Real-life safety of 5-grass pollen tablet in 5-to-9-year-old children with allergic rhinoconjunctivitis

被引:13
作者
Gerstlauer, Michael [1 ]
Szepfalusi, Zsolt [2 ]
Golden, David [3 ]
Geng, Bob [4 ,5 ]
de Blic, Jacques [6 ,7 ]
机构
[1] Med Univ Augsburg, Pediat Pneumol & Allergol Unit, Augsburg, Germany
[2] Med Univ Vienna, Dept Pediat, Vienna, Austria
[3] Medstar Franklin Sq Med Ctr, Allergy & Immunol, Baltimore, MD USA
[4] Univ Calif San Diego, Rady Childrens Hosp, Severe Asthma Clin, Div Adult, San Diego, CA 92103 USA
[5] Univ Calif San Diego, Rady Childrens Hosp, Severe Asthma Clin, Div Pediat Allergy & Immunol, San Diego, CA 92103 USA
[6] Necker Enfants Malad Hosp, Pediat Pneumol & Allergol Unit, Paris, France
[7] Univ Paris 05, Paris, France
关键词
SUBLINGUAL IMMUNOTHERAPY; CLINICAL-PRACTICE; RHINITIS; ASTHMA; EFFICACY; MANAGEMENT; SYMPTOMS; UPDATE; IMPACT;
D O I
10.1016/j.anai.2019.04.011
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Although 5-grass pollen sublingual immunotherapy has a good safety profile in controlled clinical trials, additional safety information among pediatric patients in a real-world setting would be useful. Objective: To further document the safety of 5-grass tablet among children aged 5 to 9 years with allergic rhinoconjunctivitis (ARC). Methods: This multicenter, observational study included allergy immunotherapy-naive 5- to 9-year-old children with grass pollen-induced ARC prescribed with 5-grass tablet daily (3-day dose escalation to 300 index of reactivity [IR]). Patients were followed up daily for safety and tolerability over the first 30 treatment days. Adverse events (AEs) and adverse drug reactions (ADRs) were analyzed descriptively. Results: Three hundred seven children (mean age, 7.1 years) were enrolled. Fifty-eight percent were confirmed as polysensitized, and 36% had mild-to-moderate asthma. Of 307 patients, 233 (76%) reported AEs, and 173/307 (56%) reported ADRs, most frequently mild application-site reactions (throat irritation, oral pruritus, oral paresthesia). Sixteen of 307 (5.2%) patients withdrew because of ADRs. In 143 of 173 (83%) patients, ADRs first occurred within 1 week of starting treatment. More than half of the ADRs lasted less than 2 days, and ADRs resolved spontaneously in 161 of 173 (93%) patients. Recurrences of ADRs were reported in 45 of 173 (26%) patients and were also mainly application-site reactions. No notable differences were found in ADRs related to whether patients had asthma at inclusion. Neither epinephrine use nor admission to intensive care unit was reported. Conclusion: The safety profile of 5-grass tablet in pediatric ARC patients aged 5 to 9 years was consistent with safety findings in older patients, most ADRs being at the application site and mild to moderate. (C) 2019 Published by Elsevier Inc. on behalf of American College of Allergy, Asthma & Immunology.
引用
收藏
页码:70 / 80
页数:11
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