Feasibility and Effectiveness of a Ring-Type Blood Pressure Measurement Device Compared With 24-Hour Ambulatory Blood Pressure Monitoring Device | |||
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년도 | 2024년 2월 | ||
카테고리 | 이달의 kcj Hot Article | ||
저자 | Huijin Lee, MD,1 Sungjoon Park, MD,1 Hyuktae Kwon, MD, PhD,2 Belong Cho, MD, PhD,2 Jin Ho Park, MD, PhD,2 and Hae-Young Lee, MD, PhD1,3 | ||
소속 | 1Division of Cardiology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
2Department of Family Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea. 3Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea. |
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첨부파일 1 | kcj-54-93-abf001.jpg |
This study aimed to evaluate the applicability and precision of a ring-type cuffless blood pressure (BP) measurement device, CART-I Plus, compared to conventional 24-hour ambulatory BP monitoring (ABPM).
Forty patients were recruited, and 33 participants were included in the final analysis. Each participant wore both CART-I Plus and ABPM devices on the same arm for approximately 24 hours. BP estimation from CART-I Plus, derived from photoplethysmography (PPG) signals, were compared with the corresponding ABPM measurements.
The CART-I Plus recorded systolic blood pressure (SBP)/diastolic blood pressure (DBP) values of 131.4±14.1/81.1±12.0, 132.7±13.9/81.9±11.9, and 128.7±14.6/79.3±12.2 mmHg for 24-hour, daytime, and nighttime periods respectively, compared to ABPM values of 129.7±11.7/84.4±11.2, 131.9±11.6/86.3±11.1, and 124.5±13.6/80.0±12.2 mmHg. Mean differences in SBP/DBP between the two devices were 1.74±6.69/−3.24±6.51 mmHg, 0.75±7.44/−4.41±7.42 mmHg, and 4.15±6.15/−0.67±5.23 mmHg for 24-hour, daytime, and nighttime periods respectively. Strong correlations were also observed between the devices, with r=0.725 and r=0.750 for transitions in SBP and DBP from daytime to nighttime, respectively (both p<0.001).
The CART-I Plus device, with its unique ring-type design, shows promising accuracy in BP estimation and offers a potential avenue for continuous BP monitoring in clinical practice.
ClinicalTrials.gov Identifier: NCT06084065
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