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Updated: Feb 10, 2026

Induction and Phenotyping of Acute Right Heart Failure in a Large Animal Model of Chronic Thromboembolic Pulmonary Hypertension
Published on: March 17, 2022
Severe acute heart failure - experimental model with very low mortality
1Department of Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic. Otomar.Kittnar@staff.cuni.cz.
A novel ischemic model effectively induces severe, stable acute heart failure in pigs without mortality, proving suitable for extracorporeal circulation research. This method ensures reproducible results for developing advanced life support systems.
Area of Science:
- Cardiovascular Research
- Animal Models
- Extracorporeal Circulation
Background:
- Advancements in extracorporeal circulation necessitate reliable models of acute heart failure.
- Existing models require improvement in control and reproducibility for experimental research.
Purpose of the Study:
- To develop and evaluate a reproducible model of severe, stable acute heart failure in pigs.
- To compare a hypoxic model with an ischemic model for inducing heart failure.
Main Methods:
- Two models were tested in pigs: hypoxic (n=5) and ischemic (n=9) induction of acute heart failure.
- Severe heart failure was defined by a ≥50% decrease in cardiac output, <60% mixed venous oxygen saturation, <25% ejection fraction, and ≥50% reduction in carotid artery flow.
- The ischemic model involved proximal left coronary artery closure and controlled hypoperfusion.
Main Results:
- The ischemic model successfully induced severe heart failure in 8 out of 9 animals without acute mortality.
- Significant reductions were observed in cardiac output (6.70 to 2.89 L/min), mixed venous saturation (83% to 58%), ejection fraction (50% to 19%), and carotid flow (337 to 136 mL/min) (P≤0.001).
- The hypoxic model resulted in heart failure in only one animal.
Conclusions:
- The proposed ischemic model provides a stable and reproducible method for inducing acute heart failure in pigs.
- This model is well-suited for experimental research supporting extracorporeal circulatory support systems due to its lack of acute mortality.
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