腕戴式光容积描记仪测量腹部手术患者心脏和呼吸频率的准确性:观察性前瞻性临床验证研究。

Jonna A van der Stam, Eveline H J Mestrom, Jai Scheerhoorn, Fleur E N B Jacobs, Simon Nienhuijs, Arjen-Kars Boer, Natal A W van Riel, Helma M de Morree, Alberto G Bonomi, Volkher Scharnhorst, R Arthur Bouwman
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引用次数: 0

摘要

背景:术后恶化通常以生命参数异常为前兆。因此,术后患者的重要参数由护理人员常规测量。腕戴式传感器可能为在低视力环境下测量重要参数提供另一种工具。这些设备将允许更频繁甚至连续的重要参数测量,而不依赖于耗时的人工测量,只要它们在临床人群中的准确性得到确立。目的:本研究旨在评估可穿戴式光容积脉搏波(PPG)腕带在一组术后患者中测量心率(HR)和呼吸频率(RR)的准确性。方法:对62例腹部手术后患者(平均年龄55岁,SD 15岁;中位BMI为34,IQR为25-40 kg/m2)。将可穿戴设备获得的HR和RR测量值与麻醉后或重症监护病房的参考监测器进行比较。进行Bland-Altman和Clarke误差网格分析以确定一致性和临床准确性。结果:每名患者的数据收集时间中位数为1.2小时。该设备的HR覆盖率为94%,RR覆盖率为34%,能够为大多数测量提供准确的测量,因为98%和93%的测量在参考信号的5 bpm或3 rpm范围内。此外,100%的HR和98%的RR测量在Clarke误差网格分析中是临床可接受的。结论:腕带PPG装置能够提供HR和RR的测量,可以被视为足够准确的临床应用。考虑到覆盖范围,当获得足够质量的测量时,该设备能够连续监测HR并报告RR。试验注册:ClinicalTrials.gov NCT03923127;https://www.clinicaltrials.gov/ct2/show/NCT03923127。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The Accuracy of Wrist-Worn Photoplethysmogram-Measured Heart and Respiratory Rates in Abdominal Surgery Patients: Observational Prospective Clinical Validation Study.

Background: Postoperative deterioration is often preceded by abnormal vital parameters. Therefore, vital parameters of postoperative patients are routinely measured by nursing staff. Wrist-worn sensors could potentially provide an alternative tool for the measurement of vital parameters in low-acuity settings. These devices would allow more frequent or even continuous measurements of vital parameters without relying on time-consuming manual measurements, provided their accuracy in this clinical population is established.

Objective: This study aimed to assess the accuracy of heart rate (HR) and respiratory rate (RR) measures obtained via a wearable photoplethysmography (PPG) wristband in a cohort of postoperative patients.

Methods: The accuracy of the wrist-worn PPG sensor was assessed in 62 post-abdominal surgery patients (mean age 55, SD 15 years; median BMI 34, IQR 25-40 kg/m2). The wearable obtained HR and RR measurements were compared to those of the reference monitor in the postanesthesia or intensive care unit. Bland-Altman and Clarke error grid analyses were performed to determine agreement and clinical accuracy.

Results: Data were collected for a median of 1.2 hours per patient. With a coverage of 94% for HR and 34% for RR, the device was able to provide accurate measurements for the large majority of the measurements as 98% and 93% of the measurements were within 5 bpm or 3 rpm of the reference signal. Additionally, 100% of the HR and 98% of the RR measurements were clinically acceptable on Clarke error grid analysis.

Conclusions: The wrist-worn PPG device is able to provide measurements of HR and RR that can be seen as sufficiently accurate for clinical applications. Considering the coverage, the device was able to continuously monitor HR and report RR when measurements of sufficient quality were obtained.

Trial registration: ClinicalTrials.gov NCT03923127; https://www.clinicaltrials.gov/ct2/show/NCT03923127.

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