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A Systematic and Evidence-Based Review of Published and Pending Reports of Andexanet Alfa

机译:对Andexanet Alfa发表和待定报告的系统和证据审查

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Andexanet alfa is the newly approved factor Xa inhibitor reversal agent for the treatment of life-threatening or uncontrolled bleeding from apixaban or rivaroxaban. This decoy protein directly binds factor Xa inhibitors reversing their action. A systematic and evidence-based evaluation of the available clinical trials is lacking in the literature. This research will provide a systematic and evidence-based evaluation of published clinical trials for andexanet alfa. It will also present an evaluation of active research. Reports of research were identified through multiple databases using search terms andexanet alfa, andexanet, or PRT064445. The level of evidence and strength of recommendation were accomplished using the Strength of Recommendation Taxonomy. There are 2 published articles presenting 3 clinical trials. Two trials had a low level of evidence and the third trial, a preliminary report of results, showed a moderate level of evidence. The review of active research found 3 unique studies and a preliminary results study. The level of evidence is low for 2 of these studies, moderate for a third, and potentially high for the fourth. The strength of recommendation for all 6 studies is a C. Four of the studies present disease-oriented evidence resulting in a low level of evidence. Another study is unblinded and uncontrolled but presents patient-oriented evidence resulting in a moderate level of evidence. Only one study could score high because the outcome is patient-oriented evidence, and it could achieve follow-up of 80%. There is a need for well-controlled and blinded evaluation to improve the recommendation strength.
机译:Andexanet alfa是新批准的因子Xa抑制剂逆转剂,用于治疗阿哌沙班或利伐沙班导致的危及生命或无法控制的出血。这种诱饵蛋白直接结合因子Xa抑制剂,逆转其作用。文献中缺乏对现有临床试验的系统和循证评估。这项研究将对已发表的安的松阿尔法临床试验进行系统的循证评估。它还将对活跃的研究进行评估。研究报告通过多个数据库使用搜索词andexanet alfa、andexanet或PRT064445进行识别。证据水平和推荐强度是使用推荐强度分类法完成的。有2篇发表的文章介绍了3项临床试验。两项试验的证据水平较低,第三项试验的初步结果报告显示证据水平适中。对活跃研究的回顾发现了3项独特的研究和一项初步结果研究。其中两项研究的证据水平较低,第三项研究的证据水平适中,第四项研究的证据水平可能较高。所有6项研究的推荐强度均为C。其中四项研究提供了以疾病为导向的证据,导致证据水平较低。另一项研究是非盲和不受控制的,但提供了以患者为导向的证据,从而产生了中等水平的证据。只有一项研究得分较高,因为结果是以患者为导向的证据,并且可以实现80%的随访。需要进行良好的控制和盲评估,以提高推荐强度。

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