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[药物性胰腺炎——治疗胰腺炎的药物]

[Pancreatitis from drugs-Drugs for treatment of pancreatitis].

作者信息

Hubert Max Ole, Mayerle Julia, Sirtl Simon

机构信息

Medizinische Klinik und Poliklinik II, LMU Klinikum München, Marchioninistr. 15, 81377, München, Deutschland.

出版信息

Inn Med (Heidelb). 2025 May;66(5):524-532. doi: 10.1007/s00108-025-01888-3. Epub 2025 Apr 29.

DOI:10.1007/s00108-025-01888-3
PMID:40298970
Abstract

BACKGROUND

Drugs are a rare but important cause of acute pancreatitis (AP) due to potential therapeutic consequences, accounting for up to 5% of all cases of AP. The diagnosis of drug-induced AP is challenging due to mostly weak evidence and complex diagnostic criteria.

OBJECTIVE

This review article defines drug-induced AP, summarizes the evidence for drugs associated with AP and highlights the challenges in the diagnosis of this condition. The second part of the article focuses on the main pillars of AP treatment.

CURRENT DATA

The association of most drugs associated with AP is based on case reports and case series but there are no high-quality studies. There is sufficient evidence of a causal relationship for only 40 of more than 500 drugs associated with AP and for almost none of the drugs the causal mechanism has been definitively clarified. Several classification systems and criteria have been proposed to assess whether a drug causally triggers AP, with criteria including the temporal association, the exclusion of other causes and recurrence of AP after re-exposure.

CONCLUSION

The diagnosis of drug-induced AP remains a challenge, with many common drugs being incorrectly associated with AP. There is an urgent need for the development of biomarkers to facilitate the diagnosis of drug-induced AP. Drug treatment for AP is still primarily a needs-based fluid management and efficient analgesia. New and causal therapeutic approaches need clinical validation.

摘要

背景

由于潜在的治疗后果,药物是急性胰腺炎(AP)的一种罕见但重要的病因,占所有AP病例的5%。药物性AP的诊断具有挑战性,因为证据大多薄弱且诊断标准复杂。

目的

这篇综述文章对药物性AP进行了定义,总结了与AP相关药物的证据,并强调了这种疾病诊断中的挑战。文章的第二部分重点关注AP治疗的主要支柱。

当前数据

大多数与AP相关的药物关联是基于病例报告和病例系列,但缺乏高质量研究。在500多种与AP相关的药物中,只有40种有充分证据证明存在因果关系,而且几乎没有一种药物的因果机制得到明确阐明。已经提出了几种分类系统和标准来评估一种药物是否因果性引发AP,标准包括时间关联、排除其他病因以及再次接触后AP复发。

结论

药物性AP的诊断仍然是一个挑战,许多常用药物被错误地认为与AP有关。迫切需要开发生物标志物以促进药物性AP的诊断。AP的药物治疗仍然主要是基于需求的液体管理和有效的镇痛。新的因果治疗方法需要临床验证。

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本文引用的文献

1
Systematic review of immune checkpoint inhibitor-related gastrointestinal, hepatobiliary, and pancreatic adverse events.免疫检查点抑制剂相关的胃肠道、肝胆和胰腺不良事件的系统评价。
J Immunother Cancer. 2024 Nov 14;12(11):e009742. doi: 10.1136/jitc-2024-009742.
2
Normal saline versus lactated Ringer's solution for acute pancreatitis resuscitation, an open-label multicenter randomized controlled trial: the WATERLAND trial study protocol.生理盐水与乳酸林格氏液用于急性胰腺炎复苏的比较:一项开放标签、多中心随机对照试验:WATERLAND 试验研究方案。
Trials. 2024 Oct 21;25(1):699. doi: 10.1186/s13063-024-08539-2.
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Global trends in opioid use for pain management in acute pancreatitis: A multicentre prospective observational study.
全球急性胰腺炎疼痛管理中阿片类药物使用的趋势:一项多中心前瞻性观察研究。
United European Gastroenterol J. 2024 Oct;12(8):1114-1127. doi: 10.1002/ueg2.12641. Epub 2024 Aug 14.
4
Olezarsen, Acute Pancreatitis, and Familial Chylomicronemia Syndrome.奥列扎森,急性胰腺炎和家族性乳糜微粒血症综合征。
N Engl J Med. 2024 May 16;390(19):1781-1792. doi: 10.1056/NEJMoa2400201. Epub 2024 Apr 7.
5
Insufficient secretion of pancreatic FGF21 is the toxicological mechanism and therapeutic target of asparaginase-associated pancreatitis.胰 FGF21 分泌不足是天冬酰胺酶相关胰腺炎的毒理学机制和治疗靶点。
Toxicol Appl Pharmacol. 2024 Apr;485:116920. doi: 10.1016/j.taap.2024.116920. Epub 2024 Apr 4.
6
Drug-Induced Acute Pancreatitis in Adults: Focus on Antimicrobial and Antiviral Drugs, a Narrative Review.成人药物性急性胰腺炎:聚焦于抗菌药物和抗病毒药物,一篇叙述性综述
Antibiotics (Basel). 2023 Sep 29;12(10):1495. doi: 10.3390/antibiotics12101495.
7
Prospective multicentre study of indications for surgery in patients with idiopathic acute pancreatitis following endoscopic ultrasonography (PICUS).经内镜超声检查后特发性急性胰腺炎患者行手术治疗的适应证的前瞻性多中心研究(PICUS)。
Br J Surg. 2023 Nov 9;110(12):1877-1882. doi: 10.1093/bjs/znad318.
8
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J Clin Med. 2023 Sep 19;12(18):6044. doi: 10.3390/jcm12186044.
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Clin Transl Gastroenterol. 2023 Aug 1;14(8):e00621. doi: 10.14309/ctg.0000000000000621.
10
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