Key result
Hyponatraemia on admission predicted worsening renal function in acute decompensated heart failure (OR 1.90, 95% CI 1.25-2.88) and acute myocardial infarction (OR 1.56, 95% CI 1.13-2.16).
Why the study?
Does hyponatraemia on admission predict worsening renal function in patients with acute decompensated heart failure or acute myocardial infarction?
Cohort (n=3,101)
Does hyponatraemia on admission predict worsening renal function in patients with acute decompensated heart failure or acute myocardial infarction?
Odds Ratio: 1.9 (95% CI 1.25–2.88)
p-value: p=0.003
Hyponatraemia on admission is a significant independent predictor of acute cardio-renal syndrome (worsening renal function) in patients with acute decompensated heart failure and acute myocardial infarction.
May aid risk stratification for worsening renal function; hypothesis-generating and requires prospective validation before guiding management in acute heart failure or MI.
AIMS: The acute (type 1) cardio-renal syndrome (CRS) refers to an acute worsening of heart function leading to worsening renal function (WRF), and frequently complicates acute decompensated heart failure (ADHF) and acute myocardial infarction (AMI). The aim of this study was to investigate whether hyponatraemia, a surrogate marker of congestion and haemodilution and of neurohormonal activation, could identify patients at risk for WRF. METHODS AND RESULTS: We studied the association between hyponatraemia (sodium <136 mmol/L) and WRF (defined as an increase of >0.3 mg/dL in creatinine above baseline) in two separate cohorts: patients with ADHF (n = 525) and patients with AMI (n = 2576). Hyponatraemia on admission was present in 156 patients (19.7%) with ADHF and 461 patients (17.7%) with AMI. Hyponatraemia was more frequent in patients who subsequently developed WRF as compared with patients who did not, in both the ADHF (34.6% vs. 22.2%, P = 0.0003) and AMI (29.7% vs. 21.8%, P<0.01) cohorts. In a multivariable logistic regression model, the multivariable adjusted odds ratio for WRF was 1.90 [95% confidence interval (CI) 1.25-2.88; P = 0.003] and 1.56 (95% CI 1.13-2.16; P = 0.002) in the ADHF and AMI cohorts, respectively. The mortality risk associated with hyponatraemia was attenuated in the absence of WRF. CONCLUSION: Hyponatraemia predicts the development of WRF in two clinical scenarios that frequently lead to the type I CRS. These data are consistent with the concept that congestion and neurohormonal activation play a pivotal role in the pathophysiology of acute cardio-renal failure.
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Aronson et al. (2013) conducted a cohort in Acute decompensated heart failure (ADHF) and acute myocardial infarction (AMI) (n=3,101). Hyponatraemia (sodium <136 mmol/L) vs. Absence of hyponatraemia was evaluated on Worsening renal function (increase of >0.3 mg/dL in creatinine above baseline) (OR 1.90, 95% CI 1.25-2.88, p=0.003). Hyponatraemia on admission predicted worsening renal function in acute decompensated heart failure (OR 1.90, 95% CI 1.25-2.88) and acute myocardial infarction (OR 1.56, 95% CI 1.13-2.16).
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