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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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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