What is APTIMA Combo 2 assay?
The APTIMA Combo 2 Assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis and/or Neisseria gonorrhoeae in endocervical and male urethral swab specimens, and in female and male …
What does aptima multitest swab test for?
The Aptima® Multitest Swab detects up to 7 infections or disease states at a time. Chlamydia, Gonorrhea, Mycoplasma genitalium, Trichomonas vaginalis, Candida species, C. glabrata, Bacterial vaginosis.
What is GC APTIMA?
The APTIMA® Assay for Neisseria gonorrhoeae is a target amplification. nucleic acid probe test that utilizes target capture for the in vitro. qualitative detection of ribosomal RNA (rRNA) from Neisseria. gonorrhoeae (GC) to aid in the diagnosis of gonococcal urogenital. disease.
What is an aptima?
3 The APTIMA® vaginal swab is used for tests that require vaginal sampling (ie, bacterial vaginosis). APTIMA® vaginal swabs are also used to perform high-quality NAA molecular tests for Chlamydia, Gonorrhea, Trichomonas, herpes simplex virus, bacterial vaginosis, and Mycoplasma.
How accurate are aptima test?
Overall, the Combo 2 assay showed a sensitivity and specificity of 94.2 and 97.6%, respectively, in C. trachomatis swab specimens and of 94.7 and 98.9%, respectively, in C. trachomatis FCU specimens.
What is chlamydia aptima?
The APTIMA Assay for Chlamydia trachomatis is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) in clinician-collected endocervical, vaginal and male urethral swab specimens, patient-collected …
How accurate is the aptima SARS-CoV-2 assay?
The Aptima® SARS-CoV-2 assay has been designed to minimize the likelihood of false positive test results. However, it is still possible that this test can give a false positive result, even when used in locations where the prevalence is below 5%.
Is aptima a PCR test?
With Panther® Scalable Solutions, you can run over 1000 tests in 24 hours, attaining first results in about 3 hours. The Panther Fusion® SARS-CoV-2 assay is a real-time PCR test and the Aptima® SARS-CoV-2 assay utilizes our proprietary TMA® technology.
What is Gonococcus by NAA?
The Gonorrhea, Nucleic Acid Amplification (NAA) (Urine) test examines patients for the presence of Neisseria gonorrhoeae through nucleic acid amplification technology. Positive results may require further evaluation by your physician.
How accurate is aptima?
The 95% limit of detection of the Aptima assay was estimated to be at LDT CT = 33 (equivalent to 870 copies/mL). The relative light units (RLU) × 1000 for 52 true positive clinical specimens was 962.2 ± 181.5, and that for the 186 true negative specimens was 264.6 ± 14.3.
Is Hologic aptima SARS-CoV-2 assay a PCR test?
The Panther Fusion® SARS-CoV-2 assay is a real-time PCR test and the Aptima® SARS-CoV-2 assay utilizes our proprietary TMA® technology.
How do you read chlamydia test results?
Ask your healthcare provider what your test results mean for you. Normal results are negative, meaning that no chlamydia cells were found in your sample. A positive result means that chlamydia bacteria were found and that you are likely infected with the disease.
What type of test is aptima SARS-CoV-2 assay?
The Aptima® SARS-CoV-2 assay is a nucleic acid amplification in vitro diagnostic test intended for the qualitative detection of RNA from SARS-CoV-2 isolated and purified from nasopharyngeal (NP) and oropharyngeal (OP) swab specimens, nasopharyngeal washes/aspirates or nasal aspirates (collected by a healthcare provider …
How do you read chlamydia results?
What does chlamydia Gonococcus NAA mean?
The Gonorrhea, Nucleic Acid Amplification (NAA) (Urine) test examines patients for the presence of Neisseria gonorrhoeae through nucleic acid amplification technology. Positive results may require further evaluation by your physician. Includes: 3 tests: Chlamydia trachomatis, NAA.
Is aptima SARS-CoV-2 assay FDA approved?
(COVID-19) The Aptima® SARS-CoV-2 assay is authorized for use with respiratory specimens collected from individuals consistent with the Emergency Use Authorization (EUA).
Is the Hologic aptima test a PCR test?
What does chlamydia IgM positive mean?
Presence of antibodies against chlamydia bacteria indicates active or previous infection. IgG antibodies act as marker for positive infection and this indicates past, current, or chronic infections. Positive IgM antibodies indicate recent infection.
Can you test positive for chlamydia and your partner negative?
Yes, it is possible to contract a STI from someone who tested negative (for the STIs that they were tested for)… if (and only if!) they were positive for an STI that they weren’t tested for.
How accurate is gonorrhea test?
For gonorrhea testing in women, the sensitivity and specificity were 79% and 99%, respectively, for urine samples compared to cervical samples. For gonorrhea testing in men, the sensitivity and specificity were 92% and 99%, respectively, for urine samples compared to urethral samples.
What is the best test for gonorrhea?
Gonorrhea nucleic acid amplification (NAAT) testing: NAAT testing detects the genetic material (DNA) of the gonorrhea bacteria and is considered the optimal test for gonorrhea infection. This type of test can be performed on a urine sample or a swab taken from a site of potential infection.
What is the aptima Combo 2 test?
The APTIMA Combo 2 Assay is a target amplification nucleic acid probe test that utilizes target capture for the in vitro qualitative detection and differentiation of ribosomal RNA (rRNA) from Chlamydia trachomatis (CT) and/or Neisseria
What is the Gen-Probe aptima Combo 2 assay?
PROBE APTIMA Combo 2 Assay for the detection of C. trachomatis and/or N. gonorrhoeae. The GEN-PROBE APTIMA Specimen Transfer Kit provides the necessary materials and instructions to allow for the testing of PreservCyt liquid Pap specimens in the AC2 Assay.
What is an aptima test?
APTIMA assays for the detection of Chlamydia trachomatis and/or Neisseria gonorrhoeae. The GEN-PROBE APTIMA Specimen Transfer Kit allows for APTIMA Assay testing of gynecological specimens collected and processed by the Cytyc ThinPrep 2000 Processor according to the instructions provided. Gen-Probe Incorporated
What is the sensitivity and specificity of C trachomatis in preservcyt liquid PAP specimens?
Sensitivity and specificity for C. trachomatis in PreservCyt liquid Pap specimens tested in the APTIMA Combo 2 Assay, by symptom status and overall, is presented in Table 1. For Gen-Probe Incorporated Confidential Page 9 of 16 C. trachomatis, overall sensitivity was 96.7% (87/90). In symptomatic and asymptomatic