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Oxygen consumption and carbon dioxide production during liquid ventilation

dc.contributor.authorHirschl, Ronald B.en_US
dc.contributor.authorGrover, Bretten_US
dc.contributor.authorMcCracken, Michaelen_US
dc.contributor.authorWolfson, Marla R.en_US
dc.contributor.authorShaffer, Thomas H.en_US
dc.contributor.authorBartlett, Robert H.en_US
dc.date.accessioned2006-04-10T15:49:31Z
dc.date.available2006-04-10T15:49:31Z
dc.date.issued1993-04en_US
dc.identifier.citationHirschl, Ronald B., Grover, Brett, McCracken, Michael, Wolfson, Marla R., Shaffer, Thomas H., Bartlett, Robert H. (1993/04)."Oxygen consumption and carbon dioxide production during liquid ventilation." Journal of Pediatric Surgery 28(4): 513-519. <http://hdl.handle.net/2027.42/30885>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WKP-4BNF4FB-1/2/77306fe49012674a5f24fc0c3280b9d1en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30885
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8483062&dopt=citationen_US
dc.description.abstractLiquid ventilation with perfluorocarbon (PFCV) has advantages over conventional gas ventilation (GV) in premature and lung-injured newborn animals. Indirect calorimetric measurement of both oxygen consumption (VO2) and carbon dioxide production (VCO2) during PFCV has not been previously performed. In addition, comparison to indirect calorimetric measurement of VO2 and VCO2 during GV has not been evaluated. Ten fasted normal cats weighing 2.6 to 3.9 kg were anesthetized with pentobarbital and pancuronium. Tracheostomy was performed. Gas exchange was measured across the native lung during GV and across the membrane lung of the liquid ventilator during PFCV. VO2 was measured using a modification of a previously described, indirect, closed-circuit, volumetric technique. VCO2 was analyzed by capnographic assay of the mixed-expired closed-circuit air. The VCO2/VO2 ratio (RQ) was calculated. There was no change in VO2, VCO2, or RQ during PFCV when compared with GV (VO2: GV = 5.7 +/- 0.3 mL/kg/min, PFCV = 5.6 +/- 0.5 mL/kg/min [P = NS]; VCO2 : GV = 4.9 +/- 1.1 mL/kg/min, PFCV = 4.8 +/- 0.9 mL/kg/min [P = NS]; RQ: GV = 0.85 +/- 0.21, PFCV = 0.86 +/- 0.21 [P = NS]). During GV the PaO2 was higher than during PFCV (PaO2: GV = 335 +/- 70 mm Hg, PFCV = 267 +/- 83 mm Hg [P = .04]), as is expected because of the relative reduction in the inspiratory PiO2 of the perfluorocarbon during liquid ventilation. There was no significant change in the PaCO2 (PaCO2: GV = 37.3 +/- 2.2 mm Hg, PFCV = 40.4 +/- 5.3 mm Hg [P = NS] or the pH (pH: GV = 7.34 +/- 0.04, PFCV = 7.35 +/- 0.06 [P = NS]). This study demonstrates the efficacy of measuring VO2 and VCO2 during gas and liquid ventilation using an indirect calorimetric technique. The data demonstrate that VO2 and VCO2 do not change during liquid ventilation and that excellent gas exchange can be accomplished through PFCV.en_US
dc.format.extent872960 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleOxygen consumption and carbon dioxide production during liquid ventilationen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelSurgery and Anesthesiologyen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan, Ann Arbor, MI, USA; Departments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA.en_US
dc.contributor.affiliationotherDepartments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA; Departments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA.en_US
dc.contributor.affiliationotherDepartments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA; Departments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA.en_US
dc.contributor.affiliationotherDepartments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA; Departments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA.en_US
dc.contributor.affiliationotherDepartments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA; Departments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA.en_US
dc.contributor.affiliationotherDepartments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA; Departments of Physiology and Pediatrics, Temple University School of Medicine and St Christopher's Hospital for Children, Philadelphia, PA, USA.en_US
dc.identifier.pmid8483062en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30885/1/0000553.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0022-3468(93)90608-Nen_US
dc.identifier.sourceJournal of Pediatric Surgeryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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