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Effective Date: 12/01/2011 |
Title: Magnetoenchalopgraphy (MEG)
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Revision Date: 10/01/2015
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Document: BI329:00
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CPT Code(s): 95965-95967, S8035
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Public Statement
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Effective Date:
a)
This policy
will apply to all services performed on or after the above revision date which
will become the new effective date.
b)
For all
services referred to in this policy that were performed before the revision
date, contact customer service for the rules that would apply.
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Magnetoencephalography is a
noninvasive functional imaging technique which records the weak magnetic
forces associated with the brain’s electrical activity.
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This sophisticated technique is
sometimes helpful in localizing brain function in patients preparing to
undergo brain surgery for intractable epilepsy.
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This technology is covered in
patients who meet the medical policy criteria for intractable epilepsy.
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Medical Statement
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Magnetic
source imaging (MSI) or magnetoencephalography (MEG) are considered
medically necessary for pre-surgical evaluation in persons with intractable
focal epilepsy to identify and localize areas of epileptiform activity, when
discordance or continuing questions arise from among other techniques
designed to localize a focus.
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MSI or MEG is considered
experimental and investigational when used as a stand-alone test or as the
first order of test after clinical and routine electroencephalographic (EEG)
diagnosis of epilepsy.
Codes Used In This BI:
95965 Magnetoencephalography (MEG), recording and analysis;
for spontaneous brain magnetic activity (e.g., epileptic cerebral cortex
localization)
95966 Magnetoencephalography (MEG), recording and analysis; for evoked magnetic
fields, single modality (e.g., sensory, motor, language, or visual cortex
localization)
95967 Magnetoencephalography (MEG), recording and analysis; for evoked magnetic
fields, each additional modality (e.g., sensory, motor, language, or visual
cortex localization) (List separately in addition to code for primary procedure)
S8035 Magnetic source imaging
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Limits
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1.
MSI or MEG is
considered experimental and investigational for the following indications (not
an all inclusive list):
·
Evaluation of
Alzheimer`s disease
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Evaluation of
autism
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Evaluation of
brain tumors
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Evaluation of
cognitive and mental disorders
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Evaluation of
developmental dyslexia
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Evaluation of
multiple sclerosis
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Evaluation of
Parkinson`s disease
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Evaluation of
schizophrenia
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Evaluation of
stroke rehabilitation
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Evaluation of
traumatic brain injury
·
Fetal
neurological assessment.
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Background
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Magnetic
source imaging or magnetoencephalography is a non-invasive functional imaging
technique in which the weak magnetic forces associated with the electrical
activity of the brain are monitored externally on the scalp, i.e. MSI differs
from a standard electroencephalography (EEG) in that it records the magnetic
fields instead of the electrical activity. The principal advantage of MSI is
that while the measurement of electrical activities is affected by surrounding
brain structures, the magnetic fields are not. Thus, when coupled to a MRI, MSI
allows a high-resolution functional/anatomical image.
An
assessment conducted by the BlueCross BlueShield Technology Evaluation Center
(2003) concluded that there is insufficient evidence to render conclusions
regarding the effect of MSI/MEG on health outcomes for either pre-surgical
localization of seizure origin or pre-surgical functional mapping. An assessment
of MEG from the Ontario Ministry of Health and Long Term Care Medical Advisory
Secretariat (2006) found that studies are generally of poor quality, and were
graded of low or very-low quality of evidence. Specifically with regard to the
use of MEG in epilepsy, the assessment stated that it is unclear whether MEG has
similar accuracy in localizing seizure foci as intracranial EEG.
Pataraia,
et al. (2005) studied the functional organization of the inter-ictal spike
complex in 30 patients with mesial temporal lobe epilepsy (MTLE) using combined
MEG/EEG recordings. Spikes could be recorded in 14 patients (47%) during the 2-
to 3-h MEG/EEG recording session. The MEG and EEG spikes were subjected to
separate dipole analyses; the MEG spike dipole localizations were superimposed
on MRI scans. All spike dipoles could be localized to the temporal lobe with a
clear preponderance in the medial region. Based on dipole orientations in MEG,
patients could be classified into 2 groups: (i) patients with anterior medial
vertical (AMV) dipoles, suggesting epileptic activity in the Medio basal
temporal lobe, and (ii) patients with anterior medial horizontal (AMH) dipoles,
indicating involvement of the temporal pole and the anterior parts of the
lateral temporal lobe. Whereas patients with AMV dipoles had strictly
unitemporal inter-ictal and ictal EEG changes during prolonged video-EEG
monitoring, half of patients with AMH dipoles showed evidence of bitemporal
affection on inter-ictal and ictal EEG. Nine patients underwent epilepsy surgery
so far. While all 5 patients with AMV dipoles became completely seizure-free
post-operatively (Class Ia), 2 out of 4 patients with AMH dipoles experienced
persistent auras (Class Ib). However, this difference was not statistically
significant. These researchers concluded that combined MEG/EEG dipole modeling
can identify sub compartments of the temporal lobe involved in epileptic
activity and may be helpful to differentiate between subtypes of mesial temporal
lobe epilepsy non-invasively. The results need to be confirmed in well-designed
studies with larger sample sizes.
Papanicolaou, et al. (2005) predicted the replacement of the more invasive
procedure with MEG in the near future for temporal lobe epilepsy cases,
subsequent to the optimization of the conditions under which pre-operative MEG
is performed. Furthermore, in a review on management of intractable epilepsy in
infancy and childhood, Wirrell, et al. (2006) stated that “MEG has proven to be
useful in mapping sensory cortex and may also be useful to define eloquent
cortex. The author stated that in a recent study (Stefan, et al., 2003),
magnetic source imaging proved most useful in the localization of extra-temporal
foci. The usefulness of MEG in pediatric epilepsy surgery planning remains to be
determined”. Available evidence lacks systematic comparisons to other diagnostic
techniques. Furthermore, there are no data specifically documenting how MSI/MEG
might alter surgical management (i.e., changing the surgical approach or
reducing the time needed for intra-operative mapping).
Knowlton,
et al. (2006) stated that non-invasive brain imaging tests can potentially
supplement or even replace the use of intra-cranial EEG (ICEEG) in pre-surgical
epilepsy evaluation. These investigators prospectively examined the agreement
between MSI and ICEEG localization in epilepsy surgery candidates. Patients
completing video monitoring with scalp EEG who had intractable partial epilepsy
based on ictal electro-clinico-anatomical features were screened. A total of 49
enrolled patients (mean age of 27 years; ranging from 1 to 61 years) completed
MSI and ICEEG studies. Decisions about ICEEG and surgery were made at a
consensus conference where MSI could only influence ICEEG coverage by indicating
supplemental coverage to that already planned by an original hypothesis. The
positive predictive value of MSI for seizure localization was 82 to 90 %,
depending on whether computed against ICEEG alone or in combination with
surgical outcome. The kappa score of agreement for MSI with ICEEG was 0.2744 (p
< 0.01). These researchers found that MSI yields localizing information with a
high positive predictive value in epilepsy surgery candidates who typically
require ICEEG. This finding suggested that enough clinical validity exists for
MSI to potentially replace ICEEG for seizure localization. Moreover, the
authors stated that future studies must ascertain if certain MSI results are
more predictive of accurate epilepsy localization, and if so, what other
criteria are sufficient to preclude the need for further confirmation by
ICEEG. This type of weighting will have to be measured in the context of all
other epilepsy localization test. Furthermore, how discordant results from
multiple non-invasive tests should be handled in a single surgical
decision-making score, either toward or away from surgical resection, will have
to be determined from greater outcome evidence.
Sutherling, et al. (2008) reported on preliminary results of an ongoing,
long-term clinical study in epilepsy, where MSI changed surgical decisions. The
investigators determined whether MSI changed the surgical decision in a
prospective, blinded, crossover-controlled, single-treatment, observational case
series. Sixty-nine sequential patients diagnosed with partial epilepsy of
suspected neocortical origin had video-EEG and imaging. All met criteria for
intracranial EEG (ICEEG). At a surgical conference, a decision was made before
and after presentation of MSI. Cases where MSI altered the decision were
noted. The investigators found that MSI gave nonredundant information in 23
patients (33%). MSI added ICEEG electrodes in 9 (13%) and changed the surgical
decision in another 14 (20%). Based on MSI, 16 patients (23%) were scheduled for
different ICEEG coverage. Twenty-eight have gone to ICEEG, 29 to resection, and
14 to vagal nerve stimulation, including 17 where MSI changed the decision.
Additional electrodes in 4 patients covered the correct: hemisphere in 3, lobe
in 3 and sublobar ictal onset zone in 1. MSI avoided contralateral electrodes in
2, who both localized on ICEEG. MSI added information to ICEEG in 1. The
investigators concluded that MSI provided nonredundant information in 33% of
patients. In those who have undergone surgery to date, MSI added useful
information that changed treatment in 6 (9%), without increasing complications.
The investigators stated that MSI had benefited 21% who have gone to surgery.
In a
cohort study of epilepsy surgery candidates not sufficiently localized with
noninvasive studies, Knowlton, et al. (2008) evaluated the predictive and
prognostic value of MSI, PET, and ictal SPECT as compared with intracranial
electroencephalography (ICEEG) localization in epilepsy surgery. Of 160 patients
enrolled over 4 years, 77 completed ICEEG seizure monitoring. Sensitivity,
specificity, and predictive values relative to ICEEG were computed for each
modality. Seizures were not captured in five patients. Of the 72 diagnostic
ICEEG studies, seizure localization results were 74% localized, 10% multifocal,
and 17% nonlocalized. Sixty-one percent were localized to neocortical regions.
Depending on patient subgroup pairs, sensitivity ranged from 58 to 64% (MSI), 22
to 40% (PET), and 39 to 48% (SPECT); specificity ranges were 79 to 88% (MSI), 53
to 63% (PET), and 44 to 50% (SPECT). Gains in diagnostic yield were seen only
with the combination of MSI and PET or MSI and ictal SPECT. Localization
concordance with ICEEG was greatest with MSI, but a significant difference was
demonstrated only between MSI and PET. The investigators found that conclusively
positive MSI has a high predictive value for seizures localized with ICEEG, and
that diagnostic gain may be achieved with addition of either PET or ictal SPECT
to MSI. The investigators noted that diagnostic values for imaging tests are
lower than "true values" because of the limitations of ICEEG as a gold standard.
In a
separate paper, Knowlton, et al. (2008) examined the outcomes of cohort subjects
with epilepsy who subsequently underwent surgical resection. Of 160 patients
enrolled, 62 completed ICEEG and subsequent surgical resection. Sixty-one
percent resulted in an Engel I seizure-free outcome at a minimum of one-year
follow-up (mean = 3.4 years). Sensitivity, specificity, and predictive values
were computed for each modality. Multi-variate logistical regression was used to
identify prediction of surgical outcome by imaging test. The investigators
reported that MSI sensitivity for a conclusively localized study was 55% with a
positive predictive value of 78%. Eliminating non-diagnostic MSI cases (no
spikes captured during recording) yielded a corrected negative predictive value
of 64%. With available comparison subgroups FDG-PET and ictal SPECT values were
similar to MSI. The odds ratio (adjusted for epilepsy and MRI classification)
for MSI prediction of seizure-free outcome was 4.4 (p = 0.01). In cases with
both PET and MSI, the adjusted odds ratio for PET was 7.1 (p <0.01) and for MSI
was 6.4 (p = 0.01). In the cases with all three tests (n = 27), ictal SPECT had
the highest OR of 9.1 (p = 0.05). The investigators concluded that MSI,
FDG-PET, and ictal SPECT each have clinical value in predicting seizure-free
surgical outcome in epilepsy surgery candidates who typically require ICEEG.
Rampp and
Stefan (2007) stated that while MEG systems are still expensive and complex, the
technique`s characteristics offer promising possibilities for the investigation
of epilepsy patients (e.g., for focus localization and pre-surgical functional
mapping).
Lam, et
al. (2008) conducted a systematic evidence review of evidence of the
effectiveness of MEGI in the presurgical evaluation of localization-related
epilepsies. The investigators identified studies correlating surgical outcome
(seizure freedom) with MEG source localization and resection area. The
investigators found these studies of MEG reported wide ranging sensitivities
(range: 0.20-1.0), specificities (0.06-1.00), positive likelihood ratios
(0.67-2.0), and negative likelihood ratios (0.40-2.13). Based upon the results
of their systematic review of the literature, the investigators concluded that
"there is insufficient evidence in the current literature to support the
relationship between the use of MEG in surgical planning and seizure-free
outcome after epilepsy surgery." The investigators stated that additional
studies are needed.
In a
review on interictal electromagnetic source imaging in focal epilepsy, Leijten
and Huiskamp (2008) noted that whether MEG is superior to EEG is still
unresolved, because fair comparisons are lacking. Clinical studies have not yet
adopted all technical possibilities. Localization accuracy seems high, but
studies lack uniformity regarding methods, goals and outcome parameters.
Therefore, the final place of electromagnetic source imaging in the pre-surgical
work-up is still to be determined. The diagnostic potential is probably highest
in extra-temporal epilepsies, and lowest in mesial temporal lobe epilepsy. The
authors concluded that electromagnetic source imaging has evolved technically
and can provide valuable localization information in the pre-surgical evaluation
of patients with epilepsy. However, standardization of the technique is required
before further clinical studies can better establish its role in pre-surgical
evaluation of focal epilepsy.
A
BlueCross BlueShield Association`s technology assessment on MEG and MSI for the
purpose of pre-surgical localization of epileptic lesions (2009) that "[t]he
argument that MEG improves the diagnostic yield of IC-EEG is often made, but it
is difficult to identify studies that can support this argument. Studies that
compare IC-EEG to MEG do not inform this particular question. On the other hand,
given the gravity of this particular situation, there are some possible
arguments to be made on behalf of MEG. Given that current decision making
regarding who should receive surgery and what type of surgery is done with some
uncertainty and lack of a true reference standard, an additional piece of
information that is known to correlate with seizure focus could be arguably of
some value in making difficult decisions. The diagnostic test is easy to perform
and noninvasive. Also, IC-EEG and surgery are extremely invasive procedures that
do not always provide diagnostic information. Information from MEG might
influence a patient’s decision to undergo the risks of further testing or
surgery if the outcome can be slightly better estimated. However, given that one
possible outcome of use of MEG may result in avoidance of tests and procedures
that may benefit the patient, it is not possible to rule out harm from use of
the test. The net effect of the use of MEG on patient outcomes for this
indication remains to be determined".
MEG cannot
replace, but may guide the placement of intracranial EEG and, in some patients,
avoid an unnecessary intracranial EEG (AAN, 2009). MEG is not the first order of
test after clinical and routine EEG diagnosis of epilepsy. It is one of several
advanced pre-surgical investigative technologies. The need for MEG is much lower
than surface EEG and anatomical imaging studies (AAN, 2009). MEG is not a
stand-alone test. To realize its optimum clinical potential a comprehensive team
evaluation, such as that available in comprehensive epilepsy centers, is
necessary. The team usually comprises a neurologist with expertise in epilepsy,
a neurosurgeon, MEG-physicists, psychologists, nurses and staff experienced in
treatment of seizure disorders.
Although
the literature contains some information regarding the clinical use of MSI in
the pre-surgical mapping of eloquent cortex in patients with intra-cranial
tumors or arterio-venous malformations, there is insufficient scientific
evidence regarding its effectiveness for this indication. Critical outcomes are
lacking, such as comparison of MSI with intra-operative methods and whether the
use of MSI would change the management of patients such that clinical outcomes
are improved.
Language
and memory functions may reside in both or one hemisphere in patients with
epilepsy. Determination of laterality is important to preserve as much language
and memory functions as feasible during resective surgery. The intracarotid
amobarbital test (Wada test) has long been used for language and memory
localization. It has both merits and shortcomings when compared with newer
tests. It is invasive, uncomfortable and carries certain morbidity.
Several alternatives such as neuropsychological testing, functional MRI (fMRI),
MEG, behavioral testing and SPECT-PET are available. Each has certain
advantages and disadvantages.
There is
limited evidence for the use of MEG as a substitute or supplement to the Wada
test to identify the eloquent cortex for removal of brain tumors or arterio-venous
malformations. Pelletier, et al. (2007) compared all the Wada alternatives in a
comprehensive review. MEG, while requiring patient cooperation, had the
advantage of being a non-invasive direct measure with excellent temporal
resolution. Pelletier, et al. (2007) reported that the high concordance between
the findings of the Wada test and neuroimaging techniques, especially fMRI,
MEG, functional transcranial Doppler and possibly near infrared spectroscopy, is
encouraging and holds promise that the Wada procedure will be eventually
replaced by these non-invasive techniques. Pelletier, et al. (2007) concluded,
however, that these methods still need to be refined, and certain incongruities
between the Wada procedure and these techniques have to be addressed. For
instance, fMRI provides little information regarding right hemisphere
participation in language processing in patients with bilateral speech
representation. MEG has the disadvantage that it is limited to the evaluation of
receptive language. Furthermore, to obtain conclusive and reliable activation
patterns, both fMRI and MEG require that the patient remain motionless in the
scanner and comply with the test instructions. This restricts the application of
these imaging techniques in young children and special populations. Pelletier,
et al. (2007) stated that these neuroimaging techniques vary with regard to
their spatial and temporal resolution. fMRI has good spatial resolution and
relatively poor temporal resolution. The reverse is true for MEG. Furthermore,
different techniques target different functions. The authors suggested that
a multimodal approach, combining several techniques, is therefore the safest way
to provide the surgeon with reliable information.
There is
additional evidence for the use of MEG to localize the eloquent cortex in
resections for non-epilepsy lesions. Grover, et al. (2007) reported on a
retrospective study where visual evoked cortical magnetic field (VEF) waveforms
were recorded from both hemifields in 21 patients with temporo-parieto-occipital
mass lesions to identify preserved visual pathways. Fifteen patients had visual
symptoms pre-operatively. Magnetoencephalography VEF responses were detected,
using single equivalent current dipole, in 17 of 21 patients studied. Displaced
or abnormal responses were seen in 15 patients with disruption of pathway in one
patient. Three of 21 patients had alterations in the surgical approach or the
planned resection based on the MEG findings. The investigators concluded that
the surgical outcome for these three patients suggests that the MEG study may
have played a useful role in presurgical planning.
Korjenova,
et al. (2006) prospectively evaluated MEG and functional MRI (fMRI) imaging, as
compared with intraoperative cortical mapping, to localize the central sulcus.
Fifteen patients (six men, nine women; age range, 25-58 years) with a lesion
near the primary sensorimotor cortex (13 gliomas, one cavernous hemangioma, and
one meningioma) were examined. MEG and fMRI localizations were compared with
intraoperative cortical mappings. MEG depicted the central sulcus correctly in
all 15 patients, as verified at intraoperative mapping. The fMRI localization
results agreed with the intraoperative mappings in 11 patients. The
investigators concluded that, although both MEG and fMRI can provide useful
information for neurosurgical planning, in the present study, MEG proved to be
superior for locating the central sulcus.
There
is also insufficient evidence to support the use of MSI/MEG for other
indications including the diagnosis and treatment of various neurological
conditions/diseases such as Alzheimer`s disease, autism, cognitive and mental
disorders, developmental dyslexia, multiple sclerosis, Parkinson`s disease,
schizophrenia, stroke rehabilitation, and traumatic brain injury. Currently,
there are reliable data from well designed clinical studies that report the test
performance (sensitivity, specificity, positive and negative predictive values)
and clinical utility of MSI/MEG for these indications.
Haddad and
colleagues (2011) stated that the fetal brain remains inaccessible to
neurophysiological studies. Magnetoencephalography is being assessed to fill
this gap. These researchers performed 40 fetal MEG (fMEG) recordings with
gestational ages (GA) ranging from 30 to 37weeks. The data from each recording
were divided into 15 second epochs, which in turn were classified as continuous
(CO), discontinuous (DC), or artifact. The fetal behavioral state, quiet or
active sleep, was determined using previously defined criteria based on fetal
movements and heart rate variability. These investigators studied the
correlation between the fetal state, the GA and the percentage of CO and DC
epochs. They also analyzed the spectral edge frequency (SEF) and studied its
relation with state and GA. They found that the odds of a DC epoch decreased by
6 % per week as the GA increased (p = 0.0036). This decrease was mainly
generated by changes during quiet sleep, which showed 52 % DC epochs before a
35-week GA versus 38 % after 35 weeks (p = 0.0006). Active sleep did not show a
significant change in DC epochs with GA. When both states were compared for MEG
patterns within each GA group (before and after 35 weeks), the early group was
found to have more DC epochs in quiet sleep (54 %) compared to active sleep (42
%) (p = 0.036). No significant difference in DC epochs between the two states
was noted in the late GA group. Analysis of SEF showed a significant difference
(p = 0.0014) before and after a 35-week GA, with higher SEF noted at late GA.
However, when both quiet and active sleep states were compared within each GA
group, the SEF did not show a significant difference. The authors concluded that
fMEG shows reproducible variations in gross features and frequency content,
depending on GA and behavioral state. They stated that fetal MEG is a promising
tool to investigate fetal brain physiology and maturation
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Jan 13. [Epub ahead of print]
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Application to Products
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This policy applies to all health plans administered by QualChoice, both those insured by QualChoice and those that are self-funded by the sponsoring employer, unless there is indication in this policy otherwise or a stated exclusion in your medical plan booklet. Consult the individual plan sponsor Summary Plan Description (SPD) for self-insured plans or the specific Evidence of Coverage (EOC) for those plans insured by QualChoice. In the event of a discrepancy between this policy and a self-insured customer’s SPD or the specific QualChoice EOC, the SPD or EOC, as applicable, will prevail. State and federal mandates will be followed as they apply.
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Changes: QualChoice reserves the right to alter, amend, change or supplement benefit interpretations as needed.
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