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Relevant bibliographies by topics / COMBO2

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Journal articles

Academic literature on the topic 'COMBO2'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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Journal articles on the topic "COMBO2"

1

Lavelle, S. J. "Finding, confirming, and managing gonorrhoea in a population screened for chlamydia using the Gen-Probe Aptima Combo2 assay." Sexually Transmitted Infections 82, no. 3 (2006): 221–24. http://dx.doi.org/10.1136/sti.2005.017616.

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2

Risbud, AR, G. Rao, P. Narayanan, P. Prabhakar, and A. Das. "Detection of N. gonorrhoeae and C. trachomatis infection using urine sample from symptomatic high-risk women by APTIMA Combo2 assay." Indian Journal of Medical Microbiology 31, no. 1 (2013): 96. http://dx.doi.org/10.4103/0255-0857.108756.

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3

Brinker, C. Jeffrey. "Combo combat." Nature Materials 11, no. 10 (2012): 831–32. http://dx.doi.org/10.1038/nmat3434.

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4

Cosentino, L., J. R. Schwebke, M. M. Hobbs, and S. L. Hillier. "P3-S1.32 A validation study of the Gen-Probe APTIMA Combo2 (AC2) assay for detecting Chlamydia trachomatis and Neisseria gonorrhoeae in dry swabs." Sexually Transmitted Infections 87, Suppl 1 (2011): A278. http://dx.doi.org/10.1136/sextrans-2011-050108.432.

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5

Silveira, MF, MP Bruni, D. Stauffert, D. Golparian, and M. Unemo. "Prevalence and risk factors associated with Chlamydia trachomatis, Neisseria gonorrhoeae, and Mycoplasma genitalium among women in Pelotas, Southern Brazil." International Journal of STD & AIDS 31, no. 5 (2020): 432–39. http://dx.doi.org/10.1177/0956462419898982.

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The frequently asymptomatic sexually transmitted infections (STIs) caused by Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), and Mycoplasma genitalium (MG) are poorly diagnosed in Brazil and can lead to severe complications/sequelae without timely detection and treatment. We investigated prevalence of CT, NG, and MG infections and associated demographic, behavioral, and clinical factors in consecutive women attending a gynecology and obstetrics outpatient clinic in Pelotas, Southern Brazil. Vaginal swab samples were prospectively obtained from asymptomatic and symptomatic women (n = 49

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6

Mahto, Mrinalini, and Harry Mallinson. "P026 Value of continuing pharyngeal GenProbe Aptima Combo2 Transcription Mediated Amplificaton (TMA) testing for CT/GC in addition to urogenital/rectal swabs: Abstract P026 Table 1." Sexually Transmitted Infections 92, Suppl 1 (2016): A27.3—A28. http://dx.doi.org/10.1136/sextrans-2016-052718.80.

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7

Dize, Laura, Barbara Silver, and Charlotte Gaydos. "Comparison of the Cepheid GeneXpert CT/NG assay to the Hologic Aptima Combo2 assay for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae in self-collected rectal swabs." Diagnostic Microbiology and Infectious Disease 90, no. 2 (2018): 83–84. http://dx.doi.org/10.1016/j.diagmicrobio.2017.10.013.

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8

Robinet, Sylvain, and François Parisot. "Performance assessment of the Allplex™ STI Essential real-time PCR assay for the diagnosis of Neisseria gonorrhoeae and Chlamydia trachomatis infections in genital and extra-genital sites." Journal of Laboratory Medicine 43, no. 4 (2019): 191–200. http://dx.doi.org/10.1515/labmed-2019-0030.

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Abstract Background Commercial kits performing Neisseria gonorrhoeae (NG) and Chlamydia trachomatis (CT) nucleic acid amplification tests (NAATs) for genital samples are recommended in association with culture, but the majority of real-time polymerase chain reaction (PCR) methods have not received regulatory approval for diagnostics in extra-genital sites. Since 2017, only the Hologic® Aptima Combo2 assay has an in vitro diagnostic (IVD) certification from the European Medicine Evaluation Agency. Methods We assessed the Allplex™ STI-Essential Assay (EA) for the diagnosis of NG and CT in both g

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9

Cosentino, Lisa A., Claire S. Danby, Lorna K. Rabe, et al. "Use of Nucleic Acid Amplification Testing for Diagnosis of Extragenital Sexually Transmitted Infections." Journal of Clinical Microbiology 55, no. 9 (2017): 2801–7. http://dx.doi.org/10.1128/jcm.00616-17.

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ABSTRACT Nucleic acid amplification testing (NAAT) is the preferred method to detect Chlamydia trachomatis and Neisseria gonorrhoeae , but no commercial tests are cleared by the U.S. Food and Drug Administration for use with extragenital swab samples. This study evaluated the performance of the Gen-Probe Aptima Combo2 assay (Aptima) and the Cepheid Xpert CT/NG assay (Xpert) to detect C. trachomatis and N. gonorrhoeae in rectal and pharyngeal samples from 224 men and 175 women reporting a history of anal receptive sexual intercourse. Discordant results between the NAATs were repeated using the

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10

DORSA, WARREN J., and GREGORY R. SIRAGUSA. "A Representative Microbial Sampling Method for Large Commercial Containers of Raw Beef Based on Purge†." Journal of Food Protection 61, no. 2 (1998): 162–65. http://dx.doi.org/10.4315/0362-028x-61.2.162.

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The purge from beef combos (a boxed collection of beef trimmings) was tested as a means of representatively sampling the microbial content of this raw product. In the first experiment, purge was sampled from model beef combos that had been inoculated with bovine feces. Data from this experiment indicated a strong correlation (r = 0.94) between the total aerobic bacteria counts derived from the purge samples of a model beef combo and the total aerobic bacteria present in a rinse sample of the entire model beef combo. In a second experiment, two 500-g meat pieces were inoculated with an antibiot

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