• Blood pressure monitoring · Apr 2017

    Clinical Trial

    Validation of the G.LAB MD2200 wrist blood pressure monitor according to the European Society of Hypertension, the British Hypertension Society, and the International Organization for Standardization Protocols.

    • Ze-Yu Liu, Qing-Han Zhang, Xiao-Lei Ye, Da-Peng Liu, Kang Cheng, Chun-Hai Zhang, and Yi Wan.
    • aDepartment of Health Service, School of Public Health bDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an cDepartment of Cardiology, 117 Hospital of PLA, Hangzhou, Zhejiang, China.
    • Blood Press Monit. 2017 Apr 1; 22 (2): 101-104.

    ObjectiveTo validate the G.LAB MD2200 automated wrist blood pressure (BP) monitors according to the European Society of Hypertension International Protocol (ESH-IP) revision 2010, the British Hypertension Society (BHS), and the International Organization for Standardization (ISO) 81060-2:2013 protocols.Materials And MethodsThe device was assessed on 33 participants according to the ESH requirements and was then tested on 85 participants according to the BHS and ISO 81060-2:2013 criteria. The validation procedures and data analysis followed the protocols precisely.ResultsThe G.LAB MD2200 devices passed all parts of ESH-IP revision 2010 for both systolic and diastolic BP, with a device-observer difference of 2.15±5.51 and 1.51±5.16 mmHg, respectively. The device achieved A/A grading for the BHS protocol and it also fulfilled the criteria of ISO 81060-2:2013, with mean differences of systolic and diastolic BP between the device and the observer of 2.19±5.21 and 2.11±4.70 mmHg, respectively.ConclusionThe G.LAB MD2200 automated wrist BP monitor passed the ESH-IP revision 2010 and the ISO 81060-2:2013 protocol, and achieved the A/A grade of the BHS protocol, which can be recommended for self-measurement in the general population.

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