超声溶栓治疗st段抬高型心肌梗死的新辅助疗法:系统综述

Muhammad Isra Rafidin Rayyan, Ichlasul Mahdi Fardhani, Hammam Arif Shabri
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引用次数: 0

摘要

目前标准的st段抬高型心肌梗死(STEMI)治疗,如经皮冠状动脉介入治疗(PCI)和溶栓药物治疗,仍有一些局限性。超声溶栓是一种利用超声能量分解血栓的新型治疗方式,目前被认为是治疗STEMI的一种有前景的替代治疗策略。本系统综述旨在进一步回顾近十年来超声溶栓作为STEMI辅助治疗方式的临床应用。我们系统地检索了PubMed、Cochrane图书馆和ScienceDirect数据库的研究。在根据纳入和排除标准删除重复和筛选研究后,由三名独立审稿人进行数据提取和批判性评价。研究检索和选择结果包括5项研究,614名患者和另外273名患者作为参考组。结果表明,间歇、短脉冲、高机械指数微泡输注超声溶栓治疗组st段分辨率和血管再通率明显优于其他治疗组。此外,各干预组之间的安全水平无显著差异。综上所述,超声溶栓是一种很有前景的新型治疗方法,可以作为PCI的辅助手段,有效且安全的治疗STEMI。
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Sonothrombolysis for novel adjuvant therapy in ST-elevation myocardial infarction: a systematic review
Current standard ST-segment elevation myocardial infarction (STEMI) treatments, such as percutaneous coronary intervention (PCI) and thrombolytic agent administration, still have some limitations. Sonothrombolysis is a new therapeutic modality that utilizes ultrasound energy to break up thrombus and is currently considered a promising alternative therapeutic strategy to treat STEMI. This systematic review aims to further review the clinical application of sonothrombolysis as an adjuvant therapy modality in STEMI based on the evidence available in the last ten years. We systematically searched studies on PubMed, Cochrane Library, and ScienceDirect databases. After removing duplicates and screening studies based on inclusion and exclusion criteria, data extraction and critical appraisal were performed by three independent reviewers. Study search and selection resulted in five studies with 614 patients and an additional 273 patients as a reference group. Results showed that patients treated with an intermittent, short pulse, and high mechanical index sonothrombolysis with microbubble infusion had significantly better ST-segment resolution and vessel recanalization rates than the other treatment groups. In addition, there was no significant difference in the safety level among all intervention groups. In conclusion, sonotrombolysis is a promising novel therapy that is an adjunct to PCI, which is effective and safe for treating STEMI.
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28
审稿时长
12 weeks
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