Draft Research Plan
Screening for Syphilis Infection in Nonpregnant Adults and Adolescent
November 19, 2020
Recommendations made by the USPSTF are independent of the U.S. government. They should not be construed as an official position of the Agency for Healthcare Research and Quality or the U.S. Department of Health and Human Services.
- What is the effectiveness of screening for syphilis in reducing complications of the disease and transmission or acquisition of other sexually transmitted infections in asymptomatic, nonpregnant, sexually active adolescents and adults?
- What is the effectiveness of specific screening intervals and screening among population subgroups (e.g., based upon demographic characteristics or risk factors)?
- What is the performance of risk assessment instruments or other risk stratification methods for identifying persons at increased risk for syphilis?
- What are the harms of screening (e.g., stigma, sequelae of test inaccuracy)?
Contextual questions will not be systematically reviewed and are not shown in the Analytic Framework.
- Which population subgroups are at highest risk for incident syphilis infection and syphilis-related morbidity and mortality?
- What are the benefits and tradeoffs of screening with reverse sequence testing (i.e., using a treponemal test for initial screening followed by a nontreponemal test for confirmation) compared to the traditional sequence testing algorithm (i.e., a nontreponemal test followed by a treponemal test)?
- What is the clinical test performance of rapid point-of-care antibody tests?
The Proposed Research Approach identifies the study characteristics and criteria that the Evidence-based Practice Center will use to search for publications and to determine whether identified studies should be included or excluded from the Evidence Review. Criteria are overarching as well as specific to each of the key questions (KQs).
|Populations||Asymptomatic, nonpregnant adolescents and adults who are not known to have current syphilis infection including persons who are infected with other STIs||Symptomatic patients; neonates, infants, and children; pregnant persons; other populations in which syphilis screening may be part of disease management, such as persons living with HIV|
|Interventions||KQs 1, 3: Two-step screening for syphilis with a nontreponemal and treponemal test (traditional or reverse sequence algorithm), including different screening intervals
KQ 2: Risk assessment instruments and other risk stratification methods that identify persons at increased risk for syphilis infection
KQs 1, 3: Screening tests not currently used in U.S. primary care settings
|Comparisons||KQ 1, 3: No screening
KQ 2: Reference standard (identification or diagnosis of infection)
|KQs 1, 3: No comparator or alternate screening test/algorithm|
|Outcomes||KQ 1: Complications of syphilis infection and transmission or acquisition of STIs, including HIV
KQ 2: Any measure of discrimination (e.g., AUC, c-statistic) for identification of infection
KQ 3: Harms from screening (e.g., stigma, sequelae of test inaccuracy)
|KQ 1: Outcomes that are not directly related to health outcomes (e.g., laboratory studies); cost-effectiveness or cost-related outcomes|
|Setting||Primary care and primary care–relevant settings (e.g., school-based clinics, family planning clinics, obstetrics and gynecology clinics, STI clinics, urgent care clinics, emergency departments, community settings, and correctional facilities)|
|Study Design||All KQs: Good-quality systematic reviews
KQs 1, 3: Randomized, controlled trials; observational studies with contemporaneous control groupsKQ 2: Risk prediction studies
KQs 1, 3: Observational studies without comparison groups or historical comparators; narrative reviews; editorials; case reports
|Study Quality||Good- and fair-quality||Poor-quality|
|Country||Studies conducted in countries categorized as “High” or Very High” on the 2019 Human Development Index (as defined by the United Nations Development Programme)||Studies conducted in countries categorized as less than “High” or “Very High” on the 2019 Human Development Index|
Abbreviations: AUC = area under the curve; c = concordance; HIV = human immunodeficiency virus; KQ = key question; STI = sexually transmitted infection; U.S. = United States.