Test Code FMPP2 Myocarditis/Pericarditis Panel
Specimen Required
Container/Tube: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 2 mL
Acceptable: SST
Collection Instructions: Draw blood in a plain red top tube(s), serum gel tube is acceptable. Spin down and send 2 mL of serum ambient in a plastic vial.
Secondary ID
75830Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
ECH_1 | Echovirus Antibody Panel, Serum | No | Yes |
FINFL | Influenza Types A and B Ab, Serum | No | Yes |
FFCPA | Chlamydophila pneumoniae Ab IgG/A/M | No | Yes |
Method Name
Complement Fixation (CF)/Immunofluorescence Assay (IFA)
Reporting Name
Myocarditis/Pericarditis PanelSpecimen Type
SerumSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Ambient (preferred) | 7 days | |
Frozen | 30 days | ||
Refrigerated | 14 days |
Reject Due To
Gross Hemolysis | Reject |
Gross Lipemia | Reject |
Gross Icterus | Reject |
Other reasons for rejection | Specimens other than serum collected in Red top or SST |
Reference Values
MYOCARDITIS-PERICARDITIS PANEL
ECHOVIRUS ANTIBODIES, SERUM
REFERENCE RANGE: <1:8
INTERPRETIVE CRITERIA:
<1:8 Antibody Not Detected
>or=1:8 Antibody Detected
Single titers >or=1:32 are indicative of recent infection. Titers of 1:8 and 1:16 may be indicative of either past or recent infection, since CF antibody levels persist for only a few months. A four-fold or greater increase in titer between acute and convalescent specimens confirms the diagnosis. There is considerable cross-reactivity among enteroviruses; however, the highest titer is usually associated with the infecting serotype.
INFLUENZA TYPE A AND B ANTIBODIES, SERUM
REFERENCE RANGE: <1:8
INTERPRETIVE CRITERIA:
<1:8 Antibody Not Detected
>or=1:8 Antibody Detected
Single titers of >or=1:64 are indicative of recent infection. Titers of 1:8 and 1:32 may be indicative of either past or recent infection, since CF antibody levels persist for only a few months. A four-fold or greater increase in titer between acute and convalescent specimens confirms the diagnosis.
CHLAMYDOPHILA PNEUOMIAE ANTIBODIES (IgG, IgA, IgM)
REFERENCE RANGE:
IgG <1:64
IgA <1:16
IgM <1:10
The immunofluorescent detection of specific antibodies to Chlamydophila pneumoniae may be complicated by cross-reactive antibodies, non-specific antibody stimulation, or past exposure to similar organisms such as C. psittaci and Chlamydia trachomatis. IgM titers of 1:10 or greater usually indicate recent infection, and any IgG titer may indicate past exposure. IgA is typically present at low titers during primary infection but may be elevated in recurrent exposures or in chronic infection.
Day(s) Performed
Tuesday through Saturday
Report Available
4 to 11 daysPerforming Laboratory
Quest DiagnosticsTest Classification
This test was developed, and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.CPT Code Information
86632
86631 x 2
86658 x 5
86710 x 2
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
FMPP2 | Myocarditis/Pericarditis Panel | Not Provided |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
Z2309 | Echovirus 4 Ab | 5143-3 |
Z5241 | C. pneumoniae IgG | 6913-8 |
Z0364 | Influenza A Ab | 5229-0 |
Z0365 | Influenza B Ab | 5230-8 |
Z5242 | C. pneumoniae IgA | 6912-0 |
Z2310 | Echovirus 7 Ab | 6922-9 |
Z2311 | Echovirus 9 Ab | 5147-4 |
Z5243 | C. pneumoniae IgM | 6914-6 |
Z5244 | Interpretation | 50612-1 |
Z2313 | Echovirus 11 Ab | 6708-2 |
Z2314 | Echovirus 30 Ab | 6392-5 |