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双氯芬酸和泮托拉唑所致横纹肌溶解症:一种潜在的药物相互作用

Diclofenac- and Pantoprazole-Induced Rhabdomyolysis: A Potential Drug Interaction.

作者信息

Ertekin Yusuf Haydar, Yakar Burkay, Ertekin Hülya, Uludağ Ayşegül, Tekin Murat

机构信息

Department of Family Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey.

Corum Gulabibey Family Health Center, Corum, Turkey.

出版信息

Drug Saf Case Rep. 2015 Dec;2(1):10. doi: 10.1007/s40800-015-0012-6.

Abstract

BACKGROUND

Drugs represent one of the etiologic causes of acute rhabdomyolysis (AR) with drug-induced rhabdomyolysis most commonly associated with HMG-CoA reductase inhibitors. AR etiology can also result from the use of diclofenac, a non-steroidal anti-inflammatory drug, and omeprazole, a proton pump inhibitor. Cases of AR triggered by pantoprazole have never before been reported, although it has been observed that its inclusion in multiple drug therapies can result in muscle events.

CASE PRESENTATION

A 45-year-old man presenting with complaints of fatigue and extensive body pain was diagnosed with acute rhabdomyolysis. His symptoms started on the fourth day of the concomitant use of diclofenac and pantoprazole. The patient was using diclofenac 50-mg tablets once daily for 1 month and pantoprazole 40-mg tablets once daily during the previous week for headaches and pyrosis, resulting in an increase in his creatinine kinase levels to 3114 IU/L (reference range 24-190 IU/L) on the fifth day of concomitant use. His creatinine kinase levels returned to normal and his complaints disappeared after the seventh day of discontinuation of both treatments.

DISCUSSION

A third case of diclofenac-induced rhabdomyolysis was defined in which, different from previous cases, AR was detected during the concomitant use of diclofenac and pantoprazole. The timing of the symptom development and the limited number of AR cases induced by diclofenac and pantoprazole suggested a drug interaction.

CONCLUSION

The close relationship between diclofenac and pantoprazole, and the cytochrome P450 and P-glycoprotein systems offers a strong indication that a drug interaction may be occurring. While evaluating the side effects of drugs in patients undergoing monotherapy, clinicians should also consider the mechanisms that play a part in drug absorption and distribution.

摘要

背景

药物是急性横纹肌溶解症(AR)的病因之一,药物性横纹肌溶解症最常与HMG-CoA还原酶抑制剂相关。AR的病因也可能源于使用双氯芬酸(一种非甾体抗炎药)和奥美拉唑(一种质子泵抑制剂)。尽管已观察到泮托拉唑在多种药物治疗中的应用会导致肌肉相关事件,但此前从未有过由泮托拉唑引发AR病例的报道。

病例介绍

一名45岁男性因疲劳和全身广泛疼痛就诊,被诊断为急性横纹肌溶解症。他的症状在同时使用双氯芬酸和泮托拉唑的第四天开始出现。患者每天服用一次50毫克双氯芬酸片,持续1个月,前一周每天服用一次40毫克泮托拉唑片以治疗头痛和烧心,在同时用药的第五天,其肌酸激酶水平升至3114国际单位/升(参考范围为24 - 190国际单位/升)。在两种治疗药物停用七天后,他的肌酸激酶水平恢复正常,症状也消失了。

讨论

定义了第三例双氯芬酸诱导的横纹肌溶解症,与之前的病例不同,此次在双氯芬酸和泮托拉唑同时使用期间检测到AR。症状出现的时间以及双氯芬酸和泮托拉唑诱导的AR病例数量有限提示存在药物相互作用。

结论

双氯芬酸与泮托拉唑之间的密切关系以及细胞色素P450和P-糖蛋白系统有力地表明可能存在药物相互作用。在评估接受单一疗法患者的药物副作用时,临床医生还应考虑参与药物吸收和分布的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73db/5005763/a826175e5a47/40800_2015_12_Fig1_HTML.jpg

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