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Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement
Drug hypersensitivity reactions (DHRs) to intravenous drugs can be severe and might leave patients and doctors in a difficult position where an essential treatment or intervention has to be suspended. Even if virtually any intravenous medication can potentially trigger a life-threatening DHR, chemot...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
World Allergy Organization
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163606/ https://www.ncbi.nlm.nih.gov/pubmed/35694005 http://dx.doi.org/10.1016/j.waojou.2022.100640 |
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author | Alvarez-Cuesta, Emilio Madrigal-Burgaleta, Ricardo Broyles, Ana D. Cuesta-Herranz, Javier Guzman-Melendez, Maria Antonieta Maciag, Michelle C. Phillips, Elizabeth J. Trubiano, Jason A. Wong, Johnson T. Ansotegui, Ignacio |
author_facet | Alvarez-Cuesta, Emilio Madrigal-Burgaleta, Ricardo Broyles, Ana D. Cuesta-Herranz, Javier Guzman-Melendez, Maria Antonieta Maciag, Michelle C. Phillips, Elizabeth J. Trubiano, Jason A. Wong, Johnson T. Ansotegui, Ignacio |
author_sort | Alvarez-Cuesta, Emilio |
collection | PubMed |
description | Drug hypersensitivity reactions (DHRs) to intravenous drugs can be severe and might leave patients and doctors in a difficult position where an essential treatment or intervention has to be suspended. Even if virtually any intravenous medication can potentially trigger a life-threatening DHR, chemotherapeutics, biologics, and antibiotics are amongst the intravenous drugs most frequently involved in these reactions. Admittedly, suspending such treatments may negatively impact the survival outcomes or the quality of life of affected patients. Delabeling pathways and rapid drug desensitization (RDD) can help reactive patients stay on first-choice therapies instead of turning to less efficacious, less cost-effective, or more toxic alternatives. However, these are high-complexity and high-risk techniques, which usually need expert teams and allergy-specific techniques (skin testing, in vitro testing, drug provocation testing) to ensure safety, an accurate diagnosis, and personalized management. Unfortunately, there are significant inequalities within and among countries in access to allergy departments with the necessary expertise and resources to offer these techniques and tackle these DHRs optimally. The main objective of this consensus document is to create a great benefit for patients worldwide by aiding allergists to expand the scope of their practice and support them with evidence, data, and experience from leading groups from around the globe. This statement of the Drug Hypersensitivity Committee of the World Allergy Organization (WAO) aims to be a comprehensive practical guide on the technical aspects of implementing acute-onset intravenous hypersensitivity delabeling and RDD for a wide range of drugs. Thus, the manuscript does not only focus on clinical pathways. Instead, it also provides guidance on topics usually left unaddressed, namely, internal validation, continuous quality improvement, creating a healthy multidisciplinary environment, and redesigning care (including a specific supplemental section on a real-life example of how to design a dedicated space that can combine basic and complex diagnostic and therapeutic techniques in allergy). |
format | Online Article Text |
id | pubmed-9163606 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | World Allergy Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-91636062022-06-10 Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement Alvarez-Cuesta, Emilio Madrigal-Burgaleta, Ricardo Broyles, Ana D. Cuesta-Herranz, Javier Guzman-Melendez, Maria Antonieta Maciag, Michelle C. Phillips, Elizabeth J. Trubiano, Jason A. Wong, Johnson T. Ansotegui, Ignacio World Allergy Organ J Review Drug hypersensitivity reactions (DHRs) to intravenous drugs can be severe and might leave patients and doctors in a difficult position where an essential treatment or intervention has to be suspended. Even if virtually any intravenous medication can potentially trigger a life-threatening DHR, chemotherapeutics, biologics, and antibiotics are amongst the intravenous drugs most frequently involved in these reactions. Admittedly, suspending such treatments may negatively impact the survival outcomes or the quality of life of affected patients. Delabeling pathways and rapid drug desensitization (RDD) can help reactive patients stay on first-choice therapies instead of turning to less efficacious, less cost-effective, or more toxic alternatives. However, these are high-complexity and high-risk techniques, which usually need expert teams and allergy-specific techniques (skin testing, in vitro testing, drug provocation testing) to ensure safety, an accurate diagnosis, and personalized management. Unfortunately, there are significant inequalities within and among countries in access to allergy departments with the necessary expertise and resources to offer these techniques and tackle these DHRs optimally. The main objective of this consensus document is to create a great benefit for patients worldwide by aiding allergists to expand the scope of their practice and support them with evidence, data, and experience from leading groups from around the globe. This statement of the Drug Hypersensitivity Committee of the World Allergy Organization (WAO) aims to be a comprehensive practical guide on the technical aspects of implementing acute-onset intravenous hypersensitivity delabeling and RDD for a wide range of drugs. Thus, the manuscript does not only focus on clinical pathways. Instead, it also provides guidance on topics usually left unaddressed, namely, internal validation, continuous quality improvement, creating a healthy multidisciplinary environment, and redesigning care (including a specific supplemental section on a real-life example of how to design a dedicated space that can combine basic and complex diagnostic and therapeutic techniques in allergy). World Allergy Organization 2022-05-31 /pmc/articles/PMC9163606/ /pubmed/35694005 http://dx.doi.org/10.1016/j.waojou.2022.100640 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Alvarez-Cuesta, Emilio Madrigal-Burgaleta, Ricardo Broyles, Ana D. Cuesta-Herranz, Javier Guzman-Melendez, Maria Antonieta Maciag, Michelle C. Phillips, Elizabeth J. Trubiano, Jason A. Wong, Johnson T. Ansotegui, Ignacio Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement |
title | Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement |
title_full | Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement |
title_fullStr | Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement |
title_full_unstemmed | Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement |
title_short | Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement |
title_sort | standards for practical intravenous rapid drug desensitization & delabeling: a wao committee statement |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163606/ https://www.ncbi.nlm.nih.gov/pubmed/35694005 http://dx.doi.org/10.1016/j.waojou.2022.100640 |
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