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Hemoglobin, Plasma
0020058
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Ordering Recommendation
• Identify increased concentration, which is indicative of acute intravascular destruction of erythrocytes.
• Not of clinical value in the diagnosis of chronic hemolytic disorders.
Mnemonic
HGBP
Methodology
Quantitative Spectrophotometry
Performed
Sun-Sat
Reported
1-3 days
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect
Green (sodium or lithium heparin).
Specimen Preparation
Separate plasma from cells ASAP or within 2 hours of collection (delayed separation from cells will elevate plasma hemoglobin). Transfer 2 mL plasma to an ARUP Standard Transport Tube. (Min: 0.7 mL)
Storage/Transport Temperature
Refrigerated.
Unacceptable Conditions
EDTA or citrated plasma.
Remarks
Stability
Ambient: 2 hours; Refrigerated: 1 week; Frozen: Unacceptable
Reference Interval
0.0-9.7 mg/dL
Interpretive Data
No compliance statements are in use for this test.
Note
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
N/A
CPT Codes
83051
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 0020058 | Hemoglobin, Plasma | 721-1 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
- Free Hemoglobin
Hemoglobin, Plasma
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