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机译:关键社论

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The authors present a small prospective observational study designed to test the ability of Micropower Impulse Radar technology to detect a traumatic pneumothorax at the bedside. If ultimately found to be effective, this would be a clinically relevant and practical application of this technology. Using a non–Food and Drug Administration–approved device called the PneumoScan, four locations on each hemithorax were tested for the presence of a pneumothorax, using computed tomography as the criterion standard. All patients with clinically significant pneumothoraces requiring tube thoracostomy were detected for a sensitivity of 100%. It failed however to detect two thirds of the pneumothoraces that did not require thoracostomy. Its ability to diagnose hemothorax has also not been characterized. Therefore, its role as the sole thoracic screening examination in the resuscitation area is unclear. Based on these results, a positive chest x-ray and/or ultrasonography will still be necessary. There were also several false-positive cases contributing to a specificity of only 91%, leaving the reader unsure if a confirmatory test will be required before chest tube insertion for a positive finding. Therefore, whereas there are many purported benefits including portability and repeatability, its role in the diagnostic workup of the trauma patient is unclear, especially with respect to chest x-ray and ultrasonography.
机译:作者提出了一项小规模的前瞻性观察研究,旨在测试微功率脉冲雷达技术在床边检测创伤性气胸的能力。如果最终被证明是有效的,那么这将是该技术的临床相关和实际应用。使用未经食品和药物管理局批准的称为PneumoScan的设备,使用计算机断层扫描作为标准标准,对每个半胸腔中的四个位置进行了气胸检测。检测到所有具有显着临床意义的气胸患者需要进行胸腔镜造瘘术的患者,其敏感性为100%。然而,它没有检测到不需要胸腔造口术的三分之二的气胸。其诊断血胸的能力也未得到表征。因此,它在复苏区作为唯一的胸部筛查检查的作用尚不清楚。根据这些结果,仍然需要进行胸部X线检查和/或超声检查。也有几例假阳性病例,其特异性仅为91%,这使读者不确定是否需要在插入胸管前进行确证试验以寻找阳性结果。因此,尽管有许多声称的好处,包括便携性和可重复性,但尚不清楚其在创伤患者诊断检查中的作用,尤其是在胸部X光和超声检查方面。

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