![]() |
Prof. Dr. med. Michele Curatolo E-mail
Principal investigators for individual studies: Dr. Alban Neziri, Jürg Schliessbach, Dr. A. Siegenthaler, Dr. Konrad Streitberger, Dr. Pascal Vuilleumier.
Description. The project investigates translational aspects related with alterations in pain processing in patients with chronic pain. The following issues are addressed:
Principal investigators for individual studies: Jürg Schliessbach, Dr. Patrick Willimann.
The following studies are being performed:
Principal investigator: Dr. Andreas Siegenthaler
Description. A new model for optimal combination of different drugs in individual patients is under development. At present, data on the action profile of individual drugs are being collected. Validation of the optimization method in vitro is performed in cooperation at the University Hospital of Vienna (Dr. G. Sveticic).
Principal investigator: Dr. Andreas Siegenthaler
The following projects are running:
Further projects in the field of ultrasound: Link to web site of Urs Eichenberger is coming soon
Principal investigator: Dr. Konrad Streitberger
This pilot study investigates the correlates for the success of radiofrequency denervation of the lumbar zygapophysial joints.
Dr. Konrad Maurer, Institut of Anaesthesiology, University of Zurich, Switzerland
Prof. Hanns-Ulrich Zeilhofer, Institute of Pharmacology of the University of Zürich, Switzerland
Scientific Funds of the University Department of Anaesthesiology and Pain Therapy, Inselspital Bern, Switzerland.
Principal investigators: Dr. Sebastian Brandt, Dr. Oliver Kimberger, Dr. Sandra Eipeldauer, Eliana Koepfli,
Description: This sub-project investigates effects of Norepinephrine on microcirculatory blood flow, tissue oxygen tension and metabolic changes in the intestinal tract in the immediate postoperative course.
The following issues are in the focus of the study:
Principal investigators: Sebastian Brandt, Oliver Kimberger, Eliana Koepfli
Description: This sub-project investigates effects of epidural anesthesia in the perioperative setting.
The following issues are in the focus of the study:
Principal investigators: Dr. Sebastian Brandt, Andrin Plebani, Volker Hartwich
Description: This project investigates the reliability and accuracy of several commercially available Cardiac output measurement devices under several different hemodynamic conditions such as i.e. cardiac tamponade or hemorrhagic shock.
Hiltebrand, Brandt, Kimberger
Effects of Endotoxin and Catecholamines on Hepatic Mitochondrial Respiration
Automatic algorithm for monitoring systolic pressure variation and difference in pulse pressure
Hemodynamic Parameters Change Earlier Than Tissue Oxygen Tension in Hemorrhage
Crystalloids versus colloids for goal-directed fluid therapy in major surgery
![]() |
Prof. Dr. med. Robert Greif, MME E-mail
RCTs comparing the efficacy of new supraglottic airway devices, fiberoptic intubation, and rigid fiberoptic stilts in simulated difficult airway situations.
Working Group: L. Theiler, N. Urwyler, M. Kleine-Brüggeney, Thomas Merkt, Reto Basciani, M. Wipfli, Hendrik Fischer
Evaluation of the efficacy of iv-THC on PONV, genetic influence of polimorphisms on pharmacokinetics.
Working Group: L. Theiler, M. Kleine-Brüggeney, Thomas Merkt, cooperation with W. Bernhard, Inst. Legal Medizin, University of Bern, H. Sachs, Forensic and Toxicologic Center, Munich
Evaluation of POC-Devices (measuring PT, and Thrombelastograpy) at the OR and ICU-setting and its influence on the use of bloodproducts
Dr. Natalie Urwyler, cooperation with PD Dr. A. Lorenzo Dept. Hematology, and Prof. P. Jüni, Clinical Trail Unit, ISPM, University of Bern
Laboratory investigations about possible interactions of commonly used i.v. drugs in anesthesia.
Michel Braun, R. Lauber, cooperation with Dr. K. Nemec, Hospital Pharmacy, Donauspital Vienna Austria and Dr. J. Goette, Inst. F. Hospital Pharmacy
![]() |
PD Dr. med. Martin Luginbühl E-mail
Current hypnotic and opioid concentrations are predicted based on published models on pharmacokinetics and interaction pharmacodynamics and are presented to the anaesthesiologist either in a concentration based two dimensional plot or as a nociceptive stimulus response index in a time-based manner. The concentrations are related to published hypnotic – opioid interaction isoboles to enable the anaesthesiologist to administer hypnotics and opioids on a rational basis.
Main author: Peter M. Schumacher, PhD, Dr. sc. techn.
Cooperation: Prof. M. Stryus, Department of Anaesthesia, Ghent University Hospital, Belgium and Dr. med. S. Stahlkopf and co-workers, Dräger Medical, Lübeck, Germany
The presence of pain may increase spontaneous respiration, whereas opioids induce potentially severe respiratory depression. It is not known in how far postoperative pain antagonizes opioids induced respiratory depression. In an on-going study remifentanil induced respiratory depression before and after major orthopaedic surgery is compared.
Main author: Martin Luginbühl, PD Dr. med.
Cooperation: Antonello Caruso and Manfred Morari, Professor, Automatic Control Laboratory, Swiss Federal Institute of Technology (ETH)
Peter M. Schumacher, M Sc Techn, Ph.D. SenTec AG, Therwil, Switzerland
The limitation of propofol used in conscious sedation is respiratory depression and airway collapse. The effect site propofol concentration inducing sedation and respiratory depression are both in a similar range. We are developing a control algorithm to automatically administer propofol for sedation using transcutaneous CO2 as controlled variable for a clinical proof of concept study.
Main author: Peter M. Schumacher, PhD, Dr. sc. techn.
Cooperation: Antonello Caruso, and Manfred Morari, Professor, Automatic Control Laboratory, Swiss Federal Institute of Technology (ETH)
Peter M. Schumacher, M Sc Techn, Ph.D. SenTec AG, Therwil, Switzerland
http://www.sentec.ch
http://www.amca2005.unibe.ch
http://control.ee.ethz.ch
![]() |
Dr. med. Andreas Vogt E-mail
The multiple inert gas elimination technique (MIGET) was developed for the measurement of shunt and VA’/Q’ distributions. Micropore membrane inlet mass spectrometry (MMIMS), instead of gas chromatography (GC), has been introduced for inert gas measurement and shunt determination. The single-pore version of MMIMS correlated well with Riley shunt during oxygen breathing in a porcine lavage lung model. (Anesth Analg 2009;X:●●●–●●●)
A multi pore probe as further refinement has been implemented in this developing technology to achieve an accuracy equivalent to conventional MIGET.
Multi frequency phase fluorimetry (MFPF-100, TauTheta, USA) is a recently presented technique for the measurement of oxygen partial pressure. Multi frequency phase fluorimetry provides accurate reproducibility for oxygen partial pressure measurements and agreement with Clark type sensor analysis as gold standard is acceptable.
PaO2 oscillations, detected near the left ventricular outflow tract, proceeded to the aortic bifurcation, but not to the central venous system. Further studies are planned to evaluate the impact of PaO2 oscillations in ARDS.
B. Duenges1, PhD, M. Bodenstein1, M.D., H. Wang1, M.D., PhD, St. Böhme1, M.S., B. Röhrig2, PhD, J. E. Baumgardner3, M.D., PhD, K. Markstaller1, M.D., PhD
1 Department of Anaesthesiology, Johannes Gutenberg-University, Mainz, Germany
2 Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), Johannes Gutenberg-University, Mainz, Germany
3 Oscillogy®, LLC, Folsom PA
German Research Foundation DFG Ma 2398 / 3, Swiss National Foundation SNF POIB - 117065 / 1 and an institutional grant of the Department of Anaesthesiology, Inselspital, Bern University Hospital, and University of Bern
All experiments were performed at the Department of Anaesthesiology, Johannes Gutenberg - University, Mainz Germany (Chair: Univ. - Prof. C. Werner).
![]() |
Prof. Dr. med. Frank Stüber E-mail
![]() |
PD Dr. med. Lutz Lehmann E-mail
![]() |
Dr. med. Malte Book E-mail
In two unrelated individuals the vast majority of the human genome sequence is identical. However, the rare interindividual variations in our genotype cause our different phenotypes. These differences are not limited to a human’s look, character or skills. Phenotypic differences also contain differences in the susceptibility for, or the course of, complex diseases, different kinetics of physiologic processes or different quantitative physiologic functions. An impressive example for the heritability of susceptibility was reported in 1988: The death due to infection is heritable if one parent died due to infection in the first 50 years of life. This association was shown to be much stronger compared to the usual suspects such as cancer or cardio circulatory events. Another example is that the metabolization of opioids which determines the duration of the drug effect partially depends on the individual genetic background.
The usage of individual genetic data offers the opportunity to individualize medical treatment in a completely new perception. The group of Professor Stüber is working with different project in this field.
The overall frequency of SNPs is about 1 to 1,000 to 1 to 1200 base pairs in the human genome with the most frequent being a C to T substitution. These polymorphisms are located in the entire genome. Today’s technical tools allow the characterization of 1,000,000 SNP in parallel. By using the information of so called tag-SNPs founded on linkage disequilibrium in haplotype blocks, these data can be equalized to a whole genome SNP scan. Our group has running projects in the field of severe trauma, inflammation and sepsis.
Deletions, insertions, duplications and complex multi site variants are termed as copy number polymorphisms and the length is defined as a DNA segment that is 1kb or longer and present a variable copy number in comparison with a reference genome. The importance and the consequences of these genetic variants became clear in 2003. Hollox and co workers reported about three genes on chromosome 8p23.1 which are polymorphic in copy number. In 2006 Redon and co workers reported about a first-generation CNV map of the human genome. This map was established in the 270 individuals from the HapMap population. They detected 1,447 copy number variable regions covering 12% of the human genome. One of the key questions is whether different copy numbers result in modifying gene transcription and protein release. Our group is working in the field of CNVs with a project in human Defensins which are antimicrobial molecules acting in the innate immune system and another project is working on enzymes of the Cytochrome P450 system involved in drug metabolization.
The (semi-) quantification of the genome wide gene expression in complex diseases or specific therapeutical procedures allows the discovery of the involved pathophysiological processes. This method enables researchers to define phenotypes much more precise than just by the clinical diagnosis “inflammation”. The combination of genome wide genotype data with gene expression data might improve our knowledge about individuals being at risk for special phenotypes such as hyperinflammation or wound infections. We are going to start a project assessing the gene expression in patients with hyperinflammation.
![]() |
Prof. Dr. med. Balthasar Eberle e-mail
Curriculum Vitae
Dr. Alban Neziri, wissenschaftlicher Mitarbeiter E - Mail
Anja Conrad, Study Nurse E - Mail
Volker Hartwich, Study Nurse E - Mail
Labor
Dr. Rolf Lauber, Chemiker E - Mail
Sibylle Rohrbach Wirthmüller, Chemielaborantin EFZ E - Mail
Marcel Schiff, Laborleiter E - Mail
Xianghong Zhang, Doktorand E - Mail
Lan Zhang, Doktorandin E - Mail