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The safety and efficacy of live attenuated influenza vaccine in young children with asthma or prior wheezing.

机译:减毒活流感疫苗对年幼哮喘或哮喘患者的安全性和有效性。

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In the European Union and Canada, an Ann Arbor strain live attenuated influenza vaccine (LAIV) is approved for use in children aged 2-17 years, including those with mild to moderate asthma or prior wheezing. The safety and efficacy of LAIV versus trivalent inactivated influenza vaccine (TIV) in children with asthma aged 6-17 years have been demonstrated. However, few data are available for children younger than 6 years of age with asthma or prior wheezing. Safety and efficacy data were collected for children aged 2-5 years with asthma or prior wheezing from two randomized, multinational trials of LAIV and TIV (N?=?1,940). Wheezing, lower respiratory illness, and hospitalization were not significantly increased among children receiving LAIV compared with TIV. Increased upper respiratory symptoms and irritability were observed among LAIV recipients (p?
机译:在欧盟和加拿大,已批准将Ann Arbor毒株减毒活疫苗(LAIV)用于2-17岁的儿童,包括那些患有轻度至中度哮喘或有喘息的儿童。已证明LAIV与三价灭活流感疫苗(TIV)在6-17岁哮喘儿童中的安全性和有效性。但是,很少有6岁以下哮喘或哮喘患者的数据。从两项LAIV和TIV的随机,多国试验(N≥1,940)收集了2-5岁哮喘或哮喘发作前儿童的安全性和有效性数据。与TIV相比,接受LAIV的儿童的喘息,下呼吸道疾病和住院治疗没有明显增加。在LAIV接受者中观察到上呼吸道症状和烦躁情绪增加(p <0.05)。相对功效与在总体研究人群中观察到的结果一致,这表明与TIV接受者相比,LAIV中培养证实的流感病病例更少。研究结果支持LAIV在2-17岁患有轻度至中度哮喘或有喘息史的儿童中的安全性和有效性。在疫苗接种前7天内患有严重哮喘或活动性喘息的个体中,有关LAIV使用的数据有限。

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