HPV FDA Approved screening:
women ages 21 years and older = Pap, reflex to Aptima HPV if ASC-US
women ages 30 years and older (ACOG limits age to 65) = Pap + Aptima HPV
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Our Recommended FDA HPV testing algorithm:
women ages 21-29 = Pap, reflex to HPV testing if ASC-US
women ages 30-65 = Pap + HPV (co-testing)
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Chlamydia and Gonorrhea testing:
all sexually active women ages 15-25
women at increased risk for Chlamydia and Gonorrhea
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We automatically reflex to genotyping for the oncogenic types 16 and 18/45 for HPV positive cases. These genotypes are responsible for 75% of all squamous cell cervical cancers and 94% of cervical adenocarcinomas. https://www.medscape.com/viewarticle/731407
ASCCP treatment and testing Guidelines:
http://www.asccp.org/guidelines
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We recommend the mobile app:
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Google Play:
Apple AppStore: