Chondros K, Karpathakis N, Tsetis D, Sofras F, Mamoulakis C
Department of Urology, University Hospital of Heraklion, University of Crete Medical School, Heraklion, Crete, Greece.
Department of Radiology, Unit of Interventional Radiology, University Hospital of Heraklion, University of Crete Medical School, Heraklion, Crete, Greece.
Hippokratia. 2014 Jan;18(1):67-70.
BACKGROUND/AIM: The potential association of acute renal infarction with multiple thrombophilic gene polymorphisms and the experience of treatment with tenecteplase are described for the first time in the international literature.
The case of a 50-year old male with segmental acute renal infarction potentially associated with multiple thrombophilic gene polymorphisms is presented. He was thrombolysed with a single intravenous bolus of tenecteplase in a weight-adjusted dose (0.53mg/Kg bodyweight). Within 30 minutes after drug administration, the patient's symptoms were completely relieved. Patient's clinical course was uneventful with an acceptable renal function outcome eight weeks post-treatment. The following gene polymorphisms were identified: G455A (b-fibrinogen); C677T; A1298C (methylenetetrahydropholate reductase); T196C (platelet glycoprotein IIIa); 4G/5G (plasminogen activator inhibitor-1).
Tenecteplase is a safe and simple to use thrombolytic, with favourable pharmacokinetic profile, which might be useful if administered early, especially when local thrombolysis is impossible or unavailable and therefore warrants further investigation in clinical trials. Hippokratia 2014; 18 (1): 67-70.
背景/目的:国际文献首次描述了急性肾梗死与多种血栓形成倾向基因多态性之间的潜在关联以及使用替奈普酶治疗的经验。
介绍了一名50岁男性,患有节段性急性肾梗死,可能与多种血栓形成倾向基因多态性有关。他接受了单次静脉推注替奈普酶溶栓治疗,剂量根据体重调整(0.53mg/千克体重)。给药后30分钟内,患者症状完全缓解。治疗后八周,患者临床过程平稳,肾功能结果可接受。鉴定出以下基因多态性:G455A(β-纤维蛋白原);C677T;A1298C(亚甲基四氢叶酸还原酶);T196C(血小板糖蛋白IIIa);4G/5G(纤溶酶原激活物抑制剂-1)。
替奈普酶是一种安全且使用简便的溶栓剂,具有良好的药代动力学特性,如果早期给药可能有用,尤其是在无法进行或无法获得局部溶栓时,因此值得在临床试验中进一步研究。《希波克拉底》2014年;18(1):67 - 70。