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.
Specimen Required
Patient Preparation
Collect

Random urine.

Specimen Preparation

Transfer 10 mL urine to ARUP Standard Transport Tubes. (Min: 1.2 mL)
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.

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



Compliance Category

Performed by non-ARUP Laboratory

Note

Includes: benzthiazide, bumetanide, chlorothiazide, chlorthalidone, furosemide, hydrochlorothiazide, hydroflumethiazide, and metolazone.

Hotline History
N/A
CPT Codes

80377 (Alt code: G0480)

Components
Component Test Code* Component Chart Name LOINC
0091249 Chlorothiazide 9508-3
0091250 Hydrochlorothiazide 3676-4
0091251 Hydroflumethiazide 40469-9
0091254 Benzthiazide 3399-3
0091255 Chlorthalidone 3478-5
0091256 Metolazone 12347-1
0091257 Furosemide 3660-8
0092601 Bumetanide 3409-0
0096376 Diuretic Screen 12288-7
* 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
Diuretic Screen, Urine

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