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昂丹司琼诱发的过敏性休克:对罕见不良事件的深入分析。

Ondansetron-Induced Anaphylactic Shock: An In-Depth Analysis of a Rare Adverse Event.

作者信息

Suzuki Yasuyuki, Liu Shuang, Iwata Mari, Yamamoto Hideshi, Nishida Katsuko

机构信息

Anesthesiology, Saiseikai Matsuyama Hospital, Matsuyama, JPN.

Pharmacology, Ehime University Graduate School of Medicine, Toon, JPN.

出版信息

Cureus. 2023 Aug 3;15(8):e42894. doi: 10.7759/cureus.42894. eCollection 2023 Aug.

DOI:10.7759/cureus.42894
PMID:37664335
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10474905/
Abstract

Ondansetron, a drug predominantly employed in most general anesthesia cases, is critical for mitigating postoperative nausea and vomiting prompted by anesthetics. Although infrequent side effects such as serotonin syndrome are recognized, the drug is generally acknowledged for its safety. Nonetheless, some reports showed cases of anaphylactic shock associated with ondansetron. In this context, we have meticulously analyzed an anaphylactic case triggered by ondansetron that we encountered. Our deep-dive investigation suggests that the reaction might not be a traditional type I allergic reaction, typically associated with the drug. Instead, we present the possibility that the response could be mediated through Mas-related G protein-coupled receptor X2 (MRGPRX2), a divergent pathway leading to comparatively milder symptoms of anaphylaxis. In addition to the crucial role of adrenaline in unstable hemodynamics, our case highlights the effective use of antihistamines in rapidly managing such reactions. This finding suggests a need to further examine the safety profiles of common drugs like ondansetron and the potential involvement of MRGPRX2 in drug-induced hypersensitivity reactions.

摘要

昂丹司琼是一种在大多数全身麻醉病例中主要使用的药物,对于减轻麻醉剂引起的术后恶心和呕吐至关重要。尽管已知有诸如血清素综合征等罕见副作用,但该药物总体上因其安全性而得到认可。然而,一些报告显示了与昂丹司琼相关的过敏性休克病例。在此背景下,我们对遇到的一例由昂丹司琼引发的过敏病例进行了细致分析。我们深入的调查表明,该反应可能不是典型的与该药物相关的I型过敏反应。相反,我们提出该反应可能是通过Mas相关G蛋白偶联受体X2(MRGPRX2)介导的,这是一条导致相对较轻过敏症状的不同途径。除了肾上腺素在不稳定血流动力学中的关键作用外,我们的病例还突出了抗组胺药在快速处理此类反应中的有效应用。这一发现表明有必要进一步研究昂丹司琼等常用药物的安全性概况以及MRGPRX2在药物诱导的超敏反应中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8887/10474905/ea0418851986/cureus-0015-00000042894-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8887/10474905/2b0590ef7a31/cureus-0015-00000042894-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8887/10474905/ea0418851986/cureus-0015-00000042894-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8887/10474905/2b0590ef7a31/cureus-0015-00000042894-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8887/10474905/ea0418851986/cureus-0015-00000042894-i02.jpg

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A novel MRGPRX2-targeting antagonistic DNA aptamer inhibits histamine release and prevents mast cell-mediated anaphylaxis.一种新型靶向 MRGPRX2 的拮抗 DNA 适体可抑制组胺释放并预防肥大细胞介导的过敏反应。
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