Abstract

PurposeTo assess the frequency of chronic kidney disease (CKD), define the associated demographics, and evaluate its association with use of evidence-based drug therapy in a contemporary global study of patients with stable coronary artery disease.Methods22,272 patients from the ProspeCtive observational LongitudinAl RegIstry oF patients with stable coronary arterY disease (CLARIFY) were included. Baseline estimated glomerular filtration rate (eGFR) was calculated (CKD-Epidemiology Collaboration formula) and patients categorised according to CKD stage: >89, 60–89, 45–59 and <45 mL/min/1.73 m2.ResultsMean (SD) age was 63.9±10.4 years, 77.3% were male, 61.8% had a history of myocardial infarction, 71.9% hypertension, 30.4% diabetes and 75.4% dyslipidaemia. Chronic kidney disease (eGFR<60 mL/min/1.73 m2) was seen in 22.1% of the cohort (6.9% with eGFR<45 mL/min/1.73 m2); lower eGFR was associated with increasing age, female sex, cardiovascular risk factors, overt vascular disease, other comorbidities and higher systolic but lower diastolic blood pressure. High use of secondary prevention was seen across all CKD stages (overall 93.4% lipid-lowering drugs, 95.3% antiplatelets, 75.9% beta-blockers). The proportion of patients taking statins was lower in patients with CKD. Antiplatelet use was significantly lower in patients with CKD whereas oral anticoagulant use was higher. Angiotensin-converting enzyme inhibitor use was lower (52.0% overall) and inversely related to declining eGFR, whereas angiotensin-receptor blockers were more frequently prescribed in patients with reduced eGFR.ConclusionsChronic kidney disease is common in patients with stable coronary artery disease and is associated with comorbidities. Whilst use of individual evidence-based medications for secondary prevention was high across all CKD categories, there remains an opportunity to improve the proportion who take all three classes of preventive therapies. Angiotensin-converting enzyme inhibitors were used less frequently in lower eGRF categories. Surprisingly the reverse was seen for angiotensin-receptor blockers. Further evaluation is required to fully understand these associations. The CLARIFY (ProspeCtive observational LongitudinAl RegIstry oF patients with stable coronary arterY disease) Registry is registered in the ISRCTN registry of clinical trials with the number ISRCTN43070564. http://www.controlled-trials.com/ISRCTN43070564.

Highlights

  • Chronic kidney disease (CKD) is a powerful independent predictor of adverse prognosis following myocardial infarction (MI) [1,2] or coronary revascularization [3,4]

  • Data from 14,527 patients with acute MI complicated by heart failure (Valsartan in Acute Myocardial Infarction Trial) showed that declining estimated glomerular filtration rate (eGFR) was associated with increased risk of death and nonfatal cardiovascular outcomes [1]

  • Whilst patients with eGFR,45 mL/min/1.73 m2 were at highest risk of events, the use of aspirin, beta-blockers, statins or coronary revascularization was lowest in this group

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Summary

Introduction

Chronic kidney disease (CKD) is a powerful independent predictor of adverse prognosis following myocardial infarction (MI) [1,2] or coronary revascularization [3,4]. Data from 14,527 patients with acute MI complicated by heart failure (Valsartan in Acute Myocardial Infarction Trial) showed that declining eGFR was associated with increased risk of death and nonfatal cardiovascular outcomes [1]. A retrospective cohort study of Medicare patients with acute MI showed that those with CKD stage 4 (eGFR 15–29 mL/min/1.73 m2) were infrequently prescribed aspirin with beta-blockers (27.1%) and fewer than one in 10 were prescribed the combination of aspirin, beta-blockers and angiotensin-converting enzyme (ACE) inhibitors [7]. Similar data were found in a single-centre prospective study for patients discharged after acute MI [8]

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