Now showing 1 - 10 of 15
  • 2021-03-11Journal Article Research Paper
    [["dc.bibliographiccitation.artnumber","46"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine"],["dc.bibliographiccitation.volume","29"],["dc.contributor.author","MS, Roessler"],["dc.contributor.author","Riffelmann, M"],["dc.contributor.author","Kunze-Szikszay, N."],["dc.contributor.author","Lier, M"],["dc.contributor.author","Schmid, O"],["dc.contributor.author","Haus, H"],["dc.contributor.author","Schneider, S"],["dc.contributor.author","JF, Heuer"],["dc.date.accessioned","2021-04-14T08:28:07Z"],["dc.date.accessioned","2022-08-16T12:42:16Z"],["dc.date.available","2021-04-14T08:28:07Z"],["dc.date.available","2022-08-16T12:42:16Z"],["dc.date.issued","2021-03-11"],["dc.date.updated","2022-07-29T12:17:56Z"],["dc.description.abstract","Abstract\r\n \r\n Background\r\n Spinal stabilisation is recommended for prehospital trauma treatment. In Germany, vacuum mattresses are traditionally used for spinal stabilisation, whereas in anglo-american countries, long spine boards are preferred. While it is recommended that the on-scene time is as short as possible, even less than 10 minutes for unstable patients, spinal stabilisation is a time-consuming procedure. For this reason, the time needed for spinal stabilisation may prevent the on-scene time from being brief. The aim of this simulation study was to compare the time required for spinal stabilisation between a scoop stretcher in conjunction with a vacuum mattress and a long spine board.\r\n \r\n \r\n Methods\r\n Medical personnel of different professions were asked to perform spinal immobilizations with both methods. A total of 172 volunteers were immobilized under ideal conditions as well as under realistic conditions. A vacuum mattress was used for 78 spinal stabilisations, and a long spinal board was used for 94. The duration of the procedures were measured by video analysis.\r\n \r\n \r\n Results\r\n Under ideal conditions, spinal stabilisation on a vacuum mattress and a spine board required 254.4 s (95 % CI 235.6–273.2 s) and 83.4 s (95 % CI 77.5–89.3 s), respectively (p < 0.01). Under realistic conditions, the vacuum mattress and spine board required 358.3 s (95 % CI 316.0–400.6 s) and 112.6 s (95 % CI 102.6–122.6 s), respectively (p < 0.01).\r\n \r\n \r\n Conclusions\r\n Spinal stabilisation for trauma patients is significantly more time consuming on a vacuum mattress than on a long spine board. Considering that the prehospital time of EMS should not exceed 60 minutes and the on-scene time should not exceed 30 minutes or even 10 minutes if the patient is in extremis, based on our results, spinal stabilisation on a vacuum mattress may consume more than 20 % of the recommended on-scene time. In contrast, stabilisation on a spine board requires only one third of the time required for that on a vacuum mattress.\r\n We conclude that a long spine board may be feasible for spinal stabilisation for critical trauma patients with timesensitive life threatening ABCDE-problems to ensure the shortest possible on-scene time for prehospital trauma treatment, not least if a patient has to be rescued from an open or inaccessible terrain, especially that with uneven overgrown land."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2021"],["dc.identifier.citation","Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine. 2021 Mar 11;29(1):46"],["dc.identifier.doi","10.1186/s13049-021-00854-w"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17743"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82507"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/112740"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.notes.intern","Merged from goescholar"],["dc.relation.eissn","1757-7241"],["dc.relation.orgunit","Klinik für Anästhesiologie"],["dc.rights","CC BY 4.0"],["dc.rights.holder","The Author(s)"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.subject","Long spine board"],["dc.subject","Prehospital trauma treatment"],["dc.subject","Spinal stabilisation"],["dc.subject","Vacuum mattress"],["dc.title","Vacuum mattress or long spine board: which method of spinal stabilisation in trauma patients is more time consuming? A simulation study"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]
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  • 2021Journal Article
    [["dc.bibliographiccitation.firstpage","6245"],["dc.bibliographiccitation.issue","16-17"],["dc.bibliographiccitation.journal","Applied Microbiology and Biotechnology"],["dc.bibliographiccitation.lastpage","6255"],["dc.bibliographiccitation.volume","105"],["dc.contributor.author","Kunze-Szikszay, Nils"],["dc.contributor.author","Euler, Maximilian"],["dc.contributor.author","Perl, Thorsten"],["dc.date.accessioned","2021-09-01T06:42:43Z"],["dc.date.available","2021-09-01T06:42:43Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract Diagnosis of bacterial infections until today mostly relies on conventional microbiological methods. The resulting long turnaround times can lead to delayed initiation of adequate antibiotic therapy and prolonged periods of empiric antibiotic therapy (e.g., in intensive care medicine). Therewith, they contribute to the mortality of bacterial infections and the induction of multidrug resistances. The detection of species specific volatile organic compounds (VOCs) emitted by bacteria has been proposed as a possible diagnostic approach with the potential to serve as an innovative point-of-care diagnostic tool with very short turnaround times. A range of spectrometric methods are available which allow the detection and quantification of bacterial VOCs down to a range of part per trillion. This narrative review introduces the application of spectrometric analytical methods for the purpose of detecting VOCs of bacterial origin and their clinical use for diagnosing different infectious conditions over the last decade. Key Points • Detection of VOCs enables bacterial differentiation in various medical conditions. • Spectrometric methods may function as point-of-care diagnostics in near future."],["dc.description.abstract","Abstract Diagnosis of bacterial infections until today mostly relies on conventional microbiological methods. The resulting long turnaround times can lead to delayed initiation of adequate antibiotic therapy and prolonged periods of empiric antibiotic therapy (e.g., in intensive care medicine). Therewith, they contribute to the mortality of bacterial infections and the induction of multidrug resistances. The detection of species specific volatile organic compounds (VOCs) emitted by bacteria has been proposed as a possible diagnostic approach with the potential to serve as an innovative point-of-care diagnostic tool with very short turnaround times. A range of spectrometric methods are available which allow the detection and quantification of bacterial VOCs down to a range of part per trillion. This narrative review introduces the application of spectrometric analytical methods for the purpose of detecting VOCs of bacterial origin and their clinical use for diagnosing different infectious conditions over the last decade. Key Points • Detection of VOCs enables bacterial differentiation in various medical conditions. • Spectrometric methods may function as point-of-care diagnostics in near future."],["dc.identifier.doi","10.1007/s00253-021-11469-7"],["dc.identifier.pii","11469"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/89126"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-455"],["dc.relation.eissn","1432-0614"],["dc.relation.issn","0175-7598"],["dc.title","Identification of volatile compounds from bacteria by spectrometric methods in medicine diagnostic and other areas: current state and perspectives"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]
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  • 2016Journal Article
    [["dc.bibliographiccitation.artnumber","122"],["dc.bibliographiccitation.journal","Scandinavian Journal of Trauma Resuscitation and Emergency Medicine"],["dc.bibliographiccitation.volume","24"],["dc.contributor.author","Kunze-Szikszay, Nils"],["dc.contributor.author","Krack, Lennart A."],["dc.contributor.author","Wildenauer, Pauline"],["dc.contributor.author","Wand, Saskia"],["dc.contributor.author","Heyne, Tim"],["dc.contributor.author","Walliser, Karoline"],["dc.contributor.author","Spering, Christopher"],["dc.contributor.author","Bauer, Martin"],["dc.contributor.author","Quintel, Michael"],["dc.contributor.author","Roessler, Markus"],["dc.date.accessioned","2018-11-07T10:07:07Z"],["dc.date.available","2018-11-07T10:07:07Z"],["dc.date.issued","2016"],["dc.description.abstract","Background: Hyperfibrinolysis (HF) is a major contributor to coagulopathy and mortality in trauma patients. This study investigated (i) the rate of HF during the pre-hospital management of patients with multiple injuries and (ii) the effects of pre-hospital tranexamic acid (TxA) administration on the coagulation system. Methods: From 27 trauma patients with pre-hospital an estimated injury severity score (ISS) >= 16 points blood was obtained at the scene and on admission to the emergency department (ED). All patients received 1 g of TxA after the first blood sample was taken. Rotational thrombelastometry (ROTEM) was performed for both blood samples, and the results were compared. HF was defined as a maximum lysis (ML) >15 % in EXTEM. Results: The median (min-max) ISS was 17 points (4-50 points). Four patients (15 %) had HF diagnosed via ROTEM at the scene, and 2 patients (7.5 %) had HF diagnosed via ROTEM on admission to the ED. The median ML before TxA administration was 11 % (3-99 %) vs. 10 % after TxA administration (4-18 %; p > 0.05). TxA was administered 37 min (10-85 min) before ED arrival. The ROTEM results before and after TxA administration did not significantly differ. No adverse drug reactions were observed after TxA administration. Discussion: HF can be present in severely injured patients during pre-hospital care. Antifibrinolytic therapy administered at the scene is a significant time saver. Even in milder trauma fibrinogen can be decreased to critically low levels. Early administration of TxA cannot reverse or entirely stop this decrease. Conclusions: The pre-hospital use of TxA should be considered for severely injured patients to prevent the worsening of trauma-induced coagulopathy and unnecessarily high fibrinogen consumption."],["dc.identifier.doi","10.1186/s13049-016-0314-4"],["dc.identifier.isi","000384950400003"],["dc.identifier.pmid","27724970"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/13894"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/39223"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Biomed Central Ltd"],["dc.relation.issn","1757-7241"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","The pre-hospital administration of tranexamic acid to patients with multiple injuries and its effects on rotational thrombelastometry: a prospective observational study in pre-hospital emergency medicine"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]
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  • 2021-02-28Journal Article
    [["dc.bibliographiccitation.artnumber","69"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","BMC Microbiology"],["dc.bibliographiccitation.volume","21"],["dc.contributor.author","Kunze-Szikszay, Nils"],["dc.contributor.author","Euler, Maximilian"],["dc.contributor.author","Kuhns, Martin"],["dc.contributor.author","Thieß, Melanie"],["dc.contributor.author","Groß, Uwe"],["dc.contributor.author","Quintel, Michael"],["dc.contributor.author","Perl, Thorsten"],["dc.date.accessioned","2021-04-14T08:28:09Z"],["dc.date.accessioned","2022-08-18T12:35:52Z"],["dc.date.available","2021-04-14T08:28:09Z"],["dc.date.available","2022-08-18T12:35:52Z"],["dc.date.issued","2021-02-28"],["dc.date.updated","2022-07-29T12:07:23Z"],["dc.description.abstract","Abstract\r\n \r\n Background\r\n Hospital-acquired pneumonia (HAP) is a common problem in intensive care medicine and the patient outcome depends on the fast beginning of adequate antibiotic therapy. Until today pathogen identification is performed using conventional microbiological methods with turnaround times of at least 24 h for the first results. It was the aim of this study to investigate the potential of headspace analyses detecting bacterial species-specific patterns of volatile organic compounds (VOCs) for the rapid differentiation of HAP-relevant bacteria.\r\n \r\n \r\n Methods\r\n Eleven HAP-relevant bacteria (Acinetobacter baumanii, Acinetobacter pittii, Citrobacter freundii, Enterobacter cloacae, Escherichia coli, Klebsiella oxytoca, Klebsiella pneumoniae, Pseudomonas aeruginosa, Proteus mirabilis, Staphylococcus aureus, Serratia marcescens) were each grown for 6 hours in Lysogeny Broth and the headspace over the grown cultures was investigated using multi-capillary column-ion mobility spectrometry (MCC-IMS) to detect differences in the VOC composition between the bacteria in the panel. Peak areas with changing signal intensities were statistically analysed, including significance testing using one-way ANOVA or Kruskal-Wallis test (p < 0.05).\r\n \r\n \r\n Results\r\n 30 VOC signals (23 in the positive ion mode and 7 in the negative ion mode of the MCC-IMS) showed statistically significant differences in at least one of the investigated bacteria. The VOC patterns of the bacteria within the HAP panel differed substantially and allowed species differentiation.\r\n \r\n \r\n Conclusions\r\n MCC-IMS headspace analyses allow differentiation of bacteria within HAP-relevant panel after 6 h of incubation in a complex fluid growth medium. The method has the potential to be developed towards a feasible point-of-care diagnostic tool for pathogen differentiation on HAP."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2021"],["dc.identifier.citation","BMC Microbiology. 2021 Feb 28;21(1):69"],["dc.identifier.doi","10.1186/s12866-021-02102-8"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17742"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82517"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/112945"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.notes.intern","Merged from goescholar"],["dc.publisher","BioMed Central"],["dc.relation.eissn","1471-2180"],["dc.rights","CC BY 4.0"],["dc.rights.holder","The Author(s)"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.subject","Pneumonia"],["dc.subject","Microbiological techniques"],["dc.subject","Volatile organic compound"],["dc.subject","Metabolite"],["dc.subject","Ion mobility spectrometry"],["dc.title","Headspace analyses using multi-capillary column-ion mobility spectrometry allow rapid pathogen differentiation in hospital-acquired pneumonia relevant bacteria"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]
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  • 2019Journal Article
    [["dc.bibliographiccitation.firstpage","708"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Anaesthesia"],["dc.bibliographiccitation.lastpage","713"],["dc.bibliographiccitation.volume","74"],["dc.contributor.author","Perl, T."],["dc.contributor.author","Kunze‐Szikszay, N."],["dc.contributor.author","Bräuer, A."],["dc.contributor.author","Quintel, M."],["dc.contributor.author","Röhrig, A. L."],["dc.contributor.author","Kerpen, K."],["dc.contributor.author","Telgheder, U."],["dc.date.accessioned","2021-06-01T10:47:11Z"],["dc.date.available","2021-06-01T10:47:11Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1111/anae.14601"],["dc.identifier.eissn","1365-2044"],["dc.identifier.issn","0003-2409"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/85512"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.eissn","1365-2044"],["dc.relation.issn","0003-2409"],["dc.title","Aluminium release by coated and uncoated fluid‐warming devices"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]
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  • 2017Journal Article
    [["dc.bibliographiccitation.artnumber","46"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Intensive Care Medicine Experimental"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Cambiaghi, Barbara"],["dc.contributor.author","Vasques, Francesco"],["dc.contributor.author","Mörer, Onnen"],["dc.contributor.author","Ritter, Christian"],["dc.contributor.author","Mauri, Tommaso"],["dc.contributor.author","Kunze-Szikszay, Nils"],["dc.contributor.author","Holke, Karin"],["dc.contributor.author","Collino, Francesca"],["dc.contributor.author","Maiolo, Giorgia"],["dc.contributor.author","Rapetti, Francesca"],["dc.contributor.author","Schulze-Kalthoff, Elias"],["dc.contributor.author","Tonetti, Tommaso"],["dc.contributor.author","Hahn, Günter"],["dc.contributor.author","Quintel, Michael"],["dc.contributor.author","Gattinoni, Luciano"],["dc.date.accessioned","2020-12-10T18:41:24Z"],["dc.date.available","2020-12-10T18:41:24Z"],["dc.date.issued","2017"],["dc.description.abstract","Abstract Background Severe hypoperfusion can cause lung damage. We studied the effects of regional perfusion block in normal lungs and in the lungs that had been conditioned by lavage with 500 ml saline and high V T (20 ml kg−1) ventilation. Methods Nineteen pigs (61.2 ± 2.5 kg) were randomized to five groups: controls (n = 3), the right lower lobe block alone (n = 3), lavage and high V T (n = 4), lung lavage, and high V T plus perfusion block of the right (n = 5) or left (n = 4) lower lobe. Gas exchange, respiratory mechanics, and hemodynamics were measured hourly. After an 8-h observation period, CT scans were obtained at 0 and 15 cmH2O airway pressure. Results Perfusion block did not damage healthy lungs. In conditioned lungs, the left perfusion block caused more edema in the contralateral lung (777 ± 62 g right lung vs 484 ± 204 g left; p < 0.05) than the right perfusion block did (581 ± 103 g right lung vs 484 ± 204 g left; p n.s.). The gas/tissue ratio, however, was similar (0.5 ± 0.3 and 0.8 ± 0.5; p n.s.). The lobes with perfusion block were not affected (gas/tissue ratio right 1.6 ± 0.9; left 1.7 ± 0.5, respectively). Pulmonary artery pressure, PaO2/FiO2, dead space, and lung mechanics were more markedly affected in animals with left perfusion block, while the gas/tissue ratios were similar in the non-occluded lobes. Conclusions The right and left perfusion blocks caused the same “intensity” of edema in conditioned lungs. The total amount of edema in the two lungs differed because of differences in lung size. If capillary permeability is altered, increased blood flow may induce or increase edema."],["dc.identifier.doi","10.1186/s40635-017-0161-2"],["dc.identifier.eissn","2197-425X"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/15183"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/77572"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.publisher","Springer"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Effects of regional perfusion block in healthy and injured lungs"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]
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  • 2016Journal Article
    [["dc.bibliographiccitation.firstpage","158"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Clinical Physiology and Functional Imaging"],["dc.bibliographiccitation.lastpage","162"],["dc.bibliographiccitation.volume","38"],["dc.contributor.author","Cambiaghi, B."],["dc.contributor.author","Moerer, O."],["dc.contributor.author","Kunze-Szikszay, N."],["dc.contributor.author","Mauri, T."],["dc.contributor.author","Just, A."],["dc.contributor.author","Dittmar, J."],["dc.contributor.author","Hahn, G."],["dc.date.accessioned","2020-12-10T18:27:14Z"],["dc.date.available","2020-12-10T18:27:14Z"],["dc.date.issued","2016"],["dc.identifier.doi","10.1111/cpf.12385"],["dc.identifier.issn","1475-0961"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/76282"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","A spiky pattern in the course of electrical thoracic impedance as a very early sign of a developing pneumothorax"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]
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  • 2017Journal Article
    [["dc.bibliographiccitation.firstpage","284"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","Laboratory Animals"],["dc.bibliographiccitation.lastpage","291"],["dc.bibliographiccitation.volume","51"],["dc.contributor.author","Reupke, Verena"],["dc.contributor.author","Walliser, Karoline"],["dc.contributor.author","Perl, Thorsten"],["dc.contributor.author","Kimmina, Sarah"],["dc.contributor.author","Schraepler, Anke"],["dc.contributor.author","Quintel, Michael"],["dc.contributor.author","Kunze-Szikszay, Nils"],["dc.date.accessioned","2018-11-07T10:23:32Z"],["dc.date.available","2018-11-07T10:23:32Z"],["dc.date.issued","2017"],["dc.description.abstract","The aim of this study was to evaluate a total intravenous anaesthesia (TIVA) protocol using propofol and sufentanil without neuromuscular blocking agents (NBAs) for a non-recovery lung pathology study in rabbits including 10 h of pressure-controlled ventilation. TIVA was started with 20 mg/kg/h propofol and 0.5 mg/kg/h sufentanil. The depth of anaesthesia was assessed by reflex testing and monitoring of spontaneous movements or respiratory efforts. Vital parameters were monitored to assess the effects of the TIVA protocol. The infusion rates were increased whenever reflex testing indicated inadequate depth of anaesthesia, and were reduced when vital parameters indicated unnecessarily deep levels. Median infusion rates of 35 mg/kg/h propofol and 2.0 mg/kg/h sufentanil were needed to ensure an adequate depth of anaesthesia. This protocol suppressed spontaneous movements, breathing and palpebral reflexes, but was unable to suppress corneal and pedal withdrawal reflexes. Since significant drops in arterial blood pressure (ABP) were observed and the animals were not exposed to painful procedures, positive corneal and pedal withdrawal reflexes were tolerated. In conclusion, propofol and sufentanil is a suitable combination for long-term anaesthesia in non-recovery lung pathology models in rabbits without painful procedures. ABP must be monitored carefully because of the circulatory side-effects, but it is an inappropriate surrogate marker for depth of anaesthesia. Due to the lack of neuromuscular blockade this TIVA protocol allows the adjustment of infusion rates based on reflex testing. The resulting decreased risk of unnoticed awareness is a decisive refinement in anaesthesia for similar studies including long-term mechanical ventilation in rabbits."],["dc.description.sponsorship","Faculty of Medicine of the University of Gottingen"],["dc.identifier.doi","10.1177/0023677216660337"],["dc.identifier.isi","000401251400005"],["dc.identifier.pmid","27413175"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42476"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Sage Publications Inc"],["dc.relation.issn","1758-1117"],["dc.relation.issn","0023-6772"],["dc.title","Total intravenous anaesthesia using propofol and sufentanil allows controlled long-term ventilation in rabbits without neuromuscular blocking agents"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]
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  • 2020Journal Article
    [["dc.bibliographiccitation.firstpage","834"],["dc.bibliographiccitation.issue","6"],["dc.bibliographiccitation.journal","Anaesthesia"],["dc.bibliographiccitation.lastpage","834"],["dc.bibliographiccitation.volume","75"],["dc.contributor.author","Perl, T."],["dc.contributor.author","Kunze‐Szikszay, N."],["dc.contributor.author","Bräuer, A."],["dc.contributor.author","Roy, T."],["dc.date.accessioned","2021-04-14T08:25:28Z"],["dc.date.available","2021-04-14T08:25:28Z"],["dc.date.issued","2020"],["dc.identifier.doi","10.1111/anae.15020"],["dc.identifier.eissn","1365-2044"],["dc.identifier.issn","0003-2409"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/81639"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","1365-2044"],["dc.relation.issn","0003-2409"],["dc.title","Quantified aluminium levels released into blood and fluids using the Level 1 Fast Flow Fluid Warmer"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]
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  • 2019Journal Article
    [["dc.bibliographiccitation.firstpage","9091"],["dc.bibliographiccitation.issue","21-22"],["dc.bibliographiccitation.journal","Applied Microbiology and Biotechnology"],["dc.bibliographiccitation.lastpage","9101"],["dc.bibliographiccitation.volume","103"],["dc.contributor.author","Drees, Carolin"],["dc.contributor.author","Vautz, Wolfgang"],["dc.contributor.author","Liedtke, Sascha"],["dc.contributor.author","Rosin, Christopher"],["dc.contributor.author","Althoff, Kirsten"],["dc.contributor.author","Lippmann, Martin"],["dc.contributor.author","Zimmermann, Stefan"],["dc.contributor.author","Legler, Tobias J."],["dc.contributor.author","Yildiz, Duygu"],["dc.contributor.author","Perl, Thorsten"],["dc.contributor.author","Kunze-Szikszay, Nils"],["dc.date.accessioned","2020-12-10T14:09:58Z"],["dc.date.available","2020-12-10T14:09:58Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1007/s00253-019-10181-x"],["dc.identifier.eissn","1432-0614"],["dc.identifier.issn","0175-7598"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/70625"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","GC-IMS headspace analyses allow early recognition of bacterial growth and rapid pathogen differentiation in standard blood cultures"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]
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