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[Effect of the optimal neurohormonal blockade on long-term survival in patients with chronic heart failure]
Marek Roik1, Małgorzata H Starczewska, Sławomir Stawicki
1I Katedra i Klinika Kardiologii IWL Akademii Medycznej w Warszawie. mfroik@amwaw.edu.pl
Insights
Optimal neurohormonal blockade significantly improves survival and reduces rehospitalization in chronic heart failure patients. Evidence-based treatment optimizes care and improves the prognosis for patients with chronic heart failure.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Context:
- Pharmacological treatments demonstrably improve outcomes in chronic heart failure (CHF).
- Optimal neurohormonal blockade is a key evidence-based treatment strategy for CHF.
- Understanding the impact of optimal therapy on patient survival is crucial.
Purpose:
- To assess the effect of optimal neurohormonal blockade on survival in chronic heart failure patients over a 12-month follow-up.
- To compare outcomes between patients receiving optimal versus non-optimal neurohormonal blockade.
Summary:
- This study analyzed 489 CHF patients, defining optimal therapy as beta-blocker and ACE-inhibitor (NYHA II) or beta-blocker, ACE-Inhibitor, and spironolactone (NYHA III-IV).
- The optimal therapy group (n=232) showed significantly lower mortality (12% vs. 40%) and rehospitalization rates (48% vs. 69%) compared to the non-optimal group (n=257) over 12 months.
- Cox multivariate analysis revealed a 62% reduction in mortality and 41% reduction in cardiovascular rehospitalization with optimal therapy, after adjusting for key clinical factors.
Impact:
- Optimal neurohormonal therapy demonstrates a favorable effect on patient outcomes in chronic heart failure.
- These findings strongly support the optimization of care and adherence to evidence-based treatments for CHF patients.
- Implementing optimal therapeutic strategies can significantly improve the generally poor prognosis associated with chronic heart failure.
Background:
In recent years large scale clinical trials have cleary shown that a number of pharmacological treatments can improve the outcomes of patients (pts) with chronic heart failure (CHF).
Aim:
The aim of this study was to assess the effect of optimal neurohormal blockade in pts with chronic heart failure on survival during 12 month follow-up.
Methods:
We analyzed data on 489 pts in NYHA II-IV class of HF, referred to our Dept. (mean age was 69 +/- 12). We define doptimal neurohormonal therapy as beta-blocker and ACE-inhibitor in pts with NYHA II, and beta-blocker, ACE-Inhibitor and spironolactone in patients with NYHA III-IV class. Pts were divided into groups: group 1--optimal neurohormonal blockade (n = 232, mean age, 67 +/- 11), group 2--non-optimal neurohormonal blockade (n = 257, mean age, 70 +/- 13). Pts were followed for 12 month.
Results:
Group with optimal therapy were frequent male gender, of ischemic aetiology, and NYHA class II (p < 0.05). Diabetes mellitus, hypertension, left ventricular ejection fraction did not differ the groups (p = NS). Pts with non-optimal therapy were more frequent with prior history of renal dysfunction and anemia at admission (p < 0.05). During 12 month follow-up 12% in optimal vs 40% in non-optimal therapy died (p < 0.005). The rehospitalisation rate during one-year was also significantly higher in pts receiving non-optimal therapy (69% vs 48%, p < 0.005). Cox multivariate analysis showed after adjusting for age, gender, etiology of HF, NYHA functional class, renal dysfunction, EF, had significantly 62% reduction in mortality and 41% reduction in cardiovascular rehospitalisation in pts receiving optimal therapy.
Conclusions:
The optimal neurohormonal therapy have favorable effects on outcomes in pts with CHF. This data strongly support that optimalization of care and evidence-based treatment of CHF pts can improve poor prognosis in this group.
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