The STI II PCR Profile is a comprehensive molecular test that screens for a broad range of sexually transmitted infections (STIs) using advanced polymerase chain reaction (PCR) technology. This highly sensitive diagnostic tool detects both common and less frequent pathogens with precision, ensuring early and reliable identification of infections. The test includes Chlamydia trachomatis, Neisseria gonorrhoeae, Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma urealyticum, Ureaplasma parvum, and Trichomonas vaginalis.
Who is this profile for?
This profile is suitable for individuals who:
– Are sexually active and want a detailed STI screening.
– Experience symptoms such as discharge, genital pain, itching, or unusual sores.
– Have recently had unprotected sex or multiple partners.
– Require an advanced STI screening for routine or preventive health assessments.
– Have been exposed to a partner diagnosed with STIs or are considered high-risk.
What can be detected
The STI II PCR Profile identifies seven key pathogens linked to sexually transmitted and reproductive tract infections:
– Chlamydia trachomatis: Detects chlamydia infection, which can cause discharge, painful urination, or be asymptomatic.
– Neisseria gonorrhoeae: Detects gonorrhea, a bacterial STI that can affect the genital area, throat, or rectum.
– Mycoplasma genitalium: Identifies this bacterium associated with urethritis, pelvic pain, and potential fertility complications.
– Mycoplasma hominis: Detects this organism, which can be involved in genital and urinary tract infections.
– Ureaplasma urealyticum: Detects this bacterium that may cause discomfort, discharge, or inflammation in the urinary tract.
– Ureaplasma parvum: Identifies the presence of this microorganism, sometimes linked to reproductive tract infections.
– Trichomonas vaginalis: Detects this parasite responsible for trichomoniasis, which can cause itching, discharge, or irritation.
When to get tested
This test is recommended for individuals with symptoms of STIs, those entering new relationships, or anyone seeking a comprehensive check as part of preventive sexual healthcare. It is also suitable for post-treatment follow-up to confirm the clearance of infections.
Fasting requirements
No fasting is required for this test. However, for urine-based samples, it is advised to avoid urination for at least 1–2 hours before sample collection to ensure accuracy.
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or email us at
info@vitalync-diagnosis.com
Our partner, Medical Diagnosis, is UKAS 15189 accredited and registered with the CQC. All tests are conducted to the highest standards of accuracy and reliability.
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