Widespread adoption of population-based screening has been associated with marked decreases in cervical cancer incidence and mortality in the United States over the last few decades. Despite these gains, an estimated 13 240 US women were diagnosed with cervical cancer in 2018, and 4170 died from the disease. 1 A large body of consistent evidence implicates infection with highrisk types of human papillomavirus (hrHPV) as the causative agent in cervical cancer. These infections are common, occurring in the majority of sexually active women over their lifetime. 2 While most infections resolve without clinical consequence over a period of several years, persistent infections can lead to high-grade precancerous cervical lesions (such as cervical intraepithelial neoplasia [CIN] grades 2 and 3) that can progress to cervical cancer. Approximately 30% of CIN grade 3 lesions progress to invasive cancer over a 30-year period. 2 This slow progression allows many opportunities for these lesions to be detected and treated, thereby disrupting the trajectory to cancer.In 2018, the US Preventive Services Task Force (USPSTF) updated its screening guidelines. 3 In addition to continuing to recommend triennial cytology (Papanicolaou tests) for women ages 21 to 29 years followed by either continued triennial cytology or adding a test for high-risk types of HPV every 5 years from ages 30 to 65 years, the task force endorsed a strategy of hrHPV testing alone every 5 years for women ages 30 to 65 years. The USPSTF stated that referring all women with abnormal test results directly to colposcopy would lead to a much greater number of colposcopies, but it did not recommend any particular triage strategy for women with a positive test result for hrHPV; the Society of Gynecologic Oncology recommends triaging these women with HPV genotyping (tests for HPV types 16 or 18). 4 Current screening guidelines from the USPSTF, American College of Obstetricians and Gynecologists (ACOG), 5 and American Cancer Society (ACS) and its partners 6 are described in the eTable in the Supplement. These guidelines apply to women at average risk (no prior diagnosis of a high-grade precancerous lesion or cervical cancer, women who are not immunocompromised, and women with no in utero exposure to diethylstilbestrol). Expanded screening recommendations for women with higher risk are also included. 5,7 All of these groups recommend discontinuing screening in women at average risk who have had a hysterectomy with removal of the cervix. Clinical actions following common abnormal screening test results, as recommended by professional societies, 4,5,8 are displayed in the Figure.The endorsement of 3 strategies expands screening options and accommodates a variety of clinical settings. The 2018 USPSTF