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Recommendations when to order or not order the test. May include related or preferred tests.
Identify Mycoplasma hominis in urogential specimens.
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
This test is New York state approved.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
Cervical, urethral or vaginal swab, or semen or urine.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Place swab or specimen in Mycoplasma transport media (UTM) (ARUP supply #12884). Available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800) 522-2787. (Min: 0.5 mL) Also acceptable: Any transport media validated for Mycoplasma/Ureaplasma transport, such as M4 (DO NOT USE M4 RT). Place each specimen in an individually sealed bag.
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Frozen on dry ice.
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
Specimens not in Mycoplasma/Ureaplasma transport media. Nonurogenital sources. M4 RT or bacterial transport media. Nonpatient specimens. Dry swabs.
RemarksAdditional specimen collection, transport, or test submission information.
Specimen source required.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Ambient: 8 hours; Refrigerated: 48 hours; Frozen at -20°C: Unacceptable; Frozen at -70°C: 1 month
Methodology
Process(es) used to perform the test.
Culture
Performed
Days of the week the test is performed.
Sun-Sat
Reported
Expected turnaround time for a result, beginning when ARUP has received the specimen.
1-9 days Negative culture reported at 9 days. Positive culture reported as soon as detected.
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Culture negative for Mycoplasma hominis.
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
Compliance Category
FDA
Note
Additional information related to the test.
No environmental culturing performed. This testing is not suitable for determining contamination in any cell line or tissue culture. For respiratory sources order Mycoplasma pneumoniae by PCR (test code 0060256). For Ureaplasma urealyticum and Mycoplasma hominis refer to Ureaplasma urealyticum & Mycoplasma hominis culture (0065031).
Hotline History
N/A
CPT Codes
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* 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.
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