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Test Code URRP Ureaplasma species, Molecular Detection, PCR, Varies

Reporting Name

Ureaplasma PCR

Useful For

Rapid, sensitive, and specific identification of Ureaplasma urealyticum and Ureaplasma parvum from genitourinary, reproductive, bone, spine, joint, and lower respiratory sources

 

This test is not intended for medicolegal use.

Method Name

Real-Time Polymerase Chain Reaction (PCR)

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

Varies


Necessary Information


Specimen source is required.



Specimen Required


The high sensitivity of amplification by polymerase chain reaction requires the specimen to be processed in an environment in which contamination of the specimen by Ureaplasma DNA is not likely.

 

Submit only 1 of the following specimens:

 

Specimen Type: Swab

Supplies:

-Culturette (BBL Culture Swab) (T092)

-BD E-Swab (T853)

-M4-RT (T605)

Sources: Vaginal, cervix, urethra, urogenital, chest/mediastinal; bronchus or lung (donor swab), or upper respiratory sources

Sources for infants younger than 3 months: Nasopharynx, nose, throat

Container/Tube:

Preferred: Culture swab transport system (Dacron or rayon swab with aluminum or plastic shaft with either Stuart or Amies liquid medium)

Acceptable: Swab in transport media: M4, M4-RT, M5, M6, universal transport media, or ESwab

Specimen Volume: 1 Swab

Collection Instructions:

Vaginal:

1. Collect specimen by swabbing back and forth over mucosa surface to maximize recovery of cells.

2. Place swab back into swab cylinder.

Urethra or cervical:

1. Collect specimen by inserting swab 1 to 3 cm and rotating 360 degrees.

2. Place swab back into swab cylinder.

Wound:

1. Collect specimen by swabbing back and forth over wound surface to maximize recovery of cells.

2. Place swab back into swab cylinder.

 

Specimen Type: Fluid

Sources: Pelvic, peritoneal, amniotic, prostatic secretions, semen, reproductive drainage or fluid, pleural/chest, chest tube, pericardial

Container/Tube: Sterile container

Specimen Volume: 1 to 2 mL

 

Specimen Type: Respiratory

Sources: Sputum, tracheal secretions, bronchial washings, bronchoalveolar lavage, lung fluid

Sources for infants younger than 3 months: Nasal washings (not acceptable for older patients))

Container/Tube: Sterile container

Specimen Volume: 1 to 2 mL

 

Specimen Type: Synovial fluid

Container/Tube:

Preferred: Lavender top (EDTA)

Acceptable: Pink top (EDTA), royal blue top (EDTA), sterile vial containing EDTA-derived aliquot, red top (no anticoagulant), or sterile container

Specimen Volume: 1 mL

Collection Instructions: Send fluid specimen in original tube.

 

Specimen Type: Urine-first void, kidney/bladder stone, or ureter

Container/Tube: Sterile container

Specimen Volume: 10 mL or entire specimen

Collection instructions:

Urine first void:

1. Specimen can be collected at any time during the day. The patient should not have urinated for at least 1 hour prior to specimen collection.

2. The first voided portion is the initial 20 to 30 mL of the urine stream obtained without cleaning the external urethra.

 

Specimen Type: Tissue

Sources: Placenta, products of conception, urogenital, respiratory, bronchus, chest/mediastinal, bone, spine, or joint

Container/Tube: Sterile container

Specimen Volume: 5 mm(3)

Collection Instructions:

1. Collect fresh tissue specimen.

2. Submit fresh tissue only, do not add fluid to tissue

3. Refrigerate or freeze specimen.


Reject Due To

Cotton or calcium alginate-tipped swab Reject
Wooden shaft swab Reject
Transport swab containing gel or charcoal Reject
Formalin-fixed and/or paraffin-embedded tissues Reject
Port-a-Cul tube Reject
Anaerobic fluid vials Reject
Dry swab (no pledget or sponge) Reject
Bone marrow Reject
Decalcified bone Reject
Slides Reject
Respiratory or body fluid specimens placed in viral transport medium (M4-RT, M4, or M5) Reject

Specimen Minimum Volume

Urine-first void: 2 mL; All other specimens: See Specimen Required

Specimen Stability Information

Specimen Type Temperature Time
Varies Refrigerated (preferred) 7 days
  Frozen  7 days

Reference Values

Not applicable

Day(s) Performed

Monday through Sunday

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

87798 x 2

87999 (if appropriate for government payers)

LOINC Code Information

Test ID Test Order Name Order LOINC Value
URRP Ureaplasma PCR 69934-8

 

Result ID Test Result Name Result LOINC Value
SRC80 Specimen source 31208-2
35128 Ureaplasma urealyticum PCR 51988-4
35129 Ureaplasma parvum PCR 69933-0

Report Available

3 to 4 days

Forms

If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.

Secondary ID

60758