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哮喘/荨麻疹中的药理学刺激因素。

Pharmacological stimuli in asthma/urticaria.

作者信息

Prieto-Lastra L, Iglesias-Cadarso A, Reaño-Martos M M, Pérez-Pimiento A, Rodríguez-Cabreros M I, García-Cubero A

机构信息

Allergy Service, Universitary Hospital Puerta de Hierro, Madrid. Spain.

出版信息

Allergol Immunopathol (Madr). 2006 Sep-Oct;34(5):224-7. doi: 10.1157/13094030.

Abstract

BACKGROUND

The use of opioids as analgesics is becoming increasingly widespread, which may have repercussions in patients with urticaria or asthma, as these agents frequently cause adverse reactions.

MATERIAL AND METHODS

We present three patients who developed allergic reactions after receiving codeine: two patients who developed acute urticaria, and a third asthmatic patient receiving specific immunotherapy who developed bronchospasm. Skin prick-testing (SPT) and intradermal reaction (IDR) tests with various opioids were performed, followed by controlled oral challenge. Prick tests and IDR were also carried out in 20 controls.

RESULTS

Similar SPT and IDR results were recorded in the three patients and in the controls. In the case of controlled oral challenge with codeine, patient 1 suffered bronchospasm, while patient 2 developed generalized urticaria. The test was not performed in the third patient. All of the patients tolerated tramadol 50 mg without problems. We advised the use of tramadol as analgesic and fentanyl or remifentanil as anesthetics.

DISCUSSION

In these types of manifestation, the pharmacological properties of the opioids used are highly important, particularly as regards their histamine-releasing potential. Codeine, morphine and pethidine present the greatest histamine-releasing capacity, while tramadol, fentanyl and remifentanil do not release histamine and their use is thus recommended in pulmonary disease requiring opioid administration. Cutaneous symptoms are more frequently caused by opioids than by respiratory symptoms, since these drugs act on the MTC mast cell population, which is more prevalent in the skin than in the lungs. Some of this action is inhibited by naloxone.

CONCLUSIONS

In most patients, these reactions are not IgE-mediated. Consequently, SPT and IDR are of little diagnostic value, and controlled oral challenging with the suspect drug or with one of the non-histamine releasing agents should be used. The patch test is useful in occupational contact dermatitis.

摘要

背景

阿片类药物作为镇痛药的使用日益广泛,这可能对荨麻疹或哮喘患者产生影响,因为这些药物常引起不良反应。

材料与方法

我们报告了3例在接受可待因后发生过敏反应的患者:2例发生急性荨麻疹,第3例为接受特异性免疫治疗的哮喘患者,发生了支气管痉挛。对各种阿片类药物进行了皮肤点刺试验(SPT)和皮内反应(IDR)试验,随后进行了对照口服激发试验。对20名对照者也进行了点刺试验和IDR试验。

结果

3例患者和对照者的SPT和IDR结果相似。在可待因对照口服激发试验中,患者1发生支气管痉挛,患者2出现全身性荨麻疹。第3例患者未进行该试验。所有患者均能耐受50mg曲马多,无问题。我们建议使用曲马多作为镇痛药,芬太尼或瑞芬太尼作为麻醉药。

讨论

在这些类型的表现中,所用阿片类药物的药理特性非常重要,特别是就其组胺释放潜力而言。可待因、吗啡和哌替啶具有最大的组胺释放能力,而曲马多、芬太尼和瑞芬太尼不释放组胺,因此建议在需要使用阿片类药物的肺部疾病中使用。皮肤症状比呼吸道症状更常由阿片类药物引起,因为这些药物作用于MTC肥大细胞群体,该群体在皮肤中比在肺中更普遍。这种作用的一部分可被纳洛酮抑制。

结论

在大多数患者中,这些反应不是由IgE介导的。因此,SPT和IDR的诊断价值不大,应使用可疑药物或非组胺释放剂之一进行对照口服激发试验。斑贴试验对职业性接触性皮炎有用。

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