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首页> 外文期刊>Pediatric allergy and immunology: official publication of the European Society of Pediatric Allergy and Immunology >Safety of ultra-rush titration of sublingual immunotherapy in asthmatic children with tree-pollen allergy.
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Safety of ultra-rush titration of sublingual immunotherapy in asthmatic children with tree-pollen allergy.

机译:树花粉过敏哮喘儿童舌下免疫疗法超速滴定的安全性。

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The recommendation to use sublingual-swallow immunotherapy (SLIT) in children and adults with allergic rhinitis has been established over the past decade. Recently, ultra-rush titration of SLIT has become more and more common, raising concerns about its safety in children with asthma. Fifty-four children with asthma and adolescents aged 6-14 with documented allergic disease because of tree pollen (birch and possibly alder and/or hazel) from 14 study centers in Germany participated in a randomized, double-blind, and placebo-controlled study. Twenty-seven were randomized to receive SLIT with standardized birch pollen allergen extract and the other 27 to receive placebo. An ultra-rush high-dose SLIT titration regimen reaching the maintenance dose of 300 index of reactivity (IR) within 90 min (30-90-150-300 IR) was used. The difference in mean PFR changes during ultra-rush titration between SLIT and placebo was not significant (p = 0.056). A 95% probability that SLIT does not decrease PFR during ultra-rush titration was demonstrated. Neither anaphylactic shock nor else serious systemic reactions to the study drug occurred. No serious adverse event assessed by the investigator as related to study drug treatment was reported.
机译:在过去的十年中,已经提出了对患有变应性鼻炎的儿童和成人使用舌下吞咽免疫疗法(SLIT)的建议。最近,SLIT的超急诊滴定变得越来越普遍,引起了人们对其哮喘儿童安全性的担忧。来自德国14个研究中心的54名6-14岁哮喘和青少年儿童因树木花粉(桦木,可能还有al木和/或榛树)而出现过敏性疾病,并参加了这项随机,双盲和安慰剂对照研究。 27例随机接受标准桦木花粉过敏原提取物治疗SLIT,另27例接受安慰剂治疗。使用在90分钟内(30-90-150-300 IR)达到维持反应性指数300(IR)的超冲量大剂量SLIT滴定方案。 SLIT和安慰剂之间在超冲量滴定过程中平均PFR变化的差异不显着(p = 0.056)。证明了在超冲滴定期间SLIT不会降低PFR的95%概率。对研究药物既没有过敏性休克也没有发生严重的全身反应。研究者未报告与研究药物治疗相关的严重不良事件。

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