Information was received from a manufacturer representative regarding a patient.It was initially reported that there was a possibility that the patient had an infection with their implantable neurostimulator (ins).It was further clarified that the patient did not have an infection.The manufacturer representative stated that the patient had c.Diff (clostridium difficile), which caused their fever and other symptoms of feeling ill.This was verified by the patient¿s trial and managing physician.No further complications were reported or anticipated.Indication for use is unknown.
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