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Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic
BACKGROUND: According to expert consensus, the time interval between Hymenoptera venom immunotherapy (VIT) injections can be extended up to 12 weeks, without significant impact on efficacy and safety. However, the coronavirus disease 2019 pandemic caused longer delays, and no recommendations are ava...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Academy of Allergy, Asthma & Immunology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690271/ https://www.ncbi.nlm.nih.gov/pubmed/33249121 http://dx.doi.org/10.1016/j.jaip.2020.11.030 |
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author | Bilò, M. Beatrice Braschi, M. Chiara Piga, Mario A. Antonicelli, Leonardo Martini, Matteo |
author_facet | Bilò, M. Beatrice Braschi, M. Chiara Piga, Mario A. Antonicelli, Leonardo Martini, Matteo |
author_sort | Bilò, M. Beatrice |
collection | PubMed |
description | BACKGROUND: According to expert consensus, the time interval between Hymenoptera venom immunotherapy (VIT) injections can be extended up to 12 weeks, without significant impact on efficacy and safety. However, the coronavirus disease 2019 pandemic caused longer delays, and no recommendations are available to manage this huge extension. OBJECTIVES: To provide advice on how to resume VIT safely after a long delay from the last injection considering the potential risk factors for side effects, without starting again with the induction phase. METHODS: All the patients who delayed VIT because of the pandemic were consecutively enrolled in this single-center study. The time extension was decided according to their risk profile (eg, long prepandemic time interval, severe pre-VIT reaction, older age, multitreatments), and correlation analyses were performed to find potential risk factors of side effects. RESULTS: The mean delay from the pre- (7 weeks) to the postpandemic VIT interval (15.5 weeks) was 8.5 weeks. The total amount of the prepandemic VIT maintenance dose was safely administered in 1 day in 78% of patients, whereas only 3, of 87, experienced side effects, and their potential risk factors were identified in bee venom allergy and recent VIT initiation. CONCLUSIONS: In a real-world setting, long VIT delays may be safe and well tolerated, but more caution should be paid in resuming VIT in patients with long prepandemic maintenance interval, severe pre-VIT reaction, recent VIT initiation, older age, multidrug treatments, and bee venom allergy. This is useful in any case of long, unplanned, and unavoidable VIT delay. |
format | Online Article Text |
id | pubmed-7690271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Academy of Allergy, Asthma & Immunology |
record_format | MEDLINE/PubMed |
spelling | pubmed-76902712020-11-27 Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic Bilò, M. Beatrice Braschi, M. Chiara Piga, Mario A. Antonicelli, Leonardo Martini, Matteo J Allergy Clin Immunol Pract Original Article BACKGROUND: According to expert consensus, the time interval between Hymenoptera venom immunotherapy (VIT) injections can be extended up to 12 weeks, without significant impact on efficacy and safety. However, the coronavirus disease 2019 pandemic caused longer delays, and no recommendations are available to manage this huge extension. OBJECTIVES: To provide advice on how to resume VIT safely after a long delay from the last injection considering the potential risk factors for side effects, without starting again with the induction phase. METHODS: All the patients who delayed VIT because of the pandemic were consecutively enrolled in this single-center study. The time extension was decided according to their risk profile (eg, long prepandemic time interval, severe pre-VIT reaction, older age, multitreatments), and correlation analyses were performed to find potential risk factors of side effects. RESULTS: The mean delay from the pre- (7 weeks) to the postpandemic VIT interval (15.5 weeks) was 8.5 weeks. The total amount of the prepandemic VIT maintenance dose was safely administered in 1 day in 78% of patients, whereas only 3, of 87, experienced side effects, and their potential risk factors were identified in bee venom allergy and recent VIT initiation. CONCLUSIONS: In a real-world setting, long VIT delays may be safe and well tolerated, but more caution should be paid in resuming VIT in patients with long prepandemic maintenance interval, severe pre-VIT reaction, recent VIT initiation, older age, multidrug treatments, and bee venom allergy. This is useful in any case of long, unplanned, and unavoidable VIT delay. American Academy of Allergy, Asthma & Immunology 2021-02 2020-11-26 /pmc/articles/PMC7690271/ /pubmed/33249121 http://dx.doi.org/10.1016/j.jaip.2020.11.030 Text en © 2020 American Academy of Allergy, Asthma & Immunology. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Article Bilò, M. Beatrice Braschi, M. Chiara Piga, Mario A. Antonicelli, Leonardo Martini, Matteo Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic |
title | Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic |
title_full | Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic |
title_fullStr | Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic |
title_full_unstemmed | Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic |
title_short | Safety and Adherence to Venom Immunotherapy During COVID-19 Pandemic |
title_sort | safety and adherence to venom immunotherapy during covid-19 pandemic |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690271/ https://www.ncbi.nlm.nih.gov/pubmed/33249121 http://dx.doi.org/10.1016/j.jaip.2020.11.030 |
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