Methodist Journal

IN THIS ISSUE

Adult Congenital Heart Update

Vol 15, Issue 2 (2019)


FEATURED GUEST EDITOR

ISSUE INTRO

The Growing Number of Adults Surviving with Congenital Heart Disease

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RECOGNITIONS

Drs. MacGillivray and Lin Take the Lead in Adult Congenital Heart Disease

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REVIEW ARTICLES See More

Advanced Cardiac Imaging for Complex Adult Congenital Heart Diseases

149 Fontan Conversions

Anomalous Aortic Origin of a Coronary Artery

Pulmonary Valve Replacement for Tetralogy of Fallot

Management of the Adult with Arterial Switch

Ebstein’s Anomaly

Heart Transplantation in Adults with Congenital Heart Disease

Cholesterol: Can’t Live With It, Can’t Live Without It

CASE REPORTS See More

Simultaneous Transfemoral Mitral and Tricuspid Valve in Ring Implantation: First Case Report with Edwards Sapien 3 Valve

Uneventful Follow-Up 2 Years after Endovascular Treatment of a High Flow Iatrogenic Aortocaval Fistula Causing Pulmonary Hypertension and Right Heart Failure

Device-Related Thrombus: A Reason for Concern?

Retained Coronary Balloon Requiring Emergent Open Surgical Retrieval: An Uncommon Complication Requiring Individualized Management Strategies

MUSEUM OF HMH MULTIMODALITY IMAGING CENTER See More

Do I Look Fat in This? Multimodality Imaging Findings of a Cardiac Lipoma

CLINICAL PERSPECTIVES See More

POINTS TO REMEMBER

The Kidney in Congenital Cyanotic Heart Disease

EXCERPTA

Talking Statins with Antonio Gotto

POINTS TO REMEMBER

Lipids and Renal Disease

EXCERPTA

Addressing the Feedback Loop Between Depression, Diabetes, and Cardiovascular Disease

EDITORIALS

Letter to the Editor in Response to “Cardiac Autonomic Neuropathy in Diabetes Mellitus”

Vol 13, Issue 3 (2017)

Article Full Text

CLINICAL PERSPECTIVES

Gadolinium-Induced Nephrogenic Systemic Fibrosis

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Article Citation:

Shah AH, Olivero JJ Sr. Gadolinium-Induced Neophrogenic Systemic Fibrosis. Methodist DeBakey Cardiovasc J. 2017;13(3):172-173

doi: 10.14797/mdcj-13-3-172

Keywords
nephrogenic systemic fibrosis , gadolinium contast

The column in this issue is supplied by Anita H. Shah, M.D., and Juan Jose Olivero, M.D. Dr. Shah obtained her medical degree at The University of Texas Medical Branch in Galveston and is currently an internal medicine resident at Houston Methodist Hospital. Dr. Olivero is a nephrologist at Houston Methodist Hospital and a member of the hospital’s Nephrology Training Program. He obtained his medical degree from the University of San Carlos School of Medicine in Guatemala, Central America, and completed his residency and nephrology fellowship at Baylor College of Medicine in Houston, Texas.

Nephrogenic systemic fibrosis (NSF) is a clinicopathologic syndrome that has been associated with the use of gadolinium-based contrast agents (GBCAs).1 First discovered in 1997, NSF was initially termed nephrogenic fibrosing dermopathy due to its notable skin findings in 15 dialysis patients.1 Since that time, hundreds of cases have been reported with the use of gadolinium-based contrast agents (e.g., gadopentetate dimeglumine, gadodiamide, and gadoversetamide).1,2 This systemic disorder is not only characterized by skin manifestations but can also lead to multiorgan failure and death.3 Its prevalence increased after the FDA approved the use of noniodinated contrast agents for magnetic resonance imaging studies in the late 1980s and early 1990s.3 Unaware of the possible dire consequences, physicians initially embraced the use of these newer contrast agents since they afforded a contrast-enhanced study that would circumvent iodine nephropathy, and GBCAs were considered safe for use in renal patients. However, recent studies have found a causal relationship between NSF and GBCA exposure.3 The following are 10 points to remember about nephrogenic systemic fibrosis and its link to GBCAs.

  1. Nephrogenic systemic fibrosis has no predilection for age, sex, or race. It has been reported in children and adults around the world.1
  2. Patients at increased risk for NSF include those with acute renal failure or chronic kidney disease (CKD) stages 4 or 5 with eGFR < 30 mL/min/1.73 m2; however, it has also been documented in patients with CKD stage 3. Higher than recommended doses of gadolinium contrast or repeated doses increases the risk of NSF. Patients on peritoneal dialysis have a higher incidence of NSF than those on hemodialysis, possibly because the peritoneum is less effective in clearing the contrast.4
  3. In those with renal dysfunction and GBCA exposure, the NSF risk increases in the presence of a proinflammatory state; this includes infection, ischemia, malignancy, recent surgery, thrombosis, or major trauma or injury.4
  4. A multicenter retrospective study of renal insufficient patients found that gadodiamide exposure had an odds ratio of NSF development that was 13-times higher than gadopentetate exposure. This is because gadodiamide is less stable compared to the other gadolinium agents. With decreased stability, gadodiamide dissociates from its chelate and becomes Gd3+. This cation stimulates production of profibrotic cytokines, chemokines, and collagen formation, resulting in tissue fibrosis. In patients with nondialysis-dependent CKD stage 5, the half-life of gadodiamide is 34.3 hours compared to 70 minutes in those with intact renal function. Therefore, the toxic effects of exposure increase with decreased clearance of gadolinium.3,5
  5. Clinical manifestations of NSF can occur days to years after GBCA exposure. The early clinical signs of NSF include weakness, burning pain, pruritus, and cutaneous papules and plaques accompanied by edema. As the disease progresses, the skin becomes thickened, hyperpigmented, and “peau d’orange.” The involvement of joint tissue often results in contractures. The disease can progress from distal to proximal extremities and can involve both the upper and lower extremities, sparing the face. The fibrosis eventually may involve the lungs, renal tubules, rete testes, dura mater, ocular sclerae, and cardiac and skeletal muscle. Mortality increases with respiratory involvement, particularly with diaphragm involvement. Infections also lead to higher mortality rates in these patients.3
  6. Diagnosis is made with a history, physical exam, and exclusion of other likely diagnoses. No laboratory studies support the diagnosis of NSF, and imaging may only show nonspecific enhancement in involved areas. A biopsy of any affected organ, including the skin, may reveal supportive findings.3
  7. Biopsy findings illustrate systemic fibrosis with thickened bundles of dermal collagen and increased dermal mucin. Late in the disease, histology reveals dystrophic calcifications, calcified sclerosis, and osseous metaplasia.3
  8. Since there are no tests for diagnosing NSF, other possible diagnoses must be excluded. B2-microglobulin amyloidosis is the only other condition with fibrosis in patients with advanced CKD. A few other differentials include scleromyxedema, scleroderma, and lipodermatosclerosis.3
  9. There is no known cure for NSF, although case reports have found clinical improvement with pentoxifylline, sodium thiosulfate, ultraviolet phototherapy, extracorporeal photopheresis, and intravenous immunoglobulin. Imatinib mesylate, a tyrosine kinase inhibitor, has been shown to reduce collagen formation in some patients. Other supportive measures include physical and occupational therapy as well as analgesia for painful joint contractures. Although hemodialysis after contrast exposure does increase contrast clearance, there is no evidence that it reduces the risk of NSF development. However, treatment at the earliest onset of symptoms appears to improve the disease course.1,3,4
  10. The increased risks of gadolinium- and iodine-based contrast agents in those with renal disease has prompted investigation of alternative agents. One possibility is ferumoxytol, which is currently indicated for iron deficiency anemia in patients with CKD. It is being used in magnetic resonance imaging as an off-label alternative contrast agent for renal insufficient patients in some institutions. Hopefully with time, safer contrast agents will be developed for those with renal dysfunction.6

References

  1. Galan A, Cowper SE, Bucala R. Nephrogenic systemic fibrosis (nephrogenic fibrosing dermopathy). Curr Opin Rheumatol. 2006 Nov;18(6):614-7.
  2. Cowper SE. The International Center for Nephrogenic Systemic Fibrosis Research [Internet]. New Haven, CT: Yale Dermatopathology Service; 2013 Jun 15 [cited 2017 Jun 12]. Available from: http://www.icnsfr.org.
  3. Todd DJ, Kay J. Gadolinium-induced fibrosis. Annu Rev Med. 2016;67:273-91.
  4. Schlaudecker JD, Bernheisel CR. Gadolinium-associated nephrogenic systemic fibrosis. Am Fam Physician. 2009 Oct 1;80(7):711-4.
  5. Perazella MA. Current status of gadolinium toxicity in patients with kidney disease. Clin J Am Soc Nephrol. 2009 Feb;4(2):461-9.
  6. Vasanwala SS, Nguyen K, Hope MD, et al. Safety and technique of ferumoxytol administration for MRI. Magn Reson Med. 2016 May;75(5):2107-11.

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