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Risk factors in Hymenoptera venom allergy
F Ruëff1, J Kroth1, B Przybilla1
1AllergieZentrum, Klinik und Poliklinik für Dermatologie und Allergologie, Ludwig-Maximilians-Universität, Munich, Germany.
Allergologie Select
|November 8, 2018
Summary
Identifying risk factors is crucial for offering venom immunotherapy (VIT) and managing treatment. Key factors influence severe reactions and treatment failure in Hymenoptera sting allergies.
Area of Science:
- Allergy and Immunology
- Toxicology
Background:
- Systemic anaphylactic reactions (SAR) following Hymenoptera stings pose significant health risks.
- Venom immunotherapy (VIT) is an effective treatment, but requires careful patient selection and management due to potential risks.
Purpose of the Study:
- To identify risk factors associated with severe systemic anaphylactic reactions (SAR) after Hymenoptera stings.
- To determine risk factors for SAR during VIT and treatment failure.
- To provide guidance on optimizing VIT protocols based on identified risks.
Main Methods:
- Review of clinical data and literature on Hymenoptera sting reactions and VIT.
- Analysis of patient characteristics, sting history, and treatment parameters.
- Identification of correlations between risk factors and outcomes (SAR, treatment failure).
Main Results:
- Risk factors for SAR include prior sting severity, wasp stings, elevated baseline serum tryptase concentration (BSTC), mastocytosis, older age, ACE inhibitor use, and male gender.
- During VIT, honey bee venom treatment, high BSTC (for vespid VIT), venom-specific IgE, antihypertensive medication, and ultra-rush protocols increase SAR risk.
- Treatment failure is linked to honey bee venom allergy, high BSTC (for vespid VIT), mastocytosis, and prior VIT side effects.
Conclusions:
- Risk factor assessment is essential for personalized VIT decisions and administration.
- Minimizing risks involves managing antihypertensive medications and adjusting build-up protocols.
- Increasing maintenance doses may enhance VIT efficacy, especially in high-risk patients or those with treatment failure, with 200 µg often being sufficient.
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