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Published on: November 3, 2023
Mortality, kidney disease and cardiac procedures following acute coronary syndrome
Jula K Inrig1, Uptal D Patel, Libbie P Briley
1Duke Clinical Research Institute, Duke University Medical Center, Durham, NC 27710, USA. inrig001@mc.duke.edu
Insights
For patients with chronic kidney disease (CKD) after acute coronary syndrome (ACS), the risk of death is higher than kidney function decline. Cardiac interventions do not worsen long-term kidney function.
Area of Science:
- Cardiology
- Nephrology
- Clinical Research
Background:
- Cardiac interventions are underused in patients with chronic kidney disease (CKD) post-acute coronary syndrome (ACS) due to nephrotoxicity fears.
- CKD is a significant risk factor for adverse outcomes after ACS.
Purpose of the Study:
- To evaluate the risks of cardiac interventions in ACS patients with CKD.
- To determine if cardiac interventions impact long-term renal function in CKD patients post-ACS.
Main Methods:
- Analysis of 4631 subjects with ACS from the Blockade of the Glycoprotein IIb/IIIa Receptor to Avoid Vascular Occlusion trial.
- Outcomes assessed included mortality, reduced renal function (50% eGFR decrease or ESRD), and eGFR change.
Main Results:
- Lower baseline eGFR correlated with older age, female sex, diabetes, hypertension, and heart failure.
- Each 10 ml/min/1.73 m(2) eGFR decrease below 90 increased death hazard by 15% (HR 1.15, P=0.01).
- Catheterization with or without PCI did not significantly alter long-term eGFR compared to medical therapy (P=0.09).
Conclusions:
- In ACS patients with CKD, the risk of death outweighs renal function decline.
- Cardiac interventions (catheterization +/- PCI) do not significantly impact long-term renal function.
- CKD should not deter potentially beneficial cardiac interventions; focus should be on reducing cardiovascular risk in this population.
Background:
Cardiac interventions are underutilized in patients with chronic kidney disease (CKD) following acute coronary syndrome (ACS) partly due to nephrotoxicity concerns.
Methods:
We analyzed outcomes of 4631 subjects with ACS enrolled in the Blockade of the Glycoprotein IIb/IIIa Receptor to Avoid Vascular Occlusion trial, including time to death, time to reduced renal function (50% reduction in estimated glomerular filtration rate (eGFR) or development of end-stage renal disease (ESRD)) and percent change in eGFR from baseline.
Results:
Subjects with a lower baseline eGFR were more likely to be older, female and have diabetes, hypertension, congestive heart failure or peripheral vascular disease (all P < 0.0001); they were less likely to be taking aspirin > or = 162 mg or to have undergone a percutaneous coronary intervention (PCI) prior to enrollment (P < 0.0001). As eGFR declined, the proportion of subjects experiencing death versus reduced eGFR or ESRD qualitatively increased. In adjusted analyses, every 10 ml/min/1.73 m(2) decrease in eGFR < or = 90 was associated with a 15% increased hazard of death (HR 1.15, P = 0.01). In adjusted analyses of predictors of percent change in eGFR, catheterization (cath) with or without PCI compared to medical therapy during follow-up was not associated with significant differences in long-term eGFR (P = 0.09).
Conclusions:
Among CKD subjects in this study, the risk of death greatly outweighed the risk of reduced eGFR or development of ESRD following ACS and the occurrence of cath +/- PCI was not associated with significant differences in long-term renal function. The presence of CKD should not preclude potentially beneficial interventions and research should focus on reducing the high cardiovascular burden in this population.
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