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Oral Immunotherapy for Cow's Milk Allergy: Five Years' Experience from a Single Center in Turkey
Demir, Esen; Cigerci Günaydin, Nursen; Gülen, Figen; Tanaç, Remziye.
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  • Demir E; Department of Pediatrics, Ege University School of Medicine, Izmir, Turkey
  • Cigerci Günaydin N; Department of Pediatrics, Namik Kemal University School of Medicine, Tekirdag, Turkey
  • Gülen F; Department of Pediatrics, Ege University School of Medicine, Izmir, Turkey
  • Tanaç R; Department of Pediatrics, Ege University School of Medicine, Izmir, Turkey
Balkan Med J ; 37(6): 316-323, 2020 10 23.
Article en En | MEDLINE | ID: mdl-32648410
Background: Oral immunotherapy for cow's milk allergy is an effective treatment option because of its ability to increase the threshold for clinical reactions. Aims: To present our experience of oral immunotherapy for cow's milk allergy in the pediatric allergy outpatient clinic, and to evaluate the long-term efficacy of oral immunotherapy and risk factors for adverse reactions during oral immunotherapy. Study Design: Single-center retrospective cohort study. Methods: Forty-two patients with Immunoglobulin-E-mediated cow's milk allergy who complied with the oral immunotherapy protocol were evaluated in this study. The treatment consisted of a rapid escalation phase with an oral food challenge step that included milk doses. During the build-up phase, increasing quantities of cow's milk were administered until the patient was able to consume 200 mL of cow's milk daily. Results: The mean age of starting the oral immunotherapy was 40.2±3.2 (range, 36-156) months, and 54.8% (n=23) of the patients were males. The mean duration of the build-up phase was 18.1±5.6 (range, 9-41) weeks, and the mean maintenance phase was 29.1±11.6 (range, 12-63) months. During the oral immunotherapy, 36 adverse reactions (78% mild and 22% moderate) occurred in 16 (38%) patients. There were no differences in the age of starting the oral immunotherapy (p=0.19), cow's milk-specific Immunoglobulin-E levels (p=0.17), and cumulative provocative doses of oral food challenges (p=0.78) between the two groups of patients with and without adverse reactions. The wheal diameters to cow's milk were higher in the group with adverse reactions (p=0.03). There was no difference in the oral immunotherapy onset age between patients with and without a history of anaphylaxis (p=0.38). The patients with a history of anaphylaxis had more adverse reactions (p=0.04) and a higher number of reactions during the oral immunotherapy (p=0.01), and a higher mean duration of the up-dosing phase (p=0.04) compared with patients without anaphylaxis. Conclusion: Oral immunotherapy is a treatment option in patients with cow's milk allergy because of its high efficacy. Adverse reactions occur in about 40% of cases and are mostly mild. It should be administered with caution to patients with a history of anaphylaxis and a higher wheal diameter to cow's milk in the skin prick test.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hipersensibilidad a la Leche / Inmunoterapia Tipo de estudio: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Animals / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Balkan Med J Año: 2020 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hipersensibilidad a la Leche / Inmunoterapia Tipo de estudio: Etiology_studies / Guideline / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Animals / Child / Child, preschool / Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Balkan Med J Año: 2020 Tipo del documento: Article País de afiliación: Turquía