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|
| N-terminal-pro-BNP | ||
| Order Code: PBNP
Order Form: A-1a General Lab or IPR Req |
Chemistry 6240 RCP 356-3527 |
|
Specimen |
Plasma | ||
Collection Medium: |
| ||
Minimum: |
2 mL plasma separator tube top or 2 microtubes. | ||
Rejection Criteria: |
Red top tube is not acceptable. | ||
Testing Schedule: |
Random Access | ||
Analytic Time: |
1 hour (upon receipt in laboratory) | ||
Reference Range: |
The 95th percentiles for NT-proBNP levels in pg/mL
< 45 yrs 45-54 yrs 55-64 yrs 65-74 yrs 75+ years
Males 93 138 177 229 852
Females 178 192 226 353 624
For Chronic Heart Failure patients according to NYHA Functional Class
for NT-proBNP levels in pg/mL
NYHA I NYHA II NYHA III NYHA IV
Mean: 1015 1666 3029 3465
5th percentile 33 103 126 148
95th percentile 3410 6567 10449 12188
The Stages of Heart Failure - NYHA Classification
In order to determine the best course of therapy, physicians often
assess the stage of heart failure according to the New York Heart
Association (NYHA) functional classification system. This system
relates symptoms to everyday activities and the patient's quality of
life.
Class Patient Symptoms
Class I (Mild) No limitation of physical activity. Ordinary
physical activity does not cause undue fatigue,
palpitation, or dyspnea (shortness of breath).
Class II (Mild) Slight limitation of physical activity.
Comfortable at rest, but ordinary physical
activity results in fatigue, palpitation, or
dyspnea.
Class III (Moderate) Marked limitation of physical activity.
Comfortable at rest, but less than ordinary
activity causes fatigue, palpitation, or dyspnea.
Class IV (Severe) Unable to carry out any physical activity
without discomfort. Symptoms of cardiac
insufficiency at rest. If any physical activity
is undertaken, discomfort is increased. | ||
Comments: |
The N-terminal Pro-Brain Natriuretic Peptide (Pro-BNP) is an assay used as an aid in the diagnosis of individuals suspected of having congestive heart failure. The test is further indicated for the risk stratification of patients with acute coronary syndrome and congestive heart failure. The test may also be used as an aid in the assessment of increased risk of cardiovascular events and mortality in patients at risk for heart failure who have stable coronary artery disease. NT-Pro-BNP is stable for 2 days at 2-8 degrees C, so this assay may be added to existing PST tubes during those two days. | ||
Test Limitations: |
Hemolysis H = 1400 mg/dL Lipemia L = 4000 mg/dL Icterus I = 35 mg/dL Biotin <123 nmol/L or <30 ng/mL In patients receiving therapy with high biotin >5mg/day, no sample should be taken until at least 8 hours after last biotin administration. | ||
Methodology: |
Electrochemiluminescence Imunoassay | ||
CPT Code: |
83880 |
Updated: 02/25/2008
Note: The information contained in this handbook is for use by personnel of University of Iowa Health Care. No other use is implied or intended.