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Cough suppression and HRQoL in adult people with cystic fibrosis: an unexplored correlation.
Niehammer, Ute; Steindor, Mathis; Straßburg, Svenja; Sutharsan, Sivagurunathan; Taube, Christian; Welsner, Matthias; Hirtz, Raphael; Stehling, Florian.
Afiliación
  • Niehammer U; Department of Pulmonary Medicine, Adult Cystic Fibrosis Center, University Hospital Essen - Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
  • Steindor M; Paediatric Pulmonology and Sleep Medicine, Children's Hospital, University of Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Germany.
  • Straßburg S; Department of Pulmonary Medicine, Adult Cystic Fibrosis Center, University Hospital Essen - Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
  • Sutharsan S; Department of Pulmonary Medicine, Adult Cystic Fibrosis Center, University Hospital Essen - Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
  • Taube C; Department of Pulmonary Medicine, Adult Cystic Fibrosis Center, University Hospital Essen - Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
  • Welsner M; Department of Pulmonary Medicine, Adult Cystic Fibrosis Center, University Hospital Essen - Ruhrlandklinik, University of Duisburg-Essen, Essen, Germany.
  • Hirtz R; Paediatric Endocrinology, Children's Hospital, University of Duisburg-Essen, Essen, Germany.
  • Stehling F; Paediatric Pulmonology and Sleep Medicine, Children's Hospital, University of Duisburg-Essen, Hufelandstr. 55, 45147, Essen, Germany. florian.stehling@uk-essen.de.
Health Qual Life Outcomes ; 20(1): 141, 2022 Oct 06.
Article en En | MEDLINE | ID: mdl-36203159
BACKGROUND: Cough suppression assessed by embarrassment about coughing has been shown in adolescents with cystic fibrosis (CF) and negatively affects health-related quality of life (HRQoL) and clinical indicators of disease severity in adolescent females. However, whether cough suppression exists in adults has been studied as little as its effects on clinical and psychological outcomes beyond adolescence. METHODS: Seventy-one subjects completed the self-reported 'Cystic Fibrosis Questionnaire-Revised (CFQ-R + 14)' and a self-report questionnaire about cough suppression, health-related perspectives, and therapy adherence. The status of CF disease was quantified in terms of the percentage of predicted forced expiratory volume in one second (ppFEV1), body mass index (BMI), Pseudomonas aeruginosa, pancreatic status, and CF-related diabetes (CFRD). Additional demographic data for sex, age, graduation, employment, and marital status were assessed. RESULTS: CS exists in adult CF and is associated with impaired HRQoL but not the overall CF disease status regarding BMI, ppFEV1, or health-related perspectives. Despite a higher prevalence of cough suppression in women, no effect of sex regarding either outcome measure was observed. CONCLUSION: The results of this study suggest that mental health indicators have an impact on cough suppression.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Calidad de Vida / Fibrosis Quística Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Health Qual Life Outcomes Asunto de la revista: SAUDE PUBLICA Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Calidad de Vida / Fibrosis Quística Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Health Qual Life Outcomes Asunto de la revista: SAUDE PUBLICA Año: 2022 Tipo del documento: Article