PhenX - C reactive protein (CRP) protocol 660601:-:Pt: Patient:-:PhenX

Preferred Label : PhenX - C reactive protein (CRP) protocol 660601:-:Pt: Patient:-:PhenX;

LOINC status : ACTIVE;

LOINC long common name : PhenX - C reactive protein (CRP) protocol 660601;

LOINC short name : CRP proto 660601;

Details

Origin ID

105848-6;

UMLS CUI

C5890619;

Has component
- C reactive protein [LOINC component]
- PhenX - C reactive protein (CRP) protocol 660601 [LOINC component]
- Protein [LOINC component]
Has method
- PhenX [LOINC method]
Has system
- Patient [LOINC System]
- ^Patient [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Panel of LOINC codes
- Are the dilution wells empty:Find:Pt:^Patient:Ord: [LOINC code]
- Are the specimens stored in glass or plastic vials:Find:Pt:^Patient:Ord: [LOINC code]
- Is the lowest reportable value at least 0.02 mg per dL:Find:Pt:^Patient:Ord: [LOINC code]
- Is the sample volume at least 0.3 mL:Find:Pt:^Patient:Ord: [LOINC code]
- Serum or plasma separated within 60 minutes of collection:Find:Pt:^Patient:Ord: [LOINC code]
- Specimens stored at -20 degrees Celsius or cooler:Find:Pt:^Patient:Ord: [LOINC code]
- Were bench quality control specimens used at the beginning of each analystical run:Find:Pt:^Patient:Ord: [LOINC code]
- Were lipemic specimens clarified by centrifugation at about 15,000g prior to testing:Time:Pt:^Patient:Qn: [LOINC code]
- Were specimens maintained at 20-25 degrees celsius during tesing and stored at -70 degrees celsius or lower after testing:Find:Pt:^Patient:Ord: [LOINC code]
- Were the CardioPhase, Rheumatology, and Supplementary reagents stored between 4-8 degrees Celsius and never frozen:Find:Pt:^Patient:Ord: [LOINC code]
- Were the Diluent and Rx buffer reagents stored at room temperature:Find:Pt:^Patient:Ord: [LOINC code]
- Were the QC materials stored at -20 degrees Celsius or colder before being thawed and stored at 2-8 degrees Celsius and used within 30 days:Find:Pt:^Patient:Ord: [LOINC code]
- Were the calibration standard dilutions used within 4 hours of preparation:Find:Pt:^Patient:Ord: [LOINC code]
- Were the temperatures of the controls and patient specimens brought up to room temperature before use:Find:Pt:^Patient:Ord: [LOINC code]
- Were the three levels of control ran for each test series and did not conform to quality control manual specifications:Find:Pt:^Patient:Ord: [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

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