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一名心脏移植稳定患者中氯吡格雷诱发的横纹肌溶解症。

Clopidogrel-precipitated rhabdomyolysis in a stable heart transplant patient.

作者信息

Burton Jeffrey R, Burton Ilene, Pearson Glen J

机构信息

Faculty of Medicine and Dentistry, Division of Cardiology, University of Alberta, Edmonton, AB, Canada.

出版信息

Ann Pharmacother. 2007 Jan;41(1):133-7. doi: 10.1345/aph.1H394. Epub 2007 Jan 2.

Abstract

OBJECTIVE

To report the case of an orthotopic heart transplant recipient who developed rhabdomyolysis precipitated by the addition of clopidogrel to the existing regimen of cyclosporine and atorvastatin, which had been tolerated for more than 3 years without adverse effects or laboratory evidence of myositis.

CASE SUMMARY

Fourteen years after cardiac transplantation, a 58-year-old woman began a planned 4 week course of clopidogrel 75 mg/day following coronary angioplasty and placement of a stent in the left circumflex coronary artery. Almost 4 weeks later, she presented with severe muscle pain and weakness and laboratory evidence of rhabdomyolysis, with marked elevations of plasma creatine kinase (96,000 U/L) and urine myoglobin (332,872 microg/L) as well as early acute renal failure (serum creatinine 2.9 mg/dL). Symptoms and laboratory abnormalities resolved with cessation of cyclosporine, atorvastatin, and clopidogrel. Clopidogrel was not restarted, while atorvastatin and cyclosporine were; the patient had no recurrence of symptoms up to 15 months later.

DISCUSSION

Both atorvastatin and cyclosporine, as well as clopidogrel's active thiol derivative, are metabolized by the cytochrome P450 3A4 isoenzyme. Cyclosporine is also a moderate inhibitor of this isoenzyme. We postulate that competition between atorvastatin and clopidogrel for CYP3A4 receptors, already partially inhibited by cyclosporine, led to increased atorvastatin concentrations, resulting in the acute onset of rhabdomyolysis. This theory is further supported by the patient's continued ability to tolerate the combination of atorvastatin and cyclosporine, without clopidogrel, on rechallenge. Use of the Naranjo probability scale revealed that rhabdomyolysis was probably precipitated by the addition of clopidogrel to the stable baseline regimen of cyclosporine and atorvastatin.

CONCLUSIONS

Practitioners must be conscious of the potential for adverse effects when prescribing clopidogrel to heart transplant patients who are concomitantly receiving cyclosporine and a statin. If concomitant administration is required, careful clinical and laboratory monitoring of the patient is necessary.

摘要

目的

报告一例原位心脏移植受者的病例,该患者在已有环孢素和阿托伐他汀治疗方案(已耐受3年多,无不良反应或肌炎的实验室证据)基础上加用氯吡格雷后发生横纹肌溶解。

病例摘要

心脏移植14年后,一名58岁女性在冠状动脉血管成形术及左回旋支冠状动脉置入支架后开始接受为期4周的氯吡格雷治疗,剂量为75毫克/天。近4周后,她出现严重的肌肉疼痛和无力,并有横纹肌溶解的实验室证据,血浆肌酸激酶显著升高(96,000 U/L),尿肌红蛋白升高(332,872微克/升),以及早期急性肾衰竭(血清肌酐2.9毫克/分升)。停用环孢素、阿托伐他汀和氯吡格雷后,症状和实验室异常情况得到缓解。氯吡格雷未重新使用,而阿托伐他汀和环孢素重新使用;直至15个月后,患者症状未复发。

讨论

阿托伐他汀和环孢素以及氯吡格雷的活性硫醇衍生物均通过细胞色素P450 3A4同工酶代谢。环孢素也是该同工酶的中度抑制剂。我们推测,阿托伐他汀和氯吡格雷对已被环孢素部分抑制的CYP3A4受体的竞争,导致阿托伐他汀浓度升高,从而引发横纹肌溶解的急性发作。患者在重新使用阿托伐他汀和环孢素(未使用氯吡格雷)时能够继续耐受这两种药物的联合使用,这进一步支持了这一理论。使用纳伦霍概率量表显示,横纹肌溶解可能是在环孢素和阿托伐他汀的稳定基线治疗方案中加用氯吡格雷所致。

结论

在为同时接受环孢素和他汀类药物的心脏移植患者开氯吡格雷处方时,医生必须意识到潜在的不良反应。如果需要联合用药,则有必要对患者进行仔细的临床和实验室监测。

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