Literature DB >> 19328745

Health related quality of life in cystic fibrosis: To work or not to work?

Trudy Havermans1, Kristine Colpaert, Lea Vanharen, Lieven J Dupont.   

Abstract

BACKGROUND: The present study investigated whether patients with CF who are studying or working report a better HRQoL in comparison to non-working/studying patients.
METHODS: 57 adult CF patients completed the Cystic Fibrosis Questionnaire-Revised, a CF-specific measure of HRQoL. Medical condition was quantified in terms of FEV1 % predicted, BMI, Pseudomonas aer. status, pancreatic status (PS), having an indwelling catheter device (PAC), CF Related Diabetes Mellitus and nutritional status.
RESULTS: Mean age was 26.7 years (SD 8.1), mean FEV1 % predicted was 65.09 (SD 22.18), mean BMI was 21.23 (SD 3.45). FEV1 % predicted was related to HRQoL domains Physical Functioning and General Health (r=0.27 and 0.38 respectively, p<0.05). A higher BMI was associated with better scores on Eating Disturbances (= fewer problems; r=0.44, p<0.01) and a better perception of Weight (r=0.43, p<0.01) and Body Image (r=0.28, p<0.05). Analysis of variance showed that specific domains of HRQoL were related to diabetes (Weight), taking caloric supplements (Body Image and Weight) and/or PAC (Physical Functioning, Treatment Burden, Role, Weight). Twenty-four patients worked/studied, these patients had a higher FEV1, and fewer had Pseudomonas aer. or a PAC or took high caloric supplements, compared to non-working/studying patients. After controlling for medical parameters, patients who were working/studying scored higher than non-working/studying patients on Physical Functioning, Role Functioning and Social Functioning.
CONCLUSIONS: CF patients' HRQoL is related to medical status. The non-working/studying CF patients in this sample had greater disease severity and reported a lower quality of life than their working/studying peers, even after controlling for relevant medical parameters. The decision to stop work/study for CF patients is difficult and affects patients' personal, social and financial well-being.

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Mesh:

Year:  2009        PMID: 19328745     DOI: 10.1016/j.jcf.2009.03.002

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  9 in total

1.  Relationships among health-related quality of life, pulmonary health, and newborn screening for cystic fibrosis.

Authors:  Audrey Tluczek; Tara Becker; Anita Laxova; Adam Grieve; Caroline N Racine Gilles; Michael J Rock; William M Gershan; Christopher G Green; Philip M Farrell
Journal:  Chest       Date:  2010-11-24       Impact factor: 9.410

2.  Genetic Variation Near chrXq22-q23 Is Linked to Emotional Functioning in Cystic Fibrosis.

Authors:  Eric Barbato; Barbara Daly; Sara Douglas; Mary Kerr; Paul Litman; Rebecca Darrah
Journal:  Biol Res Nurs       Date:  2020-05-11       Impact factor: 2.522

3.  Health-related quality of life in Cystic Fibrosis patients infected with transmissible Pseudomonas aeruginosa strains: cohort study.

Authors:  Abdul Ashish; Matthew Shaw; James McShane; Martin J Ledson; Martin J Walshaw
Journal:  JRSM Short Rep       Date:  2012-02-27

4.  A longitudinal study of the impact of social deprivation and disease severity on employment status in the UK cystic fibrosis population.

Authors:  David C Taylor-Robinson; Rosalind Smyth; Peter J Diggle; Margaret Whitehead
Journal:  PLoS One       Date:  2013-08-23       Impact factor: 3.240

5.  Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population.

Authors:  Leila Vahedi; Morteza Jabarpoor-Bonyadi; Morteza Ghojazadeh; Amir Vahedi; Mandana Rafeey
Journal:  Tuberc Respir Dis (Seoul)       Date:  2016-10-05

6.  FACTORS ASSOCIATED TO QUALITY OF LIFE IN CHILDREN AND ADOLESCENTS WITH CYSTIC FIBROSIS.

Authors:  Nelbe Nesi Santana; Célia Regina Moutinho de Miranda Chaves; Christine Pereira Gonçalves; Saint Clair Dos Santos Gomes Junior
Journal:  Rev Paul Pediatr       Date:  2020-06-19

7.  Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis.

Authors:  A K M Ashiqul Haque; Alexander Dewerth; Justin S Antony; Joachim Riethmüller; Georg R Schweizer; Petra Weinmann; Ngadhnjim Latifi; Hanzey Yasar; Nicoletta Pedemonte; Elvira Sondo; Brian Weidensee; Anjali Ralhan; Julie Laval; Patrick Schlegel; Christian Seitz; Brigitta Loretz; Claus-Michael Lehr; Rupert Handgretinger; Michael S D Kormann
Journal:  Sci Rep       Date:  2018-11-13       Impact factor: 4.379

8.  Exploring Associations Between Self-Compassion, Self-Criticism, Mental Health, and Quality of Life in Adults with Cystic Fibrosis: Informing Future Interventions.

Authors:  S Kauser; R Keyte; A Regan; E F Nash; G Fitch; M Mantzios; H Egan
Journal:  J Clin Psychol Med Settings       Date:  2021-11-08

9.  Health-Related Quality of Life in Adults with Cystic Fibrosis: Familial, Occupational, Social, and Mental Health Predictors.

Authors:  Julien Ancel; Claire Launois; Jeanne-Marie Perotin; Bruno Ravoninjatovo; Pauline Mulette; Jean Hagenburg; Julie Malet; Muriel Griffon; Sophie Carré; François Lebargy; Gaëtan Deslée; Sandra Dury
Journal:  Healthcare (Basel)       Date:  2022-07-21
  9 in total

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