مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

805
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Za0Using the PCR method for detection of bacterial vaginosis in women suspected of vaginosis in Guilan province

Pages

  29-36

Abstract

 Introduction: Bacterial vaginosis is the most common lower genital tract infection among women in reproductive age. Its causative agent is often the bacterium Gardnerella vaginalis which exists in synergism with other mostly anaerobic bacteria such as Atopobium vaginae, Mobiluncus curtisii and Megasphaera type I. The present study was conducted with aim of measuring molecular measurements (PCR) in the detection and diagnosis of Bacterial vaginosis in women. Methods: This descriptive study was performed on 100 women referred to Obstetrics and Gynecology Clinics of Al-Zahra Hospital and private clinics in Rasht from September 2016 to October 2017. They were examined and tested for Bacterial vaginosis. The presence of Gardnerella vaginalis was tested by five different laboratory methods based on Amsel criteria and molecular methods including determination of appearance characteristics, determination of pH, Whiff test, and observation of Clue cells in direct smear, conducting Polymerase Chain Reaction (PCR) using specific primers on DNA extracted from vaginal specimens. Data were analyzed using SPSS software (version 21) and Chi-square test. P<0. 05 was considered significant. Results: In this study, from a total of 100 suspected women who were examined for vaginal infection with use of Amsel method, 31 cases (31%) of vaginosis were confirmed. Using the molecular method of PCR in women with vaginosis (Amsel method), Gardnerella vaginosis was confirmed in 14 (45%) and Atopobioum vagine in 10 (32%). Conclusion: Using the PCR method showed that Gardenerella vaginalis and Atopobium vaginae play an important role in womenaged 18-35-year-old with bacterialvaginosis that indicates the role of these two bacteria in the development of Bacterial vaginosis.

Cites

  • No record.
  • References

    Cite

    APA: Copy

    Roohbakhsh, Esmaeil, MOJTAHEDI, ALI, KHAVARI NEJAD, RAMAZAN ALI, & AMIRMOZAFARI, NOUR. (2019). Za0Using the PCR method for detection of bacterial vaginosis in women suspected of vaginosis in Guilan province. IRANIAN JOURNAL OF OBSTETRICS, GYNECOLOGY AND INFERTILITY, 21(12 ), 29-36. SID. https://sid.ir/paper/375221/en

    Vancouver: Copy

    Roohbakhsh Esmaeil, MOJTAHEDI ALI, KHAVARI NEJAD RAMAZAN ALI, AMIRMOZAFARI NOUR. Za0Using the PCR method for detection of bacterial vaginosis in women suspected of vaginosis in Guilan province. IRANIAN JOURNAL OF OBSTETRICS, GYNECOLOGY AND INFERTILITY[Internet]. 2019;21(12 ):29-36. Available from: https://sid.ir/paper/375221/en

    IEEE: Copy

    Esmaeil Roohbakhsh, ALI MOJTAHEDI, RAMAZAN ALI KHAVARI NEJAD, and NOUR AMIRMOZAFARI, “Za0Using the PCR method for detection of bacterial vaginosis in women suspected of vaginosis in Guilan province,” IRANIAN JOURNAL OF OBSTETRICS, GYNECOLOGY AND INFERTILITY, vol. 21, no. 12 , pp. 29–36, 2019, [Online]. Available: https://sid.ir/paper/375221/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button