Prognostic and therapeutic factors influencing the clinical outcome of hepatoblastoma after liver transplantation: A single-institute experience

2018 ◽  
Vol 22 (2) ◽  
pp. e13113 ◽  
Author(s):  
Katsutsugu Umeda ◽  
Hideaki Okajima ◽  
Koji Kawaguchi ◽  
Seishiro Nodomi ◽  
Satoshi Saida ◽  
...  
Keyword(s):  
Liver Transplantation ◽  
Clinical Outcome ◽  
Therapeutic Factors ◽  
Factors Influencing

scholarly journals Bacterial DNA translocation contributes to systemic inflammation and to minor changes in the clinical outcome of liver transplantation

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Gonzalo P. Rodríguez-Laiz ◽  
◽  
Pedro Zapater ◽  
Paola Melgar ◽  
Cándido Alcázar ◽  
...  
Keyword(s):  
Liver Transplantation ◽  
Clinical Outcome ◽  
Systemic Inflammation ◽  
Dna Translocation ◽  
Bacterial Dna

scholarly journals Influence of donor liver telomere and G-tail on clinical outcome after living donor liver transplantation

PLoS ONE ◽  
2019 ◽  
Vol 14 (3) ◽  
pp. e0213462
Author(s):  
Biou Liu ◽  
Kumiko Anno ◽  
Tsuyoshi Kobayashi ◽  
Jinlian Piao ◽  
Hidetoshi Tahara ◽  
...  
Keyword(s):  
Liver Transplantation ◽  
Clinical Outcome ◽  
Living Donor ◽  
Living Donor Liver Transplantation ◽  
Donor Liver ◽  
Donor Liver Transplantation

THE EFFECT OF COAGULATIOU CHANGES ON THE OUTCOME OF GASTROINTESTINAL HAEMORRHAGE

1987 ◽  
Author(s):  
S D Blair ◽  
K K Tan ◽  
C N McCollum ◽  
R M Greenhalgh
Keyword(s):  
Blood Transfusion ◽  
Clinical Outcome ◽  
Vascular Disease ◽  
Cause Of Death ◽  
Gastrointestinal Haemorrhage ◽  
Mortality Rates ◽  
Clotting Time ◽  
Normal Range ◽  
Factors Influencing ◽  
The Relationship

Blood is hypercoagulable following GI haemorrhage [1], and vascular thrombosis has been reported to be the main cause of death [2]. To study the relationship between coagulation and clinical outcome, Impedance Clotting Time (ICT) wac measured daily using the Biobridge [1] and clinical outcome prospectively recorded in 125 patients with acute severe GI haemorrhage.Mean (±se mean) ICT on admission was markedly shortened at 4.8±0.2 mins (normal range 8-12 mins) (p<0.001, t-Cest). Sixty patients received blood transfusion within 24 hours resulting in significantly prolonged ICT of 6.2±0.4 mins compared to 4.0±0.3 mins in the 56 not transfused (p<0.01). In 23 patients who rebled, the ICT at 24 hours of 6.7±0.4 mins demonstrated reduced hypercoagulability. Twenty of these 23 patients had bee:: transfused prior to rebleeding, a significantly greater proportion than in those who did not rebleed (p<0.00l). Six patients died, 3 of myocardial infarction, 1 of stroke, and 2 of continued haemorrhage. Mean ICT in the 4 patients dying from thrombotic vascular disease was 2.3±0.1 mins although 2 had also rebled.Clinical outcome in GI haemorrhage is strongly related to coagulation changes. The main cause of death was thrombotic vascular disease.1. Blair SD, Janvrin SB, McCollum CN, Greenhalgh RM. The effect of early blood transfusion on gastrointectinal haemorrhage. Br J Surg 1986; 73: 792-4.2. Allan R, Dykes P. A study of the factors influencing mortality rates fron gastrointestinal haenorrhage. Quart JMed 1976; 180: 533-50.

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