Literature DB >> 23721854

Utilization of patient-reported outcomes as a step towards collaborative medicine.

Laura S Blackwell1, Kristen K Marciel, Alexandra L Quittner.   

Abstract

Patient-reported outcomes (PROs) have been successfully developed for a variety of chronic respiratory diseases, such as asthma and cystic fibrosis (CF). They have recently been used to evaluate the efficacy of new medications and assess current patient functioning. Although regulatory bodies have favored PROs that measures symptoms, other domains of functioning, such as treatment burden, should be considered. This review examines current guidelines for the development and application of PROs in clinical trials, describes methods for selecting appropriate measures for paediatric populations, and presents a model incorporating PROs into clinical practice. Guidance on interpretation of these measures and graphic presentation of results are illustrated. PROs can serve as the link between the health care provider and patient to foster collaborative and personalized medicine. This model promotes greater patient responsibility, facilitates communication with providers, encourages shared decision-making, and enhances adherence. Published by Elsevier Ltd.

Entities:  

Keywords:  Collaborative Medicine; EMA; FDA; Health-Related Quality of Life; Patient Reported Outcomes; cystic fibrosis

Mesh:

Year:  2013        PMID: 23721854     DOI: 10.1016/j.prrv.2013.04.003

Source DB:  PubMed          Journal:  Paediatr Respir Rev        ISSN: 1526-0542            Impact factor:   2.726


  8 in total

1.  Quality of life in children with CF: Psychometrics and relations with stress and mealtime behaviors.

Authors:  Kimberly A Driscoll; Avani C Modi; Stephanie S Filigno; Erin E Brannon; Leigh Ann Chamberlin; Lori J Stark; Scott W Powers
Journal:  Pediatr Pulmonol       Date:  2014-12-30

2.  Standardized Clinical Pathways for Hospitalized Children and Outcomes.

Authors:  K Casey Lion; Davene R Wright; Suzanne Spencer; Chuan Zhou; Mark Del Beccaro; Rita Mangione-Smith
Journal:  Pediatrics       Date:  2016-03-21       Impact factor: 7.124

3.  Interventions for promoting participation in shared decision-making for children and adolescents with cystic fibrosis.

Authors:  Helen Malone; Susan Biggar; Sheila Javadpour; Zai Edworthy; Greg Sheaf; Imelda Coyne
Journal:  Cochrane Database Syst Rev       Date:  2019-05-23

4.  Integrative analysis of longitudinal metabolomics data from a personal multi-omics profile.

Authors:  Larissa Stanberry; George I Mias; Winston Haynes; Roger Higdon; Michael Snyder; Eugene Kolker
Journal:  Metabolites       Date:  2013-09-03

Review 5.  Patient-reported outcome measures for pain in women with pelvic floor disorders: a systematic review.

Authors:  Maisie Ralphsmith; Susannah Ahern; Joanne Dean; Rasa Ruseckaite
Journal:  Int Urogynecol J       Date:  2022-03-02       Impact factor: 1.932

6.  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

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

8.  A systematic review of patient-reported outcome measures (PROMs) in cystic fibrosis.

Authors:  Irushi Ratnayake; Susannah Ahern; Rasa Ruseckaite
Journal:  BMJ Open       Date:  2020-10-01       Impact factor: 2.692

  8 in total

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