Ordering Recommendation
Mnemonic
LH
Methodology

Quantitative Electrochemiluminescent Immunoassay

Performed

Sun-Sat

Reported

Within 24 hours

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect

Serum separator tube or plasma separator tube.

Specimen Preparation

Allow specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Hemolyzed specimens.

Remarks
Stability

After separation from cells: Ambient: 5 days; Refrigerated: 2 weeks; Frozen: 6 months

Reference Interval
Females
Males
7-9 years: 0.0-0.7 IU/L
10-12 years: 0.0-6.8 IU/L
13-15 years: 0.3-23.0 IU/L
16-17 years: 0.0-26.4 IU/L
Follicular: 2.4-12.6 IU/L
Mid-cycle: 14.0-95.6 IU/L
Luteal: 1.0-11.4 IU/L
Postmenopausal: 7.7-58.5 IU/L
7-9 years: 0.0-0.7 IU/L
10-12 years: 0.0-3.4 IU/L
13-15 years: 0.3-5.6 IU/L
16-17 years: 1.1-9.0 IU/L
18 years and older: 1.7-8.6 IU/L
Effective December 1, 2014
Tanner Stage I: 0.0-2.8 IU/L
Tanner Stage II: 0.0-7.9 IU/L
Tanner Stage III: 0.0-23.0 IU/L
Tanner Stage IV-V: 0.0-25.3 IU/L
Effective December 1, 2014
Tanner Stage I: 0.0-1.0 IU/L
Tanner Stage II: 0.0-3.6 IU/L
Tanner Stage III: 0.2-6.4 IU/L
Tanner Stage IV-V: 1.1-8.5 IU/L

Interpretive Data



Compliance Category

FDA

Note
Hotline History
N/A
CPT Codes

83002

Components
Component Test Code* Component Chart Name LOINC
0070093 Luteinizing Hormone 10501-5
* 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
  • ICSH
  • Interstitial Cell Stimulating Hormone
  • Leuteotropic Hormone
  • LH
  • Luteotropic Hormone
  • lutrophin
  • lutropin
  • Pituitary gonadotropins
Luteinizing Hormone, Serum