| Literature DB >> 29386350 |
George S Stergiou1, Bruce Alpert2, Stephan Mieke2, Roland Asmar2, Neil Atkins2, Siegfried Eckert2, Gerhard Frick2, Bruce Friedman2, Thomas Graßl2, Tsutomu Ichikawa2, John P Ioannidis2, Peter Lacy2, Richard McManus2, Alan Murray2, Martin Myers2, Paolo Palatini2, Gianfranco Parati2, David Quinn2, Josh Sarkis2, Andrew Shennan2, Takashi Usuda2, Jiguang Wang2, Colin O Wu2, Eoin O'Brien2.
Abstract
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.Entities:
Keywords: accuracy; blood pressure measurement; device; monitor; protocol; standard; validation
Mesh:
Year: 2018 PMID: 29386350 DOI: 10.1161/HYPERTENSIONAHA.117.10237
Source DB: PubMed Journal: Hypertension ISSN: 0194-911X Impact factor: 10.190