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Verfasst von:Pinder, Nadine [VerfasserIn]   i
 Bruckner, Thomas [VerfasserIn]   i
 Lehmann, Monika [VerfasserIn]   i
 Motsch, Johann [VerfasserIn]   i
 Brenner, Thorsten [VerfasserIn]   i
 Larmann, Jan [VerfasserIn]   i
 Knebel, Phillip [VerfasserIn]   i
 Hoppe-Tichy, Torsten [VerfasserIn]   i
 Swoboda, Stefanie [VerfasserIn]   i
 Weigand, Markus A. [VerfasserIn]   i
 Hofer, Stefan [VerfasserIn]   i
 Zimmermann, Johannes B. [VerfasserIn]   i
Titel:Effect of physostigmine on recovery from septic shock following intra-abdominal infection - Results from a randomized, double-blind, placebo-controlled, monocentric pilot trial (Anticholium® per Se)
Verf.angabe:Nadine Pinder, Thomas Bruckner, Monika Lehmann, Johann Motsch, Thorsten Brenner, Jan Larmann, Phillip Knebel, Torsten Hoppe-Tichy, Stefanie Swoboda, Markus A. Weigand, Stefan Hofer, Johannes B. Zimmermann
E-Jahr:2019
Jahr:August 2019
Umfang:10 S.
Fussnoten:Gesehen am 10.07.2019 ; Available online 9 April 2019
Titel Quelle:Enthalten in: Journal of critical care
Ort Quelle:[Amsterdam] : Elsevier, 1986
Jahr Quelle:2019
Band/Heft Quelle:52(2019), Seite 126-135
ISSN Quelle:1557-8615
Abstract:Purpose - The cholinergic anti-inflammatory pathway has been shown to be accessible by physostigmine salicylate in animal models. However, the cholinesterase inhibitor is not approved for adjunctive therapy in sepsis, and tolerability and safety of high initial doses followed by continuous infusion have not been investigated. - Materials and methods - In this trial, 20 patients with perioperative septic shock due to intra-abdominal infection were eligible. The physostigmine group received an initial dose of 0.04mg/kg physostigmine salicylate, followed by continuous infusion of 1mg/h for 120h; the placebo group was treated with 0.9% sodium chloride. Primary outcome was the mean Sequential Organ Failure Assessment (SOFA) score during treatment and up to 14days. - Results - Administration of physostigmine salicylate was well tolerated. Mean SOFA scores were 8.9±2.5 and 11.3±3.6 (mean±SD) for physostigmine and placebo group, respectively. Adjusted for age, difference between means was not statistically significant (−2.37, 95% CI: −5.43 to 0.70, p=0.121). Norepinephrine doses required only appeared lower in the physostigmine group (p=0.064), along with a more rapid reduction from an elevated heart rate possibly indicating less hemodynamic instability. - Conclusions - Treatment with physostigmine salicylate was feasible and safe. Further studies are justified to assess the effect on recovery from septic shock. - Trial registration - EudraCT Number 2012-001650-26, ClinicalTrials.gov identifier NCT03013322.
DOI:doi:10.1016/j.jcrc.2019.04.012
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1016/j.jcrc.2019.04.012
 Volltext: http://www.sciencedirect.com/science/article/pii/S088394411930098X
 DOI: https://doi.org/10.1016/j.jcrc.2019.04.012
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Adjunctive therapy
 Antilirium
 Cholinergic anti-inflammatory pathway
 Cholinesterase inhibitor
 Perioperative sepsis
 Sequential Organ Failure Assessment (SOFA) score
K10plus-PPN:1668922738
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