Validation of the Withings BPM Core Device for Self-Blood Pressure Measurements in General Population According to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Universal Standard.

IF 2.6 Q2 PERIPHERAL VASCULAR DISEASE
Zoya Hakobyan, Parounak Zelveian, Jirar Topouchian, Lusine Hazarapetyan, Roland Asmar
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引用次数: 0

Abstract

Background: Most of the scientific societies recommend assessing the accuracy of electronic devices for blood pressure (BP) measurements using established validation protocol.

Objective: To determine the accuracy of the BP measurements using the Withings BPM Core device in the general population according to the "Universal Standard (ISO 81060-2:2018/AMD 1:2020)".

Methods: The Withings BPM Core is an oscillometric device measuring BP at the brachial level. The study was performed according to the "Universal Standard (ISO 81060-2:2018/AMD 1:2020) protocol" using the same-arm sequential BP measurement method. Subjects (n ≥ 85) fulfilling the age, gender, BP, and cuff distribution criteria of the protocol were included. Analysis was performed as required by the Universal protocol using Criterion 1 - differences between observers' mercury sphygmomanometer reference measurements and test device BP values (test versus reference) and their standard deviation (SD); and Criterion 2 - The SD of the mean BP differences between the test device and reference BP per subject.

Results: Eighty-six subjects were selected, 85 of whom were included. The mean BP differences between the simultaneous two observers' measurements were -0.2 ± 2.1 mmHg for systolic BP (SBP) and 0.3 ± 2.1 mmHg for diastolic BP (DBP). For validation criterion 1, the mean difference ± SD between the reference and device BP values was -0.6 ± 4.8 mmHg for SBP and 0.1 ± 3.7 mmHg for DBP (≤5 ± 8 mmHg for both SBP and DBP). For criterion 2, the SD of the mean BP differences between the test device and reference BP per subject was 3.2/2.6 mmHg for SBP and DBP (≤6.91/6.95 mmHg).

Conclusion: The results of this study showed that the Withings BPM Core oscillometric device for home BP measurement fulfilled the accuracy requirements of the (ISO 81060-2:2018/AMD 1:2020) Universal protocol in the general population.

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根据医疗器械进步协会/欧洲高血压学会/国际标准化组织通用标准,验证Withings BPM核心装置在普通人群中的自我血压测量。
背景:大多数科学学会推荐使用已建立的验证方案评估用于血压测量的电子设备的准确性。目的:根据“通用标准(ISO 81060-2:2018/AMD 1:2020)”确定使用Withings BPM Core设备在普通人群中测量血压的准确性。方法:Withings BPM Core是一种测量肱水平血压的振荡装置。根据“通用标准(ISO 81060-2:2018/AMD 1:2020)协议”,采用同臂顺序血压测量方法进行研究。纳入符合方案年龄、性别、血压和袖带分布标准的受试者(n≥85)。按照通用方案的要求,使用标准1——观察者的汞血压计参考测量值与测试设备的BP值(测试与参考)之间的差异及其标准差(SD)进行分析;标准2 -每位受试者测试装置和参考血压之间的平均血压差的标准差。结果:共入选受试者86例,纳入85例。两组同时测量的平均血压差异分别为收缩压(SBP) -0.2±2.1 mmHg和舒张压(DBP) 0.3±2.1 mmHg。对于验证标准1,参考血压值与装置血压值之间的平均差值±SD为收缩压-0.6±4.8 mmHg,舒张压0.1±3.7 mmHg(收缩压和舒张压均≤5±8 mmHg)。对于标准2,每位受试者的收缩压和舒张压(≤6.91/6.95 mmHg),测试装置与参考血压之间的平均血压差异的标准差为3.2/2.6 mmHg。结论:本研究结果表明,用于家庭血压测量的Withings BPM Core振荡仪在普通人群中满足(ISO 81060-2:2018/AMD 1:2020)通用协议的精度要求。
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来源期刊
Vascular Health and Risk Management
Vascular Health and Risk Management PERIPHERAL VASCULAR DISEASE-
CiteScore
4.20
自引率
3.40%
发文量
109
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal of therapeutics and risk management, focusing on concise rapid reporting of clinical studies on the processes involved in the maintenance of vascular health; the monitoring, prevention, and treatment of vascular disease and its sequelae; and the involvement of metabolic disorders, particularly diabetes. In addition, the journal will also seek to define drug usage in terms of ultimate uptake and acceptance by the patient and healthcare professional.
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