Abstract
Hymenoptera venom allergy is a potentially life-threatening allergic reaction following a honeybee, vespid, or ant sting. Systemic-allergic sting reactions have been reported in up to 7.5% of adults and up to 3.4% of children. They can be mild and restricted to the skin or moderate to severe with a risk of life-threatening anaphylaxis. Patients should carry an emergency kit containing an adrenaline autoinjector, H 1 -antihistamines, and corticosteroids depending on the severity of their previous sting reaction(s). The only treatment to prevent further systemic sting reactions is venom immunotherapy. This guideline has been prepared by the European Academy of Allergy and Clinical Immunology's (EAACI) Taskforce on Venom Immunotherapy as part of the EAACI Guidelines on Allergen Immunotherapy initiative. The guideline aims to provide evidence-based recommendations for the use of venom immunotherapy, has been informed by a formal systematic review and meta-analysis and produced using the Appraisal of Guidelines for Research and Evaluation (AGREE II) approach. The process included representation from a range of stakeholders. Venom immunotherapy is indicated in venom-allergic children and adults to prevent further moderate-to-severe systemic sting reactions. Venom immunotherapy is also recommended in adults with only generalized skin reactions as it results in significant improvements in quality of life compared to carrying an adrenaline autoinjector. This guideline aims to give practical advice on performing venom immunotherapy. Key sections cover general considerations before initiating venom immunotherapy, evidence-based clinical recommendations, risk factors for adverse events and for relapse of systemic sting reaction, and a summary of gaps in the evidence.
Original language | English |
---|---|
Pages (from-to) | 744-764 |
Number of pages | 21 |
Journal | Allergy: European Journal of Allergy and Clinical Immunology |
Volume | 73 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr 2018 |
Keywords
- Hymenoptera venom allergy
- anaphylaxis
- effectiveness
- safety
- venom immunotherapy
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In: Allergy: European Journal of Allergy and Clinical Immunology, Vol. 73, No. 4, 04.2018, p. 744-764.
Research output: Contribution to journal › Article › Research › peer-review
TY - JOUR
T1 - EAACI guidelines on allergen immunotherapy
T2 - Hymenoptera venom allergy
AU - Sturm, G. J.
AU - Varga, E. M.
AU - Roberts, G.
AU - Mosbech, H.
AU - Bilò, M. B.
AU - Akdis, C. A.
AU - Antolín-Amérigo, D.
AU - Cichocka-Jarosz, E.
AU - Gawlik, R.
AU - Jakob, T.
AU - Kosnik, M.
AU - Lange, J.
AU - Mingomataj, E.
AU - Mitsias, D. I.
AU - Ollert, M.
AU - Oude Elberink, J. N.G.
AU - Pfaar, O.
AU - Pitsios, C.
AU - Pravettoni, V.
AU - Ruëff, F.
AU - Sin, B. A.
AU - Agache, I.
AU - Angier, E.
AU - Arasi, S.
AU - Calderón, M. A.
AU - Fernandez-Rivas, M.
AU - Halken, S.
AU - Jutel, M.
AU - Lau, S.
AU - Pajno, G. B.
AU - van Ree, R.
AU - Ryan, D.
AU - Spranger, O.
AU - van Wijk, R. G.
AU - Dhami, S.
AU - Zaman, H.
AU - Sheikh, A.
AU - Muraro, A.
N1 - Funding Information: The EAACI Guideline VIT Taskforce would like to thank Stefan Vieths and Andreas Bonertz for their advice; Patrizia Bonadonna and Axel Trautmann for their expert review of the draft guideline; all the EAACI members who commented about the draft guideline on the public Web site; and EAACI and the EU for the BM4SIT project (grant number 601763) in the European Union’s Seventh Framework Programme FP7 for funding this guideline. Funding Information: G Sturm reports grants and personal fees from ALK Abello, Novartis, Stallergens, Bencard Allergy and Leti outside of the submitted work; E-M Varga reports lecture fees from ALK-Abello, Stallergenes-Greer, Allergopharma, Bencard, MEDA and Nutricia outside the submitted work; G. Roberts has a patent issued: “Use of sublingual immunotherapy to prevent the development of allergy in at risk infants”; and his university has received payments for the activities he has undertaken giving expert advice to ALK, and presenting at company symposia for ALK, Allergen Therapeutics, and Meda, and serving as a member of an Independent Data Monitoring Committee for Merck outside of this work; Dr. Mosbech reports other from ALK-Abello, outside the submitted work; Dr. Bilò reports personal fees from Alk -Abello, personal fees from Thermo Fisher - Phadia, outside the submitted work; Dr. Akdis reports grants from Actellion, grants from EU FP 7 Grants Medall and Predicta, grants from Allergopharma, grants from Swiss National Science Foundation, grants from Christine Ku€hne Center for Allergy Research and Education, outside the submitted work; Dr. Antolín-Amérigo reports personal fees from Astra-Zeneca, personal fees from ALK-Abelló, grants from Merck-Serono, personal fees from Diater Laboratorios, personal fees from Leti, grants from Pfizer, personal fees from Allergy Therapeutics, personal fees from GlaxoSmithKline, personal fees from Mundipharma, personal fees from MEDA, personal fees from Stallergenes, outside the submitted work; Dr. Jakob reports non-financial support from German Society of Allergy Clinical Immunology as member of the executive board, personal fees and non-financial support from Springer Nature as editor of Allergo Journal International, grants and personal fees from ALK Abello, Allergopharma, Novartis and Thermo Fisher Scientific, personal fees from Allergy therapeutics/Bencard, and from Leti GmbH, outside the submitted work; Dr. Ollert reports personal fees from Thermo Fisher - Phadia, personal fees from Siemens Healthineers Diagnostics, personal fees from Allergy Therapeutics/Bencard, outside the submitted work; and Scientific Co-Founder of Protein-Ligand-Structural-Design GmbH (PLS-Design), Hamburg/ Munich, Germany; G. Pajno reports grants from Stallergenes during the conduct of this work; O. Pfaar reports grants and personal fees from ALK-Abello, Allergopharma, Stallergenes Greer, HAL-Allergy Holding B.V./HAL-Allergie GmbH, Bencard Allergie GmbH/Allergy Therapeutics, Lofarma, Biotech Tools S.A., Laboratorios LETI/LETI Pharma, and Anergis S.A.; grants from Biomay, Nuvo, and Circassia; and personal fees from MEDA Pharma, Sanofi US Services, Mobile Chamber Experts (a GA2LEN Partner), Novartis Pharma and Pohl-Boskamp, outside this work; Dr. Rue€ff reports personal fees for consultancy from ALK Abelló Arzneimittel GmbH, Bencard, Thermo Fisher Scientific, Dr. Gerhard Mann chem.-pharm. Fabrik GmbH, and Novartis, payment for lectures from ALK Abelló, Astra Zeneca, Ben-card, Novartis, MEDA Pharma GmbH & Co, Novartis, and Stallerge-nes, and a research grant from Novartis outside the submitted work; E Angier reports previous advisory board membership for Staller-genes, Meda and Schering Plough plus a sponsored lecture by Meda and attendance at a ALK SOSA meeting; M. Calderon has received honorarium in advisory boards for ALK and Hal-Allergy and served as a speaker for ALK, Merck, and Stallergenes Greer; S. Halken reports personal fees from ALK-Abello and from different companies, for example, Meda, Stallergenes, Allergopharma, and ALK-Abello, outside of this work; M Fernandez-Rivas reports personal fees from ALK, Merck and GSK; S. Halken reports personal fees from ALK-Abello and from different companies, for example, Meda, Staller-genes, Allergopharma, and ALK-Abello, outside of this work. M Jutel reports personal fees from Allergopharma, Anergis, Stallergens, ALK, LETI outside the submitted work; S Lau reports a grant from Allergo-pharma plus personal fees for data monitoring committee activities for Merck; G. Pajno reports grants from Stallergenes during the conduct of this work; R van Ree reports personal fees from HAL Allergy BV and Citeq BV outside of the submitted work; D Ryan reports personal fees from Stallergenes, Thermo Fisher, MEDA outside of the submitted work; R. Gerth van Wijk reports personal fees from ALK-Abello, Circassia, and Allergopharma, during the conduct of this work.; S. Dhami reports grants from EAACI to carry out the review, during the conduct of this work; A. Sheikh reports grants from the EAACI during the conduct of this work; A. Muraro reports personal fees from Novartis, Meda, and Mylan, outside the submitted work. The other authors declare that they have no conflict of interest. Publisher Copyright: © 2017 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.
PY - 2018/4
Y1 - 2018/4
N2 - Hymenoptera venom allergy is a potentially life-threatening allergic reaction following a honeybee, vespid, or ant sting. Systemic-allergic sting reactions have been reported in up to 7.5% of adults and up to 3.4% of children. They can be mild and restricted to the skin or moderate to severe with a risk of life-threatening anaphylaxis. Patients should carry an emergency kit containing an adrenaline autoinjector, H 1 -antihistamines, and corticosteroids depending on the severity of their previous sting reaction(s). The only treatment to prevent further systemic sting reactions is venom immunotherapy. This guideline has been prepared by the European Academy of Allergy and Clinical Immunology's (EAACI) Taskforce on Venom Immunotherapy as part of the EAACI Guidelines on Allergen Immunotherapy initiative. The guideline aims to provide evidence-based recommendations for the use of venom immunotherapy, has been informed by a formal systematic review and meta-analysis and produced using the Appraisal of Guidelines for Research and Evaluation (AGREE II) approach. The process included representation from a range of stakeholders. Venom immunotherapy is indicated in venom-allergic children and adults to prevent further moderate-to-severe systemic sting reactions. Venom immunotherapy is also recommended in adults with only generalized skin reactions as it results in significant improvements in quality of life compared to carrying an adrenaline autoinjector. This guideline aims to give practical advice on performing venom immunotherapy. Key sections cover general considerations before initiating venom immunotherapy, evidence-based clinical recommendations, risk factors for adverse events and for relapse of systemic sting reaction, and a summary of gaps in the evidence.
AB - Hymenoptera venom allergy is a potentially life-threatening allergic reaction following a honeybee, vespid, or ant sting. Systemic-allergic sting reactions have been reported in up to 7.5% of adults and up to 3.4% of children. They can be mild and restricted to the skin or moderate to severe with a risk of life-threatening anaphylaxis. Patients should carry an emergency kit containing an adrenaline autoinjector, H 1 -antihistamines, and corticosteroids depending on the severity of their previous sting reaction(s). The only treatment to prevent further systemic sting reactions is venom immunotherapy. This guideline has been prepared by the European Academy of Allergy and Clinical Immunology's (EAACI) Taskforce on Venom Immunotherapy as part of the EAACI Guidelines on Allergen Immunotherapy initiative. The guideline aims to provide evidence-based recommendations for the use of venom immunotherapy, has been informed by a formal systematic review and meta-analysis and produced using the Appraisal of Guidelines for Research and Evaluation (AGREE II) approach. The process included representation from a range of stakeholders. Venom immunotherapy is indicated in venom-allergic children and adults to prevent further moderate-to-severe systemic sting reactions. Venom immunotherapy is also recommended in adults with only generalized skin reactions as it results in significant improvements in quality of life compared to carrying an adrenaline autoinjector. This guideline aims to give practical advice on performing venom immunotherapy. Key sections cover general considerations before initiating venom immunotherapy, evidence-based clinical recommendations, risk factors for adverse events and for relapse of systemic sting reaction, and a summary of gaps in the evidence.
KW - Hymenoptera venom allergy
KW - anaphylaxis
KW - effectiveness
KW - safety
KW - venom immunotherapy
UR - http://www.scopus.com/inward/record.url?scp=85037373305&partnerID=8YFLogxK
UR - https://pubmed.ncbi.nlm.nih.gov/28748641
U2 - 10.1111/all.13262
DO - 10.1111/all.13262
M3 - Article
C2 - 28748641
AN - SCOPUS:85037373305
SN - 0105-4538
VL - 73
SP - 744
EP - 764
JO - Allergy: European Journal of Allergy and Clinical Immunology
JF - Allergy: European Journal of Allergy and Clinical Immunology
IS - 4
ER -