west china medical publishers
Keyword
  • Title
  • Author
  • Keyword
  • Abstract
Advance search
Advance search

Search

find Keyword "达比加群酯" 2 results
  • Efficacy and safety of dabigatran vs. rivaroxaban for perioperative anticoagulation in atrial fibrillation catheter ablation: a meta-analysis

    ObjectivesTo systematically evaluate the efficacy and safety of dabigatran vs. rivaroxaban for perioperative anticoagulation in the ablation of nonvalvular atrial fibrillation. MethodsPubMed, EMbase, Web of Science, The Cochrane Library, WanFang Data, CNKI and VIP databases were electronically searched to collect cohort studies on the efficacy and safety of dabigatran vs. rivaroxaban for perioperative anticoagulation in the ablation of nonvalvular atrial fibrillation from inception to July 1st, 2018. Two reviewers independently screened literature, extracted data and assessed the risk of bias of included studies, then, meta-analysis was performed by RevMan 5.3 and Stata 12.0 software. ResultsA total of 12 cohort studies involving 4 051 patients were included. The results of meta-analysis showed that: there were no differences in the rate of thromboembolic (OR=0.92, 95%CI 0.36 to 2.35, P=0.86), ischemic stroke (OR=1.15, 95%CI 0.22 to 6.07, P=0.87), major bleeding (OR=0.84, 95%CI 0.43 to 1.66, P=0.61), minor bleeding (OR=0.90, 95%CI 0.60 to 1.34, P=0.60) and pericardial tamponade (OR=1.05, 95%CI 0.45 to 2.47, P=0.90) between dabigatran and rivaroxaban groups. ConclusionsCurrent evidence shows that the efficacy and safety of dabigatran vs. rivaroxaban for perioperative anticoagulation in the ablation of nonvalvular atrial fibrillation are similar. Due to limited quality and quantity of the included studies, more high quality studies are required to verify the above conclusion.

    Release date:2019-02-19 03:57 Export PDF Favorites Scan
  • 遗传性抗凝血酶缺乏症一例并文献复习

    目的 加强临床医生对遗传性抗凝血酶缺乏症的认识,促进该病的早期诊断,改善患者预后。方法总结了1例罕见的遗传性抗凝血酶缺乏症患者的临床特点及诊治经过,并以 “遗传性抗凝血酶缺乏症”“临床特征”“达比加群酯”为关键词检索万方中文数据库,以“Hereditary antithrombin deficiency”“clinical characteristics ”“dabigatran etexilate ”为关键词检索PubMed数据库予以文献复习。结果该患者青年时期即发现非寻常部位血栓(颅内静脉窦),本次就诊期间发现多部位血栓形成,低分子肝素抗凝效果不佳,多次查抗凝血酶Ⅲ明显低于正常,进一步行基因全外显子组测序提示存在遗传性抗凝血酶Ⅲ缺乏症相关的SERPINC1基因致病变异,明确诊断为遗传性抗凝血酶缺乏症后予以达比加群酯抗凝治疗好转,随访至今未再复发。检索相关文献发现,遗传性抗凝血酶缺乏症临床相对罕见,该病具有不同的临床和基因分型,诊断的建立需依据相应的流程,其治疗及预后尚缺乏统一的认识。结论遗传性抗凝血酶缺乏症系静脉系统血栓的罕见病因,对于年轻血栓形成患者、复发性血栓或有家族聚集倾向的血栓患者,需警惕此病的可能;通过对该病的早期诊断、早期合理使用抗凝药物有助于改善预后。

    Release date: Export PDF Favorites Scan
1 pages Previous 1 Next

Format

Content