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FDA orders safety studies from scope manufacturers

The Food and Drug Administration, whose headquarters in Silver, Spring, Md., are shown, is ordering manufacturers of specialized medical scopes to study how well hospital staffers follow instructions for disinfecting the scopes between uses.

The Food and Drug Administration, whose headquarters in Silver, Spring, Md., are shown, is ordering manufacturers of specialized medical scopes to study how well hospital staffers follow instructions for disinfecting the scopes between uses.

(Chad Terhune / Los Angeles Times)
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Associated Press

Federal health authorities are ordering manufacturers of specialized medical scopes to study how the reusable devices are cleaned after a series of life-threatening bacterial outbreaks at U.S. hospitals.

The Food and Drug Administration said Monday that the three companies must submit plans to study how well hospital staffers follow instructions for disinfecting the scopes between uses. The agency hopes that this information will shed light on a recent spate of infections involving antibiotic-resistant “superbugs” linked to the scopes.

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The FDA issued the instructions to Olympus American, Fuji Medical Systems and Hoya Corp. All three companies are based in Japan but do business through U.S. affiliates. Olympus American accounts for 85% of the specialized scopes sold in the United States, according to figures from the FDA.

The FDA came under fire this year after two outbreaks at Los Angeles hospitals were linked to duodenoscopes. The specialized fiber-optic scopes are threaded through the digestive tract to diagnose and treat gallstones, tumors and blockages of the pancreas and bile ducts. Officials at both hospitals said they had followed the manufacturers’ instructions for cleaning the devices.

Since 2013, there have been at least eight outbreaks of antibiotic-resistant bacteria linked to the devices at U.S. hospitals, according to government figures. Such problems have been linked to scopes from all three manufacturers that sell the devices in the United States.

Despite the links to infections, the FDA previously ruled that it would keep the devices on the market because they fill an important need in half a million procedures performed each year.

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Duodenoscopes feature a mechanized tip with movable instruments used to drain blockages and perform other procedures. The complex design makes the scopes extremely difficult to clean. Bodily fluids and other debris can stay in the device’s joints and crevices even after cleaning and disinfection.

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MORE ON THE SUPERBUG OUTBREAKS:

Superbug outbreaks: FDA issues more scope-cleaning guidance to hospitals

Superbug outbreaks: Olympus failed to report infections for 3 years, FDA says

A killer on the loose: UCLA doctors race to stop superbug outbreak and save patients

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