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. 2015 Sep 22;187(13):994. doi: 10.1503/cmaj.141264

Venom anaphylaxis

Jeffrey Alfonsi 1,, Jason K Lee 1
PMCID: PMC4577347  PMID: 26054610

Fatal venom anaphylaxis is more common in adults than in children

About 3% of adults and 0.8% of children will have a severe systemic hypersensitivity reaction to venom from honeybee, wasp, white-faced hornet, yellow jacket or yellow hornet.1 Immediate management of anaphylaxis involves prompt intramuscular administration of epinephrine (0.3 mg 1:1000 for adults, 0.15 mg 1:1000 for children < 30 kg; both doses are available in autoinjectors).2

As many as 20% of patients with anaphylaxis to insect stings have biphasic reactions

The second reaction usually occurs within 10 hours of the sting (range 1–30 h),3 with the highest risk within the first 4–6 hours. Patients need to be in a monitored setting regardless of their initial response to epinephrine.3

The diagnosis of venom allergy is made by intradermal or immunoglobulin E testing

All patients with reactions to venom should undergo assessment using intradermal venom administration (sensitivity > 97% at 1 μg/mL) or immunoglobulin E testing in vitro (sensitivity 70%–80%).4 Testing should be done 4–6 weeks after a sting; earlier testing may give a false-negative result.4

Long-term management should involve an anaphylaxis action plan

After initial treatment (Appendix 1, www.cmaj.ca/lookup/suppl/doi:10.1503/cmaj.141264/-/DC1), every patient with suspected or confirmed venom anaphylaxis should be given two epinephrine autoinjectors, be provided with resources on insect avoidance and develop an anaphylaxis action plan (see resources). Referral to a clinical immunologist and allergist is recommended.2

Venom immunotherapy is the only disease-modifying treatment for insect sting anaphylaxis

Immunotherapy involves administering multiple escalating doses of venom to induce an anergic state. A Cochrane review of 6 randomized controlled trials involving 392 patients showed the risk of subsequent systemic reaction after immunotherapy was 2.7%, compared with 39.8% in the control groups receiving placebo (risk ratio 0.10, 95% confidence interval 0.03–0.28).5 Unfortunately, administrative barriers limit widespread adoption of this therapy.

Resources.

Footnotes

Competing interests: Jason Lee reports receiving personal fees from Merck, Omega, Alcon, Pfizer and Takeda; he has received personal fees and grants from CSL Behring, AstraZeneca, Novartis and Paladin; he has received grants from GlaxoSmithKline and ALK. No other competing interests were declared.

This article has been peer reviewed.

References

  • 1.Bilò BM, Bonifazi F. Epidemiology of insect-venom anaphylaxis. Curr Opin Allergy Clin Immunol 2008; 8: 330–7. [DOI] [PubMed] [Google Scholar]
  • 2.Golden DB, Moffitt JE, Nicklas RA. Stinging insect hypersensitivity: a practice parameter update 2011. J Allergy Clin Immunol 2011;127:852–4.e1–23. [DOI] [PubMed] [Google Scholar]
  • 3.Tole JW, Lieberman P. Biphasic anaphylaxis: review of incidence, clinical predictors, and observation recommendations. Immunol Allergy Clin North Am 2007;27:309–26. [DOI] [PubMed] [Google Scholar]
  • 4.Golden DB, Kagey-Sobotka A, Norman PS, et al. Insect sting allergy with negative venom skin test responses. J Allergy Clin Immunol 2001;107:897–901. [DOI] [PubMed] [Google Scholar]
  • 5.Boyle RJ, Elremeli M, Hockenhull J, et al. Venom immunotherapy for preventing allergic reactions to insect stings. Cochrane Database Syst Rev 2012; (10): CD008838. [DOI] [PMC free article] [PubMed] [Google Scholar]

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