4.5 Review

Improving the Safety of Immunotherapy

Journal

Publisher

ELSEVIER
DOI: 10.1016/j.jaip.2013.09.017

Keywords

Desensitization; Immunologic; Hypersensitivity; Immunotherapy

Funding

  1. Agency for Healthcare Research and Quality Asthma Study
  2. American Academy of Allergy, Asthma, and Immunology/American College of Allergy, Asthma, and Immunology
  3. National Institutes of Health
  4. National Institute for Occupational Safety and Health-Centers for Disease Control
  5. Merck
  6. Merck Advisory Board

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We present a 42-year-old woman who experienced a systemic reaction (SR) after a subcutaneous immunotherapy (SCIT) injection. Her physician must make a decision, along with the patient, on how to proceed. We consider the medical evidence pertinent to specific risk factors for SRs to SCIT, including asthma control, concomitant medications and new medical diagnoses, the influence of pollen season, adjustments for large local reactions, initial testing results, type of buildup protocol, and administration and dosing errors. We next discuss the potential risk-mitigating actions that the patient and provider should consider and the available evidence that supports various approaches, including cessation of SCIT, decreasing allergen dose or altering the timing of injections, initiating or changing the medical pretreatment regimen, and changing to sublingual immunotherapy, and also the role for anaphylaxis preparedness. Finally, we highlight the key knowledge gaps identified in this review and provide management recommendations for this 42-year-old woman. (C) 2013 American Academy of Allergy, Asthma & Immunology

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