-
Je něco špatně v tomto záznamu ?
Effects of Hyperoxia During Resuscitation From Hemorrhagic Shock in Swine With Preexisting Coronary Artery Disease
C. Hartmann, M. Loconte, E. Antonucci, M. Holzhauser, T. Hölle, D. Katzsch, T. Merz, O. McCook, U. Wachter, JA. Vogt, A. Hoffmann, M. Wepler, M. Gröger, M. Matejovic, E. Calzia, M. Georgieff, P. Asfar, P. Radermacher, BL. Nussbaum,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
- MeSH
- analýza krevních plynů MeSH
- cytokiny metabolismus MeSH
- funkční vyšetření srdce MeSH
- hemodynamika MeSH
- hemoragický šok epidemiologie mortalita patofyziologie terapie MeSH
- hypercholesterolemie epidemiologie MeSH
- hyperoxie patofyziologie MeSH
- krevní tlak MeSH
- náhodné rozdělení MeSH
- nemoci koronárních tepen epidemiologie MeSH
- prasata MeSH
- prospektivní studie MeSH
- resuscitace metody MeSH
- vyšetření funkce ledvin MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
OBJECTIVES: Investigation of the effects of hyperoxia during resuscitation from hemorrhagic shock in swine with preexisting coronary artery disease. DESIGN: Prospective, controlled, randomized trial. SETTING: University animal research laboratory. SUBJECTS: Nineteen hypercholesterolemic pigs with preexisting coronary artery disease. INTERVENTIONS: Anesthetized, mechanically ventilated, and surgically instrumented pigs underwent 3 hours of hemorrhagic shock (removal of 30% of the calculated blood volume and subsequent titration of mean arterial blood pressure ≈40 mm Hg). Postshock resuscitation (48 hr) comprised retransfusion of shed blood, crystalloids (balanced electrolyte solution), and norepinephrine support. Pigs were randomly assigned to "control" (FIO2 0.3, adjusted for arterial oxygen saturation ≥ 90%) and "hyperoxia" (FIO2 1.0 for 24 hr) groups. MEASUREMENTS AND MAIN RESULTS: Before, at the end of shock and every 12 hours of resuscitation, datasets comprising hemodynamics, calorimetry, blood gases, cytokines, and cardiac and renal function were recorded. Postmortem, organs were sampled for immunohistochemistry, western blotting, and mitochondrial high-resolution respirometry. Survival rates were 50% and 89% in the control and hyperoxia groups, respectively (p = 0.077). Apart from higher relaxation constant τ at 24 hours, hyperoxia did not affect cardiac function. However, troponin values were lower (2.2 [0.9-6.2] vs 6.9 [4.8-9.8] ng/mL; p < 0.05) at the end of the experiment. Furthermore, hyperoxia decreased cardiac 3-nitrotyrosine formation and increased inducible nitric oxide synthase expression. Plasma creatinine values were lower in the hyperoxia group during resuscitation coinciding with significantly improved renal mitochondrial respiratory capacity and lower 3-nitrotyrosine formation. CONCLUSIONS: Hyperoxia during resuscitation from hemorrhagic shock in swine with preexisting coronary artery disease reduced renal dysfunction and cardiac injury, potentially resulting in improved survival, most likely due to increased mitochondrial respiratory capacity and decreased oxidative and nitrosative stress. Compared with our previous study, the present results suggest a higher benefit of hyperoxia in comorbid swine due to an increased susceptibility to hemorrhagic shock.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18016281
- 003
- CZ-PrNML
- 005
- 20180518090855.0
- 007
- ta
- 008
- 180515s2017 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1097/CCM.0000000000002767 $2 doi
- 035 __
- $a (PubMed)29028763
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Hartmann, Clair $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany. Klinik für Anästhesiologie, Universitätsklinikum Ulm, Ulm, Germany.
- 245 10
- $a Effects of Hyperoxia During Resuscitation From Hemorrhagic Shock in Swine With Preexisting Coronary Artery Disease / $c C. Hartmann, M. Loconte, E. Antonucci, M. Holzhauser, T. Hölle, D. Katzsch, T. Merz, O. McCook, U. Wachter, JA. Vogt, A. Hoffmann, M. Wepler, M. Gröger, M. Matejovic, E. Calzia, M. Georgieff, P. Asfar, P. Radermacher, BL. Nussbaum,
- 520 9_
- $a OBJECTIVES: Investigation of the effects of hyperoxia during resuscitation from hemorrhagic shock in swine with preexisting coronary artery disease. DESIGN: Prospective, controlled, randomized trial. SETTING: University animal research laboratory. SUBJECTS: Nineteen hypercholesterolemic pigs with preexisting coronary artery disease. INTERVENTIONS: Anesthetized, mechanically ventilated, and surgically instrumented pigs underwent 3 hours of hemorrhagic shock (removal of 30% of the calculated blood volume and subsequent titration of mean arterial blood pressure ≈40 mm Hg). Postshock resuscitation (48 hr) comprised retransfusion of shed blood, crystalloids (balanced electrolyte solution), and norepinephrine support. Pigs were randomly assigned to "control" (FIO2 0.3, adjusted for arterial oxygen saturation ≥ 90%) and "hyperoxia" (FIO2 1.0 for 24 hr) groups. MEASUREMENTS AND MAIN RESULTS: Before, at the end of shock and every 12 hours of resuscitation, datasets comprising hemodynamics, calorimetry, blood gases, cytokines, and cardiac and renal function were recorded. Postmortem, organs were sampled for immunohistochemistry, western blotting, and mitochondrial high-resolution respirometry. Survival rates were 50% and 89% in the control and hyperoxia groups, respectively (p = 0.077). Apart from higher relaxation constant τ at 24 hours, hyperoxia did not affect cardiac function. However, troponin values were lower (2.2 [0.9-6.2] vs 6.9 [4.8-9.8] ng/mL; p < 0.05) at the end of the experiment. Furthermore, hyperoxia decreased cardiac 3-nitrotyrosine formation and increased inducible nitric oxide synthase expression. Plasma creatinine values were lower in the hyperoxia group during resuscitation coinciding with significantly improved renal mitochondrial respiratory capacity and lower 3-nitrotyrosine formation. CONCLUSIONS: Hyperoxia during resuscitation from hemorrhagic shock in swine with preexisting coronary artery disease reduced renal dysfunction and cardiac injury, potentially resulting in improved survival, most likely due to increased mitochondrial respiratory capacity and decreased oxidative and nitrosative stress. Compared with our previous study, the present results suggest a higher benefit of hyperoxia in comorbid swine due to an increased susceptibility to hemorrhagic shock.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a analýza krevních plynů $7 D001784
- 650 _2
- $a krevní tlak $7 D001794
- 650 _2
- $a nemoci koronárních tepen $x epidemiologie $7 D003324
- 650 _2
- $a cytokiny $x metabolismus $7 D016207
- 650 _2
- $a funkční vyšetření srdce $7 D006334
- 650 _2
- $a hemodynamika $7 D006439
- 650 _2
- $a hypercholesterolemie $x epidemiologie $7 D006937
- 650 _2
- $a hyperoxie $x patofyziologie $7 D018496
- 650 _2
- $a vyšetření funkce ledvin $7 D007677
- 650 _2
- $a prospektivní studie $7 D011446
- 650 _2
- $a náhodné rozdělení $7 D011897
- 650 _2
- $a resuscitace $x metody $7 D012151
- 650 _2
- $a hemoragický šok $x epidemiologie $x mortalita $x patofyziologie $x terapie $7 D012771
- 650 _2
- $a prasata $7 D013552
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Loconte, Maurizio $u Department of Surgical Sciences and Integrated Diagnostics, AOU IRCCS San Martino IST, University of Genoa, Genoa, Italy.
- 700 1_
- $a Antonucci, Elena $u Department of Surgical Sciences and Integrated Diagnostics, AOU IRCCS San Martino IST, University of Genoa, Genoa, Italy. Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
- 700 1_
- $a Holzhauser, Michael $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Hölle, Tobias $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Katzsch, David $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Merz, Tamara $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a McCook, Oscar $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Wachter, Ulrich $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Vogt, Josef A $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Hoffmann, Andrea $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Wepler, Martin $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany. Klinik für Anästhesiologie, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Gröger, Michael $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Matejovic, Martin $u 1st Medical Department, Biomedical Centre, Faculty of Medicine in Pilsen, Charles University, Prague, Czech Republic.
- 700 1_
- $a Calzia, Enrico $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Georgieff, Michael $u Klinik für Anästhesiologie, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Asfar, Pierre $u CNRS UMR 6214, INSERM U1083, Université Angers, Angers, France. Département de Réanimation Médicale et de Médecine Hyperbare, Centre Hospitalier Universitaire, Angers, France.
- 700 1_
- $a Radermacher, Peter $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany.
- 700 1_
- $a Nussbaum, Benedikt L $u Institut für Anästhesiologische Pathophysiologie und Verfahrensentwicklung, Universitätsklinikum Ulm, Ulm, Germany. Klinik für Anästhesiologie, Universitätsklinikum Ulm, Ulm, Germany.
- 773 0_
- $w MED00009514 $t Critical care medicine $x 1530-0293 $g Roč. 45, č. 12 (2017), s. e1270-e1279
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/29028763 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20180515 $b ABA008
- 991 __
- $a 20180518091032 $b ABA008
- 999 __
- $a ok $b bmc $g 1299905 $s 1013121
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 45 $c 12 $d e1270-e1279 $i 1530-0293 $m Critical care medicine $n Crit Care Med $x MED00009514
- LZP __
- $a Pubmed-20180515