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Temporal differences in the development of organ dysfunction based on two different approaches to induce experimental intra-abdominal hypertension in swine

BACKGROUND: Intra-abdominal hypertension [IAH] occurs frequently among critically ill patients and is associated with increased mortality and organ failure. Two porcine models of IAH that cause abdominal compartment syndrome [ACS] with organ dysfunction were created. We investigated whether the two...

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Detalles Bibliográficos
Autores principales: Moller, Michael, Kjerkegaard, Ulrik K, Larsen, Jens Rolighed, Birke-Sorensen, Hanne, Stolle, Lars B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390305/
https://www.ncbi.nlm.nih.gov/pubmed/24266989
http://dx.doi.org/10.1186/2110-5820-2-S1-S16
Descripción
Sumario:BACKGROUND: Intra-abdominal hypertension [IAH] occurs frequently among critically ill patients and is associated with increased mortality and organ failure. Two porcine models of IAH that cause abdominal compartment syndrome [ACS] with organ dysfunction were created. We investigated whether the two methods used to create IAH - CO(2 )pneumoperitoneum or adding volume to the intra-abdominal space - exerted different impacts on the temporal development of organ dysfunction. METHODS: Twenty-four 40-kg female pigs were allocated to four groups: 25 mmHg IAH with CO(2 )pneumoperitoneum (n = 8), >20 mmHg IAH caused by addition of volume (n = 8), and two corresponding sham groups (each n = 4). The two sham groups were later pooled into one control group (n = 8). The animals were monitored for 12 h. Repeated serial measurements were taken of group differences over time and analyzed using analysis of variance. RESULTS: Thirty-eight percent of the animals (n = 3) in each intervention group died near the end of the 12-h experiment. Both intervention groups experienced kidney impairment: increased creatinine concentration (P <0.0001), anuria (P = 0.0005), hyperkalemia (P <0.0001), decreased abdominal perfusion pressure, and decreased dynamic lung compliance. CO(2 )pneumoperitoneum animals developed hypercapnia (P <0.0001) and acidosis (P <0.0001). CONCLUSIONS: Both methods caused ACS and organ dysfunction within 12 h. Hypercapnia and acidosis developed in the CO(2 )pneumoperitoneum group.