Literature DB >> 15752683

Associations between clinical variables and quality of life in adults with cystic fibrosis.

Louise Gee1, Janice Abbott, Anna Hart, Steven P Conway, Christine Etherington, A Kevin Webb.   

Abstract

BACKGROUND: The disease progression of cystic fibrosis (CF) is marked by an increase in clinical conditions and therapeutic interventions, which have the potential to affect health-related quality of life (HRQoL). This cross-sectional study explored associations between clinical variables and HRQoL.
METHODS: HRQoL was measured using the Cystic Fibrosis Quality of Life (CFQoL) questionnaire, which consists of nine domains: physical, social, treatment, chest symptoms, emotional functioning, concerns for the future, relationships, body image, and career concerns. The CFQoL was completed by 223 adults with CF. Clinical and demographic data collected were: age, gender, FEV1% predicted, BMI, Burkholderia cepacia status, lung transplant status, diabetic status, level of nutritional intervention, and presence of an intravenous access device. Multiple regression using forward selection was used to construct models relating these variables to each HRQoL domain.
RESULTS: Despite many of the variables being inter-related, some variables were associated with CFQoL domains even in the presence of other important clinical factors. FEV1% predicted was weakly positively associated with all nine domains. Strong evidence emerged that patients who had received a lung transplant reported a higher HRQoL in physical and social functioning, chest symptoms, and treatment issues. Females tended to report a lower quality of life for chest symptoms and career issues, but higher values for body image. Patients with an access device expressed more career concerns. There was no evidence of an association between B. cepacia and any of the nine CFQoL domains. The model for the body image domain explained a high percentage of the variance (R2=30%): negative body image was associated with lower BMI, having an access device, diabetes, and enteral feeding.
CONCLUSIONS: While important associations were identified, much of the variance in HRQoL remains unexplained. Other clinical and psychosocial variables merit investigation. A longitudinal study is required to investigate how the disease trajectory and associated treatments affect an individual's quality of life.

Entities:  

Mesh:

Year:  2005        PMID: 15752683     DOI: 10.1016/j.jcf.2004.12.005

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


  20 in total

Review 1.  Quality of life in rare genetic conditions: a systematic review of the literature.

Authors:  Julie S Cohen; Barbara B Biesecker
Journal:  Am J Med Genet A       Date:  2010-05       Impact factor: 2.802

2.  Effects of lung transplantation on inpatient end of life care in cystic fibrosis.

Authors:  Elisabeth P Dellon; Margaret W Leigh; James R Yankaskas; Terry L Noah
Journal:  J Cyst Fibros       Date:  2007-05-03       Impact factor: 5.482

3.  Self-reported physical and psychological symptom burden in adults with cystic fibrosis.

Authors:  Gregory S Sawicki; Deborah E Sellers; Walter M Robinson
Journal:  J Pain Symptom Manage       Date:  2008-01-22       Impact factor: 3.612

4.  The development and validation of a quality-of-life questionnaire for head and neck cancer patients with enteral feeding tubes: the QOL-EF.

Authors:  Christiaan Seimeon Michael Stevens; Betty Lemon; Gina A Lockwood; John N Waldron; Andrea Bezjak; Jolie Ringash
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5.  [Routine otorhinolaryngological examination in patients with cystic fibrosis].

Authors:  A Koitschev; A Wolff; C Koitschev; S Preyer; R Ziebach; M Stern
Journal:  HNO       Date:  2006-05       Impact factor: 1.284

6.  Nutritional status is associated with health-related quality of life in children with cystic fibrosis aged 9-19 years.

Authors:  Suzanne M Shoff; Audrey Tluczek; Anita Laxova; Philip M Farrell; HuiChuan J Lai
Journal:  J Cyst Fibros       Date:  2013-02-12       Impact factor: 5.482

7.  Associations between illness perceptions and health-related quality of life in adults with cystic fibrosis.

Authors:  Gregory S Sawicki; Deborah E Sellers; Walter M Robinson
Journal:  J Psychosom Res       Date:  2010-08-10       Impact factor: 3.006

8.  Family caregiver perspectives on symptoms and treatments for patients dying from complications of cystic fibrosis.

Authors:  Elisabeth P Dellon; Mitchell D Shores; Katherine I Nelson; Joanne Wolfe; Terry L Noah; Laura C Hanson
Journal:  J Pain Symptom Manage       Date:  2010-09-17       Impact factor: 3.612

Review 9.  Patient-reported outcomes in cystic fibrosis.

Authors:  Christopher H Goss; Alexandra L Quittner
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

10.  Exercise and quality of life in patients with cystic fibrosis: A 12-week intervention study.

Authors:  Anne Mette Schmidt; Ulla Jacobsen; Vibeke Bregnballe; Hanne Vebert Olesen; Thorsten Ingemann-Hansen; Mikael Thastum; Peter Oluf Schiøtz
Journal:  Physiother Theory Pract       Date:  2011-07-03       Impact factor: 2.279

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