Department of Dermatology, Ghent University Hospital, B-9000 Ghent, Belgium.
Department of Ophthalmology, Ghent University Hospital, B-9000 Ghent, Belgium.
Contact Dermatitis. 2016 Jan;74(1):18-21. doi: 10.1111/cod.12478. Epub 2015 Oct 22.
Anti-vascular endothelial growth factor (VEGF) medication, injected intravitreally, is currently the standard of care in patients with different retinal pathologies. Since its introduction in 2006, an increasing number of patients have undergone this procedure in Ghent University Hospital. Strikingly, more patients were diagnosed with contact dermatitis caused by ophthalmic products used during intravitreal injection procedure.
To identify which of the substances used during intravitreal injection is most likely to cause contact dermatitis.
PATIENTS/MATERIALS/METHODS: Sixteen patients who developed a burning and stinging sensation and swelling of the eyelids after intravitreal injection were tested. All patients were patch tested with the Belgian baseline series, as well as a cosmetic, a pharmaceutical and an ophthalmic series, including the different eye drops used during the intravitreal injection procedure.
Fourteen of 16 patients reacted to at least one of the substances used during the injection procedure. Nine patients reacted to phenylephrine (56%), 5 to iso-Betadine(®) ophthalmic solution (31%), and 3 patients to sodium metabisulfite (16%).
The most common causal allergen was phenylephrine, being positive in 56% of patients. Patients most likely become sensitized because of the high frequency of usage of phenylephrine during repeated intravitreal injections and follow-up consultations.
抗血管内皮生长因子(VEGF)药物经玻璃体内注射,目前是治疗各种视网膜病变患者的标准疗法。自 2006 年推出以来,根特大学医院接受这种治疗的患者数量不断增加。引人注目的是,在接受玻璃体内注射的患者中,越来越多的患者被诊断为接触性皮炎,这是由眼内注射过程中使用的眼科产品引起的。
确定玻璃体内注射过程中使用的哪种物质最有可能引起接触性皮炎。
患者/材料/方法:对 16 名在玻璃体内注射后出现眼睑烧灼感、刺痛和肿胀的患者进行了测试。所有患者均用比利时基础系列、化妆品系列、药物系列和眼科系列进行斑贴试验,包括玻璃体内注射过程中使用的不同眼药水。
16 名患者中有 14 名对注射过程中使用的至少一种物质有反应。9 名患者对苯肾上腺素(56%)有反应,5 名患者对异 Betadine(®)眼科溶液有反应(31%),3 名患者对亚硫酸氢钠有反应(16%)。
最常见的致敏原是苯肾上腺素,56%的患者呈阳性。由于苯肾上腺素在重复玻璃体内注射和随访期间的使用频率较高,患者最有可能致敏。