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1.
Korean Journal of Pediatrics ; : 75-78, 2019.
Article in English | WPRIM | ID: wpr-741363

ABSTRACT

Although rare, antihistamines can cause adverse effects, including drug-induced eruptions or anaphylaxis. A 4-year-old child visited the pediatric department of a hospital for skin eruptions after administration of antihistamines, (e.g., ucerax [hydroxyzine] or leptizine [levocetirizine]), for cholinergic rashes; he did not have pruritus. Skin prick, intradermal, and drug provocation tests were performed to determine the relationship between the antihistamines and eruptions. Levocetirizine induced wheals in the skin prick test and a rash in the oral drug provocation test. In contrast, ketotifen induced no reaction in the skin prick test but showed a positive reaction in the oral provocation test. Our case report highlights that children can experience the same types of adverse reactions as seen in adults, and cross-reactivity between various antihistamines can occur.


Subject(s)
Adult , Child , Child, Preschool , Humans , Anaphylaxis , Drug Eruptions , Exanthema , Histamine Antagonists , Ketotifen , Pruritus , Skin , Urticaria
2.
Allergy, Asthma & Respiratory Disease ; : 336-343, 2017.
Article in Korean | WPRIM | ID: wpr-114706

ABSTRACT

PURPOSE: Ultrarush immunotherapy (ultra-RIT) is more convenient and higher compliant than conventional immunotherapy, but it has rarely used in clinical practice due to severe systemic reactions. This study aimed to determine the safety of ultra-RIT in children and adolescents. METHODS: We investigated 19 patients who received ultra-RIT with the same schedule between January 2011 and May 2016. They were sensitized to house dust mites (HDMs) and/or pollen and had their symptoms associated with positive allergens. Over a 1-day hospitalization period, all patients received ultra-RIT subcutaneously 3 times, increasing at hourly intervals. Systemic reactions were classified according to the World Allergy Organization grade system. RESULTS: Systemic reactions occurred in 14 patients (73.7%). The mean time to adverse reactions after the last injection was 36 minutes, and the majority of systemic reactions were pruritus and urticaria. In addition, the injection of HDM alone or HDM plus pollen caused more than grade 2 systemic reactions in about 50% each of the patients. CONCLUSION: Since ultra-RIT caused a higher incidence of systemic reactions in children and adolescents, it should be carried out cautiously in the hospitalization rather than the office.


Subject(s)
Adolescent , Child , Humans , Allergens , Appointments and Schedules , Hospitalization , Hypersensitivity , Immunotherapy , Incidence , Injections, Subcutaneous , Pediatrics , Pollen , Pruritus , Pyroglyphidae , Urticaria
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