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17-OH Progesterone LC/MS, Two Specimens

Order Code
070037
CPT
83498x2
Test Details
Synonyms

17-OHP ACTH Stimulation

TAT

11 days

Methodology

Liquid chromatography/tandem mass spectrometry (LC/MS-MS)

Remarks

Special Instructions: This panel is a series panel requiring multiple tubes to be drawn at multiple time points. This panel is used to collect an initial tube (baseline) and then treat the patient with a drug (pill or shot) or other treatment (such as glucola) and then collect more tubes after the dose. If you are not giving the patient a pill or shot or other treatment after the first sample draw, do not use this panel. This series should not be collected until the clinician is contacted to determine why a series is ordered.

Performing Location

Accredited Laboratory Partner

Testing Frequency

Contact Technical Support

Test Overview

Evaluates 17-hydroxyprogesterone at two time points, typically pre- and post-stimulation. Assists in diagnosing steroid biosynthesis disorders.

Specimen Type

Serum or Plasma

Volume

1 mL (each specimen)

Specimen Container

Red-top tube, gel-barrier tube OR lavender-top (EDTA) tube

Patient Preparation

No special preparation is required for this test. You may eat, drink, and take your medications as normal, unless instructed otherwise by your healthcare provider.

Collection

This test does not require any special collection or pre-analytical handling. Follow routine specimen collection protocols.

Specimen Stability
Temperature Period
Room temperature 7 days
Refrigerated 7 days
Frozen 14 days
Order Code
070037
CPT
83498x2
Test Details
Synonyms

17-OHP ACTH Stimulation

TAT

11 days

Methodology

Liquid chromatography/tandem mass spectrometry (LC/MS-MS)

Remarks

Special Instructions: This panel is a series panel requiring multiple tubes to be drawn at multiple time points. This panel is used to collect an initial tube (baseline) and then treat the patient with a drug (pill or shot) or other treatment (such as glucola) and then collect more tubes after the dose. If you are not giving the patient a pill or shot or other treatment after the first sample draw, do not use this panel. This series should not be collected until the clinician is contacted to determine why a series is ordered.

Performing Location

Accredited Laboratory Partner

Testing Frequency

Contact Technical Support

Test Overview

Evaluates 17-hydroxyprogesterone at two time points, typically pre- and post-stimulation. Assists in diagnosing steroid biosynthesis disorders.

Specimen Type

Serum or Plasma

Volume

1 mL (each specimen)

Specimen Container

Red-top tube, gel-barrier tube OR lavender-top (EDTA) tube

Patient Preparation

No special preparation is required for this test. You may eat, drink, and take your medications as normal, unless instructed otherwise by your healthcare provider.

Collection

This test does not require any special collection or pre-analytical handling. Follow routine specimen collection protocols.

Specimen Stability
Temperature Period
Room temperature 7 days
Refrigerated 7 days
Frozen 14 days