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A comparison of the performance of two penicillin reagent kits in the diagnosis of beta-lactam hypersensitivity.

机译:比较两种青霉素试剂盒在诊断β-内酰胺超敏性方面的性能。

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BACKGROUND: Skin testing with penicilloyl polylysine (PPL) and minor determinant mixture (MDM) represents the first-line method for diagnosing beta-lactam hypersensitivity. However, in 2004, Allergopharma and Hollister-Stier announced their decision to stop the production of penicillin reagents (Allergopen and PrePen, respectively) within 1 year. Therefore, we decided to compare PPL and MDM from Allergopharma (Allergopen) with those from Diater (DAP). METHODS: We skin-tested 195 subjects with both Allergopen and DAP reagents, as well as with other beta-lactams; 74 (group A) had had immediate reactions to beta-lactams and 74 (group B) nonimmediate reactions, while 47 (group C) underwent prophylactic tests. RESULTS: One hundred two patients (52.3%) had positive skin tests; 29 (14.9%) were positive to PPL and/or MDM. Of the 102 skin-test-positive patients, 44 belonged to group A, 57 to B and 1 to C; the last was positive only to Allergopen PPL (PPL-A) and tolerated the benzylpenicillin challenge. Minor determinant mixture reagents produced identical results in the 148 patients of groups A and B, 22 (14.9%) of which were positive. Both PPL reagents produced negative results in 139 of these 148 patients and positive ones in 5; one subject was positive to DAP PPL (PPL-D) and negative to PPL-A, while three patients were positive to PPL-A and negative to PPL-D; two of the latter tolerated benzylpenicillin challenges. CONCLUSIONS: Minor determinant mixture reagents produced identical results in all 195 patients. Results of skin testing with PPL reagents were concordant in 190 (97.4%) of them. Therefore, DAP reagents are a reliable alternative to Allergopen ones.
机译:背景:用青霉酰聚赖氨酸(PPL)和次要决定簇混合物(MDM)进行皮肤测试是诊断β-内酰胺超敏反应的一线方法。但是,在2004年,Allergopharma和Hollister-Stier宣布了他们决定在1年内停止生产青霉素试剂(分别为Allergopen和PrePen)的决定。因此,我们决定将Allergopharma(Allergopen)的PPL和MDM与Diater(DAP)的进行比较。方法:我们对195名受试者进行了Allergopen和DAP试剂以及其他β-内酰胺类药物的皮肤测试; 74(A组)对β-内酰胺类有立即反应,74(B组)非直接反应,而47(C组)进行了预防性测试。结果:102例患者(52.3%)的皮肤试验阳性; PPL和/或MDM阳性29例(14.9%)。在102名皮肤试验阳性患者中,有44人属于A组,其中57人属于B组,而1人属于C组。最后一个仅对Allergopen PPL(PPL-A)呈阳性,并能耐受苄青霉素的攻击。次要决定因素混合试剂在A组和B组的148例患者中产生了相同的结果,其中22例(14.9%)为阳性。两种PPL试剂在148例患者中有139例阴性,在5例中阳性。一名受试者对DAP PPL(PPL-D)阳性,对PPL-A阴性,而三名患者对PPL-A阳性,对PPL-D阴性;后者中的两个耐受苄青霉素挑战。结论:在全部195例患者中,次决定性混合试剂产生的结果相同。用PPL试剂进行的皮肤测试结果与190(97.4%)相一致。因此,DAP试剂是Allergopen试剂的可靠替代品。

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