Garvey Lene Heise, Krøigaard Mogens, Poulsen Lars K, Skov Per Stahl, Mosbech Holger, Venemalm Lennart, Degerbeck Fredrik, Husum Bent
Danish Anaesthesia Allergy Centre, Copenhagen University Hospital, Rigshospitalet, Department of Anaesthesia 4231, Blegdamsvej 9, DK-2100 Copenhagen, Denmark.
J Allergy Clin Immunol. 2007 Aug;120(2):409-15. doi: 10.1016/j.jaci.2007.04.029. Epub 2007 Jun 7.
Investigations at the Danish Anesthesia Allergy Centre have included testing for allergy to chlorhexidine since 1999.
To investigate whether measurement of IgE and histamine release confirm an IgE-mediated mechanism for chlorhexidine allergy.
Twenty-two patients with clinical history suggestive of chlorhexidine allergy were included. Skin tests with chlorhexidine and tryptase measurements were performed during initial investigations. Sera were analyzed retrospectively for IgE and histamine release (passive sensitization) to chlorhexidine.
Twelve patients were skin test positive and 10 were skin test negative. Of the skin test-positive patients, 11 of 12 had IgE to chlorhexidine and 7 of 11 had a positive histamine release test. None of the skin test-negative patients had specific IgE or positive histamine release to chlorhexidine. Skin test-positive patients had higher median age (64 vs 49 y) and were mainly male (11/12 vs 6/10). In both groups, 8 patients had hypotension, but bronchospasm mainly appeared in skin test-negative patients (1/12 vs 6/10). Reactions occurred more often during urologic surgery in skin test-positive patients (5/12 vs 0/10). Baseline tryptase was higher in skin test-positive patients (median, 11.5 vs 3.7 microg/L), and 6 of 7 patients had elevated IgE to chlorhexidine in serum at the time of reaction.
This study confirms that chlorhexidine allergy is IgE-mediated and that measurement of specific IgE and histamine release are good adjuncts to skin testing in patients with clinical history suggesting chlorhexidine allergy.
IgE and histamine release can be used to support the diagnosis of allergy to chlorhexidine.
自1999年以来,丹麦麻醉过敏中心的调查包括对洗必泰过敏的检测。
研究免疫球蛋白E(IgE)和组胺释放的测量是否能证实洗必泰过敏的IgE介导机制。
纳入22例有洗必泰过敏临床病史的患者。在初始调查期间进行洗必泰皮肤试验和类胰蛋白酶测量。回顾性分析血清中针对洗必泰的IgE和组胺释放(被动致敏)情况。
12例患者皮肤试验阳性,10例皮肤试验阴性。在皮肤试验阳性的患者中,12例中有11例对洗必泰有IgE,11例中有7例组胺释放试验呈阳性。皮肤试验阴性的患者中,无一例对洗必泰有特异性IgE或组胺释放阳性。皮肤试验阳性的患者年龄中位数较高(64岁对49岁),且主要为男性(12例中的11例对10例中的6例)。两组中均有8例患者出现低血压,但支气管痉挛主要出现在皮肤试验阴性的患者中(12例中的1例对10例中的6例)。皮肤试验阳性的患者在泌尿外科手术期间反应更常见(12例中的5例对10例中的0例)。皮肤试验阳性的患者基线类胰蛋白酶较高(中位数,1l.5对3.7μg/L),7例患者中有6例在反应时血清中针对洗必泰的IgE升高。
本研究证实洗必泰过敏是由IgE介导的,对于有洗必泰过敏临床病史的患者,特异性IgE和组胺释放的测量是皮肤试验的良好辅助手段。
IgE和组胺释放可用于支持洗必泰过敏的诊断。