Blood Pressure Monitoring最新文献_第4页

Validation of the automated oscillometric upper-arm cuff home blood pressure monitor Prolife PA5 Comfort AF (BP 136A) in a general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Universal Standard. 根据医疗器械进步协会/欧洲高血压学会/国际标准化组织通用标准，在普通人群中验证自动振荡上臂袖带家庭血压监测仪Prolife PA5 Comfort AF （BP 136A）。

IF 1 4区医学

Blood Pressure Monitoring Pub Date : 2026-06-01 DOI: 10.1097/MBP.0000000000000793

Ariadni Menti, Vasileios Ntousopoulos, Petroula Lempidaki, Konstantina-Rozalia Bakalakou, Dimitrios Mariglis, Aikaterini Komnianou, Evangelia Ntaskagianni, Anastasios Kollias, George S Stergiou

{"title":"Validation of the automated oscillometric upper-arm cuff home blood pressure monitor Prolife PA5 Comfort AF (BP 136A) in a general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Universal Standard.","authors":"Ariadni Menti, Vasileios Ntousopoulos, Petroula Lempidaki, Konstantina-Rozalia Bakalakou, Dimitrios Mariglis, Aikaterini Komnianou, Evangelia Ntaskagianni, Anastasios Kollias, George S Stergiou","doi":"10.1097/MBP.0000000000000793","DOIUrl":"10.1097/MBP.0000000000000793","url":null,"abstract":"This study evaluated the accuracy of the automated oscillometric upper-arm cuff blood pressure (BP) measuring device Prolife PA5 Comfort AF (BP 136A) for home use in a general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2 : 2018) and its amendments (1 : 2020 and 2 : 2024). The requirements of the Universal Standardand its amendments for a validation study in a general population using the same arm sequential measurement method were applied. Participants were recruited to fulfill the age, sex, BP level, arm circumference, and cuff size distribution criteria. The test device measures BP during inflation and uses a wide-range cuff for arm circumference 22-42 cm. One-hundred-twenty-eight individuals were recruited and 85 were analyzed [mean age: 54.9 ± 15.0 (SD) years, 36 (42%) men, arm circumference: 31.7 ± 5.4 cm, range: 22.5-41.9 cm). For validation Criterion 1, the mean difference ± SD between the test device and reference BP readings ( N = 255) was -2.1 ± 7.5/-0.3 ± 5.3 mmHg (systolic/diastolic; threshold: ≤5 ± 8 mmHg). For Criterion 2, the SD of the averaged BP differences between the test device and reference BP per individual ( N = 85) were 6.44/5.07 mmHg (systolic/diastolic; threshold: ≤6.62/6.95 mmHg). The automated oscillometric home BP monitor Prolife PA5 Comfort AF (BP 136A) fulfills all the requirements of the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018) and its amendments (1 : 2020 and 2 : 2024) for a general population and can be recommended for clinical use.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"149-152"},"PeriodicalIF":1.0,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146049999","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Validation of the automated oscillometric home blood pressure monitor AViTA BPM82 in a general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2:2018). 根据医疗器械进步协会/欧洲高血压学会/国际标准化组织（AAMI/ESH/ISO）通用标准（ISO 81060-2:2018），在普通人群中验证自动振荡式家用血压监测仪AViTA BPM82。

IF 1 4区医学

Blood Pressure Monitoring Pub Date : 2026-06-01 DOI: 10.1097/MBP.0000000000000795

Ariadni Menti, Petroula Lempidaki, Dimitrios Mariglis, Eirini Chrysovalanti Antonogiannaki, Konstantina-Rozalia Bakalakou, Aikaterini Komnianou, Anastasios Kollias, George S Stergiou

{"title":"Validation of the automated oscillometric home blood pressure monitor AViTA BPM82 in a general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2:2018).","authors":"Ariadni Menti, Petroula Lempidaki, Dimitrios Mariglis, Eirini Chrysovalanti Antonogiannaki, Konstantina-Rozalia Bakalakou, Aikaterini Komnianou, Anastasios Kollias, George S Stergiou","doi":"10.1097/MBP.0000000000000795","DOIUrl":"10.1097/MBP.0000000000000795","url":null,"abstract":"Objective: To evaluate the accuracy of the automated upper-arm cuff oscillometric home blood pressure (BP) monitor AViTA BPM82 in a general population according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Universal Standard (ISO 81060-2 : 2018) and its amendments (1 : 2020 and 2 : 2024).Methods: Participants were recruited to fulfill the age, sex, BP, and arm distribution criteria of the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018) and its amendments (1 : 2020 and 2 : 2024) in a general population using the same arm sequential measurement method. A single 360° wide-range hard cuff of the test device was used for arm circumference 22-42 cm.Results: One-hundred-twelve individuals were recruited and 85 were analyzed [mean age 58.1 ± 15.2 (SD) years, 34 men, arm circumference 32 ± 5.5 cm, range: 22-42 cm]. For validation of Criterion 1, the mean difference ± SD between the test device and reference BP readings ( N 255) was -1.6 ± 7.4/-1.5 ± 5.6 mmHg (systolic/diastolic; threshold: ≤5 ± 8 mmHg). For Criterion 2, the SD of the averaged BP differences between the test device and reference BP per individual ( N 85) was 6.20/5.11 mmHg (systolic/diastolic; threshold: ≤6.76/6.78 mmHg).Conclusion: The automated oscillometric home BP monitor AViTA BPM82 fulfilled all the requirements of the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018) and its amendments (1 : 2020 and 2 : 2024) in a general population and can be recommended for home use.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"153-156"},"PeriodicalIF":1.0,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146155624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Determinants of variability in repeated auscultatory blood pressure measurements. 反复听诊血压测量变异性的决定因素。

IF 1 4区医学

Blood Pressure Monitoring Pub Date : 2026-06-01 DOI: 10.1097/MBP.0000000000000796

Shingo Yamashita, Kei Asayama, Nobuki Yakura, Kiyotaka Iwasaki

{"title":"Determinants of variability in repeated auscultatory blood pressure measurements.","authors":"Shingo Yamashita, Kei Asayama, Nobuki Yakura, Kiyotaka Iwasaki","doi":"10.1097/MBP.0000000000000796","DOIUrl":"10.1097/MBP.0000000000000796","url":null,"abstract":"Objective: Auscultation is the reference standard for validating automated blood pressure monitoring. However, its inherent variability may compromise validation reliability. This study aimed to quantify the variability in repeated auscultatory measurements and determine the relative contributions of the underlying factors.Methods: Data were analyzed from an accuracy validation study ( n = 85) conducted under the International Organization for Standardization 81060-2 : 2018+Amd 1 : 2020 standard, wherein two trained observers performed simultaneous auscultatory measurements. Using the Guide to the Expression of Uncertainty in Measurement framework, the total variability of repeated auscultatory measurements was decomposed into the proportional contributions of the blood pressure determination methodology (inherent uncertainty of identifying Korotkoff sounds during cuff deflation), observer, and participant.Results: A total of 85 participants (55.3% female), including 13 receiving antihypertensive medications, were analyzed. The mean age was 59.5 ± 10.2 years. Mean systolic/diastolic blood pressure were 124.9 ± 24.1/76.5 ± 14.2 mmHg. Repeated auscultatory measurements showed variability with SDs of 4.91 mmHg for systolic and 3.26 mmHg for diastolic blood pressure ( n = 255). The analysis identified methodology as the largest contributor to variability (systolic: 47.4%, diastolic: 46.0%), while observer and participant factors contributed less (systolic: 5.3% and 7.1%; diastolic: 16.4% and 6.8%).Conclusion: Substantial variability exists in auscultatory blood pressure measurements, even when performed under the International Organization for Standardization standard, with the determination methodology being the primary source. Our findings suggest that the inherent variability of the auscultatory method should be acknowledged as a limiting factor in identifying accurate blood pressure in clinical and research settings.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"130-137"},"PeriodicalIF":1.0,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146155961","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Effects of 20 weeks of different power training protocols involving exercises with elastic bands on cardiovascular health in hypertensive young-old adults. 20周不同力量训练方案包括弹性带运动对高血压青壮年心血管健康的影响

IF 1 4区医学

Blood Pressure Monitoring Pub Date : 2026-06-01 DOI: 10.1097/MBP.0000000000000794

Bruno Bavaresco Gambassi, Davi Grijó Viana, Eduardo Macieira, Roberto Bianco, Luiz Filipe Chaves, Benedita de Fátima Araújo Silva, Beatriz de Sá Mota, David Guilherme Marques, Daniel Yakovi Ribeiro, Vinícius Silva, Paulo Adriano Schwingel

{"title":"Effects of 20 weeks of different power training protocols involving exercises with elastic bands on cardiovascular health in hypertensive young-old adults.","authors":"Bruno Bavaresco Gambassi, Davi Grijó Viana, Eduardo Macieira, Roberto Bianco, Luiz Filipe Chaves, Benedita de Fátima Araújo Silva, Beatriz de Sá Mota, David Guilherme Marques, Daniel Yakovi Ribeiro, Vinícius Silva, Paulo Adriano Schwingel","doi":"10.1097/MBP.0000000000000794","DOIUrl":"10.1097/MBP.0000000000000794","url":null,"abstract":"Objective: This study aimed to investigate the effects of different power training protocols on pulse pressure, systolic blood pressure (SBP), diastolic blood pressure (DBP), autonomic cardiac control, and physical performance in hypertensive ung.Methods: Twenty-five participants were randomly assigned to either the dynamic power training group (DPTG; n = 13) or the power training group (PTG; n = 12). The DPTG performed dynamic power training without absolute rest intervals, whereas the PTG performed power training with short rest periods. Both protocols were carried out three times per week over 20 weeks. Pulse pressure, SBP, DBP, autonomic cardiac control, and physical performance were assessed at baseline and after 20 weeks.Results: Significant improvements were observed in pulse pressure, SBP, autonomic cardiac control, and physical performance following the 20-week intervention ( P < 0.05).Conclusion: These findings suggest that both protocols - dynamic power training (without absolute rest intervals) and power training (with short rest periods) - promoted enhancements in pulse pressure, SBP, autonomic cardiac control, lower limb functional capacity, and dynamic balance in hypertensive young-old adults. Thus, strength and conditioning professionals may consider incorporating power training protocols as a viable exercise intervention for managing systemic arterial hypertension in this population.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"121-129"},"PeriodicalIF":1.0,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146155588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Validation of the JOYTECH DBP-6286B arm-type fully automatic digital blood pressure monitor in adults or adolescents with large arm circumference according to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018 + Amd.1:2020). 根据AAMI/ESH/ISO通用标准（ISO 81060-2:2018 + Amd.1:2020 20）， JOYTECH DBP-6286B臂式全自动数字血压监测仪在成人或大臂围青少年中的验证。

IF 1 4区医学

Blood Pressure Monitoring Pub Date : 2026-06-01 DOI: 10.1097/MBP.0000000000000789

Liping He, Guiqi Wang

{"title":"Validation of the JOYTECH DBP-6286B arm-type fully automatic digital blood pressure monitor in adults or adolescents with large arm circumference according to the AAMI/ESH/ISO Universal Standard (ISO 81060-2:2018 + Amd.1:2020).","authors":"Liping He, Guiqi Wang","doi":"10.1097/MBP.0000000000000789","DOIUrl":"10.1097/MBP.0000000000000789","url":null,"abstract":"The objective of this report is to evaluate the overall effectiveness and safety of the JOYTECH DBP-6286B arm-type fully automatic digital blood pressure monitor in adults and adolescents with an arm circumference of 40-56 cm. Subjects were recruited in adults and adolescents with large arm circumference. The test device was JOYTECH DBP-6286B and the reference device was a mercury sphygmomanometer. Using BP readings obtained from the mercury sphygmomanometer as the reference standard, the accuracy of the noninvasive BP module of the test device meets the specified requirements is evaluated. This study analyzed valid BP data from 85 subjects. According to Criterion 1, the mean difference of SBP between the test and reference device was -1.09 mmHg and the SD was 3.93 mmHg. The mean difference of DBP was -0.49 mmHg and the SD was 3.43 mmHg. The mean difference of both SBP and DBP was less than ±5 mmHg, and the SD was less than 8 mmHg, which met the requirements. According to Criterion 2, SD of SBP was 2.47 mmHg, which was less than 6.86 mmHg and met the requirements. The SD of DBP was 2.48 mmHg, which was less than 6.92 mmHg and met the requirements. The JOYTECH DBP-6286B complies with Association for the Advancement of Medical Instrumentation (AAMI)/European Society of Hypertension (ESH)/International Organization for Standardization (ISO) Universal Standard (ISO 81060-2:2018 + Amd 1:2020), and the requirements of the Recognized Consensus Standards published by the FDA completely, and is recommended for BP measurement in adults and adolescents with an arm circumference of 40-56 cm for home and clinical use.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"143-148"},"PeriodicalIF":1.0,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145965016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Ambulatory blood pressure and pulse rate patterns in acute coronary syndrome patients underwent percutaneous coronary intervention. 急性冠状动脉综合征患者经皮冠状动脉介入治疗的动态血压和脉搏模式。

IF 1 4区医学

Blood Pressure Monitoring Pub Date : 2026-06-01 DOI: 10.1097/MBP.0000000000000792

Tawithep Leowattana, Supamongkol Phoopattana, Suchat Sricholwattana, Pakawat Krisnangkura, Arthit Wongsoasu, Nattapun Rattanajaruskul, Worawut Rungsangmanoon, Teeranan Angkananard

{"title":"Ambulatory blood pressure and pulse rate patterns in acute coronary syndrome patients underwent percutaneous coronary intervention.","authors":"Tawithep Leowattana, Supamongkol Phoopattana, Suchat Sricholwattana, Pakawat Krisnangkura, Arthit Wongsoasu, Nattapun Rattanajaruskul, Worawut Rungsangmanoon, Teeranan Angkananard","doi":"10.1097/MBP.0000000000000792","DOIUrl":"10.1097/MBP.0000000000000792","url":null,"abstract":"Objectives: To evaluate 24-h ambulatory systolic blood pressure (BP), diastolic BP, and pulse rate patterns in patients with acute coronary syndrome (ACS) who underwent percutaneous coronary intervention (PCI), and their association with major adverse cardiac events (MACE).Methods: We conducted a prospective cohort study in ACS patients in who ambulatory BP monitoring was recorded during 2 weeks post-PCI. Clinical and laboratory factors correlated with dipping BP and pulse rate were analyzed by multivariable logistic regression analysis. A Cox proportional hazard model was applied to find the associated factor(s) with their MACE.Results: We included 141 patients with ST-elevation myocardial infarction (STEMI) ( n = 47) and non-STEMI ( n = 94). The average age was 61.7 ± 11.1 years. Most of them are men (63.8%), had non-STEMI (66.7%), and triple vessel disease (51.1%). Upon assessment of nocturnal dipping BP, 22% were dippers, while the others were nondippers and reverse dippers (39.7 and 38.3%, respectively). Nocturnal hypertension, neutrophil-to-lymphocyte, and mean platelet volume were significantly associated with nondippers [adjusted odds ratio: 5.71, 95% confidence interval (CI): 2.51-12.99; 1.29, 95% CI: 1.01-1.63; 1.84, 95% CI: 1.16-2.93, respectively]. Nondipping pulse rate was found in 66.0% with a mean pulse rate of 75.4 ± 10.9 beats per minute (bpm) (awake) and 70.0 ± 11.2 bpm (sleep). Nondipping pulse rate was only found as an independent factor associated with MACE (hazard ratio: 2.69, 95% CI: 1.06-6.86, P = 0.04).Conclusion: This study demonstrated a significant association of MACE with nondipping pulse rate in patients with ACS who underwent PCI.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"113-120"},"PeriodicalIF":1.0,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145916739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Validation of the YuWell YE990 automatic oscillometric blood pressure monitor in mid-to-late pregnancy according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Common Criteria (AAMI/ESH/ISO 81060-2:2018/Amd.1:2020). 根据医疗器械进步协会/欧洲高血压学会/国际标准化组织通用标准（AAMI/ESH/ISO 81060-2:2018/Amd.1:2020），验证YuWell YE990妊娠中晚期自动示波血压监测仪。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2026-04-01 Epub Date: 2025-12-09 DOI: 10.1097/MBP.0000000000000787

Xue Du, Xiaoyue Wang, Xuan Li, Tengteng Li, Wenjie Lv, Zongzhi Yin

{"title":"Validation of the YuWell YE990 automatic oscillometric blood pressure monitor in mid-to-late pregnancy according to the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Common Criteria (AAMI/ESH/ISO 81060-2:2018/Amd.1:2020).","authors":"Xue Du, Xiaoyue Wang, Xuan Li, Tengteng Li, Wenjie Lv, Zongzhi Yin","doi":"10.1097/MBP.0000000000000787","DOIUrl":"10.1097/MBP.0000000000000787","url":null,"abstract":"Background: This study aimed to validate the accuracy of the YuWell YE990 automated oscillometric upper-arm blood pressure (BP) monitor in pregnant adults according to the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization Common Criteria Universal Standard (ISO 81060-2:2018 + Amd.1:2020).Methods: Participants with normotension, hypertension without proteinuria, or pre-eclampsia were enrolled in this study. BP measurements were performed using a calibrated mercury sphygmomanometer (reference) and a YE990 device (test) following a same-arm sequential protocol conducted by two trained observers.Results: A total of 46 participants (138 paired readings) were included in the final analysis. For criterion 1 of the standard, the mean difference between the test and reference devices was -2.9 ± 6.9 mmHg for systolic BP (SBP) and 0.0 ± 6.5 mmHg for diastolic BP (DBP), both within the required limits. For criterion 2, the subject-level SDs were 5.6 mmHg for SBP and 5.7 mmHg for DBP, also satisfying the ISO thresholds of 6.30 and 6.95 mmHg, respectively.Conclusion: YuWell YE990 met all accuracy criteria specified by the ISO 81060-2:2018 + Amd.1:2020 standard and is recommended for clinical use in pregnant populations.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"95-100"},"PeriodicalIF":1.2,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145773362","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Validation of the CONTEC08C oscillometric blood pressure monitor in adults according to the International Organization for Standardization 81060-2:2018 standard. 根据国际标准化组织81060-2:2018标准验证成人CONTEC08C振荡血压监测仪。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2026-04-01 Epub Date: 2025-11-03 DOI: 10.1097/MBP.0000000000000781

Mengjia Chen, Wenjie Wang, Lu Wang, Jin Bian, Wenjun Ma, Jingjing Bai, Ying Lou, Jun Cai

{"title":"Validation of the CONTEC08C oscillometric blood pressure monitor in adults according to the International Organization for Standardization 81060-2:2018 standard.","authors":"Mengjia Chen, Wenjie Wang, Lu Wang, Jin Bian, Wenjun Ma, Jingjing Bai, Ying Lou, Jun Cai","doi":"10.1097/MBP.0000000000000781","DOIUrl":"10.1097/MBP.0000000000000781","url":null,"abstract":"This study aimed to assess the accuracy of the CONTEC08C automated oscillometric upper-arm sphygmomanometer in adults for clinical use in accordance with the ISO 81060-2:2018 standard. A total of 90 normotensive and hypertensive participants aged 18-75 years were recruited, and 85 were analyzed to evaluate the accuracy of the CONTEC08C oscillometric upper-arm sphygmomanometer using the same arm sequential validation method and a standardized protocol. The mean ± standard deviation (SD) of the differences between the test device and reference blood pressure (BP) measurements was 0.5 ± 3 mmHg for SBP and 0.4 ± 3.5 mmHg for DBP, meeting validation criterion 1. For validation criterion 2, the SD of the averaged differences between the test device and reference BP measurements per subject was 1.81/2.41 mmHg (systolic/diastolic). The CONTEC08C oscillometric upper-arm blood pressure monitor fulfilled the requirements of the ISO 81060-2:2018 standard in adults in the clinical setting and can therefore be recommended for safe clinical use.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"86-89"},"PeriodicalIF":1.2,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145437069","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

A single session of multijoint exercises induces prolonged hypotension in medicated hypertensive postmenopausal women: a pilot study. 单次多关节运动可诱导绝经后服药高血压妇女持续低血压：一项初步研究。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2026-04-01 Epub Date: 2025-12-10 DOI: 10.1097/MBP.0000000000000788

José Carlos Tavares Júnior, Luan Morais Azevêdo, Rodrigo Miguel-Dos-Santos, Gilene de Jesus Pereira, Akeline Santos de Almeida, Aluísio Andrade-Lima, Rogério Brandão Wichi

{"title":"A single session of multijoint exercises induces prolonged hypotension in medicated hypertensive postmenopausal women: a pilot study.","authors":"José Carlos Tavares Júnior, Luan Morais Azevêdo, Rodrigo Miguel-Dos-Santos, Gilene de Jesus Pereira, Akeline Santos de Almeida, Aluísio Andrade-Lima, Rogério Brandão Wichi","doi":"10.1097/MBP.0000000000000788","DOIUrl":"10.1097/MBP.0000000000000788","url":null,"abstract":"Background: Isometric exercise has emerged as an effective strategy for blood pressure (BP) management, offering potential advantages over traditional exercise modalities; however, evidence regarding its 24-h effects in medicated hypertensive postmenopausal women remains limited.Objective: This study investigated the effects of a single session of multijoint isometric exercise on 24-h ambulatory hemodynamic variables in medicated hypertensive postmenopausal women.Methods: In this randomized crossover trial, 10 medicated hypertensive postmenopausal women (59 7 years) completed two experimental sessions: an isometric exercise session and a control session. The isometric exercise consisted of six multijoint exercises (upper and lower limbs), each performed for three sets of 1 min at 30% of 1-repetition maximum, with 2-min rest intervals. The control session involved sitting at rest for an equivalent duration. Following each session, 24-h ambulatory BP monitoring was conducted.Results: Significant systolic BP reductions were observed following the isometric exercise session compared with the control session at 1 h ( P < 0.05), 6 h ( P < 0.05), and 24 h ( P < 0.05). Diastolic BP was also reduced at 1 h ( P < 0.05) and 12 h ( P < 0.05). Both awake and asleep periods showed significant BP reductions for systolic and diastolic BP (all, P < 0.05).Conclusion: A single session of multijoint isometric exercise effectively reduces ambulatory BP over a 24-h period in medicated hypertensive postmenopausal women, including both awake and asleep periods. These findings support the potential clinical utility of isometric exercise as an adjunctive strategy for BP management in this population.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"71-77"},"PeriodicalIF":1.2,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145773393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Investigation of different cuffs in validation studies of electronic blood pressure monitors. 电子血压计验证研究中不同袖口的调查。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2026-04-01 Epub Date: 2025-02-25 DOI: 10.1097/MBP.0000000000000783

Ariadni Menti, Dimitrios Mariglis, Anastasios Kollias, George S Stergiou

引用次数: 0