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1.
Allergol Immunopathol (Madr) ; 52(3): 60-64, 2024.
Article in English | MEDLINE | ID: mdl-38721956

ABSTRACT

Delayed anaphylaxis after ingestion of red meat because of galactose-alpha-1,3-galactose (alpha-gal) syndrome has increased in recent years. The mechanism involves an immunoglobulin E reaction to alpha-gal, a molecule found in mammalian meat, dairy products, medications and excipients containing mammalian-derived components, and tick salivary glycans. Sensitization occurs due to the bite of a lone star tick and the transmission of alpha-gal molecules into person's bloodstream. We describe a case of alpha-gal syndrome with severe food, drug, and perioperative allergy in which anaphylaxis with hypovolemic shock occurred immediately after an emergency surgical procedure, when a gelatin-containing drug was injected. This case study confirms that the clinical manifestations of alpha-gal syndrome could be different depending on the route of administration, with immediate reactions if an alpha-gal-containing drug is injected and delayed type allergic manifestations occurring several hours after oral intake. The purpose of this report is to highlight the importance of risk communication in case of exposure to medical products and surgical procedures of patients with alpha-gal syndrome and to encourage drug manufacturers to indicate clearly the origin of excipients in product literature.


Subject(s)
Anaphylaxis , Food Hypersensitivity , Shock , Humans , Anaphylaxis/diagnosis , Anaphylaxis/therapy , Anaphylaxis/etiology , Food Hypersensitivity/diagnosis , Food Hypersensitivity/complications , Food Hypersensitivity/immunology , Shock/etiology , Shock/diagnosis , Drug Hypersensitivity/diagnosis , Drug Hypersensitivity/therapy , Male , Animals , Immunoglobulin E/immunology , Excipients/adverse effects , Disaccharides/immunology , Disaccharides/adverse effects , Female , Trisaccharides/immunology , Gelatin/adverse effects , Syndrome
2.
Pediatr Allergy Immunol ; 34(6): e13967, 2023 06.
Article in English | MEDLINE | ID: mdl-37366202

ABSTRACT

Currently available vaccines are safe, but, potentially, any vaccine can cause an allergic reaction and, albeit very rare, anaphylaxis can occur. Although its rarity, the precise diagnostic management of a suspected anaphylaxis postvaccination is of paramount importance due to the risk of a potentially serious reaction after re-exposure, while a misdiagnosis might lead to an increase in the number of children that interrupt vaccinations resulting in an unjustifiably individual and collective risk of loss of protection against immune preventable diseases. In the light that most cases of suspected allergy to a vaccine are not effectively confirmed in up to 85% of the cases referred for an allergy evaluation, patients can continue the vaccination schedule with the same formulation and tolerance of the booster doses. The patient assessment has to be done by an expert in the vaccine field, usually an allergist or an immunologist depending on the country, to select subjects at risk of allergic reactions and to perform the correct procedures for vaccine hypersensitivity diagnosis and management, in order to guarantee safe immunization practices. The aim of this review is to provide a practical guidance for the safe management of allergic children undergoing immunization procedures. The guide is referred both to the evaluation of children who have previously experienced a suspected allergic reaction to a specific vaccine and their management in case of further booster doses, and to children allergic to a component of the vaccine to be administered.


Subject(s)
Anaphylaxis , Vaccines , Child , Humans , Anaphylaxis/diagnosis , Anaphylaxis/etiology , Vaccines/adverse effects , Vaccination/adverse effects , Vaccination/methods
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