Ordering RecommendationRecommendations when to order or not order the test. May include related or preferred tests.
MnemonicUnique test identifier.
SMR INTRP
MethodologyProcess(es) used to perform the test.
Cytochemical Stain
PerformedDays of the week the test is performed.
Mon-Fri
ReportedExpected turnaround time for a result, beginning when ARUP has received the specimen.
1-2 days
New York DOH Approval StatusIndicates test has been approved by the New York State Department of Health.
Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible.
Specimen Required
Patient Preparation
Collect
Lavender (EDTA) or Green (Sodium or Lithium Heparin). Immediately invert tube several times following procurement of whole blood.
Specimen Preparation
Transport 5 mL whole blood and 6 unfixed push smears. (Min: 0.1 mL whole blood and 2 unfixed push smears)
Storage/Transport Temperature
Room temperature.
Unacceptable Conditions
Serum or plasma.
Remarks
Most recent CBC report, patient history, clinical indications and physician's name and telephone number are required. An instructional video with more information on how to make an adequate slide can be found at: https://www.youtube.com/watch?v=ca3NwrlpS40&feature=youtu.be
Reference IntervalNormal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Interpretive DataBackground information for test. May include disease information, patient result explanation, recommendations, details of testing, associated diseases, explanation of possible patient results.
Refer to report.
No compliance statements are in use for this test.
NoteAdditional information related to the test.
Further information on how to make an adequate slide, in the form of an instructional video, can be found at: https://www.youtube.com/watch?v=ca3NwrlpS40&feature=youtu.be
CPT CodesThe 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.
AliasesOther names that describe the test. Synonyms.
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