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Validation of the KANG KC-2850 oscillometric upper-arm ambulatory blood pressure monitor in general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization universal standard.
Liu, Kui; Ma, Yi-Fei; Wang, Yan; Zhang, Yang; Li, Lin-Yi; Zhang, Jie-Qiong; Jiang, Jun; Chen, Rui-Lin; Wan, Yi.
Affiliation
  • Liu K; Department of Health Services, Fourth Military Medical University.
  • Ma YF; Department of Health Services, Fourth Military Medical University.
  • Wang Y; Department of Outpatients, Xijing 986 Hospital.
  • Zhang Y; Department of Health Statistics, School of Preventive Medicine, Fourth Military Medical University.
  • Li LY; Department of Health Services, Fourth Military Medical University.
  • Zhang JQ; Department of Health Services, Fourth Military Medical University.
  • Jiang J; Department of Health Services, Fourth Military Medical University.
  • Chen RL; Department of Basic Medicine, Fourth Military Medical University, Xi'an, China.
  • Wan Y; Department of Health Services, Fourth Military Medical University.
Blood Press Monit ; 27(5): 349-352, 2022 10 01.
Article in En | MEDLINE | ID: mdl-35687039
ABSTRACT

OBJECTIVE:

To evaluate the accuracy of the KANG KC-2850 ambulatory blood pressure monitor (ABPM) for clinical blood pressure (BP) measurement according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) universal standard (ISO 81060-22018).

METHODS:

BP was sequentially measured and compared with a standard mercury sphygmomanometer in 85 eligible participants. A standard adult cuff (22-3232 cm) was used for test device measurements. A total of 255 comparison pairs were obtained and analyzed according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO universal standard.

RESULTS:

The standard requirements were followed precisely. For the validation Criterion 1, the mean ± SD of the differences between the test device and reference BP readings was -1.12 ± 5.01 and -0.33 ± 4.52 mmHg for SBP and DBP, respectively. For Criterion 2, the SD of the averaged BP differences between the test device and reference BP per subject was 3.59 and 3.60 mmHg for SBP and DBP, respectively.

CONCLUSION:

The KANG KC-2850 ABPM met all the requirements for validation by the AAMI/ESH/ISO universal standard and can be recommended for clinical use in general population.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Pressure Monitors / Hypertension Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adult / Humans Language: En Journal: Blood Press Monit Journal subject: ANGIOLOGIA Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Pressure Monitors / Hypertension Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adult / Humans Language: En Journal: Blood Press Monit Journal subject: ANGIOLOGIA Year: 2022 Document type: Article