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[BNP-guided therapy optimizes the timing of discharge and the medium term risk stratification in patients admitted
Roberto Valle1, Nadia Aspromonte, Emanuele Carbonieri
1Centro per lo scompenso cardiaco, Unità operativa complessa di Cardiologia, Ospedale civile, San Donà di Piave. robertovalle@libero.it
Insights
Plasma brain natriuretic peptide (BNP) levels can guide heart failure (HF) treatment and predict prognosis. Higher BNP levels at discharge indicate a greater risk of cardiac events and death in HF patients.
Area of Science:
- Cardiology
- Biomarkers
- Heart Failure Management
Background:
- Congestive heart failure (HF) is a leading cause of hospitalization with high readmission rates.
- Neurohormonal activation, indicated by plasma brain natriuretic peptide (BNP), correlates with HF severity and patient outcomes.
Purpose of the Study:
- To assess if plasma BNP levels can guide drug treatment in HF patients post-discharge.
- To determine if BNP levels can predict medium-term prognosis in HF patients after hospitalization.
Main Methods:
- 200 HF patients were evaluated, with echocardiography and plasma BNP levels measured on admission and after initial treatment.
- Patients were categorized into low BNP responders and high BNP non-responders based on a 240 pg/ml cutoff and/or a 30% reduction in BNP levels.
- Clinical variables, including NYHA class and ejection fraction, were analyzed alongside BNP levels.
Main Results:
- High BNP levels (>240 pg/mL) indicated clinical instability requiring intervention, while low levels allowed for earlier discharge.
- The high BNP group (42%) experienced significantly more cardiac events than the low BNP group (10%) during a 3-month follow-up.
- Plasma BNP values >500 pg/mL identified a subgroup at high risk of death.
Conclusions:
- BNP testing is crucial for risk stratification in hospitalized HF patients to guide management.
- An aggressive treatment and follow-up strategy is warranted for HF patients with high BNP levels or minimal BNP changes post-admission.
- Changes in plasma BNP levels at discharge significantly correlate with subsequent cardiac events.
Background:
Congestive heart failure (HF) is one of the most important cause of hospitalizations and is associated with high cost. Despite a consistent body of data demonstrating the benefits of drug therapy in HF, persistently high rates of readmission, especially within six months of discharge, continue to be documented. Neurohormonal activation characterizes the disease; plasma brain natriuretic peptide (BNP), is correlated with the severity of left ventricular dysfunction and relates to outcome.
Objective:
The aim of the study was to evaluate if plasma levels of BNP would provide an index to guide drug treatment and to predict medium-term prognosis in HF patients (pts) after hospital discharge.
Methods And Results:
We evaluated 200 consecutive pts (age 77 +/- 10 (35-96) years, 49% male versus 51% female) hospitalized for HF (DRG 127). Standard echocardiography was performed and left ventricular systolic/diastolic function was assessed; plasma BNP levels were measured with a rapid point-of-care assay (Triage BNP Test, Biosite Inc, San Diego, CA) on days 1 and after initial treatment. Using a cut-off of 240 pg/ml and/or changes in plasma BNP (days 2-3 after admission), 2 groups were identified: the low BNP group-responders (n = 68, BNP < 240 pg/ml and/or > or = 30% reduction) and the high BNP group-non responders (n = 132, BNP > or = 240 pg/ml and/or < 30% reduction). The high BNP group showed a different pattern of clinical variables according to the severity of the disease New York Heart Association (NYHA) functional class, left ventricular ejection fraction, ischemic etiology and age. A sustained elevation of plasma BNP (> 240 pg/mL) indicated the presence of a clinical unstable condition requiring further intervention whereas pts with low BNP values were discharged after 24 hours. During a mean follow-up period of 3 months, there were 62 cardiac events, including 15 cardiac deaths, 22 readmissions for worsening heart failure and 25 clinical decompensation requiring diuretic treatment. The incidence of clinical events was significantly greater in pts with higher levels of BNP (admission and discharge) than in those with lower levels (42% vs. 10%) and plasma values > 500 pg/ml identified a subgroup at high risk of death.
Conclusions:
The influence of BNP in the clinical course and prognosis of patients hospitalized for HF has not been studied. After initial treatment pts need to be risk stratified by means of the BNP test, to guide further management and to identify subjects with poor prognosis. An aggressive therapeutic and follow-up strategy may be justified for pts with high BNP levels and/or no changes after hospital admission for worsening HF. The changes in plasma BNP level at discharge were significantly related to cardiac events.
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