Abstract 4357058: Heart Failure Exacerbates Renal Medullary Hypoxia and Increases Acute Kidney Injury Risk After Cardiopulmonary Bypass in Sheep.

Background: Acute kidney injury (AKI) is a major unresolved complication of cardiac surgery, particularly in patients with pre-existing heart failure (HF). Mechanistic insight has been limited by the lack of large animal models replicating this complex clinical scenario. We developed a novel ovine model of HF with continuous, region-specific assessment of renal perfusion and oxygenation before, during, and after cardiopulmonary bypass (CPB). Methods: Merino ewes (30-45 kg) were instrumented to continuously measure cardiac output (CO), mean arterial pressure (MAP), renal blood flow (RBF), renal oxygen delivery (RDO 2 ), and renal cortical and medullary perfusion and oxygenation (PO 2 ) across the pre- (conscious), intra- (anesthetized) and post-CPB (conscious) phases. HF was induced via coronary artery ligation and defined by ≥30% increase in heart rate and ≥30% reduction in left ventricular ejection fraction. HF (n=9) and healthy control (n=8) animals underwent 2 h of CPB with aortic cross-clamp (pump flow 2.4 L/min/m 2 , target MAP 70 mmHg), followed by 48 h recovery. Results: Compared to the pre-CPB (conscious) state, CPB reduced RBF and RDO 2 similarly in both groups (RBF: −56% HF, −55% control; RDO 2 : −64% HF, −68% control; all p<0.01). Renal medullary perfusion and PO 2 also declined in both groups during CPB (perfusion: HF −71%, p=0.02; control −56%, p=0.08; PO 2 : HF −42%, p=0.03; control −46%, p=0.5), with no significant intergroup differences. However, by 48 h post-CPB, medullary PO 2 had recovered in controls but remained markedly suppressed in HF animals (8.0 ± 3.7 vs 30.6 ± 5.5 mmHg, p=0.02), despite similar MAP, CO, RBF, cortical perfusion, and cortical PO 2 . Postoperative AKI was more frequent in HF animals (55% vs 12.5%, OR 8.75). Across all animals, those with AKI had lower post-CPB medullary PO 2 than those without AKI (18.7 ± 3.5 vs 31.3 ± 3.5 mmHg, p=0.04). Conventional markers (urine output, creatinine clearance) did not differ significantly between groups at any stage, underscoring their limited sensitivity to early, region-specific injury. Conclusion: This is the first large-animal model to replicate the perioperative course of cardiac surgery with CPB in the setting of heart failure, enabling continuous, region-specific monitoring of renal oxygenation. Persistent medullary hypoxia emerged as a key driver of postoperative AKI, highlighting a novel and potentially targetable mechanism in high-risk patients with HF.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4357058
Primary Topic
Acute Kidney Injury Research
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article
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article

Abstract 4357058: Heart Failure Exacerbates Renal Medullary Hypoxia and Increases Acute Kidney Injury Risk After Cardiopulmonary Bypass in Sheep.

Lindsea C. Booth, Connie P. C. Ow, Jai Raman, Yugeesh R. Lankadeva et al.
Circulation
Acute Kidney Injury Research
article

Abstract 4357058: Heart Failure Exacerbates Renal Medullary Hypoxia and Increases Acute Kidney Injury Risk After Cardiopulmonary Bypass in Sheep.

Lindsea C. Booth, Connie P. C. Ow, Jai Raman, Yugeesh R. Lankadeva, Clive Newton May, Anton Lewis Trask-Marino, Peter McCall, Taku Furukawa, Andrew Donald Cochrane, Bruno Marino
article en

Abstract

Background: Acute kidney injury (AKI) is a major unresolved complication of cardiac surgery, particularly in patients with pre-existing heart failure (HF). Mechanistic insight has been limited by the lack of large animal models replicating this complex clinical scenario. We developed a novel ovine model of HF with continuous, region-specific assessment of renal perfusion and oxygenation before, during, and after cardiopulmonary bypass (CPB). Methods: Merino ewes (30-45 kg) were instrumented to continuously measure cardiac output (CO), mean arterial pressure (MAP), renal blood flow (RBF), renal oxygen delivery (RDO 2 ), and renal cortical and medullary perfusion and oxygenation (PO 2 ) across the pre- (conscious), intra- (anesthetized) and post-CPB (conscious) phases. HF was induced via coronary artery ligation and defined by ≥30% increase in heart rate and ≥30% reduction in left ventricular ejection fraction. HF (n=9) and healthy control (n=8) animals underwent 2 h of CPB with aortic cross-clamp (pump flow 2.4 L/min/m 2 , target MAP 70 mmHg), followed by 48 h recovery. Results: Compared to the pre-CPB (conscious) state, CPB reduced RBF and RDO 2 similarly in both groups (RBF: −56% HF, −55% control; RDO 2 : −64% HF, −68% control; all p<0.01). Renal medullary perfusion and PO 2 also declined in both groups during CPB (perfusion: HF −71%, p=0.02; control −56%, p=0.08; PO 2 : HF −42%, p=0.03; control −46%, p=0.5), with no significant intergroup differences. However, by 48 h post-CPB, medullary PO 2 had recovered in controls but remained markedly suppressed in HF animals (8.0 ± 3.7 vs 30.6 ± 5.5 mmHg, p=0.02), despite similar MAP, CO, RBF, cortical perfusion, and cortical PO 2 . Postoperative AKI was more frequent in HF animals (55% vs 12.5%, OR 8.75). Across all animals, those with AKI had lower post-CPB medullary PO 2 than those without AKI (18.7 ± 3.5 vs 31.3 ± 3.5 mmHg, p=0.04). Conventional markers (urine output, creatinine clearance) did not differ significantly between groups at any stage, underscoring their limited sensitivity to early, region-specific injury. Conclusion: This is the first large-animal model to replicate the perioperative course of cardiac surgery with CPB in the setting of heart failure, enabling continuous, region-specific monitoring of renal oxygenation. Persistent medullary hypoxia emerged as a key driver of postoperative AKI, highlighting a novel and potentially targetable mechanism in high-risk patients with HF.

CirculationVol. 152(Suppl_3)
Florey Institute of Neuroscience and Mental Health (AU), Townsville Hospital (AU), Stem Cells Australia (AU), Austin Health (AU)
Openalex Percentile: Top 62%
Acute Kidney Injury Research
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