Background: Decline or inadequate recovery of activities of daily living (ADL) during hospitalization is crucial for clinical prognosis. In this study we investigated the relationship between cardiac rehabilitation (CR) and ADL recovery in patients with cardiovascular disease (CVD), with the aim of exploring associations that may contribute to the development of rehabilitation interventions.
Methods and results: This study analyzed consecutive patients hospitalized with CVD. ADL was assessed using the Barthel index (BI) at the commencement of rehabilitation and discharge. As the outcome measure for ADL, relative functional gain: BI effectiveness, calculated as (discharge BI - initial BI) / (100 - initial BI), was adopted in order to compensate ceiling effect of BI. BI effectiveness ≥0.5 defined the ADL recovery group, while <0.5 defined the ADL non-recovery group. Of the 2,938 patients screened, 1,582 (median age 79 years, male 59%) were included after exclusions. The ADL recovery group consisted of 1,162 patients, the ADL non-recovery group, 420 patients. Between-group comparisons and multivariate regression analysis identified age and initial BI as highly significant ADL recovery determinants. Recursive partitioning analysis showed CR volumes of ≥75 min/day for patients ≥75 years and ≥45 min/day for those <75 years with lower initial BI were associated with ADL recovery. These CR volumes also reduced the institutionalization odds ratios (OR=0.42 and OR=0.34, P<0.001) compared to CR volumes <45 min/day.
Conclusions: CR volume was associated with ADL recovery, especially for older patients with low baseline function at admission. Optimizing CR volume based on patient background and condition may contribute to enhance ADL recovery and improved clinical prognosis.
{"title":"Relationship Between Cardiac Rehabilitation and Recovery From Decline in Activities of Daily Living in Patients Hospitalized With Cardiovascular Disease.","authors":"Masami Kimura, Masataka Nakano, Chie Shiraishi, Shota Onoda, Takashi Amari, Kento Ihara, Kentaro Watanabe, Sayuri Tanaka, Takaaki Isshiki","doi":"10.1253/circrep.CR-25-0024","DOIUrl":"10.1253/circrep.CR-25-0024","url":null,"abstract":"<p><strong>Background: </strong>Decline or inadequate recovery of activities of daily living (ADL) during hospitalization is crucial for clinical prognosis. In this study we investigated the relationship between cardiac rehabilitation (CR) and ADL recovery in patients with cardiovascular disease (CVD), with the aim of exploring associations that may contribute to the development of rehabilitation interventions.</p><p><strong>Methods and results: </strong>This study analyzed consecutive patients hospitalized with CVD. ADL was assessed using the Barthel index (BI) at the commencement of rehabilitation and discharge. As the outcome measure for ADL, relative functional gain: BI effectiveness, calculated as (discharge BI - initial BI) / (100 - initial BI), was adopted in order to compensate ceiling effect of BI. BI effectiveness ≥0.5 defined the ADL recovery group, while <0.5 defined the ADL non-recovery group. Of the 2,938 patients screened, 1,582 (median age 79 years, male 59%) were included after exclusions. The ADL recovery group consisted of 1,162 patients, the ADL non-recovery group, 420 patients. Between-group comparisons and multivariate regression analysis identified age and initial BI as highly significant ADL recovery determinants. Recursive partitioning analysis showed CR volumes of ≥75 min/day for patients ≥75 years and ≥45 min/day for those <75 years with lower initial BI were associated with ADL recovery. These CR volumes also reduced the institutionalization odds ratios (OR=0.42 and OR=0.34, P<0.001) compared to CR volumes <45 min/day.</p><p><strong>Conclusions: </strong>CR volume was associated with ADL recovery, especially for older patients with low baseline function at admission. Optimizing CR volume based on patient background and condition may contribute to enhance ADL recovery and improved clinical prognosis.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1051-1059"},"PeriodicalIF":1.1,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597247/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145491198","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: There is a substantial risk of slow flow during percutaneous coronary intervention (PCI) for the culprit lesion in acute myocardial infarction (AMI), which can lead to adverse outcomes. We hypothesized that single-step long balloon inflation during stent deployment was associated with a more favorable final Thrombolysis in Myocardial Infarction (TIMI) flow grade. This retrospective study aimed to compare both the final TIMI flow grade and the delta TIMI flow grade in intravascular ultrasound (IVUS)-guided PCI for AMI between patients with long balloon inflation and those with conventional inflation.
Methods and results: Long inflation was defined as single-step inflation ≥60 s at stent deployment. The primary endpoints were achievement of the final TIMI flow grade 3 and the delta TIMI flow grade, defined as the difference between the initial and final grades. We analyzed 336 AMI patients with attenuation plaque on IVUS, dividing them into a long inflation group (n=50) and a conventional inflation group (n=286). Despite a significantly higher TIMI thrombus grade in the long inflation group (P<0.001), the rate of the final TIMI 3 flow was similar (90% vs. 88.5%; P=1.00). However, the delta TIMI flow grade was significantly greater in the long inflation group (P=0.028).
Conclusions: Single-step long balloon inflation may be a simple and feasible method to achieve optimal final TIMI flow in IVUS-guided PCI for AMI.
{"title":"Long Inflation at Stent Deployment in Intravascular Ultrasound-Guided Percutaneous Coronary Intervention for Acute Myocardial Infarction.","authors":"Yusuke Watanabe, Kenichi Sakakura, Hiroyuki Jinnouchi, Yousuke Taniguchi, Kei Yamamoto, Masaru Seguchi, Takunori Tsukui, Taku Kasahara, Masashi Hatori, Shun Ishibashi, Hideo Fujita","doi":"10.1253/circrep.CR-25-0141","DOIUrl":"10.1253/circrep.CR-25-0141","url":null,"abstract":"<p><strong>Background: </strong>There is a substantial risk of slow flow during percutaneous coronary intervention (PCI) for the culprit lesion in acute myocardial infarction (AMI), which can lead to adverse outcomes. We hypothesized that single-step long balloon inflation during stent deployment was associated with a more favorable final Thrombolysis in Myocardial Infarction (TIMI) flow grade. This retrospective study aimed to compare both the final TIMI flow grade and the delta TIMI flow grade in intravascular ultrasound (IVUS)-guided PCI for AMI between patients with long balloon inflation and those with conventional inflation.</p><p><strong>Methods and results: </strong>Long inflation was defined as single-step inflation ≥60 s at stent deployment. The primary endpoints were achievement of the final TIMI flow grade 3 and the delta TIMI flow grade, defined as the difference between the initial and final grades. We analyzed 336 AMI patients with attenuation plaque on IVUS, dividing them into a long inflation group (n=50) and a conventional inflation group (n=286). Despite a significantly higher TIMI thrombus grade in the long inflation group (P<0.001), the rate of the final TIMI 3 flow was similar (90% vs. 88.5%; P=1.00). However, the delta TIMI flow grade was significantly greater in the long inflation group (P=0.028).</p><p><strong>Conclusions: </strong>Single-step long balloon inflation may be a simple and feasible method to achieve optimal final TIMI flow in IVUS-guided PCI for AMI.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1230-1239"},"PeriodicalIF":1.1,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688430/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727974","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: Malnutrition is a significant prognostic factor in chronic heart failure (CHF), particularly among older adults. The geriatric nutritional risk index (GNRI) is a screening tool for assessing malnutrition in this population. Although low GNRI is associated with increased deaths of patients with HF, the prognostic impact of longitudinal GNRI changes in malnourished patients remains unclear.
Methods and results: This post-hoc analysis of the KUNIUMI registry chronic cohort, a prospective observational study of patients with pre-HF/HF, assessed GNRI at baseline and 1-year follow-up. The annual GNRI change (∆GNRI) was calculated, and its association with all-cause death in malnourished patients was analyzed. The primary outcome was all-cause death, with a 2-year follow-up after the initial 1-year assessment. Among 1,242 patients (mean age: 74.4±10.9 years), 19.8% had low GNRI (<92). All-cause death was significantly higher in patients with low GNRI than in those with high GNRI (30.1% vs. 7.1%; P<0.001). In patients with low GNRI, multivariable Cox regression showed a significant association between ∆GNRI and death (hazard ratio: 0.94; 95% confidence interval: 0.91-0.96; P<0.001). Multiple linear regression indicated that nutritional counseling positively influenced ∆GNRI, but HF severity was not significantly associated.
Conclusions: ∆GNRI is a significant prognostic indicator in malnourished patients with pre-HF/HF. Serial GNRI assessments may improve risk stratification and guide nutritional interventions.
{"title":"Prognostic Impact of Annual Changes in the Geriatric Nutritional Risk Index in Malnourished Patients With Heart Failure.","authors":"Tatsuya Kitagawa, Wataru Fujimoto, Makoto Takemoto, Koji Kuroda, Soichiro Yamashita, Junichi Imanishi, Masamichi Iwasaki, Takafumi Todoroki, Masanori Okuda, Manabu Nagao, Akihide Konishi, Ryuji Toh, Kunihiro Nishimura, Masakazu Shinohara, Hiromasa Otake","doi":"10.1253/circrep.CR-25-0177","DOIUrl":"10.1253/circrep.CR-25-0177","url":null,"abstract":"<p><strong>Background: </strong>Malnutrition is a significant prognostic factor in chronic heart failure (CHF), particularly among older adults. The geriatric nutritional risk index (GNRI) is a screening tool for assessing malnutrition in this population. Although low GNRI is associated with increased deaths of patients with HF, the prognostic impact of longitudinal GNRI changes in malnourished patients remains unclear.</p><p><strong>Methods and results: </strong>This post-hoc analysis of the KUNIUMI registry chronic cohort, a prospective observational study of patients with pre-HF/HF, assessed GNRI at baseline and 1-year follow-up. The annual GNRI change (∆GNRI) was calculated, and its association with all-cause death in malnourished patients was analyzed. The primary outcome was all-cause death, with a 2-year follow-up after the initial 1-year assessment. Among 1,242 patients (mean age: 74.4±10.9 years), 19.8% had low GNRI (<92). All-cause death was significantly higher in patients with low GNRI than in those with high GNRI (30.1% vs. 7.1%; P<0.001). In patients with low GNRI, multivariable Cox regression showed a significant association between ∆GNRI and death (hazard ratio: 0.94; 95% confidence interval: 0.91-0.96; P<0.001). Multiple linear regression indicated that nutritional counseling positively influenced ∆GNRI, but HF severity was not significantly associated.</p><p><strong>Conclusions: </strong>∆GNRI is a significant prognostic indicator in malnourished patients with pre-HF/HF. Serial GNRI assessments may improve risk stratification and guide nutritional interventions.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1211-1221"},"PeriodicalIF":1.1,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688437/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145727139","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 atropine is widely recommended as the first-line treatment for symptomatic bradycardia, but because the optimal initial dose remains uncertain, the aim of this scoping review was to examine the existing literature on the efficacy and safety of intravenous atropine at specific doses in adult patients with symptomatic bradycardia and to identify gaps in evidence. A systematic search of 4 databases (PubMed, CENTRAL, Web of Science, and Ichushi-Web) was conducted from inception to December 16, 2024. Studies were included if they reported administration of a specified dose of atropine in adult patients, regardless of study design. No randomized controlled trials directly comparing 0.5 mg vs. 1.0 mg were found. A total of 19 studies were included and categorized into groups based on initial atropine dose: low (<0.5 mg), moderate (0.5 mg ≤ dose <1.0 mg), high (≥1.0 mg), and those spanning multiple categories. No consistent relationship was found between atropine dose and clinical outcomes, such as heart rate response or adverse effects. None of the moderate-dose studies reported worsening bradycardia. Moderate-dose atropine could be safe, and the current practice of using 0.5 mg as an initial dose in Japan, where 0.5 mg/mL prefilled syringes are commercially available, appears clinically reasonable. However, in the absence of high-quality comparative data, future research should apply rigorous study designs to determine the optimal atropine dose in emergency care settings.
静脉注射阿托品被广泛推荐作为对症性心动过缓的一线治疗,但由于最佳初始剂量仍不确定,本综述的目的是检查关于特定剂量静脉注射阿托品治疗对症性心动过缓成人患者的有效性和安全性的现有文献,并找出证据中的空白。系统检索了4个数据库(PubMed, CENTRAL, Web of Science, Ichushi-Web),从成立到2024年12月16日。无论研究设计如何,只要报告成人患者使用特定剂量的阿托品,就纳入研究。没有发现直接比较0.5 mg和1.0 mg的随机对照试验。共纳入19项研究,并根据阿托品的初始剂量分为两组:低(
{"title":"Initial Dose of Intravenous Atropine for Patients With Symptomatic Bradycardia - A Scoping Review.","authors":"Masashi Yokose, Mutsuko Sangawa, Hiroki Shiomi, Kazuo Sakamoto, Kenichi Iijima, Tetsuma Kawaji, Takayuki Kitai, Yukio Hosaka, Eiji Hiraoka, Teruo Noguchi, Hiroshi Takahashi, Tetsuya Matoba, Migaku Kikuchi, Yoshio Tahara, Hiroshi Nonogi, Toshikazu Funazaki","doi":"10.1253/circrep.CR-25-0169","DOIUrl":"10.1253/circrep.CR-25-0169","url":null,"abstract":"<p><p>Intravenous atropine is widely recommended as the first-line treatment for symptomatic bradycardia, but because the optimal initial dose remains uncertain, the aim of this scoping review was to examine the existing literature on the efficacy and safety of intravenous atropine at specific doses in adult patients with symptomatic bradycardia and to identify gaps in evidence. A systematic search of 4 databases (PubMed, CENTRAL, Web of Science, and Ichushi-Web) was conducted from inception to December 16, 2024. Studies were included if they reported administration of a specified dose of atropine in adult patients, regardless of study design. No randomized controlled trials directly comparing 0.5 mg vs. 1.0 mg were found. A total of 19 studies were included and categorized into groups based on initial atropine dose: low (<0.5 mg), moderate (0.5 mg ≤ dose <1.0 mg), high (≥1.0 mg), and those spanning multiple categories. No consistent relationship was found between atropine dose and clinical outcomes, such as heart rate response or adverse effects. None of the moderate-dose studies reported worsening bradycardia. Moderate-dose atropine could be safe, and the current practice of using 0.5 mg as an initial dose in Japan, where 0.5 mg/mL prefilled syringes are commercially available, appears clinically reasonable. However, in the absence of high-quality comparative data, future research should apply rigorous study designs to determine the optimal atropine dose in emergency care settings.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1044-1050"},"PeriodicalIF":1.1,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597395/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145491126","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 physician ordered advance code (PAC), a treatment code used in Japanese hospitals based on the physician orders for life sustaining treatment paradigm, plays a crucial role in guiding treatment decisions for patients with acute heart failure (AHF). However, data on the clinical characteristics, decision-making processes, and outcomes associated with PAC in Japanese patients are limited.
Methods and results: We retrospectively analyzed data from 1,203 AHF patients across multiple centers in Japan. Patients were categorized based on the presence or absence of PAC orders; clinical characteristics and mortality outcomes were compared between the 2 groups. Patients with PAC orders were significantly older, more often female, and had lower activities of daily living scores. Cognitive impairment was markedly more prevalent in the PAC than non-PAC group. PAC decisions were primarily communicated to family members rather than to patients themselves, with only 7.3% of patients directly informed. The median time from admission to final PAC order was 2 days, with 74.1% finalized within 5 days. PAC orders frequently permitted intravenous therapies, but limited resuscitative measures in only 15% of patients. In-hospital and 2-year mortality rates were substantially higher in the PAC than non-PAC group.
Conclusions: PAC designation reflected poor clinical status and was linked to significantly worse mortality outcome. Enhancing shared decision-making and aligning PAC with patient values are essential steps to optimize care for this vulnerable population.
{"title":"Status of Physician-Ordered Advance Code in Patients With Acute Heart Failure.","authors":"Kensuke Takabayashi, Shouji Kitaguchi, Tetsuhisa Kitamura, Hiroyuki Takenaka, Yoshihisa Nakagawa, Takeshi Kimura, Ryuji Nohara","doi":"10.1253/circrep.CR-25-0173","DOIUrl":"10.1253/circrep.CR-25-0173","url":null,"abstract":"<p><strong>Background: </strong>The physician ordered advance code (PAC), a treatment code used in Japanese hospitals based on the physician orders for life sustaining treatment paradigm, plays a crucial role in guiding treatment decisions for patients with acute heart failure (AHF). However, data on the clinical characteristics, decision-making processes, and outcomes associated with PAC in Japanese patients are limited.</p><p><strong>Methods and results: </strong>We retrospectively analyzed data from 1,203 AHF patients across multiple centers in Japan. Patients were categorized based on the presence or absence of PAC orders; clinical characteristics and mortality outcomes were compared between the 2 groups. Patients with PAC orders were significantly older, more often female, and had lower activities of daily living scores. Cognitive impairment was markedly more prevalent in the PAC than non-PAC group. PAC decisions were primarily communicated to family members rather than to patients themselves, with only 7.3% of patients directly informed. The median time from admission to final PAC order was 2 days, with 74.1% finalized within 5 days. PAC orders frequently permitted intravenous therapies, but limited resuscitative measures in only 15% of patients. In-hospital and 2-year mortality rates were substantially higher in the PAC than non-PAC group.</p><p><strong>Conclusions: </strong>PAC designation reflected poor clinical status and was linked to significantly worse mortality outcome. Enhancing shared decision-making and aligning PAC with patient values are essential steps to optimize care for this vulnerable population.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1079-1085"},"PeriodicalIF":1.1,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597245/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145491308","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: This study aimed to identify fall risk indicators associated with future falls among older patients with cardiovascular disease (CVD), based on a multidimensional assessment.
Methods and results: In this prospective cohort study, 129 patients aged ≥65 years with CVD were enrolled between 2021 and 2023. Participants were classified into fall and non-fall groups based on fall incidence during a 1-year follow up. We assessed physical frailty, systolic blood pressure, polypharmacy, and the Falls Efficacy Scale International (FES-I) to evaluate concern about falling. The overall 1-year fall incidence was 17.0% (22 falls), equating to 0.28 falls per person-year. Compared with the non-fall group, the fall group was older, had lower physical function and blood pressure, and higher FES-I scores. Multivariate logistic regression, adjusted with propensity scores, revealed that a FES-I score ≥28 was a significant predictor of falls (odds ratio [OR] 8.906, 95% confidence interval [CI] 2.556-13.031, P=0.001; adjusted OR 2.964, 95% CI 1.038-8.460, P=0.042). Receiver operating characteristic analysis identified a FES-I cut-off of 28, with an area under the curve of 0.684 (95% CI 0.527-0.840, P=0.017).
Conclusions: The 1-year fall incidence among older patients with CVD was comparable with rates in community-dwelling older adults. Higher concern about falling, as measured using FES-I, was significantly associated with future falls.
背景:本研究旨在基于多维评估,确定与老年心血管疾病(CVD)患者未来跌倒相关的跌倒风险指标。方法和结果:在这项前瞻性队列研究中,在2021年至2023年期间入组了129例年龄≥65岁的CVD患者。参与者根据1年随访期间的跌倒发生率分为跌倒组和非跌倒组。我们评估了身体虚弱、收缩压、多种药物以及国际跌倒功效量表(FES-I)来评估对跌倒的担忧。1年总体跌倒发生率为17.0%(22次跌倒),相当于每人每年0.28次跌倒。与非跌倒组相比,跌倒组年龄更大,身体功能和血压更低,FES-I评分更高。经倾向评分校正的多因素logistic回归显示,FES-I评分≥28是跌倒的显著预测因子(优势比[OR] 8.906, 95%可信区间[CI] 2.556 ~ 13.031, P=0.001;调整后的OR为2.964,95% CI 1.038 ~ 8.460, P=0.042)。受试者工作特征分析确定FES-I截止值为28,曲线下面积为0.684 (95% CI 0.527-0.840, P=0.017)。结论:老年CVD患者的1年跌倒发生率与社区居住老年人的发生率相当。用FES-I测量,对跌倒的高度关注与未来跌倒显著相关。
{"title":"Concern About Falling Is a Predictor of Fall Risk in Older Patients With Cardiovascular Disease - A 1-Year Longitudinal Study.","authors":"Masakazu Saitoh, Ryuichi Sawa, Kohei Shiota, Kotaro Iwatsu, Tomoyuki Morisawa, Tetsuya Takahashi, Junya Nishimura, Masamichi Mochizuki, Eriko Kitahara, Toshiyuki Fujiwara, Miho Yokoyama, Tohru Minamino","doi":"10.1253/circrep.CR-25-0097","DOIUrl":"10.1253/circrep.CR-25-0097","url":null,"abstract":"<p><strong>Background: </strong>This study aimed to identify fall risk indicators associated with future falls among older patients with cardiovascular disease (CVD), based on a multidimensional assessment.</p><p><strong>Methods and results: </strong>In this prospective cohort study, 129 patients aged ≥65 years with CVD were enrolled between 2021 and 2023. Participants were classified into fall and non-fall groups based on fall incidence during a 1-year follow up. We assessed physical frailty, systolic blood pressure, polypharmacy, and the Falls Efficacy Scale International (FES-I) to evaluate concern about falling. The overall 1-year fall incidence was 17.0% (22 falls), equating to 0.28 falls per person-year. Compared with the non-fall group, the fall group was older, had lower physical function and blood pressure, and higher FES-I scores. Multivariate logistic regression, adjusted with propensity scores, revealed that a FES-I score ≥28 was a significant predictor of falls (odds ratio [OR] 8.906, 95% confidence interval [CI] 2.556-13.031, P=0.001; adjusted OR 2.964, 95% CI 1.038-8.460, P=0.042). Receiver operating characteristic analysis identified a FES-I cut-off of 28, with an area under the curve of 0.684 (95% CI 0.527-0.840, P=0.017).</p><p><strong>Conclusions: </strong>The 1-year fall incidence among older patients with CVD was comparable with rates in community-dwelling older adults. Higher concern about falling, as measured using FES-I, was significantly associated with future falls.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1071-1078"},"PeriodicalIF":1.1,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597239/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145490486","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: Point-of-care (POC) cardiac troponin testing, although less sensitive than high-sensitivity cardiac troponin assays, allows for rapid bedside evaluation. This study assessed the diagnostic performance of POC troponin tests for both ruling in and ruling out acute myocardial infarction (AMI) at the time of patient presentation.
Methods and results: In accordance with PRISMA-DTA guidelines, we conducted a systematic review and meta-analysis using PubMed, Web of Science, and the Cochrane Library from inception through June 17, 2023. We included all studies evaluating the diagnostic accuracy of POC troponin assays for identifying AMI among adult patients. Among the 551 studies initially screened, 6 met the eligibility criteria for inclusion. A meta-analysis of diagnostic accuracy based on these 6 observational datasets demonstrated pooled sensitivity and specificity values of 47% (95% confidence interval (CI) 45-49%) and 90% (95% CI 89-90%), respectively, for AMI detection. In a subgroup meta-analysis of non-ST-segment elevation MI using 4 observational datasets, the pooled sensitivity and specificity were 48% (95% CI 45-50%) and 89% (95% CI 89-90%), respectively.
Conclusions: These findings emphasize that the clinical application of POC troponin assays in AMI diagnosis must consider the test's robust specificity (≈90%) alongside its limited sensitivity (<50%).
背景:即时护理(POC)心肌肌钙蛋白检测,虽然不如高灵敏度心肌肌钙蛋白检测灵敏,但允许快速床边评估。本研究评估了POC肌钙蛋白试验在诊断和排除急性心肌梗死(AMI)时的诊断性能。方法和结果:根据PRISMA-DTA指南,我们使用PubMed、Web of Science和Cochrane Library从成立到2023年6月17日进行了系统评价和荟萃分析。我们纳入了所有评估POC肌钙蛋白检测诊断成人AMI准确性的研究。在最初筛选的551项研究中,6项符合纳入的资格标准。基于这6个观察数据集的诊断准确性荟萃分析显示,AMI检测的总敏感性和特异性分别为47%(95%置信区间(CI) 45-49%)和90% (95% CI 89-90%)。在使用4个观察数据集的非st段抬高性心肌梗死亚组荟萃分析中,合并敏感性和特异性分别为48% (95% CI 45-50%)和89% (95% CI 89-90%)。结论:这些发现强调POC肌钙蛋白检测在AMI诊断中的临床应用必须考虑该检测的强大特异性(≈90%)及其有限的敏感性(
{"title":"Diagnostic Accuracy of the Initial Point-of-Care Troponin Tests for Patients With Chest Pain Who Were Suspected of Acute Myocardial Infarction - A Systematic Review and Meta-Analysis.","authors":"Marina Arai, Yuichiro Minami, Junichi Yamaguchi, Akihito Tanaka, Kunihiro Matsuo, Toshiaki Mano, Sunao Kojima, Kiyotaka Hao, Takuya Taniguchi, Kazuya Tateishi, Rie Aoyama, Masashi Yokose, Teruo Noguchi, Yasushi Tsujimoto, Tetsuya Matoba, Toshikazu Funazaki, Yoshio Tahara, Hiroshi Nonogi, Migaku Kikuchi","doi":"10.1253/circrep.CR-25-0163","DOIUrl":"10.1253/circrep.CR-25-0163","url":null,"abstract":"<p><strong>Background: </strong>Point-of-care (POC) cardiac troponin testing, although less sensitive than high-sensitivity cardiac troponin assays, allows for rapid bedside evaluation. This study assessed the diagnostic performance of POC troponin tests for both ruling in and ruling out acute myocardial infarction (AMI) at the time of patient presentation.</p><p><strong>Methods and results: </strong>In accordance with PRISMA-DTA guidelines, we conducted a systematic review and meta-analysis using PubMed, Web of Science, and the Cochrane Library from inception through June 17, 2023. We included all studies evaluating the diagnostic accuracy of POC troponin assays for identifying AMI among adult patients. Among the 551 studies initially screened, 6 met the eligibility criteria for inclusion. A meta-analysis of diagnostic accuracy based on these 6 observational datasets demonstrated pooled sensitivity and specificity values of 47% (95% confidence interval (CI) 45-49%) and 90% (95% CI 89-90%), respectively, for AMI detection. In a subgroup meta-analysis of non-ST-segment elevation MI using 4 observational datasets, the pooled sensitivity and specificity were 48% (95% CI 45-50%) and 89% (95% CI 89-90%), respectively.</p><p><strong>Conclusions: </strong>These findings emphasize that the clinical application of POC troponin assays in AMI diagnosis must consider the test's robust specificity (≈90%) alongside its limited sensitivity (<50%).</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"997-1004"},"PeriodicalIF":1.1,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597238/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145490429","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 Navitor valve shows excellent valve function and high deliverability. However, valve pop-up during valve implantation remains a concern.
Methods and results: We defined pop-up as an upward valve dislocation ≥3 mm after implantation. Pop-up occurred in 13 (19%) of 67 patients, with 2 (3.0%) patients requiring a second valve. The depth ratio between non- and left-coronary cusp side at the 80% release and aortic valve calcification score were identified as predictors of valve pop-up.
Conclusions: Pop-up of the Navitor valve occurred in 19% of patients. Inconsistent valve depth and severe leaflet calcification were predictors of valve pop-up.
{"title":"Incidence and Predictors of Valve Pop-up During Navitor Valve Implantation.","authors":"Ryosuke Higuchi, Itaru Takamisawa, Mitsunobu Kitamura, Makoto Ohno, Mamoru Nanasato","doi":"10.1253/circrep.CR-25-0185","DOIUrl":"10.1253/circrep.CR-25-0185","url":null,"abstract":"<p><strong>Background: </strong>The Navitor valve shows excellent valve function and high deliverability. However, valve pop-up during valve implantation remains a concern.</p><p><strong>Methods and results: </strong>We defined pop-up as an upward valve dislocation ≥3 mm after implantation. Pop-up occurred in 13 (19%) of 67 patients, with 2 (3.0%) patients requiring a second valve. The depth ratio between non- and left-coronary cusp side at the 80% release and aortic valve calcification score were identified as predictors of valve pop-up.</p><p><strong>Conclusions: </strong>Pop-up of the Navitor valve occurred in 19% of patients. Inconsistent valve depth and severe leaflet calcification were predictors of valve pop-up.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 12","pages":"1304-1305"},"PeriodicalIF":1.1,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12688419/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145728039","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 device for mechanical circulatory support (MCS) in patients with acute myocardial infarction (AMI) complicated with cardiogenic shock (CS) remains unknown. Therefore, in this study we aimed to analyze which MCS (intra-aortic balloon pumping (IABP) or IMPELLA) is associated with better outcomes in patients with AMI-related CS.
Methods and results: This systematic review and meta-analysis used a random-effects model to account for potential heterogeneity. Risk ratios (RRs) and 95% confidence intervals (CIs) were used for the dichotomous outcomes. The PubMed, Web of Science, and CENTRAL databases were searched up to April 30, 2023. The risk of bias was evaluated using the Revised Cochrane risk-of-bias tool for randomized trials (RoB2) tool, and the certainty of evidence was evaluated according to the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) tool. Two randomized controlled trials were included in the meta-analysis. For the primary outcome of 30-day survival, IMPELLA probably improves the outcome by a small amount compared with IABP (RR0.94 [95% CI 0.5-1.53], 29 fewer per 1,000 [95% CI from 204 fewer to 258 more], low certainty of evidence).
Conclusions: We could not show a survival benefit of IMPELLA compared with IABP in patients with AMI complicated by CS. Further investigation is required to resolve this issue.
背景:急性心肌梗死(AMI)合并心源性休克(CS)患者机械循环支持(MCS)的最佳装置尚不清楚。因此,在本研究中,我们旨在分析哪种MCS(主动脉内球囊泵送(IABP)或IMPELLA)与ami相关性CS患者更好的预后相关。方法和结果:本系统综述和荟萃分析使用随机效应模型来解释潜在的异质性。风险比(rr)和95%置信区间(ci)用于二分类结果。PubMed、Web of Science和CENTRAL数据库被检索到2023年4月30日。使用修订Cochrane随机试验风险偏倚工具(RoB2)评估偏倚风险,根据分级推荐评估、发展和评价(GRADE)工具评估证据的确定性。meta分析纳入两项随机对照试验。对于30天生存的主要结局,与IABP相比,IMPELLA可能有少量改善结局(RR0.94 [95% CI 0.5-1.53],每1000人中减少29人[95% CI从少204人到多258人],证据确定性低)。结论:与IABP相比,我们无法证明IMPELLA在AMI合并CS患者中的生存获益。需要进一步调查才能解决这个问题。
{"title":"Prognostic Impact of the Difference of Mechanical Circulatory Support in Patients With Acute Coronary Syndrome Complicated by Cardiogenic Shock - A Systematic Review and Meta-Analysis.","authors":"Katsutaka Hashiba, Kazuo Sakamoto, Aya Katasako-Yabumoto, Takeshi Yamamoto, Naoki Nakayama, Hiroyuki Hanada, Takahiro Nakashima, Jin Kirigaya, Tomoko Ishizu, Yumiko Hosoya, Toru Kondo, Yusuke Okazaki, Masahiro Yamamoto, Takumi Osawa, Marina Arai, Yoshio Tahara, Hiroshi Nonogi, Teruo Noguchi, Yasushi Tsujimoto, Toshikazu Funazaki, Migaku Kikuchi, Tetsuya Matoba","doi":"10.1253/circrep.CR-25-0161","DOIUrl":"10.1253/circrep.CR-25-0161","url":null,"abstract":"<p><strong>Background: </strong>The optimal device for mechanical circulatory support (MCS) in patients with acute myocardial infarction (AMI) complicated with cardiogenic shock (CS) remains unknown. Therefore, in this study we aimed to analyze which MCS (intra-aortic balloon pumping (IABP) or IMPELLA) is associated with better outcomes in patients with AMI-related CS.</p><p><strong>Methods and results: </strong>This systematic review and meta-analysis used a random-effects model to account for potential heterogeneity. Risk ratios (RRs) and 95% confidence intervals (CIs) were used for the dichotomous outcomes. The PubMed, Web of Science, and CENTRAL databases were searched up to April 30, 2023. The risk of bias was evaluated using the Revised Cochrane risk-of-bias tool for randomized trials (RoB2) tool, and the certainty of evidence was evaluated according to the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) tool. Two randomized controlled trials were included in the meta-analysis. For the primary outcome of 30-day survival, IMPELLA probably improves the outcome by a small amount compared with IABP (RR0.94 [95% CI 0.5-1.53], 29 fewer per 1,000 [95% CI from 204 fewer to 258 more], low certainty of evidence).</p><p><strong>Conclusions: </strong>We could not show a survival benefit of IMPELLA compared with IABP in patients with AMI complicated by CS. Further investigation is required to resolve this issue.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"7 11","pages":"1014-1020"},"PeriodicalIF":1.1,"publicationDate":"2025-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12597236/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145491237","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: Frailty is a crucial factor in the prognoses of patients who undergo transcatheter aortic valve implantation (TAVI); however, comprehensive assessments of this parameter are not frequently performed in this regard. This study evaluated the prognostic value of the Kihon Checklist (KCL), which covers physical, cognitive, and social domains, for patients receiving TAVI.
Methods and results: We retrospectively analyzed data from 986 patients who underwent elective TAVI between May 2017 and September 2022. Frailty was classified according to the KCL as non-frail (for scores of 0-3), pre-frail (4-7), or frail (≥8). The primary outcome measure was all-cause mortality following discharge. Kaplan-Meier, Cox regression, and classification and regression tree (CART) analyses were used. Of the overall patient cohort, 47.4% were classified as frail. Over a mean follow-up period of 968±578 days, 18.1% died. Frailty was significantly associated with higher mortality (adjusted hazard ratio 1.771; 95% confidence interval 1.096-2.862; P<0.02). Impaired socialization and physical function were also found to represent independent predictors of mortality. CART identified socialization as the primary node in the risk stratification.
Conclusions: Preoperative frailty, as defined by the KCL, was found to be independently associated with mortality after TAVI. Social and physical domains were also found to have strong prognostic relevance in this context.
{"title":"Multidimensional Frailty and Mortality in Transcatheter Aortic Valve Implantation Patients - Prognostic Value of the Kihon Checklist.","authors":"Daichi Kobayashi, Masakazu Saitoh, Kentaro Hori, Shinya Tajima, Kotaro Takizawa, Junko Sakamoto, Atsuko Nakayama","doi":"10.1253/circrep.CR-25-0221","DOIUrl":"10.1253/circrep.CR-25-0221","url":null,"abstract":"<p><strong>Background: </strong>Frailty is a crucial factor in the prognoses of patients who undergo transcatheter aortic valve implantation (TAVI); however, comprehensive assessments of this parameter are not frequently performed in this regard. This study evaluated the prognostic value of the Kihon Checklist (KCL), which covers physical, cognitive, and social domains, for patients receiving TAVI.</p><p><strong>Methods and results: </strong>We retrospectively analyzed data from 986 patients who underwent elective TAVI between May 2017 and September 2022. Frailty was classified according to the KCL as non-frail (for scores of 0-3), pre-frail (4-7), or frail (≥8). The primary outcome measure was all-cause mortality following discharge. Kaplan-Meier, Cox regression, and classification and regression tree (CART) analyses were used. Of the overall patient cohort, 47.4% were classified as frail. Over a mean follow-up period of 968±578 days, 18.1% died. Frailty was significantly associated with higher mortality (adjusted hazard ratio 1.771; 95% confidence interval 1.096-2.862; P<0.02). Impaired socialization and physical function were also found to represent independent predictors of mortality. CART identified socialization as the primary node in the risk stratification.</p><p><strong>Conclusions: </strong>Preoperative frailty, as defined by the KCL, was found to be independently associated with mortality after TAVI. Social and physical domains were also found to have strong prognostic relevance in this context.</p>","PeriodicalId":94305,"journal":{"name":"Circulation reports","volume":"8 1","pages":"153-161"},"PeriodicalIF":1.1,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12782907/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145954770","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}