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Blood pressure monitoring · Apr 2017
Clinical TrialValidation 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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