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The safety and effectiveness of low field intraoperative MRI guidance in frameless stereotactic biopsies of brain tumours—design and interim analysis of a prospective randomized trial

机译:低场术中MRI指导在脑肿瘤无框架立体定位活检中的安全性和有效性-一项前瞻性随机试验的设计和中期分析

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摘要

The aim of the study was to assess the safety and effectiveness of stereotactic brain tumour biopsy (STx biopsy) guided by low-field intraoperative magnetic resonance imaging (iMRI) in comparison with its frameless classic analogue based on a prospective randomized trial. A pilot group of 42 brain tumour patients was prospectively randomized into a low-field iMRI group and a control group that underwent a frameless STx biopsy. The primary endpoints of the analysis were postoperative complication rate and diagnostic yield, and the secondary endpoints were length of hospital stay and duration of operation. The iMRI group (21 patients) and the control group (21 patients) did not differ significantly according to demographic and epidemiological data. No major postoperative complications were noted in either group. In addition, no significant differences in the diagnostic yield (p = 1.00) and length of hospital stay (p = 0.16) were observed. The mean total OR time was 111 ± 24 min in iMRI and 78 ± 29 min in the control group (p = 0.0001). Usage of iMRI may prolong the time of the procedure but seems to be comparable in safety and effectiveness to the standard frameless STx biopsy.
机译:这项研究的目的是评估基于低场术中磁共振成像(iMRI)的立体定向脑肿瘤活检(STx活检)与无框经典类似物的安全性和有效性,该无创经典类似物基于一项前瞻性随机试验。前瞻性将42名脑肿瘤患者的试验组随机分为低视野iMRI组和接受无框架STx活检的对照组。分析的主要终点是术后并发症发生率和诊断率,次要终点是住院时间和手术时间。根据人口统计学和流行病学数据,iMRI组(21例患者)和对照组(21例)没有明显差异。两组均未发现严重的术后并发症。此外,在诊断率(p = 1.00)和住院时间(p = 0.16)上没有发现显着差异。 iMRI的平均总OR时间为111±in24 min,对照组为78±29 min(p = 0.0001)。使用iMRI可能会延长手术时间,但在安全性和有效性上似乎可以与标准无框STx活检相媲美。

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