Abbott Laboratories is adding HPV screening to its "Alinity m" family of diagnostic assays following U.S. Food & Drug Administration approval. Abbott said in a press release that the FDA approved its ...
Guidelines expanded to include self-collection for HPV testing and revised guidance for exiting cervical cancer screening.
HPV testing 8 years after negative result was comparable to risk after 3 years in cytology cohort. HealthDay News — Primary human papillomavirus (HPV) screening intervals could be extended, with the ...
According to the U.S. Centers for Disease Control (CDC), most sexually active adults will experience HPV infections; new test detects those HPV genotypes that could lead to cancer Abbott (ABT)'s new ...
(CNN) — Testing for high-risk human papillomaviruses every five years – even with a self-collected sample – is the “preferred screening strategy” for cervical cancer starting at age 30, according to a ...
The U.S. Food and Drug Administration (FDA) has approved a human papillomavirus (HPV) DNA test for women 25 and older that can be used to determine whether these women should have additional ...
Editor's Note: One hundred years ago, Dr. George Papanicolaou first put vaginal smears under the microscope to study human vaginal cytology, using samples supplied by his wife. [1] Dr. Papanicolaou ...
The Teal Wand allows you to screen yourself for cervical cancer from the comfort of your home. This is everything you need to know. Anna Gragert (she/her/hers) was previously the lifestyle editor at ...
ABBOTT PARK, Ill., Nov. 2, 2023 /PRNewswire/ -- Abbott (NYSE: ABT) has received U.S. Food and Drug Administration (FDA) approval for its molecular human papillomavirus or HPV screening solution, ...
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