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Tryptase levels in children presenting with anaphylaxis: Temporal trends and associated factors.
De Schryver, Sarah; Halbrich, Michelle; Clarke, Ann; La Vieille, Sebastien; Eisman, Harley; Alizadehfar, Reza; Joseph, Lawrence; Morris, Judy; Ben-Shoshan, Moshe.
Afiliação
  • De Schryver S; Division of Allergy and Clinical Immunology, Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada.
  • Halbrich M; Division of Paediatric Allergy and Clinical Immunology, Department of Paediatrics, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Clarke A; Division of Rheumatology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • La Vieille S; Food Directorate, Health Canada, Ottawa, Ontario, Canada.
  • Eisman H; Department of Emergency Medicine, Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada.
  • Alizadehfar R; Division of Allergy and Clinical Immunology, Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada.
  • Joseph L; Department of Epidemiology and Biostatistics, McGill University, Montreal, Quebec, Canada.
  • Morris J; Department of Emergency Medicine, Hôpital du Sacré-Cœur, Montreal, Quebec, Canada.
  • Ben-Shoshan M; Division of Allergy and Clinical Immunology, Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada. Electronic address: moshebenshoshan@gmail.com.
J Allergy Clin Immunol ; 137(4): 1138-1142, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26478007
ABSTRACT

BACKGROUND:

The diagnosis of anaphylaxis currently relies on suggestive clinical history after exposure to a potential triggering factor because no reliable diagnostic marker is available to confirm the diagnosis.

OBJECTIVES:

We aimed to evaluate tryptase levels in children with anaphylaxis and to examine predictors of elevated tryptase level (defined as ≥11.4 µg/L during reaction and for those with a baseline level, defined as a reaction level of at least 2 ng/mL + 1.2 × [postreaction tryptase level]).

METHODS:

Children presenting with anaphylaxis to the Montreal Children's Hospital were recruited over a 4-year period. Symptoms, triggers, and management of anaphylaxis were documented. Levels during the reaction and approximately 9 months after the reaction were compared on the basis of paired means using the t distribution. Multivariate linear and logistic regressions were used to evaluate the association between tryptase levels and risk factors.

RESULTS:

Over a 4-year period, 203 children had serum tryptase levels measured. Among these, 39 children (19.2%; 95% CI, 14.1%-25.4%) had elevated levels. Only severe reactions were associated with reaction levels of 11.4 µg/L or more (odds ratio, 6.5; 95% CI, 2.2-19.0). Milk-induced anaphylaxis and severe reactions were more likely associated with increased tryptase levels (beta-adjusted, 4.0; 95% CI, 0.95-7.0, and 7.5; 95% CI, 4.8-10.3, respectively). Reaction levels exceeding the threshold level of 2 ng/mL + 1.2 × (postreaction tryptase level) detected most of the anaphylactic reactions, particularly if baseline levels were taken within 2 months of the reaction.

CONCLUSIONS:

Tryptase levels are particularly useful for the diagnosis of severe and/or milk-induced anaphylaxis. Assessing the difference between reaction and postreaction tryptase levels may improve diagnostic sensitivity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triptases / Anafilaxia Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triptases / Anafilaxia Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2016 Tipo de documento: Article