āChlamydia & Gonorrhea4,5
|
- Sexually active, <25 years: annually ā
- Sexually active, ā„25 years: if at increased risk5
|
- āConsider screening more frequently if at increased risk5
- Rescreen for reinfection approximately 3 months after treatment
|
āSyphilis6
|
- At least once, repeat if at increased risk
- Co-test when screening for HIVā
|
āIncreased risk includes history of incarceration or transactional sex work, geography, race/ethnicity, methamphetamine use
|
āHIV
|
ā<65 years: at least once (opt-out), annually if at risk
|
āTest if seeking evaluation and treatment for STIs
|
āHepatitis C7
|
āā„18 years: at least once, repeat if at risk
|
āExcept in settings where the prevalence of HCV infection is <0.1%
|
āChlamydia & Gonorrhea4,5
|
- At first prenatal visit
- <25 years or at increased risk; retest at 3rd trimesterā5
|
- āConduct test of cure 4 weeks after treatment for chlamydia
- Rescreen for reinfection 3 months after treatment
|
āSyphilis6
|
- First prenatal visit
- 3rd trimester (ideally 28-32 weeks' gestation)8
-
Delivery unless low risk & negative 3rd trimester testā
|
āIncreased risk includes limited prenatal care, unstable housing, meth use, incarceration (within past year), new STI diagnosis in pregnancy and lives in area with high congenital syphilis rates3
|
āHIV
|
- At first prenatal visit (opt-out)
- At 3rd trimester if at increased risk9ā
|
āRapid testing should be performed at delivery if not previously screened during pregnancy
|
āHepatitis B7
|
- First prenatal visit of each pregnancy
- At delivery if no prior screening or if at increased riskā
|
āTest for Hepatitis B surface antigen (HBsAg). Increased risk includes injection drug use, new STI in pregnancy or HBsAg+ partner.3
|
āHepatitis C7
|
āAt first prenatal visit
|
āExcept in settings where the prevalence of HCV infection is <0.1%
|
āChlamydia & Gonorrhea
|
āIf at high risk
|
āConsider routine chlamydia screening in high prevalence settings (adolescent clinics, correctional facilities, STI/sexual health clinic)
|
āSyphilis
|
āScreen asymptomatic adults at increased risk
|
āIncrease risk includes history of incarceration or commercial sex work, geography, race/ethnicity, and age <29 years
|
āHIV
|
ā<65 years: at least once (opt-out), annually if at risk
|
āTest if seeking evaluation and treatment for STIs
|
āHepatitis C7
|
āā„18 years: at least once, repeat if at risk
|
āExcept in settings where the prevalence of HCV infection is <0.1%
|
āChlamydia & Gonorrhea
|
āAnnually at sites of sexual exposure (urethral [urine], rectum, pharynx) regardless of condom use; every 3-6 months if at increased risk
|
āIncreased risk includes patients on HIV PrEP (screen every 3-4 months) or living with HIV, if patient or sex partners has multiple partners, sex in conjunction with drug use |
āSyphilis
|
āAny age: annually, every 3-6 months if at increased risk |
Screen every 3-4 months if on HIV PrEPā |
āHIV
|
Annually if patient/partner(s) have had >1 sex partner since last HIV test; every 3-6 months if at increased riskā |
Screen every 2 months (if on injectable HIV PrEP) or 3 months (if on oral HIV PrEP)ā |
āHepatitis B7
|
At least onceā |
āTest for HBsAg, HBV core antibody, and HBV surface antibody |
āHepatitis C7
|
āā„18 years: at least once, repeat if at risk |
Except in settings where the prevalence of HCV infection is <0.1%ā |
āChlamydia & Gonorrhea
|
āAdapt screening recommendations based on anatomy
|
Consider screening for pharyngeal and rectal infections based on sexual behaviors and exposure, regardless of reproductive anatomyā |
āSyphilis
|
āConsider at least annually, repeat if at increased risk |
āNone
|
āHIV
|
ā<65 years: at least once (opt-out), annually if at risk |
āNone
|
āHepatitis C7
|
ā„18 years: at least once, repeat if at riskā |
āExcept in settings where the prevalence of HCV infection is <0.1% |
Chlamydia, Gonorrhea, & Syphilis
|
āAt first HIV evaluation, and at least annually thereafter; more frequently based on risk |
āChlamydia & gonorrhea infection should include all sites of sexual exposure (pharynx, rectum, urethral [urine], and vagina) regardless of sex |
Trichomonas
|
If receptive vaginal sex, at first HIV evaluation, then at least annuallyā |
Retest approximately 3 months after treatmentā |
āHepatitis B7
|
At least onceā |
Test for HBsAg, HBV core antibody, and HBV surface antibodyā |
āHepatitis C7
|
- Serologic testing at initial evaluation
- Annual HCV testing in MSM with HIV infectionā
|
āNone
|
1Consider trichomonas screening in high-prevalence settings (e.g., STI clinics and correctional facilities) and for asymptomatic cisgender women at high risk for infection (e.g., those with multiple sex partners, transactional sex, drug misuse, or a history of STI or incarceration). The use of highly sensitive and specific tests (e.g., a nucleic acid amplification test (NAAT)) is recommended for detecting
Trichomonas vaginalis.
4A vaginal swab (self-collected) NAAT is the optimal urogenital specimen type for women. Consider rectal chlamydia (CT) and pharyngeal and rectal gonorrhea (GC) screening for women based on reported sexual history, through shared decision-making between the patient and the provider.
5CT or GC risk factors include prior CT or GC infection, particularly in past 24 months; more than one sex partner in the past year; suspicion that a recent partner may have had concurrent partners; new sex partner in past 3 months; illicit drug use; transactional sex in the past year, and local factors (e.g., community prevalence of infection). CDPH data has shown that CT and GC rates among Black/African American females are 1.5 and 3 times higher than statewide rates among all females, respectively, which are likely due to social determinants of health and living in communities with high STI prevalence.āÆProviders should consider screening Black/African American women up to age 30.
7AB 789 requires primary care facilities in California to offer hepatitis B and hepatitis C testing based on the latest screening recommendations from the U.S. Preventive Services Task Force
828 weeks gestation recommended by the Centers for Disease Control and Prevention 2021 STI Treatment Guidelines
9High risk (for HIV infection in pregnancy) include persons who use drugs, have STIs during pregnancy, have multiple sex partners during pregnancy, have a new sex partner during pregnancy, live in areas with high HIV prevalence, or have partners with HIV
10Primary Care Guidelines for Persons with Human Immunodeficiency Virus: 2020 Update by the HIV Medicine Association of the Infectious Disease Society of America. Clinical Infectious Diseases. 6 November 2020;
https://doi.org/10.1093/cid/ciaa1391.