clinical interpretation of cardiopulmonary exercise testing in cystic fibrosis and implications for exercise counselling.

机构信息

Department of Paediatric Respiratory and Sleep Medicine, Royal Hospital for Sick Children, Edinburgh; Department of Child Life and Health, University of Edinburgh.

Department of Paediatric Respiratory and Sleep Medicine, Royal Hospital for Sick Children, Edinburgh; CAPES Foundation, Ministry of Education of Brazil, Brasília - DF, Brazil.

出版信息

Paediatr Respir Rev. 2017 Sep;24:72-78. doi: 10.1016/j.prrv.2015.09.009. Epub 2015 Oct 13.

Abstract

The measurement of exercise capacity in persons with cystic fibrosis by Cardiopulmonary Exercise Testing (CPET) offers a functional assessment of lung performance and efficiency in a dynamic setting. Exercise performance can measured against predicted values and the mechanism by which exercise limitation occurs can be identified. In healthy subjects, exercise is limited by cardiac output, such that a significant breathing reserve exists at the end of exercise. However, other mechanisms of exercise limitation which may be identified in CF subjects include ventilatory limitation, and/or limitation due to physical deconditioning. A detailed understanding of exercise capacity and the mechanism for exercise limitation may enable health professionals to tailor an individualised exercise programme for each CF patient.

摘要

心肺运动测试(CPET)可测量囊性纤维化患者的运动能力,在动态环境下对肺功能和效率进行功能性评估。可以根据预测值来衡量运动表现,并且可以确定运动受限的发生机制。在健康受试者中,运动受心输出量限制,因此在运动结束时存在显著的呼吸储备。然而,在 CF 受试者中可能存在其他运动受限的机制,包括通气受限和/或由于身体适应不良导致的限制。对运动能力和运动受限机制的详细了解,可以使健康专业人员为每个 CF 患者量身定制个性化的运动方案。

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