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Clinical research on pathogenesis and treatment of posttransplant portal hypertension and intrahepatic circulatory disorder in adult living donor liver transplantation

Clinical research on pathogenesis and treatment of posttransplant portal hypertension and intrahepatic circulatory disorder in adult living donor liver transplantation
成人活体肝移植术后门静脉高压及肝内循环障碍发病机制及治疗的临床研究
批准号:
15209042
负责人:
KIUCHI Tetsuya
金额:
$24.46万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004

项目摘要

项目成果

KIUCHI Tetsuya的其他基金

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中文摘要
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英文摘要
Portal venous pressure(PVP) early after adult living donor liver transplantation showed an inverse correlation with graft weight per body weight, although affected also by cirrhosis, hepatic arterial flow, and circulatory volume. On the other hand, PVP early days after transplantation had a causative relationship with posttransplant prognosis : recipients with averaged PVP>20 mmHg showed 50% reduction of survival. In patients with early posttransplant portal hypertension(PH), ascites and bilirubin increased and protein synthesis decreased in proportion to PVP. Incidence of gram-negative bacteremia also increased. However, its prognostic impact decreased with time Tissue congestion in the paramedian sector of right liver graft, attributable to interrupted venous outflow, gave no significant impact on PVP, i.e., it is post-sinusoidal congestion in contrast to presinusoidal PH.Thus it was suggested that increased splanchnic flow running into a small-for-size graft causes elevation of PVP and injury to intrahepatic portal system, and establishes a prolonged pathological condition. Portal venous flow volume(PVF) per unit tissue showed an inverse relationship with relative graft size However, increased PVF per se did not lead to tissue injury, but rather contributed a reduction of serum bilirubin. PVF and PVP showed a positive correlation in the native liver. But this was lost in early posttransplant period and dependent on portal venous compliance(PVC). PVC was highly variable among grafts and affected by donor age and graft warm ischemia.To prevent tissue injury due to early posttransplant PH, splenic artery ligation(SAL) or partial porto-caval shunt(PPCS) was done. SAL led to PVP reduction but not PVF reduction and PPCS also led to reduction of PVP, bilirubin, and ascites. Both led to better prognosis and reduction of medical costs due to ascites loss Impact of some reduction in graft regeneration and protein synthesis caused by PPCS is to be elucidated.(299 words)
期刊论文(50)
专著(0)
科研奖励(0)
会议论文
DOI: --
发表时间: 2004
期刊: Transplantation 77
影响因子: --
作者: [Kiuchi T, Yamamoto H, Maetan Y, Egawa H, Kaihara S, Itoh K, et al.]
通讯作者: et al.
臓器移植領域
器官移植领域
DOI: --
发表时间: 2004
期刊: 各領域における深在性真菌症の診断・治療
影响因子: --
作者: [木内哲也, 光武耕太郎]
通讯作者: 光武耕太郎
DOI: 10.1053/j.gastro.2004.09.042
发表时间: 2004-11-01
期刊: GASTROENTEROLOGY
影响因子: 29.4
作者: [Kulik, L, Abecassis, M]
通讯作者: Abecassis, M
成人生体肝移植(特集 肝疾患 病態・治療の最新の知見-コンセンサスに向けて)
成人活体肝移植(专题:肝病:病理生理学和治疗的最新发现 - 达成共识)
DOI: --
发表时间: 2004
期刊: 現代医学 52・1
影响因子: --
作者: [山本栄和, 尾池文隆, 亀井秀弥, 木内哲也]
通讯作者: 木内哲也
33
    Pathogenesis and antigen localization in immune reaction against tissue-specific antigens in liver transplantation
    • 批准号:
      17390347
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.05万
    • 财政年份:
      2005
    • 负责人:
      KIUCHI Tetsuya
    • 依托单位:
    Clinical research on the pathogenesis and treatment of portal hemodynamics and pathological regeneration in small-for-size liver grafts after living donor liver transplantation: Pathogenesis and clinical innovation
    • 批准号:
      13470253
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $8.7万
    • 财政年份:
      2001
    • 负责人:
      KIUCHI Tetsuya
    • 依托单位: