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 

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)

Chlamydia and Gonorrhea testing:

all sexually active women ages 15-25

women at increased risk for Chlamydia and Gonorrhea

 

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

We recommend the mobile app: 

 

              Google Play:                                                         Apple AppStore: