Literature DB >> 17652505

Patient-reported outcomes in cystic fibrosis.

Christopher H Goss1, Alexandra L Quittner.   

Abstract

Over the past 20 years, there has been tremendous progress in the area of patient-reported outcomes (PROs). A PRO instrument is defined as any measure of a patient's health status that is elicited directly from the patient and assesses how the patient "feels or functions with respect to his or her health condition." The advances seen in clinical research regarding PROs has been mirrored in research in cystic fibrosis (CF). A large number of instruments have been used for both therapeutic and nontherapeutic clinical research for many chronic conditions. This review will summarize a history of the development of PROs and how PROs are viewed by the U.S. Food and Drug Administration. We will then review the current state of the art of patient-reported outcomes in CF, specifically addressing the evaluation of different PRO instruments in terms of their reliability and validity. Finally, we will delineate further areas for development of PROs in CF. We believe that the future of CF research will incorporate a more diverse selection of PRO outcome measures; these outcome measures ultimately may be incorporated into clinical care to standardize symptom assessment and provide information regarding the need for specific clinical interventions to improve the quality of care delivered to these patients.

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Year:  2007        PMID: 17652505      PMCID: PMC2647603          DOI: 10.1513/pats.200703-039BR

Source DB:  PubMed          Journal:  Proc Am Thorac Soc        ISSN: 1546-3222


  91 in total

1.  Survival and quality of life of cystic fibrosis patients before and after heart-lung transplantation.

Authors:  N Caine; L D Sharples; R Smyth; J Scott; T Hathaway; T W Higenbottam; J Wallwork
Journal:  Transplant Proc       Date:  1991-02       Impact factor: 1.066

2.  Health-related quality-of-life assessments and patient-physician communication: a randomized controlled trial.

Authors:  Symone B Detmar; Martin J Muller; Jan H Schornagel; Lidwina D V Wever; Neil K Aaronson
Journal:  JAMA       Date:  2002-12-18       Impact factor: 56.272

3.  Effect of disease-related pain on the health-related quality of life of children and adolescents with cystic fibrosis.

Authors:  Tonya M Palermo; Dale Harrison; Jeffrey L Koh
Journal:  Clin J Pain       Date:  2006 Jul-Aug       Impact factor: 3.442

4.  Impact of recent pulmonary exacerbations on quality of life in patients with cystic fibrosis.

Authors:  Maria T Britto; Uma R Kotagal; Richard W Hornung; Harry D Atherton; Joel Tsevat; Robert W Wilmott
Journal:  Chest       Date:  2002-01       Impact factor: 9.410

5.  Translation and linguistic validation of a disease-specific quality of life measure for cystic fibrosis.

Authors:  A L Quittner; S Sweeny; M Watrous; P Munzenberger; K Bearss; A Gibson Nitza; L A Fisher; B Henry
Journal:  J Pediatr Psychol       Date:  2000-09

Review 6.  Methods to explain the clinical significance of health status measures.

Authors:  Gordon H Guyatt; David Osoba; Albert W Wu; Kathleen W Wyrwich; Geoffrey R Norman
Journal:  Mayo Clin Proc       Date:  2002-04       Impact factor: 7.616

7.  Prevalence of pain in adults with cystic fibrosis.

Authors:  Filippo Festini; Silvana Ballarin; Teresa Codamo; Roberta Doro; Carmen Loganes
Journal:  J Cyst Fibros       Date:  2004-03       Impact factor: 5.482

8.  The musculoskeletal complications of cystic fibrosis.

Authors:  R J Massie; S J Towns; E Bernard; J Chaitow; R Howman-Giles; P P Van Asperen
Journal:  J Paediatr Child Health       Date:  1998-10       Impact factor: 1.954

9.  Gender differences in health-related quality of life of adolescents with cystic fibrosis.

Authors:  Renata Arrington-Sanders; Michael S Yi; Joel Tsevat; Robert W Wilmott; Joseph M Mrus; Maria T Britto
Journal:  Health Qual Life Outcomes       Date:  2006-01-24       Impact factor: 3.186

Review 10.  Measuring and reporting quality of life outcomes in clinical trials in cystic fibrosis: a critical review.

Authors:  Janice Abbott; Anna Hart
Journal:  Health Qual Life Outcomes       Date:  2005-03-24       Impact factor: 3.186

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  38 in total

1.  The PROMIS initiative: involvement of rehabilitation stakeholders in development and examples of applications in rehabilitation research.

Authors:  Dagmar Amtmann; Karon F Cook; Kurt L Johnson; David Cella
Journal:  Arch Phys Med Rehabil       Date:  2011-10       Impact factor: 3.966

Review 2.  Outcome measures for development of new therapies in cystic fibrosis: are we making progress and what are the next steps?

Authors:  Bonnie W Ramsey
Journal:  Proc Am Thorac Soc       Date:  2007-08-01

Review 3.  Evidence-based assessment of health-related quality of life and functional impairment in pediatric psychology.

Authors:  Tonya M Palermo; Anna C Long; Amy S Lewandowski; Dennis Drotar; Alexandra L Quittner; Lynn S Walker
Journal:  J Pediatr Psychol       Date:  2008-04-22

4.  Lung transplantation for cystic fibrosis.

Authors:  Frederick R Adler; Paul Aurora; David H Barker; Mark L Barr; Laura S Blackwell; Otto H Bosma; Samuel Brown; D R Cox; Judy L Jensen; Geoffrey Kurland; George D Nossent; Alexandra L Quittner; Walter M Robinson; Sandy L Romero; Helen Spencer; Stuart C Sweet; Wim van der Bij; J Vermeulen; Erik A M Verschuuren; Elianne J L E Vrijlandt; William Walsh; Marlyn S Woo; Theodore G Liou
Journal:  Proc Am Thorac Soc       Date:  2009-12

5.  High treatment burden in adults with cystic fibrosis: challenges to disease self-management.

Authors:  Gregory S Sawicki; Deborah E Sellers; Walter M Robinson
Journal:  J Cyst Fibros       Date:  2008-10-26       Impact factor: 5.482

Review 6.  Determination of the minimal clinically important difference scores for the Cystic Fibrosis Questionnaire-Revised respiratory symptom scale in two populations of patients with cystic fibrosis and chronic Pseudomonas aeruginosa airway infection.

Authors:  Alexandra L Quittner; Avani C Modi; Claire Wainwright; Kelly Otto; Jean Kirihara; A Bruce Montgomery
Journal:  Chest       Date:  2009-05-15       Impact factor: 9.410

Review 7.  Measuring and improving respiratory outcomes in cystic fibrosis lung disease: opportunities and challenges to therapy.

Authors:  Edith T Zemanick; J Kirk Harris; Steven Conway; Michael W Konstan; Bruce Marshall; Alexandra L Quittner; George Retsch-Bogart; Lisa Saiman; Frank J Accurso
Journal:  J Cyst Fibros       Date:  2009-10-14       Impact factor: 5.482

8.  Primary Ciliary Dyskinesia: First Health-related Quality-of-Life Measures for Pediatric Patients.

Authors:  Sharon D Dell; Margaret W Leigh; Jane S Lucas; Thomas W Ferkol; Michael R Knowles; Adrianne Alpern; Laura Behan; Anjana M Morris; Claire Hogg; Audrey DunnGalvin; Alexandra L Quittner
Journal:  Ann Am Thorac Soc       Date:  2016-10

9.  Longitudinal trends in health-related quality of life in adults with cystic fibrosis.

Authors:  Edward J Dill; Ree Dawson; Deborah E Sellers; Walter M Robinson; Gregory S Sawicki
Journal:  Chest       Date:  2013-09       Impact factor: 9.410

10.  Health-related quality of life in children with cystic fibrosis: validation of the German CFQ-R.

Authors:  Anne Schmidt; Kerstin Wenninger; Nadja Niemann; Ulrich Wahn; Doris Staab
Journal:  Health Qual Life Outcomes       Date:  2009-12-02       Impact factor: 3.186

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