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Can Variable Plasma Volume Alterations Affect the Efficiency of the First Trimester Screening Test?
Clinical Laboratory
|June 25, 2019
Summary
Plasma volume changes, indicated by hematocrit levels, can impact first trimester screening test accuracy. Elevated hematocrit may increase false positive results for aneuploidy screening in pregnant women.
Area of Science:
- Maternal-Fetal Medicine
- Biochemistry
- Genetics
Background:
- First trimester screening is crucial for detecting fetal aneuploidy.
- Plasma volume alterations can influence biochemical marker levels.
- Hematocrit is a potential indicator of plasma volume changes.
Purpose of the Study:
- To evaluate the impact of hematocrit-determined plasma volume changes on first trimester screening biochemical parameters.
- To assess the relationship between hematocrit and false positive screening results.
Main Methods:
- 1,424 pregnant women in their first trimester were studied.
- Included ultrasonographic Nuchal Translucency measurement and serum free β-hCG and PAPP-A.
- Complete blood count was performed to assess hematocrit and rule out anemia.
Main Results:
- Serum hematocrit (Hct) significantly predicted false positive screening results (AUC: 0.839, p < 0.001).
- An optimal Hct cutoff of 30.2% demonstrated 85% sensitivity and 75% specificity for identifying false positives.
- 1.5% of the total cohort (21/1424) received false positive results.
Conclusions:
- Plasma volume alterations, reflected by hematocrit, can affect biochemical markers used in first trimester aneuploidy screening.
- Hematocrit levels may contribute to false positive results, necessitating careful interpretation.
- Further research is warranted to refine screening protocols considering plasma volume variations.
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