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  3. 3024. PCR. Neisseria gonorrhoeae (u/g scraping, qualitative determination)

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3024. PCR. Neisseria gonorrhoeae (u/g scraping, qualitative determination)

3024. PCR. Neisseria gonorrhoeae (u/g scraping, qualitative determination)

Turnaround time (days): 3

755 ₴

Important information

*Collection of urogenital biomaterial is not available in all departments.

*Before your visit, check the presence of a corresponding mark on the page of the selected branch.

Description

PCR testing for Neisseria gonorrhoeae from urogenital swabs is an accurate method for diagnosing gonorrhea. It can detect the pathogen's DNA even in asymptomatic cases or in cases with a low bacterial load. It is recommended for suspected STIs, complications, or screening.

Neisseria gonorrhoeae is a gram-negative bacterium that causes gonorrhea, one of the most common sexually transmitted infections. Gonorrhea can affect the mucous membranes of the genitourinary tract, rectum, pharynx, and eyes, and has a wide range of clinical manifestations, from severe inflammation to asymptomatic carriage.

Without proper treatment, the infection can cause dangerous complications:

  • in women – cervicitis, urethritis, endometritis, salpingitis, tuboperitoneal infertility, and an increased risk of ectopic pregnancy;
  • in men – acute urethritis, balanoposthitis, epididymitis, orchiepididymitis, and impaired fertility;
  • in both sexes – gonococcal pharyngitis, proctitis, gonococcal arthritis, mucocutaneous lesions, and generalized gonococcal infection (DGI).

A low-symptom or asymptomatic course of the disease is particularly dangerous, especially in women. This not only complicates timely diagnosis but also facilitates the spread of the pathogen among partners.

Advantages of real-time PCR:

  • Direct detection of Neisseria gonorrhoeae DNA, regardless of the viability of the bacteria.
  • High analytical sensitivity allows for the detection of infection with minimal strain.
  • Effective in cases of latent infection, reinfection, or after partial treatment;
  • Quick results, highly accurate, without the need for culture.

Sample for testing:

  • for men – urethral swab;
  • for women – cervical, cervical canal, and urethral swab.

For oropharyngeal or rectal manifestations, a swab from the appropriate areas can be tested (in a separate analysis).

When and who needs the test?

  • For STI symptoms (painful urination, abnormal discharge, lower abdominal pain).
  • Patients with recurrent urethritis, cervicitis, or colpitis.
  • In case of contact with an infected partner.
  • Couples with infertility or prior to ART (IVF, ICSI).
  • Before gynecological or urological interventions.
  • As a preventive screening in high-risk groups (frequent partner changes, HIV-positive status, etc.).

Biological material

  • Scrapes from various sites depending on the test

Preparing for urogenital sampling


Women

  • Collection of material should be carried out before the start of treatment with antibacterial/antimycotic drugs (general and local).
  • In case of treatment monitoring – 14 days after completion of the course of treatment with antibacterial/antimycotic drugs.
  • Avoid sexual intercourse for 3 days.
  • In case...

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3325. Package # 426 (Intimate health of a woman)

Number of tests: 5
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3391. Package No.38.2 (Diagnosis of vaginal discharge causes. PCR: Screening for the causes of vaginitis, Chlamydia trachomatis, Mycoplasma genitalium, Neisseria gonorrhoeae (urogenital swab). Bacterial culture. Urogenital complex)

Number of tests: 5
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3389. Package No.38 (Urogenital health: PCR. Chlamydia trachomatis, Mycoplasma hominis, Mycoplasma genitalium, Ureaplasma species, Trichomonas vaginalis, Gardnerella vaginalis, Neisseria gonorrhoeae (urogenital swab). Bacterial culture. Urogenital complex)

Number of tests: 8
Bacterial culture. Urogenital complex (Lactobacillus spp., Gardnerella vaginalis, Enterococcus spp., Staphylococcus spp., Streptococcus spp., Enterobacterales, Non-fermenters, Candida spp., and others). Automatic identification. Antimicrobial resistance pr
PCR. Neisseria gonorrhoeae (u/g scraping, qualitative determination)

Turnaround time (days): 3

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3394. Пакет №38.1 (Урогенітальне здоров'я 2: ПЛР:Chlamydia trachomatis/Mycoplasma hominis/Mycoplasma genitalium/Ureaplasma species/Trichomonas vaginalis/Gardnerella vaginalis/Neisseria gonorrhoeae/ВПЛ6/11/ВКР14 (сobas HPV FDA) (у/г зішкріб).Бакпосів.УГ.Комплекс)

Number of tests: 10
Bacterial culture. Urogenital complex (Lactobacillus spp., Gardnerella vaginalis, Enterococcus spp., Staphylococcus spp., Streptococcus spp., Enterobacterales, Non-fermenters, Candida spp., and others). Automatic identification. Antimicrobial resistance pr
PCR. HPV HCR 14 (cobas HPV FDA approved). Genotyping 16 and 18 and groups 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 (u/g scrape, qualitative)

Turnaround time (days): 3

8160 ₴

3024. PCR. Neisseria gonorrhoeae (u/g scraping, qualitative determination)

755 ₴

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