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Validation of the Omron HBP-1300 in pregnancy for medium-arm and large-arm circumferences according to the British Hypertension Society protocol

Abbud, Lamaana; Nzelu, Dianea; Salaria, Mariama; Kay, Pollya; Kametas, Nikos A.a,b

doi: 10.1097/MBP.0000000000000341
Devices and Technology

Objective The aim of this study was to validate the Omron HBP-1300 oscillometric blood pressure (BP) device according to the British Hypertension Society validation protocol, in pregnant women of both medium-arm and large-arm circumferences.

Participants and methods BP was measured sequentially in 72 women of any gestation requiring the use of a large-size (N=36, arm circumference ≥33 cm) or medium-size cuff (N=36, arm circumference <33 cm) alternating between a mercury sphygmomanometer and the Omron HBP-1300 device.

Results The Omron HBP-1300 is accurate in pregnancy with a mean device–observer difference of 3±6 and 1±6 mmHg for systolic BP and 2±5 and 3±6 mmHg for diastolic BP in women requiring the use of the medium and large cuff, respectively.

Conclusion The Omron HBP-1300-automated BP device can be recommended for use in pregnant women with medium-arm or large-arm circumferences.

aAntenatal Hypertension Clinic

bFetal Medicine Research Institute, King’s College Hospital, London, UK

Correspondence to Nikos A. Kametas, MD, Antenatal Hypertension Clinic, Fetal Medicine Research Institute, King’s College Hospital, Denmark Hill, London SE5 8BB, UK Tel: +44 203 299 2465; fax: +44 207 733 9534; e-mail: nick.kametas@kcl.ac.uk

Received February 11, 2018

Received in revised form May 31, 2018

Accepted June 19, 2018

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