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	<title>qEEGsupport.com &#187; qeeg database</title>
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	<description>Quantitative Electroencephalography (qEEG): Information &#38; Discussion</description>
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		<item>
		<title>Concern Regarding the Mitsar Amplifier</title>
		<link>http://qeegsupport.com/concern-regarding-the-mitsar-amplifier/</link>
		<comments>http://qeegsupport.com/concern-regarding-the-mitsar-amplifier/#comments</comments>
		<pubDate>Sat, 19 Dec 2009 22:41:00 +0000</pubDate>
		<dc:creator>Jay Gunkelman</dc:creator>
				<category><![CDATA[neurofeedback]]></category>
		<category><![CDATA[qEEG]]></category>
		<category><![CDATA[brain mapping]]></category>
		<category><![CDATA[mitsar]]></category>
		<category><![CDATA[qeeg amplifier]]></category>
		<category><![CDATA[qeeg database]]></category>

		<guid isPermaLink="false">http://qeegsupport.com/?p=420</guid>
		<description><![CDATA[The concern regarding the Mitsar amplifier expressed  with so much vigor by those with competing interests has met the reality test  of actual recorded data.  The concern expressed was over a theoretical time  skewing error due to the data sampling of an older version of the Mitsar  amplifier.
I suggested at the [...]]]></description>
			<content:encoded><![CDATA[<p>The concern regarding the Mitsar amplifier expressed  with so much vigor by those with competing interests has met the reality test  of actual recorded data.  The concern expressed was over a theoretical time  skewing error due to the data sampling of an older version of the Mitsar  amplifier.</p>
<p>I suggested at the time that all the emotion was merely an  example of someone yelling &#8220;the sky is falling&#8221;, like Chicken Little. There  was no real problem, just lots of crying out and hand wringing.</p>
<p>I  requested in an open international forum for anyone to send me a sample  of the problem, and none could be produced. I suspected there was no real problem, as the sample issue was concerning a 500 sample/second device having a time skew&#8230; though this was in comparison to a database  collected on a 100 sample per second device, with the waveforms interpolated  from these samples.<span id="more-420"></span></p>
<p>It was highly suspect from my technical  perspective when this issue was raised, and it was even more suspect when  nobody could produce actual data showing the coherence or phase  issue.</p>
<p>Testing now has shown that the old style Mitsar, with the  non-simultaneous sampling is identical in performance to the new style  amplifier that has simultaneous sampling, and thus no skewing error is  possible in the newest amp.  There is also an intermediate style amplifier  tested, which is one of the smaller amps, but with a more current sampling  design.</p>
<p>The data clearly show that there is no difference in coherence  between these devices.</p>
<p>The Mitsar amplifier also has been tested with  the new BranMaster  Discovery amplifier, and it also was shown to have  indenticle coherence findings with the Mitsar amplifier.</p>
<p>Clearly there  is no real issue.</p>
<p>Data rules&#8230;. the experimental details are  below.</p>
<p>Jay</p>
<p>We performed the following  experiment.</p>
<p>We took three different Mitsar amplifiers:</p>
<p>1.  Mitsar-EEG-201 &#8211; old model of amplifiers with relatively large time  shift between channels (1.75 ms maximum) 2. Mitsar-EEG-201M &#8211; new model  of amplifiers with relatively small time shift between channels  (470 microsecond maximum) 3. Mitsar-EEG-202 &#8211; 32-channels amplifiers with zero time shift between channels.</p>
<p>Than we take Electro-Cap and put it  on the head of one subject. We used linked ears referent for EEG  recording.</p>
<p>We sequentially connect Electro-Cap and referents to three  different amplifiers and perform independent recording of EEG in eyes  closed condition. The duration of recording was longer than 300  seconds.</p>
<p>When we reconnect Electro-Cap and referents from one amplifier  to another we do not touch to electrodes on the head and ears.</p>
<p>The  total time of out experiment was approximately 20 minutes. This means the  functional state of subject remain relatively stable.</p>
<p>Than we remontage  the EEG to average referent (very important for time  shift influence  measurements), compute the coherence for all three EEG recordings using the  same processing parameters and compare them. The duration of time interval  for processing was the same for these EEG recording and was equal to 300  seconds.</p>
<p>We do not find any dramatic differences in coherence  corresponding to different amplifiers. The small fluctuations can be explaned  by amplifiers noise and non-stationarity of EEG.</p>
<p><span style="font-family: Arial; font-size: x-small;"><img class="aligncenter" title="Mitsar Comparison Results" src="http://qeegsupport.com/wp-content/uploads/2009/04/comperisonresults.jpg" alt="comperisonresults Concern Regarding the Mitsar Amplifier" width="711" height="1575" /><br />
</span></p>
<p><strong>Mitsar Calibration</strong></p>
<p>The Mitsar system is calibrated at the manufacturer. There is no need to recalibrate the amplifier unless there is a serious problem from damage. The calibration button is so the user can run a test calibration signal to demonstrate that the channels are in fact correct and equal. If these were ever not correct (or equal) then the manufacturer would recalibrate the hardware device. It is blocked so that a user cannot accidentally mess the calibrations up.  So in summary the  calibration button in the software is pressed and then the button to observe EEG is pressed. Then the test calibration signal is generated and can be recorded. This is a good idea if the case is a medical or legal evaluation so that when the data is presented as evidence there is validation that a microvolt equals a microvolt.</p>
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		<title>Thalamic Involvement in the Generation of the Alpha Rhythms</title>
		<link>http://qeegsupport.com/thalamic-involvement-in-the-generation-of-the-alpha-rhythms/</link>
		<comments>http://qeegsupport.com/thalamic-involvement-in-the-generation-of-the-alpha-rhythms/#comments</comments>
		<pubDate>Tue, 07 Jul 2009 20:59:29 +0000</pubDate>
		<dc:creator>Jay Gunkelman</dc:creator>
				<category><![CDATA[Brain Science]]></category>
		<category><![CDATA[LORETA]]></category>
		<category><![CDATA[qEEG]]></category>
		<category><![CDATA[brain mapping]]></category>
		<category><![CDATA[EEG]]></category>
		<category><![CDATA[eeg databases]]></category>
		<category><![CDATA[gunkelman]]></category>
		<category><![CDATA[qeeg database]]></category>

		<guid isPermaLink="false">http://qeegsupport.com/?p=298</guid>
		<description><![CDATA[Alpha… it’s not a simple idling rhythm… let’s look at alpha generators:
The thalamic involvement in the generation of the alpha rhythm is being under-valued when looking at the LORETA images of alpha current source generators.  The alpha power may come from the sources that LORETA identifies, but the thalamus is intimately involved in alpha [...]]]></description>
			<content:encoded><![CDATA[<p>Alpha… it’s not a simple idling rhythm… let’s look at alpha generators:</p>
<p>The thalamic involvement in the generation of the alpha rhythm is being under-valued when looking at the LORETA images of alpha current source generators.  The alpha power may come from the sources that LORETA identifies, but the thalamus is intimately involved in alpha rhythm generation, and this is not part of the LORETA image of the sources.</p>
<p>The polarization within the thalamus sets the base frequency of the alpha, but the cortical rhythm requires a complex multi-layer feedback loop from the thalamus to the cortex, and back to the thalamus.  Without the cortex, there is a total disruption of the normal spatio-temporal distribution of the alpha wave’s spike trains within the thalamus, and cortical damage often disturbs coherence due to this mechanism.</p>
<p>The thalamus distributes the alpha posteriorly via specific sensory relays, which have a simple return circuit. Like the white matter relay from the lateral geniculate of the thalamus to the occipital lobe’s primary visual areas, and directly back.  This thalamo-cortical-thalamic loop is relatively faster than the loop seen frontally.  The frontal return circuitry is not simple, but the descending routes are complex and somewhat circuitous, taking more time, and thus it is common for the frontal lobe’s alpha to be at the slower end of the individual’s alpha frequency range.  The frontal lobe has a return path through the striatum.<br />
<span id="more-298"></span><br />
The five divisions of the frontal-striatal pathways are the motor circuit, the oculomotor circuit (from the frontal eye fields), the dorsolateral prefrontal circuit (cortical gating), lateral orbito-frontal circuit (emotive), and the anterior cingulate circuit (emotional and cognitive flexibility).  The striatal-thalamic pathways are divided into two descending pathways which both start from the cortex to the head of the caudate and then the putamen, and then this pathway divides between the globus pallidus and substantia nigra, and then these both go to the thalamus.  The thalamo-cortical completion of the circuit projects to both the premotor and motor cortex directly.</p>
<p>Not all circuits are simple thalamus-to-cortex-to-thalamus “echoic” returns to the original source…</p>
<p>A cortico-thalamo-cortical projection system exists which originates from the primary visual cortex, relayed by the lateral posterior nucleus of the thalamus, projecting to the suprasylvian visual area (which is involved in highest levels of visual integration and comprehension). This finding suggests that the thalamus modulates transmission of cortical signals from one cortical area to another&#8230; the coherence or “connectivity” of the cortex is not cortical-cortical, but cortical-thalamo-cortical.   </p>
<p>With maturation, the cortex provides a stimulatory effect on the alpha frequency, raising it to a slightly faster frequency tuning through feedback to the thalamus, but the basic frequencies of alpha are generated by the reticular nucleus of the thalamus providing acetylcholine to the thalamic nuclei, and by the underlying polarization within the thalamus, which is effected by the NE levels from the brainstem, and by fluctuating DC field strength levels in the brain.   The other effects are the thalamo cortical transmission times, and an effect of the cortical-thalamic processing time for any given pathway…. Longer time needed for frontal than posterior circuits.</p>
<p>Crudely stated:  The frequencies of alpha are set in the thalamus, and the spatial and temporal distribution of alpha are controlled by the cortex, with rhythmic “initiation” (phase reset) done by the DC system’s “modulatory” influence on the AC rhythms of the EEG.</p>
<p>The thalamus can provide rhythms in the range from 3 to 16, with the common range of 8-12 representing an adult group’s “average”.  Hyperpolarization of the thalamus slows the alpha, and hypopolarization speeds it up until it desynchronizes at about 16 Hz, and becomes a low voltage fast EEG.  </p>
<p>The addition of some GABA (an inhibitory neurotransmitter) easily acquired with the addition of some alcohol will slow the alpha back into a rhythmic pattern.  This basic mechanism is the reason alpha-theta training works so well on the low voltage fast EEGs seen so commonly in alcohol addiction.  </p>
<p>LORETA may show a generator in the precuneus/cuneus area for the occipital alpha component, and the posterior cingulate for the parietal component (when alpha modulators are identified with ICA analysis and then source localized)… but these localizations miss the full beauty of the real mechanism’s complexity and especially the primary importance of the thalamus.</p>
<p>The thalamus gates our perceptions into “perceptual packets”, with the “thalamic gate” being open during the negative half-wave (up-side of the waveform), and less open during the positive half wave (the downward going half).  Two stimuli presented within 75 to 100 milliseconds of each other will be “perceptually synchronized”, or though of as being instantaneously simultaneous.</p>
<p>The alpha frequency is the perceptual sampling rate… how many perceptual packets are evaluated per unit time, with a better semantic or declarative memory function seen with faster alpha frequencies.  This is from the work on IAF (individual alpha frequency) from Professor Dr. Wolfgang Klimesch’s lab in Salzburg Austria, with significant contributions from Drs Michael Doppelmayr and Simon Hanselmayr.</p>
<p>The databases have difficulty characterizing alpha frequency tuning issues, with many identifying too much power at a slower frequency (like 7 Hz)… although the power values would be healthy and normal if alpha were only faster (like 9 Hz)… the databases seldom tell you it is merely 2 Hz slow.  The normal alpha coherence values, if the alpha is slowed, are seen as hypercoherence, although they are perfectly normal for alpha.  Databases that rely on predetermined band’s peak frequency may miss a shift if it exceeds their defined band, and this will miss the mean frequency if the peak is good but the band width has less faster content than slower content.</p>
<p>Faster alpha may cause similar issues (too much 12-15 Hz power or 12-15 Hz hypercoherence) when it is not “too much” of either that is really wrong, just alpha being too fast.</p>
<p>Thus when there are tuning issues, databases often have difficulty characterizing the core issue of tuning.   When a tuning issue is noted, the coherence and power values may be “off” according to the database, when the real values are not really abnormal, just that they are too slow or too fast.</p>
<p>Theoretically, these issues may prove to be an area where Z-score training may have difficulty, flagging red herrings of power and coherence… though this is an empirical question that will be answered with time and experience</p>
<p><a class="a2a_dd addtoany_share_save" href="http://www.addtoany.com/share_save#url=http%3A%2F%2Fqeegsupport.com%2Fthalamic-involvement-in-the-generation-of-the-alpha-rhythms%2F&amp;title=Thalamic%20Involvement%20in%20the%20Generation%20of%20the%20Alpha%20Rhythms"><img src="http://qeegsupport.com/wp-content/plugins/add-to-any/share_save_171_16.png" width="171" height="16" alt="share save 171 16 Thalamic Involvement in the Generation of the Alpha Rhythms"  title="Thalamic Involvement in the Generation of the Alpha Rhythms" /></a> </p>]]></content:encoded>
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		<item>
		<title>Technical Issues in qEEG</title>
		<link>http://qeegsupport.com/technical-issues-in-qeeg/</link>
		<comments>http://qeegsupport.com/technical-issues-in-qeeg/#comments</comments>
		<pubDate>Mon, 02 Feb 2009 21:49:13 +0000</pubDate>
		<dc:creator>Jay Gunkelman</dc:creator>
				<category><![CDATA[Brain Science]]></category>
		<category><![CDATA[qEEG]]></category>
		<category><![CDATA[brain mapping]]></category>
		<category><![CDATA[EEG]]></category>
		<category><![CDATA[eeg artifacting]]></category>
		<category><![CDATA[eeg databases]]></category>
		<category><![CDATA[gunkelman]]></category>
		<category><![CDATA[neurofeedback]]></category>
		<category><![CDATA[patterns]]></category>
		<category><![CDATA[qeeg database]]></category>
		<category><![CDATA[technical issues]]></category>

		<guid isPermaLink="false">http://qeegsupport.com/?p=147</guid>
		<description><![CDATA[Three part video by Jay Gunkelman discussing Technical Issues in qEEG.
Technical Issues in qEEG Power point Presentation

 Continue Reading to see parts 2 and 3.


Part 2 Discusses Z-Scores and Standard Deviations




]]></description>
			<content:encoded><![CDATA[<p>Three part video by Jay Gunkelman discussing Technical Issues in qEEG.</p>
<p><a href="http://www.bio-medical.com/download/qeegtechnicalissues.ppt">Technical Issues in qEEG Power point Presentation</a></p>
<p><object width="410" height="341" data="http://www.veoh.com/veohplayer.swf?permalinkId=v17392502KSfSKjEf&amp;id=anonymous&amp;player=videodetailsembedded&amp;videoAutoPlay=0" type="application/x-shockwave-flash"><param name="bgcolor" value="#FFFFFF" /><param name="src" value="http://www.veoh.com/veohplayer.swf?permalinkId=v17392502KSfSKjEf&amp;id=anonymous&amp;player=videodetailsembedded&amp;videoAutoPlay=0" /><param name="allowfullscreen" value="true" /></object></p>
<p><a href="http://www.veoh.com/videos/v17392502KSfSKjEf"> </a>Continue Reading to see parts 2 and 3.</p>
<p><span id="more-147"></span></p>
<p><object width="410" height="341" data="http://www.veoh.com/veohplayer.swf?permalinkId=v1737023759Ry5DJJ&amp;id=anonymous&amp;player=videodetailsembedded&amp;videoAutoPlay=0" type="application/x-shockwave-flash"><param name="bgcolor" value="#FFFFFF" /><param name="src" value="http://www.veoh.com/veohplayer.swf?permalinkId=v1737023759Ry5DJJ&amp;id=anonymous&amp;player=videodetailsembedded&amp;videoAutoPlay=0" /><param name="allowfullscreen" value="true" /></object></p>
<p>Part 2 Discusses Z-Scores and Standard Deviations<a href="http://www.veoh.com/videos/v1737023759Ry5DJJ"><br />
</a></p>
<p><object width="410" height="341" data="http://www.veoh.com/veohplayer.swf?permalinkId=v17370245M7TrGQCj&amp;id=anonymous&amp;player=videodetailsembedded&amp;videoAutoPlay=0" type="application/x-shockwave-flash"><param name="bgcolor" value="#FFFFFF" /><param name="src" value="http://www.veoh.com/veohplayer.swf?permalinkId=v17370245M7TrGQCj&amp;id=anonymous&amp;player=videodetailsembedded&amp;videoAutoPlay=0" /><param name="allowfullscreen" value="true" /></object></p>
<p><a href="http://www.veoh.com/videos/v17370245M7TrGQCj"><br />
</a></p>
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		<title>qEEG Artifacting</title>
		<link>http://qeegsupport.com/qeeg-artifacting/</link>
		<comments>http://qeegsupport.com/qeeg-artifacting/#comments</comments>
		<pubDate>Fri, 30 Jan 2009 07:33:46 +0000</pubDate>
		<dc:creator>Jay Gunkelman</dc:creator>
				<category><![CDATA[Brain Science]]></category>
		<category><![CDATA[qEEG]]></category>
		<category><![CDATA[brain mapping]]></category>
		<category><![CDATA[discriminants]]></category>
		<category><![CDATA[eeg artifacting]]></category>
		<category><![CDATA[eeg databases]]></category>
		<category><![CDATA[gunkelman]]></category>
		<category><![CDATA[patterns]]></category>
		<category><![CDATA[qeeg database]]></category>

		<guid isPermaLink="false">http://qeegsupport.com/?p=138</guid>
		<description><![CDATA[The qEEG represents the statistical manipulation of the raw EEG, so an understanding of these manipulations should precede any discussion of the qEEGs clinical indications for protocols. Without such knowledge any given finding may be misinterpreted.
Following the careful recording of the EEG, the quantitative analysis is begun with the sampling of the data to be [...]]]></description>
			<content:encoded><![CDATA[<p><span style="font-size: 10pt; font-family: Arial; color: black;">The qEEG represents the statistical manipulation of the raw EEG, so an understanding of these manipulations should precede any discussion of the qEEGs clinical indications for protocols. Without such knowledge any given finding may be misinterpreted.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Following the careful recording of the EEG, the quantitative analysis is begun with the sampling of the data to be used in the analysis by the Fourier transform. The Fourier analysis assumes there are no transients (epileptic discharges, episodic voltage changes etc.) or state changes (light sleep, drug effect, mental task, etc.), so these must be avoided when selecting data for analysis in qEEG for eyes closed resting database comparison. There are some eyes open and task databases available more recently (Hudspeth, Sterman, Duffy etc.)<span id="more-138"></span></span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Transients are an event with a rapid onset and ending, with an increase in amplitude of greater than 50% over the ongoing activity. Epileptiform activity is one common example of this phenomenon. The only time transient discharges may validly be included is when dipole localization or “mapping” of the sources of this activity is the intent, and in this circumstance only significant discharges should be sampled, with the ongoing background treated as the state change and eliminated.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Less rigorous analysis selection standards exist for data not intended for database comparison, such as reading or other task related data. Usually these task data will only be used for gross comparison to the more carefully collected steady state data, looking for gross changes in brain function. When there is an intent to compare to an eyes closed normative database, transients will increased the variability of the dataset, but will be averaged out in the mapping unless persistent or very prominent. These transients will simultaneously alter the dataset’s standard deviation from the norm. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">State changes include typically sleep stages collected for an eyes closed awake database comparison. Stage 1 sleep is a subtle drowsy state, where people recorded will usually deny being drowsy when alerted. The alpha is beginning to wax and wane, with subtle increases in theta and occasionally slow rolling eye movements and a decreased EMG tonus. This is just prior to stage 2, where an object being held will slip from grasp, alerting the client, with most realizing the drowsing is present in stage 2. Many people doing a repetitive task or automatic pilot type task will be in stage 1 without being aware of time passing. This is a dangerous situation if response to change is needed, as there are delays in reaction time associated with this state.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The problem with stage 1 (drowsing) being added to a dataset is that it is a mixing of states, violating the FFT assumptions and making database comparison validity more than merely suspect. The inclusion invalidates comparison. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The task of artifacting is to sample enough data to provide reliable maps while maintaining the validity of the sampling, not taking state changes or transients. The amount of data acquired should provide highly repeatable or reliable mapping. The time required to achieve these results is different for each frequency. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Beta becomes reliable in the first 30 to 45 seconds, with alpha following at 60-90 seconds. The intermittent nature of theta makes it the least easily established reliability, with 120-180 seconds required. Delta is reliable at about 120 seconds. Our lab tries to get 120 seconds of data when possible.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Reliability may be established another way, with split-half replication. This actually looks at the lability within the sampled data by looking for the invariant similarity of the repeatable parts of the two data sets, with the more variable parts looked at with less confidence.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The time span or length of the epochs selected determines the sensitivity to the slower frequencies. The Fourier transform has to have a completed waveform in the data epoch sampling for the frequency to be detected and quantified. A 1/2 Hz low frequency sensitivity is thus achieved only when 2 second epoch lengths or longer are sampled. There is a downside to too long an epoch. It increases the likelihood of including state changes and transients, though when clean state stable data exists in long episodes, it should be sampled.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Some equipment has preset epoch lengths and interactions between the sampling rates and the epoch length, which is problematic in sampling data flexibly. The epochs in some equipment are not able to be adjusted in time to ’slide’ past artifacts, making the data artifacting such that it is difficult to sample the clean data in a record with intermittents like eye movement or other transients. Careful selection of the equipment should precede entry into this field.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The artifacting is mostly concerned with eliminating the more common artifacts of eye movement and EMG, as well as movement or electrode artifacts. This cleaning of the data is part of the art of doing good qEEGs, though the science of adequate sampling and the assumptions of the Fourier must be kept in mind.</span></p>
<p><a name="newartifacts"></a><strong><span style="font-family: Arial;">New artifacts introduced by the digital processing.</span></strong></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The digital recording and processing of the raw analog waveform of the EEG should be understood in technical detail to properly interpret the resultant maps and numerical tables of findings.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The EEG is digitally converted from the analog data by an analog-to-digital or A-D converter and a resultant digital dataset is derived. The digitizing sampling rate and the bit length of the computer data will determine the resolution of the resultant image and tabular datasets. The faster the sampling rate, the faster the frequency that can be resolved, with a minimal sampling frequency defined by the Nyquist principle as 2 times the frequency being resolved. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Proper reproduction of the EEG for visual perspective requires a more conservative sampling rate than the 2:1 Nyquist ratio. This greater than 2:1 ratio must be set by the individual’s preferences. Few would choose less than 128 samples per second, most would prefer 500/second to 1000/second. (The manufacturer’s with set buffer sizes for the epochs, like the Lexicor, will however need to look at the impact in loss of lower frequency sensitivity. For this situation 128 to 256 is the highest reasonable choice.)</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The channel sampling should be simultaneous, to avoid remontaging error or slew. If not simultaneous, a faster sampling rates will reduce this error (as will burst mode sampling) reducing the phase or time base error to a minimum. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The bit length of the computer “word” processed by the CPU effects the amplitude resolution in qEEG, irrespective the sampling rate. The longer the bit length, the better the resolution ( a bit length of 12 is acceptable, but 16 is preferred. Older units will have 8 bit processing and are not fully adequate without further scaling adjustments).</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The epochs selected during artifacting will all have an abrupt start and stop, without a zero voltage point at each end of all the epochs. This sudden voltage is seen by the FFT (fast Fourier transform) of the computer analysis as a square wave at the start and stop of each epoch. The resultant output of the Fourier is that all frequencies were present at that point to “reconstruct” the square wave. This is termed “leakage artifact”, or “Gibb’s artifact”. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The result of the Gibb’s artifact is that if a 10 Hz waveform was put into the FFT, a spectral plot of the output would have a rise of the baseline where all frequencies were used to reconstruct these abrupt starts and stops of the epochs. There would be a spectral peaking at 10 Hz, with a tapered response and a broadened base to the frequency plot.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">To correct for the leakage or Gibb’s artifact, a “windowing” filter is used. The result of this windowing is the return to the baseline of the generally elevated spectral plot mentioned previously. There is a residual broadening of the idealized spectral peak at 10 Hz. This residual artifact of the broadening of the spectrum following the windowing is “smearing” artifact.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The windowing used in qEEG is usually a Hanning window. This filter slowly ramps up the start and ramps down at the end, to avoid the apparent square wave the FFT sees. Other windowing techniques are triangular, Blackman, Hamming, Meyer’s , with the lack of windowing occasionally referred to as a “rectangular window”. A full discussion of these details, contrasting the different styles of windowing is outside the scope of this chapter.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">“Aliasing” is an artifact caused by a frequency source near the sampling rate (and above the nyquist sampling rate) so that a beat frequency is created as an alias of the source frequency/sampling rate interaction. Aliasing filters are used to control for this artifact in all modern devices.</span></p>
<p><a name="databaseissues"></a><strong><span style="font-family: Arial;">Database issues</span></strong></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The datasets derived from the artifacted EEG are the starting point for the comparison of these data points to the databases used in qEEG analysis. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The databases are the means and standard deviations used to establish the significance probabilities for the observed measurements. These will be represented as Z-Scores, roughly these may be seen as the standard<br />
deviations from the normative database of the data points in the dataset. They are calculated as the patient mean minus the database mean, divided by the standard deviation of the population.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Z-scores are reported in tabular form and may be mapped. Significance probability mapping ( a term derived by Frank Duffy, M.D. of Harvard’s Children’s Hospital) allows the interpreting individual to view the spatial distribution and extent of deviation in an easily discernible display. 1.96 Z-score deviation is equal to 2 standard deviations, and 3.08 Z-score deviation is three standard deviations.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Normative databases are constructed with highly screened normal individuals with an age range establishing the limits of the database. The database is constructed controlling for socio-economic and other demographic influences. Importantly, the databases must be established with different norms for male and female, to account for the significantly different neurophysiologic structures and rates of development of the male and female brains.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The database used should be selected to match the end use and population to be seen. The age range may be critical for those seeing children or the elderly. For others, the presence of multivariate stepwise discriminants used in determining the likelihood of membership in one of two or more clinical groupings will be critical in the selection.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">For others, the presence of an eyes open database for use in clinical eyes open work, or the task related data will be critical.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The database from E.Roy John, Ph.D. of NYU’s Brain Reasearch Laboratory contains more than univariate measures, with multivariate parametric statistical evaluations of normal and many clinical subgroups. This has stepwise discriminant analysis associated with it. Discriminants for head trauma are also available from Thatcher. The Duffy database is used, though is not is commercial distribution now that the Nicholet BEAM instrumentation does not carry it. Sterman has an age limited performance based database available, with new databases such as </span><span style="font-size: 10pt; font-family: Arial;"><span style="color: windowtext;">Hudspeth</span>’s<span style="color: black;"> coming into availability recently as well.</span></span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">In using the discriminants, if available in a database, care should be exercised to assure the applicability of the discriminant to the client being evaluated. The client must fit the conditions that were set for the construction of the discriminant. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">If a discriminant is set up to decide the likelihood of being a member of group A or group B, a member of another group, C, will be classified as A or B, not properly identified as another type, type C. This weakness of discriminants must be controlled in the selection and use of the discriminant, not after it has been performed. </span></p>
<p><a name="displays"></a><strong><span style="text-decoration: underline;"><span style="font-family: Arial;">Displays </span></span></strong></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The displays in the qEEG report will be presented as a progressive analysis of the data. The displays may be sorted into those that are closer to and farther from the raw EEG, being farther from the EEG as more statistical manipulations are performed. The farther from the raw data one goes, the easier it is to mistakenly interpret artifacts as real or misinterpret relational data.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">To avoid these easy and eventually certain mistakes, the full visual interpretation of the EEG must precede any review of the analyzed data. Only then should this be followed by a review of the raw amplitude mapping, in as detailed a frequency display as possible. This may be followed by broad band analysis. The amplitude mapping should be followed by the power and then the relative power analysis. Only after this step-wise evaluation this should absolute or relative power Z score or other database comparisons be done.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">Following the spectral evaluation, the statistically extracted measures of symmetry, coherence and phase are evaluated, without being as likely to make a mistake.</span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">The presence of artifact should be expected in clinical work. In clinical work the luxury of prolonged recordings and rejection from a study due to artifacts is not present as it is in academic situations. The progressive step by step evaluation will control for these situations as best they may be. </span></p>
<p><span style="font-size: 10pt; font-family: Arial; color: black;">To err may be human, but it should be controlled and accounted for with methodologic routine to the extent humanly possible.</span></p>
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