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Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options

BACKGROUND: Chronic spontaneous urticaria (CSU) can be extremely debilitating to the patient and challenging for the treating clinician. The National Institute of Health and Clinical Excellence (NICE) in the United Kingdom (UK) recommendation of omalizumab for patients who fail to respond to high-do...

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Autores principales: Khan, Sujoy, Chopra, Charu, Mitchell, Alaistair, Nakonechna, Alla, Yong, Patrick, Karim, Mohammed Yousuf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791268/
https://www.ncbi.nlm.nih.gov/pubmed/36578314
http://dx.doi.org/10.1177/21526575221144951
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author Khan, Sujoy
Chopra, Charu
Mitchell, Alaistair
Nakonechna, Alla
Yong, Patrick
Karim, Mohammed Yousuf
author_facet Khan, Sujoy
Chopra, Charu
Mitchell, Alaistair
Nakonechna, Alla
Yong, Patrick
Karim, Mohammed Yousuf
author_sort Khan, Sujoy
collection PubMed
description BACKGROUND: Chronic spontaneous urticaria (CSU) can be extremely debilitating to the patient and challenging for the treating clinician. The National Institute of Health and Clinical Excellence (NICE) in the United Kingdom (UK) recommendation of omalizumab for patients who fail to respond to high-dose anti-histamines has improved treatment options and quality of life. However, there is still lack of clear guidelines for treatment of patients resistant to standard and anti-IgE therapies. METHODS: We discuss the therapeutic strategies employed among nine extremely resistant CSU cases and the heterogeneity between guidelines from different societies. RESULTS: Patients with anti-histamine-resistant urticaria either remained on omalizumab or started on immunosuppressive drugs (dapsone or ciclosporin) when they stopped responding to omalizumab. We used clinical assessment, skin biopsies (when available) and previous published reports to consider dapsone (for predominantly neutrophilic infiltration), or ciclosporin at doses between 2 and 4 mg/kg/day. One patient with ciclosporin-resistant urticaria responded to mycophenolate mofetil. Two patients remain on long-term omalizumab due to its relative safety and efficacy including 1 patient with underlying antibody deficiency where omalizumab was preferred over risks of using immunosuppressive medications. CONCLUSIONS: These case studies bring to light the real-world difficulties in managing patients with resistant CSU and the need for generating the evidence base on alternative therapeutic options such as synergistic use of biologics and immunosuppressive drugs.
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spelling pubmed-97912682022-12-27 Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options Khan, Sujoy Chopra, Charu Mitchell, Alaistair Nakonechna, Alla Yong, Patrick Karim, Mohammed Yousuf Allergy Rhinol (Providence) Review BACKGROUND: Chronic spontaneous urticaria (CSU) can be extremely debilitating to the patient and challenging for the treating clinician. The National Institute of Health and Clinical Excellence (NICE) in the United Kingdom (UK) recommendation of omalizumab for patients who fail to respond to high-dose anti-histamines has improved treatment options and quality of life. However, there is still lack of clear guidelines for treatment of patients resistant to standard and anti-IgE therapies. METHODS: We discuss the therapeutic strategies employed among nine extremely resistant CSU cases and the heterogeneity between guidelines from different societies. RESULTS: Patients with anti-histamine-resistant urticaria either remained on omalizumab or started on immunosuppressive drugs (dapsone or ciclosporin) when they stopped responding to omalizumab. We used clinical assessment, skin biopsies (when available) and previous published reports to consider dapsone (for predominantly neutrophilic infiltration), or ciclosporin at doses between 2 and 4 mg/kg/day. One patient with ciclosporin-resistant urticaria responded to mycophenolate mofetil. Two patients remain on long-term omalizumab due to its relative safety and efficacy including 1 patient with underlying antibody deficiency where omalizumab was preferred over risks of using immunosuppressive medications. CONCLUSIONS: These case studies bring to light the real-world difficulties in managing patients with resistant CSU and the need for generating the evidence base on alternative therapeutic options such as synergistic use of biologics and immunosuppressive drugs. SAGE Publications 2022-12-21 /pmc/articles/PMC9791268/ /pubmed/36578314 http://dx.doi.org/10.1177/21526575221144951 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Khan, Sujoy
Chopra, Charu
Mitchell, Alaistair
Nakonechna, Alla
Yong, Patrick
Karim, Mohammed Yousuf
Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options
title Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options
title_full Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options
title_fullStr Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options
title_full_unstemmed Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options
title_short Resistant Chronic Spontaneous Urticaria – A Case Series Narrative Review of Treatment Options
title_sort resistant chronic spontaneous urticaria – a case series narrative review of treatment options
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791268/
https://www.ncbi.nlm.nih.gov/pubmed/36578314
http://dx.doi.org/10.1177/21526575221144951
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