Pulmonary rehabilitation in idiopathic pulmonary fibrosis

被引:3
作者
Dowman, Leona M. [1 ,2 ,3 ]
Holland, Anne E. [1 ,3 ,4 ]
机构
[1] Monash Univ, Sch Translat Med, Melbourne, Australia
[2] Austin Hlth, Dept Physiotherapy & Resp & Sleep Med, Heidelberg, Australia
[3] Alfred Hlth, Inst Breathing & Sleep, Melbourne, Australia
[4] Alfred Hlth, Dept Physiotherapy & Resp Med, Melbourne, Vic, Australia
关键词
idiopathic pulmonary fibrosis; interstitial lung diseases; rehabilitation; RESPIRATORY SOCIETY; DISEASE; DIAGNOSIS; GUIDELINES; MANAGEMENT; STATEMENT;
D O I
10.1097/MCP.0000000000001094
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose of reviewThis review synthesizes the expanding evidence for pulmonary rehabilitation that has led to its recommended inclusion in the holistic care of people with idiopathic pulmonary fibrosis (IPF), as well as discussing strategies that may maximize and sustain benefits.Recent findingsPulmonary rehabilitation is an effective intervention leading to significant improvements in exercise tolerance, symptoms, and quality of life for people with IPF. Improvements in symptoms and quality of life can persist longer term, whereas functional capacity does not; therefore, strategies to preserve functional capacity are an important area of research. Referral early in the disease course is encouraged to promote longer lasting effects. Evidence that high-intensity interval training may optimize benefits of exercise training is emerging. Supplemental oxygen is frequently used to manage exercise-induced desaturation, although its use as an adjunct therapy requires more evidence.SummaryCurrent evidence strongly supports the inclusion of pulmonary rehabilitation in the standard holistic care of IPF, with early participation encouraged. Further research is needed to establish the optimal exercise strategies, modalities and adjunct therapies that enhance outcomes of pulmonary rehabilitation and promote longer lasting effects.
引用
收藏
页码:516 / 522
页数:7
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