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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Detection and prognostic impact of renal dysfunction in patients with chronic heart failure and normal serum
Domenico Scrutinio1, Andrea Passantino, Rocco Lagioia
1Division of Cardiology and Cardiac Rehabilitation, S Maugeri Foundation, IRCCS, Institute of Cassano Murge, Bari, Italy. domenico.scrutinio@fsm.it
Insights
In chronic heart failure patients with normal serum creatinine, the Cockcroft-Gault formula normalized for body-surface area (eCrCl(BSA)) better predicts mortality risk than other formulas. This identifies a high-risk subgroup needing closer monitoring.
Area of Science:
- Cardiology
- Nephrology
- Clinical Risk Assessment
Background:
- Accurate renal dysfunction (RD) identification is vital for chronic heart failure (CHF) risk stratification.
- CHF patients are at increased risk of RD, even with normal serum creatinine (SCr), due to reduced creatinine generation.
- Standard renal function equations are less accurate at low SCr levels.
Purpose of the Study:
- To assess and compare the prognostic value of different renal function estimation formulas in CHF patients with normal SCr.
- To identify the most accurate formula for predicting mortality in this specific patient group.
Main Methods:
- Study included 462 patients with systolic CHF and normal SCr.
- Estimated creatinine clearance using Cockcroft-Gault (eCrCl) and MDRD equation (eGFR).
- Calculated eCrCl normalized for body-surface area (eCrCl(BSA)).
- Primary outcome was 2-year all-cause mortality.
Main Results:
- The eCrCl(BSA) was the only significant predictor of mortality (p = 0.006).
- Patients in the lowest eCrCl(BSA) quartile had a 2.1-fold increased mortality risk.
- Two-year survival was significantly lower in the lowest eCrCl(BSA) quartile (70.4%) compared to the referent quartile (89.7%).
- Other mortality predictors included ischemic etiology, NYHA class, low LVEF, and anemia.
Conclusions:
- A significant proportion of CHF patients with normal SCr have prognostically relevant RD.
- The Cockcroft-Gault formula corrected for BSA (eCrCl(BSA)) more accurately identifies this high-risk subgroup than the MDRD equation.
- These findings highlight the importance of using appropriate formulas for renal function assessment in CHF management.
Background:
Accurate identification of renal dysfunction (RD) is crucial to risk stratification in chronic heart failure (CHF). Patients with CHF are at special risk of having RD despite normal serum creatinine (SCr), owing to a decreased Cr generation. At low levels of SCr, the equations estimating renal function are less accurate. This study was aimed to assess and compare the prognostic value of formulas estimating renal function in CHF patients with normal SCr.
Methods:
We studied 462 patients with systolic CHF and normal SCr. Creatinine clearance was estimated by the Cockcroft-Gault (eCrCl) and glomerular filtration rate by the 4-variable MDRD equation (eGFR); eCrCl normalized for body-surface area (eCrCl(BSA)) was calculated. The primary outcome was all-cause mortality at 2 years.
Results:
Seventy five patients died. At multivariate Cox regression analysis, only eCrCl(BSA) was significantly associated with mortality (p = 0.006); eGFR (p = 0.24), eCrCl (p = 0.09) and BUN (p = 0.14) were not statistically significant predictors. The patients in the lowest eCrCl(BSA) quartile had an adjusted 2.1-fold (CI: 1.06-4.1) increased risk of mortality, compared with those in the referent quartile. Two-year survival was 70.4% in the lowest eCrCl(BSA) quartile and 89.7% in the referent quartile. Other independent predictors of mortality were ischemic etiology (RR: 2.16 [CI: 1.3-3.5], p = 0.0017), NYHA III/IV class (RR: 2.45 [CI: 1.51-3.97], p = 0.0003), LVEF <0.25 (RR: 3.38 [CI: 1.69-6.75], p = 0.014), and anemia (RR: 1.86 [CI: 1.16-2.99], p = 0.009).
Conclusions:
A sizeable proportion of CHF patients have prognostically significant RD despite normal SCr. Such patients represent a high-risk subgroup and can more accurately be identified by the CG formula corrected for BSA than the MDRD.
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