B-Type Natriuretic Peptide and Pro-B-Type Natriuretic Peptide
BNP and proBNP.
To assist in diagnosing and managing heart failure (HF).
There are no food, fluid, activity, or medication restrictions unless by medical direction.
Method: Chemiluminescent immunoassay for BNP; electrochemiluminescent immunoassay for proBNP.
|BNP||Conventional Units||SI Units (Conventional Units × 1)|
|Male and Female||Less than 100 pg/mL||Less than 100 ng/L|
|0–74 yr||Less than 125 pg/mL||Less than 125 ng/L|
|Greater than 75 yr||Less than 449 pg/mL||Less than 449 ng/L|
|BNP levels are increased in older adults.|
Critical Findings and Potential Interventions
Overview(Study type: Blood collected in a lavender-top [EDTA] tube; related body system: Circulatory system.) The peptides B-type natriuretic peptide (BNP) and atrial natriuretic peptide (ANP) are antagonists of the renin-angiotensin-aldosterone system; they assist in the regulation of electrolytes, fluid balance, and blood pressure. BNP, proBNP, and ANP are useful markers in the diagnosis of heart failure (HF). BNP, first isolated in the brain of pigs, is a neurohormone synthesized primarily in the ventricles of the human heart in response to increases in ventricular pressure and volume. Circulating levels of BNP and proBNP increase in proportion to the severity of heart failure. A rapid BNP point-of-care immunoassay may be performed, in which a venous blood sample is collected, placed on a strip, and inserted into a device that measures BNP. Results are completed in 10 to 15 min.
Galectin-3 protein levels are considered a prognostic tool in the assessment of diagnosed HF. Elevations in blood specimens greater than 17.8 ng/mL (as measured by enzyme immunoassay) are predictive of increased risk for progression of the disease.
Soluble ST-2 is another prognostic biomarker measured in blood samples, used to predict increased risk for progression of HF—elevations in patients identified with chronic heart failure predict elevated risk of disease progression ST-2 is an interleukin family receptor secreted by cardiac muscle in response to mechanical stress. Elevations in blood specimens greater than 35 ng/mL (as measured by enzyme immunoassay) are considered clinically significant.
CAD and MI are the most common causes of heart disease and most common causes of HF. Hypertension is another significant contributing factor in the development of HF. Other conditions that can contribute to the development or acceleration of HF include anemia, congenital heart defect, diabetes, kidney disease, and thyroid disease. Emphasis on preventive care, including the administration of aspirin, statins, β—blockers, ACE inhibitors, and the diuretic aldactone is becoming more important after CAD or MI have been diagnosed to offer protection to the damaged heart muscle.
Until 2017 patients with advanced HF had few alternatives to extend their lives if a heart transplant was not a timely option. The left ventricular assist device (LVAD), approved by the FDA, is a system comprised of an implanted pump and an external battery powered pump controller designed to work in unison with the patient’s weakened left ventricle to provide additional blood flow.
- Assist in determining the prognosis and therapy of patients with heart failure.
- Assist in the diagnosis of heart failure.
- Assist in differentiating heart failure from pulmonary disease.
- Cost-effective screen for left ventricular dysfunction; positive findings would point to the need for echocardiography and further assessment.
Patients receiving nesiritide. Nesiritide (Natrecor) is a recombinant form of BNP that may be given therapeutically by IV to patients in acutely decompensated heart failure; with some assays, BNP levels may be transiently and significantly elevated at the time of administration and must be interpreted with caution. The testing laboratory should be consulted to verify whether test measurements are affected by nesiritide.
Factors that may alter the results of the study
- Age: BNP levels are increased in older adults
Potential Medical Diagnosis: Clinical Significance of Results
BNP is secreted in response to increased hemodynamic load caused by physiological stimuli, as with ventricular stretch or endocrine stimuli from the aldosterone/renin system. Increasing BNP levels would indicate a worsening condition.
- Acute kidney injury
- Cardiac inflammation (myocarditis, cardiac allograft rejection)
- Chronic kidney disease
- Cushing syndrome
- Heart failure
- Kawasaki disease
- Left ventricular hypertrophy
- Myocardial infarction
- Primary hyperaldosteronism
- Primary pulmonary hypertension
- Ventricular dysfunction
Decreasing BNP levels would indicate improvement.
Potential Nursing Problems Assessment and Nursing Diagnosis
|Problems||Signs and Symptoms|
|Cardiac output (decreased) (related to altered preload [increased/decreased], increased afterload, impaired cardiac contractility, cardiac muscle disease, altered cardiac conduction, side effects of medication)||Decreased peripheral pulses; decreased urinary output; cool, clammy skin; tachypnea; dyspnea; edema; altered level of consciousness; abnormal heart sounds; crackles in lungs; decreased activity tolerance; weight gain; edema; fatigue; hypoxia; hypotension|
|Fluid volume (excess) (related to decreased cardiac output; decreased renal perfusion)||Edema; shortness of breath; increased weight; ascites, rales, and rhonchi; diluted laboratory values; increased blood pressure; positive jugular venous distention (JVD); orthopnea; cough; restlessness; tachycardia; pulmonary congestion with x-ray; decreased urinary output; ascites; hypertension|
|Gas exchange (inadequate) (related to altered alveolar and capillary exchange secondary to fluid in the alveoli)||Decreased activity tolerance, increased shortness of breath with activity, weakness, orthopnea, cyanosis, cough, increased heart rate, weight gain, edema in the lower extremities, increased respiratory rate, use of respiratory accessory muscles|
|Tissue perfusion (inadequate) (related to compromised cardiac contractility, interrupted blood flow)||Hypotension, dizziness, cool extremities, capillary refill greater than 3 sec, weak pedal pulses, altered level of consciousness|
Before the Study: Planning and Implementation
Teaching the Patient What to Expect
- Inform the patient this test can assist in diagnosing heart failure.
- Explain that a blood sample is needed for the test.
After the Study: Potential Nursing Actions
- Cardiac Output (decreased): Assess peripheral pulses and capillary refill. Monitor blood pressure and check for orthostatic changes (dizziness) related to fluid loss. Assess respiratory rate, breath sounds, orthopnea, skin color temperature, moisture, and level of consciousness. Assess heart sounds for abnormal beats. Monitor urinary output, sodium and potassium levels, and BNP levels. Administer ordered oxygen and use pulse oximetry to monitor oxygen saturation. Assess for shortness of breath with activity. Administer ordered medications aldosterone antagonists, angiotensin-converting enzyme (ACE) inhibitors, beta blockers, diuretics, inotropic drugs, and vasodilators. Explain the importance of taking prescribed medications to support cardiac health. Increase fluids for decreased cardiac preload, decrease fluids for increased cardiac preload as ordered by HCP.
- Fluid Volume (excess): Daily weight with monitoring of trends. Limit fluid as appropriate. Assess for peripheral edema (legs, feet, ankles, sacrum), and JVD. Assess for shortness of breath and adventitious lung sounds such as crackles. Monitor blood pressure, heart rate, and intake versus output. Administer prescribed diuretics, restrict sodium intake, and order a low-sodium diet. Monitor laboratory values that reflect alterations in fluid status and manage underlying cause of fluid alteration.
- Gas Exchange (inadequate): Auscultate and trend breath sounds. Assess respiratory rate and administer ordered oxygen with pulse oximetry to monitor oxygen saturation. Collaborate with the health-care provider (HCP) to consider intubation and/or mechanical ventilation as appropriate. Place the head of the bed in high Fowler position. Administer ordered diuretics and vasodilators. Monitor potassium levels.
- Tissue Perfusion (inadequate): Monitor blood pressure for hypotension, and heart for increased rate and skipped beats. Assess for dizziness, pedal pulses, delayed capillary refill, and skin for pallor and warmth. Monitor for sensorium changes; confusion, stupor, lethargy, coma as well as restlessness and anxiety.
- Instruct patients to consume a variety of foods within the basic food groups, eat foods high in potassium when taking diuretics, eat a diet high in fiber (25–35 g/day), maintain a healthy weight, be physically active, limit salt intake to 2,000 mg/day, limit alcohol intake, and be a nonsmoker.
- Recommend consultation with a registered dietitian, consider cultural implications of diet recommendations.
- Encourage, as ordered, high-potassium foods (bananas, strawberries, oranges; cantaloupes; green leafy vegetables such as spinach and broccoli; dried fruits such as dates, prunes, and raisins; legumes such as peas and pinto beans; nuts and whole grains), which can offset the loss of potassium from taking diuretics.
- Emphasize the importance of limiting dietary salt to recommended daily amount.
Followup Evaluation and Desired Outcomes
- Details the purpose of taking prescribed medications: diuretic, ACE inhibitor, and/or beta blocker.
- Acknowledges the importance of limiting fluids to decrease cardiac stress, including strategies to limit fluid intake and notify the HCP for excessive weight gain.
- Safely self-administers ordered oxygen and can state symptoms of hypoxia reportable to the HCP.
- Demonstrates how to keep an accurate intake and output and acknowledges the importance of a daily weight to monitor fluid fluctuations.
- Understands the importance of reporting life-threatening changes such as cool extremities, pallor, and diaphoresis to HCP immediately.
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