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Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey

BACKGROUND: Generalized pustular psoriasis (GPP) is a rare disease characterized by episodic worsening (flares). Knowledge of the burden of GPP and the experience of affected individuals is limited. AIMS: To conduct a survey of people living with GPP to understand how they experience GPP flares, whi...

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Autores principales: Reisner, Dale V., Johnsson, Frida Dunger, Kotowsky, Nirali, Brunette, Steven, Valdecantos, Wendell, Eyerich, Kilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777175/
https://www.ncbi.nlm.nih.gov/pubmed/35061229
http://dx.doi.org/10.1007/s40257-021-00663-y
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author Reisner, Dale V.
Johnsson, Frida Dunger
Kotowsky, Nirali
Brunette, Steven
Valdecantos, Wendell
Eyerich, Kilian
author_facet Reisner, Dale V.
Johnsson, Frida Dunger
Kotowsky, Nirali
Brunette, Steven
Valdecantos, Wendell
Eyerich, Kilian
author_sort Reisner, Dale V.
collection PubMed
description BACKGROUND: Generalized pustular psoriasis (GPP) is a rare disease characterized by episodic worsening (flares). Knowledge of the burden of GPP and the experience of affected individuals is limited. AIMS: To conduct a survey of people living with GPP to understand how they experience GPP flares, which therapies they have received and are receiving, and how GPP impacts their activities of daily living. METHODS: The online survey consisted of 43 questions answered by individuals recruited from an opt-in market research database. The research team performed a targeted outreach to identify individuals with GPP. The survey included screening questions to determine if potential participants qualified for inclusion. Eligible individuals were US residents aged ≥ 18 years who self-reported that they had been diagnosed with GPP. Respondents provided consent to participate and received compensation (fair market value) for their time. RESULTS: Between August 4 and 14, 2020, 66 people living with GPP in the USA were surveyed. Most participants were female, aged 40–59 years, had been diagnosed ≥ 1 year previously, and had experienced ≥ 2 flares in the past year. A substantial proportion of respondents had symptoms for years, had consulted multiple healthcare professionals, and experienced misdiagnoses before receiving a diagnosis of GPP. Emotional stress was the most common cause of flares and many respondents reported a fear of flares. Respondents defined flares by the presence of itching, an increase in the size of the affected area, more crusts or pustules, and fatigue. A change in mood was the most burdensome symptom. Most respondents were receiving topical corticosteroids and only approximately one-third felt their condition was well controlled. GPP had an impact on activities of daily living even in the absence of flares and many respondents felt that their physician did not understand the level of emotional, psychological, or physical pain caused by GPP. CONCLUSIONS: GPP imposes a substantial emotional burden on patients, with wide-ranging impacts on activities of daily living beyond the physical discomfort of skin lesions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40257-021-00663-y.
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spelling pubmed-87771752022-01-21 Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey Reisner, Dale V. Johnsson, Frida Dunger Kotowsky, Nirali Brunette, Steven Valdecantos, Wendell Eyerich, Kilian Am J Clin Dermatol Original Research Article BACKGROUND: Generalized pustular psoriasis (GPP) is a rare disease characterized by episodic worsening (flares). Knowledge of the burden of GPP and the experience of affected individuals is limited. AIMS: To conduct a survey of people living with GPP to understand how they experience GPP flares, which therapies they have received and are receiving, and how GPP impacts their activities of daily living. METHODS: The online survey consisted of 43 questions answered by individuals recruited from an opt-in market research database. The research team performed a targeted outreach to identify individuals with GPP. The survey included screening questions to determine if potential participants qualified for inclusion. Eligible individuals were US residents aged ≥ 18 years who self-reported that they had been diagnosed with GPP. Respondents provided consent to participate and received compensation (fair market value) for their time. RESULTS: Between August 4 and 14, 2020, 66 people living with GPP in the USA were surveyed. Most participants were female, aged 40–59 years, had been diagnosed ≥ 1 year previously, and had experienced ≥ 2 flares in the past year. A substantial proportion of respondents had symptoms for years, had consulted multiple healthcare professionals, and experienced misdiagnoses before receiving a diagnosis of GPP. Emotional stress was the most common cause of flares and many respondents reported a fear of flares. Respondents defined flares by the presence of itching, an increase in the size of the affected area, more crusts or pustules, and fatigue. A change in mood was the most burdensome symptom. Most respondents were receiving topical corticosteroids and only approximately one-third felt their condition was well controlled. GPP had an impact on activities of daily living even in the absence of flares and many respondents felt that their physician did not understand the level of emotional, psychological, or physical pain caused by GPP. CONCLUSIONS: GPP imposes a substantial emotional burden on patients, with wide-ranging impacts on activities of daily living beyond the physical discomfort of skin lesions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40257-021-00663-y. Springer International Publishing 2022-01-21 2022 /pmc/articles/PMC8777175/ /pubmed/35061229 http://dx.doi.org/10.1007/s40257-021-00663-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research Article
Reisner, Dale V.
Johnsson, Frida Dunger
Kotowsky, Nirali
Brunette, Steven
Valdecantos, Wendell
Eyerich, Kilian
Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey
title Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey
title_full Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey
title_fullStr Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey
title_full_unstemmed Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey
title_short Impact of Generalized Pustular Psoriasis from the Perspective of People Living with the Condition: Results of an Online Survey
title_sort impact of generalized pustular psoriasis from the perspective of people living with the condition: results of an online survey
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777175/
https://www.ncbi.nlm.nih.gov/pubmed/35061229
http://dx.doi.org/10.1007/s40257-021-00663-y
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