The digene HPV Test

Article provided by QIAGEN

The digene HPV Test is the leading test approved by the U.S. Food and Drug Administration (FDA) that directly detects the presence of high-risk types of the HPV virus. When used along with a Pap to screen women 30 and older, it more accurately identifies who is at risk of developing cervical cancer than the Pap alone.

Here's are the reasons why:

• The Pap test (or Pap smear) has helped diagnose many women with cervical cancer or pre-cancerous conditions. A trained lab professional looks through a microscope at a sample of your cervical cells to determine if any abnormalities are present that could signal the presence of disease.
• The digene HPV Test – which can be run by the lab on the same sample of cells used for the Pap – uses molecular technology to detect the presence of high-risk types of HPV (human papillomavirus), which is what causes cervical cells to become abnormal in the first place.
• For women over 30 years old, who are most at risk of cervical cancer, getting both the Pap and HPV tests together provides the best assurance of finding cervical disease before it becomes cancer. Studies show that, on average, the combination of the digene HPV Test and the Pap identifies 95-100 percent of advanced cervical disease (CIN 2, CIN 3, or cancer). It is important to remember, however, that the presence of HPV does not mean you have cervical disease. An additional exam is needed to determine whether disease exists.
• It is recommended that younger women (20-30), in whom HPV infections are common but usually temporary, get an HPV test only if their Pap smear looks "inconclusive" or "borderline," to help their doctor or nurse determine whether further examination is needed.

QIAGEN, the maker of the digene HPV test for women age 30+ together with the Pap, developed the test to more accurately identity the cancer-causing types of the HPV virus and identify women at increased risk of cervical cancer. For more information please go here: www.theHPVtest.com.