TY - JOUR
T1 - A Universal Standard for the Validation of Blood Pressure Measuring Devices
T2 - Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Collaboration Statement
AU - Stergiou, George S
AU - Alpert, Bruce
AU - Mieke, Stephan
AU - Asmar, Roland
AU - Atkins, Neil
AU - Eckert, Siegfried
AU - Frick, Gerhard
AU - Friedman, Bruce
AU - Graßl, Thomas
AU - Ichikawa, Tsutomu
AU - Ioannidis, John P
AU - Lacy, Peter
AU - McManus, Richard
AU - Murray, Alan
AU - Myers, Martin
AU - Palatini, Paolo
AU - Parati, Gianfranco
AU - Quinn, David
AU - Sarkis, Josh
AU - Shennan, Andrew
AU - Usuda, Takashi
AU - Wang, Jiguang
AU - Wu, Colin O
AU - O'Brien, Eoin
N1 - © 2018 American Heart Association, Inc., and Wolters Kluwer Health, Inc.
PY - 2018/3
Y1 - 2018/3
N2 - In the past 30 years, several organizations, such as the US Association for the Advancement of Medical Instrumentation (AAMI), the British Hypertension Society, the European Society of Hypertension (ESH) Working Group on Blood Pressure (BP) Monitoring, and the International Organization for Standardization (ISO), have developed protocols for clinical validation of BP measuring devices. However, it is recognized that science, as well as patients, consumers, and manufacturers, would be best served if all BP measuring devices were assessed for accuracy according to an agreed single validation protocol that had global acceptance. Therefore, an international initiative was taken by the AAMI, ESH, and ISO experts who agreed to develop a universal standard for device validation. This statement presents the key aspects of a validation procedure, which were agreed by the AAMI, ESH, and ISO representatives as the basis for a single universal validation protocol. As soon as the AAMI/ESH/ISO standard is fully developed, this will be regarded as the single universal standard and will replace all other previous standards/protocols.
AB - In the past 30 years, several organizations, such as the US Association for the Advancement of Medical Instrumentation (AAMI), the British Hypertension Society, the European Society of Hypertension (ESH) Working Group on Blood Pressure (BP) Monitoring, and the International Organization for Standardization (ISO), have developed protocols for clinical validation of BP measuring devices. However, it is recognized that science, as well as patients, consumers, and manufacturers, would be best served if all BP measuring devices were assessed for accuracy according to an agreed single validation protocol that had global acceptance. Therefore, an international initiative was taken by the AAMI, ESH, and ISO experts who agreed to develop a universal standard for device validation. This statement presents the key aspects of a validation procedure, which were agreed by the AAMI, ESH, and ISO representatives as the basis for a single universal validation protocol. As soon as the AAMI/ESH/ISO standard is fully developed, this will be regarded as the single universal standard and will replace all other previous standards/protocols.
KW - Blood Pressure Determination/standards
KW - Blood Pressure Monitors/standards
KW - Consensus
KW - Europe
KW - Humans
KW - International Cooperation
KW - Practice Guidelines as Topic/standards
KW - Reference Standards
KW - Reproducibility of Results
KW - Societies, Medical/standards
U2 - 10.1161/HYPERTENSIONAHA.117.10237
DO - 10.1161/HYPERTENSIONAHA.117.10237
M3 - Review article
C2 - 29386350
VL - 71
SP - 368
EP - 374
JO - Hypertension
JF - Hypertension
SN - 0194-911X
IS - 3
ER -