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Hum. Reprod. Advance Access originally published online on January 5, 2007
Human Reproduction 2007 22(4):1149-1155; doi:10.1093/humrep/del482
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© The Author 2007. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Peritoneal tissue-oxygen tension during a carbon dioxide pneumoperitoneum in a mouse laparoscopic model with controlled respiratory support

Nicolas Bourdel1,2, Sachiko Matsuzaki1,2,4, Jean-Etienne Bazin1,3, Jean-Luc Pouly1,2, Gérard Mage1,2 and Michel Canis1,2

1 Université d'Auvergne – Clermont I, Centre d'Endoscopie et des Nouvelles Techniques Interventionnelles (CENIT), Faculté de Médecine, Clermont-Ferrand, France 2 CHU Clermont-Ferrand, Polyclinique-Hôtel-Dieu, Gynécologie Obstétrique et Médecine de la Reproduction, France 3 CHU Clermont-Ferrand, Hotêl Dieu, Service d'Anesthésie Réanimation, France

4 To whom correspondence should be addressed at: CHU Clermont-Ferrand, Polyclinique-Hôtel-Dieu, Gynécologie Obstétrique et Médecine de la Reproduction, Boulevard Léon Malfreyt, 63058 Clermont-Ferrand, France. Tel.: +33 4 7375 0138; Fax: +33 4 7393 1706; E-mail: sachikoma{at}aol.com

BACKGROUND: Previous animal studies suggested that the peritoneal environment during a carbon dioxide (CO2) pneumoperitoneum is hypoxic and that this may contribute to the formation of intra-abdominal adhesions or the growth of malignant cells. There is no study, however, that investigates the relationship between anaesthesia, ventilation and the laparoscopic peritoneal environment to the development of hypoxia. The objective of this study is to monitor the peritoneal tissue-oxygen tension (PitO2) under various conditions including anaesthesia alone, during a CO2 pneumoperitoneum at both low and high intraperitoneal pressure (IPP), and laparotomy, in animal models with controlled respiratory support (CRS).

METHODS: C57BL6 mice were divided into eight groups (n = 5) consisting of anaesthesia alone or with CO2 pneumoperitoneum at low (2 mmHg) or high (8 mmHg) IPP or undergoing laparotomy. Groups were further subdivided into those with or without CRS with endotracheal intubation and mechanical ventilation. Over the course of the 1 h procedure, PitO2 was continuously monitored.

RESULTS: Protocol 1. The PitO2 levels (104.2 ± 7.8 mmHg, mean ± SEM) in non-injured peritoneum during a CO2 pneumoperitoneum at a low IPP were elevated ~2-fold over the levels during laparotomy (49.8 ± 15.0 mmHg) in ventilated mice. Protocol 2. After insufflation with CO2, the PitO2 was immediately elevated and maintained at a higher level. Following laparotomy, it decreased immediately. This elevation was not seen with air insufflation.

CONCLUSION: In mice, a significant elevation in PitO2 occurs during a CO2 pneumoperitoneum at low IPP with CRS.

Key words: anaesthesia/laparoscopy/peritoneal environment/pneumoperitoneum/tissue-oxygen tension

Submitted on July 28, 2006; resubmitted on October 9, 2006; resubmitted on November 20, 2006; accepted on November 29, 2006.


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S. Matsuzaki, M. Canis, J.-E. Bazin, C. Darcha, J.-L. Pouly, and G. Mage
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