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News / Nation & World

Device touted to treat pain hurting patients

Many spinal-cord simulators shock, burn recipients

By Associated Press
Published: November 25, 2018, 7:53pm
2 Photos
Jim Taft watches The History Channel from the confines of his bed Nov. 16 at his home in West Columbia, S.C. Taft has experienced debilitating health issues after a neurosurgeon implanted Boston Scientific’s Precision spinal cord stimulator in his back in 2014.
Jim Taft watches The History Channel from the confines of his bed Nov. 16 at his home in West Columbia, S.C. Taft has experienced debilitating health issues after a neurosurgeon implanted Boston Scientific’s Precision spinal cord stimulator in his back in 2014. Sean Rayford/Associated Press Photo Gallery

COLUMBIA, South Carolina — Desperate for relief after years of agony, Jim Taft listened intently as his pain management doctor described a medical device that could change his life.

It wouldn’t fix the nerve damage in his mangled right arm, Taft and his wife recalled the doctor saying, but a spinal-cord stimulator would cloak his pain, making him “good as new.”

But Taft’s surgically implanted stimulator failed when a wire along his spine broke. After an operation to repair it, he said the device shocked him so many times that he couldn’t sleep and even fell down a flight of stairs. Today, the 45-year-old Taft is a prisoner in his own bed, barely able to get to the bathroom by himself.

“I thought I would have a wonderful life,” he said. “But look at me.”

For years, medical device companies and doctors have touted spinal-cord stimulators as a panacea for millions of patients suffering from a wide range of pain disorders, making them one of the fastest-growing products in the $400 billion medical device industry. Companies and doctors aggressively push them as a safe antidote to the deadly opioid crisis in the U.S. and as a treatment for an aging population in need of chronic pain relief.

But the stimulators — devices that use electrical currents to block pain signals before they reach the brain — are more dangerous than many patients know, an Associated Press investigation found. They account for the third-highest number of medical device injury reports to the U.S. Food and Drug Administration, with more than 80,000 incidents flagged since 2008.

Patients report that they have been shocked or burned or have suffered spinal-cord nerve damage ranging from muscle weakness to paraplegia, FDA data shows. Among the 4,000 types of devices tracked by the FDA, only metal hip replacements and insulin pumps have logged more injury reports.

The FDA data contains more than 500 reports of people with spinal-cord stimulators who died, but details are scant, making it difficult to determine if the deaths were related to the stimulator or implant surgery.

Medical device manufacturers insist spinal-cord stimulators are safe — some 60,000 are implanted annually — and doctors who specialize in these surgeries say they have helped reduce pain for many of their patients.

Most of these devices have been approved by the FDA with little clinical testing, however, and the agency’s data shows that spinal-cord stimulators have a disproportionately higher number of injuries compared to hip implants, which are far more plentiful.

Devices are rarely pulled from the market, even when major problems emerge.

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