Literature DB >> 19176710

Health-related quality of life measurement in cystic fibrosis: advances and limitations.

J Abbott1.   

Abstract

Health-related quality of life (HRQoL) measurement in cystic fibrosis (CF) allows the inclusion of the patient's perspective in research and clinical practice. HRQoL scales have been used for many purposes and this review focuses on how HRQoL measurement has been implemented in CF research and care. Specifically, the review considers 1) the instruments used to measure HRQoL, 2) the factors that influence how people report HRQoL, 3) the monitoring of HRQoL in clinical practice, 4) HRQoL as an outcome measure in interventions and clinical trials and 5) whether HRQoL can predict survival. The challenge for the future is to use the available information to develop and evaluate psychological interventions that would be expected to improve HRQoL in children and adults with CF.

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Year:  2009        PMID: 19176710     DOI: 10.1177/1479972308098159

Source DB:  PubMed          Journal:  Chron Respir Dis        ISSN: 1479-9723            Impact factor:   2.444


  7 in total

1.  Self-esteem and its relationship to mental health and quality of life in adults with cystic fibrosis.

Authors:  Melanie Jane Platten; Emily Newman; Ethel Quayle
Journal:  J Clin Psychol Med Settings       Date:  2013-09

2.  How about your peers? Cystic fibrosis questionnaire data from healthy children and adolescents.

Authors:  Marijke M Tibosch; Coosje J J C M Sintnicolaas; Jeannette B Peters; Peter J F M Merkus; Jan-Bart L Yntema; Christianne M Verhaak; Jan H Vercoulen
Journal:  BMC Pediatr       Date:  2011-10-11       Impact factor: 2.125

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.  Cough suppression and HRQoL in adult people with cystic fibrosis: an unexplored correlation.

Authors:  Raphael Hirtz; Florian Stehling; Ute Niehammer; Mathis Steindor; Svenja Straßburg; Sivagurunathan Sutharsan; Christian Taube; Matthias Welsner
Journal:  Health Qual Life Outcomes       Date:  2022-10-06       Impact factor: 3.077

5.  Acceptability of patient reported outcome measures (PROMs) in a cystic fibrosis data registry.

Authors:  Irushi Ratnayake; Susannah Ahern; Rasa Ruseckaite
Journal:  BMJ Open Respir Res       Date:  2021-07

6.  Sensitivity to Change and Minimal Important Differences of the LupusQoL in Patients With Systemic Lupus Erythematosus.

Authors:  Kathleen McElhone; Janice Abbott; Chris Sutton; Montana Mullen; Peter Lanyon; Anisur Rahman; Chee-Seng Yee; Mohammed Akil; Ian N Bruce; Yasmeen Ahmad; Caroline Gordon; Lee-Suan Teh
Journal:  Arthritis Care Res (Hoboken)       Date:  2016-09-02       Impact factor: 4.794

7.  Patient-Reported Outcome Measures in Cystic Fibrosis: Protocol for a Systematic Review.

Authors:  Irushi Ratnayake; Susannah Ahern; Rasa Ruseckaite
Journal:  JMIR Res Protoc       Date:  2020-05-06
  7 in total

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