Nephrogenic Fibrosing Dermopathy
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Nephrogenic Fibrosing Dermopathy
Nephrogenic Fibrosing Dermopathy (NFD) is the most recent name given to a severe disease that has appeared as a side effect for some people who have had MRI exams using a gadolinium based contrast dye. When the disease was formally identified in 2000, it was initially called nephrogenic systemic fibrosis (NSF). Today, the disease is routinely referred to as NSF/NFD.
They symptoms of nephrogenic fibrosing dermopathy include hardening of the skin, accompanied by stiffness and pain in the joints. Range of motion is reduced, and weakness in the limbs develops – in some cases, to the point where the patient is wheelchair bound. It is a severe, life altering disease with no known cure.
Gadolinium was approved for MRI studies in 1988 because it has unique properties that provide an extremely clear outline of the area being examined. After nephrogenic fibrosing dermopathy was identified, a body of evidence began to build that showed the disease occurring almost exclusively in patients who have had gadolinium MRI exams, particularly those with kidney disease.
In 2007, the FDA asked the manufacturers of gadolinium contrast material to label their products with a warning about the dangers of nephrogenic fibrosing dermopathy, emphasizing the higher risk for those with kidney problems. In July of 2007 the FDA issued a Public Health Advisory about gadolinium MRIs and sent out a formal warning to medical professionals across the country.
Some victims of nephrogenic fibrosing dermopathy have sought legal recourse. If you have experienced some of these symptoms following an MRI, you may be eligible for compensation. One of the medical/legal professionals in our office is always available to go over your case with you in detail, and free of charge. Just call or send us an email and we’ll connect you to the right person.
