Background: Inflammation in epicardial adipose tissue (EAT) has been hypothesized to influence heart structure and function, thereby contributing to aortic valve (AV) disease. However, it remains unclear how the biological state of EAT is related to AV hemodynamics.
Methods and results: We studied 50 patients with AV calcification who underwent elective cardiac surgery (cardiac valve surgery and/or coronary artery bypass graft). Echocardiographic data (AV area index [AVAI] and peak transvalvular AV velocity [PAVV]), were acquired before surgery. During cardiac surgery, 2 EAT samples were obtained for immunohistochemistry and the number of CD68- and CD11c-positive macrophages and osteocalcin-positive cells was counted in 6 random high-power fields (×400 magnification). PAVV, but not AVAI, was positively correlated with the number of CD11c-positive macrophages and osteocalcin-positive cells in EAT in patients with clinical AV stenosis (AS), defined as PAVV ≥2.5 m/s. On multivariate analysis adjusted for left ventricular function, the number of osteocalcin-positive cells in EAT was independently correlated with increased PAVV (β=0.42; P=0.013) and the presence of clinical AS (odds ratio per 1-unit increase 1.14; P=0.011), whereas there was no correlation between increased PAVV or the presence of clinical AS and the number of CD68- and CD11c-positive macrophages in EAT.
Conclusions: The biological activities of EAT, which are characterized mainly by osteogenic activity, are associated with AV hemodynamics and may contribute to AS progression.
{"title":"Associations of Inflammatory and Osteogenic Activities in Epicardial Adipose Tissue With Aortic Valve Hemodynamic.","authors":"Toshiro Kitagawa, Kazuhiro Sentani, Shinichi Norimura, Yuki Ikegami, Taiichi Takasaki, Shinya Takahashi, Shinji Mii, Yukiko Nakano","doi":"10.1253/circrep.CR-25-0189","DOIUrl":"10.1253/circrep.CR-25-0189","url":null,"abstract":"<p><strong>Background: </strong>Inflammation in epicardial adipose tissue (EAT) has been hypothesized to influence heart structure and function, thereby contributing to aortic valve (AV) disease. However, it remains unclear how the biological state of EAT is related to AV hemodynamics.</p><p><strong>Methods and results: </strong>We studied 50 patients with AV calcification who underwent elective cardiac surgery (cardiac valve surgery and/or coronary artery bypass graft). Echocardiographic data (AV area index [AVAI] and peak transvalvular AV velocity [PAVV]), were acquired before surgery. During cardiac surgery, 2 EAT samples were obtained for immunohistochemistry and the number of CD68- and CD11c-positive macrophages and osteocalcin-positive cells was counted in 6 random high-power fields (×400 magnification). PAVV, but not AVAI, was positively correlated with the number of CD11c-positive macrophages and osteocalcin-positive cells in EAT in patients with clinical AV stenosis (AS), defined as PAVV ≥2.5 m/s. On multivariate analysis adjusted for left ventricular function, the number of osteocalcin-positive cells in EAT was independently correlated with increased PAVV (β=0.42; P=0.013) and the presence of clinical AS (odds ratio per 1-unit increase 1.14; P=0.011), whereas there was no correlation between increased PAVV or the presence of clinical AS and the number of CD68- and CD11c-positive macrophages in EAT.</p><p><strong>Conclusions: </strong>The biological activities of EAT, which are characterized mainly by osteogenic activity, are associated with AV hemodynamics and may contribute to AS progression.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1259-1268"},"PeriodicalIF":1.1,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688424/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145728041","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-15eCollection Date: 2025-12-10DOI: 10.1253/circrep.CR-25-0123
Koichiro Kuwahara, Ataru Igarashi, Takanori Tsuchiya, Russell Miller, You Won Seong, Yusuke Nakamura
Background: Chronic heart failure (CHF) affects millions worldwide, posing a significant burden on healthcare resources. For patients with HF with reduced ejection fraction (HFrEF) following a worsening event, vericiguat is a promising new treatment. In this study we evaluated the budgetary impact on Japan's health system with the introduction of vericiguat as an add-on to standard of care (SoC) for chronic HFrEF after a worsening event.
Methods and results: An economic model was developed comparing SoC to a scenario in which vericiguat is introduced as an add-on therapy over a 5-year time horizon. A literature review, medical claims data and clinical trial data were used to derive inputs. Total healthcare costs after introducing vericiguat were estimated to increase <1% over 5 years compared to the SoC scenario showing a cumulated budget impact of US$41,027,304. Increases were driven by drug and medical costs, but were partially offset by decreasing costs for hospitalizations, terminal care, and urgent HF visits. In the sensitivity analyses, the hospitalization rate had the largest effect on the overall budget impact.
Conclusions: This analysis highlighted the minimal budgetary impact of vericiguat and its potential to reduce hospitalizations in Japan. Although drug and monitoring costs increased, reductions in acute care expenses helped offset these costs. Further research is needed on long-term cost-effectiveness and real-world outcomes.
{"title":"Budget Impact of Vericiguat for Treating Chronic Heart Failure in Japan.","authors":"Koichiro Kuwahara, Ataru Igarashi, Takanori Tsuchiya, Russell Miller, You Won Seong, Yusuke Nakamura","doi":"10.1253/circrep.CR-25-0123","DOIUrl":"10.1253/circrep.CR-25-0123","url":null,"abstract":"<p><strong>Background: </strong>Chronic heart failure (CHF) affects millions worldwide, posing a significant burden on healthcare resources. For patients with HF with reduced ejection fraction (HFrEF) following a worsening event, vericiguat is a promising new treatment. In this study we evaluated the budgetary impact on Japan's health system with the introduction of vericiguat as an add-on to standard of care (SoC) for chronic HFrEF after a worsening event.</p><p><strong>Methods and results: </strong>An economic model was developed comparing SoC to a scenario in which vericiguat is introduced as an add-on therapy over a 5-year time horizon. A literature review, medical claims data and clinical trial data were used to derive inputs. Total healthcare costs after introducing vericiguat were estimated to increase <1% over 5 years compared to the SoC scenario showing a cumulated budget impact of US$41,027,304. Increases were driven by drug and medical costs, but were partially offset by decreasing costs for hospitalizations, terminal care, and urgent HF visits. In the sensitivity analyses, the hospitalization rate had the largest effect on the overall budget impact.</p><p><strong>Conclusions: </strong>This analysis highlighted the minimal budgetary impact of vericiguat and its potential to reduce hospitalizations in Japan. Although drug and monitoring costs increased, reductions in acute care expenses helped offset these costs. Further research is needed on long-term cost-effectiveness and real-world outcomes.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1222-1229"},"PeriodicalIF":1.1,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688427/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145728000","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Sex differences exist in atherosclerotic cardiovascular disease, partly due to the anti-atherosclerotic properties of estrogens in women. While polyvascular disease (PolyVD) exhibits worse outcomes, it is unknown whether women have an impact on cardiovascular outcomes of PolyVD.
Methods and results: We analyzed 678 coronary artery disease patients receiving PCI. PolyVD was defined as the concomitance of ischemic stroke and/or lower extremity arterial disease (LEAD). The occurrence of 3-year major adverse cardiovascular events (MACE; i.e., all-cause death + non-fatal myocardial infarction + ischemic stroke + ischemic-driven non-culprit lesion revascularization + LEAD) was compared between men and women with and without PolyVD, respectively. Women accounted for 17.8% and 21.1% of patients with and without PolyVD, respectively (P=0.34). In patients without PolyVD, women presented marginally higher on-treatment low-density lipoprotein cholesterol (LDL-C) levels (101.5 vs. 93.0 mg/dL; P=0.05). However, women exhibited a lower 3-year MACE risk (adjusted hazard ratio [HR] 0.31; 95% confidence interval [CI] 0.11-0.88; P=0.02). In patients with PolyVD, women exhibited higher LDL-C levels (103.0 vs. 82.0 mg/dL; P=0.04). Furthermore, even after adjusting clinical demographics and risk factor control, the 3-year MACE risk did not differ between males and females (adjusted HR 0.67; 95% CI 0.29-1.57; P=0.36).
Conclusions: Women without PolyVD were less likely to experience 3-year MACE, whereas cardiovascular outcomes in women with PolyVD were similar to men with PolyVD. These findings suggest a need to intensify anti-atherosclerotic management in both men and women with PolyVD.
背景:动脉粥样硬化性心血管疾病存在性别差异,部分原因是女性雌激素的抗动脉粥样硬化特性。虽然多血管疾病(PolyVD)表现出较差的结局,但尚不清楚女性是否对PolyVD的心血管结局有影响。方法与结果:对678例接受PCI治疗的冠心病患者进行分析。PolyVD被定义为伴有缺血性卒中和/或下肢动脉疾病(LEAD)。比较男女合并和不合并PolyVD患者3年主要心血管不良事件(MACE,即全因死亡+非致死性心肌梗死+缺血性卒中+缺血性非元凶病变血运重建术+ LEAD)的发生情况。女性分别占有和无PolyVD患者的17.8%和21.1% (P=0.34)。在没有PolyVD的患者中,女性治疗时低密度脂蛋白胆固醇(LDL-C)水平略高(101.5 vs 93.0 mg/dL; P=0.05)。然而,女性表现出较低的3年MACE风险(校正风险比[HR] 0.31; 95%可信区间[CI] 0.11-0.88; P=0.02)。在PolyVD患者中,女性表现出更高的LDL-C水平(103.0 vs 82.0 mg/dL; P=0.04)。此外,即使在调整临床人口统计学和危险因素控制后,3年MACE风险在男性和女性之间也没有差异(调整HR 0.67; 95% CI 0.29-1.57; P=0.36)。结论:没有PolyVD的女性经历3年MACE的可能性较小,而患有PolyVD的女性心血管结局与患有PolyVD的男性相似。这些发现提示有必要加强对男性和女性PolyVD患者的抗动脉粥样硬化管理。
{"title":"Sex Differences in Polyvascular Disease - Implications for Lipid-Lowering Management and Cardiovascular Outcomes.","authors":"Aya Katasako-Yabumoto, Yu Kataoka, Eri Kiyoshige, Kunihiro Nishimura, Stephen J Nicholls, Rishi Puri, Kota Murai, Takamasa Iwai, Kenichiro Sawada, Hideo Matama, Satoshi Honda, Kensuke Takagi, Masashi Fujino, Shuichi Yoneda, Fumiyuki Otsuka, Kazuhiro Nakao, Kensaku Nishihira, Itaru Takamisawa, Yasuhide Asaumi, Kenichi Tsujita, Teruo Noguchi","doi":"10.1253/circrep.CR-25-0178","DOIUrl":"10.1253/circrep.CR-25-0178","url":null,"abstract":"<p><strong>Background: </strong>Sex differences exist in atherosclerotic cardiovascular disease, partly due to the anti-atherosclerotic properties of estrogens in women. While polyvascular disease (PolyVD) exhibits worse outcomes, it is unknown whether women have an impact on cardiovascular outcomes of PolyVD.</p><p><strong>Methods and results: </strong>We analyzed 678 coronary artery disease patients receiving PCI. PolyVD was defined as the concomitance of ischemic stroke and/or lower extremity arterial disease (LEAD). The occurrence of 3-year major adverse cardiovascular events (MACE; i.e., all-cause death + non-fatal myocardial infarction + ischemic stroke + ischemic-driven non-culprit lesion revascularization + LEAD) was compared between men and women with and without PolyVD, respectively. Women accounted for 17.8% and 21.1% of patients with and without PolyVD, respectively (P=0.34). In patients without PolyVD, women presented marginally higher on-treatment low-density lipoprotein cholesterol (LDL-C) levels (101.5 vs. 93.0 mg/dL; P=0.05). However, women exhibited a lower 3-year MACE risk (adjusted hazard ratio [HR] 0.31; 95% confidence interval [CI] 0.11-0.88; P=0.02). In patients with PolyVD, women exhibited higher LDL-C levels (103.0 vs. 82.0 mg/dL; P=0.04). Furthermore, even after adjusting clinical demographics and risk factor control, the 3-year MACE risk did not differ between males and females (adjusted HR 0.67; 95% CI 0.29-1.57; P=0.36).</p><p><strong>Conclusions: </strong>Women without PolyVD were less likely to experience 3-year MACE, whereas cardiovascular outcomes in women with PolyVD were similar to men with PolyVD. These findings suggest a need to intensify anti-atherosclerotic management in both men and women with PolyVD.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1199-1210"},"PeriodicalIF":1.1,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688431/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Intravenous magnesium is commonly used in clinical practice for treating Torsade de Pointes (TdP), although supporting evidence remains limited. This scoping review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension guidelines. Four online databases were searched for relevant studies published as of November 27, 2024, but only 4 observational studies met the inclusion criteria. TdP resolved in a substantial proportion of patients treated with intravenous magnesium (78.3% [N=36/46]), although most studies lacked a control group. No serious adverse events related to magnesium were reported (0% [N=0/46]). Despite several limitations that preclude firm conclusions, intravenous magnesium appears to be a relatively safe and effective treatment for TdP. However, TdP progressed to ventricular fibrillation (VF) in 21.7% (N=10/46) of patients, underscoring the need for readiness to perform immediate electrical defibrillation during treatment. Further high-quality studies are warranted to validate these findings.
{"title":"Safety and Efficacy of Intravenous Magnesium for Torsade de Pointes - A Scoping Review.","authors":"Mutsuko Sangawa, Hiroki Shiomi, Eiji Hiraoka, Kazuo Sakamoto, Kenichi Iijima, Tetsuma Kawaji, Takayuki Kitai, Yukio Hosaka, Masashi Yokose, Teruo Noguchi, Hiroshi Takahashi, Tetsuya Matoba, Migaku Kikuchi, Yoshio Tahara, Hiroshi Nonogi, Toshikazu Funazaki","doi":"10.1253/circrep.CR-25-0175","DOIUrl":"10.1253/circrep.CR-25-0175","url":null,"abstract":"<p><p>Intravenous magnesium is commonly used in clinical practice for treating Torsade de Pointes (TdP), although supporting evidence remains limited. This scoping review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension guidelines. Four online databases were searched for relevant studies published as of November 27, 2024, but only 4 observational studies met the inclusion criteria. TdP resolved in a substantial proportion of patients treated with intravenous magnesium (78.3% [N=36/46]), although most studies lacked a control group. No serious adverse events related to magnesium were reported (0% [N=0/46]). Despite several limitations that preclude firm conclusions, intravenous magnesium appears to be a relatively safe and effective treatment for TdP. However, TdP progressed to ventricular fibrillation (VF) in 21.7% (N=10/46) of patients, underscoring the need for readiness to perform immediate electrical defibrillation during treatment. Further high-quality studies are warranted to validate these findings.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1037-1043"},"PeriodicalIF":1.1,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597394/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145491363","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: The optimal period for discontinuing tafamidis in wild-type transthyretin amyloid cardiomyopathy (ATTRwt-CM) patients based on cost-effectiveness is unknown.
Methods and results: A retrospective analysis of 80 tafamidis-treated ATTRwt-CM patients was conducted. The median follow up was 26.4 months; 17 patients permanently discontinued tafamidis, and 12 patients died after a median of 1.0 month following tafamidis discontinuation. Discontinuation was mainly due to non-cardiovascular hospitalization; deaths were mostly non-cardiovascular and occurred early after discontinuation.
Conclusions: The period from tafamidis discontinuation to death was shorter in ATTRwt-CM patients hospitalized for non-cardiovascular diseases. Discussions of the right period for discontinuation are needed.
{"title":"Discontinuation of Tafamidis in Wild-Type Transthyretin Amyloid Cardiomyopathy Patients.","authors":"Yuichi Baba, Yuri Ochi, Toru Kubo, Juri Kawaguchi, Naohito Yamasaki, Hiroaki Kitaoka","doi":"10.1253/circrep.CR-25-0181","DOIUrl":"10.1253/circrep.CR-25-0181","url":null,"abstract":"<p><strong>Background: </strong>The optimal period for discontinuing tafamidis in wild-type transthyretin amyloid cardiomyopathy (ATTRwt-CM) patients based on cost-effectiveness is unknown.</p><p><strong>Methods and results: </strong>A retrospective analysis of 80 tafamidis-treated ATTRwt-CM patients was conducted. The median follow up was 26.4 months; 17 patients permanently discontinued tafamidis, and 12 patients died after a median of 1.0 month following tafamidis discontinuation. Discontinuation was mainly due to non-cardiovascular hospitalization; deaths were mostly non-cardiovascular and occurred early after discontinuation.</p><p><strong>Conclusions: </strong>The period from tafamidis discontinuation to death was shorter in ATTRwt-CM patients hospitalized for non-cardiovascular diseases. Discussions of the right period for discontinuation are needed.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1301-1303"},"PeriodicalIF":1.1,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688423/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145728044","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Electrode catheter placement into the coronary sinus (CS) is critical for electrophysiologic studies. Although central venous approaches (e.g., internal jugular or subclavian) are well documented, peripheral venous approaches like the cubital vein are not. This study evaluated the feasibility and safety of CS catheter placement via the right cubital vein during atrial fibrillation (AF) ablation.
Methods and results: Of 1,363 consecutive patients who underwent first-time AF ablation at Sakurabashi Watanabe Advanced Healthcare Hospital between January 2019 and December 2021, 1,274 underwent at least 1 right cubital vein puncture attempt. The success rate, causes of failure, and complications were analyzed. CS catheters were successfully placed via the right cubital vein in 1,214 (95.3%) patients, whereas placements were unsuccessful in 60 (4.7%) patients. Although older patients were more likely to experience unsuccessful placements, there were no significant differences in other baseline characteristics between the 2 groups. Unsuccessful placements were attributed to failure in venipuncture or sheath insertion (n=49) and failure to advance the CS catheter through the vein (n=11). No major complications were reported.
Conclusions: CS catheter placement via the right cubital vein demonstrated high feasibility and safety, with a 95% success rate and minimal complications. This approach offers a practical and technically straightforward alternative for placing CS catheters, particularly in patients with adequate vein development.
{"title":"Placement of the Coronary Sinus Catheter via the Right Cubital Vein During Atrial Fibrillation Ablation.","authors":"Kohei Iwasa, Masato Okada, Koji Tanaka, Yuko Hirao, Naoko Miyazaki, Heitaro Watanabe, Yoshitaka Iwanaga, Atsunori Okamura, Yasushi Sakata, Nobuaki Tanaka","doi":"10.1253/circrep.CR-25-0187","DOIUrl":"10.1253/circrep.CR-25-0187","url":null,"abstract":"<p><strong>Background: </strong>Electrode catheter placement into the coronary sinus (CS) is critical for electrophysiologic studies. Although central venous approaches (e.g., internal jugular or subclavian) are well documented, peripheral venous approaches like the cubital vein are not. This study evaluated the feasibility and safety of CS catheter placement via the right cubital vein during atrial fibrillation (AF) ablation.</p><p><strong>Methods and results: </strong>Of 1,363 consecutive patients who underwent first-time AF ablation at Sakurabashi Watanabe Advanced Healthcare Hospital between January 2019 and December 2021, 1,274 underwent at least 1 right cubital vein puncture attempt. The success rate, causes of failure, and complications were analyzed. CS catheters were successfully placed via the right cubital vein in 1,214 (95.3%) patients, whereas placements were unsuccessful in 60 (4.7%) patients. Although older patients were more likely to experience unsuccessful placements, there were no significant differences in other baseline characteristics between the 2 groups. Unsuccessful placements were attributed to failure in venipuncture or sheath insertion (n=49) and failure to advance the CS catheter through the vein (n=11). No major complications were reported.</p><p><strong>Conclusions: </strong>CS catheter placement via the right cubital vein demonstrated high feasibility and safety, with a 95% success rate and minimal complications. This approach offers a practical and technically straightforward alternative for placing CS catheters, particularly in patients with adequate vein development.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1181-1189"},"PeriodicalIF":1.1,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688425/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145728026","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Electrical storm (ES) is defined as a condition in which ventricular tachycardia (VT) or ventricular fibrillation (VF) episodes requiring electrical shock or implantable cardioverter-defibrillator (ICD) shocks occur ≥3 times within 24 h. It is a life-threatening condition, and treatment options include antiarrhythmic drugs, sedation, circulatory support, and catheter ablation. Sedation is conventionally performed for repeated electrical shocks; however, evidence for its effectiveness in ES suppression remains limited. This scoping review aimed to assess whether the use of sedatives is beneficial for ES suppression.
Methods and results: This scoping review followed the PRISMA extension for scoping reviews (PRISMA-ScR) guidelines. Three online databases were searched to identify studies published from the inception of each database until September 18, 2024. To date, no randomized or quasi-randomized controlled trials or observational analytical studies have met the inclusion criteria for the use of sedation in patients with ES.
Conclusions: This scoping review underscores the need for high-quality studies to enhance the level of evidence and bridge knowledge gaps, ultimately aiming to shift the care paradigm for patients with ES.
{"title":"Should Sedative Administration Be Recommended as an Antiarrhythmic Therapy to Suppress Ventricular Fibrillation and Ventricular Tachycardia in Patients With Electrical Storm? - A Scoping Review.","authors":"Takayuki Kitai, Tetsuma Kawaji, Yukio Hosaka, Mutsuko Sangawa, Hiroki Shiomi, Eiji Hiraoka, Kazuo Sakamoto, Kenichi Iijima, Masashi Yokose, Teruo Noguchi, Hiroshi Takahashi, Tetsuya Matoba, Migaku Kikuchi, Yoshio Tahara, Hiroshi Nonogi, Toshikazu Funazaki","doi":"10.1253/circrep.CR-25-0176","DOIUrl":"10.1253/circrep.CR-25-0176","url":null,"abstract":"<p><strong>Background: </strong>Electrical storm (ES) is defined as a condition in which ventricular tachycardia (VT) or ventricular fibrillation (VF) episodes requiring electrical shock or implantable cardioverter-defibrillator (ICD) shocks occur ≥3 times within 24 h. It is a life-threatening condition, and treatment options include antiarrhythmic drugs, sedation, circulatory support, and catheter ablation. Sedation is conventionally performed for repeated electrical shocks; however, evidence for its effectiveness in ES suppression remains limited. This scoping review aimed to assess whether the use of sedatives is beneficial for ES suppression.</p><p><strong>Methods and results: </strong>This scoping review followed the PRISMA extension for scoping reviews (PRISMA-ScR) guidelines. Three online databases were searched to identify studies published from the inception of each database until September 18, 2024. To date, no randomized or quasi-randomized controlled trials or observational analytical studies have met the inclusion criteria for the use of sedation in patients with ES.</p><p><strong>Conclusions: </strong>This scoping review underscores the need for high-quality studies to enhance the level of evidence and bridge knowledge gaps, ultimately aiming to shift the care paradigm for patients with ES.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1149-1153"},"PeriodicalIF":1.1,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688421/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727445","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: We developed the SaFIS, a structured self-administered food intake survey for patients with cardiovascular diseases needing dietary improvements.
Methods and results: The SaFIS comprised questions on 31 items, including staple foods (7 items) and food ingredients (24 items), based on the foods recommended by the Japanese Atherosclerosis Society for the Prevention of Arteriosclerotic Disease. To evaluate reproducibility, SaFIS was administered twice with a 1-month interval using the intraclass correlation coefficient (ICC [1,1]). Validity was assessed by comparing energy and nutrient content from a weighed dietary record (WDR) with the first SaFIS survey using Bland-Altman plots. Reproducibility values were energy (ICC 0.90, 95% confidence interval: 0.80-0.95), protein (0.90, 0.80-0.95), fat (0.76, 0.54-0.88), saturated fatty acids (0.78, 0.58-0.89), monounsaturated fatty acids (0.76, 0.56-0.88), polyunsaturated fatty acids (0.82, 0.66-0.91), carbohydrates (0.89, 0.79-0.95), and dietary fiber (0.86, 0.71-0.93). Bland-Altman values indicated SaFIS-based energy, protein, carbohydrate, monounsaturated fatty acids, and dietary fiber were 67.2 kJ, 5.7 g, 3.9 g, 0.5 g, and 1.8 g greater than WDR-based values, respectively. SaFIS-based fat, saturated, and polyunsaturated fatty acid values were 0.7 g, 1.3 g, and 0.39 g less than WDR-based values, respectively.
Conclusions: SaFIS demonstrated high reproducibility and validity with clinical potential. Subsequent introduction to digital health from the usability perspective is planned.
{"title":"Reproducibility and Validity of a Food Intake Survey Developed for Implementation via Digital Health for Patients With or at Risk for Cardiovascular Disease.","authors":"Daisuke Moriyama, Takuji Adachi, Kuya Funaki, Hironobu Ashikawa, Ken Harada, Sumio Yamada","doi":"10.1253/circrep.CR-25-0032","DOIUrl":"10.1253/circrep.CR-25-0032","url":null,"abstract":"<p><strong>Background: </strong>We developed the SaFIS, a structured self-administered food intake survey for patients with cardiovascular diseases needing dietary improvements.</p><p><strong>Methods and results: </strong>The SaFIS comprised questions on 31 items, including staple foods (7 items) and food ingredients (24 items), based on the foods recommended by the Japanese Atherosclerosis Society for the Prevention of Arteriosclerotic Disease. To evaluate reproducibility, SaFIS was administered twice with a 1-month interval using the intraclass correlation coefficient (ICC [1,1]). Validity was assessed by comparing energy and nutrient content from a weighed dietary record (WDR) with the first SaFIS survey using Bland-Altman plots. Reproducibility values were energy (ICC 0.90, 95% confidence interval: 0.80-0.95), protein (0.90, 0.80-0.95), fat (0.76, 0.54-0.88), saturated fatty acids (0.78, 0.58-0.89), monounsaturated fatty acids (0.76, 0.56-0.88), polyunsaturated fatty acids (0.82, 0.66-0.91), carbohydrates (0.89, 0.79-0.95), and dietary fiber (0.86, 0.71-0.93). Bland-Altman values indicated SaFIS-based energy, protein, carbohydrate, monounsaturated fatty acids, and dietary fiber were 67.2 kJ, 5.7 g, 3.9 g, 0.5 g, and 1.8 g greater than WDR-based values, respectively. SaFIS-based fat, saturated, and polyunsaturated fatty acid values were 0.7 g, 1.3 g, and 0.39 g less than WDR-based values, respectively.</p><p><strong>Conclusions: </strong>SaFIS demonstrated high reproducibility and validity with clinical potential. Subsequent introduction to digital health from the usability perspective is planned.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1109-1115"},"PeriodicalIF":1.1,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597241/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145491327","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-04eCollection Date: 2025-12-10DOI: 10.1253/circrep.CR-25-0164
Yukio Shiina, Atsuhito Fukushima, Migaku Kikuchi
Background: This study retrospectively evaluated the safety of resuscitation training during the Coronavirus Disease 2019 (COVID-19) pandemic under Japan Resuscitation Council (JRC) guidance.
Methods and results: From 2018 to 2024, all participating staff were monitored by the Infection Prevention and Control Center. Although learner numbers declined in 2020, training sessions increased, and numbers returned to prepandemic levels. The Resuscitation Quality Improvement program enabled flexible, contactless training, further boosting participation. Notably, no COVID-19 cases were linked to training sessions.
Conclusions: These findings demonstrate that resuscitation training can be conducted safely by adhering to JRC guidance, even during a public health crisis.
{"title":"Resuscitation Training Amid the Coronavirus Disease 2019 Pandemic - A Safe Approach.","authors":"Yukio Shiina, Atsuhito Fukushima, Migaku Kikuchi","doi":"10.1253/circrep.CR-25-0164","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0164","url":null,"abstract":"<p><strong>Background: </strong>This study retrospectively evaluated the safety of resuscitation training during the Coronavirus Disease 2019 (COVID-19) pandemic under Japan Resuscitation Council (JRC) guidance.</p><p><strong>Methods and results: </strong>From 2018 to 2024, all participating staff were monitored by the Infection Prevention and Control Center. Although learner numbers declined in 2020, training sessions increased, and numbers returned to prepandemic levels. The Resuscitation Quality Improvement program enabled flexible, contactless training, further boosting participation. Notably, no COVID-19 cases were linked to training sessions.</p><p><strong>Conclusions: </strong>These findings demonstrate that resuscitation training can be conducted safely by adhering to JRC guidance, even during a public health crisis.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1298-1300"},"PeriodicalIF":1.1,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688420/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727166","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-01eCollection Date: 2025-11-10DOI: 10.1253/circrep.CR-25-0203
Junichi Yokota
{"title":"Exploring the Optimal Amount of Cardiac Rehabilitation During Hospitalization for Recovery of Activities of Daily Living.","authors":"Junichi Yokota","doi":"10.1253/circrep.CR-25-0203","DOIUrl":"10.1253/circrep.CR-25-0203","url":null,"abstract":"","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1060-1061"},"PeriodicalIF":1.1,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597235/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145491161","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}