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低剂量氯吡格雷和阿司匹林联用致血尿 被引量:3

Hematuria due to concomitant use of low dose clopidogrel and aspirin
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摘要 1例76岁男性急性冠状动脉综合征患者行经皮冠状动脉支架置入术后规律口服阿司匹林(0.1g、1次/d)、氯吡格雷(50 mg、1次/d)、阿托伐他汀钙(20 mg、1次/d)和单硝酸异山梨酯(10 mg、2次/d).2个月后突发左侧腰痛伴肉眼血尿.实验室检查:尿隐血(+++),红细胞235个/μl,红细胞19个/高倍视野.泌尿系统超声和肾功能检查未见明显异常.停用氯吡格雷和阿司匹林,并给予对症治疗.2d后患者尿液恢复正常,左侧腰痛明显好转,尿红细胞阴性.细胞色素P450 (CYP)2C19基因多态性检测显示患者携带CYP2C19* 17等位基因,即CYP2C19酶为超快代谢型.继续给予患者阿司匹林等口服治疗,患者未再出现血尿. A 76-year-old male patient with acute coronary syndrome received regularly aspirin (0.1 g once daily),clopidogrel (50 mg once daily),atorvastatin calcium (20 mg once daily),and isosorbide mononitrate (10 mg twice daily) by mouth after undergoing percutaneous coronary intervention.He suffered from left lumbago with gross hematuria after 2 months of treatments.Laboratory tests showed the following values:urine occult blood(+++),235 red blood cells per microlitre and 17 red blood cells per high power field.Urinary system ultrasonography and renal function detection showed no abnormalities.Aspirin and clopidogel were withdrawn and the symptomatic treatments were given.Two days later,the patient’s urine recovered to normal,his left lumbago was alleviated,and the red blood cell in his urine was negative.Gene polymorphism detection of cytochrome P-450 (CYP)2C19 showed that the patient carried CYP2C19 *17(CT) allele and CYP2C19 enzyme had ultra rapid metabolism.Aspirin was given orally and the hematuria did not appear again.
作者 刘俊 朱艳虹
出处 《药物不良反应杂志》 CSCD 2015年第1期60-61,共2页 Adverse Drug Reactions Journal
关键词 氯吡格雷 阿司匹林 血尿 Clopidogrel Aspirin Hematuria
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  • 1杜健鹏,史大卓,李田昌,徐浩,陈浩.冠心病稳定期血瘀证与冠状动脉病变特点的相关性[J].中西医结合学报,2010,8(9):848-852. 被引量:11
  • 2徐浩,鹿小燕,陈可冀,史大卓.血瘀证及其兼证与冠脉造影所示病变及介入治疗后再狭窄的相关性研究[J].中国中西医结合杂志,2007,27(1):8-13. 被引量:73
  • 3Sire SC, Risinger C, Dahl ML, Akiillu E, Christensen M, Bertilsson L, Ingelman-Sundberg M. A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants. Clin Pharmacol Ther. 2006; 79(1): 103-113.
  • 4Mendis S, Thygesen K, Kuulasmaa K, Giampaoli S, Mahonen M, Ngu Blackett K, Lisheng L; Writing group on behalf of the participating experts of the WHO consultation for revision of WHO definition of myocardial infarction. World Health Organization definition of myocardial infarction: 2008-09 revision. Int J Epidemiol. 2011 ; 40 (1) : 139-146.
  • 5翁维良.血瘀证及活血化瘀中西医结合研究新进展一第二届全国活血化瘀研究学术会议纪要[J].中国中西医结合杂志,1987,7(3):190-191.
  • 6Angiolillo DJ, Shoemaker SB, Desai B, Yuan H, Charlton RK, Bernardo E, Zenni MM, Guzman LA, Bass TA, Costa MA. Randomized comparison of a high clopidogrel maintenance dose in patients with diabetes mellitus and coronary artery disease: results of the Optimizing Antiplatelet Therapy in Diabetes Mellitus (OPTIMUS) study. Circulation. 2007; 115(6): 708-716.
  • 7Chesebro JH, Knatterud G, Roberts R, Borer J, Cohen LS, Dalen J, Dodge HT, Francis CK, Hillis D, Ludbrook P, Markis JE, Mueller H, Passamani ER, Powers ER, Rao AK, Robertson T, Ross A, Ryan TJ, Sobel BE, Willerson J, Williams DO, Zaret BL, Braunwald E. Thrombolysis in Myocardial Infarction (TIMI) Trial, Phase I : A comparison between intravenous tissue plasminogen activator and intravenous streptokinase. Clinical findings through hospital discharge. Circulation. 1987; 76(1): 142-154.
  • 8Desta Z, Zhao X, Shin JG, Flockhart DA. Clinical significance of the cytochrome P450 2C19 genetic polyrnorphism. Clin Pharmacokinet. 2002; 41 (12) : 913-958.
  • 9Savi P, Herbert JM. Clopidogrel and ticlopidine: P2Y12 adenosine diphosphate-reeeptor antagonists for the prevention of atherothrombosis. Semin Thromb Hemost. 2005; 31(2): 174-183.
  • 10Geiger J, Brich J, Honig-Liedl P, Eigenthaler M, Schanzenbacher P, Herbert JM, Walter U. Specific impairment of human platelet P2Y(AC) ADP receptor- mediated signaling by the antiplatelet drug clopidogrel. Arterioscler Thromb Vasc Biol. 1999; 19(8): 2007-2011.

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