The Food and Drug Administration has approved a testing protocol that allows patients to collect their own vaginal samples for human papillomavirus (HPV) screening in healthcare settings—including urgent care. It’s significant because it allows for HPV primary testing without the need for a traditional Pap smear performed with a speculum. The self-collected samples must still be sent to labs for analysis. While a Pap smear can potentially detect abnormalities in the cervix, the new HPV …
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