Clinical Trial Center.
Department of Cardiovascular Medicine, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Blood Press Monit. 2021 Oct 1;26(5):396-399. doi: 10.1097/MBP.0000000000000541.
To evaluate the accuracy of the YuWell YE900 oscillometric upper-arm professional office blood pressure monitor in adults and children 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).
Subjects were recruited to fulfill the age, sex, blood pressure and cuff distribution criteria of the AAMI/ESH/ISO Universal Standard in adults and children (aged 3-12 years) using the same arm sequential blood pressure measurement method. Three cuffs of the test device were used for arm circumference 18-22 cm (small), 22-32 cm (medium) and 32-42 cm (large).
Ninety-two subjects were recruited, and 85 (50 adults and 35 children) were analyzed. For validation criterion 1, the mean ± SD of the differences between the test device and reference blood pressure readings was 1.7 ± 6.62/3.1 ± 5.76 mmHg (systolic/diastolic). For validation criterion 2, the SD of the averaged blood pressure differences between the test device and reference blood pressure per subject was 5.25/5.13 mmHg (systolic/diastolic).
The YuWell YE900 professional electronic blood pressure monitor has passed the requirements of the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018) in adults and children and can be recommended for clinical use.
根据医疗器械促进协会/欧洲高血压学会/国际标准化组织(AAMI/ESH/ISO)通用标准(ISO 81060-2:2018)评估 YuWell YE900 腕式电子血压计在成人和儿童中的准确性。
采用相同手臂顺序血压测量法,根据 AAMI/ESH/ISO 通用标准中成人和儿童(年龄 3-12 岁)的年龄、性别、血压和袖带分布标准招募受试者。使用三种测试设备袖带,臂围 18-22cm(小)、22-32cm(中)和 32-42cm(大)。
共招募 92 名受试者,85 名(50 名成人和 35 名儿童)进行了分析。对于验证标准 1,测试设备和参考血压读数之间差值的平均值±SD 为 1.7±6.62/3.1±5.76mmHg(收缩压/舒张压)。对于验证标准 2,每个受试者测试设备和参考血压平均差值的 SD 为 5.25/5.13mmHg(收缩压/舒张压)。
YuWell YE900 专业电子血压计已通过 AAMI/ESH/ISO 通用标准(ISO 81060-2:2018)在成人和儿童中的要求,可以推荐用于临床使用。