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Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism
INTRODUCTION: A patient-reported outcome (PRO) measure specific to chronic hypoparathyroidism is lacking to facilitate the evaluation of treatment. A PRO measure that followed the recommendations of the US Food and Drug Administration (FDA) PRO guidance was created to address key hypoparathyroidism...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822864/ https://www.ncbi.nlm.nih.gov/pubmed/31183782 http://dx.doi.org/10.1007/s12325-019-00999-2 |
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author | Martin, Susan Chen, Kristina Harris, Nimanee Vera-Llonch, Montserrat Krasner, Alan |
author_facet | Martin, Susan Chen, Kristina Harris, Nimanee Vera-Llonch, Montserrat Krasner, Alan |
author_sort | Martin, Susan |
collection | PubMed |
description | INTRODUCTION: A patient-reported outcome (PRO) measure specific to chronic hypoparathyroidism is lacking to facilitate the evaluation of treatment. A PRO measure that followed the recommendations of the US Food and Drug Administration (FDA) PRO guidance was created to address key hypoparathyroidism symptoms. METHODS: A literature review was conducted to identify symptoms of hypoparathyroidism and any existing PRO measures appropriate for evaluating these symptoms, followed by concept elicitation interviews involving six individuals with hypoparathyroidism. On the basis of the results of the literature review and interviews, a draft item pool was developed and refined through two sets of cognitive debriefing interviews with six additional patients. A translatability assessment was also conducted to evaluate concepts, phrases, or components of the items that could be problematic in future translations and to identify culturally specific phrasing. RESULTS: No PRO measures appropriate to address hypoparathyroidism symptoms documented in the literature were identified. Qualitative research participants included 11 women and one man, with an average age of 49 years; the majority (10) of these participants were white. Concept elicitation interview results were generally consistent with the results of the literature review; the most commonly reported symptoms included issues with cognition, often described as “brain fog” (n = 6), muscle cramping (n = 5), tingling (n = 5), and muscle spasms or twitching (n = 4). The initial draft item pool included 20 items; based upon participant feedback, the final Hypoparathyroidism Symptom Diary comprised 13 items and was found to be easily understood and relevant to the participants. No significant issues were identified by the translatability assessment. CONCLUSION: The Hypoparathyroidism Symptom Diary was developed following the recommendations of the FDA’s PRO guidance. The measure addresses a comprehensive set of symptoms, as well as key impacts of hypoparathyroidism deemed important by patients. FUNDING: Shire Human Genetic Therapies, Inc., Lexington, MA, USA, a member of the Takeda group of companies. |
format | Online Article Text |
id | pubmed-6822864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-68228642019-11-06 Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism Martin, Susan Chen, Kristina Harris, Nimanee Vera-Llonch, Montserrat Krasner, Alan Adv Ther Original Research INTRODUCTION: A patient-reported outcome (PRO) measure specific to chronic hypoparathyroidism is lacking to facilitate the evaluation of treatment. A PRO measure that followed the recommendations of the US Food and Drug Administration (FDA) PRO guidance was created to address key hypoparathyroidism symptoms. METHODS: A literature review was conducted to identify symptoms of hypoparathyroidism and any existing PRO measures appropriate for evaluating these symptoms, followed by concept elicitation interviews involving six individuals with hypoparathyroidism. On the basis of the results of the literature review and interviews, a draft item pool was developed and refined through two sets of cognitive debriefing interviews with six additional patients. A translatability assessment was also conducted to evaluate concepts, phrases, or components of the items that could be problematic in future translations and to identify culturally specific phrasing. RESULTS: No PRO measures appropriate to address hypoparathyroidism symptoms documented in the literature were identified. Qualitative research participants included 11 women and one man, with an average age of 49 years; the majority (10) of these participants were white. Concept elicitation interview results were generally consistent with the results of the literature review; the most commonly reported symptoms included issues with cognition, often described as “brain fog” (n = 6), muscle cramping (n = 5), tingling (n = 5), and muscle spasms or twitching (n = 4). The initial draft item pool included 20 items; based upon participant feedback, the final Hypoparathyroidism Symptom Diary comprised 13 items and was found to be easily understood and relevant to the participants. No significant issues were identified by the translatability assessment. CONCLUSION: The Hypoparathyroidism Symptom Diary was developed following the recommendations of the FDA’s PRO guidance. The measure addresses a comprehensive set of symptoms, as well as key impacts of hypoparathyroidism deemed important by patients. FUNDING: Shire Human Genetic Therapies, Inc., Lexington, MA, USA, a member of the Takeda group of companies. Springer Healthcare 2019-06-10 2019 /pmc/articles/PMC6822864/ /pubmed/31183782 http://dx.doi.org/10.1007/s12325-019-00999-2 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Martin, Susan Chen, Kristina Harris, Nimanee Vera-Llonch, Montserrat Krasner, Alan Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism |
title | Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism |
title_full | Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism |
title_fullStr | Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism |
title_full_unstemmed | Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism |
title_short | Development of a Patient-Reported Outcome Measure for Chronic Hypoparathyroidism |
title_sort | development of a patient-reported outcome measure for chronic hypoparathyroidism |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6822864/ https://www.ncbi.nlm.nih.gov/pubmed/31183782 http://dx.doi.org/10.1007/s12325-019-00999-2 |
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