A pilot study of the usefulness and safety of a ready-to-use atopy patch test (Diallertest) versus a comparator (Finn Chamber) during cow's milk allergy in children

被引:60
作者
Kalach, N
Soulaines, P
de Boissieu, D
Dupont, C
机构
[1] Cochin St Vincent de Paul Hosp, Dept Pediat Neonatol, Pediat Gastroenterol & Nutr Unit, F-75674 Paris 14, France
[2] Catholic Univ Lille, St Vincent de Paul Hosp, Clin Pediat St Antoine, Lille, France
[3] Univ Paris 05, Paris, France
关键词
cow's milk allergy; children; ready-to-use atopy patch test;
D O I
10.1016/j.jaci.2005.08.033
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Patch testing is used in the diagnosis of food allergy, especially during delayed manifestations. Objective: A ready-to-use atopy patch test (APT), the Diallertest, was compared with another APT device, the Finn Chamber, in pediatric cow's milk allergy. Methods: This prospective study involved 49 children (34.3 +/- 17 [mean +/- SD] months of age), with cow's milk allergy manifested by atopic dermatitis (10.2%), digestive manifestations (40.8%), or both (49%). All children underwent both APT techniques, with a reading 72 hours after application, followed by a milk elimination diet for 4 to 6 weeks and open cow's milk challenge. Results: A positive result was seen in 22 (44.8%) versus 13 (26.5%) patients with the ready-to-use and the comparator APTs, respectively. No side effects were recorded. Both techniques were concordant in 67.3% of patients. Of the total 41 open cow's milk challenges, 60.9% had positive results, with 8 patients lost to follow-up. The performances of the ready-to-use and comparator APTs were as follows: sensitivity, 76% (95% CI, 59.2% to 92.7%) versus 44% (95% CI, 24.5% to 63.4%; P = .02); specificity, 93.8% (95% CI, 81.9% to 100%) versus 93.8% (95% CI, 81.9% to 100%); positive predictive value, 95 % (95% CI, 85.4% to 100 %; 1 false-positive result) versus 91.7% (95% CI, 76% to 100%; 1 false-positive result); negative predictive value, 71.4% (95% CI, 52% to 90.7%; 6 false-negative results) versus 51.7% (95% Cl, 33.5% to 69.8%; 14 false-negative results); and test accuracy, 82.9% (95% Cl, 71.3% to 94.5%) versus 63.4% (95% CI, 48.6% to 78.1 %; P = .05). Conclusion: The ready-to-use APT exhibited a good sensitivity and specificity, with no side effects.
引用
收藏
页码:1321 / 1326
页数:6
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