Omron HBP-1100 (HBP-1100-E)
The technology used in the Omron HBP-1100 (HBP-1100-E), to measure blood pressure, has been compared to a clinically validated device but not according to a protocol compliant with (EU) 2017/745 and MEDDEV 2.7/1 rev 4.
|Medaval||None||Although equivalence to another device is claimed, this has not been tested to MDR requirements.|
|ESH (Europe)||Professional use for adults and children||Published evidence|
Note: This is a provisional list, as equivalence according to EU Regulation 2017/745 (e.g. MEDDEV 2.7/1 rev 4) is not proven. Accordingly, these publications are not used in the assessment of star-ratings.
Omron HBP-1300 (HBP-1300-E)
Cao X, Song C, Guo L, Yang J, Deng S, Xu Y, Chen X, Sapa WB, Wang K. Quality Control and Validation of Oscillometric Blood Pressure Measurements Taken During an Epidemiological Investigation. Medicine (Baltimore). 2015 Sep;94(37):e1475. doi: 10.1097/MD.0000000000001475. PMID: 26376388.
Ad Hoc protocol General population (Note: Modified protocols)
Meng L, Zhao D, Pan Y, Ding W, Wei Q, Li H, Gao P. Validation of Omron HBP-1300 professional blood pressure monitor based on auscultation in children and adults. BMC Cardiovasc Disord. 2016 Jan 13;16(9):5. Epub: 2016 Jan 13. doi: 10.1186/s12872-015-0177-z. PMID: 26758197. Available from: bmccardiovascdisord.biomedcentral.com.
81060-2:2013 - Pass Adults and chlidren
Abbud L, Nzelu D, Salaria M, Kay P, Kametas NA. Validation of the Omron HBP-1300 in pregnancy for medium-arm and large-arm circumferences according to the British Hypertension Society protocol. Blood Press Monit. 2018 Oct;23(5):277-80. Epub: 2018 Jul 9. doi: 10.1097/MBP.0000000000000341. PMID: 29994925.
BHS:1993 Pregnancy; Arm circumference 24 cm to 32 cm (n=36) (Note: Confusingly, the results would suggest that the device should have an A/A grade but this is not stated in the paper and no reason is provided for the omission.)
BHS:1993 Pregnancy; Arm circumference 33 cm to 43 cm (n=36) (Note: Confusingly, the device appears to pass with an A/A grade but this is not stated in the paper and no reason is provided for the omission.)
Even though the study is stated to have been carried out according to the BHS protocol, the BHS grades are omitted. Means and standard deviations are provided and the device is recommended but there is no reference as to the basis for this recommendation. These are serious anomalies that should have been resolved during the review process. Without this resolution, the hypothesis that the results are invalid cannot be rejected.