Our dysfunctional federal government’s bungling is killing people.
Example: Every year, more than half a million patients undergoing a common medical procedure risk getting a superbug infection because their doctor is using a contaminated instrument. A doctor inserts a thin, tubular scope down your throat and into your digestive system to treat cancer and other problems. You assume the tube is clean. Think again.
The scope’s defective design allows bacteria to grow even after it’s rigorously cleaned between patients. The Food and Drug Administration, whose job is to ensure the safety of medical devices, has known about this problem since 2012 but dawdled while patients died. Three months ago, Olympus, the manufacturer of most of these specialized scopes (duodenoscopes), began recalling them.
Yet numerous hospitals are still using them, and patients are still getting infected and dying – eight more infections and two more deaths according to last month’s FDA data.
Even at prestigious institutions such as UCLA Medical Center, New York-Presbyterian, Hartford Hospital in Connecticut, Massachusetts General in Boston and Thomas Jefferson University Hospital in Philadelphia, patients have been infected with superbugs from contaminated duodenoscopes.
When hospitals fail to warn patients about the risk, it makes a mockery of the idea that patients are giving “informed consent” before the procedure, says medical-safety expert Lawrence Muscarella.
Worse, the FDA and another federal agency, the Centers for Disease Control and Prevention, go along with the hush-up about which hospitals are having a problem. These agencies are supposed to work for us – the public – but clearly they’re siding with the hospitals. The FDA is stonewalling about where the two most recent deaths occurred.