氟康唑引起的固定药疹

T. N. Myasnikova, T. Latysheva, T. Romanova, V. V. Smirnov
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摘要

目的:描述一组由氟康唑引起的固定药物红斑(FDE)患者的特征,以确定局部刺激性应用试验(LPAT)的敏感性和特异性,并评估与唑类其他抗真菌药物的交叉过敏反应性。347名迟发性药物过敏(DDH)患者接受了会诊,86名患者(24.8%)疑似患有FDE,其中23名患者由氟康唑引起(26.8%)。我们纳入了疑似氟康唑 FDE 患者(23 人)。结果:男女比例为 1:6.3,平均年龄为(30.39±10.23)岁。有 1 名患者撤销了氟康唑引起的 FDE 诊断。反应次数1例--2名患者(9.1%),不止1例--20名患者(90.9%)。4 名患者(18.2%)有过敏反应。LPAT 诊断氟康唑引起的 FDE DDH 的敏感性为 41.7%,特异性为 100%,假阴性率为 58.3%,阳性预测值为 100%。使用酮康唑、伊曲康唑进行 DPT 检测,100% 的病例均为阴性。结论:根据所获得的结果,我们可以得出结论,氟康唑引起的 FDE 绝大多数发生在 19 至 30 岁的女性身上。由于氟康唑引起的 FDE 患者对酮康唑和伊曲康唑的耐受性良好,因此她们很有可能从氟康唑转用这两种药物中的一种。在诊断由氟康唑引起的皮肤过敏时,应使用 LPAT,因为它对患者绝对安全,而且 42% 的患者可以避免使用 DPT。重要的是,90%以上的病例都得到了及时和正确的诊断,从而避免了对氟康唑的重复反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fixed drug eruption caused by fluconazole
Objective: to characterize a group of patients with fixed drug erythema (FDE) caused by fluconazole to determine the sensitivity and specificity of the local provocative application test (LPAT) and to evaluate cross-allergenic reactivity with other antifungal drugs of the azole group.Materials and methods: a prospective study was conducted in the period from 2012 to 2022. 347 patients with delayed drug hypersensitivity (DDH) were consulted, FDE could be suspected in 86 patients (24.8%), of which 23 patients were caused by fluconazole (26.8%). We included patients with suspected fluconazole FDE (n=23). LPAT with fluconazole was performed in 12 patients, drug provocation test (DPT) with ketoconazole – 17, DPT with itraconazole – 15, DPT with fluconazole – 1.Results: the ratio of men and women was 1:6.3, the average age was 30.39±10.23 years. In 1 patient, the diagnosis of FDE caused by fluconazole was withdrawn. Number of reactions: 1 – in 2 patients (9.1%), more than one reaction – in 20 (90.9%). 4 patients (18.2%) had atopy. Sensitivity of LPAT for diagnosing DDH in FDE caused by fluconazole was 41.7%, specificity – 100%, false-negative rate – 58.3%, positive predictive value – 100%. DPT with ketoconazole, itraconazole was negative in 100% of cases.Conclusions: the results obtained allow us to conclude that FDE caused by fluconazole in the vast majority of cases developed in women aged 19 to 30 years. Since patients with FDE caused by fluconazole tolerate ketoconazole and itraconazole well, it is highly likely that they can switch from fluconazole to one of these drugs. LPAT should be used for diagnosing FDE caused by fluconazole, since it was absolutely safe for the patient and allowed avoiding DPT in 42% of patients. Importantly that the timely and correct diagnosis in more than 90% of cases, it was possible to prevent the development of a repeated reaction to fluconazole.
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