对肌肉松弛剂过敏:皮肤试验是合理的。

Allergie et immunologie Pub Date : 2002-09-01
D A Moneret-Vautrin, G Kanny
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引用次数: 0

摘要

肌肉松弛剂(MR)的ige依赖性过敏发生率估计为1 / 6500全身麻醉(GA)。手术期间62%的过敏反应是由于MR过敏反应。所有的分子都是二价的,携带两个NH4+表位(季铵离子),无论是在结构上还是在体内快速质子化(维库溴铵)后。皮试的优异综合性能使其成为诊断类过敏反应的金标准。技术包括皮内试验和针刺试验。目前的定位是前臂和背部。针刺试验阳性标准为3毫米。对于IDTs,标准是注射量为0.02 ~ 0.04 ml时,注射丘疹的大小增加一倍:8 mm。推荐浓度不是假阴性。商业浓度可通过点刺试验进行测试,但稀释度为1:10的微量和阿曲库铵除外。建议IDT的浓度范围从1:10 000开始,直到正常无反应浓度:100微克/毫升(琥珀胆碱),200微克/毫升(胆碱),10微克/毫升(阿曲库铵),2微克/毫升(米维库铵),200微克/毫升(潘库溴铵),400微克/毫升(维库溴铵),1000微克/毫升(罗库溴铵),200微克/毫升(顺式阿曲库铵)。皮肤试验对MRs的特异性和敏感性均大于95%。多年来的重现率为88%。PT与IDR的总体一致性为97%。两种类型的测试都可用于诊断。为了寻找交叉增敏,必须进行IDT。84%的患者确实对MRs有交叉致敏,但只有16%的患者对所有MRs都有反应。由阴性IDTs选择的MRs的进一步使用已被证明是安全的。
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Anaphylaxis to muscle relaxants: rational for skin tests.

IgE-dependent allergy to muscle relaxants (MR) has an estimated prevalence of 1 out of 6500 General Anesthesias (GA). 62% of anaphylaxis during surgery are due to MR anaphylaxis. All the molecules are divalent, carrying two NH4+ epitopes (quaternary ammonium ions), either structurally or after rapid in vivo protonization (vecuronium). The excellent overall performance of skin test makes them the golden standard for the diagnosis of anaphylactoid reactions. Techniques include intradermal tests and prick-tests. The current localizations are the forearm and the back. Positivity criteria are 3 mm for prick-tests. For IDTs, the criterium is the doubling of the size of the injection papula, when 0.02 to 0.04 ml is injected: 8 mm. The recommended concentrations are not falsely negative. Commercial concentrations can be tested by prick tests, except for mivacurium and atracurium tested of 1:10 dilution. A scale of concentrations is advised for IDT starting with 1:10,000, up to a normally non reactive concentration that is: 100 micrograms/ml (succinylcholine), 200 micrograms/ml (gallamine), 10 micrograms/ml (atracurium), 2 micrograms/ml (mivacurium), 200 micrograms/ml (pancuronium), 400 micrograms/ml (vecuronium), 1,000 micrograms/ml (rocuronium), 200 micrograms/ml (cis atracurium). The specificity and sensitivity of the skin tests to MRs are greater than 95%. The reproducibility over years is 88%. The overall concordance of PT and IDR is 97%. Both types of tests can be used for the diagnosis. IDT have to be carried out for the search of the cross sensitization. 84% of patients do have cross sensitization to MRs but only 16% react to all MRs. The further use of MRs selected by negative IDTs has been proved to be safe.

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