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Diuretic Screen, Urine
0091258
Ordering Recommendation
Mnemonic
DIURETIC U
Methodology
Qualitative High Performance Liquid Chromatography/Ultraviolet Detection
Performed
Varies
Reported
5-14 days
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
ARUP Consult®
Disease Topics
Specimen Required
Patient Preparation
 
Collect
Random urine. 
Specimen Preparation
Transfer 10 mL urine to ARUP Standard Transport Tubes. (Min: 1.2 mL) 
Storage/Transport Temperature
Refrigerated. Also acceptable: Frozen. 
Unacceptable Conditions
 
Remarks
 
Stability
Ambient: 72 hours; Refrigerated: 2 weeks; Frozen: 6 months 
Reference Interval
By report
Interpretive Data


Note
Includes: benzthiazide, bumetanide, chlorothiazide, chlorthalidone, furosemide, hydrochlorothiazide, hydroflumethiazide, and metolazone.
CPT Code(s)
Components
Component Test Code*Component Chart NameLOINC
0091249Chlorothiazide9508-3
0091250Hydrochlorothiazide3676-4
0091251Hydroflumethiazide40469-9
0091254Benzthiazide3399-3
0091255Chlorthalidone3478-5
0091256Metolazone12347-1
0091257Furosemide3660-8
0092601Bumetanide3409-0
0096376Diuretic Screen12288-7
* 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.
Aliases
  • Thiazide

Performed at Medtox