17 Alpha Hydroxyprogesterone (17-OHP)
Clinical Biochemistry
Sample and container requirements
Serum (preferred) Lithium Heparin Plasma (paediatrics only)
Minimum volume required
300 µL serum/plasma
Special requirements
Time of collection MUST be stated.
Patient preparation
No specific patient preparation is required. Specimens from neonates for 17-OHP analysis should not be collected until 48 hours after birth and prior to any steroid therapy being commenced.
Sample viability
Turnaround time
5 working days
Reference range
Adults: Adult males: 1.2 – 3.7 nmol/L Adult females: 0.6 – 4.0 nmol/L (follicular phase) and 1.0 – 6.0 nmol/L (luteal phase) Paediatrics: Neonates (>48 hrs): <8.0 nmol/L (For neonates please record gestational age, birth weight and sex. Premature or small babies can have inappropriately high values.) Tanner stage 1 males/females: <5.0 nmol/L (Source: locally derived)
Clinical guidance
Please refer to LabTestsOnlineUK to learn more about 17-OHP. https://labtestsonline.org.uk/tests/17-hydroxyprogesterone
Notes
Images to go here
This information was last updated on 19 August 2026