Association between lung function, thoracoabdominal mobility and posture in cystic fibrosis: pilot study

Author:

Pinto Francisca Pereira1ORCID,Souza Gustavo Vieira Paterlini de2ORCID,Sarro Karine Jacon3ORCID,Garcia Cintia Carvalho Bragança4ORCID,Paro Flávia Marini1ORCID

Affiliation:

1. Universidade Federal do Espírito Santo, Brazil

2. Universidade Federal do Espírito Santo, Brazil; Faculdade Estácio de Sá de Vitória, Brazil

3. Universidade Estadual de Campinas, Brazil

4. Hospital Infantil Nossa Senhora da Glória, Brazil

Abstract

Abstract Introduction: Deterioration of lung function is the main cause of mortality in cystic fibrosis (CF), so it is essential to study different related factors. Objective: To assess the association of pulmonary function with thoracoabdominal mobility and postural alignment in individuals with CF. Method: A cross-sectional study was performed in individuals with CF (8-17 years). Pulmonary function was assessed by spirometry. Thoracoabdominal mobility and postural alignment were evaluated by photogrammetry using the Postural Assessment Software (PAS/Sapo). Pearson correlation coefficient analysis was performed, and p < 0.05 was considered significant. Results: The following spirometric variables showed a decrease compared to predicted values: FEV1, FEV1/FVC, PEF and FEF25-75%. Postural assessment showed alterations in head horizontal alignment (HHA; 2.71 ± 2.23o), acromion horizontal alignment (AHA; 1.33 ± 1.35o), anterior superior iliac spine (ASIS) horizontal alignment (ASISHA; 1.11 ± 0.89o), angle between acromia and ASIS (AAASIS; 0.89 ± 0.39o), scapula horizontal asymmetry - T3 (SHAT3; 16.95 ± 12.03%), and asymmetry of the projection of the center of gravity within the base of support in the frontal (11.45 ± 8.10%) and sagittal (48.98 ± 18.55%) planes. A strong positive correlation was found between pulmonary function and thoracoabdominal mobility in the variables anteroposterior mobility of the upper chest (APMUC) and FVC (r = 0.818, p = 0.024), APMUC and FEV1 (r = 0.874, p = 0.010), and APMUC and FEF25-75% (r = 0.797, p = 0.032). A strong negative correlation was detected between FEV1/FVC and AHA (r = -0.761, p = 0.047). Conclusion: Our study showed in CF a reduction in pulmonary function, strong positive correlation between APMUC and pulmonary function, high prevalence of kyphoscoliosis and strong negative correlation between AHA and pulmonary function.

Publisher

FapUNIFESP (SciELO)

Reference39 articles.

1. Cystic fibrosis;Elborn JS;Lancet,2016

2. Longitudinal impact of demographic and clinical variables on health-related quality of life in cystic fibrosis;Abbott J;BMJ Open,2015

3. Qualidade de vida de crianças e adolescentes com fibrose cística importância da imagem corporal e impacto do estado nutricional, idade e raça/cor na percepção dos pacientes e responsáveis;Silva LA;Demetra,2018

4. A systematic review of studies examining the rate of lung function decline in patients with cystic fibrosis;Harun SN;Paediatr Respir Rev,2016

5. Diretrizes brasileiras de diagnóstico e tratamento da fibrose cística;Athanazio RA;J Bras Pneumol,2017

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3