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首页> 外文期刊>Current respiratory medicine reviews >Persistent Allergic Minimum Phlogosis as Mechanistic Link Between Recurrent Respiratory Infections and Atopy: A Single Center Pilot Study
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Persistent Allergic Minimum Phlogosis as Mechanistic Link Between Recurrent Respiratory Infections and Atopy: A Single Center Pilot Study

机译:持续过敏的最小植物,作为复发性呼吸道感染与特性的机械联系:单一中心试验研究

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Background: Recurrent respiratory infections (RRIs) are very common in early life, and constituting a social problem concerning the family, the paediatrician and pharma-economy. Although the relation between atopy and RRIs has been evaluated in several studies, the data are not stillconclusive. Objectives: The aim of the study were: (i) to determine the type, the number and the total duration of RRIs recorded during follow-up study in atopic and non-atopic groups; (ii) the multiplicity and strength of sensitization as a further risk factor for developing RRIs. Patients and Methods: 10,200 children were prospectively and consecutively monitored when they were 12 years old. All children were assessed for SPT, serum total and specific IgE levels for common food and inhalant allergens. Parental report of each physician-diagnosed respiratory illnesswas also analyzed. Results: Of the 10,200 children who started the study, information was obtained until the end of the study for 7,568 (74.2%). Of these, 3,294 children (43.52%) resulted affected by RRIs. Atopy was found in 1888 of 3294 children (57.31%). RRIs symptoms occurred morefrequently in atopic children than in non atopic ones (p Conclusions: Our results provide evidence that atopy and the multiplicity and strength of sensitization modify the risk respiratory infections.
机译:背景:复发性呼吸道感染(RRIS)在早期生命中非常普遍,并构成了一个关于家庭,儿科医生和制药经济的社会问题。虽然在几项研究中评估了特性和RRI之间的关系,但数据并不依赖于依赖性。目的:该研究的目的是:(i)确定在特应性和非特征群体的后续研究中记录的类型,数量和总持续时间; (ii)致敏的多重性和强度作为发展RRI的进一步危险因素。患者和方法:每天12岁,预先监测10,200名儿童。所有孩子均针对SPT,血清和特异性IgE水平评估普通食物和吸入剂过敏原。还分析了每个医生诊断的呼吸道疾病的父母报告。结果:在开始研究的10,200名儿童中,在研究结束时获得了7,568(74.2%)。其中,3,294名儿童(43.52%)导致RRIS影响。在3294名儿童的1888年(57.31%)发现了特性。 Atopic症状在特应性儿童中发生了比非特应性的症状(P:P:我们的结果提供了证据,提供了特殊性和多种致敏强度和强度改变风险呼吸道感染。

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