FDA Adds Contrast Agent Label Warning
The U.S. Food and Drug Administration has set label requirements for gadolinium-based contrast agents used in MR imaging to minimize causing the rare but serious kidney dysfunction condition called nephrogenic systemic fibrosis.
"These label changes are intended to help ensure these drugs are used appropriately, and that patients at risk for NSF who receive GBCAs are actively monitored for the development of NSF," the agency says.
Symptoms that hospitals and physicians are asked to monitor include scaling, hardening and tightening of the skin, red or dark patches on the skin and stiffness. NSF also can cause fibrosis of internal organs, which may lead to death, and there is no effective treatment for NSF. So far, all reports of NSF have been in patients who already have abnormal kidney function.
In addition to abnormal kidney function, other factors that appear to put patients at greater risk include its use in patients who have an impaired ability to eliminate the drug, including patients with acute kidney injury, and repeat doses or higher than recommended doses of gadolinium contrast agents.
He American College of Radiology in June also issued guidelines.
According to the revised FDA-required label, health professionals will be required to:
- Two-Midnight Rule Must be Fixed or Replaced, Say Providers
- The Secret to Physician Engagement? It's Not Better Pay
- Hospital Groups Strike Back at Hospital Rating Systems
- AHIP: Enormity of HIX Challenges Sinks In
- Don't Underestimate Emotional Intelligence
- 4 Reasons PCMH Principles Aren't Going Away
- Yale New Haven Health Partners with Tenet Healthcare in CT
- Evidence-Based Practice and Nursing Research: Avoiding Confusion
- Care Coordination Tough to Define, Measure
- SCOTUS Review of NC Board Case 'A Very Big Deal' to Providers