Nocturnal Blood Pressure Dipping in Adults: A Comparison Between Cuffless and Ambulatory Blood Pressure Monitoring.

IF 2.9 3区 医学 Q2 PERIPHERAL VASCULAR DISEASE
C Hove, T M Seeberg, K G Bøtker-Rasmussen, E Westgaard, S Heimark, B Waldum-Grevbo, A C K Larstorp
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引用次数: 0

Abstract

Background: Cuffless blood pressure (BP) devices have demonstrated potential in estimating daytime BP but have not been able to predict nocturnal BP precisely, creating difficulties when the intended use is ambulatory BP monitoring (ABPM). We evaluated the ability of a photoplethysmography-based cuffless BP device, with the intended use 24-hour ABPM, to estimate nocturnal BP compared to a cuff-based oscillometric device.

Methods: Participants underwent 24-hour ABPM with the cuffless device placed on the non-dominant upper arm and a validated cuff-based oscillometric device on the dominant arm. The difference between mean awake and asleep BP (awake-asleep BP change) was calculated for both devices and used in the analyses. The statistical analyses were guided by the Awake/Asleep test (European Society of Hypertension 2023 Recommendations), however, there were methodological deviances from these recommendations. Most importantly, we used only cuffless BP values that were obtained simultaneously with the reference device.

Results: Data from 50 participants, aged 18-80 years, with mean (standard deviation; SD) inclusion office systolic/diastolic BP (SBP/DBP) 120.1 (11.5)/75.3 (7.9), were analyzed. The cuffless device achieved a mean difference [95% limits of agreement] of 1.6 [-8.0, 11.2] mmHg for SBP and 1.2 [-6.7, 9.1] mmHg for DBP in awake-asleep BP changes compared to the reference. Pearson correlation coefficients (95% confidence interval) for SBP/DBP were 0.75 (0.59, 0.85)/0.74 (0.58, 0.84). Our population had an overrepresentation of normal and low BP.

Conclusion: Although the cuffless device shows promise in successfully tracking nocturnal BP, full validation is required before clinical use.

成人夜间血压下降:无袖带和动态血压监测的比较。
背景:无袖带血压(BP)装置在估计白天血压方面有潜力,但不能准确预测夜间血压,当预期用途是动态血压监测(ABPM)时,会产生困难。我们评估了基于光容积描记仪的无袖带血压装置的能力,与基于袖带的振荡装置相比,使用24小时ABPM来估计夜间血压。方法:参与者接受24小时ABPM,无袖带装置放置在非优势上臂,有效的基于袖带的振荡装置放置在优势上臂。计算两种设备平均清醒和睡眠血压的差异(清醒-睡眠血压变化)并用于分析。统计分析以清醒/睡眠测试(欧洲高血压协会2023建议)为指导,然而,这些建议在方法上存在偏差。最重要的是,我们只使用与参考装置同时获得的无断口BP值。结果:分析了50名年龄在18-80岁的参与者的数据,平均(标准差;SD)收缩压/舒张压(SBP/DBP)为120.1(11.5)/75.3(7.9)。与参考文献相比,无袖带装置的收缩压平均差异为1.6 [-8.0,11.2]mmHg,舒张压平均差异为1.2 [-6.7,9.1]mmHg。收缩压/舒张压的Pearson相关系数(95%置信区间)为0.75(0.59,0.85)/0.74(0.58,0.84)。我们的人群中血压正常和低血压的比例过高。结论:尽管无袖带装置有望成功跟踪夜间血压,但在临床使用前需要充分验证。
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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来源期刊
American Journal of Hypertension
American Journal of Hypertension 医学-外周血管病
CiteScore
6.90
自引率
6.20%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The American Journal of Hypertension is a monthly, peer-reviewed journal that provides a forum for scientific inquiry of the highest standards in the field of hypertension and related cardiovascular disease. The journal publishes high-quality original research and review articles on basic sciences, molecular biology, clinical and experimental hypertension, cardiology, epidemiology, pediatric hypertension, endocrinology, neurophysiology, and nephrology.
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