Lewis Katz School of Medicine at Temple University, Department of Emergency Medicine, Philadelphia, Pennsylvania.
Capital Health, Department of Emergency Medicine, Pennington, New Jersey.
West J Emerg Med. 2024 Mar;25(2):268-274. doi: 10.5811/westjem.17822.
Numerous studies have demonstrated the accuracy of point-of-care ultrasound (POCUS). Portable, handheld devices have expanded the clinical scope of POCUS at a fraction of the cost of traditional, cart-based models. There is a paucity of data assessing the diagnostic accuracy of portable devices. Our objective in this study was to compare the diagnostic accuracy of a portable device with a cart-based model.
This was an institutional review board-approved, observational, prospective, randomized clinical trial (NCT05196776) of a convenience sample of adult patients who presented to a university-based health system. Patients who required a cardiac, lung, renal, aorta, or biliary POCUS were randomized to a portable device or to a cart-based model. We hypothesized that the cart-based model would have a 90% diagnostic accuracy vs 70% for the handheld device. To detect a 20% difference, the sample size was calculated to be 98, with 49 patients randomized to each arm. We used standard 2x2 tables to calculate test characteristics with 95% confidence intervals (CI).
A total of 110 patients were enrolled, with 56 patients randomized to the cart-based model and 54 to the handheld device. The sensitivity, specificity, and diagnostic accuracy of the cart-based vs handheld were 77.8% (40-97.2) vs 92.9% (66.1-99.8), 91.5% (79.6-97.6) vs 92.3% (79.1-98.4%), and 89.3% (78.1-96) vs 92.5% (81.8-97.9), respectively.
The diagnostic accuracy of a portable, handheld device is similar to that of a cart-based model.
大量研究表明,即时床旁超声(POCUS)具有准确性。便携式、手持式设备以传统推车式模型的一小部分成本扩展了 POCUS 的临床应用范围。评估便携式设备诊断准确性的数据很少。本研究的目的是比较便携式设备与推车式模型的诊断准确性。
这是一项机构审查委员会批准的、观察性、前瞻性、随机临床试验(NCT05196776),纳入了方便抽样的成年患者,他们在一个基于大学的医疗系统就诊。需要进行心脏、肺部、肾脏、主动脉或胆道 POCUS 的患者被随机分配到便携式设备或推车式模型组。我们假设推车式模型的诊断准确性为 90%,而手持式设备为 70%。为了检测 20%的差异,计算样本量为 98 例,每组随机分配 49 例患者。我们使用标准的 2x2 表计算具有 95%置信区间(CI)的检验特征。
共纳入 110 例患者,其中 56 例患者随机分配到推车式模型组,54 例患者随机分配到手持式设备组。推车式与手持式设备的敏感性、特异性和诊断准确性分别为 77.8%(40-97.2)与 92.9%(66.1-99.8),91.5%(79.6-97.6)与 92.3%(79.1-98.4%),89.3%(78.1-96)与 92.5%(81.8-97.9)。
便携式手持式设备的诊断准确性与推车式模型相似。