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Adherence to inhalation therapy and quality of life in children with cystic fibrosis : a cross-sectional study
dc.contributor.author | Peruch, Thais | pt_BR |
dc.contributor.author | Feiten, Taiane dos Santos | pt_BR |
dc.contributor.author | Flores, Josani Silva | pt_BR |
dc.contributor.author | Dalcin, Paulo de Tarso Roth | pt_BR |
dc.contributor.author | Ziegler, Bruna | pt_BR |
dc.date.accessioned | 2021-04-28T04:30:03Z | pt_BR |
dc.date.issued | 2020 | pt_BR |
dc.identifier.issn | 2357-9730 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/10183/220284 | pt_BR |
dc.description.abstract | Introduction: Inhalation therapy is a crucial part of the cystic fibrosis (CF) treatment regimen. Drugs that assist in mucociliary clearance and inhaled antibiotics are used by most patients. Methods: This is a cross-sectional study where patients with CF and their caregivers answered questionnaires regarding their adherence to inhalation therapy and QoL. Demographic, spirometric, and bacteriological data, as well as S-K scores and hospitalization frequencies were also collected. Results: We included 66 patients in this study; participants had a mean age of 12.3 years and Z-scores of -1.4 for forced expiratory volume in 1 second and 48.6 for body mass index. Patients were divided into 2 groups according to their self-reported adherence to inhalation therapy: high adherence (n = 46) and moderate/low adherence (n = 20). When comparing both groups, there was no statistically significant differences in age, sex, family income, and S-K score (p > 0.05). The high-adherence group had had shorter hospitalization periods in the previous year (p = 0.016) and presented better scores in the following domains of the QoL questionnaire: emotion (p = 0.006), eating (p = 0.041), treatment burden (p = 0.001), health perception (p = 0.001), and social (p = 0.046). Conclusions: A low self-reported adherence to inhalation therapy recommendations was associated with longer hospitalizations in the previous year and with a decrease in QoL in pediatric patients with CF. | en |
dc.format.mimetype | application/pdf | pt_BR |
dc.language.iso | eng | pt_BR |
dc.relation.ispartof | Clinical and biomedical research. vol. 40, no. 2 (2020), p. 105-110. | pt_BR |
dc.rights | Open Access | en |
dc.subject | Cystic fibrosis | en |
dc.subject | Fibrose cística | pt_BR |
dc.subject | Criança | pt_BR |
dc.subject | Adherence | en |
dc.subject | Qualidade de vida | pt_BR |
dc.subject | Nebulization | en |
dc.subject | Quality of life | en |
dc.subject | Cooperação e adesão ao tratamento | pt_BR |
dc.subject | Terapia respiratória | pt_BR |
dc.subject | Oxigenoterapia | pt_BR |
dc.title | Adherence to inhalation therapy and quality of life in children with cystic fibrosis : a cross-sectional study | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dc.identifier.nrb | 001123673 | pt_BR |
dc.type.origin | Nacional | pt_BR |
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