Nephrogenic fibrosing dermopathy

Jump to navigation Jump to search

WikiDoc Resources for Nephrogenic fibrosing dermopathy

Articles

Most recent articles on Nephrogenic fibrosing dermopathy

Most cited articles on Nephrogenic fibrosing dermopathy

Review articles on Nephrogenic fibrosing dermopathy

Articles on Nephrogenic fibrosing dermopathy in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Nephrogenic fibrosing dermopathy

Images of Nephrogenic fibrosing dermopathy

Photos of Nephrogenic fibrosing dermopathy

Podcasts & MP3s on Nephrogenic fibrosing dermopathy

Videos on Nephrogenic fibrosing dermopathy

Evidence Based Medicine

Cochrane Collaboration on Nephrogenic fibrosing dermopathy

Bandolier on Nephrogenic fibrosing dermopathy

TRIP on Nephrogenic fibrosing dermopathy

Clinical Trials

Ongoing Trials on Nephrogenic fibrosing dermopathy at Clinical Trials.gov

Trial results on Nephrogenic fibrosing dermopathy

Clinical Trials on Nephrogenic fibrosing dermopathy at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Nephrogenic fibrosing dermopathy

NICE Guidance on Nephrogenic fibrosing dermopathy

NHS PRODIGY Guidance

FDA on Nephrogenic fibrosing dermopathy

CDC on Nephrogenic fibrosing dermopathy

Books

Books on Nephrogenic fibrosing dermopathy

News

Nephrogenic fibrosing dermopathy in the news

Be alerted to news on Nephrogenic fibrosing dermopathy

News trends on Nephrogenic fibrosing dermopathy

Commentary

Blogs on Nephrogenic fibrosing dermopathy

Definitions

Definitions of Nephrogenic fibrosing dermopathy

Patient Resources / Community

Patient resources on Nephrogenic fibrosing dermopathy

Discussion groups on Nephrogenic fibrosing dermopathy

Patient Handouts on Nephrogenic fibrosing dermopathy

Directions to Hospitals Treating Nephrogenic fibrosing dermopathy

Risk calculators and risk factors for Nephrogenic fibrosing dermopathy

Healthcare Provider Resources

Symptoms of Nephrogenic fibrosing dermopathy

Causes & Risk Factors for Nephrogenic fibrosing dermopathy

Diagnostic studies for Nephrogenic fibrosing dermopathy

Treatment of Nephrogenic fibrosing dermopathy

Continuing Medical Education (CME)

CME Programs on Nephrogenic fibrosing dermopathy

International

Nephrogenic fibrosing dermopathy en Espanol

Nephrogenic fibrosing dermopathy en Francais

Business

Nephrogenic fibrosing dermopathy in the Marketplace

Patents on Nephrogenic fibrosing dermopathy

Experimental / Informatics

List of terms related to Nephrogenic fibrosing dermopathy

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]

Please Join in Editing This Page and Apply to be an Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [3] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Overview

Nephrogenic fibrosing dermopathy or nephrogenic systemic fibrosis is a rare and serious syndrome that involves fibrosis of skin, joints, eyes, and internal organs. Its cause is not fully understood, but it seems to be associated with exposure to gadolinium (which is frequently used as a contrast substance for MRIs) in patients with severe kidney failure. It does not have a genetic basis.

Historical Background

NFD was first identified in 1997 as a fibrotic disorder of the skin in patients with renal failure (1). Since then, systemic involvement has been described in some patients with NFD, resulting in use of the term nephrogenic systemic fibrosis (NSF); NFD and NSF have been used to describe the same condition (3). No clear etiology has been established for NFD, and little is known about its pathogenesis or natural history. This report describes the largest geographic cluster of NFD that has been identified and provides evidence that exposure to a gadolinium-containing contrast agent is a risk factor for the development of the disease.

Although risk factors for NFD have not been studied extensively, possible correlations with severity of renal failure, thrombotic episodes, edema, and vascular procedures have been reported (2,4). Recently, medication exposures such as erythropoietin and gadolinium-containing contrast agents have been identified as potential risk factors for NFD (5,6). In May 2006, the Danish Medicines Agency reported 25 cases of NFD diagnosed in Europe among patients with recent exposure to gadolinium-containing contrast. In response, the Food and Drug Administration (FDA) issued a public health advisory in June 2006 regarding the use of these contrast agents in patients with renal failure (7). As of December 25, 2006, the FDA MedWatch system had received 90 reports of NFD possibly related to gadolinium-containing contrast agents.

Intravenously administered contrast agents are used routinely for MRI studies; the contrast agents contain gadolinium (a paramagnetic heavy metal), which is bound to a chelating agent. The mechanism for possible gadolinium-associated NFD is unknown; however, one hypothesis is that the gadolinium ions might dissociate from the chelate and result in a fibrotic reaction (5). Five gadolinium-based contrast agents are available in the United States; the first was approved for use in 1988 (7). Adverse events associated with these agents typically are minor (e.g., nausea); severe effects such as allergic reactions or tissue necrosis as a result of extravasation are rare. In addition, gadolinium-containing contrast agents are believed to be less nephrotoxic than iodinated contrast agents used for computed tomography (CT) imaging (8). Excretion of gadolinium-containing contrast agents primarily occurs renally; the amount of contrast eliminated from the body after dialysis has not been well-evaluated. Two studies suggest that 65%--78% of gadolinium-containing contrast might be cleared after one hemodialysis session and 98% after three sessions (9,10). Peritoneal dialysis might achieve less effective gadolinium-contrast clearance than hemodialysis. In one study, 69% of total gadolinium-containing contrast was excreted after 22 days in patients undergoing continuous ambulatory peritoneal dialysis (9). Delayed clearance might prolong the duration of gadolinium-containing contrast exposure among patients undergoing peritoneal dialysis. However, patients undergoing peritoneal dialysis have not been previously reported to be at higher risk for NFD than patients undergoing hemodialysis. The chronic peritoneal dialysis outpatients in this investigation had higher estimated NFD attack rates than chronic hemodialysis outpatients. No controls who had gadolinium-containing contrast exposure underwent primarily peritoneal dialysis.

Clinical Presentations

In NFD, patients develop large areas of hardened skin with fibrotic nodules and plaques. Flexion contractures with an accompanying limitation of range of motion can also occur. NFD resembles scleromyxedema at the histologic (microscopic) level; it shows a proliferation of dermal fibroblasts and dendritic cells, thickened collagen bundles, increased elastic fibers, and deposits of mucin. [1]

Treatment

Most patients with NFD have undergone hemodialysis for renal failure, some have never undergone dialysis and others have received only peritoneal dialysis. Many patients have taken immunosuppressive medications and have other diseases, such as hepatitis C. Four of the five FDA-approved gadolinium contrast agents have been principally implicated in NFD, including Omniscan, Multihance, Magnevist, and OptiMARK.

Classification

The European authorities have classified the gadolinium-containing contrast agents in three groups:[2]

  • Least likely (safest) to release free gadolinium ions Gd3+ in the body have a cyclical structure: Dotarem, Gadovist and ProHance
  • Intermediate have a ionic linear structure: Magnevist, MultiHance, Primovist and Vasovist
  • Most likely to release Gd3+ have a linear non-ionic structure: Omniscan and OptiMARK

It can be noted that this classification was released after another proposition would have left the safest category (ionic cyclical structure) with only one agent (Dotarem). The intermediate category would have been either ionic linear structure or non-ionic cyclical structure. The third category most at risk was unchanged (linear non-ionic).[3]

References

  1. Scheinfeld, NS; Cowper, S; Kovarik, CL; Butler, DF. "Nephrogenic Fibrosing Dermatopathy." Emedicine. [1]
  2. http://www.mhra.gov.uk/home/idcplg?IdcService=GET_FILE&dID=35149&noSaveAs=0&Rendition=WEB
  3. http://www.ismrm.org/special/EMEA2.pdf

de:Nephrogene systemische Fibrose

Template:SIB

Template:WH Template:WS