Six-minute walk test and factors affecting exercise capacity in children with cystic fibrosis

被引:1
作者
Toopchizadeh, Vahideh [1 ]
Nezamoleslami, Elaheh [1 ]
Rafeey, Mandana [2 ]
Jahanjoo, Fatemeh [3 ]
Khabbaz, Mohammad Sadegh [4 ]
Jafari-Rouhi, Amir Hossein [5 ]
机构
[1] Tabriz Univ Med Sci, Phys Med & Rehabil Res Ctr, Tabriz 5166615556, Iran
[2] Tabriz Univ Med Sci, Liver & Gastrointestinal Dis Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Road Traff Injury Res Ctr, Tabriz, Iran
[4] Guilan Univ Med Sci, Rasht, Iran
[5] Tabriz Univ Med Sci, Tabriz Childrens Hosp, Pediat Hlth Res Ctr, Tabriz, Iran
关键词
Cystic fibrosis; physical capacity; six-minute walk test; chest physical therapy; LUNG-FUNCTION; ADOLESCENTS; ADULTS; MANAGEMENT; DYSPNEA;
D O I
10.3233/PRM-210089
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
PURPOSE: This study aimed to compare the result of the six-minute walk test (6MWT) in patients with cystic fibrosis (CF) aged < 20 years old and individuals without CF. METHODS: In this cross-sectional study, 50 children and adolescents with CF and 20 children and adolescents without CF underwent the 6MWT. Vital signs before and immediately after the 6MWT and six-minute walk distance (6MWD) were evaluated. RESULTS: The mean change in heart rate, percentage of peripheral oxygen saturation (SpO2%), systolic blood pressure, respiratory rate, and dyspnea severity during the 6MWT was significantly higher in patients with CF. In the case group, 6MWD was associated with regular chest physical therapy (CPT) and forced expiratory volume (FEV)>80%. Patients with CF receiving regular CPT or mechanical vibration and with FEV in the first second >80% showed better physical capacity during the 6MWT (smaller Sp02% decline and lower dyspnea perception). CONCLUSION: Children and adolescents with CF have lower physical capacity compared to individuals without CF. CPT and mechanical vibration could be used to increase physical capacity in this population.
引用
收藏
页码:517 / 528
页数:12
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