5 research outputs found
Standardized intensive care unit management in an anhepatic pig model: new standards for analyzing liver support systems
A simple dummy liver assist device prolongs anhepatic survival in a porcine model of total hepatectomy by slight hypothermia
<p>Abstract</p> <p>Background</p> <p>Advances in intensive care support such as therapeutic hypothermia or new liver assist devices have been the mainstay of treatment attempting to bridge the gap from acute liver failure to liver transplantation, but the efficacy of the available devices in reducing mortality has been questioned. To address this issue, the present animal study was aimed to analyze the pure clinical effects of a simple extracorporeal dummy device in an anhepatic porcine model of acute liver failure.</p> <p>Methods</p> <p>Total hepatectomy was performed in ten female pigs followed by standardized intensive care support until death. Five animals (dummy group, n = 5) underwent additional cyclic connection to an extracorporeal dummy device which consisted of a plasma separation unit. The separated undetoxified plasma was completely returned to the pigs circulation without any plasma substitution or exchange in contrast to animals receiving intensive care support alone (control group, n = 5). All physiological parameters such as vital and ventilation parameters were monitored electronically; laboratory values and endotoxin levels were measured every 8 hours.</p> <p>Results</p> <p>Survival of the dummy device group was 74 Ā± 6 hours in contrast to 53 Ā± 5 hours of the control group which was statistically significant (p < 0.05). Body temperature 24 hours after hepatectomy was significantly lower (36.5 Ā± 0.5Ā°C vs. 38.2 Ā± 0.7Ā°C) in the dummy device group. Significant lower values were measured for blood lactate (1.9 Ā± 0.2 vs. 2.5 Ā± 0.5 mM/L) from 16 hours, creatinine (1.5 Ā± 0.2 vs. 2.0 Ā± 0.3 mg/dL) from 40 hours and ammonia (273 Ā± 122 vs. 1345 Ā± 700 Ī¼g/dL) from 48 hours after hepatectomy until death. A significant rise of endotoxin levels indicated the onset of sepsis at time of death in 60% (3/5) of the dummy device group animals surviving beyond 60 hours from hepatectomy.</p> <p>Conclusions</p> <p>Episodes of slight hypothermia induced by cyclic connection to the extracorporeal dummy device produced a significant survival benefit of more than 20 hours through organ protection and hemodynamic stabilisation. Animal studies which focus on a survival benefit generated by liver assist devices should especially address the aspect of slight transient hypothermia by extracorporeal cooling.</p
Effectiveness and Safety of Dorsal Root Ganglion Stimulation for the Treatment of Chronic Pain:A Pooled Analysis
Porcine model characterizing various parameters assessing the outcome after acetaminophen intoxication induced acute liver failure
AIM:
To investigate the changes of hemodynamic and laboratory parameters during the course of acute liver failure following acetaminophen overdose.
METHODS:
Eight pigs underwent a midline laparotomy following jejunal catheter placement for further acetaminophen intoxication and positioning of a portal vein Doppler flow-probe. Acute liver failure was realized by intrajejunal acetaminophen administration in six animals, two animals were sham operated. All animals were invasively monitored and received standardized intensive care support throughout the study. Portal blood flow, hemodynamic and ventilation parameters were continuously recorded. Laboratory parameters were analysed every eight hours. Liver biopsies were sampled every 24 h following intoxication and upon autopsy.
RESULTS:
Acute liver failure (ALF) occurred after 28 Ā± 5 h resulted in multiple organ failure and death despite maximal support after further 21 Ā± 1 h (study end). Portal blood flow (baseline 1100 Ā± 156 mL/min) increased to a maximum flow of 1873 Ā± 175 mL/min at manifestation of ALF, which was significantly elevated (P 0.01).
CONCLUSION:
Declining portal blood flow and subsequent severe thrombocytopenia after acetaminophen intoxication precede fatality in a porcine acute liver failure model