Jan-Steffen Pooth

Dr. Jan-Steffen Pooth

University Medical Center Freiburg, Freiburg, Germany
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Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 July 2021 in Nature Reviews Neuroscience
Verified
Journal Article
Closed access
SDStefano G. Daniele
Stefano G. Daniele
GTGeorg Trummer
Georg Trummer
KHKonstantin A. Hossmann
Konstantin A. Hossmann
ZVZvonimir Vrselja
Zvonimir Vrselja
CBChristoph Benk
Christoph Benk
NSNenad Sestan
Nenad Sestan

23 November 2022 in Perfusion
Verified
Journal Article
Open access
APAlois Philipp
Alois Philipp
JPJan-Steffen Pooth
Jan-Steffen Pooth
CBChristoph Benk
Christoph Benk
TMThomas Mueller
Thomas Mueller
DLDirk Lunz
Dirk Lunz
Introduction: There is increasing evidence for extracorporeal cardiopulmonary resuscitation (ECPR) as a rescue therapy for selected patients in refractory cardiac arrest (CA). Besides patient selection, the control of reperfusion parameters is of eminent importance. Especially in out-of-hospital CA, monitoring and individualized, targeted reperfusion remains a great challenge for emergency personnel. The CARL® system is designed to enable an early control of a variety of reperfusion parameters and to pursue a targeted reperfusion strategy in ECPR. Case presentation: We report the first 10 ECPR applications of the CARL® system in Regensburg, Germany. Early blood gas analysis, oxygen titration and pressure monitoring were feasible and enabled an individualized and targeted reperfusion strategy in all patients. After suffering from refractory CA and prolonged resuscitation attempts, five out of the first 10 patients survived and were successfully discharged from the hospital (CPC one on hospital discharge). Conclusion: Application of the CARL® system contributed to early monitoring and control of reperfusion parameters. Whether targeted ECPR may have the potential to improve outcomes in refractory OHCA remains the subject of future investigations.

21 December 2023 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
GTGeorg Trummer
Georg Trummer
CBChristoph Benk
Christoph Benk
JPJan-Steffen Pooth
Jan-Steffen Pooth
TWTobias Wengenmayer
Tobias Wengenmayer
ASAlexander Supady
Alexander Supady
OGon behalf of the Extracorporeal Multi-Organ Repair Study Group
on behalf of the Extracorporeal Multi-Organ Repair Study Group
Background: Survival following cardiac arrest (CA) remains poor after conventional cardiopulmonary resuscitation (CCPR) (6–26%), and the outcomes after extracorporeal cardiopulmonary resuscitation (ECPR) are often inconsistent. Poor survival is a consequence of CA, low-flow states during CCPR, multi-organ injury, insufficient monitoring, and delayed treatment of the causative condition. We developed a new strategy to address these issues. Methods: This all-comers, multicenter, prospective observational study (69 patients with in- and out-of-hospital CA (IHCA and OHCA) after prolonged refractory CCPR) focused on extracorporeal cardiopulmonary support, comprehensive monitoring, multi-organ repair, and the potential for out-of-hospital cannulation and treatment. Result: The overall survival rate at hospital discharge was 42.0%, and a favorable neurological outcome (CPC 1+2) at 90 days was achieved for 79.3% of survivors (CPC 1+2 survival 33%). IHCA survival was very favorable (51.7%), as was CPC 1+2 survival at 90 days (41%). Survival of OHCA patients was 35% and CPC 1+2 survival at 90 days was 28%. The subgroup of OHCA patients with pre-hospital cannulation showed a superior survival rate of 57.1%. Conclusions: This new strategy focusing on repairing damage to multiple organs appears to improve outcomes after CA, and these findings should provide a sound basis for further research in this area.

11 April 2022 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
SBSam Brixius
Sam Brixius
JPJan-Steffen Pooth
Jan-Steffen Pooth
JHJörg Haberstroh
Jörg Haberstroh
DDDamjanovic Damjanovic
Damjanovic Damjanovic
CSChristian Scherer
Christian Scherer
GTGeorg Trummer
Georg Trummer
Survival and neurological outcomes after out-of-hospital cardiac arrest (OHCA) remain low. The further development of prehospital extracorporeal resuscitation (ECPR) towards Controlled Automated Reperfusion of the Whole Body (CARL) has the potential to improve survival and outcome in these patients. In CARL therapy, pulsatile, high blood-flow reperfusion is performed combined with several modified reperfusion parameters and adjusted defibrillation strategies. We aimed to investigate whether pulsatile, high-flow reperfusion is feasible in refractory OHCA and whether the CARL approach improves heart-rhythm control during ECPR. In a reality-based porcine model of refractory OHCA, 20 pigs underwent prehospital CARL or conventional ECPR. Significantly higher pulsatile blood-flow proved to be feasible, and critical hypotension was consistently prevented via CARL. In the CARL group, spontaneous rhythm conversions were observed using a modified priming solution. Applying potassium-induced secondary cardioplegia proved to be a safe and effective method for sustained rhythm conversion. Moreover, significantly fewer defibrillation attempts were needed, and cardiac arrhythmias were reduced during reperfusion via CARL. Prehospital CARL therapy thus not only proved to be feasible after prolonged OHCA, but it turned out to be superior to conventional ECPR regarding rhythm control.

27 January 2025 in Artificial Organs
Verified
Journal Article
Open access
JPJan-Steffen Pooth
Jan-Steffen Pooth
JFJil Kristin Förster
Jil Kristin Förster
CBChristoph Benk
Christoph Benk
PDPatric Diel
Patric Diel
SBSam Joé Brixius
Sam Joé Brixius
JBJulia Benk
Julia Benk
Introduction: Veno‐venous extracorporeal membrane oxygenation (V‐V ECMO) is increasingly used in the treatment of severe respiratory failure. Despite a significant increase in the worldwide use of extracorporeal lung assist devices recirculation remains a common complication and is associated with a reduced effectiveness of ECMO support and increased hemolysis. In this observational study we aimed to investigate the impact of cannula configuration and extracorporeal flow on recirculation. Materials and Methods: An observational retrospective study was performed, which included all patients, who received V‐V ECMO and recirculation measurements at the University Medical Center Freiburg between August 2021 and June 2023. Recirculation and extracorporeal flow were determined using ultrasonic indicator dilution technology. Patients were divided into subgroups according to their type of cannulation (dual lumen single‐site vs. bifemoral vs. femoro‐jugular). Results: A total of 215 recirculation measurements in 47 patients were performed. Dual lumen single‐site cannulation was associated with significantly lower recirculation rates (8.7% [0.0; 12.0]) compared to single lumen dual‐site cannulation (femoro‐jugular: 17.6% [0.0; 25.8]; bifemoral: 27.9% ± 13.4%). In addition, a positive linear correlation was observed between extracorporeal flow and recirculation in all subgroups. Recirculation increased significantly with rising extracorporeal flow in all subgroups. Conclusion: Recirculation is a common complication in V‐V ECMO and can lead to a reduction of ECMO effectiveness. Particular attention should be paid to optimal positioning of the cannulas in patients with more than one cannula. The ultrasonic indicator dilution method is a simple and quick method for measuring recirculation in V‐V ECMO and can be used at an early stage if effectiveness decreases.

23 May 2022 in Journal of Translational Medicine
Verified
Journal Article
Open access
PDF file
PBPatrick Bernhard
Patrick Bernhard
BBBerit Amelie Bretthauer
Berit Amelie Bretthauer
SBSam Joé Brixius
Sam Joé Brixius
HBHannah Bügener
Hannah Bügener
JGJohannes Elias Groh
Johannes Elias Groh
JPJan-Steffen Pooth
Jan-Steffen Pooth
Background: Only a small number of patients survive an out-of-hospital cardiac arrest (CA) and can be discharged from hospital alive with a large percentage of these patients retaining neurological impairments. In recent years, extracorporeal cardiopulmonary resuscitation (ECPR) has emerged as a beneficial strategy to optimize cardiac arrest treatment. However, ECPR is still associated with various complications. To reduce these problems, a profound understanding of the underlying mechanisms is required. This study aims to investigate the effects of CA, conventional cardiopulmonary resuscitation (CPR) and ECPR using a whole-body reperfusion protocol (controlled and automated reperfusion of the whole body—CARL) on the serum proteome profiles in a pig model of refractory CA. Methods: N = 7 pigs underwent 5 min of untreated CA followed by 30 min CPR and 120 min perfusion with CARL. Blood samples for proteomic analysis were drawn at baseline, after CPR and at the end of the CARL period. Following albumin-depletion, proteomic analysis was performed using liquid chromatography–tandem mass spectrometry. Results: N = 21 serum samples were measured resulting in the identification and quantification of 308–360 proteins per sample and 388 unique proteins in total. The three serum proteome profiles at the investigated time points clustered individually and segregated almost completely when considering a 90% confidence interval. Differential expression analysis showed significant abundance changes in 27 proteins between baseline and after CPR and in 9 proteins after CARL compared to CPR. Significant findings were further validated through a co-abundance cluster analysis corroborating the observed abundance changes. Conclusions: The presented data highlight the impact of systemic ischemia and reperfusion on the entire serum proteome during resuscitation with a special focus on changes regarding haemolysis, coagulation, inflammation, and cell-death processes. Generally, the observed changes contribute to post-ischemic complications. Better understanding of the underlying mechanisms during CA and resuscitation may help to limit these complications and improve therapeutic options.