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Medical Policy Search



Printer Friendly Version Magnetic Resonance Spectroscopy

Magnetic Resonance Spectroscopy

 

DESCRIPTION

Magnetic resonance spectroscopy (MRS) is a noninvasive technique that can be used to measure the concentrations of different chemical components within tissues. The technique is based on the same physical principles as magnetic resonance imaging (MRI) and the detection of energy exchange between external magnetic fields and specific nuclei within atoms. With MRI, this energy exchange, measured as a radiofrequency signal, is then translated into the familiar anatomic image by assigning different gray values according to the strength of the emitted signal. The principal difference between MRI and MRS is that in MRI the emitted radiofrequency is based on the spatial position of nuclei, while MRS detects the chemical composition of the scanned tissue. The information produced by MRS is displayed graphically as a spectrum with peaks consistent with the various chemicals detected. MRS may be performed as an adjunct to MRI. An MRI image is first generated, and then MRS spectra are developed at the site of interest, termed the voxel. While an MRI provides an anatomic image of the brain, MRS provides a functional image related to underlying dynamic physiology. MRS can be performed with existing MRI equipment and modified with additional software and hardware.

MRS has been studied most extensively in a variety of brain pathologies. In the brain, both 1-H (i.e., proton) and 31-P are present in concentrations high enough to detect and thus have been used extensively to study brain chemistry. For example, proton MRS of the healthy brain reveals 5 principal spectra:

  • Arising from N-acetyl groups, especially n-acetylaspartate (NAA). NAA intensity is thought to be a marker of neuronal integrity and is the most important proton signal in studying central nervous system (CNS) pathology. Decreases in the NAA signal are associated with neuronal loss.
  • Arising from choline-containing compounds (Cho) such as membrane phospholipids (e.g., phosphocholine and glycerophosphocholine). Choline levels increase in acute demyelinating disease. Brain tumors may also have high signals from Cho.
  • Arising from creatine and phosphocreatine. In the brain, creatine is a relatively constant element of cellular energetic metabolism and thus is sometimes used as an internal standard.
  • Arising from lipid
  • Arising from lactate. Normally this spectrum is barely visible, but lactate may increase to detectable levels when anaerobic metabolism is present. Lactate may accumulate in necrotic areas, in inflammatory infiltrates, and in brain tumors.

Different patterns of the above spectra, in both the healthy and diseased brain, are the basis of clinical applications of MRS. The MRS findings characteristically associated with non-necrotic brain tumors include elevated choline (Cho) levels and reduced N-acetylaspartate (NAA) levels. The International Network for Pattern Recognition using Magnetic Resonance (http://azizu.uab.es/INTERPRET/index.html) has developed a user-friendly computer program for spectral classification and a database of 300 tumor spectra with histologically validated diagnoses to aid radiologists in MRS diagnosis.

Peripheral applications of MRS include the study of myocardial ischemia, peripheral vascular disease, and skeletal muscle. Applications in non-CNS oncologic evaluation have also been explored. New nomograms for prostate cancer are being developed that incorporate MRI and MRS results.

Multiple software packages for performing proton MRS have received clearance by the U.S. Food and Drug Administration (FDA) through the 510(k) process since 1993.

 

POLICY

Magnetic resonance spectroscopy is considered investigational.

 

POLICY EXCEPTIONS

Federal Employee Program (FEP) may dictate that all FDA-approved devices, drugs or biologics may not be considered investigational and thus these devices may be assessed only on the basis of their medical necessity.

 

POLICY GUIDELINES

Investigative service is defined as the use of any treatment procedure, facility, equipment, drug, device, or supply not yet recognized by certifying boards and/or approving or licensing agencies or published peer review criteria as standard, effective medical practice for the treatment of the condition being treated and as such therefore is not considered medically necessary.

The coverage guidelines outlined in the Medical Policy Manual should not be used in lieu of the Member's specific benefit plan language.

 

POLICY HISTORY

5/28/2008: Policy added

12/28/2010: Policy description and statement unchanged.  Add FEP verbiage to the Policy Exceptions section.

01/18/2012: Policy reviewed; no changes.

04/01/2013: Policy reviewed; no changes.

 

SOURCE(S)

Blue Cross & Blue Shield Association Policy # 6.01.24

 

CODE REFERENCE

This is not an all-inclusive list of non-covered procedure codes.

All codes billed for this procedure are considered investigational and not eligible for coverage. 

Non-Covered Codes

Code Number

Description

CPT-4

76390Magnetic resonance spectroscopy

ICD-9 Procedure

 

 

ICD-9 Diagnosis

 

 

HCPCS

  



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