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A pilot study of respiratory rate derived from a wearable biosensor compared with capnography in emergency department patients

机译:急诊科患者通过可穿戴式生物传感器与二氧化碳图比较呼吸频率的初步研究

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Purpose: Respiratory rate is assessed less frequently than other vital signs, and documented respiratory rates are often erroneous. This pilot study compared respiratory rates derived from a wearable biosensor to those derived from capnography. Methods: Emergency department patients with respiratory complaints were enrolled and had capnography via nasal cannula and a wireless, wearable biosensor from Philips applied for approximately one hour. Respiratory rates were obtained from both of these methods. We determined the difference between median respiratory rates obtained from the biosensor and capnography and the proportion of biosensor-derived respiratory rates that were within three breaths/minute of the capnography-derived respiratory rates for each patient. A Spearman correlation coefficient was calculated to assess the strength of the correlation between mean respiratory rates derived from both methods. Plots of minute-by-minute respiratory rates, per patient, for each monitoring method were shown to two physicians. The physicians identified time periods in which the respiratory rates appeared invalid. The proportion of time with invalid respiratory rates for each patient, for each method, was calculated and averaged. Results: We analyzed data for 17 patients. Median biosensor-derived respiratory rate was 20?breaths/minute (range: 7–40?breaths/minute) and median capnography-derived respiratory rate was 25?breaths/minute (range: 0–58?breaths/minute). Overall, 72.8% of biosensor-derived respiratory rates were within three breaths per minute of the capnography-derived respiratory rates. Overall mean difference was 3.5?breaths/minute (±5.2?breaths/minute). Respiratory rates appeared invalid 0.7% of the time for the biosensor and 5.0% of the time for capnography. Conclusion: Our pilot study suggests that the Philips wearable biosensor can continuously obtain respiratory rates that are comparable to capnography-derived respiratory rates among emergency department patients with respiratory complaints.
机译:目的:评估呼吸频率的频率低于其他生命体征,并且记录的呼吸频率通常是错误的。这项先导研究将可穿戴式生物传感器的呼吸频率与二氧化碳图的呼吸频率进行了比较。方法:登记急诊科有呼吸系统不适的患者,并通过鼻插管进行二氧化碳描记,并使用飞利浦的无线可穿戴生物传感器进行大约一小时的随访。从这两种方法均获得了呼吸频率。我们确定了每位患者从生物传感器和二氧化碳图获得的中值呼吸频率与由二氧化碳传感器得出的呼吸频率在三呼吸/分钟以内的生物传感器得出的呼吸频率之间的比例之间的差异。计算Spearman相关系数,以评估两种方法得出的平均呼吸频率之间的相关强度。向每位患者显示了每种监测方法每分钟的分钟呼吸频率图。医生确定了呼吸频率无效的时间段。对于每种方法,对每个患者计算无效呼吸频率的时间比例均应计算并取平均值。结果:我们分析了17例患者的数据。由生物传感器得出的呼吸频率中位数为20呼吸/分钟(范围:7-40呼吸/分钟),由二氧化碳分析得出的中位呼吸频率为25呼吸/分钟(范围:0-58呼吸/分钟)。总体而言,生物传感器得出的呼吸频率的72.8%处于二氧化碳分析仪得出的呼吸频率的每分钟3次呼吸之内。总体平均差异为3.5呼吸/分钟(±5.2呼吸/分钟)。对于生物传感器来说,呼吸频率无效的时间占0.7%,对于二氧化碳分析而言,呼吸时间的无效时间为5.0%。结论:我们的初步研究表明,飞利浦可穿戴式生物传感器可以连续获得与急诊科有呼吸系统不适的患者以二氧化碳图得出的呼吸频率相当的呼吸频率。

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