Background: The clinical differences between intra-aortic balloon pumping (IABP) and a microaxial flow pump (Impella) for left ventricular (LV) unloading in patients with fulminant myocarditis (FM) supported with venoarterial extracorporeal membrane oxygenation (VA-ECMO) remain unclear.
Methods and results: In this single-center, retrospective cohort study, we analyzed 27 consecutive patients with lymphocytic FM who received VA-ECMO support. Patients were stratified by the LV unloading device that was used: IABP (n=15); or Impella (n=12). The primary endpoint was a composite of all-cause mortality or implantation of an extracorporeal ventricular assist device (exVAD) within 30 days of VA-ECMO initiation. Temporal changes in laboratory and hemodynamic parameters during the first 7 days of support were also assessed. Baseline characteristics, including LV ejection fraction (IABP 16% vs. Impella 18%; P=0.814) and QRS duration (139 vs. 105 ms; P=0.805), were comparable between groups. Nine patients met the primary endpoint (mortality [n=7]; exVAD implantation [n=2]). Kaplan-Meier analysis revealed a significantly lower incidence of the primary endpoint in the Impella group (log-rank P=0.018). The Impella group also showed a significantly greater improvement in cardiac power output (group×time interaction, P=0.040). Hemolysis, elevated total bilirubin, and increased serum creatinine were more pronounced in the Impella group.
Conclusions: In patients with FM requiring VA-ECMO, LV unloading with Impella was associated with improved short-term clinical outcomes compared with IABP.
背景:在静脉动脉体外膜氧合(VA-ECMO)支持下,主动脉内球囊泵(IABP)和微轴流泵(Impella)用于暴发性心肌炎(FM)患者左室(LV)卸载的临床差异尚不清楚。方法和结果:在这项单中心、回顾性队列研究中,我们分析了27例接受VA-ECMO支持的淋巴细胞性FM患者。采用左室卸荷装置对患者进行分层:IABP (n=15);或Impella (n=12)。主要终点是VA-ECMO开始后30天内全因死亡率或植入体外心室辅助装置(exVAD)的综合指标。还评估了支持前7天的实验室和血流动力学参数的时间变化。基线特征,包括左室射血分数(IABP 16% vs Impella 18%, P=0.814)和QRS持续时间(139 vs 105 ms, P=0.805),组间具有可比性。9例患者达到主要终点(死亡[n=7]; exVAD植入[n=2])。Kaplan-Meier分析显示Impella组的主要终点发生率显著降低(log-rank P=0.018)。Impella组的心功率输出也有显著性改善(group×time交互作用,P=0.040)。溶血、总胆红素升高和血清肌酐升高在Impella组更为明显。结论:在需要VA-ECMO的FM患者中,与IABP相比,使用Impella卸载左室可改善短期临床结果。
{"title":"Short-Term Outcomes of Intra-Aortic Balloon Pump vs. Microaxial Flow Pump for Fulminant Myocarditis Supported by Venoarterial Extracorporeal Membrane Oxygenation.","authors":"Saeko Iikura, Yuki Ikeda, Shohei Nakahara, Yuki Watanabe, Yosuke Haruki, Yu Takigami, Yuko Eda, Yuichiro Iida, Takeru Nabeta, Shunsuke Ishii, Junya Ako","doi":"10.1253/circrep.CR-25-0283","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0283","url":null,"abstract":"<p><strong>Background: </strong>The clinical differences between intra-aortic balloon pumping (IABP) and a microaxial flow pump (Impella) for left ventricular (LV) unloading in patients with fulminant myocarditis (FM) supported with venoarterial extracorporeal membrane oxygenation (VA-ECMO) remain unclear.</p><p><strong>Methods and results: </strong>In this single-center, retrospective cohort study, we analyzed 27 consecutive patients with lymphocytic FM who received VA-ECMO support. Patients were stratified by the LV unloading device that was used: IABP (n=15); or Impella (n=12). The primary endpoint was a composite of all-cause mortality or implantation of an extracorporeal ventricular assist device (exVAD) within 30 days of VA-ECMO initiation. Temporal changes in laboratory and hemodynamic parameters during the first 7 days of support were also assessed. Baseline characteristics, including LV ejection fraction (IABP 16% vs. Impella 18%; P=0.814) and QRS duration (139 vs. 105 ms; P=0.805), were comparable between groups. Nine patients met the primary endpoint (mortality [n=7]; exVAD implantation [n=2]). Kaplan-Meier analysis revealed a significantly lower incidence of the primary endpoint in the Impella group (log-rank P=0.018). The Impella group also showed a significantly greater improvement in cardiac power output (group×time interaction, P=0.040). Hemolysis, elevated total bilirubin, and increased serum creatinine were more pronounced in the Impella group.</p><p><strong>Conclusions: </strong>In patients with FM requiring VA-ECMO, LV unloading with Impella was associated with improved short-term clinical outcomes compared with IABP.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"580-588"},"PeriodicalIF":1.1,"publicationDate":"2026-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13070792/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147694689","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: Drug-coated balloon (DCB) is a novel treatment option for percutaneous coronary intervention (PCI). The presence of heart failure (HF) in patients with coronary artery disease (CAD) is associated with a poor prognosis. However, the clinical significance of DCB-based PCI in CAD patients with HF is unknown.
Methods and results: This was a retrospective analysis of a cohort study from a prospective, single center registry from 2015 to 2024. We enrolled 258 CAD patients with chronic HF who underwent PCI with DCB or in combination with a drug-eluting stent (DES). Propensity score matching analysis was performed between the DCB-based PCI and DES-only PCI groups. The primary endpoint of this study was all-cause mortality. Baseline clinical characteristics were comparable between the groups. The total DES number and length were significantly reduced in patients with DCB-based PCI than in those with DES-only PCI. Kaplan-Meier analysis revealed that the DCB-based PCI group had a significantly lower rate of all-cause mortality compared with the DES-only group (log-rank test, P=0.04).
Conclusions: In CAD patients with chronic HF, DCB-based PCI was associated with a lower risk of mortality compared with DES-only PCI.
{"title":"Clinical Impact of Drug-Coated Balloon-Based Percutaneous Coronary Intervention in Coronary Artery Disease Patients With Chronic Heart Failure.","authors":"Tetsuya Takahashi, Taiga Ishigaki, Wataru Katawaki, Taku Toshima, Yu Kumagai, Tamon Yamanaka, Masafumi Watanabe","doi":"10.1253/circrep.CR-25-0320","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0320","url":null,"abstract":"<p><strong>Background: </strong>Drug-coated balloon (DCB) is a novel treatment option for percutaneous coronary intervention (PCI). The presence of heart failure (HF) in patients with coronary artery disease (CAD) is associated with a poor prognosis. However, the clinical significance of DCB-based PCI in CAD patients with HF is unknown.</p><p><strong>Methods and results: </strong>This was a retrospective analysis of a cohort study from a prospective, single center registry from 2015 to 2024. We enrolled 258 CAD patients with chronic HF who underwent PCI with DCB or in combination with a drug-eluting stent (DES). Propensity score matching analysis was performed between the DCB-based PCI and DES-only PCI groups. The primary endpoint of this study was all-cause mortality. Baseline clinical characteristics were comparable between the groups. The total DES number and length were significantly reduced in patients with DCB-based PCI than in those with DES-only PCI. Kaplan-Meier analysis revealed that the DCB-based PCI group had a significantly lower rate of all-cause mortality compared with the DES-only group (log-rank test, P=0.04).</p><p><strong>Conclusions: </strong>In CAD patients with chronic HF, DCB-based PCI was associated with a lower risk of mortality compared with DES-only PCI.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"626-633"},"PeriodicalIF":1.1,"publicationDate":"2026-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065455/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679877","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 prognosis of acute myocarditis (AM) is difficult to predict due to its variable presentation. We investigated the prognosticators of AM patients requiring hospitalization.
Methods and results: We conducted a multicenter observational study including 80 hospitalized AM patients. The primary endpoint was a composite of all-cause death, heart transplantation, and implantation of ventricular assist devices during the index hospitalization. Thirteen (16%) patients reached the endpoint. Longer QRS duration at admission independently predicted adverse outcomes, with an optimal cut-off of 130 ms.
Conclusions: Prolonged QRS duration at admission might predict in-hospital prognosis in AM patients regardless of whether or not it was fulminant.
{"title":"Baseline Prolonged QRS Duration May Predict In-Hospital Outcomes of Patients With Acute Myocarditis: Multicenter Observational Study.","authors":"Ayano Yoshida, Takuma Takada, Eiji Shibahashi, Takuro Abe, Kensuke Shimazaki, Takanori Kawamoto, Motoko Kametani, Natsuko Satomi, Kazuho Kamishima, Takashi Saito, Erina Tomari, Atsushi Honda, Atsushi Takagi, Kyomi Ashihara, Junichi Yamaguchi, Kentaro Jujo","doi":"10.1253/circrep.CR-25-0306","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0306","url":null,"abstract":"<p><strong>Background: </strong>The prognosis of acute myocarditis (AM) is difficult to predict due to its variable presentation. We investigated the prognosticators of AM patients requiring hospitalization.</p><p><strong>Methods and results: </strong>We conducted a multicenter observational study including 80 hospitalized AM patients. The primary endpoint was a composite of all-cause death, heart transplantation, and implantation of ventricular assist devices during the index hospitalization. Thirteen (16%) patients reached the endpoint. Longer QRS duration at admission independently predicted adverse outcomes, with an optimal cut-off of 130 ms.</p><p><strong>Conclusions: </strong>Prolonged QRS duration at admission might predict in-hospital prognosis in AM patients regardless of whether or not it was fulminant.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"674-676"},"PeriodicalIF":1.1,"publicationDate":"2026-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065449/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679948","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: Drug-coated balloon (DCB) angioplasty has shown short-term feasibility for large-vessel coronary artery disease (CAD; ≥3 mm); however, long-term outcomes remain unclear. This study aimed to evaluate the 5-year cardiovascular outcomes of DCB angioplasty vs. drug-eluting stents (DES) for de novo large-vessel CAD.
Methods and results: This single-center retrospective study analyzed patients undergoing percutaneous coronary intervention (PCI) with either DCB (SeQuent Please) or DES (Xience Alpine) between January 2016 and December 2018. The primary outcomes were cardiovascular events (CVE), defined as a composite of cardiac death, non-fatal myocardial infarction, and target lesion revascularization (TLR). Secondary outcomes included minimal lumen diameter (MLD), diameter stenosis (DS), and late lumen loss (LLL), assessed at the index PCI and at the 1-year angiographic follow up. Overall, 114 patients (122 lesions) in the DCB group and 269 patients (293 lesions) in the DES group were analyzed, with similar median follow-up durations (1,678 vs. 1,825 days; P=0.687). At 5 years, TLR and CVE rates were comparable between the DCB and DES groups (7.9% vs. 4.5%, P=0.239; and 11.4% vs. 10.4%, P=0.773, respectively). No significant differences in MLD, DS, or LLL were observed between the groups at the 1-year follow up.
Conclusions: With careful lesion selection and preparation, DCB angioplasty could serve as a feasible treatment option for de novo large-vessel CAD in clinical practice.
背景:药物包被球囊(DCB)血管成形术已显示出短期内治疗大血管冠状动脉疾病(CAD;≥3mm)的可行性;然而,长期结果仍不明朗。本研究旨在评估DCB血管成形术与药物洗脱支架(DES)治疗新生大血管CAD的5年心血管预后。方法和结果:本单中心回顾性研究分析了2016年1月至2018年12月期间接受DCB (SeQuent Please)或DES (Xience Alpine)经皮冠状动脉介入治疗(PCI)的患者。主要结局是心血管事件(CVE),定义为心源性死亡、非致死性心肌梗死和靶病变血运重建术(TLR)的复合。次要结果包括最小管腔直径(MLD)、直径狭窄(DS)和晚期管腔损失(LLL),通过PCI指数和1年血管造影随访进行评估。总体而言,DCB组分析了114例患者(122个病变),DES组分析了269例患者(293个病变),中位随访时间相似(1,678天对1,825天;P=0.687)。5年时,DCB组和DES组的TLR和CVE率具有可比性(分别为7.9% vs. 4.5%, P=0.239; 11.4% vs. 10.4%, P=0.773)。在1年随访中,两组间MLD、DS或LLL无显著差异。结论:经过精心的病变选择和准备,DCB血管成形术可作为临床治疗新生大血管CAD的可行选择。
{"title":"Long-Term Efficacy of Drug-Coated Balloon Angioplasty vs. Drug-Eluting Stent for De Novo Large-Vessel Coronary Arteries.","authors":"Mayuka Masuda, Hiroyuki Yamamoto, Shinsuke Nakano, Nobuyuki Takahashi, Taishi Miyata, Tomohiro Inoue, Tomofumi Takaya","doi":"10.1253/circrep.CR-25-0322","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0322","url":null,"abstract":"<p><strong>Background: </strong>Drug-coated balloon (DCB) angioplasty has shown short-term feasibility for large-vessel coronary artery disease (CAD; ≥3 mm); however, long-term outcomes remain unclear. This study aimed to evaluate the 5-year cardiovascular outcomes of DCB angioplasty vs. drug-eluting stents (DES) for de novo large-vessel CAD.</p><p><strong>Methods and results: </strong>This single-center retrospective study analyzed patients undergoing percutaneous coronary intervention (PCI) with either DCB (SeQuent Please) or DES (Xience Alpine) between January 2016 and December 2018. The primary outcomes were cardiovascular events (CVE), defined as a composite of cardiac death, non-fatal myocardial infarction, and target lesion revascularization (TLR). Secondary outcomes included minimal lumen diameter (MLD), diameter stenosis (DS), and late lumen loss (LLL), assessed at the index PCI and at the 1-year angiographic follow up. Overall, 114 patients (122 lesions) in the DCB group and 269 patients (293 lesions) in the DES group were analyzed, with similar median follow-up durations (1,678 vs. 1,825 days; P=0.687). At 5 years, TLR and CVE rates were comparable between the DCB and DES groups (7.9% vs. 4.5%, P=0.239; and 11.4% vs. 10.4%, P=0.773, respectively). No significant differences in MLD, DS, or LLL were observed between the groups at the 1-year follow up.</p><p><strong>Conclusions: </strong>With careful lesion selection and preparation, DCB angioplasty could serve as a feasible treatment option for de novo large-vessel CAD in clinical practice.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"564-571"},"PeriodicalIF":1.1,"publicationDate":"2026-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065446/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679656","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 : 2026-02-14eCollection Date: 2026-04-10DOI: 10.1253/circrep.CR-25-0314
Yoko M Nakao, Atsushi Takayama, Koji Kawakami
Background: Day-to-day home blood pressure variability (BPV) is associated with cardiovascular risk and influenced by environmental conditions. However, it is unclear whether short-term increases in day-to-day BPV can be predicted from personal sensor data. In this study, our aim is to develop and validate a machine-learning prediction model for short-term increases in day-to-day BPV using personal sensor data on behavioral and environmental exposure.
Methods and results: We will conduct a 30-day monitoring study in community-dwelling adults. Participants will measure home BP twice daily, while a portable sensor and an activity tracker record environmental conditions and physical activity. The primary outcome is an episode of increased systolic day-to-day BPV, defined as a rolling 5-day coefficient of variation ≥11.0%. Candidate predictors will be derived from the preceding 5-day exposure window. We will construct window-level data, allocate participants to training and test sets, and train machine-learning models with participant-level cross-validation. We will evaluate performance using the area under the receiver operating characteristic curve, calibration, Brier score, and decision-curve analysis, and interpret the XGBoost model with Shapley additive explanations to quantify the predictor contributions.
Conclusions: This protocol outlines a framework for predicting short-term increases in day-to-day BPV from personally experienced environmental exposure and behaviors, supporting future personalized interventions targeting modifiable environmental and behavioral factors.
{"title":"Development and Internal Validation of Machine-Learning Models for Short-Term Prediction of Day-to-Day Home Blood Pressure Variability Using IoT-Based Environmental and Activity Data: Protocol for the AURA-BPV Study.","authors":"Yoko M Nakao, Atsushi Takayama, Koji Kawakami","doi":"10.1253/circrep.CR-25-0314","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0314","url":null,"abstract":"<p><strong>Background: </strong>Day-to-day home blood pressure variability (BPV) is associated with cardiovascular risk and influenced by environmental conditions. However, it is unclear whether short-term increases in day-to-day BPV can be predicted from personal sensor data. In this study, our aim is to develop and validate a machine-learning prediction model for short-term increases in day-to-day BPV using personal sensor data on behavioral and environmental exposure.</p><p><strong>Methods and results: </strong>We will conduct a 30-day monitoring study in community-dwelling adults. Participants will measure home BP twice daily, while a portable sensor and an activity tracker record environmental conditions and physical activity. The primary outcome is an episode of increased systolic day-to-day BPV, defined as a rolling 5-day coefficient of variation ≥11.0%. Candidate predictors will be derived from the preceding 5-day exposure window. We will construct window-level data, allocate participants to training and test sets, and train machine-learning models with participant-level cross-validation. We will evaluate performance using the area under the receiver operating characteristic curve, calibration, Brier score, and decision-curve analysis, and interpret the XGBoost model with Shapley additive explanations to quantify the predictor contributions.</p><p><strong>Conclusions: </strong>This protocol outlines a framework for predicting short-term increases in day-to-day BPV from personally experienced environmental exposure and behaviors, supporting future personalized interventions targeting modifiable environmental and behavioral factors.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"683-687"},"PeriodicalIF":1.1,"publicationDate":"2026-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065445/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679915","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: Postoperative declines in activities of daily living (ADL) are concerning in older adults undergoing cardiovascular surgeries. Sarcopenia represents a determinant of such adverse outcomes. We examined whether preoperative sarcopenia and its components predicted postoperative ADL decline in older patients who underwent elective cardiovascular surgeries.
Methods and results: This retrospective cohort study included 589 patients aged ≥65 years who underwent elective coronary artery bypass grafting, heart valve surgery, or thoracic aortic surgery. Sarcopenia was defined according to the Asian Working Group for Sarcopenia 2019 criteria. ADLs were assessed using the Barthel Index, with in-hospital ADL decline being defined as a ≥10-point reduction. Thirty-three (5.6%) patients had sarcopenia preoperatively. ADL decline was significantly higher in the patients with sarcopenia compared with those without (15.2% vs. 5.0%; P=0.014). Multivariable logistic regression analyses demonstrated that sarcopenia was independently associated with ADL decline (odds ratio 3.094; 95% confidence interval 1.067-8.968; P=0.038). Each sarcopenia component - low muscle mass, low muscle strength, and slow gait speed - was also independently associated with ADL decline (all P<0.050). Age-adjusted receiver operating characteristic analyses showed that sarcopenia demonstrated moderate discrimination for predicting postoperative ADL decline, with an area under the curve of 0.707.
Conclusions: Preoperative sarcopenia and its individual components independently predicted in-hospital ADL decline following cardiovascular surgery. Preoperative assessments may help identify high-risk patients.
背景:在接受心血管手术的老年人中,术后日常生活活动(ADL)的下降令人担忧。肌肉减少症是这些不良结果的决定因素。我们研究了术前肌肉减少症及其成分是否能预测接受选择性心血管手术的老年患者术后ADL下降。方法和结果:这项回顾性队列研究包括589例年龄≥65岁的患者,他们接受了择期冠状动脉搭桥术、心脏瓣膜手术或胸主动脉手术。肌少症是根据2019年亚洲肌少症工作组的标准定义的。使用Barthel指数评估ADL,住院ADL下降定义为下降≥10点。术前肌少症33例(5.6%)。肌少症患者的ADL下降明显高于无肌少症患者(15.2% vs. 5.0%; P=0.014)。多变量logistic回归分析显示,肌肉减少症与ADL下降独立相关(优势比3.094;95%可信区间1.067 ~ 8.968;P=0.038)。肌肉减少症的每一个组成部分——低肌肉质量、低肌肉力量和慢步态速度——也与ADL下降独立相关(所有结论:术前肌肉减少症及其单个组成部分独立预测心血管手术后住院ADL下降。术前评估有助于识别高危患者。
{"title":"Preoperative Sarcopenia and Postoperative Activities of Daily Living Decline in Patients Undergoing Elective Cardiovascular Surgery.","authors":"Tomohiro Kato, Yuta Ozaki, Shigefumi Honda, Yusuke Uemura, Kenji Takemoto, Masato Watarai, Toyoaki Murohara","doi":"10.1253/circrep.CR-25-0299","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0299","url":null,"abstract":"<p><strong>Background: </strong>Postoperative declines in activities of daily living (ADL) are concerning in older adults undergoing cardiovascular surgeries. Sarcopenia represents a determinant of such adverse outcomes. We examined whether preoperative sarcopenia and its components predicted postoperative ADL decline in older patients who underwent elective cardiovascular surgeries.</p><p><strong>Methods and results: </strong>This retrospective cohort study included 589 patients aged ≥65 years who underwent elective coronary artery bypass grafting, heart valve surgery, or thoracic aortic surgery. Sarcopenia was defined according to the Asian Working Group for Sarcopenia 2019 criteria. ADLs were assessed using the Barthel Index, with in-hospital ADL decline being defined as a ≥10-point reduction. Thirty-three (5.6%) patients had sarcopenia preoperatively. ADL decline was significantly higher in the patients with sarcopenia compared with those without (15.2% vs. 5.0%; P=0.014). Multivariable logistic regression analyses demonstrated that sarcopenia was independently associated with ADL decline (odds ratio 3.094; 95% confidence interval 1.067-8.968; P=0.038). Each sarcopenia component - low muscle mass, low muscle strength, and slow gait speed - was also independently associated with ADL decline (all P<0.050). Age-adjusted receiver operating characteristic analyses showed that sarcopenia demonstrated moderate discrimination for predicting postoperative ADL decline, with an area under the curve of 0.707.</p><p><strong>Conclusions: </strong>Preoperative sarcopenia and its individual components independently predicted in-hospital ADL decline following cardiovascular surgery. Preoperative assessments may help identify high-risk patients.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"537-543"},"PeriodicalIF":1.1,"publicationDate":"2026-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065460/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679573","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: Because snowfall may affect the acute outcomes of severe cardiovascular diseases by prolonging emergency medical service (EMS) response times, we investigated the association between snowfall and EMS response times for out-of-hospital cardiac arrests (OHCAs) in the regions of Japan.
Methods and results: We used the Utstein database, a nationwide population-based registry that collects data on all OHCA patients in Japan, during winter from 2009 to 2019. A prefecture-specific logistic regression model was applied to estimate odds ratios (ORs) of prolongation of EMS response time (≥7 min), which was associated with poorer neurological outcomes, on days with moderate/heavy snowfall compared to no-snowfall days. A random-effects meta-analysis model was applied to obtain pooled ORs in both overall and subgroup analyses ("heavy snowfall prefectures" and "non-heavy snowfall prefectures"). Among 94,428 bystander-witnessed cardiogenic OHCA patients, the ORs of prolonged EMS response time were 1.05 (95% confidence interval (CI): 0.96, 1.14) on moderate snowfall days and 1.22 (95% CI: 1.07, 1.40) on heavy snowfall days, compared to no-snowfall days. Subgroup analysis revealed no statistical difference between heavy snowfall prefectures and non-heavy snowfall prefectures, although ORs were higher for heavy snowfall prefectures.
Conclusions: Snowfall prolongs EMS response time to cardiogenic OHCA in both areas with heavy snowfall and those with less snowfall, which may also impact survival and neurological outcomes.
{"title":"Impact of Snowfall on Ambulance Response Times to Out-of-Hospital Cardiac Arrest - Nationally-Representative Population-Based Registry Analysis, 2009-2019.","authors":"Hirokuni Wataki, Xerxes Tesoro Seposo, Athicha Uttajug, Toshihisa Anzai, Isao Yokota, Kayo Ueda, Naohiro Yonemoto, Yoshio Tahara, Tetsuya Matoba, Takanori Ikeda","doi":"10.1253/circrep.CR-25-0129","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0129","url":null,"abstract":"<p><strong>Background: </strong>Because snowfall may affect the acute outcomes of severe cardiovascular diseases by prolonging emergency medical service (EMS) response times, we investigated the association between snowfall and EMS response times for out-of-hospital cardiac arrests (OHCAs) in the regions of Japan.</p><p><strong>Methods and results: </strong>We used the Utstein database, a nationwide population-based registry that collects data on all OHCA patients in Japan, during winter from 2009 to 2019. A prefecture-specific logistic regression model was applied to estimate odds ratios (ORs) of prolongation of EMS response time (≥7 min), which was associated with poorer neurological outcomes, on days with moderate/heavy snowfall compared to no-snowfall days. A random-effects meta-analysis model was applied to obtain pooled ORs in both overall and subgroup analyses (\"heavy snowfall prefectures\" and \"non-heavy snowfall prefectures\"). Among 94,428 bystander-witnessed cardiogenic OHCA patients, the ORs of prolonged EMS response time were 1.05 (95% confidence interval (CI): 0.96, 1.14) on moderate snowfall days and 1.22 (95% CI: 1.07, 1.40) on heavy snowfall days, compared to no-snowfall days. Subgroup analysis revealed no statistical difference between heavy snowfall prefectures and non-heavy snowfall prefectures, although ORs were higher for heavy snowfall prefectures.</p><p><strong>Conclusions: </strong>Snowfall prolongs EMS response time to cardiogenic OHCA in both areas with heavy snowfall and those with less snowfall, which may also impact survival and neurological outcomes.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 3","pages":"479-485"},"PeriodicalIF":1.1,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12971214/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147438748","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 : 2026-02-10eCollection Date: 2026-04-10DOI: 10.1253/circrep.CR-25-0335
Naoto Yabu, Tomoyuki Minami, Shota Yasuda, Yoshiyuki Kobayashi, Aya Saito
Background: Postoperative atrial fibrillation (POAF) after cardiac surgery requires prompt intervention. We compared landiolol with verapamil for POAF treatment.
Methods and results: This randomized trial enrolled 179 patients; 45 developed POAF. Landiolol achieved higher sinus rhythm conversion at 8 h (73.3% vs 16.7%; P=0.0016), but not at 12 h. No differences were observed in recurrence, adverse events, or intensive care unit stay.
背景:心脏手术后心房颤动(POAF)需要及时干预。我们比较了兰地洛尔和维拉帕米治疗POAF的效果。方法和结果:该随机试验入组179例患者;45人发展为POAF。兰地洛尔在8小时获得了更高的窦性心律转换(73.3% vs 16.7%; P=0.0016),但在12小时没有。在复发、不良事件或重症监护病房住院时间方面没有观察到差异。结论:兰地洛尔促进早期心律转换,但短期临床效果不明显。
{"title":"Comparison of Landiolol and Verapamil for Postoperative Atrial Fibrillation: A Prospective Randomized Study.","authors":"Naoto Yabu, Tomoyuki Minami, Shota Yasuda, Yoshiyuki Kobayashi, Aya Saito","doi":"10.1253/circrep.CR-25-0335","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0335","url":null,"abstract":"<p><strong>Background: </strong>Postoperative atrial fibrillation (POAF) after cardiac surgery requires prompt intervention. We compared landiolol with verapamil for POAF treatment.</p><p><strong>Methods and results: </strong>This randomized trial enrolled 179 patients; 45 developed POAF. Landiolol achieved higher sinus rhythm conversion at 8 h (73.3% vs 16.7%; P=0.0016), but not at 12 h. No differences were observed in recurrence, adverse events, or intensive care unit stay.</p><p><strong>Conclusions: </strong>Landiolol facilitates earlier rhythm conversion without clear short-term clinical benefit.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"680-682"},"PeriodicalIF":1.1,"publicationDate":"2026-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065448/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679861","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 clinical impact of left QRS axis deviation (LAD) during new-onset left bundle branch block (LBBB) after transcatheter aortic valve replacement (TAVR) remains unclear.
Methods and results: This single-center retrospective study analyzed 254 patients who developed new-onset LBBB during hospitalization after TAVR. Clinical and echocardiographic outcomes were compared between patients with LBBB and LAD (LBBBLAD) and those with LBBB and a normal QRS axis (LBBBNA). 96 patients (38%) had LBBBLAD, defined as a QRS axis <-30°. A more leftward preprocedural QRS axis independently predicted LBBBLAD (odds ratio 1.20 per 10° decrement; 95% confidence interval (CI) 1.09-1.33; P<0.01). At 3 years, there were no significant differences between groups in all-cause death (28% vs. 19%; P=0.14), cardiovascular death (6% vs. 5%; P=0.73), or heart failure rehospitalization (18% vs. 10%; P=0.07). However, LBBBLAD was associated with a higher incidence of permanent pacemaker implantation (PPI) for atrioventricular conduction disorder (16% vs. 6%; P=0.02) and remained an independent predictor of PPI (Cox hazard ratio 2.46; 95% CI 1.06-5.73; P=0.04). Echocardiographic measures, including left ventricular ejection fraction, chamber size, and mitral regurgitation severity showed no significant longitudinal differences between groups.
Conclusions: Compared to post-TAVR LBBBNA, post-TAVR LBBBLAD is associated with an increased need for PPI, but not with adverse mortality or heart failure outcomes at 3-year follow-up. Closer and extended rhythm monitoring may be warranted in this subgroup.
背景:经导管主动脉瓣置换术(TAVR)后新发左束支阻滞(LBBB)中左QRS轴偏差(LAD)的临床影响尚不清楚。方法和结果:这项单中心回顾性研究分析了254例TAVR术后住院期间发生新发LBBB的患者。比较LBBB合并LAD患者(LBBBLAD)与LBBB合并QRS轴正常患者(LBBBNA)的临床和超声心动图结果。96例(38%)患者患有LBBBLAD,定义为QRS轴LAD(优势比1.20 / 10°递减;95%置信区间(CI) 1.09-1.33;PLAD与房室传导障碍患者永久性起搏器植入(PPI)的较高发生率相关(16% vs. 6%; P=0.02),并且仍然是PPI的独立预测因子(Cox风险比2.46;95% CI 1.06-5.73; P=0.04)。超声心动图测量,包括左心室射血分数、心室大小和二尖瓣反流严重程度,在两组之间没有显著的纵向差异。结论:与tavr后LBBBNA相比,tavr后LBBBLAD与PPI需求增加有关,但与3年随访的不良死亡率或心力衰竭结局无关。在这个亚组中可能需要更密切和更广泛的节律监测。
{"title":"Left vs. Normal QRS Axis During Left Bundle Branch Block Induced by Transcatheter Aortic Valve Replacement: 3-Year Outcomes.","authors":"Kenichi Sasaki, Shingo Kuwata, Masaki Izumo, Yukio Sato, Takahiko Kai, Taishi Okuno, Tetsu Tanaka, Masahiro Sekiguchi, Yoshihiro J Akashi","doi":"10.1253/circrep.CR-25-0249","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0249","url":null,"abstract":"<p><strong>Background: </strong>The clinical impact of left QRS axis deviation (LAD) during new-onset left bundle branch block (LBBB) after transcatheter aortic valve replacement (TAVR) remains unclear.</p><p><strong>Methods and results: </strong>This single-center retrospective study analyzed 254 patients who developed new-onset LBBB during hospitalization after TAVR. Clinical and echocardiographic outcomes were compared between patients with LBBB and LAD (LBBB<sub>LAD</sub>) and those with LBBB and a normal QRS axis (LBBB<sub>NA</sub>). 96 patients (38%) had LBBB<sub>LAD</sub>, defined as a QRS axis <-30°. A more leftward preprocedural QRS axis independently predicted LBBB<sub>LAD</sub> (odds ratio 1.20 per 10° decrement; 95% confidence interval (CI) 1.09-1.33; P<0.01). At 3 years, there were no significant differences between groups in all-cause death (28% vs. 19%; P=0.14), cardiovascular death (6% vs. 5%; P=0.73), or heart failure rehospitalization (18% vs. 10%; P=0.07). However, LBBB<sub>LAD</sub> was associated with a higher incidence of permanent pacemaker implantation (PPI) for atrioventricular conduction disorder (16% vs. 6%; P=0.02) and remained an independent predictor of PPI (Cox hazard ratio 2.46; 95% CI 1.06-5.73; P=0.04). Echocardiographic measures, including left ventricular ejection fraction, chamber size, and mitral regurgitation severity showed no significant longitudinal differences between groups.</p><p><strong>Conclusions: </strong>Compared to post-TAVR LBBB<sub>NA</sub>, post-TAVR LBBB<sub>LAD</sub> is associated with an increased need for PPI, but not with adverse mortality or heart failure outcomes at 3-year follow-up. Closer and extended rhythm monitoring may be warranted in this subgroup.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"657-667"},"PeriodicalIF":1.1,"publicationDate":"2026-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065458/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679650","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: Data on the clinical outcomes and hemodynamic performance of the smallest commercially available bioprostheses (19 mm) in Japan for aortic valve replacement (AVR) remain limited.
Methods and results: We analyzed the data of 187 adults (median age, 76 [interquartile range (IQR): 73-80] years; 165 women [88%]; median follow-up, 65 [IQR: 32-95] months) with symptomatic aortic valve stenosis, regurgitation, and valve deterioration who underwent surgical AVR between January 2015 and July 2024 with the Avalus (n=7), Magna (n=77), Epic (n=26), Inspiris (n=58), or Mosaic (n=27) bioprosthesis because of having small aortic annuli. The primary and secondary endpoints were all-cause death and major adverse cardiac events, respectively. Moderate-to-severe prosthesis-patient mismatch occurred in 53 patients (28%). The overall survival rates (95% confidence interval [CI]) at 1, 3, and 5 years after valve replacement were 93.0% (88.3-95.9%), 87.0% (81.0-91.2%), and 85.7% (79.5-90.1%), respectively. The rates of freedom from major adverse cardiac and cerebrovascular events (95% CI) at 1, 3, and 5 years were 96.2% (92.1-98.2%), 90.2(84.5-93.9%), and 88.7(82.5-92.7%), respectively. Four patients required re-intervention (3, re-AVR and 1, medication). No significant differences were observed in either outcomes or hemodynamics among the different aortic bioprostheses.
Conclusions: Surgical replacement with 19-mm third-generation aortic valve bioprostheses for small aortic annuli is feasible with favorable early and mid-term hemodynamics.
{"title":"Mid-Term Clinical Outcomes and Hemodynamic Performance of 19-mm Bioprostheses Following Aortic Valve Replacement: A Single-Institution 10-Year Experience.","authors":"Takayuki Gyoten, Yuta Kanazawa, Yu Kumagai, Takayuki Akatsu, Yuko Gatate, Takahide Arai, Shintaro Nakano, Akihiro Yoshitake","doi":"10.1253/circrep.CR-25-0307","DOIUrl":"https://doi.org/10.1253/circrep.CR-25-0307","url":null,"abstract":"<p><strong>Background: </strong>Data on the clinical outcomes and hemodynamic performance of the smallest commercially available bioprostheses (19 mm) in Japan for aortic valve replacement (AVR) remain limited.</p><p><strong>Methods and results: </strong>We analyzed the data of 187 adults (median age, 76 [interquartile range (IQR): 73-80] years; 165 women [88%]; median follow-up, 65 [IQR: 32-95] months) with symptomatic aortic valve stenosis, regurgitation, and valve deterioration who underwent surgical AVR between January 2015 and July 2024 with the Avalus (n=7), Magna (n=77), Epic (n=26), Inspiris (n=58), or Mosaic (n=27) bioprosthesis because of having small aortic annuli. The primary and secondary endpoints were all-cause death and major adverse cardiac events, respectively. Moderate-to-severe prosthesis-patient mismatch occurred in 53 patients (28%). The overall survival rates (95% confidence interval [CI]) at 1, 3, and 5 years after valve replacement were 93.0% (88.3-95.9%), 87.0% (81.0-91.2%), and 85.7% (79.5-90.1%), respectively. The rates of freedom from major adverse cardiac and cerebrovascular events (95% CI) at 1, 3, and 5 years were 96.2% (92.1-98.2%), 90.2(84.5-93.9%), and 88.7(82.5-92.7%), respectively. Four patients required re-intervention (3, re-AVR and 1, medication). No significant differences were observed in either outcomes or hemodynamics among the different aortic bioprostheses.</p><p><strong>Conclusions: </strong>Surgical replacement with 19-mm third-generation aortic valve bioprostheses for small aortic annuli is feasible with favorable early and mid-term hemodynamics.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 4","pages":"572-579"},"PeriodicalIF":1.1,"publicationDate":"2026-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13065456/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147679653","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}