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

Journal Paper

Paper Information

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:

987
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:

1

Information Journal Paper

Title

COMPARISON OF DIRECT MICROSCOPIC EXAMINATION AND CULTURE METHODS SENSITIVITY FOR DIAGNOSIS OF TRICHOMONAS VAGINALIS IN TABRIZ HEALTH CARE CENTERS VISITORS

Pages

  63-68

Abstract

 Background: TRICHOMONAS VAGINALIS is a common pathogen with worldwide distribution. It is estimated that worldwide 180 million people are infected annually. TRICHOMONIASIS is associated with vaginitis, cervicitis, low birth weight, and preterm delivery in pregnant women; in addition, it is a cofactor in HIV transmission. Diagnosis of disease is traditionally depends on the microscopic observation of motile protozoa in vaginal discharge, with the sensitivity of 38% up to 80%. Culture of organism is the current gold standard and its sensitivity is 85-95%. In this study we used these two methods for comparative detection of T. vaginalis in vaginal discharge.Materials and methods: A total of 2630 visitors attending the health care centers in Tabriz were eXa.mh'1edT.wo cotton swabs were used to obtain vaginal discharge. First swab was used for direct microscopic examination. Cultivation was performed in Kupferberg trichomonas medium (QUELAB, Canada) using second swab.Results: Clinical examination of 2630 health center visitors showed that 1575 person (59.88%) had vaginal signs and 1055 person were asymptomatic. 92 out of 2630 patients were positive for T. vaginalis by wet mount examination (3.46%). The growth of T. vaginalis was observed in 120 samples (4.56%).Conclusion: Although wet preparation is the only test widely available for diagnosis of T. vaginalis, its sensitivity is poor. In this study, using culture as a gold standard, the sensitivity of wet preparation was 75% and specificity was 99%. The results suggest that direct examination with parasite cultivation can be the method of choice for detection of TRICHOMONIASIS.

Cites

References

Cite

APA: Copy

JAMALI, R., ZAREI KAR, B., GHAZANCHAEI, A., & YOUSEFI, SABER. (2007). COMPARISON OF DIRECT MICROSCOPIC EXAMINATION AND CULTURE METHODS SENSITIVITY FOR DIAGNOSIS OF TRICHOMONAS VAGINALIS IN TABRIZ HEALTH CARE CENTERS VISITORS. YAFTEH, 8(4 (30)), 63-68. SID. https://sid.ir/paper/408337/en

Vancouver: Copy

JAMALI R., ZAREI KAR B., GHAZANCHAEI A., YOUSEFI SABER. COMPARISON OF DIRECT MICROSCOPIC EXAMINATION AND CULTURE METHODS SENSITIVITY FOR DIAGNOSIS OF TRICHOMONAS VAGINALIS IN TABRIZ HEALTH CARE CENTERS VISITORS. YAFTEH[Internet]. 2007;8(4 (30)):63-68. Available from: https://sid.ir/paper/408337/en

IEEE: Copy

R. JAMALI, B. ZAREI KAR, A. GHAZANCHAEI, and SABER YOUSEFI, “COMPARISON OF DIRECT MICROSCOPIC EXAMINATION AND CULTURE METHODS SENSITIVITY FOR DIAGNOSIS OF TRICHOMONAS VAGINALIS IN TABRIZ HEALTH CARE CENTERS VISITORS,” YAFTEH, vol. 8, no. 4 (30), pp. 63–68, 2007, [Online]. Available: https://sid.ir/paper/408337/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