Safety and Effectiveness of a 3-Day Rush Insect Venom Immunotherapy Protocol.


Journal

International archives of allergy and immunology
ISSN: 1423-0097
Titre abrégé: Int Arch Allergy Immunol
Pays: Switzerland
ID NLM: 9211652

Informations de publication

Date de publication:
2020
Historique:
received: 25 06 2019
accepted: 08 10 2019
pubmed: 4 12 2019
medline: 11 2 2020
entrez: 4 12 2019
Statut: ppublish

Résumé

Venom immunotherapy (VIT) is an established and effective treatment for patients with Hymenoptera venom allergies. Especially during the build-up of VIT, systemic allergic reactions are a key issue. To investigate the safety and effectiveness of a 3-day rush insect VIT protocol and a strategy for the management of individuals with VIT-induced anaphylaxis. In this retrospective monocentric study, 11-year data regarding build-up cycles of VIT were retrieved from institutional records. The following parameters of VIT-induced anaphylaxis were analyzed: frequency, severity, time of occurrence within the build-up cycle, and impact on the success of VIT. The effectiveness of VIT was assessed by the results of sting challenges (SCs) by the culprit insect. In total, 1,317 initial build-up cycles of VIT were evaluated in this study, and the frequency of VIT-induced anaphylaxis was 6.6%. Anaphylaxis occurred most frequently when the daily cumulative venom dose was ≥100 µg. A group (n = 65) of patients with VIT-induced anaphylaxis in this dose range temporarily received a reduced maintenance dose, and without additional co-medications or complications, the target dose was reached after a second build-up in 91% of the cycles. After completing the VIT build-up, SCs were performed in 76.9% of the cohort, and the effectiveness of VIT was confirmed by 98.5% of the tests. In this study, we report a 3-day VIT rush protocol with a reasonable rate of VIT-induced anaphylaxis and excellent effectiveness of VIT.

Sections du résumé

BACKGROUND
Venom immunotherapy (VIT) is an established and effective treatment for patients with Hymenoptera venom allergies. Especially during the build-up of VIT, systemic allergic reactions are a key issue.
OBJECTIVE
To investigate the safety and effectiveness of a 3-day rush insect VIT protocol and a strategy for the management of individuals with VIT-induced anaphylaxis.
METHODS
In this retrospective monocentric study, 11-year data regarding build-up cycles of VIT were retrieved from institutional records. The following parameters of VIT-induced anaphylaxis were analyzed: frequency, severity, time of occurrence within the build-up cycle, and impact on the success of VIT. The effectiveness of VIT was assessed by the results of sting challenges (SCs) by the culprit insect.
RESULTS
In total, 1,317 initial build-up cycles of VIT were evaluated in this study, and the frequency of VIT-induced anaphylaxis was 6.6%. Anaphylaxis occurred most frequently when the daily cumulative venom dose was ≥100 µg. A group (n = 65) of patients with VIT-induced anaphylaxis in this dose range temporarily received a reduced maintenance dose, and without additional co-medications or complications, the target dose was reached after a second build-up in 91% of the cycles. After completing the VIT build-up, SCs were performed in 76.9% of the cohort, and the effectiveness of VIT was confirmed by 98.5% of the tests.
CONCLUSIONS
In this study, we report a 3-day VIT rush protocol with a reasonable rate of VIT-induced anaphylaxis and excellent effectiveness of VIT.

Identifiants

pubmed: 31794966
pii: 000503965
doi: 10.1159/000503965
doi:

Substances chimiques

Allergens 0
Arthropod Venoms 0
Immunologic Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111-118

Informations de copyright

© 2019 S. Karger AG, Basel.

Auteurs

Paula Kranert (P)

Department of Dermatology, Faculty of Medicine, Eberhard Karls University, Tübingen, Germany.

Stephan Forchhammer (S)

Department of Dermatology, Faculty of Medicine, Eberhard Karls University, Tübingen, Germany.

Sebastian Volc (S)

Department of Dermatology, Faculty of Medicine, Eberhard Karls University, Tübingen, Germany.

Franziska Stenger (F)

Department of Dermatology, Faculty of Medicine, Eberhard Karls University, Tübingen, Germany.

Martin Schaller (M)

Department of Dermatology, Faculty of Medicine, Eberhard Karls University, Tübingen, Germany.

Jörg Fischer (J)

Department of Dermatology, Faculty of Medicine, Eberhard Karls University, Tübingen, Germany, joerg.fischer@med.uni-tuebingen.de.

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