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Exp Ther Med. 2017 Aug;14(2):1157-1162. doi: 10.3892/etm.2017.4604. Epub 2017 Jun 14.
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本文引用的文献

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Associations of CYP3A4, NR1I2, CYP2C19 and P2RY12 polymorphisms with clopidogrel resistance in Chinese patients with ischemic stroke.CYP3A4、NR1I2、CYP2C19和P2RY12基因多态性与中国缺血性脑卒中患者氯吡格雷抵抗的相关性
Acta Pharmacol Sin. 2016 Jul;37(7):882-8. doi: 10.1038/aps.2016.41. Epub 2016 May 2.
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Influence of UGT2B7, CYP3A4, and OPRM1 Gene Polymorphisms on Transdermal Buprenorphine Pain Control in Patients with Critical Lower Limb Ischemia Awaiting Revascularization.UGT2B7、CYP3A4和OPRM1基因多态性对等待血运重建的严重下肢缺血患者经皮丁丙诺啡疼痛控制的影响。
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Warfarin dosage response related pharmacogenetics in Chinese population.中国人群中与华法林剂量反应相关的药物遗传学
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Fever as a risk factor for increased response to vitamin K antagonists: a review of the evidence and potential mechanisms.发热作为维生素K拮抗剂反应增强的风险因素:证据及潜在机制综述
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Development and comparison of a new personalized warfarin stable dose prediction algorithm in Chinese patients undergoing heart valve replacement.一种用于接受心脏瓣膜置换术的中国患者的新型华法林稳定剂量预测算法的开发与比较
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Integrating interacting drugs and genetic variations to improve the predictability of warfarin maintenance dose in Chinese patients.整合相互作用的药物和遗传变异,以提高中国患者华法林维持剂量的可预测性。
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急性肢体缺血患者中与CYP3A4功能丧失突变相关的华法林诱导的危及生命的出血:病例报告及文献复习

Warfarin-induced life-threatening bleeding associated with a CYP3A4 loss-of-function mutation in an acute limb ischemia patient: Case report and review of the literature.

作者信息

Ma Xiao-Wei, Hao Chang-Ning, Gu Zhi-Chun, Ye Meng, Li Min, Zhang Lan

机构信息

Department of Clinical Laboratory, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, P.R. China.

Department of Vascular Surgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, P.R. China.

出版信息

Exp Ther Med. 2017 Aug;14(2):1157-1162. doi: 10.3892/etm.2017.4604. Epub 2017 Jun 14.

DOI:10.3892/etm.2017.4604
PMID:28810573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5525648/
Abstract

Patients with acute limb ischemia, deep venous thrombosis and pulmonary artery embolism may be treated with warfarin. The dose-response interaction of warfarin is associated with numerous factors, depending on which an uncommon life-threatening bleeding may occur. The present case study reported on a patient with acute limb ischemia and a history of warfarin-induced bleeding ten years previously and who again developed life threatening bleeding associated with warfarin treatment and received vascular surgery. In this patient, a cytochrome P450 3A4 loss-of-function mutation decreased the effective dose of warfarin. Although this was a rare case, clinicians should be alert to the bleeding risk associated with such rare genetic mutations.

摘要

急性肢体缺血、深静脉血栓形成和肺动脉栓塞患者可用华法林治疗。华法林的剂量反应相互作用与多种因素有关,据此可能会发生罕见的危及生命的出血。本病例研究报告了一名急性肢体缺血患者,该患者十年前有华法林所致出血史,此次再次出现与华法林治疗相关的危及生命的出血并接受了血管手术。在该患者中,细胞色素P450 3A4功能缺失突变降低了华法林的有效剂量。尽管这是一例罕见病例,但临床医生应警惕与此类罕见基因突变相关的出血风险。