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The FDA: Doctors, Change the Way You Perform Uterine Surgery

By HERWriter
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FDA: surgeons, change how you perform uterine surgery MonkeyBusiness Images/PhotoSpin

The Food and Drug Administration is asking doctors to stop using a procedure performed on tens of thousands of American women each year during uterine surgery, because it poses a risk of spreading cancerous tissue.

In an FDA safety advisory, surgeons are discouraged from using a powered cutting tool -- power morcellators -- to remove uterine fibroids.

With laparoscopic power morcellation, a tube-shaped blade is used to grind and shred uterine tissue so it can be removed through a small incision in the abdomen. The technique is widely used to treat painful uterine fibroids, either by removing the noncancerous growths themselves or the entire uterus.

According to the Wall Street Journal, morcellators, introduced in the 1990s, help gynecologists perform about 50,000 fibroid-removal procedures each year through tiny holes rather than longer incisions that can lead to bigger scars and a longer recovery time.

Based on an analysis of currently available data, the FDA has determined that approximately 1 in 350 women who undergo hysterectomy or myomectomy for fibroids have an unsuspected type of uterine cancer called uterine sarcoma.

If laparoscopic power morcellation is performed on these women, there is a risk that the procedure will spread the cancerous tissue within the abdomen and pelvis, significantly worsening the patient’s likelihood of long-term survival.

Since uterine sarcoma can't be reliably detected before they are removed, they can be mistaken for fibroids. The cancer is typically discovered only after the mass has been removed and tissue sent to a pathologist.

Between 500,000 and 600,000 women each year undergo hysterectomies, up to 40 percent for painful uterine fibroids. It’s unclear how many involve morcellation but it’s estimated to be between 50,000 and 150,000.

Dr. William Maisel, deputy director for science and chief scientist at the Center for Devices and Radiological Health told the New York Times that although the FDA had the authority to ban power morcellators, it chose not to because some women may still see the procedure as a good option.

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We value and respect our HERWriters' experiences, but everyone is different. Many of our writers are speaking from personal experience, and what's worked for them may not work for you. Their articles are not a substitute for medical advice, although we hope you can gain knowledge from their insight.

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