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Recommendations when to order or not order the test. May include related or preferred tests.
Detect Acanthamoeba spp and Naegleria fowleri in various specimen types.
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.
Corneal scrapings, vitreous fluid or tissue.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Place corneal scrapings, vitreous fluid, or tissue in 2 mL of Page Amoeba Saline (ARUP supply #31917). Available online through eSupply using ARUP Connect™ or contact Client Services at (800) 522-2787.
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Room temperature.
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
Specimens in media or preservatives.
RemarksAdditional specimen collection, transport, or test submission information.
Specimen source preferred.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Expected turnaround time for a result, beginning when ARUP has received the specimen.
2-10 days
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Negative
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
This culture will detect free-living amoeba such as Acanthamoeba species and Naegleria fowleri but will NOT detect Balamuthia mandrillaris.
Compliance Category
Standard
Note
Additional information related to the test.
For CSF refer to Acanthamoeba and Naegleria Culture and Stain, CSF (ARUP test code 3000878).For Entamoeba histolytica detection refer to Entamoeba histolytica Antigen, EIA(ARUP test code 0058001).
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.