Your browser doesn't support javascript.
loading
Hypersensitivity to dipyrone in aspirin-exacerbated respiratory disease patients is associated with urticaria.
Agondi, Rosana Câmara; Dias, Gabriella Melo Fontes Silva; Assis, Joao Paulo de; Pacheco, Rosilane; Kalil, Jorge; Giavina-Bianchi, Pedro.
Afiliación
  • Agondi RC; Clinical Immunology and Allergy Division, University of Sao Paulo School of Medicine, São Paulo, Brazil; Laboratory of Immunology (LIM19), Heart Institute (InCor), School of Medicine, University of São Paulo, São Paulo, Brazil. Electronic address: rosana.agondi@hc.fm.usp.br.
  • Dias GMFS; Clinical Immunology and Allergy Division, University of Sao Paulo School of Medicine, São Paulo, Brazil. Electronic address: gabriellamfs@gmail.com.
  • Assis JP; Clinical Immunology and Allergy Division, University of Sao Paulo School of Medicine, São Paulo, Brazil. Electronic address: jpadelfim@yahoo.com.br.
  • Pacheco R; Clinical Immunology and Allergy Division, University of Sao Paulo School of Medicine, São Paulo, Brazil. Electronic address: rosilanepacheco@hotmail.com.
  • Kalil J; Clinical Immunology and Allergy Division, University of Sao Paulo School of Medicine, São Paulo, Brazil; Laboratory of Immunology (LIM19), Heart Institute (InCor), School of Medicine, University of São Paulo, São Paulo, Brazil. Electronic address: jkalil@usp.br.
  • Giavina-Bianchi P; Clinical Immunology and Allergy Division, University of Sao Paulo School of Medicine, São Paulo, Brazil. Electronic address: pbianchi@usp.br.
Respir Med ; 170: 106041, 2020.
Article en En | MEDLINE | ID: mdl-32843172
OBJECTIVE: To phenotype patients with aspirin-exacerbated respiratory disease (AERD) according to the presence of atopy, urticaria and level of peripheral eosinophils. METHODS: This study included adult asthmatic patients with AERD followed up at a tertiary hospital. They were classified according to atopy and/or urticaria, assessing clinical and laboratorial differences among the groups in order to identify possible aggravating factors of the disease. RESULTS: We included 73 patients, 78.1% being female with a mean age of 54.0 years. Severe asthma was observed in 68.5% and respiratory exacerbation with dipyrone in 67.1% of these patients. They had median total serum IgE of 191.6 IU/mL, mean peripheral eosinophils of 718.5 cells/mm3, and 50.7% were atopic. Urticaria was observed in 32.9% of them, and exacerbations were more often triggered by dipyrone (p = .016). Atopic patients were younger than nonatopic patients (p = .023), and had, on average, higher total serum IgE levels (p = .022). We observed a good correlation between asthma severity and peripheral eosinophils count (r2 = 026; p = .021). CONCLUSIONS: In this study, severe asthma was highly prevalent in AERD patients. Likewise, urticaria was quite prevalent and its presence was associated with dipyrone induced hypersensitivity reaction. Atopy was found in half of the patients, with no association with asthma severity. Patients with higher levels of peripheral eosinophils had more severe asthma. Dypirone hypersensitivity may be a marker for concomitant respiratory and cutaneous hypersensitivity reactions.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Urticaria / Antiinflamatorios no Esteroideos / Aspirina / Dipirona / Hipersensibilidad a las Drogas / Asma Inducida por Aspirina / Hipersensibilidad Inmediata Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Respir Med Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Urticaria / Antiinflamatorios no Esteroideos / Aspirina / Dipirona / Hipersensibilidad a las Drogas / Asma Inducida por Aspirina / Hipersensibilidad Inmediata Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Respir Med Año: 2020 Tipo del documento: Article