根据美国医疗器械进步协会/欧洲高血压学会/国际标准化组织通用标准(国际标准化协会81060-2:2018)和国际标准化联合会,YuWell YE660D示波上臂血压计在普通人群中用于临床和家庭的验证标准化修正案1。2020

IF 1.2 4区 医学 Q4 PERIPHERAL VASCULAR DISEASE
Blood Pressure Monitoring Pub Date : 2023-10-01 Epub Date: 2023-06-22 DOI:10.1097/MBP.0000000000000658
Hui-Jie Zhang, Yue Peng, Juan Zhang, Jin Zhang, Li-Ni Teng, Shu-Juan Zhang, De-Jun Zhou, Ming-Zhi Long
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引用次数: 0

摘要

目的:根据医疗器械进步协会/欧洲高血压学会/国际标准化组织(AAMI/ESH/ISO)通用标准(ISO 81060-2),评估YuWell YE660D示波上臂血压监测仪在普通人群中(用于成人临床和家庭血压测量)的准确性 : 2018)及其修正案1。方法:招募受试者,使用相同的臂序血压测量方法,在普通人群中满足AAMI/ESH/ISO通用标准的年龄、性别、血压和袖带分布标准。测试装置的两个袖带用于手臂周长22-32 cm(标准)和22-45 cm(宽范围)。结果:共招募92名受试者,对85名受试人进行分析。对于验证标准1,平均值 ± 测试装置和参考血压读数之间的差异SD为0.3 ± 7.2/2.2 ± 5.5 mmHg(收缩压/舒张压)。对于验证标准2,每个受试者的测试装置和参考BP之间的平均BP差异的SD为6.1/4.8 结论:YuWell YE660D示波上臂电子血压计已通过AAMI/ESH/ISO通用标准(ISO 81060-2)的要求 : 2018)及其修正案1。2020年在成人中使用,因此可以推荐用于家庭和临床。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Validation of the YuWell YE660D oscillometric upper-arm blood pressure monitor for clinic and home in general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Universal Standard (International Organization for Standardization 81060-2:2018) and the International Organization for Standardization Amendment 1. 2020.

Objective: To evaluate the accuracy of the YuWell YE660D oscillometric upper-arm blood pressure (BP) monitor in general population (for clinic and home BP measurements in adults) according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2 : 2018) and its Amendment 1. 2020.

Methods: Subjects were recruited to fulfill the age, sex, BP and cuff distribution criteria of the AAMI/ESH/ISO Universal Standard in general population using the same arm sequential BP measurement method. Two cuffs of the test device were used for arm circumferences 22-32 cm (standard) and 22-45 cm (wide range).

Results: Ninety-two subjects were recruited and 85 subjects were analyzed. For validation criterion 1, the mean ± SD of the differences between the test device and reference BP readings was 0.3 ± 7.2/2.2 ± 5.5 mmHg (systolic/diastolic). For validation criterion 2, the SD of the averaged BP differences between the test device and reference BP per subject was 6.1/4.8 mmHg (systolic/diastolic).

Conclusion: The YuWell YE660D oscillometric upper-arm electronic BP monitor has passed the requirements of the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018) and its Amendment 1. 2020 in adults and hence can be recommended for home and clinical use.

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来源期刊
Blood Pressure Monitoring
Blood Pressure Monitoring 医学-外周血管病
CiteScore
2.00
自引率
7.70%
发文量
110
审稿时长
>12 weeks
期刊介绍: Blood Pressure Monitoring is devoted to original research in blood pressure measurement and blood pressure variability. It includes device technology, analytical methodology of blood pressure over time and its variability, clinical trials - including, but not limited to, pharmacology - involving blood pressure monitoring, blood pressure reactivity, patient evaluation, and outcomes and effectiveness research. This innovative journal contains papers dealing with all aspects of manual, automated, and ambulatory monitoring. Basic and clinical science papers are considered although the emphasis is on clinical medicine. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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