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Medical Devices: Evidence and Research Volume 11, 2018 - Issue

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Original Research

Validation of BP devices QardioArm^® in the general population and Omron M6 Comfort^® in type II diabetic patients according to the European Society of Hypertension International Protocol (ESH-IP)

Mirna N Chahine1 Faculty of Medical Sciences, Lebanese University, Hadath, Lebanon;2 Foundation-Medical Research Institutes (F-MRI), Beirut, Lebanon

Jirar Topouchian3 Preventive Cardiology Center, Yerevan, Armenia;4 Diagnostic Center, Hotel-Dieu Hospital, Paris, France

Parounak Zelveian3 Preventive Cardiology Center, Yerevan, Armenia

Zoya Hakobyan3 Preventive Cardiology Center, Yerevan, Armenia

Arevik Melkonyan3 Preventive Cardiology Center, Yerevan, Armenia

Alaa Azaki1 Faculty of Medical Sciences, Lebanese University, Hadath, Lebanon

Reem Diab1 Faculty of Medical Sciences, Lebanese University, Hadath, Lebanon

Aya Harb1 Faculty of Medical Sciences, Lebanese University, Hadath, Lebanon

Roland Asmar1 Faculty of Medical Sciences, Lebanese University, Hadath, Lebanon;2 Foundation-Medical Research Institutes (F-MRI), Beirut, LebanonCorrespondence[email protected]

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Pages 11-20 | Published online: 27 Dec 2017

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Validation of BP devices QardioArm^® in the general population and Omron M6 Comfort^® in type II diabetic patients according to the European Society of Hypertension International Protocol (ESH-IP)

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Validation of BP devices QardioArm® in the general population and Omron M6 Comfort® in type II diabetic patients according to the European Society of Hypertension International Protocol (ESH-IP)

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Validation of BP devices QardioArm^® in the general population and Omron M6 Comfort^® in type II diabetic patients according to the European Society of Hypertension International Protocol (ESH-IP)