首页 > 最新文献

Artificial organs最新文献

英文 中文
Upcoming Meetings 即将到来的会议
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-18 DOI: 10.1111/aor.70012
{"title":"Upcoming Meetings","authors":"","doi":"10.1111/aor.70012","DOIUrl":"https://doi.org/10.1111/aor.70012","url":null,"abstract":"","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":"49 10","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145538071","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hydraulic In Vitro Characterization of MR-Conditional Blood Pumps. 核磁共振条件血泵的体外液压特性研究。
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-17 DOI: 10.1111/aor.70041
Dominik T Schulte, Marcel Renggli, Henning Richter, Francesca Del Chicca, Michael Hofmann, Martin O Schmiady, Marianne Schmid Daners

Background: Many cardiac surgical procedures use cardiopulmonary bypass (CPB), which in neonates requires the heart-lung machine (HLM) to be positioned close to the patient due to their small circulating blood volume. The absence of an MR-compatible blood pump to be used in CPB remains a key challenge for studying perioperative brain injury mechanisms in this high-risk group. This study aims to take the first step toward MR-conditional HLMs by developing hardware, verifying pump hydraulics, and ensuring MR compatibility.

Methods: This study presents three MR-conditional blood pump prototypes: a roller pump, a non-occlusive roller pump, and a centrifugal pump. MR compatibility was assessed by monitoring for imaging interference during scanning. Hydraulic performance was evaluated with pressure-flow diagrams using a mock circulation test bench.

Results: None of the prototypes interfered with MR imaging, and although SNR was reduced by -8.43% ± 7.96%, image quality remained sufficient for reliable assessment of relevant brain regions. Roller and non-occlusive pumps maintained stable flow across pressure heads, with reductions of -4.46 ± 8.02 and -119.33 ± 18.22 mL/min, respectively. The centrifugal pump exhibited pressure-dependent performance (slope -2.21 ± 0.45 mmHg/[L/min]). All pumps generated non-pulsatile flow (SHE < 1000 erg/cm3).

Conclusion: All three pumps meet basic MR-conditionality and flow requirements, supporting their potential for use in MRI-guided studies during neonatal cardiac surgery.

背景:许多心脏外科手术使用体外循环(CPB),由于新生儿的循环血容量小,需要心肺机(HLM)靠近患者。缺乏核磁共振兼容的血泵用于CPB仍然是研究这一高危人群围手术期脑损伤机制的关键挑战。本研究旨在通过开发硬件、验证泵液压和确保核磁共振兼容性,向核磁共振条件高阶机械迈出第一步。方法:本研究提出了三种磁共振条件血泵原型:滚轴泵,非闭塞滚轴泵和离心泵。通过监测扫描过程中的成像干扰来评估MR兼容性。利用模拟循环试验台的压力流图对其水力性能进行了评价。结果:所有原型都没有干扰MR成像,尽管信噪比降低了-8.43%±7.96%,但图像质量仍然足以可靠地评估相关脑区。滚柱泵和非闭塞泵在压力头之间保持稳定的流量,分别减少-4.46±8.02和-119.33±18.22 mL/min。离心泵表现出压力依赖性(斜率为-2.21±0.45 mmHg/[L/min])。所有泵都产生非脉动流(SHE 3)。结论:所有三种泵都满足基本的mri条件和流量要求,支持它们在新生儿心脏手术期间mri引导研究中的潜在应用。
{"title":"Hydraulic In Vitro Characterization of MR-Conditional Blood Pumps.","authors":"Dominik T Schulte, Marcel Renggli, Henning Richter, Francesca Del Chicca, Michael Hofmann, Martin O Schmiady, Marianne Schmid Daners","doi":"10.1111/aor.70041","DOIUrl":"https://doi.org/10.1111/aor.70041","url":null,"abstract":"<p><strong>Background: </strong>Many cardiac surgical procedures use cardiopulmonary bypass (CPB), which in neonates requires the heart-lung machine (HLM) to be positioned close to the patient due to their small circulating blood volume. The absence of an MR-compatible blood pump to be used in CPB remains a key challenge for studying perioperative brain injury mechanisms in this high-risk group. This study aims to take the first step toward MR-conditional HLMs by developing hardware, verifying pump hydraulics, and ensuring MR compatibility.</p><p><strong>Methods: </strong>This study presents three MR-conditional blood pump prototypes: a roller pump, a non-occlusive roller pump, and a centrifugal pump. MR compatibility was assessed by monitoring for imaging interference during scanning. Hydraulic performance was evaluated with pressure-flow diagrams using a mock circulation test bench.</p><p><strong>Results: </strong>None of the prototypes interfered with MR imaging, and although SNR was reduced by -8.43% ± 7.96%, image quality remained sufficient for reliable assessment of relevant brain regions. Roller and non-occlusive pumps maintained stable flow across pressure heads, with reductions of -4.46 ± 8.02 and -119.33 ± 18.22 mL/min, respectively. The centrifugal pump exhibited pressure-dependent performance (slope -2.21 ± 0.45 mmHg/[L/min]). All pumps generated non-pulsatile flow (SHE < 1000 erg/cm<sup>3</sup>).</p><p><strong>Conclusion: </strong>All three pumps meet basic MR-conditionality and flow requirements, supporting their potential for use in MRI-guided studies during neonatal cardiac surgery.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534326","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Trends in Left Ventricular Assist Device Utilization and Survival Outcomes Following the Donor Allocation Policy Change. 供体分配政策改变后左室辅助装置使用和生存结果的趋势
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-17 DOI: 10.1111/aor.70046
Christopher D Pritting, Daler Rahimov, Matthew P Weber, Eugene Storozynsky, Howard J Eisen, J Eduardo Rame, Rene J Alvarez, Keshava Rajagopal, John W Entwistle, Vakhtang Tchantchaleishvili

Background: We sought to estimate left ventricular assist device use (LVAD) with waitlist and post-transplant survival trends in patients supported on durable LVAD in relation to the UNOS donor heart allocation policy revision.

Methods: Adult patients implanted with HeartMate II LVAD, HeartWare HVAD, or HeartMate 3 LVAD, and listed for isolated heart transplantation between October 18, 2013, and June 16, 2023, were identified in the UNOS database and were stratified into pre- and post-policy revision groups. Patients on temporary circulatory support, right, or biventricular assist devices, total artificial hearts, recipients of donation after circulatory death (DCD) hearts, and those undergoing simultaneous multiorgan transplants were excluded. Waitlist and post-transplant survival were compared between the groups.

Results: Policy revision was associated with a decrease in LVAD use both at the time of listing (pre: 28% vs. post: 24.5%, p < 0.01) and at the time of transplant (pre: 45.8% vs. post: 31.7%, p < 0.01). For those listed with an LVAD, more patients eventually underwent transplantation (pre: 89.6% vs. post: 94.3%, p < 0.01) following the policy change. Overall waitlist and post-transplant survival among patients supported on LVAD worsened following the policy change, both showing statistical significance (p < 0.01).

Conclusion: In the post-policy era, a decline in durable LVAD utilization was observed, along with worse waitlist and post-transplant outcomes among LVAD-supported patients.

背景:我们试图评估与UNOS供体心脏分配政策修订相关的持久左室辅助装置(LVAD)支持患者的等待名单和移植后生存趋势。方法:在2013年10月18日至2023年6月16日期间,在UNOS数据库中识别植入HeartMate II LVAD、HeartWare HVAD或HeartMate 3 LVAD并列入孤立心脏移植的成年患者,并将其分为政策修订前和政策修订后两组。排除使用临时循环支持装置、右心室辅助装置或双心室辅助装置的患者、全人工心脏、循环死亡(DCD)心脏捐赠接受者以及同时接受多器官移植的患者。比较两组患者的等待名单和移植后生存率。结果:政策修订与上市时LVAD使用率的下降有关(前:28% vs后:24.5%,p结论:在政策后时代,观察到持久LVAD使用率的下降,以及LVAD支持患者的等待名单和移植后结果更差。
{"title":"Trends in Left Ventricular Assist Device Utilization and Survival Outcomes Following the Donor Allocation Policy Change.","authors":"Christopher D Pritting, Daler Rahimov, Matthew P Weber, Eugene Storozynsky, Howard J Eisen, J Eduardo Rame, Rene J Alvarez, Keshava Rajagopal, John W Entwistle, Vakhtang Tchantchaleishvili","doi":"10.1111/aor.70046","DOIUrl":"https://doi.org/10.1111/aor.70046","url":null,"abstract":"<p><strong>Background: </strong>We sought to estimate left ventricular assist device use (LVAD) with waitlist and post-transplant survival trends in patients supported on durable LVAD in relation to the UNOS donor heart allocation policy revision.</p><p><strong>Methods: </strong>Adult patients implanted with HeartMate II LVAD, HeartWare HVAD, or HeartMate 3 LVAD, and listed for isolated heart transplantation between October 18, 2013, and June 16, 2023, were identified in the UNOS database and were stratified into pre- and post-policy revision groups. Patients on temporary circulatory support, right, or biventricular assist devices, total artificial hearts, recipients of donation after circulatory death (DCD) hearts, and those undergoing simultaneous multiorgan transplants were excluded. Waitlist and post-transplant survival were compared between the groups.</p><p><strong>Results: </strong>Policy revision was associated with a decrease in LVAD use both at the time of listing (pre: 28% vs. post: 24.5%, p < 0.01) and at the time of transplant (pre: 45.8% vs. post: 31.7%, p < 0.01). For those listed with an LVAD, more patients eventually underwent transplantation (pre: 89.6% vs. post: 94.3%, p < 0.01) following the policy change. Overall waitlist and post-transplant survival among patients supported on LVAD worsened following the policy change, both showing statistical significance (p < 0.01).</p><p><strong>Conclusion: </strong>In the post-policy era, a decline in durable LVAD utilization was observed, along with worse waitlist and post-transplant outcomes among LVAD-supported patients.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
AI-Assisted Decision-Making for End-Stage Organ Failure: Opportunities and Ethical Concerns. 终末期器官衰竭的人工智能辅助决策:机会和伦理问题。
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-17 DOI: 10.1111/aor.70027
John W Haller, Olga D Brazhnik, Kathleen N Fenton

AI holds significant promise for guiding clinical decisions in end-stage organ failure, where treatment options now include medical management, transplantation, mechanical support devices, and palliative care. This paper discusses current applications of AI in healthcare, emphasizing the complex decision-making necessary for patients with organ failure. It outlines how AI can support risk stratification, patient selection, and outcome prediction, particularly in transplantation practices that increasingly rely on robust data to inform care pathways. By analyzing large datasets from electronic health records, imaging, and patient-reported outcomes, AI can help physicians forecast long-term survival and quality of life, and potentially assist clinicians in modifying treatment strategies before adverse trajectories take hold. There is a need for standardized, high-quality data, rigorous validation, and transparent algorithms to mitigate biases that could exacerbate disparities in care. Ethical considerations demand attention to equitable access, patient privacy, and the preservation of the human element in patient-clinician relationships. Patients generally view AI with cautious optimism, recognizing its potential to augment care but also voicing concerns about data protection and the risk of losing compassionate, personal care. Importantly, AI can help with "alignment," or fitting treatment recommendations to patients' values, and promote sustainable and patient-centered outcomes. Ultimately, the successful integration of AI into daily practice requires multidisciplinary collaboration among developers, clinicians, ethicists, and regulators. Deep stakeholder engagement, continuous algorithmic refinement, and user-friendly design are pivotal to ensuring that AI serves as a practical decision-support tool that complements, rather than replaces, clinical expertise and shared decision-making.

人工智能在指导终末期器官衰竭的临床决策方面具有重要的前景,目前的治疗选择包括医疗管理、移植、机械支持装置和姑息治疗。本文讨论了人工智能在医疗保健中的当前应用,强调了器官衰竭患者所需的复杂决策。它概述了人工智能如何支持风险分层、患者选择和结果预测,特别是在越来越依赖于可靠数据来指导护理路径的移植实践中。通过分析来自电子健康记录、成像和患者报告结果的大型数据集,人工智能可以帮助医生预测长期生存和生活质量,并可能帮助临床医生在不良轨迹出现之前修改治疗策略。需要标准化、高质量的数据、严格的验证和透明的算法来减轻可能加剧护理差距的偏见。伦理方面的考虑要求关注公平获取、患者隐私以及在医患关系中保留人的因素。患者普遍对人工智能持谨慎乐观的态度,他们认识到人工智能有可能增强护理,但也表达了对数据保护和失去富有同情心的个人护理的风险的担忧。重要的是,人工智能可以帮助“调整”,或使治疗建议符合患者的价值观,并促进可持续和以患者为中心的结果。最终,将人工智能成功整合到日常实践中需要开发人员、临床医生、伦理学家和监管机构之间的多学科合作。利益相关者的深度参与、持续的算法改进和用户友好的设计对于确保人工智能作为一种实用的决策支持工具,补充而不是取代临床专业知识和共同决策至关重要。
{"title":"AI-Assisted Decision-Making for End-Stage Organ Failure: Opportunities and Ethical Concerns.","authors":"John W Haller, Olga D Brazhnik, Kathleen N Fenton","doi":"10.1111/aor.70027","DOIUrl":"https://doi.org/10.1111/aor.70027","url":null,"abstract":"<p><p>AI holds significant promise for guiding clinical decisions in end-stage organ failure, where treatment options now include medical management, transplantation, mechanical support devices, and palliative care. This paper discusses current applications of AI in healthcare, emphasizing the complex decision-making necessary for patients with organ failure. It outlines how AI can support risk stratification, patient selection, and outcome prediction, particularly in transplantation practices that increasingly rely on robust data to inform care pathways. By analyzing large datasets from electronic health records, imaging, and patient-reported outcomes, AI can help physicians forecast long-term survival and quality of life, and potentially assist clinicians in modifying treatment strategies before adverse trajectories take hold. There is a need for standardized, high-quality data, rigorous validation, and transparent algorithms to mitigate biases that could exacerbate disparities in care. Ethical considerations demand attention to equitable access, patient privacy, and the preservation of the human element in patient-clinician relationships. Patients generally view AI with cautious optimism, recognizing its potential to augment care but also voicing concerns about data protection and the risk of losing compassionate, personal care. Importantly, AI can help with \"alignment,\" or fitting treatment recommendations to patients' values, and promote sustainable and patient-centered outcomes. Ultimately, the successful integration of AI into daily practice requires multidisciplinary collaboration among developers, clinicians, ethicists, and regulators. Deep stakeholder engagement, continuous algorithmic refinement, and user-friendly design are pivotal to ensuring that AI serves as a practical decision-support tool that complements, rather than replaces, clinical expertise and shared decision-making.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534318","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Early-Stage Feasibility Testing of a Nutating Disc for Innovative Cardiovascular Applications. 创新心血管应用的旋转盘的早期可行性测试。
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-17 DOI: 10.1111/aor.70051
Gretel Monreal, Steven C Koenig, Joshua G Crane, Mark S Slaughter, David M Lancisi, Robert Mastromattei, Richard K Wampler

Background: Magvad LLC is developing an innovative total artificial heart (TAH) based on a single nutating (nonrotating, "wobbling") disc pump design to provide up to 8 L/min pulsatile flow at 100 mmHg pressure in children and adults with end-stage heart failure (HF). We present an early-stage in vitro study to demonstrate proof-of-concept of a nutating disc mechanism for future cardiovascular applications.

Methods: A commercially available single nutating disc water meter (Recordall, Badger Meter 25-3/4″) was modified and connected to a motor via a shaft coupler and controlled via software to regulate disc "wobbles" per minute. The nutating disc pump was integrated into static and HF-tuned dynamic mock loops and operated at shaft rotational speeds of 25-225 rpm.

Results: Pressure-flow (H-Q) curves demonstrated the pump generated 7 L/min flow at 100 mmHg (225 rpm). Pump flow, motor work, hemodynamic work, and pump efficiency increased with increasing wobble speed. The pump restored hemodynamics in the dynamic HF mock loop by increasing mean arterial flow and pressure, augmenting pulsatility, and decreasing venous pressure with increasing wobble speed.

Conclusions: These results demonstrate proof-of-concept and very early-stage feasibility of a single nutating disc to function as a novel low-speed volume displacement pulsatile flow mechanism for future cardiovascular applications including the development of an innovative TAH.

背景:Magvad LLC正在开发一种创新的全人工心脏(TAH),基于单张动(不旋转,“摆动”)圆盘泵设计,为患有终末期心力衰竭(HF)的儿童和成人在100mmhg压力下提供高达8l /min的脉动流量。我们提出了一项早期的体外研究,以证明未来心血管应用的旋转盘机制的概念验证。方法:将市售的单转盘式水表(Recordall, Badger meter 25-3/4″)进行修改,并通过轴耦合器连接到电机上,通过软件控制以调节每分钟的盘“摆动”。旋转盘式泵被集成到静态和高频调节的动态模拟回路中,并在25-225 rpm的轴转速下运行。结果:压力-流量(H-Q)曲线显示泵在100 mmHg (225 rpm)下产生7 L/min流量。泵流量、马达功、血流动力学功和泵效率随着摆动速度的增加而增加。随着摆动速度的增加,泵通过增加平均动脉流量和压力,增加脉动性,降低静脉压来恢复动态HF模拟环路中的血流动力学。结论:这些结果证明了单个旋转盘作为一种新型低速容积置换脉动流机制的概念验证和非常早期的可行性,可用于未来的心血管应用,包括创新TAH的开发。
{"title":"Early-Stage Feasibility Testing of a Nutating Disc for Innovative Cardiovascular Applications.","authors":"Gretel Monreal, Steven C Koenig, Joshua G Crane, Mark S Slaughter, David M Lancisi, Robert Mastromattei, Richard K Wampler","doi":"10.1111/aor.70051","DOIUrl":"https://doi.org/10.1111/aor.70051","url":null,"abstract":"<p><strong>Background: </strong>Magvad LLC is developing an innovative total artificial heart (TAH) based on a single nutating (nonrotating, \"wobbling\") disc pump design to provide up to 8 L/min pulsatile flow at 100 mmHg pressure in children and adults with end-stage heart failure (HF). We present an early-stage in vitro study to demonstrate proof-of-concept of a nutating disc mechanism for future cardiovascular applications.</p><p><strong>Methods: </strong>A commercially available single nutating disc water meter (Recordall, Badger Meter 25-3/4″) was modified and connected to a motor via a shaft coupler and controlled via software to regulate disc \"wobbles\" per minute. The nutating disc pump was integrated into static and HF-tuned dynamic mock loops and operated at shaft rotational speeds of 25-225 rpm.</p><p><strong>Results: </strong>Pressure-flow (H-Q) curves demonstrated the pump generated 7 L/min flow at 100 mmHg (225 rpm). Pump flow, motor work, hemodynamic work, and pump efficiency increased with increasing wobble speed. The pump restored hemodynamics in the dynamic HF mock loop by increasing mean arterial flow and pressure, augmenting pulsatility, and decreasing venous pressure with increasing wobble speed.</p><p><strong>Conclusions: </strong>These results demonstrate proof-of-concept and very early-stage feasibility of a single nutating disc to function as a novel low-speed volume displacement pulsatile flow mechanism for future cardiovascular applications including the development of an innovative TAH.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Delayed Surgical Closure of Post-Infarct Ventricular Septal Defect With Transaxillary Microaxial Flow Pump Bridging. 经腋窝微轴流泵桥接延迟手术封闭梗死后室间隔缺损。
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-10 DOI: 10.1111/aor.70043
Sarah Madira, Mehran Rahimi, Sophia Roberts-Pyeatte, Aaron Guo, Takuya Wada, John M Lasala, Justin Vader, Jonathan Moreno, Joel Schilling, Michael Pasque, Kunal Kotkar, Muhammad F Masood, Ralph J Damiano, Tsuyoshi Kaneko, Amit Pawale

Background: Ventricular septal defects are catastrophic complications of acute myocardial infarction associated with poor prognosis and high in-hospital mortality. Transaxillary microaxial flow pump (tMAFP) support may provide hemodynamic stabilization and serve as an effective bridge to delayed surgical repair with improved survival outcomes. We aimed to describe perioperative management and outcomes of surgical post-infarct ventricular septal defects (PIVSD) repair with and without tMAFP bridging, hypothesizing that tMAFP support would facilitate delayed repair with favorable operative and survival outcomes.

Methods: We retrospectively reviewed 34 patients diagnosed with PIVSD at a single tertiary center between January 2018 and May 2025, stratified by the use of tMAFP. This report focuses on the surgical repair subgroup, describing perioperative management and outcomes with or without tMAFP bridging.

Results: Of 20 surgical patients, nine were bridged with tMAFP. These patients had a longer stabilization period before repair (median 14 vs. 3 days), shorter cardiopulmonary bypass times, higher preoperative mobility, and no in-hospital mortality, compared with five deaths among 11 patients repaired without tMAFP bridging. None in the tMAFP group required postoperative VA-ECMO, and no device-related complications were observed.

Conclusions: In this retrospective cohort study, tMAFP support allowed delayed surgical repair in PIVSD with favorable perioperative outcomes and survival.

背景:室间隔缺损是急性心肌梗死的灾难性并发症,预后差,住院死亡率高。经腋窝微轴流泵(tMAFP)支持可以提供血流动力学稳定,并作为延迟手术修复的有效桥梁,改善生存结果。我们的目的是描述有和没有tMAFP桥接的梗死后室间隔缺损(PIVSD)手术修复的围手术期管理和结果,假设tMAFP支持可以促进延迟修复,并具有良好的手术和生存结果。方法:我们回顾性分析了2018年1月至2025年5月在单一三级中心诊断为PIVSD的34例患者,按使用tMAFP进行分层。本报告的重点是手术修复亚组,描述围手术期的处理和有无tMAFP桥接的结果。结果:20例手术患者中,9例采用tMAFP桥接。这些患者在修复前有更长的稳定期(中位14天vs. 3天),更短的体外循环时间,更高的术前活动能力,并且没有住院死亡率,而在11例没有tMAFP桥接的修复患者中有5例死亡。tMAFP组无术后VA-ECMO,无器械相关并发症。结论:在这项回顾性队列研究中,tMAFP支持可使PIVSD的延迟手术修复具有良好的围手术期结果和生存率。
{"title":"Delayed Surgical Closure of Post-Infarct Ventricular Septal Defect With Transaxillary Microaxial Flow Pump Bridging.","authors":"Sarah Madira, Mehran Rahimi, Sophia Roberts-Pyeatte, Aaron Guo, Takuya Wada, John M Lasala, Justin Vader, Jonathan Moreno, Joel Schilling, Michael Pasque, Kunal Kotkar, Muhammad F Masood, Ralph J Damiano, Tsuyoshi Kaneko, Amit Pawale","doi":"10.1111/aor.70043","DOIUrl":"https://doi.org/10.1111/aor.70043","url":null,"abstract":"<p><strong>Background: </strong>Ventricular septal defects are catastrophic complications of acute myocardial infarction associated with poor prognosis and high in-hospital mortality. Transaxillary microaxial flow pump (tMAFP) support may provide hemodynamic stabilization and serve as an effective bridge to delayed surgical repair with improved survival outcomes. We aimed to describe perioperative management and outcomes of surgical post-infarct ventricular septal defects (PIVSD) repair with and without tMAFP bridging, hypothesizing that tMAFP support would facilitate delayed repair with favorable operative and survival outcomes.</p><p><strong>Methods: </strong>We retrospectively reviewed 34 patients diagnosed with PIVSD at a single tertiary center between January 2018 and May 2025, stratified by the use of tMAFP. This report focuses on the surgical repair subgroup, describing perioperative management and outcomes with or without tMAFP bridging.</p><p><strong>Results: </strong>Of 20 surgical patients, nine were bridged with tMAFP. These patients had a longer stabilization period before repair (median 14 vs. 3 days), shorter cardiopulmonary bypass times, higher preoperative mobility, and no in-hospital mortality, compared with five deaths among 11 patients repaired without tMAFP bridging. None in the tMAFP group required postoperative VA-ECMO, and no device-related complications were observed.</p><p><strong>Conclusions: </strong>In this retrospective cohort study, tMAFP support allowed delayed surgical repair in PIVSD with favorable perioperative outcomes and survival.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145487552","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Follow-Up of Left-Ventricular Assist Device Patients With Telemonitoring: A National Retrospective Multicentric Study on the Satelia LVAD Web Application. 远程监测左室辅助装置患者的随访:一项关于卫星左室辅助装置Web应用的全国性回顾性多中心研究。
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-08 DOI: 10.1111/aor.70038
Clément Delmas, Anne-Sophie Simoni, Céline Goeminne, Aude Boignard, Anne-Céline Martin, Fabrice Vanhuyse, Erwan Flecher, Catherine Nafeh-Bizet, Romain Itier, Nicolas Pages, Sophie Nisse-Durgeat, Pascal Battistella, Karine Nubret-le-Coniat

Background: Left-ventricular assist devices (LVADs) are a major therapeutic option in advanced heart failure (adHF), improving survival rates and quality of life (QoL). Complications, however, can alter their prognosis. Specialized telemonitoring could facilitate LVAD follow-ups and improve outcomes. This study aimed to evaluate the usefulness of telemonitoring for LVAD patients.

Methods: Patients, followed up with a web application (SateliaLVAD), were included in a national retrospective study at nine tertiary hospitals in France. Characteristics and detected hospitalization risk alerts data were collected. The risk of hospitalization was categorized based on a clinical algorithm (green: no risk, orange: heightened risk, and red: emergent contact with patient and possible hospitalization).

Results: In total, 161 patients were included (male: 82.0%, mean age: 62.2 years). Indications for LVAD were mainly ischemic cardiomyopathy (82.0%) and bridge to transplant (50.3%). The mean follow-up duration lasted 19.9 [1-45] months with 76 (47.2%) patients continuing telemonitoring. Compliance was high (79.0%). The main reason for cessation was death (30.6%). Total hospitalization risk alerts detected by telemonitoring were: orange alerts (n = 8265, 72.3%) and red alerts (n = 1613, 14.1%) with 48.5% of cases resolved (orange: 50.8% vs. red: 54.8%). The most frequent type of resolved alert was for a measured risk of cardiac decompensation (orange: 2227 vs. red: 382).

Conclusion: To our knowledge, this is the first extensive study to describe the follow-up of LVAD patients by a dedicated telemonitoring application. Telemonitoring as a specific follow-up tool may be feasible for this subpopulation. Future randomized studies on specific prospective evaluations such as survival and QoL are needed.

背景:左心室辅助装置(lvad)是晚期心力衰竭(adHF)的主要治疗选择,可提高生存率和生活质量(QoL)。然而,并发症可以改变他们的预后。专门的远程监测可以促进LVAD的随访并改善结果。本研究旨在评估远程监护对LVAD患者的有用性。方法:采用SateliaLVAD网络应用程序对法国9家三级医院的患者进行回顾性研究。收集特征和检测到的住院风险警报数据。根据临床算法对住院风险进行分类(绿色:无风险,橙色:风险增加,红色:紧急接触患者并可能住院)。结果:共纳入161例患者,其中男性占82.0%,平均年龄62.2岁。LVAD的适应症主要为缺血性心肌病(82.0%)和移植桥(50.3%)。平均随访时间为19.9[1-45]个月,76例(47.2%)患者继续远程监测。依从性高(79.0%)。戒烟的主要原因是死亡(30.6%)。远程监控检测到的住院风险警报总数为:橙色警报(n = 8265, 72.3%)和红色警报(n = 1613, 14.1%),其中48.5%的病例得到解决(橙色:50.8%,红色:54.8%)。最常见的预警类型是测量心脏失代偿风险(橙色:2227,红色:382)。结论:据我们所知,这是第一个通过专门的远程监测应用来描述LVAD患者随访的广泛研究。远程监测作为一种特殊的随访工具对这一人群可能是可行的。未来需要对具体的前瞻性评估(如生存和生活质量)进行随机研究。
{"title":"Follow-Up of Left-Ventricular Assist Device Patients With Telemonitoring: A National Retrospective Multicentric Study on the Satelia LVAD Web Application.","authors":"Clément Delmas, Anne-Sophie Simoni, Céline Goeminne, Aude Boignard, Anne-Céline Martin, Fabrice Vanhuyse, Erwan Flecher, Catherine Nafeh-Bizet, Romain Itier, Nicolas Pages, Sophie Nisse-Durgeat, Pascal Battistella, Karine Nubret-le-Coniat","doi":"10.1111/aor.70038","DOIUrl":"https://doi.org/10.1111/aor.70038","url":null,"abstract":"<p><strong>Background: </strong>Left-ventricular assist devices (LVADs) are a major therapeutic option in advanced heart failure (adHF), improving survival rates and quality of life (QoL). Complications, however, can alter their prognosis. Specialized telemonitoring could facilitate LVAD follow-ups and improve outcomes. This study aimed to evaluate the usefulness of telemonitoring for LVAD patients.</p><p><strong>Methods: </strong>Patients, followed up with a web application (SateliaLVAD), were included in a national retrospective study at nine tertiary hospitals in France. Characteristics and detected hospitalization risk alerts data were collected. The risk of hospitalization was categorized based on a clinical algorithm (green: no risk, orange: heightened risk, and red: emergent contact with patient and possible hospitalization).</p><p><strong>Results: </strong>In total, 161 patients were included (male: 82.0%, mean age: 62.2 years). Indications for LVAD were mainly ischemic cardiomyopathy (82.0%) and bridge to transplant (50.3%). The mean follow-up duration lasted 19.9 [1-45] months with 76 (47.2%) patients continuing telemonitoring. Compliance was high (79.0%). The main reason for cessation was death (30.6%). Total hospitalization risk alerts detected by telemonitoring were: orange alerts (n = 8265, 72.3%) and red alerts (n = 1613, 14.1%) with 48.5% of cases resolved (orange: 50.8% vs. red: 54.8%). The most frequent type of resolved alert was for a measured risk of cardiac decompensation (orange: 2227 vs. red: 382).</p><p><strong>Conclusion: </strong>To our knowledge, this is the first extensive study to describe the follow-up of LVAD patients by a dedicated telemonitoring application. Telemonitoring as a specific follow-up tool may be feasible for this subpopulation. Future randomized studies on specific prospective evaluations such as survival and QoL are needed.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.3,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145470287","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison of the Construction Methods of Parathyroid Organoids and Functional Influence of Calcium on Organoids. 甲状旁腺类器官构建方法的比较及钙对类器官功能的影响。
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-01 Epub Date: 2025-07-05 DOI: 10.1111/aor.15048
Chuanbo Xu, Huajiang Liu, Jiantao She, Tao Xu, Yuan Zhou, Xuebo Yan, Tiangang Li, Bin Dai

Objective: This study aimed to determine the more suitable method for constructing parathyroid organoids.

Methods: Parathyroid organoids were established using two different culture conditions, and organoid morphology and ATP activity were assessed to evaluate their performance. Organoid identity and function were confirmed by STR profiling, histology, immunofluorescence, and ELISA. Organoids were further treated with different calcium concentrations, and changes in morphology, ATP activity, intracellular calcium, CaSR expression, and PTH secretion were examined.

Results: Organoids cultured in VEGF-121- and angiotensin-negative medium showed no noticeable morphological change from Day 1 to Day 3, and ATP activity declined over the same period. In contrast, organoids in VEGF-121+ and angiotensin-positive medium exhibited increased number and ATP activity over the same period. These organoids shared the same mutation profile and structural features as the original tissues and expressed PTH, GCM2, CaSR, and CHGA. PTH secretion remained stable across passages. Low calcium had minimal impact on morphology, viability, and PTH release but reduced intracellular calcium levels and CaSR expression. High calcium promoted ATP activity and elevated intracellular calcium, while suppressing PTH secretion and upregulating CaSR expression.

Conclusions: VEGF-121+ and angiotensin-positive medium better supported the generation and maintenance of functional parathyroid organoids. This provides an in vitro model for further investigation into parathyroid-related signaling and applications in regenerative medicine.

目的:探讨构建甲状旁腺类器官的合适方法。方法:在两种不同的培养条件下建立甲状旁腺类器官,并对类器官形态和ATP活性进行评价。通过STR分析、组织学、免疫荧光和ELISA证实了类器官的身份和功能。进一步用不同钙浓度处理类器官,观察其形态学、ATP活性、细胞内钙、CaSR表达和甲状旁腺激素分泌的变化。结果:在VEGF-121和血管紧张素阴性培养基中培养的类器官从第1天到第3天没有明显的形态学变化,ATP活性在同一时期下降。相比之下,VEGF-121+和血管紧张素阳性培养基中的类器官在同一时期表现出增加的数量和ATP活性。这些类器官与原始组织具有相同的突变谱和结构特征,表达PTH、GCM2、CaSR和CHGA。甲状旁腺激素分泌保持稳定。低钙对形态、活力和甲状旁腺激素释放的影响最小,但降低了细胞内钙水平和CaSR表达。高钙促进ATP活性和细胞内钙升高,抑制PTH分泌,上调CaSR表达。结论:VEGF-121+和血管紧张素阳性培养基能更好地支持功能性甲状旁腺类器官的生成和维持。这为进一步研究甲状旁腺相关信号传导及其在再生医学中的应用提供了体外模型。
{"title":"Comparison of the Construction Methods of Parathyroid Organoids and Functional Influence of Calcium on Organoids.","authors":"Chuanbo Xu, Huajiang Liu, Jiantao She, Tao Xu, Yuan Zhou, Xuebo Yan, Tiangang Li, Bin Dai","doi":"10.1111/aor.15048","DOIUrl":"10.1111/aor.15048","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to determine the more suitable method for constructing parathyroid organoids.</p><p><strong>Methods: </strong>Parathyroid organoids were established using two different culture conditions, and organoid morphology and ATP activity were assessed to evaluate their performance. Organoid identity and function were confirmed by STR profiling, histology, immunofluorescence, and ELISA. Organoids were further treated with different calcium concentrations, and changes in morphology, ATP activity, intracellular calcium, CaSR expression, and PTH secretion were examined.</p><p><strong>Results: </strong>Organoids cultured in VEGF-121- and angiotensin-negative medium showed no noticeable morphological change from Day 1 to Day 3, and ATP activity declined over the same period. In contrast, organoids in VEGF-121+ and angiotensin-positive medium exhibited increased number and ATP activity over the same period. These organoids shared the same mutation profile and structural features as the original tissues and expressed PTH, GCM2, CaSR, and CHGA. PTH secretion remained stable across passages. Low calcium had minimal impact on morphology, viability, and PTH release but reduced intracellular calcium levels and CaSR expression. High calcium promoted ATP activity and elevated intracellular calcium, while suppressing PTH secretion and upregulating CaSR expression.</p><p><strong>Conclusions: </strong>VEGF-121+ and angiotensin-positive medium better supported the generation and maintenance of functional parathyroid organoids. This provides an in vitro model for further investigation into parathyroid-related signaling and applications in regenerative medicine.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":"1623-1632"},"PeriodicalIF":2.3,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144566950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dobutamine Use in Patients With Extracorporeal Cardiopulmonary Resuscitation Following Out-of-Hospital Cardiac Arrest: A Secondary Analysis of the SAVE-J II Study. 院外心脏骤停后体外心肺复苏患者多巴酚丁胺的使用:SAVE-J II研究的二次分析
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-01 Epub Date: 2025-07-03 DOI: 10.1111/aor.15055
Tasuku Hada, Toru Hifumi, Hiromu Okano, Kasumi Shirasaki, Shutaro Isokawa, Akihiko Inoue, Tetsuya Sakamoto, Yasuhiro Kuroda, Norio Otani

Background: The effects of dobutamine on outcomes in patients experiencing out-of-hospital cardiac arrest (OHCA), treated with extracorporeal cardiopulmonary resuscitation (ECPR), remain unclear. In this study, we aimed to evaluate the association between dobutamine use within 24 h and clinical outcomes in patients with OHCA who underwent ECPR.

Methods: A post hoc analysis was conducted on the registry data from the SAVE-J II study (2013-2018). To address potential confounding variables related to dobutamine administration, 1:3 propensity score matching was employed using the patients' baseline characteristics. Following the matching, the dobutamine and non-dobutamine groups were compared, focusing on in-hospital mortality and neurological outcomes assessed using the cerebral performance category (CPC) scale.

Results: Of the 2157 registered cases, 581 cases of cardiogenic OHCA treated with targeted temperature management were included in this analysis. Eighty-eight patients who received dobutamine were compared with 264 who did not after propensity score matching. The in-hospital mortality rate was 60.2% in the dobutamine group, compared with 58.3% in the non-dobutamine group (p = 0.80). The proportion of patients with a CPC score of 3-5 at hospital discharge was 79.5% in the dobutamine group, compared with 78.0% in the non-dobutamine group (p = 0.88). A Kaplan-Meier analysis demonstrated no significant differences in survival rates between the two groups (42.1 vs. 43.6%, log-rank p = 0.79).

Conclusion: In patients with OHCA who underwent ECPR, dobutamine administration within 24 h was not significantly associated with in-hospital mortality and neurological outcomes.

背景:多巴酚丁胺对院外心脏骤停(OHCA)患者经体外心肺复苏(ECPR)治疗后预后的影响尚不清楚。在这项研究中,我们旨在评估接受ECPR的OHCA患者24小时内多巴酚丁胺使用与临床结果之间的关系。方法:对SAVE-J II研究(2013-2018)的注册表数据进行事后分析。为了解决与多巴酚丁胺给药相关的潜在混杂变量,采用1:3倾向评分匹配患者的基线特征。匹配后,比较多巴酚丁胺组和非多巴酚丁胺组,重点关注住院死亡率和使用脑功能类别(CPC)量表评估的神经预后。结果:在2157例登记病例中,581例心源性OHCA经靶向温度管理纳入本分析。在倾向评分匹配后,88名接受多巴酚丁胺治疗的患者与264名未接受多巴酚丁胺治疗的患者进行比较。多巴酚丁胺组住院死亡率为60.2%,而非多巴酚丁胺组为58.3% (p = 0.80)。多巴酚丁胺组CPC评分为3-5分的患者出院比例为79.5%,而非多巴酚丁胺组为78.0% (p = 0.88)。Kaplan-Meier分析显示两组患者的生存率无显著差异(42.1 vs 43.6%, log-rank p = 0.79)。结论:在接受ECPR的OHCA患者中,24小时内给药多巴酚丁胺与住院死亡率和神经系统预后无显著相关性。
{"title":"Dobutamine Use in Patients With Extracorporeal Cardiopulmonary Resuscitation Following Out-of-Hospital Cardiac Arrest: A Secondary Analysis of the SAVE-J II Study.","authors":"Tasuku Hada, Toru Hifumi, Hiromu Okano, Kasumi Shirasaki, Shutaro Isokawa, Akihiko Inoue, Tetsuya Sakamoto, Yasuhiro Kuroda, Norio Otani","doi":"10.1111/aor.15055","DOIUrl":"10.1111/aor.15055","url":null,"abstract":"<p><strong>Background: </strong>The effects of dobutamine on outcomes in patients experiencing out-of-hospital cardiac arrest (OHCA), treated with extracorporeal cardiopulmonary resuscitation (ECPR), remain unclear. In this study, we aimed to evaluate the association between dobutamine use within 24 h and clinical outcomes in patients with OHCA who underwent ECPR.</p><p><strong>Methods: </strong>A post hoc analysis was conducted on the registry data from the SAVE-J II study (2013-2018). To address potential confounding variables related to dobutamine administration, 1:3 propensity score matching was employed using the patients' baseline characteristics. Following the matching, the dobutamine and non-dobutamine groups were compared, focusing on in-hospital mortality and neurological outcomes assessed using the cerebral performance category (CPC) scale.</p><p><strong>Results: </strong>Of the 2157 registered cases, 581 cases of cardiogenic OHCA treated with targeted temperature management were included in this analysis. Eighty-eight patients who received dobutamine were compared with 264 who did not after propensity score matching. The in-hospital mortality rate was 60.2% in the dobutamine group, compared with 58.3% in the non-dobutamine group (p = 0.80). The proportion of patients with a CPC score of 3-5 at hospital discharge was 79.5% in the dobutamine group, compared with 78.0% in the non-dobutamine group (p = 0.88). A Kaplan-Meier analysis demonstrated no significant differences in survival rates between the two groups (42.1 vs. 43.6%, log-rank p = 0.79).</p><p><strong>Conclusion: </strong>In patients with OHCA who underwent ECPR, dobutamine administration within 24 h was not significantly associated with in-hospital mortality and neurological outcomes.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":"1688-1698"},"PeriodicalIF":2.3,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144551821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Novel Numerical Study on the Development and Implementation of a Physiological Control Strategy for HeartMate 3 LVAD. 心脏伴侣3型LVAD生理控制策略开发与实现的数值研究。
IF 2.3 3区 医学 Q3 ENGINEERING, BIOMEDICAL Pub Date : 2025-11-01 Epub Date: 2025-08-21 DOI: 10.1111/aor.15052
Amin Khorshid Savar, Fang Chen, Yunzhang Cheng

Purpose: With the rising prevalence of heart disease and the limited availability of heart transplants, the demand for Left Ventricular Assist Devices (LVADs) is growing. While LVADs significantly improve the quality of life for heart failure patients, conventional models operate at a fixed speed, failing to adapt to varying blood flow demands. The Power Ratio Control (PRC) method offers a promising approach to adjusting blood flow according to activity levels dynamically, improving LVAD adaptability. This research investigates the application of PRC to enhance LVAD performance.

Method: To the best of our knowledge, this study presents the first implementation of PRC on the HeartMate 3. We also develop a model to incorporate clinically relevant parameters and peripheral components into an advanced model. This framework simulates real-world conditions, integrating dynamic factors like preload, contractility, and heart rate variations to evaluate the device's performance.

Results: Results show that PRC significantly improves HeartMate 3's dynamic response to physiological changes, allowing it to mimic the behavior of a healthy heart closely. Under PRC, the LVAD achieves better fluid responsiveness, stable cardiac output (CO), and efficient adaptation to varying activity levels. These findings highlight the potential clinical benefits of PRC, offering a more personalized approach to heart failure management.

Conclusion: This research represents a significant advancement in LVAD technology, pioneering the use of PRC in the HeartMate 3 and enhancing modeling accuracy. These innovations underscore the potential for adaptive control strategies to improve LVAD performance, paving the way for broader future advancements in mechanical circulatory support.

目的:随着心脏病患病率的上升和心脏移植的有限可用性,对左心室辅助装置(lvad)的需求正在增长。虽然lvad显著改善了心力衰竭患者的生活质量,但传统的模式运行速度固定,无法适应不断变化的血流需求。功率比控制(PRC)方法提供了一种很有前途的方法,可以根据活动水平动态调节血流,提高LVAD的适应性。本研究探讨了PRC在LVAD性能提升中的应用。方法:据我们所知,本研究首次在HeartMate 3上实现了PRC。我们还开发了一个模型,将临床相关参数和外围成分纳入一个先进的模型。该框架模拟了现实世界的条件,整合了预负荷、收缩力和心率变化等动态因素,以评估设备的性能。结果:PRC显著改善了HeartMate 3对生理变化的动态反应,使其能够接近健康心脏的行为。在PRC下,LVAD获得更好的液体反应,稳定的心输出量(CO),以及对不同活动水平的有效适应。这些发现强调了PRC的潜在临床益处,为心力衰竭管理提供了更个性化的方法。结论:本研究代表了LVAD技术的重大进步,开创了PRC在HeartMate 3中的应用,并提高了建模精度。这些创新强调了自适应控制策略提高LVAD性能的潜力,为机械循环支持的更广泛未来发展铺平了道路。
{"title":"A Novel Numerical Study on the Development and Implementation of a Physiological Control Strategy for HeartMate 3 LVAD.","authors":"Amin Khorshid Savar, Fang Chen, Yunzhang Cheng","doi":"10.1111/aor.15052","DOIUrl":"10.1111/aor.15052","url":null,"abstract":"<p><strong>Purpose: </strong>With the rising prevalence of heart disease and the limited availability of heart transplants, the demand for Left Ventricular Assist Devices (LVADs) is growing. While LVADs significantly improve the quality of life for heart failure patients, conventional models operate at a fixed speed, failing to adapt to varying blood flow demands. The Power Ratio Control (PRC) method offers a promising approach to adjusting blood flow according to activity levels dynamically, improving LVAD adaptability. This research investigates the application of PRC to enhance LVAD performance.</p><p><strong>Method: </strong>To the best of our knowledge, this study presents the first implementation of PRC on the HeartMate 3. We also develop a model to incorporate clinically relevant parameters and peripheral components into an advanced model. This framework simulates real-world conditions, integrating dynamic factors like preload, contractility, and heart rate variations to evaluate the device's performance.</p><p><strong>Results: </strong>Results show that PRC significantly improves HeartMate 3's dynamic response to physiological changes, allowing it to mimic the behavior of a healthy heart closely. Under PRC, the LVAD achieves better fluid responsiveness, stable cardiac output (CO), and efficient adaptation to varying activity levels. These findings highlight the potential clinical benefits of PRC, offering a more personalized approach to heart failure management.</p><p><strong>Conclusion: </strong>This research represents a significant advancement in LVAD technology, pioneering the use of PRC in the HeartMate 3 and enhancing modeling accuracy. These innovations underscore the potential for adaptive control strategies to improve LVAD performance, paving the way for broader future advancements in mechanical circulatory support.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":"1633-1641"},"PeriodicalIF":2.3,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144940443","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Artificial organs
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1