Sign in →

Test Code BNP NT-proBNP

Additional Codes

Cerner

NextGen

NT-proBNP II

NT-proBNP II

BNP

Brain Type Natriuretic Peptide (NT-proBNP)

Alternate Name(s)

Brain Type Natriuretic Peptide

BNP

NT-proBNP II

N-terminal fragment NT-proBNP

Useful For

Left ventricular dysfunction can occur as part of coronary heart disease, arterial hypertension, valvular disease, and primary myocardial disease.  If the left ventricular dysfunction remains untreated and is progressive, the potential for mortality is high, e.g., due to sudden cardiac death.  Initial studies reveal that natriuretic peptides can be used for diagnostic clinical problems associated with left ventricular dysfunction.

 

In subjects with left ventricular dysfunction, serum and plasma concentrations of BNP increase, as do the concentrations of the biologically inactive prohormone, proBNP.  ProBNP is secreted mainly by the left ventricle of the heart and, in this process, is cleaved into pysiologically active BNP and the N-terminal fragment NT-proBNP. The concentration of NT-proBNP in serum and plasma indicates the prognosis for left ventricular dysfunction.  It is also useful in assigning symptoms to cardiac or non-cardiac causes. NT-proBNP determination helps to identify subjects with left ventricular dysfunction and changes in concentration can be used to evaluate the success of treatment in patients with left ventricular dysfunction.

 

NT-proBNP levels are increased in patients with unstable angina and following myocardial infarction.  Studies indicate NT-proBNP measurements, although not diagnostic for these conditions, provide prognostic information for the short- and long-term risk stratification of patients with unstable angina or myocardial infarction.

Methodology

(Vitros) Chemiluminescent

Patient Preparation

None

Collection Instructions

Standard phlebotomy practices.

Specimen Requirements

Container

Specimen Type

Tube

Lithium Heparin Plasma

PST

 or  or 

Serum

 or 

SST

 or  or 

 

Stability

Storage

Temperature

Stability

Room Temperature

18-25°C

≤ 1 day

Refrigerated

 2-8°C

≤ 4 days

Frozen

≤-20 °C

≤26 weeks

Thaw up to 3 times

Rejection Criteria

Gross Hemolysis

Turbid Specimens

Result Reporting and Reference Values

Reported in pg/mL

Setting

Age

Decision Threshold

Outpatient

<150 years

<125 Negative: Heart Failure Unlikely

Outpatient

<150 years

≥125 Possible Heart failure or other causes such as acute coronary syndrome, pulmonary embolism, pulmonary hypertension, sepsis, stroke, or renal dysfunction

Emergency

 

See Interpretative data below

 

Interpretative data:

The normal reference range reflects the negative cutoff value for the primary care (Outpatient) setting.

The following range is more pertinent for acute congestive heart failure in the Emergency department setting:

  • NT-proBNP <300 pg/mL: Acute CHF unlikely
  • NT-proBNP 300-1800 pg/mL: Consider age stratified cutoff values below.

Proposed algorithms for NT-proBNP state that congestive heart failure is likely if:

  •  Age 22 to 49         NT-proBNP >449 pg/mL
  •  Age 50 to 74         NT-proBNP >899 pg/mL
  •  Age >74                NT-proBNP >1799 pg/mL

Serum concentrations of natriuretic peptides may be elevated in patients with acute myocardial infarction and renal insufficiency. Factors such as these should be considered when interpreting results.

Reflex Testing

None

Limitations

  • Ortho reports a bias with the following:
    • Cefoxitin sodium has shown a possible negative 10-24% bias
    • Sodium azide can cause a negative 12% bias         
  • Ortho reports no significant effect with the following:
    • Bilirubin up to 20 mg/dL
    • Biotin does not interfere