NT-proBNP in the Management of Discharged Patients With Acutely Decompensated Heart Failure and Preserved Ejection Fraction

Heart Failure Clinical Trial

Official title:

NT-proBNP in the Management of Discharged Patients With Acutely Decompensated Heart Failure and Preserved Ejection Fraction

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02807168
• Other study ID #: NICE-preserve
• Status: Completed
• Phase: N/A
• Start date: June 2015
• Est. completion date: August 2019

Study information

• Verified date: August 2019
• Source: Hospital Universitario Virgen de la Arrixaca
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Acute decompensated heart failure (ADHF) is a health problem of great magnitude, because it is the most frequent cause of hospitalization of patients over 65 years old. Of these patients, more than 50% will be readmitted within the next six months with the consequent worsening prognosis, increased mortality and high costs associated. In fact, two-third parts of the costs of this condition are due to hospitalizations. Hence the increased importance of ADHF and its associated hospitalizations as an essential event in the natural history of the disease on to address therapeutic efforts.

However, at the present time there is a change of scenario that makes that more than half of these patients show HF with preserved ejection fraction (PEF), so that acute heart failure with preserved ejection fraction (AHF-PEF) is a fact with high prevalence and epidemiological relevance. To this the investigators must add that, unlike patients with depressed EF, HF-PEF has no therapeutic strategies that may have proven a recovery of the affected patients. All this makes that overall heart failure with PEF and AHF-PEF represent a major health problem.

However, despite of the lack of effective treatments, there are also opportunities for improvement both in terms of morbidity and mortality that should be evaluated. Rather than looking for therapies or new specific drugs, these opportunities may be in the use of management strategies among which the use of biomarkers and their monitoring could be key. In this regard, NT-proBNP has been shown to correlate with severity and prognosis, including the risk of decompensation. Nevertheless, whilst the latest guidelines for heart failure management recommend its use in the diagnosis of HF, the use of biomarkers to monitor and guide treatment has not been included yet.

The assumption of this study is that the use of NT-proBNP may serve as a therapeutic and management guideline for the in-patient with HF-PEF who is to be discharged, allowing a reduction of decompensations and hospitalizations as well as a better functional situation at 6 months.

Several criteria have been proposed to define the syndrome of HFpEF according to the 2013 ACCF/AHA Heart Failure Guideline including (a) clinical signs or symptoms of HF; (b) evidence of preserved or normal LVEF; and (c) evidence of abnormal LV diastolic dysfunction that can be determined by Doppler echocardiography or cardiac catheterization The assay N‑terminal proB‑type natriuretic peptid is indicated as an aid in the diagnosis of individuals suspected of having congestive heart failure and detection of mild forms of cardiac dysfunction. The test also aids in the assessment of heart failure severity in patients diagnosed with congestive heart failure. This assay is further indicated for the risk stratification of patients with acute coronary syndrome and congestive heart failure, and it can also be used for monitoring the treatment in patients with left ventricular dysfunction.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 167
• Est. completion date: August 2019
• Est. primary completion date: August 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients who are discharged after hospitalizations for AHF which is defined by:

• Dyspnea at rest or with minimal effort

• Pulmonary congestion on chest X ray

• NT-pro-BNP levels in the first 24 hours after admission:

<50 years: >450 pg/ml 50-75 years: >900 pg/mL >75 years: >1800 pg/mL

2. -Administration of at least 40 mg IV furosemide (or equivalent) at admission

3. -Preserved ejection fraction (LVEF>50%) in echocardiography performed at admission and evidence of diastolic dysfunction defined according to following parameters

• e´ <8 cm/s septal or <10 cm/s lateral (TDI mitral annulus)

• E/e' ratio >15

• A mitral-A pulmon > 30 msg

• Left atrial volumen index=34 mL/m2

• left ventricular mass index >95 g/m2 (woman) o >115 g/m2 (man)

4. -Ability to sign the informed consent

Exclusion Criteria:

1. Significant lung disease demonstrated by spirometry

2. Life´s prognosis < 6 months

3. Patients who does not have adhesion at the different visits of the study

Related Conditions & MeSH terms

• Heart Failure
• Preserved Left Ventricular Ejection Fraction

Intervention

Other:
• NT-proBNP (Cardiac Biomarkers)

Locations

Country	Name	City	State
Spain	Hospital Virgen de La Arrixaca	Murcia

Sponsors (7)

Lead Sponsor	Collaborator
Hospital Universitario Virgen de la Arrixaca	Alfonso Varela Román, Antoni Bayés Genís, Juan Cinca Cuscullola, Manuel Martinez Selles, Pablo García Pavía, Pedro Luis Sánchez Fernández

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Decrease of rehospitalizations due to acute heart failure at 6 months after discharge.	To assess if a clinical management strategy that includes the monitoring of NT-proBNP concentrations after hospital discharge of patients with AHF-PEF reduces rehospitalizations due to AHF at 6 months after discharge (defined as unplanned hospital admission lasting for at least 24 h and due to HF decompensation).	6 months