Blood Pressure Monitoring最新文献_第3页

High job stress evaluated using the Brief Job Stress Questionnaire as an independent risk factor for hypertension among a Japanese male occupational population. 使用简要工作压力问卷评估高工作压力作为日本男性职业人群高血压的独立危险因素。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-12-18 DOI: 10.1097/MBP.0000000000000730

Hiromitsu Sekizuka, Hirohisa Kato, Toshiya Ishii, Satoko Nagumo

{"title":"High job stress evaluated using the Brief Job Stress Questionnaire as an independent risk factor for hypertension among a Japanese male occupational population.","authors":"Hiromitsu Sekizuka, Hirohisa Kato, Toshiya Ishii, Satoko Nagumo","doi":"10.1097/MBP.0000000000000730","DOIUrl":"10.1097/MBP.0000000000000730","url":null,"abstract":"Objective: Stress and working environments are risk factors for hypertension. A new occupational health policy called the Stress Check Program was started in Japan in 2015. Therefore, we clarified whether the presence or absence of high job stress (HJS) as determined using the Brief Job Stress Questionnaire (BJSQ) is related to the comorbidity of hypertension.Methods: The results of a single year's BJSQ and medical examinations were investigated for 18 629 active Japanese male office workers who were 30-59 years old. The presence or absence of HJS was assessed using the BJSQ and investigated using a personal computer in a medical interview. Furthermore, the relationships between HJS and hypertension comorbidity were analyzed.Results: The mean age of the subjects was 43.8 ± 10.3 years old, and the proportion of subjects with HJS was 10%. After adjustment for age and lifestyle habits, HJS was associated with a risk of hypertension comorbidity (odds ratio, 1.18; 95% confidence interval, 1.02-1.36; P = 0.022). HJS was a significant hypertensive comorbidity factor.Conclusion: HJS measured using the BJSQ independently contributed to hypertension comorbidity among male office workers.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":"30 1","pages":"24-29"},"PeriodicalIF":1.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142913825","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

Effect of wearing N95 masks for 10 hours on ambulatory blood pressure in healthy adults. 佩戴 N95 口罩 10 小时对健康成年人活动血压的影响。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-09-27 DOI: 10.1097/MBP.0000000000000729

Zachary Zeigler, Anthony Acevedo, Isiaha Mews, Dalton Lesser, Abby Koornneef

{"title":"Effect of wearing N95 masks for 10 hours on ambulatory blood pressure in healthy adults.","authors":"Zachary Zeigler, Anthony Acevedo, Isiaha Mews, Dalton Lesser, Abby Koornneef","doi":"10.1097/MBP.0000000000000729","DOIUrl":"10.1097/MBP.0000000000000729","url":null,"abstract":"The impact of wearing a face mask for an extended duration is unknown. This study aimed to determine if wearing a face mask for 10 h impacts blood pressure (BP) and arterial stiffness. Subjects received an ambulatory blood pressure cuff and were asked to wear it for 10 h while readings were taken every 15 min. During the face mask trial, subjects wore an N95 mask for 10 h. During the control, subjects did not wear a mask. Subjects were randomized to start their trial. An accelerometer was given to ensure no physical activity differences. Linear mixed models were used to determine group differences, and McNemar test was used to assess frequency differences when determining BP load. Twelve college-aged (20.5 ± 1.5 years) male ( n = 5) and female ( n = 7) individuals with normal BP participated in this study. There were no differences in time spent in any physical activity domain (all P > 0.05). There was no difference in brachial SBP ( P = 0.688), brachial DBP ( P = 0.063), central SBP ( P = 0.875), central DBP ( P = 0.246), heart rate ( P = 0.125), and augmentation pressure ( P = 0.158) between conditions. During mask condition, augmentation pressure was reduced by 5.2 ± 3.1% compared to control ( P < 0.001). There were no frequency differences in the number of BP readings above 140 mmHg for SBP ( P = 0.479) and >90 mmHg for DBP ( P = 0.212). The current study found that wearing an N95 mask for 10 h did not affect brachial or central BP but significantly decreased augmentation pressure.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"18-23"},"PeriodicalIF":1.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142457189","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 G.LAB MD6300 upper arm blood pressure monitor in different positions according to the AAMI/ESH/ISO Universal Standard (ISO81060-2:2018+AMD1:2020). 根据 AAMI/ESH/ISO 通用标准（ISO81060-2:2018+AMD1:2020），对 G.LAB MD6300 上臂血压计的不同位置进行验证。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-10-24 DOI: 10.1097/MBP.0000000000000732

Rui Cheng, Linyi Li, Jinfeng Chen, Jie Ren, Yi Wan

{"title":"Validation of the G.LAB MD6300 upper arm blood pressure monitor in different positions according to the AAMI/ESH/ISO Universal Standard (ISO81060-2:2018+AMD1:2020).","authors":"Rui Cheng, Linyi Li, Jinfeng Chen, Jie Ren, Yi Wan","doi":"10.1097/MBP.0000000000000732","DOIUrl":"10.1097/MBP.0000000000000732","url":null,"abstract":"Objective: To validate the accuracy of the G.LAB MD6300 oscillometric upper arm blood pressure monitor in the sitting, supine, and right lateral decubitus position in the 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+AMD1 : 2020).Methods: The qualified participants were recruited in the study and the same left-arm sequential method was used for blood pressure measurement according to the Universal Standard. The validation results were assessed for the three positions and the Bland-Altman scatter plot was used to show the difference between the test device and reference results.Results: A total of 85 participants were included in the analysis. The mean differences between the test device and reference readings were 0.95 ± 6.76/0.47 ± 6.71 mmHg, 0.55 ± 6.73/-0.20 ± 6.72 mmHg, and - 0.71 ± 7.11/-0.86 ± 7.06 mmHg for SBP and DBP for the validation criterion 1 in the sitting position, supine with upward palm position, and right lateral decubitus position with downward left palm flat on left side position, respectively. Furthermore, the mean differences and their standard deviations for SBP and DBP calculated according to criterion 2 in the ISO81060-2 : 2018+AMD1 : 2020 were acceptable in all three positions.Conclusion: The G.LAB MD6300 upper arm blood pressure monitor fulfilled the validation criteria of the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018+AMD1 : 2020) in the sitting position, and its accuracy in the supine and right lateral decubitus position was acceptable and roughly equivalent to that in the sitting position. Therefore, it can be recommended for clinical use and self-measurement in the general population.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"30-35"},"PeriodicalIF":1.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142680716","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

Screening for orthostatic hypotension and de-escalation of antihypertensives: insight into confounding factors, alternative methods of diagnosis, and recent studies. 筛查体位性低血压和降压药物的降级：对混杂因素、替代诊断方法和最新研究的见解。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-12-18 DOI: 10.1097/MBP.0000000000000720

Rhea Trivedi, Sameer Ahmad, Aayush Visaria

引用次数: 0

Unattended versus conventional blood pressure measurements in hospitalized hypertensive patients. 住院高血压患者的无人值守血压测量与常规血压测量的比较。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-09-17 DOI: 10.1097/MBP.0000000000000727

Zhe Hu, Rui Chu, Yang Gao, Xin Chen, Chang-Sheng Sheng

{"title":"Unattended versus conventional blood pressure measurements in hospitalized hypertensive patients.","authors":"Zhe Hu, Rui Chu, Yang Gao, Xin Chen, Chang-Sheng Sheng","doi":"10.1097/MBP.0000000000000727","DOIUrl":"10.1097/MBP.0000000000000727","url":null,"abstract":"Background: This study aims to compare the differences between unattended and conventional blood pressure measurements in hospitalized hypertensive patients.Methods: In fall of 2019, hypertensive patients at Ruijin Hospital underwent two rounds of unattended and conventional (nurse-monitored) blood pressure measurement. Both rounds used the same electronic blood pressure monitor with measurements taken three times, 30 s apart. Comparison was made using intra-class correlation coefficients, Bland-Altman plots, paired t -tests, etc.Results: Among the 92 subjects in the study, the median age was 50 years old, with women accounting for 33.7%. Among the subjects, the median duration of hypertension was 8.0 years. The prevalence of diabetes, coronary heart disease, and stroke were 26.1%, 5.4%, and 6.5%, respectively. Whether unattended or conventional measurements were taken first, the average blood pressure measured first was slightly higher than the one measured later, but the difference was within 1-2 mmHg. Except that the average DBP during the round of conventional blood pressure measurements was significantly reduced by 1.6 mmHg compared to the conventional DBP, there were no other significant differences. Subgroup analysis by age, gender, BMI, and diabetes showed no significant difference in blood pressure measurement results between unattended and conventional methods.Conclusion: No significant difference was observed between unattended and conventional methods of blood pressure measurement in hospitalized hypertensive patients. Unattended blood pressure measurement can be adopted as the current standard for blood pressure management in hospitalized patients.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"11-17"},"PeriodicalIF":1.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142280091","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 JAMR upper-arm pressure monitor B23 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）对 JAMR 上臂压力监测仪 B23 进行验证。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-07-30 DOI: 10.1097/MBP.0000000000000719

Jing Li, Li-Hong Han, Ru Feng, Li-Hao Wu, Jie Cai, Tian-Ying Zeng, Hui Liu, Lei Wang, Ju-Yun Li, Zhong-Qun Zhan

{"title":"Validation of the JAMR upper-arm pressure monitor B23 according to the AAMI/ESH/ISO Universal Standard (ISO 81060- 2:2018/AMD 1:2020).","authors":"Jing Li, Li-Hong Han, Ru Feng, Li-Hao Wu, Jie Cai, Tian-Ying Zeng, Hui Liu, Lei Wang, Ju-Yun Li, Zhong-Qun Zhan","doi":"10.1097/MBP.0000000000000719","DOIUrl":"10.1097/MBP.0000000000000719","url":null,"abstract":"The aim of this study was to evaluate the accuracy of the JAMR upper-arm blood pressure monitor B23 in the general population according to the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018/AMD 1 : 2020). The study recruited participants who met the criteria of the AAMI/ESH/ISO Universal Standard in terms of their number, sex, age, limb size, and blood pressure (BP) distribution. The study involved measuring BP, including both SBP and DBP, using both the test device and a standard mercury sphygmomanometer in sequential measurements. Of 90 participants, 85 qualified participants were analyzed. A total of 255 sets of comparison data (three sets for each subject) were obtained and analyzed. For the validation criterion 1, the mean ± SD of the differences between the JAMR B23 and mercury sphygmomanometer BP readings was -0.24 ± 6.52/-2.67 ± 5.6 mmHg (SBP/DBP). For criterion 2, the SD of the averaged BP (SBP/DBP) differences between the JAMR B23 and reference BP (SBP/DBP) per participant was 5.61/5.13 mmHg (the requirement was ≤6.95/6.43 mmHg by calculation). The JAMR B23 passed all the requirements of the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018/AMD 1 : 2020) and can be recommended for clinical and self/home use in the general population.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"40-43"},"PeriodicalIF":1.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11654443/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141892806","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Validation of TMB-2285-BT wrist blood pressure monitor in general population according to the ISO 81060-2:2018 + Amd.1:2020 Protocol. 根据 ISO 81060-2:2018 + Amd.1:2020 协议对 TMB-2285-BT 普通人群腕式血压计进行验证。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-09-13 DOI: 10.1097/MBP.0000000000000724

Zijian Xie, Bin Peng, Jia Hu, Xinda Wang, Xiaoqin Du, Chaoya Li, Jiahui Liang

{"title":"Validation of TMB-2285-BT wrist blood pressure monitor in general population according to the ISO 81060-2:2018 + Amd.1:2020 Protocol.","authors":"Zijian Xie, Bin Peng, Jia Hu, Xinda Wang, Xiaoqin Du, Chaoya Li, Jiahui Liang","doi":"10.1097/MBP.0000000000000724","DOIUrl":"10.1097/MBP.0000000000000724","url":null,"abstract":"The objective of this study is to evaluate the accuracy of the wrist blood pressure (BP) monitor (TMB-2285-BT) in general population according to international standard of ISO 81060-2:2018+Amd.1:2020. The TMB-2285-BT BP monitor is an oscillometric device measuring BP from wrist. A single cuff for wrist sizes of 13.5-21.5 cm was used for the test device. The study was performed according to the 'International Standard (ISO 81060-2:2018 + Amd.1:2020) protocol' using the same-arm sequential BP measurement method. Subjects ( n ≥ 85) fulfilling the age, gender, BP, and cuff distribution criteria of the protocol were enrolled. For criterion 1, the mean difference of SBP and DBP between the test device and the reference device was -0.27 mmHg and -0.80 mmHg, respectively. For criterion 2, the SD of the averaged paired determinations of SBP and DBP for the test device and the reference device was 2.60 and 2.06 mmHg, respectively, both of which were less than 6.95 and 6.89 mmHg. The accuracy of the test device fulfilled the requirements of the criterion 1 and 2 of ISO 81060-2:2018 + Amd.1:2020. The TMB-2285-BT wrist BP monitor can be recommended for home BP measurement for general population.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"44-47"},"PeriodicalIF":1.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142280092","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 DBP-8278B Wrist-type Fully Automatic Blood Pressure Monitor in the general population according to the ISO 81060-2:2018/AMD 1:2020 protocol. 根据 ISO 81060-2:2018/AMD 1:2020 协议，在普通人群中验证 DBP-8278B 腕式全自动血压计。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2025-02-01 Epub Date: 2024-07-16 DOI: 10.1097/MBP.0000000000000717

Qi Zhou

{"title":"Validation of the DBP-8278B Wrist-type Fully Automatic Blood Pressure Monitor in the general population according to the ISO 81060-2:2018/AMD 1:2020 protocol.","authors":"Qi Zhou","doi":"10.1097/MBP.0000000000000717","DOIUrl":"10.1097/MBP.0000000000000717","url":null,"abstract":"The aim of this study was to evaluate the accuracy of the DBP-8278B Wrist-type Fully Automatic Blood Pressure Monitor in the general population according to the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018/AMD 1 : 2020). The test monitor was used to measure SBP and DBP and pulse rate in the wrists using the oscillometric method. According to this protocol using the same-arm sequential blood pressure measurement method, subjects were recruited to fulfill the age, sex, blood pressure, and cuff distribution criteria of the Universal Standard. A single cuff for wrist sizes of 13.5-21.5 cm was used. A total of 85 subjects were included in this study. According to Criterion 1, the mean difference in SBP between the test device and the reference device was 0.89 mmHg, with a SD of 7.76 mmHg. The mean difference of DBP was -1.44 mmHg, with a SD of 6.23 mmHg. The mean difference between SBP and DBP was less than 5.0 mmHg, and the SD was less than 8.0 mmHg, which met the requirements. According to Criterion 2, the SD of the mean differences of SBP between the test device and the reference device per subject was 5.65 mmHg, which was less than 6.88 mmHg and met the requirements. The SD of the mean differences of DBP between the test device and the reference device per subject was 5.61 mmHg, which was less than 6.78 mmHg and met the requirements. The DBP-8278B Wrist-type Fully Automatic Blood Pressure Monitor met the requirements of the AAMI/ESH/ISO Universal Standard (ISO 81060-2 : 2018/AMD 1 : 2020). It can be recommended for home and clinical use.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"36-39"},"PeriodicalIF":1.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11654442/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141619222","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Could soluble ST2 levels be used to detect nondipper hypertensive subgroup in newly diagnosed hypertension patients. 可溶性 ST2 水平是否可用于检测新诊断的高血压患者中的非非高血压亚组。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2024-12-01 Epub Date: 2024-06-24 DOI: 10.1097/MBP.0000000000000714

Emrah Ozdemir, Berna Stavileci, Bahar Ozdemir, Faik Alper Aksoy, Ceyla Zeynep Colakoglu Gevher, Ali Dogan, Murat Ziyrek

{"title":"Could soluble ST2 levels be used to detect nondipper hypertensive subgroup in newly diagnosed hypertension patients.","authors":"Emrah Ozdemir, Berna Stavileci, Bahar Ozdemir, Faik Alper Aksoy, Ceyla Zeynep Colakoglu Gevher, Ali Dogan, Murat Ziyrek","doi":"10.1097/MBP.0000000000000714","DOIUrl":"10.1097/MBP.0000000000000714","url":null,"abstract":"Aim: ST2 receptor is a member of toll-like/interleukin-1 receptor family. After the activation of IL-33/ST2 signaling pathway clinically detectable amount of soluble form of ST2 (sST2) is released into the circulation. Previous studies showed that sST2 levels were significantly higher in hypertension patients than in controls. In this prospective study, we aimed to analyze this relation and test the predictive accuracy of the sST2 level in diagnosis of nondipping hypertension in newly diagnosed hypertension patients.Methods: Three hundred thirty-seven patients (150 normal, 187 hypertension) who presented with symptoms of hypertension were included in the study. All patients underwent 24-h ambulatory blood pressure monitoring and sST2 measurement.Results: Of 187 hypertension patients, 92 of them had nondipping and 95 of them had dipping pattern. sST2 level was significantly higher in nondipping group compared to dipping group and control group (40.79 ± 7.77 vs. 32.47 ± 6.68; P < 0.0001 and 40.79 ± 7.77 vs. 20.09 ± 7.09; P < 0.0001 respectively). Binary logistic regression analysis revealed that; only sST2 level was an independent risk factor for hypertension [ P < 0.0001, β : 1.258, odds ratio (OR) (95% confidence interval (CI)): 1.158-1.366]. and also nondipping hypertension [ P < 0.0001, β : 1.208, OR (95% CI): 1.108-1.317].Conclusion: Based on the present study it could be concluded that sST2 level is significantly associated with the newly diagnosed hypertension and nondipping hypertension. Hence it could reliably be used to diagnose hypertension and nondipping hypertension with high sensitivity and specificity.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"284-289"},"PeriodicalIF":1.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141490727","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

Psychological distress, forced awakening, and morning blood pressure surge. 心理困扰、强迫觉醒和早晨血压飙升。

IF 1.2 4区医学

Blood Pressure Monitoring Pub Date : 2024-12-01 Epub Date: 2024-07-22 DOI: 10.1097/MBP.0000000000000718

Yeonsu Kim, Jill Howie Esquivel, Meghan Kathleen Mattos, Eric M Davis, Jeongok Logan

{"title":"Psychological distress, forced awakening, and morning blood pressure surge.","authors":"Yeonsu Kim, Jill Howie Esquivel, Meghan Kathleen Mattos, Eric M Davis, Jeongok Logan","doi":"10.1097/MBP.0000000000000718","DOIUrl":"10.1097/MBP.0000000000000718","url":null,"abstract":"Background: Morning blood pressure surge (MBPS) has been recognized as an independent predictor of cardiovascular disease events. Psychological distress, including anxiety, depression, and perceived stress, and behavioral risk factors, such as poor sleep quality, have been associated with increased MBPS. Elevations in sympathetic activity induced by forced awakening may also contribute to further increases in MBPS. Yet, no examination of the interrelationships among psychological distress, sleep quality, awakening mode (natural vs. forced awakenings), and MBPS has been undertaken.Objective: This pilot study aimed: (1) to examine if MBPS differs by awakening mode and (2) to investigate whether psychological distress is associated with MBPS difference between natural and forced awakenings, independent of sleep quality.Methods: Thirty-two healthy adults were included in this cross-sectional study. Blood pressure was measured using a beat-to-beat blood pressure monitor over two nights, consisting of one night of natural awakening and one night of forced awakening. Psychological distress and sleep quality were assessed using questionnaires. We conducted paired t -tests (aim 1) and multiple linear regressions (aim 2).Results: MBPS was significantly greater during forced awakening compared with natural awakening. In addition, the MBPS difference between natural and forced awakenings was significantly greater in participants with higher anxiety levels, independent of sleep quality.Conclusion: We found that augmentation of MBPS by forced awakening was significantly greater in individuals who reported higher anxiety levels. Additional research is needed to examine the potential impacts of forced awakening and anxiety on MBPS in a larger sample of individuals at risk for cardiovascular disease.","PeriodicalId":8950,"journal":{"name":"Blood Pressure Monitoring","volume":" ","pages":"277-283"},"PeriodicalIF":1.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141858927","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