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Updated: Jan 31, 2026

Murine Nasal Lavage Fluid Collection without Blood Contamination
Published on: July 11, 2025
Effect of blood contamination on amniotic fluid detection in vitro using immunoassays
Elisa T Bushman1,2, Lauren H Theilen1,2, Martha Monson1,2
1Department of Obstetrics & Gynecology, University of Utah Health, Salt Lake City, UT, USA.
Insights
ROM Plus® demonstrates superior accuracy in detecting amniotic fluid proteins, even with blood contamination, outperforming Amnisure® and Actim® PROM tests. This finding is crucial for accurate diagnosis of ruptured membranes in clinical settings.
Area of Science:
- Clinical diagnostics
- Biomarker detection
- Obstetrics and Gynecology
Background:
- Accurate diagnosis of ruptured membranes is critical in obstetrics.
- Blood contamination can interfere with diagnostic tests for ruptured membranes.
- Existing tests like Amnisure® and Actim® PROM have limitations in the presence of blood.
Purpose of the Study:
- To evaluate the diagnostic accuracy of Actim PROM®, Amnisure®, and ROM Plus® tests for amniotic fluid proteins.
- To assess the impact of blood contamination on the performance of these tests.
- To compare the efficacy of ROM Plus® against Amnisure® and Actim® PROM in detecting ruptured membranes.
Main Methods:
- Commercially available immunoassays (Actim PROM®, Amnisure®, ROM Plus®) were used.
- Amniotic fluid was spiked with varying concentrations of whole blood (1-50%).
- Tests were performed in duplicate and interpreted by blinded obstetricians.
- Accuracy, sensitivity, specificity, and concordance were calculated and compared using Fisher exact test.
Main Results:
- No false positive results were observed for any test.
- ROM Plus® exhibited the highest overall accuracy (97.9%), significantly outperforming Amnisure® (80.7%) and Actim® PROM (78.3%).
- ROM Plus® demonstrated significantly higher sensitivity (p < .0001) compared to the other two tests.
- Intra- and interobserver concordance were high (98-100%) across all tested methods.
Conclusions:
- ROM Plus® maintains robust diagnostic performance for amniotic fluid proteins in the presence of blood contamination.
- ROM Plus® significantly outperforms Amnisure® and Actim® PROM tests when blood is present.
- These findings support ROM Plus® as a reliable option for diagnosing ruptured membranes, even with blood-tinged samples.
Abstract:
Objective: To determine the accuracy of Actim PROM®, Amnisure®, and ROM Plus® tests for detecting amniotic fluid proteins in the setting of blood contamination.Methods: IGFBP-1 and AFP are proteins present in high concentrations in amniotic fluid, and are detected by three commercially-available immunoassays used for diagnosing ruptured membranes: Actim PROM®, Amnisure®, and ROM Plus®. We used whole blood samples and diluted these with amniotic fluid (containing known concentrations of amniotic fluid proteins) to whole blood levels of 50, 20, 10, 5, and 1%. Actim PROM®, Amnisure®, and ROM Plus® tests were performed on each sample in duplicate according to package insert instructions. Results were interpreted independently at 5, 10, 15, and 20 min by two obstetricians who were blinded to the concentrations of blood and amniotic fluid proteins in each sample. Results of each test were determined to be true positive, false negative, false positive, or true negative based on physician interpretation and whether amniotic fluid had been spiked into the samples in detectable concentrations. Overall accuracy, intraobserver concordance, and interobserver concordance, sensitivity, specificity, and predictive values for each test were calculated. Fisher exact test was used to compare test characteristics, with a p-value of <.05 considered significant.Results: Out of 120 tests performed, there were no false positive results for any test. Overall, ROM Plus® had better accuracy (97.9%) than Amnisure® (80.7%) or Actim® PROM (78.3%). Intra- and interobserver concordance were similar for all three tests (98-100%). ROM Plus® had significantly higher sensitivity than Amnisure® and Actim® PROM (p < .0001). There was no significant difference in sensitivity between Amnisure® and Actim® PROM (p = .51).Conclusion: ROM Plus® maintains strong test characteristics for the detection of amniotic fluid proteins in the setting of blood contamination, and performs significantly better than Amnisure® and Actim® PROM tests in the presence of blood.
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