Background: The Emergency Bypass System (EBS, Terumo Corporation) and Permanent Life Support (PLS, MAQUET Cardiopulmonary GmbH) platforms differ in pump design and surface coating, which may influence hemocompatibility. This study compared the longitudinal hematological profiles and transfusion requirements of these systems. Methods: Adult patients who underwent extracorporeal membrane oxygenation were analyzed using 1:1 propensity score matching (74 matched pairs). The primary endpoints included hemoglobin and platelet trajectories during the first 5 days, which were analyzed using linear mixed-effects models. Results: In the matched cohort, both groups demonstrated statistically similar longitudinal declines in hemoglobin and platelet counts (p=0.525 and p=0.501, respectively). However, this apparent stability in the EBS group was achieved at a significantly higher hematological cost. Within 5 days, the EBS group required 25.5% more red blood cell transfusions (p<0.001) and 34.2% more platelet transfusions (p<0.001) than the PLS group. Multivariable analysis confirmed that the use of the PLS system was independently associated with a lower transfusion demand. Conclusion Although laboratory trajectories were comparable during the acute phase, patients supported by EBS experienced a substantially higher transfusion burden. These findings suggest a masking effect, in which compensatory transfusions may obscure the accelerated blood cell consumption associated with EBS. Therefore, clinicians should remain vigilant regarding the potential hidden hematologic costs of EBS support, even when laboratory parameters appear stable.

Background and Objectives: Atrial septal defect (ASD) often accompanies atrial fibrillation (AF). AF is usually treated with radiofrequency catheter ablation (RFCA) before transcatheter ASD closure. However, there is still no established consensus on the treatment of AF after transcatheter ASD closure, as the deployed occluder makes access to the left atrium during RFCA more challenging. We report 9 cases of totally thoracoscopic ablation (TTA) for atrial tachyarrhythmia following transcatheter ASD closure. Methods: From 2012 to 2021, 9 patients underwent TTA for atrial tachyarrhythmia that developed or recurred after transcatheter ASD closure. TTA, a type of video-assisted thoracoscopic surgery, was performed to achieve transmural ablation of the atria. Results: Seven patients had been diagnosed with atrial tachyarrhythmia before transcatheter ASD closures; 3 had undergone RFCA, and 4 had received direct-current cardioversion.All 9 patients were in sinus rhythm at the time of transcatheter ASD closure. During a mean follow-up of 44.9 ± 39.4 months after closure, atrial tachyarrhythmia developed or recurred in all patients. After TTA, every patient was discharged without atrial tachyarrhythmia. The mean follow-up duration after TTA was 58.7 ± 41.1 months. Atrial arrhythmia recurred in 2 patients; in one, sinus rhythm was restored after post-TTA RFCA. A cerebral infarction occurred in one patient despite maintaining sinus rhythm after TTA. N-terminal pro brain natriuretic peptide levels significantly decreased after TTA (P = 0.021). Conclusions TTA can be performed without interference from the ASD occluder and therefore represents a safe and feasible treatment option for AF after transcatheter ASD closure.

Background: Pump-controlled retrograde trial off (PCRTO) is a safe, simple, and reversible method for weaning patients from veno-arterial extracorporeal membrane oxygenation (VA-ECMO). However, few studies have compared PCRTO to conventional weaning methods. This retrospective study aimed to compare PCRTO to non-PCRTO methods. Methods: This study included patients who were weaned from VA-ECMO from January 2016 to December 2022 at our medical center. Demographic data, ECMO management, ECMO complications, survival to discharge, and cardiogenic shock after VA-ECMO weaning were compared between the 2 groups. Results: Seventy patients who were weaned from VA-ECMO using PCRTO and 85 patients who were weaned with conventional methods were compared. Patient characteristics were not significantly different between the 2 groups. The rate of survival to discharge was significantly higher in the PCRTO group than in the non-PCRTO group (90% vs. 72%, p=0.01). The rates of freedom from all-cause mortality at 10, 30, and 50 days after weaning from ECMO were 75%, 55%, and 35% in the non-PCRTO group and 62%, 60%, and 58% in the PCRTO group, respectively (p=0.1). The incidence of cardiogenic shock after weaning from VA-ECMO was significantly higher in the non-PCRTO group (16% vs. 5%, p=0.04). In logistic regression analysis, PCRTO was a significant factor for survival to discharge (odds ratio, 2.42; 95% confidence interval, 1.29–5.28; p=0.02). Conclusion Compared to conventional methods, PCRTO is a feasible and reversible method, and it serves as a useful predictor of successful VA-ECMO weaning through a preload stress test.

Background: We aimed to analyze the impact of concomitant Maze procedure on the clinical and rhythm outcomes, and echocardiographic parameters in tricuspid repair for patients with severe tricuspid regurgitation (TR) and persistent atrial fibrillation (AF). Methods: Patients who had severe TR and persistent AF and underwent tricuspid valve (TV) repair were included in the study. Both primary TR and secondary TR were included in the current study. The study population was stratified according to Maze procedure. The primary outcome was major adverse cardiovascular and cerebrovascular event (MACCE) at 15 years postsurgery. Propensity-score matching analyses was performed to adjust baseline differences. Results: Three hundred seventy-one patients who underwent tricuspid repair for severe TR and persistent AF from 1994 to 2021 were included, and 198 patients (53.4%) underwent concomitant Maze procedure. The maze group showed 10-year sinus rhythm (SR) restoration rate of 55%. In the matched cohort, the maze group showed a lower cumulative incidence of cardiac death (4.6% vs. 14.4%, P = 0.131), readmission for heart failure (8.1% vs. 22.2%, P = 0.073), and MACCE (21.1% vs. 42.1%, P = 0.029) at 15 years compared to the non-maze group. Left atrial (LA) diameter significantly decreased in the maze group at 5 years (53.3 vs. 59.6 mm, P < 0.001) after surgery compared to preoperative level, and there was a significant difference in the change of LA diameter over time between the two groups (P = 0.013). Conclusion The Maze procedure during TV repair in patients with severe TR and persistent AF showed acceptable SR rates and lower MACCE rates compared to those without the procedure, while also promoting LA reverse remodeling.

The indication of pannus removal in patients with mitral valve (MV) replacement has not been determined. In the present study, four patients underwent secondary open cardiac surgery for MV pannus removal concomitant with tricuspid annuloplasty. After the first open cardiac surgery, these patients presented with gradual elevation in the transmitral pressure gradient (TMPG) and pulmonary artery systolic pressure (PASP) with aggravation of tricuspid regurgitation related to pannus formation in the prosthetic MV. Notably, the function of the prosthetic valve was normal in all patients. We performed tricuspid annuloplasty concomitant with pannus removal in the prosthetic MV alone. Pannus in the prosthetic MV was successfully removed without valve replacement, and improvement was noted in hemodynamic parameters, including TMPG and PASP after the operation. Herein, we share our experience and opinions about pannus removal in the prosthetic MV concomitant with tricuspid valve surgery.

Atrial functional mitral regurgitation (AFMR) is a newly discovered condition associated with long-standing atrial fibrillation (AF). This retrospective study analyzed the outcomes of the maze procedure and mitral regurgitation surgery in patients with AFMR and compared them with those in patients without AFMR. Patients who underwent the maze procedure at a single center were included (July 2012–August 2021). After excluding patients aged <18 years and those with infective endocarditis, 36 patients with AFMR (AFMR group) and 248 without AFMR (non-AFMR group) were enrolled in the study. The outcomes were compared using propensity score matching (PSM). After PSM, there were 36 patients in each group. The rates of freedom from AF at 1, 3, and 5 years postoperatively were 64.5%, 62.5%, and 60.0%, respectively, in the AFMR group, and were not significantly different from those in the non-AFMR group (p = 0.07). However, significantly more patients with AFMR exhibited junctional rhythm after the maze procedure than those without AFMR (p = 0.001) and significantly more underwent permanent pacemaker insertion in the AFMR group than in the non-AFMR group (p = 0.021). The groups demonstrated no significant differences in cardiac operation results. Patients with AFMR required close observation for sinus nodal dysfunction with bradycardia after the maze procedure. However, the results of cardiac surgery, including mitral valve repair, were comparable to those in patients without AFMR.

Background and Objectives: The left atrial appendage (LAA) can contribute significantly to LA mechanical contraction. Nevertheless, the preventive effect of LAA occlusion during the maze procedure against cerebral infarction remains controversial. In this study, we compared the surgical, cardiac hemodynamic, and neurologic outcomes between LAA preservation and occlusion performed during the maze procedure. Methods: Between January 2015 and August 2021, 252 patients underwent the maze procedure using cryoablation at our medical center. After excluding patients according to our exclusion criteria (i.e., mechanical prosthesis implantation, preexisting LAA thrombus), LAA was preserved in 113 patients (non-occlusion group) and occluded in 75 patients (occlusion group). Outcomes were compared using propensity score matching (PSM). Results: PSM did not reveal significant intergroup differences in baseline characteristics between the non-occlusion (n=53) and occlusion (n=53) groups. During a median follow-up of 44 months, 2 patients in the non-occlusion group (3.8%) experienced ischemic strokes.There was no significant difference in the rate of freedom from stroke (p=0.19) and major adverse cardiac events (p=0.43) between the 2 groups. Through echocardiography at 1-year follow-up, a statistically significant difference in LA mechanical contraction was observed between the non-occlusion group and occlusion group (24 of 33 [72.7%] vs. 18 of 37 [48.6%], respectively; p=0.04). Conclusions In this study, preservation of the LAA during the maze procedure resulted in better LA function than LAA occlusion, with similar rates of stroke.