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Research Paper| Volume 43, ISSUE 1, P18-26, January 2016

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Evaluation of tissue hemoglobin saturation (StO2) using near-infrared spectroscopy during hypoxemia and hyperoxemia in Beagle dogs

  • Noah D Pavlisko
    Correspondence
    Correspondence: Noah D Pavlisko, Department of Small Animal Clinical Sciences, Virginia-Maryland Regional College of Veterinary Medicine, Duckpond Drive, Blacksburg, 24061 VA, USA
    Affiliations
    Department of Small Animal Clinical Sciences, Virginia-Maryland Regional College of Veterinary Medicine, Blacksburg, VA, USA
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  • Maria Killos
    Affiliations
    Department of Small Animal Clinical Sciences, Virginia-Maryland Regional College of Veterinary Medicine, Blacksburg, VA, USA
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  • Natalia Henao-Guerrero
    Affiliations
    Department of Small Animal Clinical Sciences, Virginia-Maryland Regional College of Veterinary Medicine, Blacksburg, VA, USA
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  • Carolina H Riccó
    Affiliations
    Department of Small Animal Clinical Sciences, Virginia-Maryland Regional College of Veterinary Medicine, Blacksburg, VA, USA

    Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA
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  • Stephen Werre
    Affiliations
    Laboratory for Study Design and Statistical Analysis, Virginia-Maryland Regional College of Veterinary Medicine, Blacksburg, VA, USA
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      Abstract

      Objective

      To determine the relationship between tissue oxygen saturation (StO2) and oxygen delivery ( D . O 2 ) during hypoxemia and hyperoxemia.

      Study design

      Prospective, randomized study.

      Animals

      Eight purpose-bred Beagle dogs.

      Methods

      Dogs were anesthetized with isoflurane, ventilated to eucapnia, and instrumented for thermodilution cardiac output, invasive mean arterial pressure (MAP), sartorius muscle StO2 and airway gas monitoring. Dogs were administered rocuronium to facilitate mechanical ventilation and esmolol to minimize anesthetic effects on cardiac output. Instrumentation and baseline data collection were at 0.21 fractional inspired oxygen (FIO2). Dogs were evaluated at high (0.40 then 0.95) and low (0.15 then 0.10) FIO2 sequences in random order with a 60 minute rest period at FIO2 0.21 between sequences. Target FIO2 was achieved by manipulating nitrogen and oxygen flow rates. Data collected at each FIO2, after a 10 minute period of stabilization, included heart rate (HR), MAP, cardiac index (CI) and StO2. Arterial oxygen content (CaO2) and oxygen delivery index ( D . O 2 I ) were calculated at each FIO2. Data analysis included Pearson’s correlation analysis and mixed-model anova (p < 0.05).

      Results

      There were no significant differences in HR, MAP or CI across all FIO2 values. Significant decreases occurred in mean ± standard deviation StO2 (90 ± 4% to 69 ± 18%; p = 0.0001), D . O 2 I (458 ± 70 to 281 ± 100 mL minute−1 m−2; p = 0.0008) and CaO2 (13.2 ± 1.53 to 8.4 ± 2.05 mL dL−1; p = 0.0001) from FIO2 0.21 to 0.10, but not at remaining FIO2 values. The correlation between StO2 and D . O 2 I across all FIO2 values was strong (r = 0.97; p = 0.0013) and linear.

      Conclusions and clinical relevance

      In this model of hypoxemia and hyperoxemia, the strong correlation between StO2 and D . O 2 I suggests that StO2 can be used to estimate D . O 2 .

      Keywords

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