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首页> 外文期刊>Contact dermatitis >Adverse cutaneous reaction to diabetic glucose sensors and insulin pumps: Irritant contact dermatitis or allergic contact dermatitis?
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Adverse cutaneous reaction to diabetic glucose sensors and insulin pumps: Irritant contact dermatitis or allergic contact dermatitis?

机译:对糖尿病葡萄糖传感器和胰岛素泵的不良反应:刺激性接触皮炎或过敏性接触皮炎?

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Abstract Background Adverse cutaneous reactions to diabetes medical devices (glucose sensors and insulin pumps) are described, notably allergic contact dermatitis (ACD) with isobornyl acrylate (IBOA) and N,N dimethylacrylamide (DMAA) as the main allergen. Objectives To determine if all cases of adverse cutaneous reactions observed with diabetes medical devices (ie FreeStyle Libre, Enlite sensors or insulin pumps), referred to our department with suspected allergies are confirmed as ACD. Patients and methods Fifty‐two patients who presented skin reactions to diabetes medical devices were patch tested with the European baseline series, a plastic and glues series, a (meth) acrylates series, a piece of the adhesive part of the device, as well as IBOA 0.1% and DMAA 0.1% pet. Results Seventeen patients had no positive reaction to IBOA nor to the adhesive part of the device; 11 of these also tested with DMAA with negative result. No other relevant allergen was identified. Conclusion Some cutaneous reactions, otherwise very similar to those of patients sensitized to IBOA, can be explained either by the presence of an untested allergen not yet discovered, or by irritant contact dermatitis. Therefore, European legislation on the full labelling of ingredients by manufacturers, in order to facilitate the identification of allergens and irritants, is imperative.
机译:摘要背景描述了对糖尿病医疗装置(葡萄糖传感器和胰岛素泵)的不良皮肤反应,特别是用异丙醇(IboA)和N,N二甲基丙烯酰胺(DMAA)作为主要过敏原的过敏接触皮炎(ACD)。目的是用糖尿病医疗器械(即自由式Libre,GenaTA传感器或胰岛素泵)观察到所有患有糖尿病医疗器械(IE自由度,传感器或胰岛素泵)的案例,以怀疑过敏术称为ACD。患者和方法将皮肤反应的患者和方法呈现给糖尿病医疗装置的皮肤反应是用欧洲基线系列,塑料和胶水系列,一种(甲基)丙烯酸酯系列,一块粘合剂部分,以及装置IBOA 0.1%和DMAA 0.1%PET。结果17名患者对IBOA没有阳性反应,也不是该装置的粘合剂部分;其中11种也用DMAA测试,具有阴性结果。没有确定其他相关过敏原。结论一些皮肤反应,否则与对IBOA致敏的患者非常相似,可以通过存在未发现未发现的过敏原,或通过刺激性接触皮炎来解释。因此,欧洲立法通过制造商全部标记成分,以便于鉴定过敏原和刺激物,是必要的。

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