Publications by authors named "Ko Yoshizumi"

Radiofrequency ablation procedures for atrial fibrillation are occasionally associated with pulmonary vein stenosis (PVS). A common treatment for PVS is catheter intervention; however, because of the high restenosis rate, it is not suitable for young patients. The case presented herein is of a young male patient with severe bilateral PVS who underwent successful surgical pulmonary vein repair by sutureless technique.

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A combination of tetralogy of Fallot( TOF) and total anomalous pulmonary venous return(TAPVR) is rare and results in chronic volume and pressure load of the right side of the heart and underfilling of the left heart. We report a successful 2-staged surgical correction of TOF associated with TAPVR and atrial septal defect. The patient was unsuitable for total primary intracardiac correction because the volume of the left ventricle was considered to be small.

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Myxoma is the most common primary cardiac tumor in adults; however, it is extremely rare in infants. Acute occlusion of the abdominal aorta by a cardiac myxoma is also rare. We report the case of an infant with acute occlusion of the suprarenal abdominal aorta by a left ventricular myxoma.

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  • Hypoplastic left heart syndrome (HLHS) is a serious heart condition, and recent research suggests that using autologous cardiosphere-derived cells (CDCs) might improve heart function in affected patients.
  • This study aimed to determine the safety and feasibility of delivering CDCs directly into the coronary arteries of patients with HLHS.
  • The results showed that CDC treatment was safe, led to significant improvements in right ventricular function after three months, and was associated with better growth and heart failure status compared to control patients at 18 months post-treatment.
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Objectives: In cases of severe Ebstein's anomaly, it is essential to determine whether biventricular repair (BVR) or single-ventricle palliation is feasible. Since 1999, in our institution, we have used the novel technique comprising tricuspid valve (TV) closure and right ventricular and right atrial (RV/RA) exclusion to reduce the deleterious effects of an enlarged RV in patients with severe Ebstein's anomaly. However, in cases with good RV function, primary BVR is performed.

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  • The study investigates how pulmonary root translocation affects the left ventricular outflow tract in a 6-year-old boy with complex heart defects.
  • After the procedure, imaging showed an improvement in the left ventricular outflow's natural shape compared to before surgery.
  • The technique avoids the need for coronary transfer and maintains the aortic root's structure, but further evaluation of long-term outcomes is necessary.
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  • - A 40-year-old woman with systemic lupus erythematosus experienced serious complications, including cerebral infarction and alveolar hemorrhage.
  • - Upon examination, she was found to have severe aortic insufficiency and diagnosed with Libman-Sacks syndrome, which is associated with lupus.
  • - Surgery was performed due to left ventricular dilatation and fatigue, revealing distinctive holes of 4-mm and 5-mm in the aortic valve's cusps during pathology analysis.
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  • A 26-year-old woman with Marfan syndrome and severe mitral valve regurgitation aimed to have children while managing her health condition.
  • To prepare for necessary cardiovascular surgery, the medical team conducted a mitral annuloplasty using a right anterior thoracotomy approach.
  • Repairing the mitral valve through this technique is highly effective for patients with Marfan syndrome, offering significant benefits.
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Apicoaortic bypass for left ventricular outflow tract obstruction has been performed with acceptable mid-term mortality. However, sometimes it is difficult to anastomose the distal end of the conduit to the calcified descending aorta in patients with a porcelain aorta. We report an aortic non-touch modification of the apicoaortic bypass in an 80-year-old woman with valvular aortic stenosis and a porcelain aorta extending from the ascending to abdominal aorta.

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Objective: Tricuspid valve size is the major determinant of outcomes for patients with pulmonary atresia with intact ventricular septum. Lack of right ventricle-pulmonary artery continuity is associated with poor tricuspid valve growth (decrement in Z-value). However, most reports did not show evidence for disproportionate growth of the tricuspid valve after establishment of right ventricle-pulmonary artery continuity.

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The cognitive impairment and hemodynamic instability after neonatal cardiac surgery with cardiopulmonary bypass (CPB) might be exacerbated by hemodilution. Therefore, this study investigated the impact of different bloodless prime volumes on the hemodynamics and the inflammatory response by a miniaturized CPB system in neonatal piglets. The bypass circuit consisted of a Capiox RX05 (Capiox Baby RX, Terumo Corp.

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  • The study analyzed the outcomes of 29 patients with impaired ventricular function who underwent the Fontan operation between 1991 and 2007, focusing on the impact of their condition on mortality and morbidity.
  • The research found that, despite the high-risk status of these patients, there were no early deaths, and while late complications included two fatalities and re-operations, significant improvements in heart function and oxygen saturation were observed over time.
  • At a median follow-up of 7.5 years, the patients maintained a stable ejection fraction and showed reductions in abnormal ventricular volume, although some experienced issues like congestive heart failure, arrhythmias, and protein-losing enteropathy.
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Blood priming is necessary for cardiopulmonary bypass (CPB) in neonates to avoid excessive hemodilution; however, transfusion-related inflammation affects postCPB outcomes in neonatal open-heart surgery. We hypothesized that ultrafiltration of priming blood before CPB may reduce inflammatory mediators in priming blood and postCPB inflammatory responses, thereby improving cardiopulmonary function. Twelve 1-week-old piglets (3.

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  • This study reviewed blood transfusion-free open-heart surgeries in 536 children weighing 5-20 kg from 2004 to 2007, utilizing a miniaturized cardiopulmonary bypass (CPB) circuit with specific priming volumes based on flow rates.
  • Nearly half (49.3%) of the patients avoided transfusions during surgery, with the rate varying significantly according to weight and complexity of the congenital heart condition.
  • Factors like body weight, preoperative hematocrit, and characteristics of the CPB circuit were found to predict the need for transfusions, suggesting that improvements in CPB technology could help reduce transfusion rates, especially for smaller or more complex cases.
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  • Adult patients undergoing total cavopulmonary connection (TCPC) face high risks due to various risk factors, with a study reviewing 25 such cases aged 16-52 showing diverse challenges.
  • The study found that patients with 6 or more risk factors had significantly higher mortality rates compared to those with fewer than 6, although no specific risk factors were statistically decisive for late death.
  • Overall, while many candidates tolerated the TCPC procedure early on, the accumulation of multiple risk factors indicates a need for careful monitoring and possibly alternative approaches in high-risk cases.
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Background: The purpose of this study was to describe the experience with staged surgical reconstruction of the hypoplastic left heart syndrome (HLHS) with a right ventricle to pulmonary artery conduit and to identify the risk factors that influence late outcome.

Methods: Between February 1998 and June 2007, 62 patients with HLHS underwent a Norwood procedure by using right ventricle to pulmonary artery conduit (median age, 9 days [range, 1 to 57]; median body weight 2.7 kg [range, 1.

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Background: The purpose of the present study was to evaluate the effect of modified ultrafiltration (MUF) on neonates with transposition of the great arteries (TGA) undergoing arterial switch operation.

Methods And Results: The current study included 36 neonates who underwent an arterial switch operation between 1998 and 2006. Arterio-venous MUF was done in 15 patients (MUF-treated group) and the other 21 patients were controls.

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This study was undertaken to determine the impact of miniaturization of a cardiopulmonary bypass (CPB) circuit on blood transfusion and hemodynamics in neonatal open-heart surgery. Neonates (n = 102) undergoing open-heart surgery between 2002 and 2006 were included and divided into three groups: group 1 (n = 28), Dideco 902 oxygenator + 5/16" line; group 2 (n = 29), Dideco 901 oxygenator + 1/4" line; group3 (n = 45), Dideco 901 oxygenator + 3/16" arterial + 1/4" venous line. Amount of priming volume, blood and bicarbonate sodium use during CPB, and hemodynamics were compared.

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  • Single-ventricle palliation without cardiopulmonary bypass is beneficial in minimizing systemic edema and inflammation, yet simple clamping of the superior vena cava (SVC) can negatively affect cerebral blood flow.
  • The study involved 14 children with single-ventricle physiology, using a centrifugal pump-assisted temporary shunt to connect the SVC to the right atrium, allowing for improved blood flow during the bidirectional cavopulmonary shunt (BCPS) procedure.
  • Results showed that all patients tolerated the procedure well, maintaining stable central venous pressure and oxygen saturation without needing blood transfusions or experiencing postoperative neurological complications.
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To minimize myocardial ischemia, we repaired aortic arch obstruction with ventricular septal defect, using two different techniques of cerebral and myocardial perfusion. Seventy-one infants, ages 3 to 137 days, underwent primary repair of coarctation of the aorta (n = 49)/interruption of the aortic arch (n = 22) with ventricular septal defect. In 65 patients, an end-to-end arch anastomosis was performed with cerebral and myocardial perfusion through the innominate or the ascending arterial cannula (non-working beating heart: NWBH).

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Atrioventricular valve repair with artificial chordal replacement has been widely used for congenital and acquired mitral valve abnormalities, but not for tricuspid valve abnormalities. A case is presented of dysplastic tricuspid valve that was successfully repaired using artificial chordae. A 2-year-old female presented with poor weight gain.

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Objectives: The purpose of this study is to provide short- and mid-term results of open aortic valvotomy (OAV) for patients with critical aortic stenosis (AS).

Methods: Between December 1993 and June 1996, 6 patients with critical AS underwent an OAV in our unit. Their ages and body weights at operation ranged from 1 to 65 days (median age, 9 days) and from 2.

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  • - A rare condition, congenital left ventricular diverticulum with mitral regurgitation (MR), was observed in a 5-month-old female infant.
  • - The infant underwent a surgical procedure known as the Dor procedure, which involved excluding a large diverticulum using an endoventricular circular patch.
  • - This approach preserved the left ventricular cavity and improved the positioning of the papillary muscles, ultimately leading to a successful repair of the mitral valve.
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