
|
Role of MRI in Central Nervous System (CNS) Disease |
|
MRI has established itself as an important clinical tool in the diagnosis of central nervous system diseases. While MRI indications in the body are expanding, evaluation of CNS diseases remains the most common application of MRI today. The complete imaging evaluation of patients with CNS neoplasms includes detection, characterization, and determination of tumor extent (or metastatic spread). Also, secondary effects such as hydrocephalus, compartmental herniation or vascular compromise can be discerned. The role of MRI in CNS inflammatory disease or infection is also well established.
MRI techniques are well suited to the CNS setting. Compared to CT, MRI offers superior contrast resolution and does not involve ionizing radiation. MRI is not compromised by adjacent osseous structures, making it particularly valuable in evaluating the posterior fossa and spine. In short, MRI provides greater sensitivity and specificity for the majority of CNS disease states compared to other radiologic modalities.
Why are contrast agents necessary given the good resolution of unenhanced MRI images?
- Relaxation characteristics of normal and pathologic tissues are not always different enough to produce obvious differences in signal intensity.
- Pathology which is sometimes occult on unenhanced images becomes obvious in the presence of contrast.
- Enhancement significantly increases MRI sensitivity.
- In addition to improving delineation between normal and abnormal tissues, the pattern of contrast enhancement can improve diagnostic specificity by facilitating characterization of the lesion(s) in question.
- Contrast can yield physiologic and functional information in addition to lesion delineation.
Considerable investigational work is being done in the area of MRI contrast agents, but at present the majority of products employed in CNS or body studies are all gadolinium compounds such as MAGNEVIST® (gadopentetate dimeglumine) injection produced by Bayer HealthCare Pharmaceuticals.
Common Indications
Contrast-enhanced MRI has numerous indications in the CNS including:
Brain
- CNS infections
- Noninfectious inflammatory disease (e.g., MS, etc.)
- Preoperative/pretreatment evaluation of brain tumors
- Postoperative evaluation of brain tumor therapy
- Meningeal disease
Spine
- Infection/inflammatory disease
- Primary tumors
- Drop metastases
- Initial evaluation of syrinx
- Postoperative evaluation of lumbar spine: disk vs. scar
Evaluation of Stroke
An important neuroradiological indication for MRI is evaluation of stroke via perfusion and diffusion imaging. These MRI techniques have become critical in the management of so-called "brain attack." Diffusion imaging can demonstrate the central effect of a stroke on the brain, whereas perfusion imaging visualizes the larger "second ring" delineating blood flow and blood volume. Diffusion and perfusion MRI are becoming increasingly critical in the management of incipient or acute stroke as neuroprotective agents are more widely studied.
Infection
Inflammatory disease can be especially difficult to detect along the ependyma or meninges, but contrast-enhanced MRI techniques can delineate and localize infection. Abscesses can be confirmed by visualization of capsule formation via contrast-enhanced MRI, a particularly important indication since attempts to drain a focal infection prior to completion of capsule formation are associated with considerable risk.
Brain Neoplasms
Brain NeoplasmsDetecting and monitoring brain neoplasms remains one of the chief indications for MRI in neuroradiology. MRI is used for initial diagnosis, to stage disease, to plan surgery, and to evaluate postinterventional results.
Primary brain tumors are generally well demonstrated on unenhanced MRI, but early parenchymal or subarachnoid metastatic disease usually requires enhancement for optimal diagnosis. Approximately half of all low-grade gliomas do not disrupt the blood brain barrier and therefore are not better enhanced with contrast agents. These can be well established with non-contrast MRI and hence primary intra-axial neoplasm generally does not require a contrast study. However, enhanced studies are particularly sensitive for the detection of small extra-axial neoplasms such as meningiomas and vestibular schwannomas.
Generally, if a primary brain tumor is discovered on an unenhanced study, a contrast-enhanced study will be performed prior to institution of therapy to help fully characterize and delineate the extent of the lesion and thereby help inform the therapeutic intervention.
Contrast studies are central to the detection of secondary brain neoplasms, e.g., metastases. Enhancing metastases can be detected even before significant edema or mass effects are present.
MRI is also a critical tool for post interventional monitoring, after the patient has undergone surgery, radiation, chemotherapy or any combination thereof. Changes in enhancement patterns in post-operative compared to pre-operative images provide information about residual or recurrent neoplasm or confirms if the therapy has successfully eradicated the lesion.
Indications in the Spine
Contrast-enhanced techniques delineate infections vs. malignancies in the spine. Evaluation of a syrinx cavity in the spinal cord is also performed with contrast techniques.
MRI is commonly employed in the evaluation of the lumbar spine pre- and postoperatively. After surgery for disk disease, significant fibrosis can occur in the lumbar spine. This scarring can mimic residual disk herniation. Enhanced MRI differentiates these two conditions reliably.
Based on the slower uptake into cartilage, negatively charged ionic contrast agents have been shown to further delineate disk and scar tissue.
The exact relationship between MRI findings and the clinical status of patients is not completely understood.
|
|
You need to have the Adobe®
Acrobat Reader installed on your computer to view some of
the documents on this site.
You can download a copy of the Adobe®
Acrobat Reader by clicking the icon below.

INDICATIONS and IMPORTANT SAFETY INFORMATION
MAGNEVIST® (gadopentetate dimeglumine) Injection
INDICATIONS AND USAGE
Central Nervous System: MAGNEVIST® (gadopentetate dimeglumine) Injection is indicated for use with magnetic resonance imaging (MRI) in adults, and pediatric patients (2 years of age and older) to visualize lesions with abnormal vascularity in the brain (intracranial lesions), spine and associated tissues. MAGNEVIST Injection has been shown to facilitate visualization of intracranial lesions including but not limited to tumors.
Extracranial/Extraspinal Tissues: MAGNEVIST is indicated for use with MRI in adults and pediatric patients (2 years of age and older) to facilitate the visualization of lesions with abnormal vascularity in the head and neck.
Body: MAGNEVIST Injection is indicated for use in MRI in adults and pediatric patients (2 years of age and older) to facilitate the visualization of lesions with abnormal vascularity in the body (excluding the heart).
IMPORTANT SAFETY INFORMATION
WARNING: NEPHROGENIC SYSTEMIC FIBROSIS
Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with:
- acute or chronic severe renal insufficiency (glomerular filtration rate < 30 mL/min/1.73m2), or
- acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period.
In these patients, avoid use of gadolinium-based contrast agents unless the diagnostic information is essential and not available with non-contrast enhanced magnetic resonance imaging (MRI). NSF may result in fatal or debilitating systemic fibrosis affecting the skin, muscle and internal organs. Screen all patients for renal dysfunction by obtaining a history and/or laboratory tests. When administering a gadolinium-based contrast agent, do not exceed the recommended dose and allow a sufficient period of time for elimination of the agent from the body prior to any readministration.
The possibility of serious or life-threatening anaphylactic or anaphylactoid reactions, including cardiovascular, respiratory, and/or cutaneous manifestations, should always be considered. As with other paramagnetic contrast agents, caution should be exercised in patients with renal insufficiency due to the possibility of further deterioration in renal function. As with other injectable products, cases of phlebitis and thrombophlebitis have been reported; assessment of the dosed limb for the development of injection site reactions is recommended.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
For important risk and use information, please see the full prescribing information.
EOVIST® (gadoxetate disodium) Injection
INDICATIONS AND USAGE
EOVIST® (gadoxetate disodium) Injection is a gadolinium-based contrast agent indicated for intravenous use in T1-weighted magnetic resonance imaging (MRI) of the liver to detect and characterize lesions in adults with known or suspected focal liver disease.
IMPORTANT SAFETY INFORMATION
WARNING: NEPHROGENIC SYSTEMIC FIBROSIS
Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with:
- acute or chronic severe renal insufficiency (glomerular filtration rate < 30 mL/min/1.73m2), or
- acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period.
In these patients, avoid use of gadolinium-based contrast agents unless the diagnostic information is essential and not available with non-contrast enhanced magnetic resonance imaging (MRI). NSF may result in fatal or debilitating systemic fibrosis affecting the skin, muscle and internal organs. Screen all patients for renal dysfunction by obtaining a history and/or laboratory tests. When administering a gadolinium-based contrast agent, do not exceed the recommended dose and allow a sufficient period of time for elimination of the agent from the body prior to any readministration.
The possibility of serious or life-threatening anaphylactoid/hypersensitivity reactions with cardiovascular, respiratory and/or cutaneous manifestations should always be considered. The most common adverse reactions observed in clinical trials at the recommended dose included feeling hot, nausea and headache.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
For important risk and use information, please see the full prescribing information.
ULTRAVIST® (iopromide) Injection
INDICATIONS AND USAGE
ULTRAVIST® (iopromide) Injection is an iodinated contrast agent indicated for:
Intra-arterial Procedures*: 150 mgI/mL for intra-arterial digital subtraction angiography (IA-DSA); 300 mgI/mL for cerebral arteriography and peripheral arteriography; 370 mgI/mL for coronary arteriography and left ventriculography, visceral angiography, and aortography.
Intravenous Procedures*: 240 mgI/mL for peripheral venography; 300 mgI/mL for excretory urography; 300 mgI/mL and 370 mgI/mL for contrast Computed Tomography (CT) of the head and body (intrathoracic, intra-abdominal and retroperitoneal regions) for the evaluation of neoplastic and non-neoplastic lesions. The usefulness of contrast enhancement for the investigation of the retrobulbar space and of low grade or infiltrative glioma has not been demonstrated.
*For information on the concentrations and doses for the Pediatric Population [see Dosage and Administration (2.3) and Use in Specific Populations (8.4) in the full prescribing information].
IMPORTANT SAFETY INFORMATION
WARNING: NOT FOR INTRATHECAL USE Inadvertent intrathecal administration may cause death, convulsions, cerebral hemorrhage, coma, paralysis, arachnoiditis, acute renal failure, cardiac arrest, seizures, rhabdomyolysis, hyperthermia, and brain edema.
CONTRAINDICATIONS ULTRAVIST Injection is contraindicated for intrathecal use.
Preparatory dehydration (e.g. prolonged fasting and the administration of a laxative before ULTRAVIST Injection) is contraindicated in pediatric patients because of risk of renal failure.
WARNINGS AND PRECAUTIONS Life-threatening or fatal anaphylactoid reactions may occur during or after Ultravist administration. Acute renal failure may occur following ULTRAVIST administration, particularly in patients with renal insufficiency, diabetes, multiple myeloma. Hemodynamic disturbances including shock and cardiac arrest may occur during or shortly after administration of ULTRAVIST. Angiography may be associated with local and distal organ damage, ischemia, thromboembolism and organ failure.
MOST COMMON ADVERSE REACTIONS Most common adverse reactions (>1%) are headache, dysguesia, abnormal vision, chest pain, vasodilatation, nausea, vomiting, back pain, urinary urgency, injection site and infusion site reactions, and pain.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
For important risk and use information, please see the full prescribing information.
|
|
|