Background: Although the COVID-19 pandemic altered hospitalization trends for acute cardiovascular diseases (CVD) in Japan, the effects of a concomitant COVID-19 diagnosis on mortality in this high-risk population remains unclear. We investigated the association between COVID-19 infection and 30-day mortality among patients hospitalized for acute CVD using a nationwide database.
Methods and results: This retrospective cohort study used data from the Japanese Registry of All Cardiac and Vascular Diseases-Diagnosis Procedure Combination (JROAD-DPC) database from January 2020 to March 2022. We included patients hospitalized for acute myocardial infarction, acute heart failure, aortic rupture, or venous thromboembolism. We compared patients with and without COVID-19, with 30-day mortality as the primary outcome. We used 1 : 1 propensity score matching to balance baseline patient and hospital characteristics. Of 395,671 eligible patients in the JROAD-DPC database, 41,794 (10.6%) had a concomitant COVID-19 diagnosis. In the matched cohort of 41,794 pairs, the risk of 30-day mortality was significantly higher patients for patients with than without COVID-19 (6.6% vs. 5.8%; odds ratio 1.14; 95% confidence interval 1.08-1.21; P<0.001). This increased risk was consistent across all major diagnostic subgroups (P for interaction >0.3).
Conclusions: In this large nationwide study of patients hospitalized for acute CVD in Japan, concomitant COVID-19 infection was associated with a significant increase in 30-day mortality. These findings suggest that COVID-19 infection is associated with increased mortality in this vulnerable patient population.
背景:尽管COVID-19大流行改变了日本急性心血管疾病(CVD)的住院趋势,但在这一高危人群中,合并COVID-19诊断对死亡率的影响尚不清楚。我们使用全国数据库调查了COVID-19感染与急性心血管疾病住院患者30天死亡率之间的关系。方法和结果:这项回顾性队列研究使用了2020年1月至2022年3月日本所有心血管疾病诊断程序组合登记处(JROAD-DPC)数据库的数据。我们纳入了因急性心肌梗死、急性心力衰竭、主动脉破裂或静脉血栓栓塞住院的患者。我们比较了患有和未患有COVID-19的患者,以30天死亡率作为主要结局。我们使用1:1倾向评分匹配来平衡基线患者和医院特征。在JROAD-DPC数据库中的395,671例符合条件的患者中,41,794例(10.6%)合并了COVID-19诊断。在41794对配对队列中,感染COVID-19的患者30天死亡风险显著高于未感染COVID-19的患者(6.6% vs. 5.8%;优势比1.14;95%置信区间1.08-1.21;P0.3)。结论:在这项针对日本急性心血管疾病住院患者的大型全国性研究中,合并的COVID-19感染与30天死亡率显着增加相关。这些发现表明,COVID-19感染与这一弱势患者群体的死亡率增加有关。
{"title":"Association of Concomitant COVID-19 Infection With Outcomes in Patients With Acute Cardiovascular Diseases - Nationwide Study Using the JROAD Database in Japan.","authors":"Tadafumi Sugimoto, Atsushi Mizuno, Daisuke Yoneoka, Shingo Matsumoto, Chisa Matsumoto, Yuya Matsue, Mari Ishida, Koshiro Kanaoka, Yoshitaka Iwanaga, Yoshihiro Miyamoto, Koichi Node","doi":"10.1253/circrep.CR-25-0245","DOIUrl":"10.1253/circrep.CR-25-0245","url":null,"abstract":"<p><strong>Background: </strong>Although the COVID-19 pandemic altered hospitalization trends for acute cardiovascular diseases (CVD) in Japan, the effects of a concomitant COVID-19 diagnosis on mortality in this high-risk population remains unclear. We investigated the association between COVID-19 infection and 30-day mortality among patients hospitalized for acute CVD using a nationwide database.</p><p><strong>Methods and results: </strong>This retrospective cohort study used data from the Japanese Registry of All Cardiac and Vascular Diseases-Diagnosis Procedure Combination (JROAD-DPC) database from January 2020 to March 2022. We included patients hospitalized for acute myocardial infarction, acute heart failure, aortic rupture, or venous thromboembolism. We compared patients with and without COVID-19, with 30-day mortality as the primary outcome. We used 1 : 1 propensity score matching to balance baseline patient and hospital characteristics. Of 395,671 eligible patients in the JROAD-DPC database, 41,794 (10.6%) had a concomitant COVID-19 diagnosis. In the matched cohort of 41,794 pairs, the risk of 30-day mortality was significantly higher patients for patients with than without COVID-19 (6.6% vs. 5.8%; odds ratio 1.14; 95% confidence interval 1.08-1.21; P<0.001). This increased risk was consistent across all major diagnostic subgroups (P for interaction >0.3).</p><p><strong>Conclusions: </strong>In this large nationwide study of patients hospitalized for acute CVD in Japan, concomitant COVID-19 infection was associated with a significant increase in 30-day mortality. These findings suggest that COVID-19 infection is associated with increased mortality in this vulnerable patient population.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 2","pages":"236-243"},"PeriodicalIF":1.1,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12885533/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146159854","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: Cancer therapy-related cardiac dysfunction (CTRCD) is a recognized complication of breast cancer treatment. Although early detection using cardiac biomarkers such as cardiac troponin I (cTnI) is recommended, the impact of CTRCD on cancer prognosis remains unclear.
Methods and results: We conducted a prospective observational study of 273 patients with breast cancer treated with anthracycline-based chemotherapy and/or human epidermal growth factor receptor 2 (HER2)-targeted therapy at Fukushima Medical University between January 2016 and July 2022. Serial measurements of cTnI, B-type natriuretic peptide (BNP), and echocardiographic parameters were performed at baseline and at 3, 6, 12, and 24 months. CTRCD was defined based on declines in left ventricular ejection fraction (LVEF) and categorized as mild, moderate, or severe. CTRCD occurred in 40 (14.7%) patients. Even mild CTRCD was associated with greater reductions in LVEF at 12 months in patients with elevated cTnI, although recovery was observed by 24 months. Kaplan-Meier analysis revealed significantly shorter progression-free survival in the CTRCD group. In multivariable analysis, CTRCD was an independent predictor of cancer progression (hazard ratio 2.50; 95% confidence interval 1.17-5.36; P=0.018).
Conclusions: CTRCD following cardiotoxic chemotherapy was associated with reduced progression-free survival in patients with breast cancer. These findings underscore the importance of early CTRCD detection not only for cardiac protection but also as a prognostic indicator in cancer management.
{"title":"Development of Cancer Therapy-Related Cardiac Dysfunction Is Associated With Disease Progression in Breast Cancer.","authors":"Fumika Haga, Masayoshi Oikawa, Tetsuya Tani, Tetsuro Yokokawa, Tomofumi Misaka, Takashi Kaneshiro, Akiomi Yoshihisa, Kazunoshin Tachibana, Tohru Otake, Takafumi Ishida, Yasuchika Takeishi","doi":"10.1253/circrep.CR-25-0220","DOIUrl":"10.1253/circrep.CR-25-0220","url":null,"abstract":"<p><strong>Background: </strong>Cancer therapy-related cardiac dysfunction (CTRCD) is a recognized complication of breast cancer treatment. Although early detection using cardiac biomarkers such as cardiac troponin I (cTnI) is recommended, the impact of CTRCD on cancer prognosis remains unclear.</p><p><strong>Methods and results: </strong>We conducted a prospective observational study of 273 patients with breast cancer treated with anthracycline-based chemotherapy and/or human epidermal growth factor receptor 2 (HER2)-targeted therapy at Fukushima Medical University between January 2016 and July 2022. Serial measurements of cTnI, B-type natriuretic peptide (BNP), and echocardiographic parameters were performed at baseline and at 3, 6, 12, and 24 months. CTRCD was defined based on declines in left ventricular ejection fraction (LVEF) and categorized as mild, moderate, or severe. CTRCD occurred in 40 (14.7%) patients. Even mild CTRCD was associated with greater reductions in LVEF at 12 months in patients with elevated cTnI, although recovery was observed by 24 months. Kaplan-Meier analysis revealed significantly shorter progression-free survival in the CTRCD group. In multivariable analysis, CTRCD was an independent predictor of cancer progression (hazard ratio 2.50; 95% confidence interval 1.17-5.36; P=0.018).</p><p><strong>Conclusions: </strong>CTRCD following cardiotoxic chemotherapy was associated with reduced progression-free survival in patients with breast cancer. These findings underscore the importance of early CTRCD detection not only for cardiac protection but also as a prognostic indicator in cancer management.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 2","pages":"244-253"},"PeriodicalIF":1.1,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12885535/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146159780","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 impact of emergency surgery for acute type A aortic dissection (ATAAD) on renal function in patients with autosomal dominant polycystic kidney disease (ADPKD) remains unclear.
Methods and results: The renal function of 4 patients with ADPKD undergoing emergency ATAAD surgery remained unchanged up to 30 days postoperatively. During follow-up of 2 patients, 1 progressed from Stage 4 chronic kidney disease (CKD) preoperatively to Stage 5 at 3 years postoperatively, while the other progressed from Stage 3b CKD preoperatively to Stage 4 at 5 years postoperatively.
Conclusions: Emergency surgery for ATAAD had no effect on renal function.
{"title":"Impact of Emergency Surgery for Acute Type A Aortic Dissection on Postoperative Renal Function in Patients With Autosomal Dominant Polycystic Kidney Disease.","authors":"Naoto Fukunaga, Taiki Takanishi, Tatsuto Wakami, Akio Shimoji, Otohime Mori, Nobushige Tamura","doi":"10.1253/circrep.CR-25-0255","DOIUrl":"10.1253/circrep.CR-25-0255","url":null,"abstract":"<p><strong>Background: </strong>The impact of emergency surgery for acute type A aortic dissection (ATAAD) on renal function in patients with autosomal dominant polycystic kidney disease (ADPKD) remains unclear.</p><p><strong>Methods and results: </strong>The renal function of 4 patients with ADPKD undergoing emergency ATAAD surgery remained unchanged up to 30 days postoperatively. During follow-up of 2 patients, 1 progressed from Stage 4 chronic kidney disease (CKD) preoperatively to Stage 5 at 3 years postoperatively, while the other progressed from Stage 3b CKD preoperatively to Stage 4 at 5 years postoperatively.</p><p><strong>Conclusions: </strong>Emergency surgery for ATAAD had no effect on renal function.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 2","pages":"353-355"},"PeriodicalIF":1.1,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12885534/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146159729","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: Several studies have reported that age influences the severity of hospitalization-associated disability (HAD) after cardiac surgery. However, age-specific differences in the incidence and characteristics of HAD remain unclear. Therefore, this study aimed to clarify the incidence and characteristics of HAD according to age group.
Methods and results: This prospective, multicenter observational study included 604 patients who underwent elective cardiac surgery at 12 acute-care hospitals. HAD was defined as a decrease of ≥5 points in the Barthel Index score from the preoperative assessment to the discharge assessment. The HAD incidence rate was 6.8% for patients aged 65-74 years, 14.5% for patients aged 75-89 years, and 10.4% overall. The characteristics varied by age group. In the 65-74 age group, the incidence of HAD was influenced by a higher prevalence of comorbidities, level of prehospital nursing care, preoperative left ventricular ejection fraction, intubation time, and physical function. In the 75-89 age group, HAD incidence was associated with Kihon Checklist score, level of nursing care, the use of rehabilitation services, preoperative physical function, and intubation time.
Conclusions: The incidence of HAD in post-cardiac surgery patients was 10.4%, increasing with age. Factors affecting the incidence of HAD differed by age group.
{"title":"Characteristics of Hospitalization-Associated Disability After Cardiac Surgery by Age Group.","authors":"Satomi Kusaka, Masakazu Saitoh, Tomoyuki Morisawa, Kentaro Iwata, Masami Inokuma, Go Takamura, Akira Minei, Yusuke Ochi, Koji Sakurada, Yu Hojo, Junichi Nishikawa, Kenta Kamisaka, Masayuki Tahara, Yosuke Takahashi, Tetsuya Takahashi","doi":"10.1253/circrep.CR-25-0080","DOIUrl":"10.1253/circrep.CR-25-0080","url":null,"abstract":"<p><strong>Background: </strong>Several studies have reported that age influences the severity of hospitalization-associated disability (HAD) after cardiac surgery. However, age-specific differences in the incidence and characteristics of HAD remain unclear. Therefore, this study aimed to clarify the incidence and characteristics of HAD according to age group.</p><p><strong>Methods and results: </strong>This prospective, multicenter observational study included 604 patients who underwent elective cardiac surgery at 12 acute-care hospitals. HAD was defined as a decrease of ≥5 points in the Barthel Index score from the preoperative assessment to the discharge assessment. The HAD incidence rate was 6.8% for patients aged 65-74 years, 14.5% for patients aged 75-89 years, and 10.4% overall. The characteristics varied by age group. In the 65-74 age group, the incidence of HAD was influenced by a higher prevalence of comorbidities, level of prehospital nursing care, preoperative left ventricular ejection fraction, intubation time, and physical function. In the 75-89 age group, HAD incidence was associated with Kihon Checklist score, level of nursing care, the use of rehabilitation services, preoperative physical function, and intubation time.</p><p><strong>Conclusions: </strong>The incidence of HAD in post-cardiac surgery patients was 10.4%, increasing with age. Factors affecting the incidence of HAD differed by age group.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"77-92"},"PeriodicalIF":1.1,"publicationDate":"2025-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782916/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954707","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: Atrial fibrillation (AF) after bioprosthetic valve (BPV) replacement is common in older patients with multiple comorbidities and is associated with a heightened risk of thromboembolism. Anticoagulation therapy is often indicated, but renal impairment and other comorbidities elevate bleeding risk, making clinical decisions complex. This study compared clinical outcomes between warfarin and direct oral anticoagulants (DOACs) in this high-risk population.
Methods and results: This subgroup analysis of the BPV-AF Registry included 612 patients treated with oral anticoagulants after BPV replacement, stratified by renal function: normal or mild impairment (creatinine clearance [CCr] ≥50 mL/min), mild-to-moderate impairment (30 mL/min ≤ CCr < 50 mL/min), and moderate-to-severe impairment (15 mL/min ≤ CCr < 30 mL/min). Baseline characteristics and outcomes were analyzed within each stratum. The composite outcome of stroke, systemic embolism, and cardiovascular events was numerically less frequent in the DOAC than warfarin group across all strata, although the differences were not statistically significant. Major bleeding also tended to be lower in the DOAC group.
Conclusions: In this study from a Japanese nationwide registry comparing outcomes of AF patients after BPV replacement with severe renal impairment between those treated with DOACs and those treated with warfarin, comparative conclusions between DOACs and warfarin cannot be drawn because of the small sample size. Nonetheless, both anticoagulants may be acceptable in clinical practice, highlighting the need for individualized decision-making based on patient risk.
{"title":"Clinical Outcomes of Anticoagulation Therapy With Direct Oral Anticoagulants or Warfarin in Patients With Atrial Fibrillation and Renal Impairment After Bioprosthetic Valve Replacement.","authors":"Miwa Ito, Misa Takegami, Yutaka Furukawa, Makoto Miyake, Tomoyuki Fujita, Tadaaki Koyama, Hidekazu Tanaka, Kenji Ando, Tatsuhiko Komiya, Masaki Izumo, Hiroya Kawai, Kiyoyuki Eishi, Kiyoshi Yoshida, Takeshi Kimura, Ryuzo Nawada, Tomohiro Sakamoto, Yoshisato Shibata, Toshihiro Fukui, Kenji Minatoya, Yasushi Sakata, Masayuki Fukuzawa, Kunihiro Nishimura, Shozo Kaneko, Tadashi Hoshiyama, Hisanori Kanazawa, Kenichi Tsujita, Chisato Izumi","doi":"10.1253/circrep.CR-25-0156","DOIUrl":"10.1253/circrep.CR-25-0156","url":null,"abstract":"<p><strong>Background: </strong>Atrial fibrillation (AF) after bioprosthetic valve (BPV) replacement is common in older patients with multiple comorbidities and is associated with a heightened risk of thromboembolism. Anticoagulation therapy is often indicated, but renal impairment and other comorbidities elevate bleeding risk, making clinical decisions complex. This study compared clinical outcomes between warfarin and direct oral anticoagulants (DOACs) in this high-risk population.</p><p><strong>Methods and results: </strong>This subgroup analysis of the BPV-AF Registry included 612 patients treated with oral anticoagulants after BPV replacement, stratified by renal function: normal or mild impairment (creatinine clearance [CCr] ≥50 mL/min), mild-to-moderate impairment (30 mL/min ≤ CCr < 50 mL/min), and moderate-to-severe impairment (15 mL/min ≤ CCr < 30 mL/min). Baseline characteristics and outcomes were analyzed within each stratum. The composite outcome of stroke, systemic embolism, and cardiovascular events was numerically less frequent in the DOAC than warfarin group across all strata, although the differences were not statistically significant. Major bleeding also tended to be lower in the DOAC group.</p><p><strong>Conclusions: </strong>In this study from a Japanese nationwide registry comparing outcomes of AF patients after BPV replacement with severe renal impairment between those treated with DOACs and those treated with warfarin, comparative conclusions between DOACs and warfarin cannot be drawn because of the small sample size. Nonetheless, both anticoagulants may be acceptable in clinical practice, highlighting the need for individualized decision-making based on patient risk.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"58-67"},"PeriodicalIF":1.1,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782906/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954738","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}
Despite advances in the treatment of cardiogenic shock (CS), it remains associated with high mortality rates. To improve patient outcomes, management in a dedicated care center has been proposed. However, the definition of a dedicated CS center has not been systematically examined, and no consensus exists across major societies or guidelines. The aim of this scoping review was to identify key elements defining CS centers linked to better patient outcomes and guide future research. This review was conducted in accordance with the PRISMA extension for scoping reviews. The PubMed, Cochrane, and Web of Science electronic databases were systematically searched to identify studies published from inception to July 19, 2023. Twenty observational studies examining hospital characteristics and patient outcomes with CS were included. Higher volumes of CS patients, more board-certified cardiologists, percutaneous coronary intervention (PCI) availability 24/7, and the presence of cardiovascular intensive care units, left ventricular assist device (LVAD) centers, and hub-and-spoke systems were associated with better outcomes. Inconsistent associations were observed for the number of PCIs, extracorporeal membrane oxygenation, and percutaneous microaxial ventricular assist device procedures, and LVAD case volume and the availability of cardiac surgical support were not associated with improved outcomes. This scoping review identified candidate elements of CS centers linked to better outcomes, providing a foundation for developing an optimal CS care system.
尽管心源性休克(CS)的治疗取得了进展,但它仍然与高死亡率有关。为了提高患者的治疗效果,建议在专门的护理中心进行管理。然而,专门的CS中心的定义尚未被系统地审查,并且在主要协会或指南中没有达成共识。本综述的目的是确定与更好的患者预后相关的CS中心的关键因素,并指导未来的研究。该审查是根据PRISMA扩展范围审查进行的。系统地检索PubMed、Cochrane和Web of Science电子数据库,以确定从成立到2023年7月19日发表的研究。纳入了20项观察性研究,检查了CS的医院特征和患者结局。更多的CS患者、更多的委员会认证的心脏病专家、24/7的经皮冠状动脉介入治疗(PCI)的可用性、心血管重症监护病房、左心室辅助装置(LVAD)中心和轮辐系统的存在与更好的结果相关。pci的数量、体外膜氧合和经皮微轴心室辅助装置手术观察到不一致的关联,LVAD病例量和心脏手术支持的可用性与改善的结果无关。该范围审查确定了与更好的结果相关的CS中心候选元素,为开发最佳CS护理系统提供了基础。
{"title":"Defining a Cardiogenic Shock Center and Its Relationship to Outcomes Among Patients With Cardiogenic Shock - A Scoping Review.","authors":"Yusuke Okazaki, Jin Kirigaya, Takeshi Yamamoto, Toru Kondo, Akihito Tanaka, Takahiro Nakashima, Masahiro Yamamoto, Naoki Nakayama, Hiroyuki Hanada, Katsutaka Hashiba, Tomoko Ishizu, Yumiko Hosoya, Aya Katasako-Yabumoto, Takumi Osawa, Kazuo Sakamoto, Marina Arai, Teruo Noguchi, Yoshio Tahara, Kunihiro Matsuo, Junichi Yamaguchi, Toshiaki Mano, Sunao Kojima, Toshikazu Funazaki, Hiroshi Nonogi, Migaku Kikuchi, Tetsuya Matoba","doi":"10.1253/circrep.CR-25-0194","DOIUrl":"10.1253/circrep.CR-25-0194","url":null,"abstract":"<p><p>Despite advances in the treatment of cardiogenic shock (CS), it remains associated with high mortality rates. To improve patient outcomes, management in a dedicated care center has been proposed. However, the definition of a dedicated CS center has not been systematically examined, and no consensus exists across major societies or guidelines. The aim of this scoping review was to identify key elements defining CS centers linked to better patient outcomes and guide future research. This review was conducted in accordance with the PRISMA extension for scoping reviews. The PubMed, Cochrane, and Web of Science electronic databases were systematically searched to identify studies published from inception to July 19, 2023. Twenty observational studies examining hospital characteristics and patient outcomes with CS were included. Higher volumes of CS patients, more board-certified cardiologists, percutaneous coronary intervention (PCI) availability 24/7, and the presence of cardiovascular intensive care units, left ventricular assist device (LVAD) centers, and hub-and-spoke systems were associated with better outcomes. Inconsistent associations were observed for the number of PCIs, extracorporeal membrane oxygenation, and percutaneous microaxial ventricular assist device procedures, and LVAD case volume and the availability of cardiac surgical support were not associated with improved outcomes. This scoping review identified candidate elements of CS centers linked to better outcomes, providing a foundation for developing an optimal CS care system.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"4-12"},"PeriodicalIF":1.1,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782917/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954704","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: Heart failure (HF) is an increasing public health concern in Japan, largely related to the aging population. This protocol describes the rationale, objectives, and methods of the Hokuriku-plus Heart Failure Registry (HpHFR), designed to establish a comprehensive clinical and digital database to assess novel prognostic indicators in patients with HF.
Methods and results: HpHFR is a prospective, multicenter observational cohort study that has enrolled patients with acute or chronic HF from 5 Japanese centers. Eligible patients provided informed consent and underwent baseline clinical, laboratory, and biometric assessment, including digital phonocardiography and wearable device data. Follow-up assessment will be conducted at 4, 12, 26, and 52 weeks. Primary outcomes include all-cause death, HF-related hospitalization, and worsening HF. Secondary outcomes are the changes in clinical parameters over time. A digital substudy will investigate continuous biometric monitoring, and a genomic substudy explores the loss of chromosome Y as a prognostic biomarker.
Conclusions: In conclusion, this study protocol summarizes the development of a valuable prospective cohort resource. This registry will provide a unique dataset enabling multifaceted investigations to improve HF prediction and management by systematically integrating comprehensive clinical and laboratory data with biometric indicators derived from digital devices and genomic markers.
{"title":"Hokuriku-plus Heart Failure Registry Study - Rationale and Study Design.","authors":"Yasuaki Takeji, Masaya Shimojima, Akihiro Nomura, Masahiro Noguchi, Tamami Kamiya, Miho Ohira, Tadayuki Hirai, Masayuki Mori, Chiaki Goten, Hirofumi Okada, Takashi Kusayama, Shohei Yoshida, Mika Mori, Hayato Tada, Shin-Ichiro Takashima, Takeshi Kato, Kenji Sakata, Kenshi Hayashi, Noboru Fujino, Ikufumi Takahashi, Shizuko Takahara, Shuji Sugimoto, Keisuke Ohtani, Toshihiko Yasuda, Yusuke Takeda, Kanako Yamamoto, Chieko Kato, Takahiro Saeki, Masanobu Namura, Taiji Yoshida, Shumpei Saito, Soichiro Usui, Masayuki Takamura","doi":"10.1253/circrep.CR-25-0160","DOIUrl":"10.1253/circrep.CR-25-0160","url":null,"abstract":"<p><strong>Background: </strong>Heart failure (HF) is an increasing public health concern in Japan, largely related to the aging population. This protocol describes the rationale, objectives, and methods of the Hokuriku-plus Heart Failure Registry (HpHFR), designed to establish a comprehensive clinical and digital database to assess novel prognostic indicators in patients with HF.</p><p><strong>Methods and results: </strong>HpHFR is a prospective, multicenter observational cohort study that has enrolled patients with acute or chronic HF from 5 Japanese centers. Eligible patients provided informed consent and underwent baseline clinical, laboratory, and biometric assessment, including digital phonocardiography and wearable device data. Follow-up assessment will be conducted at 4, 12, 26, and 52 weeks. Primary outcomes include all-cause death, HF-related hospitalization, and worsening HF. Secondary outcomes are the changes in clinical parameters over time. A digital substudy will investigate continuous biometric monitoring, and a genomic substudy explores the loss of chromosome Y as a prognostic biomarker.</p><p><strong>Conclusions: </strong>In conclusion, this study protocol summarizes the development of a valuable prospective cohort resource. This registry will provide a unique dataset enabling multifaceted investigations to improve HF prediction and management by systematically integrating comprehensive clinical and laboratory data with biometric indicators derived from digital devices and genomic markers.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"168-173"},"PeriodicalIF":1.1,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782937/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954761","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: Hospitalization-associated disability (HAD) is linked to poor post-discharge outcomes in older individuals with heart failure (HF). We investigated whether HAD could be predicted by physical activity measured using a wearable device.
Methods and results: We retrospectively analyzed data from 104 older individuals with HF whose physical activity was recorded for 3 consecutive days after initiating cardiac rehabilitation. Physical activity was categorized as sedentary behavior (≤1.5 metabolic equivalents [METs]), light-intensity physical activity (LPA; 1.6-2.9 METs), and moderate-to-vigorous physical activity (≥3.0 METs). HAD was observed in 31 (29.8%) individuals. LPA duration was significantly shorter in the HAD than non-HAD group (mean [±SD] 45.7±24.9 vs. 121.2±67.4 min/day; P<0.0001). In receiver operating characteristic curve analysis, the optimal LPA cut-off was 68 min/day, with 87.1% sensitivity and 80.8% specificity (area under the curve=0.888; P<0.0001).
Conclusions: Physical activity measured using a wearable device may be useful in predicting HAD in older individuals with HF.
背景:住院相关残疾(HAD)与老年心力衰竭(HF)患者出院后预后不良有关。我们研究了HAD是否可以通过使用可穿戴设备测量的身体活动来预测。方法和结果:我们回顾性分析了104例老年HF患者的数据,这些患者在开始心脏康复后连续3天记录身体活动。体力活动被分类为久坐行为(≤1.5代谢当量[METs])、低强度体力活动(LPA; 1.6-2.9 METs)和中高强度体力活动(≥3.0 METs)。31例(29.8%)患者有HAD。HAD组LPA持续时间明显短于非HAD组(平均[±SD] 45.7±24.9 vs 121.2±67.4分钟/天)。结论:使用可穿戴设备测量身体活动可能有助于预测老年HF患者的HAD。
{"title":"Wearable Device-Measured Physical Activity for Predicting Hospitalization-Associated Disability in Older Patients With Heart Failure.","authors":"Yosuke Yoshida, Satoshi Okayama, Daisuke Fujihara, Megumi Fukui, Midori Taniyama, Ayami Yamada, Naoki Doi, Runa Takahashi, Shingo Ogaki, Yumi Kondo, Tomohito Inoue, Sho Ishizuka, Rina Onishi, Mayu Watanabe, Satoharu Hattori, Atsushi Iwai, Daisuke Kamon, Yutaka Goryo, Hajime Fujimoto, Megumi Suzuki, Michitaka Nakamura, Makoto Watanabe, Naofumi Doi, Yoshihiko Saito","doi":"10.1253/circrep.CR-25-0099","DOIUrl":"10.1253/circrep.CR-25-0099","url":null,"abstract":"<p><strong>Background: </strong>Hospitalization-associated disability (HAD) is linked to poor post-discharge outcomes in older individuals with heart failure (HF). We investigated whether HAD could be predicted by physical activity measured using a wearable device.</p><p><strong>Methods and results: </strong>We retrospectively analyzed data from 104 older individuals with HF whose physical activity was recorded for 3 consecutive days after initiating cardiac rehabilitation. Physical activity was categorized as sedentary behavior (≤1.5 metabolic equivalents [METs]), light-intensity physical activity (LPA; 1.6-2.9 METs), and moderate-to-vigorous physical activity (≥3.0 METs). HAD was observed in 31 (29.8%) individuals. LPA duration was significantly shorter in the HAD than non-HAD group (mean [±SD] 45.7±24.9 vs. 121.2±67.4 min/day; P<0.0001). In receiver operating characteristic curve analysis, the optimal LPA cut-off was 68 min/day, with 87.1% sensitivity and 80.8% specificity (area under the curve=0.888; P<0.0001).</p><p><strong>Conclusions: </strong>Physical activity measured using a wearable device may be useful in predicting HAD in older individuals with HF.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"68-76"},"PeriodicalIF":1.1,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782908/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145992535","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}
{"title":"Anomalous Left Atrial Band Identified by Multimodality Imaging in a Patient Undergoing Atrial Fibrillation Ablation.","authors":"Takuya Nishimura, Toshihiro Nakamura, Mitsuru Wada, Kengo Kusano","doi":"10.1253/circrep.CR-25-0236","DOIUrl":"10.1253/circrep.CR-25-0236","url":null,"abstract":"","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 2","pages":"366-367"},"PeriodicalIF":1.1,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12885542/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146159868","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}