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Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies

BACKGROUND: Hereditary Angioedema (HAE), a rare genetic disease, manifests as intermittent, painful attacks of angioedema. Attacks vary in frequency and severity and include skin, abdominal and life-threatening laryngeal swellings. This study aimed to develop a patient reported outcome (PRO) tool fo...

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Autores principales: Bonner, Nicola, Abetz-Webb, Linda, Renault, Lydie, Caballero, Teresa, Longhurst, Hilary, Maurer, Marcus, Christiansen, Sandra, Zuraw, Bruce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487558/
https://www.ncbi.nlm.nih.gov/pubmed/26129930
http://dx.doi.org/10.1186/s12955-015-0292-7
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author Bonner, Nicola
Abetz-Webb, Linda
Renault, Lydie
Caballero, Teresa
Longhurst, Hilary
Maurer, Marcus
Christiansen, Sandra
Zuraw, Bruce
author_facet Bonner, Nicola
Abetz-Webb, Linda
Renault, Lydie
Caballero, Teresa
Longhurst, Hilary
Maurer, Marcus
Christiansen, Sandra
Zuraw, Bruce
author_sort Bonner, Nicola
collection PubMed
description BACKGROUND: Hereditary Angioedema (HAE), a rare genetic disease, manifests as intermittent, painful attacks of angioedema. Attacks vary in frequency and severity and include skin, abdominal and life-threatening laryngeal swellings. This study aimed to develop a patient reported outcome (PRO) tool for the assessment of HAE attacks, including their management and impact on patients’ lives, for use in clinical studies, or by physicians in general practice. METHODS: The results of open-ended face to face concept elicitation interviews with HAE patients in Argentina (n = 10) and the US (n = 33) were used to develop the first draft questionnaire of the HAE patient reported outcomes questionnaire (HAE PRO). Subsequently, in-depth cognitive debriefing interviews were performed with HAE patients in the UK (n = 10), Brazil (n = 10), Germany (n = 11) and France (n = 12). Following input from eight multinational clinical experts further cognitive interviews were conducted in the US (n = 12) and Germany (n = 12). Patients who experienced abdominal, cutaneous or laryngeal attacks of varying severity levels were included in all rounds of interviews. Across the rounds of interviews patients discussed their HAE attack symptoms, impacts and treatments. Cognitive debriefing interviews explored patient understanding and relevance of questionnaire items. All interviews were conducted face to face following a pre-defined semi-structured interview guide in the patient’s native language. RESULTS: Patients reported a variety of HAE symptoms, attack triggers, warning signs, attack impacts and treatment options which were used to develop the HAE PRO. The HAE PRO was revised and refined following input from patients and clinical experts. The final 18-item HAE PRO provides an assessment of the HAE attack experience including symptoms, impacts, treatment requirements, healthcare resource use and loss of productivity caused by HAE attacks. CONCLUSIONS: Patient and expert input has contributed to the development of a content valid questionnaire that assesses concepts important to HAE patients globally. HAE patients across cultures consider the HAE PRO a relevant and appropriate assessment of HAE attacks and treatment.
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spelling pubmed-44875582015-07-02 Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies Bonner, Nicola Abetz-Webb, Linda Renault, Lydie Caballero, Teresa Longhurst, Hilary Maurer, Marcus Christiansen, Sandra Zuraw, Bruce Health Qual Life Outcomes Research Article BACKGROUND: Hereditary Angioedema (HAE), a rare genetic disease, manifests as intermittent, painful attacks of angioedema. Attacks vary in frequency and severity and include skin, abdominal and life-threatening laryngeal swellings. This study aimed to develop a patient reported outcome (PRO) tool for the assessment of HAE attacks, including their management and impact on patients’ lives, for use in clinical studies, or by physicians in general practice. METHODS: The results of open-ended face to face concept elicitation interviews with HAE patients in Argentina (n = 10) and the US (n = 33) were used to develop the first draft questionnaire of the HAE patient reported outcomes questionnaire (HAE PRO). Subsequently, in-depth cognitive debriefing interviews were performed with HAE patients in the UK (n = 10), Brazil (n = 10), Germany (n = 11) and France (n = 12). Following input from eight multinational clinical experts further cognitive interviews were conducted in the US (n = 12) and Germany (n = 12). Patients who experienced abdominal, cutaneous or laryngeal attacks of varying severity levels were included in all rounds of interviews. Across the rounds of interviews patients discussed their HAE attack symptoms, impacts and treatments. Cognitive debriefing interviews explored patient understanding and relevance of questionnaire items. All interviews were conducted face to face following a pre-defined semi-structured interview guide in the patient’s native language. RESULTS: Patients reported a variety of HAE symptoms, attack triggers, warning signs, attack impacts and treatment options which were used to develop the HAE PRO. The HAE PRO was revised and refined following input from patients and clinical experts. The final 18-item HAE PRO provides an assessment of the HAE attack experience including symptoms, impacts, treatment requirements, healthcare resource use and loss of productivity caused by HAE attacks. CONCLUSIONS: Patient and expert input has contributed to the development of a content valid questionnaire that assesses concepts important to HAE patients globally. HAE patients across cultures consider the HAE PRO a relevant and appropriate assessment of HAE attacks and treatment. BioMed Central 2015-07-01 /pmc/articles/PMC4487558/ /pubmed/26129930 http://dx.doi.org/10.1186/s12955-015-0292-7 Text en © Bonner et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bonner, Nicola
Abetz-Webb, Linda
Renault, Lydie
Caballero, Teresa
Longhurst, Hilary
Maurer, Marcus
Christiansen, Sandra
Zuraw, Bruce
Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies
title Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies
title_full Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies
title_fullStr Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies
title_full_unstemmed Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies
title_short Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies
title_sort development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487558/
https://www.ncbi.nlm.nih.gov/pubmed/26129930
http://dx.doi.org/10.1186/s12955-015-0292-7
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