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Variations of renal tissue oxygenation during abdominal compartment syndrome and sepsis.

TitleVariations of renal tissue oxygenation during abdominal compartment syndrome and sepsis.
Publication TypeJournal Article
Year of Publication2017
AuthorsKalfadis, S., Nalbanti V., Ioannidis O., Porfiriou G., Botsios D., & Tsalis K.
JournalAdv Med Sci
Volume62
Issue1
Pagination177-185
Date Published2017 Mar
ISSN1898-4002
KeywordsAnimals, Carbon Dioxide, Dogs, Female, Intra-Abdominal Hypertension, Kidney, Male, Oxygen, Sepsis
Abstract

PURPOSE: This experimental study was designed to evaluate the renal tissue oxygenation under the coexistence of abdominal compartment syndrome and sepsis.MATERIAL AND METHODS: Fourteen non-breed dogs were divided into two groups: the control group (8) and the study group (6). Sepsis was established with intravenous endotoxin infusion at 100μg/kg for over 30min. Insufflation of CO in the peritoneal cavity was used for the increase in intra-abdominal pressure (IAP). A special catheter placed and fixed in the renal cortex at a depth of 3mm from the renal capsule was used for the measurement of renal tissue oxygenation.RESULTS: Study parameters were recorded at the starting phase, at IAP of 15mmHg and 30mmHg and after decompression of the abdomen in the control group, and at the same intervals plus the induction of sepsis, prior to increasing abdominal pressure, in the study group. With the elevation of the IAP a reduction of renal tissue oxygenation presents itself, which is more pronounced in the presence of sepsis, especially for IAP over 15mmHg. Like other parameters, after abdominal decompression the renal tissue oxygenation returns to the initial levels, independently of sepsis.CONCLUSIONS: The afferent arterioles vasoconstriction, which takes place during sepsis, and the intra-renal shunt, which occurs and leads to blood diversion to the medulla from the renal cortex due to the combination of intra-abdominal hypertension (IAH) and sepsis, seem to explain this finding.

DOI10.1016/j.advms.2016.08.004
Alternate JournalAdv Med Sci
PubMed ID28282605

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