Feedback
Diuretic Survey Quantitative, Serum or Plasma
2007763
Ordering Recommendation
Mnemonic
DIURET SP
Methodology
Quantitative High Performance Liquid Chromatography - Tandem Mass Spectrometry
Performed
Varies
Reported
3-9 days
N/A
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
ARUP Consult®
Disease Topics
Specimen Required
Patient Preparation
 
Collect
Plain red, lavender (EDTA), or pink (K2EDTA). 
Specimen Preparation
Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.4 mL) 
Storage/Transport Temperature
Refrigerated. Also acceptable: Room temperature or frozen. 
Unacceptable Conditions
Separator tubes. 
Remarks
 
Stability
Ambient: 1 week; Refrigerated: 1 month; Frozen: 1 month 
Reference Interval
By report
Interpretive Data


Components
Component Test Code*Component Chart NameLOINC
2007764Chlorothiazide, Serum or Plasma3464-5
2007765Hydrochlorothiazide, Serum or Plasma3675-6
2007766Furosemide, Serum or Plasma3659-0
* 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
  • Chlorothiazide
  • Diuril{R}
  • Furosemide
  • HCTZ
  • Hydrochlorothiazide
  • HydroDiuril{R}
  • Lasix{R}
  • Thiazide (Diuretic Survey Quantitative, Serum or Plasma)

Performed at National Medical Services (NMS)