Patient reported outcome measures in rare diseases: a narrative review

Abstract Background Rare diseases can lead to a significant reduction in quality of life for patients and their families. Ensuring the patients voice is central to clinical decision making is key to delivering, evaluating and understanding the efficacy of therapeutic interventions. Patient reported...

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Main Authors: Anita Slade, Fatima Isa, Derek Kyte, Tanya Pankhurst, Larissa Kerecuk, James Ferguson, Graham Lipkin, Melanie Calvert
Format: Article
Language:English
Published: BMC 2018-04-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13023-018-0810-x
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spelling doaj-3a9f790d61844c2092be93b5cbdf7a8e2020-11-25T02:26:01ZengBMCOrphanet Journal of Rare Diseases1750-11722018-04-011311910.1186/s13023-018-0810-xPatient reported outcome measures in rare diseases: a narrative reviewAnita Slade0Fatima Isa1Derek Kyte2Tanya Pankhurst3Larissa Kerecuk4James Ferguson5Graham Lipkin6Melanie Calvert7Centre for Patient Reported Outcome Research, College of Medical and Dental Sciences, University of Birmingham EdgbastonPublic Health EnglandCentre for Patient Reported Outcome Research, College of Medical and Dental Sciences, University of Birmingham EdgbastonCentre for Patient Reported Outcome Research, College of Medical and Dental Sciences, University of Birmingham EdgbastonCentre for Patient Reported Outcome Research, College of Medical and Dental Sciences, University of Birmingham EdgbastonCentre for Patient Reported Outcome Research, College of Medical and Dental Sciences, University of Birmingham EdgbastonCentre for Patient Reported Outcome Research, College of Medical and Dental Sciences, University of Birmingham EdgbastonCentre for Patient Reported Outcome Research, College of Medical and Dental Sciences, University of Birmingham EdgbastonAbstract Background Rare diseases can lead to a significant reduction in quality of life for patients and their families. Ensuring the patients voice is central to clinical decision making is key to delivering, evaluating and understanding the efficacy of therapeutic interventions. Patient reported outcome measures (PROMs) are used to capture the patient’s views about their health status and facilitate our understanding of the impact of these diseases and their treatments on patient’s quality of life and symptoms. Main text This review explores some of the current issues around the utilisation of PROMs in rare diseases, including small patient populations and dearth of valid PROMs. Difficulties in validating new or current PROMs for use in clinical trials and research are discussed. The review highlights potential solutions for some of the issues outlined in the review and the implementation of PROMs in research and clinical practice are discussed. Conclusion Patient input throughout the development of PROMs including qualitative research is essential to ensure that outcomes that matter to people living with rare disease are appropriately captured. Given the large number of rare diseases, small numbers of patients living with each condition and the cost of instrument development, creative and pragmatic solutions to PROM development and use may be necessary. Solutions include qualitative interviews, modern psychometrics and resources such as item banking and computer adaptive testing. Use of PROMs in rare disease research and clinical practice offers the potential to improve patient care and clinical outcomes.http://link.springer.com/article/10.1186/s13023-018-0810-xRare diseasesRare disordersPatient reported outcome measuresOutcome assessmentsQuality of life
collection DOAJ
language English
format Article
sources DOAJ
author Anita Slade
Fatima Isa
Derek Kyte
Tanya Pankhurst
Larissa Kerecuk
James Ferguson
Graham Lipkin
Melanie Calvert
spellingShingle Anita Slade
Fatima Isa
Derek Kyte
Tanya Pankhurst
Larissa Kerecuk
James Ferguson
Graham Lipkin
Melanie Calvert
Patient reported outcome measures in rare diseases: a narrative review
Orphanet Journal of Rare Diseases
Rare diseases
Rare disorders
Patient reported outcome measures
Outcome assessments
Quality of life
author_facet Anita Slade
Fatima Isa
Derek Kyte
Tanya Pankhurst
Larissa Kerecuk
James Ferguson
Graham Lipkin
Melanie Calvert
author_sort Anita Slade
title Patient reported outcome measures in rare diseases: a narrative review
title_short Patient reported outcome measures in rare diseases: a narrative review
title_full Patient reported outcome measures in rare diseases: a narrative review
title_fullStr Patient reported outcome measures in rare diseases: a narrative review
title_full_unstemmed Patient reported outcome measures in rare diseases: a narrative review
title_sort patient reported outcome measures in rare diseases: a narrative review
publisher BMC
series Orphanet Journal of Rare Diseases
issn 1750-1172
publishDate 2018-04-01
description Abstract Background Rare diseases can lead to a significant reduction in quality of life for patients and their families. Ensuring the patients voice is central to clinical decision making is key to delivering, evaluating and understanding the efficacy of therapeutic interventions. Patient reported outcome measures (PROMs) are used to capture the patient’s views about their health status and facilitate our understanding of the impact of these diseases and their treatments on patient’s quality of life and symptoms. Main text This review explores some of the current issues around the utilisation of PROMs in rare diseases, including small patient populations and dearth of valid PROMs. Difficulties in validating new or current PROMs for use in clinical trials and research are discussed. The review highlights potential solutions for some of the issues outlined in the review and the implementation of PROMs in research and clinical practice are discussed. Conclusion Patient input throughout the development of PROMs including qualitative research is essential to ensure that outcomes that matter to people living with rare disease are appropriately captured. Given the large number of rare diseases, small numbers of patients living with each condition and the cost of instrument development, creative and pragmatic solutions to PROM development and use may be necessary. Solutions include qualitative interviews, modern psychometrics and resources such as item banking and computer adaptive testing. Use of PROMs in rare disease research and clinical practice offers the potential to improve patient care and clinical outcomes.
topic Rare diseases
Rare disorders
Patient reported outcome measures
Outcome assessments
Quality of life
url http://link.springer.com/article/10.1186/s13023-018-0810-x
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