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Hem 7130

Manufactured by Omron
Sourced in Japan, China

The HEM-7130 is an automated digital blood pressure monitor. It measures and displays the user's systolic and diastolic blood pressure, as well as their pulse rate. The device is designed for home use.

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23 protocols using hem 7130

1

Automated Resting Blood Pressure

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Resting blood pressure will be assessed after 5 min of rest by an automated device (Omron HEM-7130®). Two readings will be taken with a difference of 3 min between each one. With the participant seated, left arm will be placed on the table and the bracelet will be fitted around the arm, above the elbow, and aligned with brachial artery. A pediatric bracelet will be used when necessary.
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2

Brachial Artery Blood Pressure Measurement

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Participants were placed in a sitting position and brachial artery blood pressure was measured using a sphygmomanometer (HEM‐7130, OMRON, Kyoto, Japan) before and immediately after exercise. The test–retest reliability of the systolic and diastolic blood pressure measurements showed CV values of 6.1% and 8.1%, respectively.
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3

Arterial Pressure Measurement Protocol

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Arterial pressures were recorded at the baseline and after the treatment of DRS. The participant’s arterial pressure was indirectly measured by the oscillatory sphygmomanometer method using an automated device (HEM7130, Omron Healthcare Brazil, São Paulo, Brazil); three measurements were performed at 5 min intervals recording the systolic and diastolic arterial pressure.
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4

Physiological Measurements for Healthy Subjects

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The volunteers were asked to abstain from taking alcoholic beverages, caffeine or CNS stimulating substances for at least 48 hr, and refrain from exercise for at least 24 hr before the tests. They should have had neither food nor water for at least 4 hr, and abstained form diuretics for at least 7 days, and they also were asked to empty their bladder at least 30 min before the tests (Pereira et al., 2018 (link)). All of the subjects had their blood pressure (BP) recorded in the sitting position by using a cuff BP machine (HEM-7130, Omron Healthcare Co. Ltd., Kyoto, Japan). Bioelectrical impedance analysis (HBF 375, Omron Healthcare Co. Ltd., Kyoto, Japan) was used to measure body composition (i.e., fat-free mass, body and visceral fat percentages) in a room with controlled temperature. Their hands and feet were cleaned before standing on a platform throughout the test with their arms raised and elbows extended straight out (Oshima et al., 2010 ).
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5

Comprehensive Cardiometabolic Assessment Protocol

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The participants’ BP was measured using an automated device (OMRON HEM-7130) after they rested for ≥5 min in a sitting position. The right cuff size was selected based on the participant’s mid-arm circumference (small (arm circumference <23 cm), standard (23 to <33 cm) and large (≥33 cm)). Weight, height and waist circumference (WC) were also measured for each participant following the WHO protocol. WC was defined as ‘desirable’ (men <90 cm; women <80 cm), ‘high’ (men 90 to <102 cm; women 80 to <88 cm) and ‘very high’ (men ≥102 cm; women ≥88 cm) according to the WHO definition.30 Central obesity was defined as WC ≥102 cm in men and WC ≥88 cm in women.31 (link) Body mass index (BMI) was calculated as Weight(kg)[Heightm]2 , and categorized using Asian-specific thresholds of ‘underweight and normal’ (BMI<23 kg/m2), ‘overweight’ (23–<27.5 kg/m2) and ‘obese’ (≥27.5 kg/m2) according to the WHO definition.32 (link) Waist-to-height ratio (WHtR) was calculated as WC(cm)Height(cm) . The history of CVD and stroke were obtained from the baseline interview. Lastly, the lipid profile consisting of serum total cholesterol (TC), high-density lipoprotein cholesterol (HDL-c), low-density lipoprotein cholesterol (LDL-c) and triglycerides was measured for each participant.
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6

Weekly Blood Pressure Monitoring

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Participants attended follow-up appointments in the hospital once a week. Blood pressure was measured three times by trained professionals between 8 and 9 a.m., with an interval of about 2 min. The average of the last two blood pressure measurements was used for the analysis. According to the oscillometer technique, automated upper-arm cuff devices were used (Omron, Dalian, Co., Ltd. Product name: “Omron” electronic sphygmomanometer; model: HEM-7130).
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7

Epidemiological and Anthropometric Assessment Protocol

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The methods for completing the epidemiological questionnaires and for anthropometric measurements were based on a standard protocol [13 (link), 14 (link)]. Interviews were performed by trained enumerators who used a questionnaire to collect information on demographic status, socioeconomic status, medical history, family medical history, smoking status, and physical activity levels. The anthropometric measurements included height, weight, and body mass index (BMI). Height measurements were accurate to 1 cm and weight measurements to 1 kg. BMI was calculated as body weight (kg) divided by height squared (m2).
Blood pressure and heart rate were measured using a digital sphygmomanometer (OMRON HEM-7130 made in Japan) with a cuff of appropriate size following the standard recommended procedures. Three blood pressure readings were taken three times at 5-minute intervals after 5 minutes of rest in the sitting position with positioning of the arm, with the average used for data analysis. Random blood glucose rates were measured using the pin-prick method and portable glucometers (FreeStyle Optium Neo) [16 ].
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8

Comprehensive Geriatric Assessment Protocol

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Standardised questionnaires will be administered with a face-to-face interview by trained interviewers. Data collected will include socio-demographic (living arrangement, marital status, education, lifetime occupation), smoking, alcohol consumption, medical history, use of medications (prescribed and non-prescribed), hearing and visual impairment, falls, fear of falling (assessed with the Fall Efficacy Scale-International, FES-I) [46 (link)], cognitive function (assessed using the Montreal Cognitive Assessment, MoCA) [47 (link)], depressive symptoms (Geriatric Depression Scale, GDS) [48 (link)], anthropometric measures (height, weight, body composition (Tanita Scale BC 545N), circumference of the waist, hip, calf and mid arm), and blood pressure (Omron HEM7130).
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9

Comprehensive Cardiovascular Evaluation

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Participants visited our institute and answered medical history, physical activity, and MRI safety questionnaires. Height and body mass were measured to calculate body mass index (BMI). Blood pressure and heart rate were measured at rest in the seated position (HEM-7130, Omron Corporation, Japan) and were used for screening hypertension. Subsequently, MRI data were collected on a 3-Tesla scanner (Ingenia, Philips Medical Systems, Netherlands) using a 32-channel head coil (dStream Head) for radiofrequency signal reception and a quad body coil for signal transmission. Maximal oxygen uptake (VO2max) was measured on a separate day in the athlete group to determine the aerobic fitness level.
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10

Comprehensive Cardiometabolic Assessment Protocol

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Medical history and medications used were obtained by interviewing. Body weight, percentage of body fat, and percentage of visceral fat were measured using a body composition monitor (Omron Karada Scan Body Composition Monitor HBF-214, Japan). Body mass index (BMI) was calculated as body weight in kilograms divided by the square of height in meters. Waist circumference was measured at the approximate midpoint between the lower margin of the last rib and the top of the iliac crest and hip circumference was measured at the widest point of the buttocks in the standing position.21 Blood pressure and heart rate were measured twice using an automatic brachial sphygmomanometer (HEM-7130, Omron, Japan). The participants were seated and relaxed for 5 minutes before the measurement. Blood tests were performed after a 12-hour fast including the lipid profile, creatinine, fasting blood sugar, and HbA1c. Estimated glomerular filtration rate was calculated from creatinine using the CKD-EPI creatinine equation. The blood test was performed according to the manufacturer’s protocols (Human Diagnostics Worldwide, Germany).
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