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Test ID: MPC
Mycoplasma Pneumoniae Culture

Secondary ID A test code used for billing and in test definitions created prior to November 2011

80422

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Mycoplasma Pneumoniae Culture

Aliases Lists additional common names for a test, as an aid in searching

M. pneumoniae culture FORWARD
Mycoplasma Pneumoniae Culture FORWARD

Specimen Type Describes the specimen type needed for testing

Varies

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

3 mL Sputum, Bronchial Washings, Tracheal Aspirate, Broncoalveolar Lavage, Nasopharyngeal Aspirate, Respiratory Fluid, 1 Throat Swab or 1 Nasopharyngeal Swab.

 

Collect respiratory specimen in mycoplasma transport media (Supply T187) supplied, Universal transport medium, M4 or M5. Specimen must be placed in transport media within 2 hours of collection.  Send specimen frozen.

 

Note: 1. Specimen source is required.

         2. Separate specimens must be submitted when multiple tests are ordered.

Specimen Minimum Volume Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.

1 mL

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis

NA

Thawing

Warm reject; Cold reject

Lipemia

NA

Icterus

NA

Other

-Unacceptable:M4-RT

-Unacceptable: Lung Tissue, Sterile Body Fluids (Pleural Fluid, Pericardial Fluid, or others) Due to stability (Refrigerate 48 hours\Frozen NO\Ambient NO)

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
VariesFrozen30 days

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Mycoplasma pneumoniae is one of the principal etiologic agents responsible for primary atypical pneumonia (often called walking pneumonia) as well as more mild forms of upper respiratory illness. Primary atypical pneumonia may be a severely debilitating disease and may infect otherwise healthy individuals.

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Culture methods for M. pneumoniae are relatively insensitive and a negative result does not exclude mycoplasma infection. Molecular detection with PCR is more sensitive in the acute phase of illness.

 

Test Performed by: Focus Diagnostics, Inc.

                            5785 Corporate Avenue

                            Cypress, CA   90630-4750

Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

Monday through Sunday

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

28-30 days

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

30-32 days

Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

4 weeks

Performing Laboratory Location The location of the laboratory that performs the test

Focus Diagnositics, Inc.

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

87109

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
Z2074SourceIn Process
Z0352Culture StatusIn Process
Z0353M Pneumoniae CultureIn Process