Ordering RecommendationRecommendations when to order or not order the test. May include related or preferred tests.
Use for nutritional assessment of vitamin K1.
MnemonicUnique test identifier.
VIT K
MethodologyProcess(es) used to perform the test.
Quantitative High Performance Liquid Chromatography
PerformedDays of the week the test is performed.
Sun-Fri
ReportedExpected turnaround time for a result, beginning when ARUP has received the specimen.
2-5 days
New York DOH Approval StatusIndicates test has been approved by the New York State Department of Health.
This test is New York DOH approved.
Specimen Required
Patient Preparation
Patient should fast overnight for 12 hours and should not consume alcohol for 24 hours prior to blood draw.
Collect
Plain red or serum separator tube. Also acceptable: Lavender (EDTA) or pink (K2EDTA).
Specimen Preparation
Protect from light during collection, storage, and shipment. Separate serum or plasma from cells within 1 hour of collection. Transfer 1 mL serum or plasma to an ARUP Amber Transport Tube. (Min: 0.6 mL)
Storage/Transport Temperature
Frozen. Separate specimens must be submitted when multiple tests are ordered.
Unacceptable Conditions
Any specimen other than serum or EDTA plasma. Hemolyzed specimens.
Remarks
Stability
After separation from cells: Ambient: Unacceptable; Refrigerated: 1 month; Frozen: 6 months
Reference IntervalNormal range/expected value(s) for a specific disease state. May also include abnormal ranges.
0.22-4.88 nmol/L
Interpretive DataBackground information for test. May include disease information, patient result explanation, recommendations, details of testing, associated diseases, explanation of possible patient results.
Vitamin K concentration is reported as nanomoles per liter (nmol/L). To convert concentration to nanograms per milliliter (ng/mL), multiply the result by 0.45.
Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
NoteAdditional information related to the test.
Hotline History
N/A
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.
Chat
Feedback
