A5075195484- Congenital Diaphragmatic Hernia Studies
- Neonatal Respiratory Health Research
- Esophageal and GI Pathology
- Tracheal and airway disorders
- Congenital Anomalies and Fetal Surgery
- Hernia repair and management
- Pediatric Hepatobiliary Diseases and Treatments
- Intestinal Malrotation and Obstruction Disorders
- Congenital Heart Disease Studies
- Gallbladder and Bile Duct Disorders
- Appendicitis Diagnosis and Management
- Gastroesophageal reflux and treatments
- Abdominal Surgery and Complications
- Airway Management and Intubation Techniques
- Gastrointestinal disorders and treatments
- Tumors and Oncological Cases
- Dysphagia Assessment and Management
- Neonatal Health and Biochemistry
- Organ Transplantation Techniques and Outcomes
- Clinical Nutrition and Gastroenterology
- Minimally Invasive Surgical Techniques
- Pleural and Pulmonary Diseases
- Child Nutrition and Feeding Issues
- Pelvic and Acetabular Injuries
- Renal cell carcinoma treatment
Shizuoka Children's Hospital
2016-2025
Hospital for Sick Children
2019-2023
Juntendo University Urayasu Hospital
2023
Chiba University
2022-2023
Nagoya University Hospital
2022-2023
Kanagawa Children's Medical Center
2022-2023
Sonoda Women's University
2023
Juntendo University
2023
Osaka Women's and Children's Hospital
2022-2023
Osaka University
2022-2023
Abstract Necrotizing enterocolitis (NEC) is a devastating disease of premature infants with high mortality rate, indicating the need for precision treatment. NEC characterized by intestinal inflammation and ischemia, as well derangements in microcirculation. Remote ischemic conditioning (RIC) has emerged promising tool protecting distant organs against ischemia-induced damage. However, effectiveness RIC unknown. To address this gap, we aimed to determine efficacy mechanism action...
Abstract Background To retrospectively investigate the developmental outcomes at 3 years of age in patients with congenital diaphragmatic hernia (CDH) using a multicenter collaborative research approach. Methods We evaluated CDH and no other malformations born between 2010 2016 seven facilities Japanese Research Group. The quotient (DQ) was Kyoto Scale Psychological Development 2001, most standardized scale Japan. Factors associated DQ score < 85 were also analyzed. Results Of 196...
Background: Double aortic arch is the most constrictive type of vascular ring, completely encircling trachea and esophagus, can cause severe respiratory failure, dysphagia, or devastating esophageal hemorrhage. Although surgical repair usually recommended shortly after diagnosis, surgery in extremely preterm infants presents significant challenges. The optimal timing management complications that arise while awaiting are not well understood. Case presentation: We report case an Asian female...
Aim: To define the role of laparoscopy for treating malrotation in children. Materials and Methods: The Ladd procedure (9 laparoscopic [lap-Ladd], 17 open [open-Ladd]; n=26) was performed children up to including 30 days age (neonatal [Group N]) older (Group C). These groups were compared retrospectively. Results: Group N (n=14) comprised 3 lap-Ladd 11 open-Ladd patients. C (n=12) 6 No case had ischemic bowel preoperatively. Intestinal volvulus confirmed 9 patients N, with 5 (P=not...
Abstract Congenital diaphragmatic hernia (CDH) is a birth defect of the diaphragm in which abdominal organs herniate through into thoracic cavity. The main pathophysiology respiratory distress and persistent pulmonary hypertension because hypoplasia caused by compression elevated organs. Recent progress prenatal diagnosis postnatal care has led to an increase survival rate patients with CDH. However, some survivors experience mid‐ long‐term disabilities complications requiring treatment...
Treatment modalities for neonates with congenital diaphragmatic hernia (CDH) have greatly improved in recent years, a concomitant increase survival. However, long-term outcomes restrict the identification of optimal care pathways CDH survivors adolescence and adulthood. Therefore, we evaluated within Japanese Study Group (JCDHSG).Participants were born between 2006 2018 according to JCDHSG. Participants enrolled database at 1.5, 3, 6, 12 years old. Follow-up items included complications,...
Abstract Background The aim of the present study was to investigate characteristics, management, and outcomes congenital biliary dilatation ( CBD ) in neonates infants (<1 year old) a single institution over past 20 years. Methods From 1997 2016, 21 patients <1 old underwent definitive surgery for . Open OS performed between 2008, laparoscopic LS has been since 2009. Results bile duct showed cystic all patients. Sixteen (76.2%) were diagnosed prenatally, incidence increased with time...
Abstract Introduction In children with choledochal cysts ( CC ), obstruction of the discharge bile or pancreatic juice is frequently observed, and biliary perforation severe pancreatitis may occur. such cases, temporary drainage necessary to stabilize these patients. We employed laparoscopic cholecystostomy followed by cyst excision in cases complicated . Methods Between 2009 2013, emergency for was performed seven girls whom conservative treatment failed ameliorate abdominal pain, vomiting,...