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Biomarkers · Chemical

PrEP hCG, Total, Quantitative

LOINC codes
21198-7
Tests that measure PrEP hCG, Total, Quantitative
Quest Diagnostics 13

Ranges

Each lab publishes a reference range for the population groups it tests, usually the middle 95% of results. These intervals describe that population, not an optimal or healthy target. How ranges differ

Quest Diagnostics, PrEP hCG, Total, Quantitative 13696

PopulationInterval
Male<5 mIU/mL
Postmenopausal<10 mIU/mL
Nonpregnant or Premenopausal<5 mIU/mL
FemaleNot stated

Quest Diagnostics test catalog, 13696

Quest Diagnostics, hCG with Gestational Table 19485

PopulationInterval
(mIU/mL), <1 Week5-50
(mIU/mL), 1-2 Weeks50-500
(mIU/mL), 2-3 Weeks100-5000
(mIU/mL), 3-4 Weeks500-10000
(mIU/mL), 4-5 Weeks1000-50000
(mIU/mL), 5-6 Weeks10000-100000
(mIU/mL), 6-8 Weeks15000-200000
(mIU/mL), 2-3 Months10000-100000
Gestational AgeExpected hCG Values (mIU/mL)

Quest Diagnostics test catalog, 19485

Quest Diagnostics, hCG, Total, Quantitative 8396

PopulationInterval
Male<5 mIU/mL
Postmenopausal<10 mIU/mL
Non-pregnant or Premenopausal<5 mIU/mL
FemaleNot stated

Quest Diagnostics test catalog, 8396

Tests

Check the catalog code, specimen, method and preparation for every test that measures PrEP hCG, Total, Quantitative. Select up to five tests to compare them side by side.

Quest Diagnostics 13 tests

Single-analyte tests

  • hCG with Gestational Table 19485

    Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA)
    Quest Diagnostics catalog page
  • hCG, Total with HAMA Treatment 19720

    Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA)
    Reference notes
    hCG, Total, Quantitative HAMA Treated See below hCG, Total, Quantitative Untreated Males: <5 mIU/mL Females: Non-pregnant or Premenopausal: <5 mIU/mL Postmenopausal: <10 mIU/mL
    Quest Diagnostics catalog page
  • hCG, Total, Quantitative 8396

    Serum · Fasting not stated · Turnaround Set up: Sun-Fri; Report available: 3 days

    Method and collection
    Method
    Immunoassay (IA)
    Quest Diagnostics catalog page
  • PrEP hCG, Total, Quantitative 13696

    Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA)
    Quest Diagnostics catalog page

Panels that include this biomarker

  • First Trimester Screen, hCG 16145

    2 analytes · Serum · Fasting not stated · Turnaround Set up: Mon-Fri

    Method and collection
    Method
    Calculation (CALC) • Chemiluminescence (CL) • Immunoassay (IA)
    Quest Diagnostics catalog page
  • Sequential Integrated Screen, Part 1 16131

    2 analytes · Serum · Fasting not stated

    Method and collection
    Method
    Chemiluminescence (CL) • Immunoassay (IA)
    Collection
    Collect between 10.0 weeks to 13.9 weeks. Must complete patient demographic information using the Maternal Serum Screen Requisition. Additional information: NT measurement, when provided by the physician, will be used for additional interpretation.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page
  • Stepwise, Part 1 16463

    2 analytes · Serum · Fasting not stated · Turnaround Set up: Mon-Sat

    Method and collection
    Method
    Chemiluminescence (CL) • Immunoassay (IA)
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page
  • Quad Screen 30294

    4 analytes · Serum · Fasting not stated · Turnaround Set up: Mon-Fri (Day shift); Report available: 4 days

    Method and collection
    Method
    Immunoassay (IA)
    Collection
    For manual orders use "Maternal Serum Screen Requisition" The Quad test in pregnant women should be performed between 14.0 and 22.9 weeks gestational age, although the optimal period is 15.0-16.9 weeks. This time frame allows sufficient opportunity for further diagnostic studies if the initial Quad Screen test results are abnormal. Specimens submitted before 14.0 weeks or after 22.9 weeks gestation cannot be properly evaluated for open neural tube defects, Down Syndrome or Trisomy 18. The Maternal Serum Screen Requisition designed to obtain patient data and the patient's informed consent must be utilized when ordering the Quad Screen test. Because the Quad Screen test results are influenced by certain patient characteristics, the following data must be provided with the specimen in order to permit accurate interpretation of results: date of collection, patient's (maternal) date of birth, patient's estimated date of delivery, patient's weight, patient's race, patient's diabetic status (is patient insulin dependent prior to pregnancy), number of fetuses, and whether this is a repeat sample.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page
  • Sequential Integrated Screen, Part 2 16133

    4 analytes · Serum · Fasting not stated

    Method and collection
    Method
    Chemiluminescence (CL) • Immunoassay (IA)
    Collection
    Collect between 14.0 to 22 6/7 weeks. Maternal date of birth (mm/dd/yy), Estimated Date of Delivery by US/LMP/PE, weight, race, insulin-dependent diabetes status, repeat sample (Y/N), number of fetuses, and neural tube defect history must be provided for interpretation of results. Must complete patient demographic information using the Maternal Serum Screen Requisition.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page

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Sources

Verify these ranges and sources

We compile this page from named laboratory catalogs, guidelines and studies. Labs calculate reference intervals from the people they test, for one assay method and one population group, so an interval describes that population rather than an optimal target.

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