Invasive Hemodynamic Monitoring of Aortic and Pulmonary Artery Hemodynamics in a Large Animal Model of ARDS

J Vis Exp. 2018 Nov 26:(141). doi: 10.3791/57405.

Abstract

One of the leading causes of morbidity and mortality in patients with heart failure is right ventricular (RV) dysfunction, especially if it is due to pulmonary hypertension. For a better understanding and treatment of this disease, precise hemodynamic monitoring of left and right ventricular parameters is important. For this reason, it is essential to establish experimental pig models of cardiac hemodynamics and measurements for research purpose. This article shows the induction of ARDS by using oleic acid (OA) and consequent right ventricular dysfunction, as well as the instrumentation of the pigs and the data acquisition process that is needed to assess hemodynamic parameters. To achieve right ventricular dysfunction, we used oleic acid (OA) to cause ARDS and accompanied this with pulmonary artery hypertension (PAH). With this model of PAH and consecutive right ventricular dysfunction, many hemodynamic parameters can be measured, and right ventricular volume load can be detected. All vital parameters, including respiratory rate (RR), heart rate (HR) and body temperature were recorded throughout the whole experiment. Hemodynamic parameters including femoral artery pressure (FAP), aortic pressure (AP), right ventricular pressure (peak systolic, end systolic and end diastolic right ventricular pressure), central venous pressure (CVP), pulmonary artery pressure (PAP) and left arterial pressure (LAP) were measured as well as perfusion parameters including ascending aortic flow (AAF) and pulmonary artery flow (PAF). Hemodynamic measurements were performed using transcardiopulmonary thermodilution to provide cardiac output (CO). Furthermore, the PiCCO2 system (Pulse Contour Cardiac Output System 2) was used to receive parameters such as stroke volume variance (SVV), pulse pressure variance (PPV), as well as extravascular lung water (EVLW) and global end-diastolic volume (GEDV). Our monitoring procedure is suitable for detecting right ventricular dysfunction and monitoring hemodynamic findings before and after volume administration.

Publication types

  • Video-Audio Media

MeSH terms

  • Animals
  • Blood Pressure / physiology
  • Cardiac Output / drug effects
  • Cardiac Output / physiology
  • Disease Models, Animal*
  • Female
  • Heart Failure / chemically induced
  • Heart Failure / physiopathology
  • Hemodynamic Monitoring / methods*
  • Hemodynamics / drug effects
  • Hemodynamics / physiology*
  • Humans
  • Hypertension, Pulmonary / chemically induced
  • Hypertension, Pulmonary / physiopathology
  • Male
  • Oleic Acid / toxicity
  • Pulmonary Artery / drug effects
  • Pulmonary Artery / physiopathology*
  • Respiratory Distress Syndrome / chemically induced
  • Respiratory Distress Syndrome / physiopathology*
  • Stroke Volume / drug effects
  • Stroke Volume / physiology
  • Swine
  • Ventricular Dysfunction, Right / chemically induced
  • Ventricular Dysfunction, Right / physiopathology

Substances

  • Oleic Acid