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FDA Approves Medtronic's Melody Transcatheter Pulmonary Valve and Ensemble Delivery System

机译:FDA批准美敦力(Medtronic)的Melody经导管肺动脉瓣和集合体输送系统

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The Food and Drug Administration (FDA) approved Medtronic Inc's Melody Transcatheter Pulmonary Valve and Ensemble Delivery System, January 25,2010-the first heart valve to be implanted through a catheter, or tube, in a leg vein and guided up to the heart. This new approach to the treatment of adults and children with previously implanted, poorly functioning pulmonary valve conduits can delay the need for open-heart surgery. The company is located in Minneapolis, Minnesota. Conduits are surgically implanted valves used to treat congenital heart defects of the pulmonary valve. Patients with congenital heart defects have narrowed, leaky, or missing pulmonary valves that impede the proper flow of blood from the heart's right ventricle to the pulmonary artery, which then sends the blood on to the lungs for oxygenation.
机译:美国食品药品监督管理局(FDA)批准了美敦力公司的Melody经导管肺动脉瓣和集合体输送系统,2010年1月25日,这是第一个通过导管或管子植入腿部静脉并被引导至心脏的心脏瓣膜。这种对以前植入的功能不佳的肺动脉导管进行治疗的成人和儿童的新方法可以延迟进行心脏直视手术的时间。该公司位于明尼苏达州的明尼阿波利斯。导管是通过外科手术植入的瓣膜,用于治疗先天性心脏瓣膜的心脏缺陷。先天性心脏缺陷患者的肺动脉瓣狭窄,渗漏或缺失,这阻碍了血液从心脏右心室到肺动脉的正常流动,然后血液被输送到肺中进行充氧。

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