根据欧洲高血压学会国际方案对格朗威MD2301数字式自动血压计进行验证。

Validation of the Grandway MD2301 digital automatic blood pressure monitor according to the European Society of Hypertension International Protocol.

作者信息

Chen Wan, Zeng Zhao-Lin, Bing Sen, Li Lin-Yi, Wang Rui, Wan Yi

机构信息

aDepartment of Cardiology, People's Hospital of Jiulongpo District, Chongqing bDepartment of Cardiology, Second Hospital of Xi'an City cDepartment of Cardiology, Xijing Hospital dDepartment of Health Service, School of Public Health, Fourth Military Medical University, Xi'an, Shaanxi, China.

出版信息

Blood Press Monit. 2016 Aug;21(4):259-61. doi: 10.1097/MBP.0000000000000191.

DOI:10.1097/MBP.0000000000000191

PMID:27093703

Abstract

OBJECTIVE

The aim of the present study was to validate the Grandway MD2301 digital automatic blood pressure monitor according to the European Society of Hypertension International Protocol (ESH-IP) revision 2010.

METHODS

The ESH-IP revision 2010 for the validation of blood pressure-measuring devices in adults was followed precisely. Systolic and diastolic blood pressure (SBP and DBP, respectively) were measured sequentially in 33 adult patients and compared with a standard mercury sphygmomanometer (two observers). A total of 99 comparison pairs were obtained.

RESULTS

The device produced 78, 95 and 99 measurements within 5, 10, and 15 mmHg for SBP and 83, 96, and 99 for DBP, respectively. The average device-observer difference was -1.81±4.22 mmHg for SBP and -0.15±3.93 mmHg for DBP. All of the data were within the standards requirements to pass the testing.

CONCLUSION

The Grandway MD2301 digital automatic blood pressure monitor meets the standards of the ESH-IP revision 2010 and can be recommended for self/home measurement in the general population.

摘要