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74 protocols using hbp 1300

1

Validating Omron HBP-1300 Blood Pressure Monitor

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Variables were defined as follows for ease of analysis: “A” refers to the Omron HBP-1300, “B” refers to mercury sphygmomanometer, and “M” denotes the mean value of the 3 measurements. Thus, SBPA1, SBPA2, and SBPA3 denote the 1st, 2nd, and 3rd systolic measurements taken by using the Omron HBP-1300; while SBPB1, SBPB2, and SBPB3 denote the 1st, 2nd, and 3rd systolic measurements taken by using a mercury sphygmomanometer, respectively. Accordingly, DBPA1, DBPA2, and DBPA3 denote the 3 diastolic measurements taken by using the Omron HBP-1300; while DBPB1, DBPB2, and DBPB3 denote the 3 diastolic measurements taken by using a mercury sphygmomanometer. MSBPA and MDBPA denote the mean SBP and DBP values of the 3 repeated measurements taken using the Omron HBP-1300, while MSBPB and MDBPB denote the mean SBP and DBP values taken using a mercury sphygmomanometer, respectively.
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2

Standardized Blood Pressure Measurement Protocol

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Community health workers (CHW) serving as clinic staff measured blood pressure and entered it into the electronic medical record at the beginning of each visit per routine. A physician sat with CHWs and assisted in measuring approximately 500 patient blood pressures to demonstrate proper technique. Patients were seated in a chair with the arm supported at the level of the heart. Blood pressure was measured using Omron HBP-1300™ automated cuffs. Blood pressure was repeated by a clinician approximately 30–60 minutes later using Omron HBP-1300™ (Omron Healthcare, Inc. Lake Forest, IL, USA) automated cuffs. Hypertension was defined by the average of these two measurements and categorized as defined by the Joint National Committee14 . Stage 1 is SBP ≥ 140mmHG but < 160mmHg and/or DBP ≥ 90mmHg but < 100mmHg; stage 2 is SBP ≥ 160mmHg and/or DBP ≥ 100mmHg.
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3

Accurate Blood Pressure and Metabolic Measurements

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BP was measured in the sitting position using an automated BP monitor (Omron HBP‐1300, Omron Corp., Kyoto, Japan), a well‐known device for measuring BP. A study by Meng et al. (2016 (link)) reported that the average discrepancy between manual readings by professional doctors and those obtained with the Omron HBP‐1300 was within acceptable limits: 1.4 ± 3.2 mmHg for SBP and 1.0 ± 3.9 mmHg for diastolic blood pressure (DBP); that is, the device's SBP readings have an average deviation of approximately 1.4 mmHg with a standard error margin of ±3.2 mmHg, and for DBP the average deviation is around 1.0 mmHg with a standard error margin of ±3.9 mmHg. These findings are consistent in both children and adults. The following metabolic parameters were measured from fasting venous blood samples: lipid profile, including total cholesterol (enzymatic method), HDL‐C and LDL‐C (direct‐enzymatic method), and non‐HDL‐C; and glucose tolerance indicators, such as blood glucose (immobilized enzyme electrode method) and HbA1c (HPLC method). Blood samples were analyzed at local clinical laboratories (Tsukuba i‐Laboratory LLP, Ibaraki, Japan).
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4

Reliable Blood Pressure Measurement Technique

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Blood pressure was measured using the Omron HBP-1300 professional portable blood pressure monitor (HBP-1300, Omron Corp, Kyoto, Japan). The reliability of the measurement tool was ICC=.94 in SBP and ICC=.92 in diastolic blood pressure (DBP) [25 (link)]. Measurements were taken after the participants arrived at the laboratory, sat, and rested for at least 5 min. The cuff was leveled with the heart, then tightly wrapped around the upper arm 2 cm above the elbow, and placed over the brachial artery.
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5

Standardized Blood Pressure Measurement

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Digital blood pressure monitor was used to measure blood pressure (Omron HBP-1300, Kyoto, Japan). The sensitivity and specificity of the Omron HBP-1300 used were 86.2% and 98.0%, respectively. Blood pressure was measured in the morning during urine bottle collection from the participants’ house. The participants were to be seated and asked to rest for at least 5 min before the measurement starts. The cuff used was wrapped to a tightness that allows two fingers to be inserted in between the cuff and the arm. The arm was placed at the same height as the heart during measurement. Three measurements with an interval of one to 2 min between each measurement were taken. The average of the last two readings was recorded.
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6

Blood Pressure and Anthropometric Measurements

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All participants, after resting in a seated position for at least five minutes, systolic blood pressure (SBP) and diastolic blood pressure (DBP) were measured from the right arm by OMRON HBP-1300 (OMRON Healthcare Co., Ltd., Kyoto, Japan), at 5-minute intervals. Three readings were taken, and the average of the three measurements was computed for subsequent analysis. The height was measured with an RGZ-160 measurement device (Jiangsu Suhong Medical Instruments Co., Ltd., Jiangsu, China), and the weight of the participants wearing light clothing, without hats, shoes, coats, or any extra weights in the pockets, was measured using the InBody H20B measurement instrument (InBody Co., Ltd., Seoul, South Korea). Body mass index (BMI) was calculated by dividing a person’s weight (kg) divided by the square of their height (m) [41 (link)], and was categorized as underweight (BMI < 18.5 kg/m2), normal (BMI: 18.5–23.9 kg/m2), overweight (BMI: 23-24.9 kg/m2) and obese (BMI≥25 kg/m2), respectively.
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7

Comprehensive Health Screening Protocol

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During the initial screening stage, each participant received face-to-face questionnaire interview, physical examination and laboratory measurement.
The questionnaire included information on: (1) sex, age and other general demographic data; (2) smoking and drinking status; (3) education and annual household income; (4) history of diseases and treatment. Anthropometric measurements included height, weight and waist circumference (WC). Participants were required to wear light clothes, with no shoes and no headgear while being measured for height and weight. Body mass index (BMI) was calculated by dividing weight (kg) by height (m2). Seated blood pressure was measured twice on the right upper arm after 5 min of rest with an automatic digital sphygmomanometer (Omron HBP-1300; Omron Corporation, Kyoto, Japan). If the difference between the two SBP readings was greater than 10 mmHg, a third measurement was obtained and the average of the last 2 readings was used. Fasting vein blood glucose test was performed by a rapid glucose analyzer (BeneCheck PD-G001-2; General Life Biotechnology Co., Ltd., Taiwan, China) and total cholesterol (TC), triglyceride (TG), HDL-C and LDL-C is performed by a rapid lipid analyzer (CardioChek PA Analyzer; Polymer Technology Systems, Indiana, USA). LDL-C is calculated using the values of TC, HDL-C and TG levels in the Friedewald equation.
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8

Standardized Hypertension Measurement Protocol

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Study procedures have been described in detail previously.6 At each study visit, a standardized questionnaire and physical examination were administered. Automated BP was measured using an OMRON HBP‐1300 (OMRON Healthcare) professional BP monitor. High clinic BP was defined as BP measurements (≥140/90 mmHg) on at least two consecutive visits according to the International Society of Hypertension (ISH) threshold.7
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9

Orthostatic Blood Pressure Measurement Protocol

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All participants were instructed to have a light diet on the day of assessment. All BP tests were performed at noon to decrease the impact of circadian rhythms on hemodynamics and were evaluated in a quiet room by the same cardiovascular physician. All BP tests were performed with a fully automatic electronic sphygmomanometer (Omron HBP‐1300; Omron Healthcare, Dalian, China). The BP was recorded after a 5‐min rest and a second measurement was performed immediately after the first assessment. The average of the two measurements was taken as the supine BP value. The participants were then asked to stand up as soon as possible and their orthostatic BP was measured immediately at 0, 1, 2, and 3 min. MOH was defined as an SBP drop of 20–30 mmHg or a DBP drop of 10–15 mmHg within 3 min of standing. SOH was designated as an SBP decrease of more than 30 mmHg or a DBP decrease of more than 15 mmHg within 3 min of standing.
5 (link) NOH was defined as a decrease in SBP of less than 20 mmHg and a decrease in DBP of less than 10 mmHg within 3 min of the posture change from supine to orthostatic position.
5 (link) The ΔSBP represents the SBP after standing minus the SBP when lying on the back. Similarly, ΔDBP represents the DBP after standing minus the DBP when lying on the back. Negative values indicate lower blood pressure after standing.
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10

Hypertension Measurement Protocol

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The CHS obtained BP measurements from individuals, and hypertension was defined as a systolic BP (SBP) at least 140 mmHg and/or diastolic BP (DBP) at least 90 mmHg or current treatment [18 (link)]. BP was measured three times on the right arm positioned at heart level, and there were 30 s between each measurement. Measurements were conducted using the OMRON HBP-1300 professional portable BP monitor (OMRON, Kyoto, Japan), the accuracy of which was verified in our prior study [25 (link)]. The average of the three measurements was used for analysis.
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