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Haemoglobin predicts survival in patients with chronic heart failure: a substudy of the ELITE II trial
Rakesh Sharma1, Darrel P Francis, Bertram Pitt
1Department of Clinical Cardiology, National Heart and Lung Institute, Imperial College School of Medicine, London SW3 6LY, UK.
Insights
Hemoglobin levels impact survival in chronic heart failure (CHF) patients. Both anemia and polycythemia are linked to worse outcomes, with optimal survival around 14.5 g/dL.
Area of Science:
- Cardiology
- Hematology
Background:
- Anemia correction in chronic heart failure (CHF) may improve symptoms and cardiac function.
- The prognostic significance of hemoglobin levels in CHF patients requires further investigation.
Purpose of the Study:
- To investigate the relationship between hemoglobin concentration and survival in patients with chronic heart failure.
Main Methods:
- Analysis of hemoglobin concentrations in 3044 patients from the ELITE II trial.
- Survival data was collected and analyzed using univariate and polynomial regression models.
- Patient characteristics including age, NYHA class, and ejection fraction were considered.
Main Results:
- Hemoglobin was not a significant predictor of survival as a continuous variable (P=0.26).
- A non-linear relationship was observed, with optimal survival around 14.5 g/dL hemoglobin.
- Anemia and polycythemia were associated with significantly worse survival, independent of other factors.
Conclusions:
- Hemoglobin concentration is an independent predictor of mortality in CHF patients.
- Both low (anemia) and high (polycythemia) hemoglobin levels are associated with increased mortality risk.
- Maintaining hemoglobin levels around 14.5 g/dL may be crucial for improving survival in CHF.
Aims:
The correction of anaemia in chronic heart failure (CHF) has been suggested to be associated with an improvement in symptoms and cardiac function. We aimed to investigate the relationship between the concentration of haemoglobin and survival in CHF.
Methods And Results:
We analysed haemoglobin concentrations in 3044 patients recruited in the Evaluation of Losartan In The Elderly (ELITE II) trial. Patients of mean age 71.5 +/- 6.8 years (+/-SD) and New York Heart Association (NYHA) class 2.5 +/- 0.6 were enrolled from June 1997 to May 1998 and followed-up for survival (range 1-780 days, median 551). In univariate analysis, age, NYHA class, serum creatinine, left ventricular ejection fraction (all P<0.0001) and sex (P=0.046) all predicted survival. Haemoglobin as a continuous variable for all patients was not a significant prognostic marker (P=0.26). However, sub-dividing patients according to 1.0 g/dL increments of haemoglobin revealed that the survival relationship was non-linear. The results from the polynomial regression suggest that the optimal interval is a symmetric one centred around 14.5 g/dL. This was independent of age, sex, NYHA class, left ventricular ejection fraction, creatinine, co-existing chronic obstructive pulmonary disease and treatment allocation (P<0.001). There was a minor fall in plasma haemoglobin at the 12-month follow-up (mean change for all patients 0.3 +/- 2.2 g/dL, P<0.0001), with no difference between captopril and losartan groups (P>0.3).
Conclusion:
Haemoglobin is an independent predictor of mortality in CHF patients, with anaemic and polycythaemic patients having the worst survival.
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