基本情報
- 所属
- 自治医科大学 外科学講座(小児外科部門) 教授
- 学位
- Stat3はMn-SODを介して肝細胞における低酸素再酸素化傷害を抑制する(2005年3月 千葉大学)
- J-GLOBAL ID
- 201601010421619629
- researchmap会員ID
- B000250759
- 外部リンク
研究キーワード
11研究分野
1経歴
2-
2023年10月 - 現在
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2015年
学歴
1-
1992年4月 - 1998年3月
論文
209-
Pediatric surgery international 40(1) 240-240 2024年8月22日PURPOSE: This study aimed to clarify surgical complications associated with open surgery for congenital diaphragmatic hernia (CDH). METHODS: We performed an exploratory data analysis of the clinical characteristics of surgical complications of neonates with CDH who underwent laparotomy or thoracotomy between 2006 and 2021. Data of these patients were obtained from the database of the Japanese CDH Study Group. RESULTS: Among 1,111 neonates with left or right CDH, 852 underwent open surgery (laparotomy or thoracotomy). Of these 852 neonates, 51 had the following surgical complications: organ injury (n = 48; 6% of open surgeries); circulatory failure caused by changes in the organ location (n = 2); and skin burns (n = 1). Injured organs included the spleen (n = 30; 62% of organ injuries), liver (n = 7), lungs (n = 4), intestine (n = 4), adrenal gland (n = 2), and thoracic wall (n = 2). Fourteen of the patients who experienced organ injury required a blood transfusion (2% of open surgeries). The adjusted odds ratio of splenic injury for patients with non-direct closure of the diaphragm was 2.2 (95% confidence interval, 1.1-4.9). CONCLUSION: Of the patients who underwent open surgery for CDH, 2% experienced organ injury that required a blood transfusion. Non-direct closure of the diaphragmatic defect was a risk factor for splenic injury.
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Journal of pediatric surgery 59(8) 1451-1457 2024年8月BACKGROUND: We aimed to investigate the clinical characteristics and outcomes of patients with isolated left-sided congenital diaphragmatic hernia (CDH) who developed preoperative pneumothorax and determine its risk factors. METHODS: We performed an international cohort study of patients with CDH enrolled in the Congenital Diaphragmatic Hernia Study Group registry between January 2015 and December 2020. The main outcomes assessed included survival to hospital discharge and preoperative pneumothorax development. The cumulative incidence of pneumothorax was estimated by the Gray test. The Fine and Gray competing risk regression model was used to identify the risk factors for pneumothorax. RESULTS: Data for 2858 neonates with isolated left-sided CDH were extracted; 224 (7.8%) developed preoperative pneumothorax. Among patients with a large diaphragmatic defect, those with pneumothorax had a significantly lower rate of survival to discharge than did those without. The competing risks model demonstrated that a patent ductus arteriosus with a right-to-left shunt flow after birth (hazard ratio [HR]: 1.78; 95% confidence interval [CI]: 1.21-2.63; p = 0.003) and large defects (HR: 1.65; 95% CI: 1.13-2.42; p = 0.01) were associated with an increased risk of preoperative pneumothorax. Significant differences were observed in the cumulative incidence of pneumothorax depending on defect size and shunt direction (p < 0.001). CONCLUSIONS: Pneumothorax is a significant preoperative complication associated with increased mortality in neonates with CDH, particularly in cases with large defects. Large diaphragmatic defects and persistent pulmonary hypertension were found to be risk factors for preoperative pneumothorax development. LEVEL OF EVIDENCE: LEVEL Ⅲ Retrospective Comparative Study.
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Surgery today 2024年7月31日PURPOSE: This pilot study evaluated indocyanine green-guided near-infrared fluorescence (ICG-NIRF) imaging of testicular blood flow to predict long-term testicular atrophy after testicular torsion (TT) surgery. METHODS: The subjects of this retrospective study were patients who underwent surgery for TT at our hospital between December, 2020 and July, 2022. After detorsion, testicular blood flow was evaluated by ICG-NIRF imaging and classified into three categories: fluorescence detected, no fluorescence detected, and fluorescence detected only in the tunica albuginea vessels. Testicular volume was measured by ultrasonography up to 12 months after surgery to evaluate long-term outcomes. RESULTS: Twelve patients were included in this analysis. We found a 100% correlation between the absence of ICG-NIRF signals and subsequent testicular atrophy. In three patients without an ICG-NIRF signal, the median testis size 12 months postoperatively was significantly smaller (16.5% of the contralateral testis; range 13-20%) than that in six patients with an ICG-NIRF signal (96%; 89-115%) (p = 0.013). Mild atrophy (74.5%; 73-76%) was also observed in the three patients for whom an ICG-NIRF signal was detected only in the tunica albuginea vessels. CONCLUSIONS: Our pilot study highlights the potential of ICG-NIRF imaging as a prognostic tool for guiding surgical decision-making for patients with TT, by predicting postoperative testicular atrophy.
MISC
705-
AMERICAN JOURNAL OF TRANSPLANTATION 4 392-392 2004年
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日本小児外科学会雑誌 38(5) 782-786 2002年8月20日成因が異なると考えられる限局性腸管拡張症(本症)の2例を経験した.症例1は6カ月, 男児である.胆汁性嘔吐を認め, 小腸狭窄の術前診断にて開腹した.空腸に限局性拡張を認め, 拡張腸管切除・端々吻合を施行した.拡張腸管の病理組織像は正常で, 拡張腸管の原因となるような所見は認められなかった.症例2は9歳, 男児である.間歇性の腹痛, 胆汁性嘔吐を認め, 緊急手術を施行した.回腸に限局性拡張を認め, 拡張腸管切除・端々吻合を施行した.拡張腸管は著明な筋層低形成を呈し, 中央部においては粘膜下層の外周がほとんど欠損している部分も見られた.腸管壁の菲薄化, 脆弱化が腸管拡張の原因と考えられた.本症の病因は不明だが, 1)筋層低形成, 2)胎生期の一時的な腸閉塞, 3)脊索の内胚葉からの分離障害, 等が成因論として考えられている.それぞれの説に合致する症例が存在するため, 本症の疾患概念の中には複数の病態が存在していると考えられた.
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日本小児放射線学会雑誌 = Journal of Japanese Society of Pediatric Radiology 17(3) 169-173 2001年12月1日
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日本小児放射線学会雑誌 = Journal of Japanese Society of Pediatric Radiology 17 56-56 2001年5月1日
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日本小児放射線学会雑誌 = Journal of Japanese Society of Pediatric Radiology 16 26-26 2000年5月1日
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日本小児外科学会雑誌 36(2) 396-396 2000年4月20日
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日本小児外科学会雑誌 36(2) 403-404 2000年4月20日
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日本小児外科学会雑誌 36(1) 138-138 2000年2月20日
共同研究・競争的資金等の研究課題
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日本学術振興会 科学研究費助成事業 2024年4月 - 2029年3月
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日本学術振興会 科学研究費助成事業 2023年4月 - 2026年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2022年4月 - 2025年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2021年4月 - 2024年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2021年4月 - 2024年3月