对麻醉和手术所用药物的过敏反应和其他不良反应

Brian A. Baldo
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引用次数: 0

摘要

患者在围手术期和术后可能接触到的药物可能非常多。其中包括诱导剂、神经肌肉阻滞药(NMBDs)、阿片类药物、抗生素、舒格迈司、胶体、局部麻醉剂、多肽、抗纤维蛋白溶解剂、肝素和相关抗凝剂、蓝色染料、洗必泰,以及一系列其他药物,这取决于与患者个人临床状况和术后恢复期进展有关的多个因素。为避免对特定药物(如曲马多和可待因)代谢不良或超速代谢或可能出现的药物不良反应(ADR),手术期间或术后可能需要避免使用某些药物。对于有过敏性休克史或对已知药物有其他不良反应/不耐受史的患者,就属于这种情况。其他药物也可能在手术前停用一段时间,例如:增加出血机会的抗凝剂;急性肾功能衰竭患者的利尿剂;大血管手术后肾脏损伤的降压药;以及血清素能药物,这些药物与某些阿片类药物一起可能会罕见地诱发血清素中毒。通过基因分型和表型对种系变异进行研究,以确定ADRs的遗传易感性,为个体化药物治疗提供了一种日益重要的方法。人类白细胞抗原(HLA)基因与一些严重的迟发性免疫介导反应的关联研究正在进行中,药物代谢细胞色素CYP450酶、P-糖蛋白和儿茶酚-O-甲基转移酶的变异也为评估药物(尤其是阿片类药物和其他镇痛药)的不良反应和非反应带来了希望。越来越多的机构开展的 ADR 调查通常只涉及少量患者,属于回顾性调查,无法明确确定罪魁祸首药物,也不能充分区分免疫介导和非免疫介导的过敏性反应。在所进行的多项调查中,我们对麻醉和手术过程中和手术后发现的大量药物进行了研究,以确定其是否涉及过敏反应。药物分为最常涉及的药物(NMBD 和抗生素);越来越常涉及的药物,即抗生素(尤其是替考拉宁)和蓝色染料;越来越少涉及的药物;以及较少涉及围术期和术后不良反应的药物,但对于偶尔有潜在敏感性的病人来说,这些药物仍然重要且有必要牢记。临床医生应了解药物诱导的真正过敏性 IgE/FcεRI 型 ADR 与假性过敏性 MRGPRX2 介导的 ADR 之间的相似之处、每种 ADR 的临床特征及其区别特征。讨论了识别 MRGPRX2 激动剂以及诊断和区分假性过敏与过敏反应机制的程序。
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Allergic and other adverse reactions to drugs used in anesthesia and surgery

The list of drugs patients may be exposed to during the perioperative and postoperative periods is potentially extensive. It includes induction agents, neuromuscular blocking drugs (NMBDs), opioids, antibiotics, sugammadex, colloids, local anesthetics, polypeptides, antifibrinolytic agents, heparin and related anticoagulants, blue dyes, chlorhexidine, and a range of other agents depending on several factors related to individual patients’ clinical condition and progress in the postoperative recovery period. To avoid poor or ultrarapid metabolizers to a particular drug (for example tramadol and codeine) or possible adverse drug reactions (ADRs), some drugs may need to be avoided during or after surgery. This will be the case for patients with a history of anaphylaxis or other adverse events/intolerances to a known drug. Other drugs may be ceased for a period before surgery, e.g., anticoagulants that increase the chance of bleeding; diuretics for patients with acute renal failure; antihypertensives relative to kidney injury after major vascular surgery; and serotonergic drugs that together with some opioids may rarely induce serotonin toxicity. Studies of germline variations shown by genotyping and phenotyping to identify a predisposition of genetic factors to ADRs offer an increasingly important approach to individualize drug therapy. Studies of associations of human leukocyte antigen (HLA) genes with some serious delayed immune-mediated reactions are ongoing and variations of drug-metabolizing cytochrome CYP450 enzymes, P-glycoprotein, and catechol-O-methyltransferase show promise for the assessment of ADRs and non-responses to drugs, particularly opioids and other analgesics. Surveys of ADRs from an increasing number of institutions often cover small numbers of patients, are retrospective in nature, fail to clearly identify culprit drugs, and do not adequately distinguish immune-mediated from non-immune-mediated anaphylactoid reactions. From the many surveys undertaken, the large list of agents identified during and after anesthesia and surgery are examined for their ADR involvement. Drugs are classified into those most often involved, (NMBD and antibiotics); drugs that are becoming more frequently implicated, namely antibiotics (particularly teicoplanin), and blue dyes; those becoming less frequently involved; and drugs more rarely involved in perioperative, and postoperative adverse reactions but still important and necessary to keep in mind for the occasional potential sensitive patient. Clinicians should be aware of the similarities between drug-induced true allergic type I IgE/FcεRI- and pseudoallergic MRGPRX2-mediated ADRs, the clinical features of each, and their distinguishing characteristics. Procedures for identifying MRGPRX2 agonists and diagnosing and distinguishing pseudoallergic from allergic reaction mechanisms are discussed.

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