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Flow cytometry of ethanol-fixed versus fresh bladder barbotage specimens
The Journal of Urology
|June 1, 1985
Summary
Flow cytometry deoxyribonucleic acid (DNA) analysis of bladder washings is reliable using ethanol-fixed cells, matching fresh cell results in 88% of cases. This allows for consistent, reproducible sample analysis at flow cytometry centers.
Area of Science:
- Urology
- Cytometry
- Molecular Biology
Background:
- Flow cytometry is a valuable tool for analyzing cellular DNA content.
- Standardization of sample preparation techniques is crucial for accurate diagnostic results.
- Bladder washings are commonly used for cytological and molecular analyses.
Purpose of the Study:
- To compare the accuracy and reproducibility of deoxyribonucleic acid (DNA) analyses from fresh versus ethanol-fixed saline bladder barbotage specimens.
- To determine if ethanol-fixed bladder washings are suitable for flow cytometry analysis.
Main Methods:
- Saline bladder barbotage specimens were collected from 99 patients.
- Deoxyribonucleic acid (DNA) content was analyzed using flow cytometry.
- Two cell preparation techniques were compared: fresh cells and ethanol-fixed cells.
Main Results:
- Flow cytometric DNA analyses showed consistency between fresh and ethanol-fixed specimens in 87 out of 99 cases (88% agreement).
- The agreement between the two methods was statistically significant (p < 0.0001) based on the Kappa statistic.
- The findings indicate high concordance between the preparation techniques.
Conclusions:
- Accurate and reproducible deoxyribonucleic acid (DNA) analyses can be obtained from ethanol-fixed bladder washings.
- Ethanol-fixed bladder washings are a viable option for flow cytometry analysis.
- This standardization allows for reliable sample submission to flow cytometry centers, improving diagnostic accessibility.