Detection of Brain Activation in Unresponsive Patients With Acute
Brain InjuryClaassen J, Doyle K, Matory A, et al. New England Journal of
Medicine 2019;380:2497-2505. doi:10.1056/NEJMoa1812757.
Background:
Brain activation in response to spoken motor commands can be detected
by electroencephalography (EEG) in clinically unresponsive patients.
The prevalence and prognostic importance of dissociation between
commanded motor behavior and brain activation in the first few days
after brain injury is not well understood.
Methods:
We studied a prospective, consecutive series of patients in a single
intensive care unit who had acute brain injury from a variety of
causes and who were unresponsive to spoken commands, including some
patients with the ability to localize painful stimuli or to fixate
on or track visual stimuli. Machine learning was applied to EEG
recordings to detect brain activation in response to commands that
patients move their hands. The functional outcome at 12 months was
determined with the Glasgow Outcome Scale–Extended (GOS-E; levels
range from 1-8, with higher levels indicating better outcomes).
Results:
A total of 16 (15%) of 104 unresponsive patients had brain activation
detected by EEG at a median of 4 days after injury. The condition in
8 (50%) of these 16 patients and in 23 (26%) of 88 patients without
brain activation improved such that they were able to follow
commands before discharge. At 12 months, 7 (44%) of 16 patients with
brain activation and 12 (14%) of 84 patients without brain
activation had a GOS-E level of 4 or higher, denoting the ability to
function independently for 8 hours (odds ratio: 4.6; 95% confidence
interval: 1.2-17.1).
Conclusions:
A dissociation between the absence of behavioral responses to motor
commands and the evidence of brain activation in response to these
commands in EEG recordings was found in 15% of patients in a
consecutive series of patients with acute brain injury (supported by
the Dana Foundation and the James S. McDonnell Foundation).
Commentary
Families of patients in coma often feel that their loved ones can hear them, even if
medical professionals find no outward signs of such sensory perception. There are
many news reports of patients “waking up” after weeks or months of coma and
confirming that they could hear harrowing conversations of their own condition. Such
reports have fueled the desire to have better and more accurate tools for coma
prognostication.Although the clinical neurologic examination is one of the most important tools used
to prognosticate coma outcome, the value of clinical neurophysiology cannot be
overstated. For many decades, neurophysiologic tests have been used to augment the
clinical examination. These tests are often very useful in predicting futility and
an unfavorable outcome. While this is very helpful, the ability to predict good
outcome would be very welcome as well. Encouraging neurophysiological tests would
help clinicians provide families with appropriate encouragement about their loved
ones.A recent study by Claassen and colleagues evaluated patients in various stages of
coma to determine whether they had “cognitive motor dissociation” and whether this
would predict outcomes.[1] Cognitive motor dissociation is a coma state in which a patient is able to
perceive sensory input without the ability to demonstrate it with motor output. They
evaluated 104 patients with acute brain injury admitted to their neurologic
intensive care unit who were in coma of varying severity and undergoing
electroencephalography (EEG) monitoring. All patients were unresponsive to spoken
commands, but some could localize painful stimuli or track visual stimuli. The
patients were administered standard auditory stimuli (various commands), and the EEG
was analyzed quantitatively for activation. Eight (50%) of 16 patients in whom brain
activation was detected (ie, cognitive motor dissociation present) and 23 (26%) of
88 patients in whom it was not able to follow commands before discharge (odds ratio
[OR]: 2.8; 95% confidence interval [CI]: 1.0-8.4). After 12 months, 7 (44%) of 16
patient with cognitive motor dissociation and 12 (14%) of 84 patients without brain
activation to auditory stimulation were capable of functioning independently (OR:
4.6; 95% CI: 1.2-17.1).[1]The study by Claassen and colleagues demonstrates that verbal command–induced brain
activation, as detected by sophisticated quantitative EEG analysis, is a favorable
prognostic indicator in comatosepatients. Such patients with cognitive motor
dissociation are considerably more likely than those without brain activation to
have meaningful recovery. Having a reliable neurophysiologic marker for favorable
outcome from coma is a welcome addition.The clinical neurophysiologist has several tests that can assist with unfavorable and
favorable prognosis from coma. Many of these have been evaluated in anoxic coma, and
most have been reappraised after the widespread use of therapeutic hypothermia (TH).[2] One of the most widely used and reliable neurophysiologic tests used for
predicting poor outcome from coma is median somatosensory-evoked potentials (SEPs).
Bilateral absence of cortical N20 waveforms of the median SEP study as early as 24
hours after onset of coma is highly correlated with a poor outcome (0%-5%
false-positive rate [FPR]); with the use of TH, this reliability has not changed.[2,3] Brainstem auditory-evoked potentials (BAEP) have also been evaluated in
anoxic coma but have been found to have limited value in prognosticating poor outcomes.[4]Electroencephalography, obtained continuously or serially, can also have indicators
of poor prognosis.[5,6] The absence of EEG reactivity to painful stimulation is highly suggestive of
poor prognosis during TH (FPR 1%-7%) and after (FPR 0%-3%).[2] Other EEG features indicative of a poor prognosis include a suppressed EEG
with amplitude <20 µV (FPR 0%-7%), prolonged epileptiform activity (FPR 0%-6%),
and a burst suppression pattern with identical bursts after TH (FPR 0%).[7,8] A recent study has challenged the association of prolonged status epilepticus
with poor prognosis in patients undergoing TH. In this study, 54% of patients with
status epilepticus were alive at 6 months and 43% had a good outcome.[9] Burst suppression during TH is not strongly associated with poor prognosis,
and some of these patients can make a full recovery.[10] Several other EEG features that are often associated with a poor prognosis,
but lack as much data, are α/θ coma, spindle coma, generalized periodic discharges,
and stimulus-induced rhythmic, periodic, or ictal discharges.[11]A few EEG features have also been associated with a favorable prognosis. Early
reactivity to painful stimuli and early continuous background have a greater than
70% positive predictive value (PPV).[12] Rhythmic delta activity has also been associated with good outcomes.[11]Although the absence of cortical waveforms of short latency median SEPs has been used
to prognosticate poor prognosis in coma, middle and late latency-evoked potentials
have been shown to predict favorable outcomes. These latter evoked potentials likely
represent secondary processing of sensory stimuli. The N70 potential, a middle
latency potential, normally obtained approximately 70 ms after stimulation of the
median nerve at the wrist, if present with a latency of less than 130 ms was
associated with a favorable prognosis in 35 (97%) of 36 of patients.[13] Conversely, if the N70 is absent or delayed beyond 130 ms, it is highly
associated with a poor prognosis (FPR 15%).[14]The auditory mismatch negativity (MMN) potential has also shown value in identifying
anoxic comapatients with favorable prognosis. In the pre-TH era, patients who had
an MMN had a PPV for favorable outcome of 69.8%; the MMN was a more reliable
predictor of favorable outcome than Glasgow Coma Scale and BAEP.[15] With TH, MMN improvement between when the patient is hypothermic to
normothermic suggests favorable outcome; 100% of patients with improved MMN survived
anoxic coma while only 40% of those without MMN improvement survived.[16]The novelty P300 potential has also been associated with a favorable prognosis. This
potential is obtained approximately 220 to 380 ms after auditory stimulus delivery
and is induced in response to a “novel” stimulus, presented at a frequency of less
than 5%. This tests higher cognitive processing without active participation by the
patient, making use of this test possible in coma. The novel stimulus can be an
auditory stimulus that is of different tone and pitch than the usual, or it can be
more specific, like the patient’s own name spoken by a loved one. The more specific
the novelty stimulus to the patient, the more likely the P300 will be present.[17] The P300 has a high sensitivity (71%), specificity (85%), and PPV (81%) for
awakening from anoxic coma.[18]The auditory stimulus used to determine brain activation in Claassen and colleagues
study joins these other neurophysiologic tests in determining prognosis for patients
in coma. The EEG changes detected in this study were done with quantitative EEG
analysis using a machine learning algorithm. Such tools are likely not readily
available in most laboratories, and whether the EEG activation can be seen visually
is not certain. Additionally, whether this auditory stimulus–induced brain
activation is different than painful stimulus–induced EEG reactivity (something
routinely tested in comatosepatients) is not clear. These issues notwithstanding,
this study does add another very useful tool to help determine prognosis of comatosepatients.With the variety of neurophysiologic tests now available, clinical neurophysiologists
are in a position to not only determine poor prognosis but can also estimate
favorable outcomes. Continuous EEG (or serial routine EEGs) and median SEP can
identify indicators of unfavorable outcome. If no such indicators are present,
evaluating the EEG for brain activation in response to auditory stimulus, using
novelty auditory stimuli to identify the novelty P300, or using other middle or late
latency-evoked potentials may be considered to identify patients who have a high
chance of recovery. When appropriate these techniques can be combined with other
nonneurophysiologic techniques, such as neuroimaging and serologic testing, used for prognostication.[2] It should be remembered that most prognostic evaluations have been studied in
anoxic coma, and their applicability to other causes of coma may be limited.As we improve our ability to identify the comapatient who is likely to make a
favorable recovery as well as those who are not, we can offer families more accurate
information. We may be able to validate that their loved one can “hear” them or we
may be able to more convincingly assure them that they cannot. Indeed, as important
as caring for the comatosepatient is managing the family’s expectations.
Authors: Susan T Herman; Nicholas S Abend; Thomas P Bleck; Kevin E Chapman; Frank W Drislane; Ronald G Emerson; Elizabeth E Gerard; Cecil D Hahn; Aatif M Husain; Peter W Kaplan; Suzette M LaRoche; Marc R Nuwer; Mark Quigg; James J Riviello; Sarah E Schmitt; Liberty A Simmons; Tammy N Tsuchida; Lawrence J Hirsch Journal: J Clin Neurophysiol Date: 2015-04 Impact factor: 2.177
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Authors: Jan Claassen; Kevin Doyle; Adu Matory; Caroline Couch; Kelly M Burger; Angela Velazquez; Joshua U Okonkwo; Jean-Rémi King; Soojin Park; Sachin Agarwal; David Roh; Murad Megjhani; Andrey Eliseyev; E Sander Connolly; Benjamin Rohaut Journal: N Engl J Med Date: 2019-06-27 Impact factor: 91.245
Authors: Jeannette Hofmeijer; Marleen C Tjepkema-Cloostermans; Michel J A M van Putten Journal: Clin Neurophysiol Date: 2013-10-26 Impact factor: 3.708