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 ...

10.12.2012 Aufrufe

278 Verner/Schneider/Gebel/Panning/Wiese/Tröger/Breitmeier, Blood ethanol concentrations and inebriation symptoms following percutaneous ethanol injection therapy (PEIT) carried out on patients suffering from hepatocellular carcinoma Fig. 2: Positiv relationship between the maximum of the blood ethanol concentration and the amount of ethanol administered in all 14 patients. Solid line indicates the theoretic curve based on the 3-parameter logistic model: y=A/(1+B*exp(–C*x)), where x is the amount of administered ethanol, and y is the maximal blood ethanol concentration. The theoretic curve indicates the model of a non-linear regression analysis, which fitted the data best. This non-linear logarithmic model demonstrates the most accurate match compared to all other linear and non-linear models tested. The coefficient of determination for the nonlinear logarithmic model was R 2 = 0.417 and r = 0.6432. Discussion To our knowledge, the systemic effects of ethanol by patients with HCC undergoing percutaneous ethanol injection have not been studied. In many other publications [24, 25, 26, 27, 28, 29], where healthy, mostly male test persons are given amounts of alcohol intravenously in a dose that has been defined in advance and where the intervals at which blood is taken, has also been defined. In our cases the procedure of ethanol instillation has been carried out on hospitalised patients suffering from hepatocellular carcinoma. In the form of high volume ethanol therapy (PEI) it was injected directly into the tumour using ultrasound as a guide. It must be taken into consideration that in order to analyse the data the alcohol has to be injected directly into the liver (tumour), resulting thus in the avoidance of gastric or rather hepatic first-pass-effects in the liver. The alcohol will then flow directly from the tumour via the hepatic veins, or through direct puncture of the hepatic veins instead of the tumour into the vascular system. This explains the partly rapid increase of the blood ethanol concentration with an extremly fast distribution of ethanol in the body, especially into the central nervous system, which leads to substantial inebriation symptoms by the patients subsequent to percutaneous ethanol injection therapy. In our BLUTALKOHOL VOL. 42/2005

Verner/Schneider/Gebel/Panning/Wiese/Tröger/Breitmeier, Blood ethanol concentrations and inebriation symptoms following percutaneous ethanol injection therapy (PEIT) carried out on patients suffering from hepatocellular carcinoma opinion the clinical symptoms after percutaneous ethanol injection were not effected by the anaesthetics. At the time of examination the anaesthetics had been broken down completely. By some authors it would mentioned, that acutely elevated alcohol levels can put the patient at risk of atrial fibrillation, atrial flutter, and ventricular tachycardia [30, 31]. In addition, acute alcohol consumption is also associated with myocardial depression and a risk of developing angina pectoris in adults [30]. TSOKOS et al. couldn’t found any association between treatment-assiciated complications and systemic blood ethanol concentration following percutaneous ethanol injection therapy (PEIT) measured in minipigs [32]. Other authors [33,34] mentioned about acute cardiovascular instability, bradycardia, sudden hypotension, and sinus arrest to be connected with percutaneous ethanol injection therapy for hepatocellular carcinoma. Without further investigations in this therapy it is at the moment impossible to forecast how much and at which interval alcohol is released into the hepatic veins and distributed systemically. Due to this route of ethanol administration and compared to the normal methods such as oral intake this method effects a very short time till the maximum BEC is reached. During this study after the commencement of the instillation therapy the maximum blood ethanol concentration was recorded to be between 5 and 25 minutes. The average was measured at 13 minutes ± 4.9 minutes. The patients in this study were devided in Child A and B, Okuda I and II (one patient with Okuda III), and all patients did only have moderate cirrhosis. The elimination rate wasn’t slowed in patients with liver cancer treated with PEI. The rate of ethanol disappearence probably corresponded to normal healthy people. Additional studies with a longer period of blood taking time after PEI are necessary to determine the accurate elemination rate in patients with HCC treated by PEI. In addition there was often plateau formation during the distribution and elemination of the alcohol due to the fact that the tumour was for example subjected to continuous alcohol doses over a longer period of time (Fig. 1). Or rather there were several peak formations as the tumour dispersed alcohol into vascular system at different intervals in time (Fig. 1). For this very reason it is not possible to fulfil normal kinetic requirements using this method of alcohol induction. The result of this study could possibly only be compared to subjects drinking different volumes of alcohol at several different intervals in this case several peaks can be observed. Similarly by alcohol instillation into the tumour using the above mentioned method, the dispersed amount or rather the time period in which the alcohol is dispersed is not calculable due to the fact that the distribution of alcohol takes place through the tumour itself. In nine cases the BEC reached peak values of measured c max higher than the values of calculated c max . This is due to the fact that the ethanol was injected directly into the liver veins instead of the tumour. In five cases the main part of the injection was deposited into the tumour and the release was rather slow resulting thus, in the calculated c max being higher than the measured c max. The main reason for the variance in the venous blood alcohol levels could be due to the variable amount and unknown time course of alcohol release from the tumor into the intervascular compartment. It can be concluded from the findings of this study, that the ethanol distribution and elimination follows the recognised process of distribution and elimination only after complete release of ethanol out of the tumour into hepatic veins. For that reason the traditional elimination kinetic of alcohol can not be applied immediate in 279 BLUTALKOHOL VOL. 42/2005

278<br />

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 />

Fig. 2: Positiv relationship between the max<strong>im</strong>um of the blood ethanol concentration and<br />

the amount of ethanol administered in all 14 patients. Solid line indicates the theoretic<br />

curve based on the 3-parameter logistic model: y=A/(1+B*exp(–C*x)), where x is the<br />

amount of administered ethanol, and y is the max<strong>im</strong>al blood ethanol concentration.<br />

The theoretic curve indicates the model of a non-linear regression analysis, which fitted<br />

the data best. This non-linear logarithmic model demonstrates the most accurate match<br />

compared to all other linear and non-linear models tested. The coefficient of determination<br />

for the nonlinear logarithmic model was R 2 = 0.417 and r = 0.6432.<br />

Discussion<br />

To our knowledge, the systemic effects of ethanol by patients with HCC <strong>und</strong>ergoing<br />

percutaneous ethanol injection have not been studied. In many other publications [24, 25,<br />

26, 27, 28, 29], where healthy, mostly male test persons are given amounts of alcohol intravenously<br />

in a dose that has been defined in advance and where the intervals at which<br />

blood is taken, has also been defined. In our cases the procedure of ethanol instillation has<br />

been carried out on hospitalised patients suffering from hepatocellular carcinoma. In the<br />

form of high volume ethanol therapy (PEI) it was injected directly into the tumour using<br />

ultraso<strong>und</strong> as a guide. It must be taken into consideration that in order to analyse the data<br />

the alcohol has to be injected directly into the liver (tumour), resulting thus in the avoidance<br />

of gastric or rather hepatic first-pass-effects in the liver. The alcohol will then flow<br />

directly from the tumour via the hepatic veins, or through direct puncture of the hepatic<br />

veins instead of the tumour into the vascular system. This explains the partly rapid increase<br />

of the blood ethanol concentration with an extremly fast distribution of ethanol in<br />

the body, especially into the central nervous system, which leads to substantial inebriation<br />

symptoms by the patients subsequent to percutaneous ethanol injection therapy. In our<br />

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

Hurra! Ihre Datei wurde hochgeladen und ist bereit für die Veröffentlichung.

Erfolgreich gespeichert!

Leider ist etwas schief gelaufen!