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Real-world safety and effectiveness evidence of a microcrystalline tyrosine-associated mite allergoid in children and adolescents with allergic rhinitis

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dc.contributor.author Sala-Cunill, Anna
dc.contributor.author Almeida-Sánchez, Zulay-M
dc.contributor.author García-Núñez, Ignacio
dc.contributor.author Lain, Sofia
dc.contributor.author Martínez-Tadeo, Juan-A
dc.contributor.author Martos, María-D
dc.contributor.author Núñez, Ramón
dc.contributor.author Ramírez, Mercedes
dc.contributor.author Boronat, Anna
dc.contributor.author Toran-Barona, Carla
dc.contributor.author Justicia, José-Luis
dc.date.accessioned 2025-11-20T12:48:36Z
dc.date.available 2025-11-20T12:48:36Z
dc.date.issued 2021
dc.identifier.citation Sala-Cunill A, Almeida-Sánchez ZM, García-Núñez I, Laín S, Martínez-Tadeo JA, Martos MD, et al. Real-world safety and effectiveness evidence of a microcrystalline tyrosine-associated mite allergoid in children and adolescents with allergic rhinitis. aei. 1 de julio de 2021;49(4):98-108.
dc.identifier.issn 0301-0546
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/21751
dc.description.abstract Evidence regarding allergen immunotherapy (AIT) in pediatric population is scarce. We have assessed safety and effectiveness of subcutaneous AIT with a microcrystalline tyrosine (MCT)-associated mite allergoid, Acarovac Plus(®), in children and adolescents with allergic rhinitis (AR), with and without asthma, in the real-world setting. This was a retrospective, multicenter study including children and adolescents aged 5 years to 17 years with AR, with and without asthma, and sensitized to mites, receiving AIT with Acarovac Plus(®) during ?6 months. Primary and secondary objectives were safety and effectiveness, respectively. Effectiveness variables were assessed during 12 months before and after AIT and included unscheduled visits to the healthcare center and emergency room admissions, rhinitis and asthma symptoms according to ARIA and GEMA classifications, respectively, medication use, and patients' and physicians' disease perception graded on a visual analog scale (VAS). All 79 patients included had a mean (SD) age of 12.7 (3.3) years. Two patients experienced systemic adverse reactions (none severe). Unscheduled visits to the healthcare center and emergency room admissions decreased (mean (SD) 3.02 [2.48] and 0.63 [1.35] vs. 1.08 [1.38] and 0.09 [0.38], before and after treatment, p < 0.001 and p = 0.001, respectively). After AIT, rhinitis and asthma classification changed (p < 0.0001 for all classifications), showing improvements in symptoms and a significant decrease in rhinitis and use of medication for asthma and VAS scores grading patients' and physicians' disease perception (p < 0.001). In conclusion, these results show that AIT with an MCT-associated mite allergoid appears safe and effective in children and adolescents with AR treated in the real-world setting.
dc.language.iso eng
dc.publisher CODON PUBLICATIONS
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0 *
dc.subject.mesh Adolescent
dc.subject.mesh Allergoids
dc.subject.mesh Animals
dc.subject.mesh Asthma/epidemiology/therapy
dc.subject.mesh Child
dc.subject.mesh Desensitization, Immunologic
dc.subject.mesh Humans
dc.subject.mesh Mites
dc.subject.mesh Retrospective Studies
dc.subject.mesh Rhinitis, Allergic/epidemiology/therapy
dc.subject.mesh Tyrosine
dc.title Real-world safety and effectiveness evidence of a microcrystalline tyrosine-associated mite allergoid in children and adolescents with allergic rhinitis
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 34224224
dc.relation.publisherversion https://all-imm.com/index.php/aei/article/view/195
dc.identifier.doi 10.15586/aei.v49i4.195
dc.journal.title Allergologia Et Immunopathologia
dc.identifier.essn 1578-1267


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