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dc.contributor.authorCaliskan, E.
dc.contributor.authorKoksal, M. O.
dc.contributor.authorKeceli, S. A.
dc.contributor.authorCakiroglu, Y.
dc.contributor.authorAgacfidan, A.
dc.contributor.authorKeskin, F.
dc.contributor.authorCiftci, S.
dc.date.accessioned2021-03-04T17:34:08Z
dc.date.available2021-03-04T17:34:08Z
dc.date.issued2018
dc.identifier.citationKeskin F., Ciftci S., Keceli S. A. , Koksal M. O. , Caliskan E., Cakiroglu Y., Agacfidan A., "Comparison of Culture and Real-time Polymerase Chain Reaction Methods for Detection of Mycoplasma hominis in Amniotic Fluids Samples", NIGERIAN JOURNAL OF CLINICAL PRACTICE, cilt.21, sa.9, ss.1127-1131, 2018
dc.identifier.issn1119-3077
dc.identifier.othervv_1032021
dc.identifier.otherav_864f9585-3cff-4518-a4e8-e3c888cbd151
dc.identifier.urihttp://hdl.handle.net/20.500.12627/91266
dc.identifier.urihttps://doi.org/10.4103/njcp.njcp_230_17
dc.description.abstractBackground: Mycoplasma hominis is often present in the amniotic cavity with microbial invasion associated with spontaneous preterm labor. Conventional culture method is the gold standard for detection of Mycoplasmas, but real-time polymerase chain reaction (real-time PCR) has revolutionized the diagnosis of M. hominis. Objective: The purpose of this study is the comparison of the culture methodology with real-time PCR for the detection of M. hominis in amniotic fluid samples. Methods: Amniotic fluid samples were collected from 65 pregnant women (age range: 25-45 years) previously followed at an infertility clinic. They were collected by transabdominal genetic amniocentesis during 16-21 weeks of gestation. Amniotic fluids were inoculated in SP4 broth for 48-72 h, and after becoming alkaline, culture suspension was spread on A7 agar plate for 1 week till the typical colonies seen in "fried-egg" morphology under stereomicroscope. DNA was extracted using a QIAGEN Mini DNA kit. The real-time-PCR was performed using Rotor-Gene Q Real-time PCR instrument. A melting-curve analysis was also performed. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were measured by real-time PCR by taking culture as gold standard. Results: Sixty-five women in 16-21 weeks of gestation, with a mean age of 33 +/- 5.06 years, were enrolled into this study. M. hominis detected by culture and real-time PCR assay was 72% (47/65) and 69% (45/65), respectively. 66% (43/65) specimens were positive by both methods. Real-time PCR sensitivity was 91.5%, specificity 88.9%, PPV 95.6%, and NPV 80%. Conclusion: Rapid detection of Mycoplasmas causing maternal complications such as neonatal infections and preterm labor in pregnancy by real-time PCR may be important and necessary. The high sensitivity and shorter time requirement of real-time PCR support its further development for diagnosis of Mycoplasma infections.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectTemel Tıp Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.titleComparison of Culture and Real-time Polymerase Chain Reaction Methods for Detection of Mycoplasma hominis in Amniotic Fluids Samples
dc.typeMakale
dc.relation.journalNIGERIAN JOURNAL OF CLINICAL PRACTICE
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume21
dc.identifier.issue9
dc.identifier.startpage1127
dc.identifier.endpage1131
dc.contributor.firstauthorID256044


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