{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,8]],"date-time":"2026-10-08T12:07:25Z","timestamp":1791461245507,"version":"4.3.4"},"reference-count":27,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2019,2,25]],"date-time":"2019-02-25T00:00:00Z","timestamp":1551052800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Omron Healthcare"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J of Clinical Hypertension"],"published-print":{"date-parts":[[2019,6]]},"abstract":"<jats:p>There is growing evidence of the clinical significance of daytime masked hypertension (MHT) and blood pressure (BP) variability (BPV). Recently, watch\u2010type wearable devices for self\u2010BP measurement have become available. Such devices might be promising tools to identify patients with daytime MHT or large BPV in their real\u2010life conditions. The present study aimed to validate the accuracy of the Omron HEM\u20106410T\u2010ZM and the Omron HEM\u20106410T\u2010ZL, which are automatic watch\u2010type wearable devices for self\u2010BP measurement, according to the American National Standards Institute, Inc\/Association for the Advancement of Medical Instrumentation\/International Organization for Standardization (ANSI\/AAMI\/ISO) 81060\u20102:2013 guideline. Watches were held with the wrist at heart level. The mean differences between reference BPs and HEM\u20106410T\u2010ZM readings were \u22120.9\u00a0\u00b1\u00a07.6\/\u20101.1\u00a0\u00b1\u00a06.1\u00a0mm\u00a0Hg for systolic BP (SBP)\/diastolic BP (DBP) for criterion 1, and \u22120.9\u00a0\u00b1\u00a06.8\/\u20101.1\u00a0\u00b1\u00a05.5\u00a0mm\u00a0Hg for SBP\/DBP for criterion 2. The mean differences between reference BPs and HEM\u20106410T\u2010ZL readings were 2.4\u00a0\u00b1\u00a07.3\/0.7\u00a0\u00b1\u00a07.0\u00a0mm\u00a0Hg for SBP\/DBP for criterion 1, and 2.4\u00a0\u00b1\u00a06.5\/0.7\u00a0\u00b1\u00a06.5\u00a0mm\u00a0Hg for SBP\/DBP for criterion 2. The Omron HEM\u20106410T\u2010ZM and the Omron HEM\u20106410T\u2010ZL both fulfilled both validation criteria 1 and 2 of the ANSI\/AAMI\/ISO 81060\u20102:2013 guidelines.<\/jats:p>","DOI":"10.1111\/jch.13499","type":"journal-article","created":{"date-parts":[[2019,2,26]],"date-time":"2019-02-26T01:16:05Z","timestamp":1551143765000},"page":"853-858","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":132,"title":["Validation of two watch\u2010type wearable blood pressure monitors according to the ANSI\/AAMI\/ISO81060\u20102:2013 guidelines: Omron HEM\u20106410T\u2010ZM and HEM\u20106410T\u2010ZL"],"prefix":"10.1111","volume":"21","author":[{"given":"Mitsuo","family":"Kuwabara","sequence":"first","affiliation":[{"name":"Division of Cardiovascular Medicine, Department of Medicine Jichi Medical University School of Medicine Tochigi Japan"},{"name":"Omron Healthcare Co., Ltd. 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