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儿童期特应性疾病的发展及其由Phadiatop儿科进行的预测。

Development of atopic disease during childhood and its prediction by Phadiatop Paediatric.

作者信息

Lilja G, Oman H, Johansson S G

机构信息

Sachs' Children's Hospital, Karolinska Institute, Stockholm, Sweden.

出版信息

Clin Exp Allergy. 1996 Sep;26(9):1073-9.

PMID:8889263
Abstract

BACKGROUND

Evaluating in vivo and/or in vitro tests for 'early' prediction of childhood allergy is of interest in paediatric allergology.

OBJECTIVE

To determine whether the measurement of Phadiatop Paediatric (PP) during early childhood could be used to predict the development of atopic disease during the first 5 years of life among infants with a family history of atopic disease.

METHODS

Phadiatop Paediatric was evaluated in 134 infants. The analysis was performed at 6 months, at 18 months and at 5 years of age and the numbers of available serum samples were 61, 85 and 134, respectively. The potential capacity of the test to predict the development of atopic disease was studied by relating the result of the test, a positive or a negative score, to the accumulated incidence of atopic diseases from birth to 18 months of age and from birth to 5 years of age.

RESULTS

Three of four children with a positive PP at 6 months of age developed clinical signs/symptoms of atopic disease before 18 months and all four before 5 years of age. The predictive value of a positive test at 18 months for symptoms before 5 years of age was 80% (12/15). If the diagnostic criterion, instead of clinical signs/symptoms of atopic disease, was at least one positive skin-prick test to major food or inhalant allergens, the predictive value of a positive PP-test at 18 months decreased to 53% (8/15).

CONCLUSION

Although the presence of circulating IgE antibodies, as detected by Phadiatop Paediatric, can predict the development of atopic diseases during childhood, the usefulness of the test is limited by its low sensitivity (22-47%).

摘要

背景

在儿科过敏学领域,评估体内和/或体外试验以“早期”预测儿童过敏具有重要意义。

目的

确定在幼儿期测量小儿Phadiatop(PP)是否可用于预测有特应性疾病家族史的婴儿在生命的前5年中特应性疾病的发生情况。

方法

对134名婴儿进行小儿Phadiatop评估。分别在6个月、18个月和5岁时进行分析,可用血清样本数量分别为61份、85份和134份。通过将试验结果(阳性或阴性评分)与出生至18个月以及出生至5岁的特应性疾病累积发病率相关联,研究该试验预测特应性疾病发生的潜在能力。

结果

6个月时PP呈阳性的4名儿童中,有3名在18个月前出现了特应性疾病的临床体征/症状,4名在5岁前均出现了相关症状。18个月时试验呈阳性对5岁前症状的预测价值为80%(12/15)。如果诊断标准不是特应性疾病的临床体征/症状,而是对主要食物或吸入性过敏原至少有一次阳性皮肤点刺试验,那么18个月时PP试验阳性的预测价值降至53%(8/15)。

结论

尽管小儿Phadiatop检测到的循环IgE抗体的存在可预测儿童期特应性疾病的发生,但其低敏感性(22 - 47%)限制了该试验的实用性。

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