Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Standards for practical intravenous rapid drug desensitization & delabeling : A WAO committee statement. / Steering Committee Authors; Review Panel Members.

I: World Allergy Organization Journal, Bind 15, Nr. 6, 100640, 06.2022.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Steering Committee Authors & Review Panel Members 2022, 'Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement', World Allergy Organization Journal, bind 15, nr. 6, 100640. https://doi.org/10.1016/j.waojou.2022.100640

APA

Steering Committee Authors, & Review Panel Members (2022). Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement. World Allergy Organization Journal, 15(6), [100640]. https://doi.org/10.1016/j.waojou.2022.100640

Vancouver

Steering Committee Authors, Review Panel Members. Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement. World Allergy Organization Journal. 2022 jun.;15(6). 100640. https://doi.org/10.1016/j.waojou.2022.100640

Author

Steering Committee Authors ; Review Panel Members. / Standards for practical intravenous rapid drug desensitization & delabeling : A WAO committee statement. I: World Allergy Organization Journal. 2022 ; Bind 15, Nr. 6.

Bibtex

@article{87fcb3587c2a4a18a25f8971aba9ca96,
title = "Standards for practical intravenous rapid drug desensitization & delabeling: A WAO committee statement",
abstract = "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).",
keywords = "Antibiotic desensitization, Antibiotics, Betalactams, Biological agents, Chemotherapy, Delabeling, Drug allergy, Drug challenge, Drug desensitization, Drug provocation test, Penicillins, Personalized medicine, Precision medicine, Risk stratification, Skin test",
author = "Ricardo Madrigal-Burgaleta and Emilio Alvarez-Cuesta and Broyles, {Ana D.} and Javier Cuesta-Herranz and Guzman-Melendez, {Maria Antonieta} and Maciag, {Michelle C.} and Phillips, {Elizabeth J.} and Trubiano, {Jason A.} and Wong, {Johnson T.} and Ignacio Ansotegui and Ali, {F. Runa} and Denisse Angel-Pereira and Aleena Banerji and Berges-Gimeno, {Maria Pilar} and Lorena Bernal-Rubio and Knut Brockow and {Cardona Villa}, Ricardo and Castells, {Mariana C.} and Caubet, {Jean Christoph} and Chang, {Yoon Seok} and Ensina, {Luis Felipe} and Manana Chikhladze and Chiriac, {Anca Mirela} and Chung, {Weng Hung} and Motohiro Ebisawa and Bryan Fernandes and Garvey, {Lene Heise} and Maximiliano Gomez and {Gomez Vera}, Javier and {Gonzalez Diaz}, Sandra and Hong, {David I.} and Ivancevich, {Juan Carlos} and Kang, {Hye Ryun} and Khan, {David A.} and Merin Kuruvilla and {Larco Sousa}, {Jose Ignacio} and Patricia Latour-Staffeld and Liu, {Anne Y.} and Eric Macy and Malling, {Hans Jorgen} and Jorge Maspero and May, {Sara M.} and Cristobalina Mayorga and Park, {Miguel A.} and Jonathan Peter and Matthieu Picard and Tito Rodriguez-Bouza and Antonino Romano and Tanno, {Luciana Kase} and Torres, {Maria Jose} and {Steering Committee Authors} and {Review Panel Members}",
note = "Publisher Copyright: {\textcopyright} 2022 The Authors",
year = "2022",
month = jun,
doi = "10.1016/j.waojou.2022.100640",
language = "English",
volume = "15",
journal = "The World Allergy Organization Journal",
issn = "1939-4551",
publisher = "BioMed Central Ltd.",
number = "6",

}

RIS

TY - JOUR

T1 - Standards for practical intravenous rapid drug desensitization & delabeling

T2 - A WAO committee statement

AU - Madrigal-Burgaleta, Ricardo

AU - Alvarez-Cuesta, Emilio

AU - Broyles, Ana D.

AU - Cuesta-Herranz, Javier

AU - Guzman-Melendez, Maria Antonieta

AU - Maciag, Michelle C.

AU - Phillips, Elizabeth J.

AU - Trubiano, Jason A.

AU - Wong, Johnson T.

AU - Ansotegui, Ignacio

AU - Ali, F. Runa

AU - Angel-Pereira, Denisse

AU - Banerji, Aleena

AU - Berges-Gimeno, Maria Pilar

AU - Bernal-Rubio, Lorena

AU - Brockow, Knut

AU - Cardona Villa, Ricardo

AU - Castells, Mariana C.

AU - Caubet, Jean Christoph

AU - Chang, Yoon Seok

AU - Ensina, Luis Felipe

AU - Chikhladze, Manana

AU - Chiriac, Anca Mirela

AU - Chung, Weng Hung

AU - Ebisawa, Motohiro

AU - Fernandes, Bryan

AU - Garvey, Lene Heise

AU - Gomez, Maximiliano

AU - Gomez Vera, Javier

AU - Gonzalez Diaz, Sandra

AU - Hong, David I.

AU - Ivancevich, Juan Carlos

AU - Kang, Hye Ryun

AU - Khan, David A.

AU - Kuruvilla, Merin

AU - Larco Sousa, Jose Ignacio

AU - Latour-Staffeld, Patricia

AU - Liu, Anne Y.

AU - Macy, Eric

AU - Malling, Hans Jorgen

AU - Maspero, Jorge

AU - May, Sara M.

AU - Mayorga, Cristobalina

AU - Park, Miguel A.

AU - Peter, Jonathan

AU - Picard, Matthieu

AU - Rodriguez-Bouza, Tito

AU - Romano, Antonino

AU - Tanno, Luciana Kase

AU - Torres, Maria Jose

AU - Steering Committee Authors

AU - Review Panel Members

N1 - Publisher Copyright: © 2022 The Authors

PY - 2022/6

Y1 - 2022/6

N2 - 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).

AB - 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).

KW - Antibiotic desensitization

KW - Antibiotics

KW - Betalactams

KW - Biological agents

KW - Chemotherapy

KW - Delabeling

KW - Drug allergy

KW - Drug challenge

KW - Drug desensitization

KW - Drug provocation test

KW - Penicillins

KW - Personalized medicine

KW - Precision medicine

KW - Risk stratification

KW - Skin test

U2 - 10.1016/j.waojou.2022.100640

DO - 10.1016/j.waojou.2022.100640

M3 - Review

C2 - 35694005

AN - SCOPUS:85134599289

VL - 15

JO - The World Allergy Organization Journal

JF - The World Allergy Organization Journal

SN - 1939-4551

IS - 6

M1 - 100640

ER -

ID: 327941684