Publication:
Safety and efficacy of ant rush immunotherapy in children

dc.contributor.authorWiparat Manuyakornen_US
dc.contributor.authorSuwat Benjaponpitaken_US
dc.contributor.authorWasu Kamchaisatianen_US
dc.contributor.authorCherapat Sasisakulpornen_US
dc.contributor.authorWanlapa Jotikasthiraen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-12-21T07:54:02Z
dc.date.accessioned2019-03-14T08:03:46Z
dc.date.available2018-12-21T07:54:02Z
dc.date.available2019-03-14T08:03:46Z
dc.date.issued2017-09-01en_US
dc.description.abstract© 2017, Allergy and Immunology Society of Thailand. All rights reserved. Background: The Rush Immunotherapy (RIT) protocol is a valid alternative in order to reach the maintenance phase early. However, there are scarce studies in the literature that have evaluated the safety and the efficacy of an ant RIT process in children. Objective: To evaluate the safety and the efficacy of an ant RIT protocol and to identify the risk factors for systemic reactions (SRs) during an RIT procedure in children. Method: A retrospective review was conducted for those children who were receiving an ant RIT procedure. The 3-day RIT protocol consisted of hourly subcutaneous injections in order to achieve a 0.5 ml maintenance dose of a 1:100 weight/ volume (wt/vol) of the Solenopsis invicta whole body extract. The safety for an RIT procedure was monitored by using the World Allergy Organization Subcutaneous Immunology Systemic Reaction Grading System. The efficacy was assessed by the reactions after a field ant re-sting. Results: A total of 20 children who were receiving an ant RIT therapy were reviewed. The mean age was 9.5±3.07 years. There were 6 systemic reactions (SRs) from 324 injections during the RIT procedure (1.85%). All of the systemic reactions were Grade 1-2. There were no associations of SRs regarding age, gender, an atopic history, or the levels of immunoglobulin E (IgE) sensitization to the ants. Among the 14 patients who experienced a field ant re-sting, 4 (28.5%) patients developed Grade 3 SRs. These Grade 3 reactions were resolved after an increase of the maintenance dose to 0.5 ml of a 1:50 wt/vol. There was a significant difference in the mean age of those children who had ant re-sting systemic reactions and those who had no reactions (6.75±0.95 year vs. 10.8±3.29, p=0.036). Conclusions: Rush immunotherapy with ant in children is safe and it has a low occurrence of severe systemic reactions. It is an alternative treatment for those patients requiring a rapid protectionen_US
dc.identifier.citationAsian Pacific Journal of Allergy and Immunology. Vol.35, No.3 (2017), 156-160en_US
dc.identifier.doi10.12932/AP0831en_US
dc.identifier.issn22288694en_US
dc.identifier.issn0125877Xen_US
dc.identifier.other2-s2.0-85034596493en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/42737
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85034596493&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titleSafety and efficacy of ant rush immunotherapy in childrenen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85034596493&origin=inwarden_US

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