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Walter Reed Infuse Bone Graft Study Under Scrutiny

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More bad news surrounding Medtronic Inc.’s Infuse Bone Graft.  Now it seems a former surgeon at Walter Reed Army Medical Center in Washington D.C. forged colleagues’ signatures and falsified data in a study conducted there.

According to The New York Times, the surgeon in question,  Dr. Timothy R. Kuklo, is a paid consultant for Medtronic, and had also given talks on Infuse while at Walter Reed.  A Medtronic official also confirmed to the Times that the company financially supported some of Kuklo’s research at Walter Reed, but said the Infuse study was not funded by Medtronic.  The official would not say when Kuklo was hired as a consultant, nor how much he has been paid, the Times said. Kuklo is now an associate professor at the Washington University medical school in St. Louis.

According to The  Wall Street Journal, Kuklo’s Walter Reed Infuse study claimed to showed that wounded soldiers’ leg injuries healed better when the product was used.  But  Walter Reed was unable to verify its conclusions. According to a report in the St. Louis Post-Dispatch, the study cited higher numbers of patients and injuries than the hospital could account for.   According to The Wall Street Journal, investigators at Walter Reed have also concluded that Kuklo forged his co-authors signatures on the study.  Kuklo also did not obtain the Army’s required permission to conduct the study.

Infuse Bone Graft contains recombinant human Bone Morphogenetic Protein (rhBMP-2), a protein released naturally by the body.  It is approved to treat a spinal condition called Degenerative Disc Disease, as well as open fractures of the tibia.  It is also approved for use in two dental bone grafting procedures: sinus augmentation and localized alveolar ridge augmentation.

In July, the Food & Drug Administration (FDA) warned that the use of Infuse Bone Graft and similar products had caused serious problems when they were used off-label in cervical spine (neck) surgeries.   Patients reported difficulty swallowing, breathing and speaking. Several required emergency treatment, including tracheotomies and the insertion of feeding tubes, as well as second surgeries.

The Kuklo affair is just the latest incident to raise questions about Infuse, as well as Medtronic’s relationships with doctor consultants.   In September, the Wall Street Journal reported that at least three-quarters of the roughly 200 “adverse events” reported to the FDA involve off-label uses of Infuse Bone Graft. According to the Journal, doctors paid consulting fees by Medtronic have promoted off-label use of Infuse by, among other things, authoring articles that present unapproved uses in a favorable light.

Doctors are free to use approved medical devices in anyway they see fit.  However, manufacturers are forbidden from promoting any use that has not received FDA approval – known as off-label use.

A Senate committee has been looking into Medtronic’s promotion of Infuse, as has the U.S. Justice Department.

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