In patients with left ventricular assist device (LVAD), concomitant mechanical valve is contraindicated for fear of thromboembolism. It is recommended that mechanical valves be replaced with biological valves or that mechanical valves be permanently closed when LVAD is indicated. Recently, a novel mechanical valve has proven safety in terms of valve thrombosis or thromboembolism in patients with valvular disease, though limited data is available regarding the performance of the valve in patients receiving LVAD therapy. In this report, we describe a case of successful bridge with extracorporeal LVAD to durable LVAD therapy without thromboembolism for postoperative cardiogenic shock after aortic root replacement using an On-X mechanical valve.
{"title":"Successful bridge with extracorporeal left ventricular assist device in a patient with aortic mechanical valve prosthesis.","authors":"Yusuke Misumi, Daisuke Yoshioka, Takuji Kawamura, Ai Kawamura, Shin Yajima, Shunsuke Saito, Shigeru Miyagawa","doi":"10.1007/s10047-025-01530-x","DOIUrl":"10.1007/s10047-025-01530-x","url":null,"abstract":"<p><p>In patients with left ventricular assist device (LVAD), concomitant mechanical valve is contraindicated for fear of thromboembolism. It is recommended that mechanical valves be replaced with biological valves or that mechanical valves be permanently closed when LVAD is indicated. Recently, a novel mechanical valve has proven safety in terms of valve thrombosis or thromboembolism in patients with valvular disease, though limited data is available regarding the performance of the valve in patients receiving LVAD therapy. In this report, we describe a case of successful bridge with extracorporeal LVAD to durable LVAD therapy without thromboembolism for postoperative cardiogenic shock after aortic root replacement using an On-X mechanical valve.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"10"},"PeriodicalIF":1.3,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145549527","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-14DOI: 10.1007/s10047-025-01535-6
Mahmut Yesin, Macit Kalçık, Emrah Bayam, Ahmet Güner, Mustafa Ozan Gürsoy, Semih Kalkan, Sabahattin Gündüz, Mehmet Özkan
Genetic and numerous epidemiologic studies have identified lipoprotein (a) [Lp(a)] as a risk factor for atherothrombotic diseases. The structure of Lp(a) is similar to plasminogen and tissue plasminogen activator and it competes with plasminogen for its binding site, leading to reduced fibrinolysis. Furthermore, since Lp(a) stimulates the secretion of plasminogen activator inhibitor-1, it may lead to thrombogenesis. In this cross-sectional study, we aimed to investigate Lp(a) levels in patients with mechanical prosthetic valve thrombosis (MPVT). Blood samples for Lp(a) determination were obtained from 80 MPVT patients (median age: 48.5 (39-59.75) years; 47 male) and 75 age and sex matched controls (median age: 52 (39-63) years; 44 male) with normally functioning mechanical prosthetic valves. The Lp(a) levels in the PVT group were significantly higher than in the controls [22(16.2-39.4) vs. 6.9(2.9-24.6) mg/dL, p < 0.001]. Elevated Lp(a) levels, recent history of subtherapeutic anticoagulation, history of cerebrovascular accidents (CVA) and a low value of international normalized ratio on admission were found to be the independent predictors of PVT. Lp(a) levels above 19.6 mg/dL predicted PVT with a sensitivity of 65% and a specificity of 71% (AUC:0.767; 95%CI: 0.687 to 0.847; p < 0.001). Lp(a) levels were significantly higher in PVT patients with a history of CVA [42.0 (23.6-53.6) vs. 21.1 (16.1- 36.2) mg/dL, p = 0.012]. Elevated Lp(a) levels may be associated with MPVT. The assessment of plasma Lp(a) levels in patients with prosthetic heart valves may provide additive information regarding the risk of PVT and CVA.
遗传学和许多流行病学研究已经确定脂蛋白(a) [Lp(a)]是动脉粥样硬化性血栓疾病的危险因素。Lp(a)的结构与纤溶酶原和组织纤溶酶原激活剂相似,与纤溶酶原竞争结合位点,导致纤溶酶减少。此外,由于Lp(a)刺激纤溶酶原激活物抑制剂-1的分泌,它可能导致血栓形成。在这项横断面研究中,我们旨在研究机械性人工瓣膜血栓形成(MPVT)患者的Lp(a)水平。80例MPVT患者(中位年龄:48.5(39-59.75)岁;47名男性)和75名年龄和性别匹配的对照组(中位年龄:52(39-63)岁;44名男性)带有功能正常的机械假体瓣膜。PVT组Lp(a)水平显著高于对照组[22(16.2-39.4)vs. 6.9(2.9-24.6) mg/dL, p < 0.001]。Lp(a)水平升高、近期亚治疗抗凝史、脑血管意外史和入院时国际标准化比值低值是PVT的独立预测因素,Lp(a)水平高于19.6 mg/dL预测PVT的敏感性为65%,特异性为71% (AUC:0.767; 95%CI: 0.687 ~ 0.847; p < 0.001)。有CVA病史的PVT患者Lp(a)水平明显较高[42.0 (23.6-53.6)vs. 21.1 (16.1- 36.2) mg/dL, p = 0.012]。Lp(a)水平升高可能与MPVT有关。人工心脏瓣膜患者血浆Lp(a)水平的评估可以提供关于PVT和CVA风险的附加信息。
{"title":"Lipoprotein (a) as a risk factor for prosthetic heart valve thrombosis.","authors":"Mahmut Yesin, Macit Kalçık, Emrah Bayam, Ahmet Güner, Mustafa Ozan Gürsoy, Semih Kalkan, Sabahattin Gündüz, Mehmet Özkan","doi":"10.1007/s10047-025-01535-6","DOIUrl":"https://doi.org/10.1007/s10047-025-01535-6","url":null,"abstract":"<p><p>Genetic and numerous epidemiologic studies have identified lipoprotein (a) [Lp(a)] as a risk factor for atherothrombotic diseases. The structure of Lp(a) is similar to plasminogen and tissue plasminogen activator and it competes with plasminogen for its binding site, leading to reduced fibrinolysis. Furthermore, since Lp(a) stimulates the secretion of plasminogen activator inhibitor-1, it may lead to thrombogenesis. In this cross-sectional study, we aimed to investigate Lp(a) levels in patients with mechanical prosthetic valve thrombosis (MPVT). Blood samples for Lp(a) determination were obtained from 80 MPVT patients (median age: 48.5 (39-59.75) years; 47 male) and 75 age and sex matched controls (median age: 52 (39-63) years; 44 male) with normally functioning mechanical prosthetic valves. The Lp(a) levels in the PVT group were significantly higher than in the controls [22(16.2-39.4) vs. 6.9(2.9-24.6) mg/dL, p < 0.001]. Elevated Lp(a) levels, recent history of subtherapeutic anticoagulation, history of cerebrovascular accidents (CVA) and a low value of international normalized ratio on admission were found to be the independent predictors of PVT. Lp(a) levels above 19.6 mg/dL predicted PVT with a sensitivity of 65% and a specificity of 71% (AUC:0.767; 95%CI: 0.687 to 0.847; p < 0.001). Lp(a) levels were significantly higher in PVT patients with a history of CVA [42.0 (23.6-53.6) vs. 21.1 (16.1- 36.2) mg/dL, p = 0.012]. Elevated Lp(a) levels may be associated with MPVT. The assessment of plasma Lp(a) levels in patients with prosthetic heart valves may provide additive information regarding the risk of PVT and CVA.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"7"},"PeriodicalIF":1.3,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145522757","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-14DOI: 10.1007/s10047-025-01538-3
Maria Yamamoto, Shin Yajima, Takuji Kawamura, Daisuke Yoshioka, Ai Kawamura, Yusuke Misumi, Shunsuke Saito, Takashi Yamauchi, Shigeru Miyagawa
Herein, we present the case of a 23-year-old woman with fulminant myocarditis that led to severe biventricular failure and cardiogenic shock. Despite high-dose inotropes and mechanical support with venoarterial extracorporeal membrane oxygenation plus and Impella CP, the patient's cardiac function did not recover. After upgrading to extracorporeal left ventricular assist device support, persistent right heart failure prevented weaning off venoarterial extracorporeal membrane oxygenation. Chest computed tomography revealed a leftward ascending aorta, prompting left mini-thoracotomy for extracorporeal biventricular assist device surgery, thereby preserving the sternum. Perioperatively, a large aortic thrombus was discovered and removed under deep hypothermic circulatory arrest. An extracorporeal left ventricular assist device was established by draining the left ventricle and perfusing the ascending aorta via the subxiphoid area, whereas the right ventricular assist device was drained from the right subclavian vein into the pulmonary outflow graft through the left second intercostal space. Ultimately, the patient underwent durable left ventricular assist device implantation with concurrent extracorporeal right ventricular assist device support via sternotomy. Preserving the sternum offers several advantages including reduced adhesion and simpler subsequent open procedures. Our experience indicates that extracorporeal biventricular assist device surgery through a left mini-thoracotomy is a viable option for selecting patients, particularly if future sternotomy is anticipated.
{"title":"Extracorporeal biventricular support through left mini-thoracotomy.","authors":"Maria Yamamoto, Shin Yajima, Takuji Kawamura, Daisuke Yoshioka, Ai Kawamura, Yusuke Misumi, Shunsuke Saito, Takashi Yamauchi, Shigeru Miyagawa","doi":"10.1007/s10047-025-01538-3","DOIUrl":"https://doi.org/10.1007/s10047-025-01538-3","url":null,"abstract":"<p><p>Herein, we present the case of a 23-year-old woman with fulminant myocarditis that led to severe biventricular failure and cardiogenic shock. Despite high-dose inotropes and mechanical support with venoarterial extracorporeal membrane oxygenation plus and Impella CP, the patient's cardiac function did not recover. After upgrading to extracorporeal left ventricular assist device support, persistent right heart failure prevented weaning off venoarterial extracorporeal membrane oxygenation. Chest computed tomography revealed a leftward ascending aorta, prompting left mini-thoracotomy for extracorporeal biventricular assist device surgery, thereby preserving the sternum. Perioperatively, a large aortic thrombus was discovered and removed under deep hypothermic circulatory arrest. An extracorporeal left ventricular assist device was established by draining the left ventricle and perfusing the ascending aorta via the subxiphoid area, whereas the right ventricular assist device was drained from the right subclavian vein into the pulmonary outflow graft through the left second intercostal space. Ultimately, the patient underwent durable left ventricular assist device implantation with concurrent extracorporeal right ventricular assist device support via sternotomy. Preserving the sternum offers several advantages including reduced adhesion and simpler subsequent open procedures. Our experience indicates that extracorporeal biventricular assist device surgery through a left mini-thoracotomy is a viable option for selecting patients, particularly if future sternotomy is anticipated.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"5"},"PeriodicalIF":1.3,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145522619","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-14DOI: 10.1007/s10047-025-01529-4
Julia K Kaniuk, Yudai Miyashita, Amanda Kamar, Taisuke Kaiho, Matthew J Schipma, Chitaru Kurihara
Bridging critically ill patients to lung transplantation with veno-venous extracorporeal membrane oxygenation (VV-ECMO) may increase infection risk, yet its impact on post-transplant outcomes remains unclear. We evaluated the incidence, timing, and risk factors for respiratory and bloodstream infections in patients supported with pre-operative VV-ECMO and assessed one-year survival. We conducted a retrospective cohort study of 293 adult lung transplant recipients at a single center between January 2018 and June 2023. Thirty-seven patients received pre-transplant VV-ECMO, and 256 did not. We compared the incidence and median time to first respiratory and bloodstream infections and estimated one-year survival. Cox proportional hazard models identified independent predictors of infection. VV-ECMO patients were younger (median 53.0 vs 63.0 years) and more often underwent bilateral transplantation for acute respiratory distress syndrome. Respiratory infections occurred in 64.9% of the VV-ECMO group versus 56.6% of controls (p = 0.38), with a shorter median time to first respiratory infection (8 vs 63 days). Bacterial bloodstream infections were more frequent after VV-ECMO (18.9% vs 6.3%, p = 0.016) and occurred earlier (99 vs 162 days). In multivariate analysis, VV-ECMO independently predicted bloodstream infection (HR 2.36, 95% CI 1.00-5.53; p = 0.049) but not a respiratory infection. One-year survival was equivalent (81.1% vs 89.8%; p = 0.16). Pre-transplant VV-ECMO is associated with earlier and increased bloodstream infections but does not compromise one-year survival, supporting its continued use as a bridge to lung transplantation.
通过静脉-静脉体外膜氧合(VV-ECMO)桥接危重患者进行肺移植可能会增加感染风险,但其对移植后预后的影响尚不清楚。我们评估了术前VV-ECMO患者呼吸道和血液感染的发生率、时间和危险因素,并评估了一年生存率。我们于2018年1月至2023年6月在单个中心对293名成人肺移植受者进行了回顾性队列研究。37例患者接受了移植前VV-ECMO, 256例未接受。我们比较了首次呼吸道和血液感染的发生率和中位时间,并估计了一年的生存期。Cox比例风险模型确定了感染的独立预测因子。VV-ECMO患者更年轻(中位年龄为53.0岁vs 63.0岁),更常因急性呼吸窘迫综合征接受双侧移植。VV-ECMO组发生呼吸道感染的比例为64.9%,对照组为56.6% (p = 0.38),首次呼吸道感染的中位时间较短(8天对63天)。VV-ECMO后细菌性血流感染更频繁(18.9% vs 6.3%, p = 0.016),发生时间更早(99 vs 162天)。在多变量分析中,VV-ECMO独立预测血流感染(HR 2.36, 95% CI 1.00-5.53; p = 0.049),但不能预测呼吸道感染。一年生存率相等(81.1% vs 89.8%; p = 0.16)。移植前VV-ECMO与早期和增加的血流感染相关,但不影响一年生存率,支持其继续作为肺移植的桥梁。
{"title":"Impact of pre-transplant veno-venous extracorporeal membrane oxygenation on post-lung transplant infections.","authors":"Julia K Kaniuk, Yudai Miyashita, Amanda Kamar, Taisuke Kaiho, Matthew J Schipma, Chitaru Kurihara","doi":"10.1007/s10047-025-01529-4","DOIUrl":"10.1007/s10047-025-01529-4","url":null,"abstract":"<p><p>Bridging critically ill patients to lung transplantation with veno-venous extracorporeal membrane oxygenation (VV-ECMO) may increase infection risk, yet its impact on post-transplant outcomes remains unclear. We evaluated the incidence, timing, and risk factors for respiratory and bloodstream infections in patients supported with pre-operative VV-ECMO and assessed one-year survival. We conducted a retrospective cohort study of 293 adult lung transplant recipients at a single center between January 2018 and June 2023. Thirty-seven patients received pre-transplant VV-ECMO, and 256 did not. We compared the incidence and median time to first respiratory and bloodstream infections and estimated one-year survival. Cox proportional hazard models identified independent predictors of infection. VV-ECMO patients were younger (median 53.0 vs 63.0 years) and more often underwent bilateral transplantation for acute respiratory distress syndrome. Respiratory infections occurred in 64.9% of the VV-ECMO group versus 56.6% of controls (p = 0.38), with a shorter median time to first respiratory infection (8 vs 63 days). Bacterial bloodstream infections were more frequent after VV-ECMO (18.9% vs 6.3%, p = 0.016) and occurred earlier (99 vs 162 days). In multivariate analysis, VV-ECMO independently predicted bloodstream infection (HR 2.36, 95% CI 1.00-5.53; p = 0.049) but not a respiratory infection. One-year survival was equivalent (81.1% vs 89.8%; p = 0.16). Pre-transplant VV-ECMO is associated with earlier and increased bloodstream infections but does not compromise one-year survival, supporting its continued use as a bridge to lung transplantation.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"6"},"PeriodicalIF":1.3,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12618338/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145522802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The relationship between the physical activity status of patients with left ventricular assist devices (LVAD) and their quality of life (QOL) remains unclear. The aim of this study was to determine the association between physical activity status and QOL and to identify the factors influencing walking activity time in LVAD patients. Thirty outpatients with LVAD were included. Physical activity was measured using a triaxial accelerometer. QOL was assessed using the Kansas City Cardiomyopathy Questionnaire (KCCQ). Multiple regression analysis was used to examine the relationship between QOL and activity duration. Physical activity measurement revealed that sedentary behavior of 1.5 metabolic equivalents or less accounted for 72.6% of total activity time. The KCCQ was positively correlated with walking activity time (r = 0.60, p = 0.0005), but not with daily activity time (r = 0.12, p = 0.55). Regression analysis revealed that regular employment (p = 0.0013), low depression score (p = 0.0005), low C-reactive protein level (p = 0.016), and high peak oxygen uptake (p = 0.019) was associated with increased walking activity time. LVAD patients had low physical activity, and walking activity time was significantly associated with their QOL. Comprehensive management may play an important role in improving the QOL in LVAD patients.
左心室辅助装置(LVAD)患者的身体活动状况与生活质量(QOL)之间的关系尚不清楚。本研究的目的是确定身体活动状况与生活质量之间的关系,并确定影响LVAD患者步行活动时间的因素。纳入30例LVAD门诊患者。使用三轴加速度计测量身体活动。使用堪萨斯城心肌病问卷(KCCQ)评估生活质量。采用多元回归分析,考察生活质量与活动持续时间的关系。身体活动测量显示,1.5代谢当量或更少的久坐行为占总活动时间的72.6%。KCCQ与步行活动时间呈正相关(r = 0.60, p = 0.0005),与日常活动时间不相关(r = 0.12, p = 0.55)。回归分析显示,正常工作(p = 0.0013)、低抑郁评分(p = 0.0005)、低c反应蛋白水平(p = 0.016)和高峰值摄氧量(p = 0.019)与步行活动时间的增加有关。LVAD患者体力活动较低,步行活动时间与生活质量显著相关。综合管理可能对改善LVAD患者的生活质量起到重要作用。
{"title":"Daily physical activity and quality of life in patients with left ventricular assist devices.","authors":"Tomoyuki Nezu, Tomomi Ide, Takeo Fujino, Takeshi Tohyama, Tae Higuchi, Yuta Nagatomi, Hitoshi Komman, Masayo Toyosawa, Takuya Nagata, Yusuke Ishikawa, Masataka Ikeda, Toru Hashimoto, Shintaro Kinugawa, Hiroyuki Tsutsui, Akira Shiose, Kohtaro Abe","doi":"10.1007/s10047-025-01536-5","DOIUrl":"https://doi.org/10.1007/s10047-025-01536-5","url":null,"abstract":"<p><p>The relationship between the physical activity status of patients with left ventricular assist devices (LVAD) and their quality of life (QOL) remains unclear. The aim of this study was to determine the association between physical activity status and QOL and to identify the factors influencing walking activity time in LVAD patients. Thirty outpatients with LVAD were included. Physical activity was measured using a triaxial accelerometer. QOL was assessed using the Kansas City Cardiomyopathy Questionnaire (KCCQ). Multiple regression analysis was used to examine the relationship between QOL and activity duration. Physical activity measurement revealed that sedentary behavior of 1.5 metabolic equivalents or less accounted for 72.6% of total activity time. The KCCQ was positively correlated with walking activity time (r = 0.60, p = 0.0005), but not with daily activity time (r = 0.12, p = 0.55). Regression analysis revealed that regular employment (p = 0.0013), low depression score (p = 0.0005), low C-reactive protein level (p = 0.016), and high peak oxygen uptake (p = 0.019) was associated with increased walking activity time. LVAD patients had low physical activity, and walking activity time was significantly associated with their QOL. Comprehensive management may play an important role in improving the QOL in LVAD patients.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"3"},"PeriodicalIF":1.3,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145512942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Danon disease is a rare inherited disorder, and its prognosis is significantly impacted by cardiac complications. Because of the severe shortage of donors, a ventricular assist device (VAD) is necessary as a bridge to heart transplantation. However, reports on VAD implantation for cardiomyopathy in Danon disease patients are limited. Herein, we report a successful pediatric case with nearly 800-day of biventricular assistance as a bridge to heart transplantation. A 12-year-old girl with severe heart failure due to hypertrophic cardiomyopathy associated with Danon disease underwent left implantation of a Heartware VAD (Heartware Inc., Miami Lakes, FL, USA). Owing to severe right ventricular failure, she was unable to be weaned off the cardiopulmonary bypass, and a right VAD implantation was undertaken using a Gyro pump (Kyosera, Kyoto, Japan). However, the right ventricular function did not recover postoperatively, and she subsequently underwent right implantation of a Heartware VAD on postoperative day 34. Despite several VAD-related complications, including aortic and pulmonary valve insufficiency and a driveline infection requiring hospitalization, the patient was able to attend junior high school during the waiting period for a heart transplantation. After a total waiting period of 882 days, including 791 days of biventricular Heartware VAD assistance, the patient underwent a heart transplantation.
{"title":"Bridge to heart transplantation with nearly 800-day intracorporeal biventricular assistance in a pediatric patient with Danon disease: a case report.","authors":"Takayuki Takehara, Takashi Kido, Masaki Taira, Takuji Watanabe, Jun Narita, Hidekazu Ishida, Ryo Ishii, Takayoshi Ueno, Shigeru Miyagawa","doi":"10.1007/s10047-025-01534-7","DOIUrl":"https://doi.org/10.1007/s10047-025-01534-7","url":null,"abstract":"<p><p>Danon disease is a rare inherited disorder, and its prognosis is significantly impacted by cardiac complications. Because of the severe shortage of donors, a ventricular assist device (VAD) is necessary as a bridge to heart transplantation. However, reports on VAD implantation for cardiomyopathy in Danon disease patients are limited. Herein, we report a successful pediatric case with nearly 800-day of biventricular assistance as a bridge to heart transplantation. A 12-year-old girl with severe heart failure due to hypertrophic cardiomyopathy associated with Danon disease underwent left implantation of a Heartware VAD (Heartware Inc., Miami Lakes, FL, USA). Owing to severe right ventricular failure, she was unable to be weaned off the cardiopulmonary bypass, and a right VAD implantation was undertaken using a Gyro pump (Kyosera, Kyoto, Japan). However, the right ventricular function did not recover postoperatively, and she subsequently underwent right implantation of a Heartware VAD on postoperative day 34. Despite several VAD-related complications, including aortic and pulmonary valve insufficiency and a driveline infection requiring hospitalization, the patient was able to attend junior high school during the waiting period for a heart transplantation. After a total waiting period of 882 days, including 791 days of biventricular Heartware VAD assistance, the patient underwent a heart transplantation.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"4"},"PeriodicalIF":1.3,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145512917","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-13DOI: 10.1007/s10047-025-01539-2
Austin Chang, Yudai Miyashita, Benjamin Louis Thomae, Amanda Kamar, Taisuke Kaiho, Chitaru Kurihara
Background: Lung transplantation improves survival in advanced lung disease, but calculated Panel Reactive Antibody (cPRA) positive patients are at higher risk for adverse outcomes. It is unclear if sensitization poses additional risks in patients bridged to transplantation with venovenous extracorporeal membrane oxygenation (VV-ECMO). This study compares outcomes between cPRA-positive and -negative patients bridged with VV-ECMO.
Methods: Among 411 transplant recipients from an institutional lung transplantation database (January 2018-March 2025), 52 patients were bridged with VV-ECMO. Of these, 14 were cPRA-positive and 38 were cPRA-negative. Univariate and multivariate analyses evaluated early post-transplant complications and survival outcomes in cPRA-positive and -negative groups.
Results: Rates of post-transplant complications such as primary graft dysfunction (PGD) in any grade (85.7% cPRA-positive vs. 76.4% cPRA-negative, p = 0.48), PGD grade 3 (35.7% vs. 50.0%, p = 0.53), acute kidney injury (AKI) (64.3% vs. 68.4%, p = 1.00), dialysis requirement (21.4% vs. 34.2%, p = 0.51), deep vein thrombosis (DVT) (71.4% vs. 55.3%, p = 0.35), and pulmonary embolism (PE) (7.1% vs. 18.4%, p = 0.42) were similar. 1-year survival rate (85.1% vs. 82.9%) and overall survival (p = 0.81) were not significantly different.
Conclusions: Post-transplant outcomes and survival were similar between cPRA-positive and -negative groups, suggesting that PRA status in VV-ECMO bridged lung transplant recipients is not associated with worse outcomes. VV-ECMO may remain a viable bridge to lung transplantation, even in sensitized patients.
{"title":"Outcomes of venovenous-extracorporeal membrane oxygenation bridging in lung transplant recipients with panel reactive antibody positivity.","authors":"Austin Chang, Yudai Miyashita, Benjamin Louis Thomae, Amanda Kamar, Taisuke Kaiho, Chitaru Kurihara","doi":"10.1007/s10047-025-01539-2","DOIUrl":"10.1007/s10047-025-01539-2","url":null,"abstract":"<p><strong>Background: </strong>Lung transplantation improves survival in advanced lung disease, but calculated Panel Reactive Antibody (cPRA) positive patients are at higher risk for adverse outcomes. It is unclear if sensitization poses additional risks in patients bridged to transplantation with venovenous extracorporeal membrane oxygenation (VV-ECMO). This study compares outcomes between cPRA-positive and -negative patients bridged with VV-ECMO.</p><p><strong>Methods: </strong>Among 411 transplant recipients from an institutional lung transplantation database (January 2018-March 2025), 52 patients were bridged with VV-ECMO. Of these, 14 were cPRA-positive and 38 were cPRA-negative. Univariate and multivariate analyses evaluated early post-transplant complications and survival outcomes in cPRA-positive and -negative groups.</p><p><strong>Results: </strong>Rates of post-transplant complications such as primary graft dysfunction (PGD) in any grade (85.7% cPRA-positive vs. 76.4% cPRA-negative, p = 0.48), PGD grade 3 (35.7% vs. 50.0%, p = 0.53), acute kidney injury (AKI) (64.3% vs. 68.4%, p = 1.00), dialysis requirement (21.4% vs. 34.2%, p = 0.51), deep vein thrombosis (DVT) (71.4% vs. 55.3%, p = 0.35), and pulmonary embolism (PE) (7.1% vs. 18.4%, p = 0.42) were similar. 1-year survival rate (85.1% vs. 82.9%) and overall survival (p = 0.81) were not significantly different.</p><p><strong>Conclusions: </strong>Post-transplant outcomes and survival were similar between cPRA-positive and -negative groups, suggesting that PRA status in VV-ECMO bridged lung transplant recipients is not associated with worse outcomes. VV-ECMO may remain a viable bridge to lung transplantation, even in sensitized patients.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"2"},"PeriodicalIF":1.3,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12615553/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145512904","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Endovascular repair (EVAR) for abdominal aortic aneurysm and iliac aneurysm is a safe and valid treatment. However, it is associated with some different complications that may require reinterventions. Among these complications, abdominal endograft proximal collapse is an infrequent event. We report a case of acute type A aortic dissection and abdominal endograft proximal collapse in a patient previously treated with EVAR.
{"title":"Abdominal endograft collapse due to acute type A aortic dissection.","authors":"Satoki Nakamura, Tomoaki Kudo, Junki Yokota, Noriko Kodani, Masatoshi Hata, Toru Kuratani","doi":"10.1007/s10047-025-01533-8","DOIUrl":"10.1007/s10047-025-01533-8","url":null,"abstract":"<p><p>Endovascular repair (EVAR) for abdominal aortic aneurysm and iliac aneurysm is a safe and valid treatment. However, it is associated with some different complications that may require reinterventions. Among these complications, abdominal endograft proximal collapse is an infrequent event. We report a case of acute type A aortic dissection and abdominal endograft proximal collapse in a patient previously treated with EVAR.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":"29 1","pages":"1"},"PeriodicalIF":1.3,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12611976/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145504542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-23DOI: 10.1007/s10047-025-01527-6
{"title":"Acknowledgments to reviewers.","authors":"","doi":"10.1007/s10047-025-01527-6","DOIUrl":"https://doi.org/10.1007/s10047-025-01527-6","url":null,"abstract":"","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145124677","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-01Epub Date: 2025-01-08DOI: 10.1007/s10047-024-01486-4
M Foltan, D Dinh, M Gruber, T Müller, C Hart, L Krenkel, C Schmid, K Lehle
Neutrophil extracellular traps (NETs) were detected in blood samples and in cellular deposits of oxygenator membranes during extracorporeal membrane oxygenation (ECMO) therapy and may be responsible for thrombogenesis. The aim was to evaluate the effect of the base material of gas fiber (GF, polymethylpentene) and heat exchange (HE) membranes and different antithrombogenic coatings on isolated granulocytes from healthy volunteers under static culture conditions. Contact of granulocytes with membranes from different ECMO oxygenators (with different surface coatings) and uncoated-GFs allowed detection of adherent cells and NETotic nuclear structures (normal, swollen, ruptured) using nuclear staining. Flow cytometry was used to identify cell activation (CD11b/CD62L, oxidative burst) of non-adherent cells. Uncoated-GFs were used as a reference. Within 3 h, granulocytes adhered to the same extent on all surfaces. In contrast, the ratio of normal to NETotic cells was significantly higher for uncoated-GFs (56-83%) compared to all coated GFs (34-72%) (p < 0.001) with no difference between the coatings. After material contact, non-adherent cells remained vital with unchanged oxidative burst function and the proportion of activated cells remained low. The expression of activation markers was independent of the origin of the GF material. In conclusion, the polymethylpentene surfaces of the GFs already induce NET formation. Antithrombogenic coatings can already reduce the proportion of NETotic nuclei. However, it cannot be ruled out that NET formation can induce thrombotic events. Therefore, new surfaces or coatings are required for future ECMO systems and long-term implantable artificial lungs.
{"title":"Incidence of neutrophil extracellular traps (NETs) in different membrane oxygenators: pilot in vitro experiments in commercially available coated membranes.","authors":"M Foltan, D Dinh, M Gruber, T Müller, C Hart, L Krenkel, C Schmid, K Lehle","doi":"10.1007/s10047-024-01486-4","DOIUrl":"10.1007/s10047-024-01486-4","url":null,"abstract":"<p><p>Neutrophil extracellular traps (NETs) were detected in blood samples and in cellular deposits of oxygenator membranes during extracorporeal membrane oxygenation (ECMO) therapy and may be responsible for thrombogenesis. The aim was to evaluate the effect of the base material of gas fiber (GF, polymethylpentene) and heat exchange (HE) membranes and different antithrombogenic coatings on isolated granulocytes from healthy volunteers under static culture conditions. Contact of granulocytes with membranes from different ECMO oxygenators (with different surface coatings) and uncoated-GFs allowed detection of adherent cells and NETotic nuclear structures (normal, swollen, ruptured) using nuclear staining. Flow cytometry was used to identify cell activation (CD11b/CD62L, oxidative burst) of non-adherent cells. Uncoated-GFs were used as a reference. Within 3 h, granulocytes adhered to the same extent on all surfaces. In contrast, the ratio of normal to NETotic cells was significantly higher for uncoated-GFs (56-83%) compared to all coated GFs (34-72%) (p < 0.001) with no difference between the coatings. After material contact, non-adherent cells remained vital with unchanged oxidative burst function and the proportion of activated cells remained low. The expression of activation markers was independent of the origin of the GF material. In conclusion, the polymethylpentene surfaces of the GFs already induce NET formation. Antithrombogenic coatings can already reduce the proportion of NETotic nuclei. However, it cannot be ruled out that NET formation can induce thrombotic events. Therefore, new surfaces or coatings are required for future ECMO systems and long-term implantable artificial lungs.</p>","PeriodicalId":15177,"journal":{"name":"Journal of Artificial Organs","volume":" ","pages":"374-382"},"PeriodicalIF":1.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12373553/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142949352","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}