Pulse Oximeter Plethysmograph Variation During Hemorrhage in Beta-Blocker-Treated Swine

J Surg Res. 2020 Dec:256:468-475. doi: 10.1016/j.jss.2020.07.004. Epub 2020 Aug 13.

Abstract

Background: Beta-blockers blunt the stress response to hemorrhage. Our aim was to investigate the feasibility of noninvasive pulse oximeter plethysmographic waveform variation (PoPV) for predicting blood volume loss in an esmolol-treated swine hemorrhagic shock model.

Materials and methods: Controlled hemorrhage was induced in eight male domestic pigs. In four pigs, a total of 15% and 30% blood volume was drawn step-by-step over 10 min in each step (controlled hemorrhage-only pigs). In the other four pigs, the heart rate (HR) was reduced and maintained by 30% from baseline by esmolol infusion before controlled hemorrhage (esmolol-treated pigs). Diagnostic abilities of HR, pulse pressure variation (PPV), PoPV, and mean arterial pressure for 15% and 30% blood volume loss were determined by the area under the receiver operating characteristic curve (AUC).

Results: PoPV was well correlated with PPV in controlled hemorrhage-only pigs (r = 0.717) and esmolol-treated pigs (r = 0.532). In controlled hemorrhage-only pigs, HR (AUC = 0.841 and 0.864), PPV (0.878 and 0.843), and PoPV (0.779 and 0.793) accurately predicted 15% and 30% of blood volume loss. In esmolol-treated pigs, the diagnostic ability of HR was decreased (AUC = 0.766 and 0.733). However, diagnostic abilities of PPV (0.848 and 0.804) and PoPV (0.808 and 0.842) were not deteriorated.

Conclusions: The diagnostic ability of HR for blood volume loss was blunted by esmolol. However, those of PPV and PoPV were not altered. PoPV may be considered to be a useful noninvasive tool to predict blood volume loss in injured patients taking beta-blockers.

Keywords: Adrenergic beta-antagonists; Hemorrhagic; Oximetry; Pulse wave analysis; Shock; Swine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure / drug effects*
  • Blood Pressure / physiology
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Feasibility Studies
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Humans
  • Male
  • Oximetry / instrumentation
  • Oximetry / methods*
  • Oxygen / blood
  • Plethysmography / instrumentation
  • Plethysmography / methods
  • Propanolamines / administration & dosage*
  • Shock, Hemorrhagic / diagnosis*
  • Shock, Hemorrhagic / drug therapy
  • Shock, Hemorrhagic / physiopathology
  • Sus scrofa

Substances

  • Propanolamines
  • esmolol
  • Oxygen