首页> 外文期刊>Circulation. Cardiovascular interventions >Magnetic resonance-guided cardiac interventions using magnetic resonance-compatible devices: a preclinical study and first-in-man congenital interventions.
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Magnetic resonance-guided cardiac interventions using magnetic resonance-compatible devices: a preclinical study and first-in-man congenital interventions.

机译:使用磁共振兼容设备进行磁共振引导的心脏干预:临床前研究和先天先天性干预。

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BACKGROUND: Percutaneous cardiac interventions are currently performed under x-ray guidance. Magnetic resonance imaging (MRI) has been used to guide intravascular interventions in the past, but mainly in animals. Translation of MR-guided interventions into humans has been limited by the lack of MR-compatible and safe equipment, such as MR guide wires with mechanical characteristics similar to standard guide wires. The aim of the present study was to evaluate the safety and efficacy of a newly developed MR-safe and compatible passive guide wire in aiding MR-guided cardiac interventions in a swine model and describe the 2 first-in-man solely MR-guided interventions. METHODS AND RESULTS: In the preclinical trial, the new MR-compatible wire aided the performance of 20 interventions in 5 swine. These consisted of balloon dilation of nondiseased pulmonary and aortic valves, aortic arch, and branch pulmonary arteries. After ethics and regulatory authority approval, the 2 first-in-man MR-guided interventions were performed in a child and an adult, both with elements of valvar pulmonary stenosis. Catheter manipulations were monitored with real-time MRI sequence with interactive modification of imaging plane and slice position. Temporal resolution was 11 to 12 frames/s. Catheterization procedure times were 110 and 80 minutes, respectively. Both patients had successful relief of the valvar stenosis and no procedural complications. CONCLUSIONS: The described preclinical study and case reports are encouraging that with the availability of the new MR-compatible and safe guide wire, certain percutaneous cardiac interventions will become feasible to perform solely under MR guidance in the future. A clinical trial is underway in our institution.
机译:背景:经皮心脏干预目前是在X射线引导下进行的。过去,磁共振成像(MRI)已用于指导血管内干预,但主要用于动物。由于缺乏与MR兼容且安全的设备,例如MR导丝的机械特性类似于标准导丝,因此MR导引的干预措施向人类的转化受到了限制。本研究的目的是评估新开发的MR安全且兼容的被动导丝在猪模型中辅助MR引导的心脏干预中的安全性和有效性,并描述2种首次在MR引导下进行的首次人工干预。方法和结果:在临床前试验中,新的MR兼容线帮助5头猪进行了20次干预。这些包括无病变的肺动脉和主动脉瓣,主动脉弓和分支肺动脉的球囊扩张。经伦理和监管机构批准后,在儿童和成人中均进行了2例首次MR引导的干预,均具有瓣膜性肺动脉狭窄。导管操作通过实时MRI序列与成像平面和切片位置的交互式修改进行监控。时间分辨率为11到12帧/秒。导管插入时间分别为110分钟和80分钟。两名患者均成功缓解了瓣膜狭窄,无手术并发症。结论:所描述的临床前研究和病例报告令人鼓舞,随着新的MR兼容且安全的新导丝的问世,某些经皮心脏干预将可能在将来仅在MR指导下进行。我们机构正在进行一项临床试验。

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