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#Beckman coulter pregnancy test manual

The CLINITEK Status+ Analyzer precisely times the reading of results, eliminating hands-on waiting time. The analyzer reports qualitative hCG results as negative (hCG level is ≤ 5 mIU/mL), positive (hCG level is ≥ 25 mIU/mL) or borderline (hCG level is between 5 and 25 mIU/mL).

The cassette is then automatically drawn into the analyzer. After mounting the cassette on a test table, the urine sample is added to the sample well. It eliminates hands-on waiting time, which improves workflow and increases the time for patient care. This CLIA-waived CLINITEST hCG pregnancy test indicates a positive result in two minutes and a negative result in five minutes.

confirm that the test has been properly completed.

create error flags when such conditions are not met, and.

perform automatic quality checks for proper sample flow and adequate sample which helps improve QC.

The CLINITEST hCG pregnancy test employs an easy-to-use cassette that is utilized with the CLINITEK Status family of analyzers. The sensitive CLINITEST hCG pregnancy test from Siemens provides fast and reliable instrument-read-and-reported test results. The test is used to see if a woman is pregnant and can be done as part of a screening test for birth defects. The hCG pregnancy test is done to check for the hormone hCG in blood or urine. Please refer to the NHANES Analytic Guidelines and the on-line NHANES Tutorial for further details on the use of sample weights and other analytic issues.The human chorionic gonadotropin (hCG) hormone, which appears soon after conception, is an excellent and reliable marker for the early detection of pregnancy.

Analytic NotesĮxam sample weights should be used for analyses. Read the General Documentation on Laboratory Data file for detailed QA/QC protocols.Ī detailed description of the quality assurance and quality control procedures can be found on the NHANES website.

#Beckman coulter pregnancy test manual

Detailed QA/QC instructions are discussed in the NHANES Laboratory/Medical Technologists Procedures Manual (LPM).

The NHANES quality control and quality assurance protocols (QA/QC) meet the 1988 Clinical Laboratory Improvement Act mandates. Laboratory Quality Assurance and Monitoring Instructions on data processing and editing can be found on the NHANES website. The test utilizes a combination of monoclonal and polyclonal antibodies to selectively detect elevated levels of hCG in urine or serum.Ī detailed description of the laboratory method used can be found on the NHANES website. The Icon 25 hCG test kit (Beckman Coulter) is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in urine or serum to aid in the early detection of pregnancy. Detailed specimen collection and processing instructions are discussed in the NHANES Laboratory/Medical Technologists Procedures Manual (LPM). Urine and serum specimens were tested in the NHANES mobile examination centers. However, due to disclosure risks only females between 20 and 44 have urine pregnancy results in this file. Eligible SampleĪ pregnancy test was completed on female participants aged 12–59 years and menstruating females aged 8–11 years. All positive test results excluded pregnant women from the DXA and cardiovascular fitness components of the mobile examination center. If the urine pregnancy test was positive on any female participants aged 8 -17 years, the result was confirmed using a serum test. A urine test was performed on survey participants 8 years and older.