首页> 外文期刊>The Journal of Allergy and Clinical Immunology >The immunostimulant OM-85 BV prevents wheezing attacks in preschool children.
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The immunostimulant OM-85 BV prevents wheezing attacks in preschool children.

机译:免疫刺激剂OM-85 BV可防止学龄前儿童喘息发作。

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BACKGROUND: No reagents have been shown to be effective in preventing wheezing attacks provoked by acute respiratory tract illnesses (ARTIs) in preschool children. New therapeutic agents and preventive strategies are needed. OBJECTIVES: We assessed the effect of OM-85 BV (Broncho-Vaxom; OM Pharma, Geneva, Switzerland) in preventing ARTI-provoked wheezing attacks in preschool children with recurrent wheezing. METHODS: A randomized, double-blind, placebo-controlled, parallel-group study was carried out between August 2007 and September 2008. The study included 75 children with recurrent wheezing who were 1 to 6 years old. Participants were randomly assigned to groups given either OM-85 BV or a placebo (1 capsule per day for 10 days each month for 3 consecutive months) at the start of the trial. Participants were followed for 12 months, which included the administration period of the test article. RESULTS: Subjects given OM-85 BV had a lower rate of wheezing attacks. The cumulative difference in wheezing attacks between the 2 groups was 2.18 wheezing attacks per patient in 12 months; there was a 37.9% reduction in the group given OM-85 BV compared with the group given placebo (P < .001). Stepwise multiple (linear) regression analysis showed that the main difference between the OM-85 BV and placebo groups was a reduction the number of ARTIs (R = -0.805, P < .001). The duration of each wheezing attack was 2 days shorter in the group given OM-85 BV than in the group given placebo (P = .001). CONCLUSION: Administration of OM-85 BV significantly reduced the rate and duration of wheezing attacks in preschool children with ARTIs.
机译:背景:尚未显示出能有效预防学龄前儿童因急性呼吸道疾病(ARTIs)引起的喘息发作的试剂。需要新的治疗剂和预防策略。目的:我们评估了OM-85 BV(Broncho-Vaxom; OM Pharma,瑞士日内瓦)在预防反复发作的学龄前儿童预防ARTI引起的喘息发作中的作用。方法:于2007年8月至2008年9月之间进行了一项随机,双盲,安慰剂对照,平行组研究。该研究包括75例1至6岁的反复喘息儿童。在试验开始时,将参与者随机分配至接受OM-85 BV或安慰剂(每天1粒,每月10天,连续3个月)的组。参与者被追踪了12个月,其中包括受试物品的给药期。结果:给予OM-85 BV的受试者发生喘息的几率较低。两组之间的喘息发作累积差异在12个月内为每名患者2.18例。与给予安慰剂的组相比,给予OM-85 BV的组减少了37.9%(P <.001)。逐步多元(线性)回归分析表明,OM-85 BV组与安慰剂组之间的主要区别在于ARTI的数量减少(R = -0.805,P <.001)。给予OM-85 BV的组,每次喘息发作的持续时间比给予安慰剂的组短2天(P = .001)。结论:OM-85 BV的使用显着降低了学龄前儿童ARTIs喘息发作的发生率和持续时间。

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