Regional Medical Laboratory

MySwab™ is powered by robust and reliable nucleic acid amplification methodology that you can trust. Our test menu is specifically designed to target the most common genital pathogens affecting women's health and sexually transmitted diseases, evaluated on a single Aptima swab.

The MySwab™ approach is comprehensive, cost effective and reliable.

Simplify collection with a single swab

	Bacterial Vaginosis • Gardnerella vaginalis • Lactobacillus species Candida Vaginitis • C. albicans • C. tropicalis • C. dubliniensis • C. parapsilosis • C. glabrata Sexually Transmitted Pathogens • Chlamydia trachomatis • Neisseria gonorrhoeae • Trichomonas vaginalis • Herpes Simplex Virus 1 and 2
Vaginal swab collected with the APTIMA collection kit. Stability: Room Temperature and Refrigerated = 30 days.

Test name	Clinical presentation	Components	Test number
	Symptoms of vaginosis, including discomfort and discharge, with low risk for sexually transmitted infections	Bacterial Vaginosis Candida Vaginitis	6987003
	Symptoms of vaginosis, including discomfort and discharge, and at risk for coinfection with Trichomonas	Bacterial Vaginosis Candida Vaginitis Trichomonas Vaginalis	6987004
	Symptoms of vaginosis, including discomfort and discharge, and at risk for coinfection with Trichomonas, Chlamydia and/or Gonorrhea	Bacterial Vaginosis Candida Vaginitis Trichomonas Vaginalis Chlamydia Trachomatis Neisseria Gonorrhoeae	6987005
	Patients with pain and/or visible lesions and potential for coinfection with other sexually transmitted infections	Trichomonas Vaginalis Chlamydia Trachomatis Neisseria Gonorrhoeae Herpes Simplex Virus 1&2**	6987006
	Option to order test components a la carte	Candida Vaginitis	6987000
		Bacterial Vaginosis	6987001
		Trichomonas Vaginalis	6910121
		Chlamydia Trachomatis	6910109
		Neisseria Gonorrhoeae	6910115
		Herpes Simplex Virus 1&2**	6987002
**This assay is only FDA approved for clinician-collected swab specimens from anogenital lesions. Swab collections from other locations or in absence of visible lesions are considered an off label use and have not been validated at this laboratory. Results should not be used as the sole means for diagnosis and should be correlated with the clinical presentation.