Frontiers in cellular and infection microbiology · 2026
Application of microfluidic chip-based multiplex PCR in diagnosing reproductive tract pathogens among patients with premature rupture of membranes.
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Zhang Liuyan, Shao Zhoujie
Аннотация
OBJECTIVE: To evaluate the diagnostic performance of a microfluidic chip-based multiplex PCR method for detecting common reproductive tract pathogens in patients with premature rupture of membranes (PROM).
METHODS: A total of 200 patients with PROM were recruited from January 2020 to December 2024. Clinical samples were collected and analyzed using a microfluidic chip-based multiplex PCR method to detect six common reproductive tract pathogens. Clinical etiological diagnosis was used as the reference standard to assess the diagnostic efficacy of the method. Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and consistency were calculated using 2 × 2 contingency tables. Receiver operating characteristic (ROC) curve analysis was performed to further evaluate the diagnostic performance.
RESULTS: The mean age of the patients was 30.5 years ± 4.2 years, and the mean gestational age was 32.7 ± 3.4 weeks. The most frequently detected pathogen was Escherichia coli (28.0%), followed by Candida albicans (21.0%) and Chlamydia trachomatis (19.0%). The microfluidic chip-based multiplex PCR method demonstrated high sensitivity (95.6%), specificity (98.2%), PPV (94.2%), and NPV (97.8%). ROC curve analysis revealed excellent diagnostic performance for all pathogens, with area under the curve (AUC) values ranging from 0.93 to 0.98.
CONCLUSION: The microfluidic chip-based multiplex PCR method provides a highly sensitive, specific, and reliable diagnostic tool for detecting reproductive tract pathogens in patients with PROM.
METHODS: A total of 200 patients with PROM were recruited from January 2020 to December 2024. Clinical samples were collected and analyzed using a microfluidic chip-based multiplex PCR method to detect six common reproductive tract pathogens. Clinical etiological diagnosis was used as the reference standard to assess the diagnostic efficacy of the method. Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and consistency were calculated using 2 × 2 contingency tables. Receiver operating characteristic (ROC) curve analysis was performed to further evaluate the diagnostic performance.
RESULTS: The mean age of the patients was 30.5 years ± 4.2 years, and the mean gestational age was 32.7 ± 3.4 weeks. The most frequently detected pathogen was Escherichia coli (28.0%), followed by Candida albicans (21.0%) and Chlamydia trachomatis (19.0%). The microfluidic chip-based multiplex PCR method demonstrated high sensitivity (95.6%), specificity (98.2%), PPV (94.2%), and NPV (97.8%). ROC curve analysis revealed excellent diagnostic performance for all pathogens, with area under the curve (AUC) values ranging from 0.93 to 0.98.
CONCLUSION: The microfluidic chip-based multiplex PCR method provides a highly sensitive, specific, and reliable diagnostic tool for detecting reproductive tract pathogens in patients with PROM.