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Blutalkohol 2005 - BADS (Bund gegen Alkohol und Drogen im ...

Blutalkohol 2005 - BADS (Bund gegen Alkohol und Drogen im ...

Blutalkohol 2005 - BADS (Bund gegen Alkohol und Drogen im ...

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Verner/Schneider/Gebel/Panning/Wiese/Tröger/Breitmeier,<br />

Blood ethanol concentrations and inebriation symptoms following percutaneous ethanol injection<br />

therapy (PEIT) carried out on patients suffering from hepatocellular carcinoma<br />

opinion the clinical symptoms after percutaneous ethanol injection were not effected by<br />

the anaesthetics. At the t<strong>im</strong>e of examination the anaesthetics had been broken down completely.<br />

By some authors it would mentioned, that acutely elevated alcohol levels can put the patient<br />

at risk of atrial fibrillation, atrial flutter, and ventricular tachycardia [30, 31]. In addition,<br />

acute alcohol consumption is also associated with myocardial depression and a risk of<br />

developing angina pectoris in adults [30]. TSOKOS et al. couldn’t fo<strong>und</strong> any association<br />

between treatment-assiciated complications and systemic blood ethanol concentration following<br />

percutaneous ethanol injection therapy (PEIT) measured in minipigs [32]. Other<br />

authors [33,34] mentioned about acute cardiovascular instability, bradycardia, sudden<br />

hypotension, and sinus arrest to be connected with percutaneous ethanol injection therapy<br />

for hepatocellular carcinoma. Without further investigations in this therapy it is at the<br />

moment <strong>im</strong>possible to forecast how much and at which interval alcohol is released into the<br />

hepatic veins and distributed systemically. Due to this route of ethanol administration and<br />

compared to the normal methods such as oral intake this method effects a very short t<strong>im</strong>e<br />

till the max<strong>im</strong>um BEC is reached. During this study after the commencement of the instillation<br />

therapy the max<strong>im</strong>um blood ethanol concentration was recorded to be between 5 and<br />

25 minutes. The average was measured at 13 minutes ± 4.9 minutes.<br />

The patients in this study were devided in Child A and B, Okuda I and II (one patient<br />

with Okuda III), and all patients did only have moderate cirrhosis. The el<strong>im</strong>ination rate<br />

wasn’t slowed in patients with liver cancer treated with PEI. The rate of ethanol disappearence<br />

probably corresponded to normal healthy people. Additional studies with a<br />

longer period of blood taking t<strong>im</strong>e after PEI are necessary to determine the accurate elemination<br />

rate in patients with HCC treated by PEI.<br />

In addition there was often plateau formation during the distribution and elemination of<br />

the alcohol due to the fact that the tumour was for example subjected to continuous alcohol<br />

doses over a longer period of t<strong>im</strong>e (Fig. 1). Or rather there were several peak formations<br />

as the tumour dispersed alcohol into vascular system at different intervals in t<strong>im</strong>e<br />

(Fig. 1). For this very reason it is not possible to fulfil normal kinetic requirements using<br />

this method of alcohol induction. The result of this study could possibly only be compared<br />

to subjects drinking different volumes of alcohol at several different intervals in this case<br />

several peaks can be observed. S<strong>im</strong>ilarly by alcohol instillation into the tumour using the<br />

above mentioned method, the dispersed amount or rather the t<strong>im</strong>e period in which the<br />

alcohol is dispersed is not calculable due to the fact that the distribution of alcohol takes<br />

place through the tumour itself.<br />

In nine cases the BEC reached peak values of measured c max higher than the values of<br />

calculated c max . This is due to the fact that the ethanol was injected directly into the liver<br />

veins instead of the tumour. In five cases the main part of the injection was deposited into<br />

the tumour and the release was rather slow resulting thus, in the calculated c max being higher<br />

than the measured c max.<br />

The main reason for the variance in the venous blood alcohol levels could be due to the<br />

variable amount and unknown t<strong>im</strong>e course of alcohol release from the tumor into the intervascular<br />

compartment. It can be concluded from the findings of this study, that the<br />

ethanol distribution and el<strong>im</strong>ination follows the recognised process of distribution and<br />

el<strong>im</strong>ination only after complete release of ethanol out of the tumour into hepatic veins. For<br />

that reason the traditional el<strong>im</strong>ination kinetic of alcohol can not be applied <strong>im</strong>mediate in<br />

279<br />

BLUTALKOHOL VOL. 42/<strong>2005</strong>

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