<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JBM</journal-id><journal-title-group><journal-title>Journal of Biosciences and Medicines</journal-title></journal-title-group><issn pub-type="epub">2327-5081</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbm.2019.711005</article-id><article-id pub-id-type="publisher-id">JBM-96233</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Frequency of Neurological Disorders and Related EEG Finding in a Tertiary Care Hospital of Karachi
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Danish</surname><given-names>Mohammad</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Syeda</surname><given-names>Saba Zaidi</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bina</surname><given-names>Fawad</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Muhammad</surname><given-names>Fazal Hussain Qureshi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Zain</surname><given-names>Jawed Abubaker</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Muhammad</surname><given-names>Zubair Shaikh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Muzna</surname><given-names>Shah</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mahira</surname><given-names>Lakhani</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sara</surname><given-names>Sadiq</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Neurology, Liaquat National Hospital, Karachi, Pakistan</addr-line></aff><aff id="aff4"><addr-line>Department of Physiology, CMH Institute of Medical Sciences, Bahawalpur, Pakistan</addr-line></aff><aff id="aff1"><addr-line>Ziauddin University, Karachi, Pakistan</addr-line></aff><aff id="aff3"><addr-line>Department of Community Health Sciences, Ziauddin University, Karachi, Pakistan</addr-line></aff><pub-date pub-type="epub"><day>23</day><month>10</month><year>2019</year></pub-date><volume>07</volume><issue>11</issue><fpage>56</fpage><lpage>64</lpage><history><date date-type="received"><day>3,</day>	<month>October</month>	<year>2019</year></date><date date-type="rev-recd"><day>4,</day>	<month>November</month>	<year>2019</year>	</date><date date-type="accepted"><day>7,</day>	<month>November</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Background: Electroencephalogram (EEG) is defined as a method of detecting brain waves signifying the electrical conductivity of the brain. Globally, EEG is used to further classify neuropsychiatric disorders. 
  Objective: To evaluate the prevalence of abnormal EEGs and related neurological disorders and it’s correlation with age and gender. 
  Methodology: A descriptive cross sectional study was conducted in Neurology department, Ziauddin hospital, Karachi, Pakistan from June 2018 to May 2019. A total of 440 individuals based on inclusion criteria were selected through Non-probability consecutive sampling. Informed consent was obtained from study participants. A self-designed structured questionnaire and EEG record were used for data collection. Data were entered and analyzed using SPSS v 20. Mean and standard deviation was calculated for numerical variable and frequency and percentages were calculated for categorical variable. Independent t-test and chi square was used to check association of abnormal EEG with age and gender. P value of ≤0.05 was considered statistically significant. 
  Results: The mean age of study participants was 52.98 &#177; 22.68 years. There were 54.5% (n = 240) males. Approximately 45.2% (n = 199) participants had predisposing condition which can lead to abnormal EEG. EEG records of 39.8% (n = 175) of the patients was normal while 60.2% (n = 265) had abnormal records. Diffuse neuronal dysfunction consistent with encephalopathy was found in 45.2%. Mild neuronal dysfunction consistent with encephalopathy accounted for 33.5% of cases. Significant difference was found in Abnormal EEG among different age group (p = 0.01). Chi square shows an association between abnormal EEG and male gender (p = 0.025). 
  Conclusion: EEG plays a vital role in the diagnosis of neuropsychiatric conditions in developing countries. EEGs can further help to determine the relationship of different neuropsychiatric conditions and can help in early diagnosis and better prognosis.
 
</p></abstract><kwd-group><kwd>Neurological Disorders</kwd><kwd> EEG</kwd><kwd> Association</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Electroencephalogram (EEG) is defined as a method of detecting brain waves signifying the electrical conductivity of the brain using small metal electrodes recorded as wavy lines on EEG recording paper [<xref ref-type="bibr" rid="scirp.96233-ref1">1</xref>]. EEG waves consist of alternating excitatory and inhibitory synaptic potentials generated in the pyramidal cells of the cerebral cortex [<xref ref-type="bibr" rid="scirp.96233-ref2">2</xref>]. EEG waves are classified as following: Alpha (α), Beta (β), Theta (θ), and Delta (δ). Alpha waves are seen at frequencies between 18 and 30 cycles/sec. They are found predominantly in healthy adults while awake or in resting states of cerebration. Beta waves are seen at frequencies between 14 to 80 cycles/sec and are found when a person is directed towards specific mental activity. Theta waves are seen at frequencies between 4 and 7 cycles/min. They are predominantly found in children, but can also be found during states of emotional stress in adults. They are also markers of degenerative brain disorders. Delta waves are seen at frequencies below 3.5 cycles/sec. They are markers of deep sleep and organic brain disease [<xref ref-type="bibr" rid="scirp.96233-ref3">3</xref>].</p><p>Physicians have declared EEG as a gold standard diagnostic test for seizures and epilepsy [<xref ref-type="bibr" rid="scirp.96233-ref4">4</xref>]. Globally, EEG is used to further classify neuropsychiatric disorders. Furthermore, studies have focused on analysing the significance of different algorithms and techniques for EEG. Khanna et al. examines microstates in resting state EEG for diagnosis of multiple neurological disorders such as schizophrenia, dementia, and depression [<xref ref-type="bibr" rid="scirp.96233-ref5">5</xref>]. In addition, wavelength based EEG have been established, as the most effective automated method for seizures and epilepsy [<xref ref-type="bibr" rid="scirp.96233-ref6">6</xref>]. Moreover, physicians are trying to prove brain death with the help of EEG reports [<xref ref-type="bibr" rid="scirp.96233-ref7">7</xref>]. Multiple methods have been developed to diagnose encephalitis using EEG [<xref ref-type="bibr" rid="scirp.96233-ref8">8</xref>].</p><p>Even though EEG is important for diagnosis but limited studies have been carried out in Pakistan. Most of the studies conducted have been used to analyse better treatment and diagnosis of disorder [<xref ref-type="bibr" rid="scirp.96233-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.96233-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.96233-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.96233-ref12">12</xref>]. Very few articles assess the demographic and etiological trend of disease [<xref ref-type="bibr" rid="scirp.96233-ref13">13</xref>]. However, there is minimal research on observation of the basic trends of EEG and the use of EEG in our setup. Therefore, the objective of this study is to evaluate the prevalence of abnormal EEGs and related neurological disorders and it’s correlation with age and gender.</p></sec><sec id="s2"><title>2. Methodology</title><p>A descriptive cross sectional study was conducted in neurological department of Ziauddin Hospital. The study duration was one year i.e. June 2018 to May 2019. The actual sample size was 384 individuals, which was calculated by using the standard formula for calculating sample size on the basis of prevalence. Prevalence was taken at 50% because no relevant data was available. The bound of error was 5% with a 95% confidence interval. The sample size was inflated to exclude non-response and poorly filled questionnaires.</p><p>Non probability consecutive sampling technique was used. Inclusion criteria consisted of all patients referred for EEG to neurology department while those were excluded who either refused to give consent for participation or from Paediatric age group or Unconscious patients or patients with altered mental status. A self-designed questionnaire was used for collection of data. Questionnaire contained information including demographics (age, gender), pertinent history (drug, family, substance abuse), source of referral, activation procedure if performed during EEG, EEG findings, provisional diagnosis made by physician referring for EEG, Conclusion and then EEG correlation with the provisional diagnosis. The EEG records were reviewed. Socio demographic data, clinical data and the neurologist’s comments on the EEG recordings were extracted and recorded on the proforma. Consent was obtained from every participant. Ethical approval was taken from Institutional review board before conducting study.</p><p>The data was analysed using Statistical Package for the Social Sciences (SPSS) version 20. Quantitative variables were presented as mean and standard deviation while qualitative variables were presented as frequency and percentages. Outcome variable was EEG correlation with the provisional diagnosis. Independent t-test and chi square was calculated to check association of abnormal EEG with age and gender.</p></sec><sec id="s3"><title>3. Results</title><p>A total of 440 patients referred for EEG were included in the study. Majority 240 (54.5%) of them were males, mean age was 52.98 &#177; 22.68 years. The age distributions of the patients were as follows: Majority, 196 (44.5%) were in the age bracket 25 - 64 years, 172 (39.9%) were 65+ years, 69 (16.3%) were between 15 - 24 years. About 98% of participants have no history of addictions. Referrals from neuro department were 86.1% while the rest of the 13.9% were from medicine, surgery and other departments as shown in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>About 44% (191) participants were on medications which include Lerace, Epival, Rivotril, midazolam, Keppra, phenytoin, Valium and hitop. Looking over the predisposing conditions that can lead to abnormal EEG findings, approximately 45.2% (199) participants were prone, as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>.</p><p>The EEG diagnosis based on the interpretation of the EEG records by the neurologists showed that 175 (39.8%) of the patients had normal records while 265 (60.2%) had abnormal records. The breakdown of the abnormal records</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Socio-demographics of participants</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle"  colspan="2"  >Male</th><th align="center" valign="middle"  colspan="2"  >Female</th><th align="center" valign="middle"  colspan="2"  >Combined</th></tr></thead><tr><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >n</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >n</td><td align="center" valign="middle" >%</td></tr><tr><td align="center" valign="middle" >Youth (15 - 24)</td><td align="center" valign="middle" >36</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >36</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >72</td><td align="center" valign="middle" >16.36</td></tr><tr><td align="center" valign="middle" >Adults (25 - 64)</td><td align="center" valign="middle" >106</td><td align="center" valign="middle" >44.16</td><td align="center" valign="middle" >90</td><td align="center" valign="middle" >45</td><td align="center" valign="middle" >196</td><td align="center" valign="middle" >44.54</td></tr><tr><td align="center" valign="middle" >Senior (65+)</td><td align="center" valign="middle" >98</td><td align="center" valign="middle" >40.83</td><td align="center" valign="middle" >74</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" >172</td><td align="center" valign="middle" >39.09</td></tr><tr><td align="center" valign="middle"  colspan="7"  >Family History</td></tr><tr><td align="center" valign="middle" >Positive</td><td align="center" valign="middle" >01</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >01</td><td align="center" valign="middle" >0.4</td><td align="center" valign="middle" >02</td><td align="center" valign="middle" >0.5</td></tr><tr><td align="center" valign="middle" >Negative</td><td align="center" valign="middle" >239</td><td align="center" valign="middle" >99.6</td><td align="center" valign="middle" >199</td><td align="center" valign="middle" >99.6</td><td align="center" valign="middle" >438</td><td align="center" valign="middle" >99.5</td></tr><tr><td align="center" valign="middle"  colspan="7"  >Addiction History</td></tr><tr><td align="center" valign="middle" >None</td><td align="center" valign="middle" >232</td><td align="center" valign="middle" >96.7</td><td align="center" valign="middle" >200</td><td align="center" valign="middle" >100</td><td align="center" valign="middle" >432</td><td align="center" valign="middle" >98.2</td></tr><tr><td align="center" valign="middle" >Alcohol</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >2.1</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1.1</td></tr><tr><td align="center" valign="middle" >Smoking</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >1.3</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle"  colspan="7"  >Referral Department</td></tr><tr><td align="center" valign="middle" >Neuro</td><td align="center" valign="middle" >213</td><td align="center" valign="middle" >88.8</td><td align="center" valign="middle" >166</td><td align="center" valign="middle" >83</td><td align="center" valign="middle" >379</td><td align="center" valign="middle" >86.1</td></tr><tr><td align="center" valign="middle" >Others</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >11.3</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >61</td><td align="center" valign="middle" >13.9</td></tr></tbody></table></table-wrap><p>showed that diffuse neuronal dysfunction consistent with encephalopathy accounted for 27.2% while Mild neuronal dysfunction consistent with encephalopathy accounted for 20.2% of cases. EEG findings resulted in a change of diagnosis in the majority of patients (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Further, to check association of abnormal EEG with age independent sample t test was used, which shows strong significant difference with p value less than 0.01. Chi-Square was applied to check significance among abnormal EEG and gender which shows significant relationship with males with p value to 0.025.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> EEG procedure and diagnosis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >N</th><th align="center" valign="middle"  colspan="3"  >%</th></tr></thead><tr><td align="center" valign="middle"  colspan="5"  >Activation Procedure</td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >177</td><td align="center" valign="middle"  colspan="3"  >40.2</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >263</td><td align="center" valign="middle"  colspan="3"  >59.8</td></tr><tr><td align="center" valign="middle"  colspan="5"  >Provisional diagnosis provided</td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >114</td><td align="center" valign="middle"  colspan="3"  >25.9</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >326</td><td align="center" valign="middle"  colspan="3"  >74.1</td></tr><tr><td align="center" valign="middle"  colspan="5"  >EEG findings confirmed provisional diagnosis:</td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >0</td><td align="center" valign="middle"  colspan="3"  >0</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >440</td><td align="center" valign="middle"  colspan="3"  >100</td></tr><tr><td align="center" valign="middle"  colspan="5"  >EEG Diagnosis</td></tr><tr><td align="center" valign="middle"  rowspan="2"  ></td><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >Female</td><td align="center" valign="middle"  colspan="2"  >Combined</td></tr><tr><td align="center" valign="middle" >n</td><td align="center" valign="middle" >n</td><td align="center" valign="middle" >N</td><td align="center" valign="middle" >%</td></tr><tr><td align="center" valign="middle" >Normal</td><td align="center" valign="middle" >84</td><td align="center" valign="middle" >91</td><td align="center" valign="middle" >175</td><td align="center" valign="middle" >39.8</td></tr><tr><td align="center" valign="middle" >Abnormal</td><td align="center" valign="middle" >156</td><td align="center" valign="middle" >109</td><td align="center" valign="middle" >265</td><td align="center" valign="middle" >60.2</td></tr><tr><td align="center" valign="middle"  colspan="5"  >Specific diagnosis of the abnormal EEG record (n = 265)</td></tr><tr><td align="center" valign="middle" >Diffuse neuronal dysfunction consistent with encephalopathy</td><td align="center" valign="middle" >73</td><td align="center" valign="middle" >47</td><td align="center" valign="middle" >120</td><td align="center" valign="middle" >45.2</td></tr><tr><td align="center" valign="middle" >Mild neuronal dysfunction consistent with encephalopathy</td><td align="center" valign="middle" >49</td><td align="center" valign="middle" >40</td><td align="center" valign="middle" >89</td><td align="center" valign="middle" >33.5</td></tr><tr><td align="center" valign="middle" >Generalized seizure disorder</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >6.7</td></tr><tr><td align="center" valign="middle" >Epileptogenic Waves</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >5.2</td></tr><tr><td align="center" valign="middle" >intermittent slowing with excessive beta activity</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >3.7</td></tr><tr><td align="center" valign="middle" >Rare right sharp waves</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >2.2</td></tr><tr><td align="center" valign="middle" >Rare left fronto parietal sharp waves</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >Status Epilepticus</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >Rare left sided epileptiform</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.3</td></tr><tr><td align="center" valign="middle" >focal seizure disorder</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >mild non-encephalopathy neuronal dysfunction</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0.7</td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>The outcome of our study seems predictable with a couple interesting findings. The study shows that in our particular setup 60.2% of EEGs were considered abnormal whereas 39.8% were denounced normal. Initially, more seizure disorders were predicted before the study. However, after the study we see that the majority of patients suffer diffused or mild neuronal dysfunction with encephalopathy leading up to 47.4% of the cases. The mean age for patients using EEG came out to be approximately 53 years. Further observations point out that the main predisposing factors patients have are diabetes and hypertension and 74% of the time no provisional diagnosis is mentioned before a study.</p><p>More abnormal EEGs were the outcome. Our study shows that 60.2% of patients having abnormal readings. Compared to other studies it seems to be the norm to have more abnormal EEGs than normal ones. One Nigeria based study showed 56 percent of patients having epileptiform activity [<xref ref-type="bibr" rid="scirp.96233-ref14">14</xref>]. On the other hand, Nigeria seemed to have 32.4% abnormal EEGs [<xref ref-type="bibr" rid="scirp.96233-ref15">15</xref>]. Even though this particular study is out of the norm one thing to know is that normal EEGs do not rule out any epileptic disorders. For example, a study by Ahmed et al. showed that 35.6% of epileptic patients showed normal reading [<xref ref-type="bibr" rid="scirp.96233-ref16">16</xref>]. This reinforces the fact that even though the abnormal reading for our results were 60.2%, there could be several more patients in the normal readings with seizure disorders.</p><p>The mean age for our study seemed to be older than the normal. Majority of the patients were between the age brackets 25 - 64 which comprise of 44.54% of patients. In addition to this, 39.9% of patients were above 65 in our setup. This finding is unusual because most EEG studies seem to have patients younger than 30. For example a study by Ahmed et al. suggests that the majority of the patients were predominantly below 20 years of age [<xref ref-type="bibr" rid="scirp.96233-ref16">16</xref>]. Another study from Kathmandu suggests that 50 percent of patients ranged from 11 - 30 years [<xref ref-type="bibr" rid="scirp.96233-ref17">17</xref>]. This may be because most of the patients in these studies were found to have seizure disorder, whereas our particular setup had more patients with neuronal dysfunction and encephalopathy. This points out that our setup may simply have less seizure disorders which is why we have more people ranging 25 and above.</p><p>Out of the abnormal EEGs the main diagnosis seemed to be either 45.2% diffuse neuronal dysfunction with encephalopathy or 33.5% mild neuronal dysfunction with encephalopathy. These stats show that few patients in our setup had seizure disorders. However, several other studies have more seizure disorder patients during EEG. Not much research has been conducted on seizure disorders in Pakistan. Only one study looks at the aetiology of status epilepticus in patients [<xref ref-type="bibr" rid="scirp.96233-ref18">18</xref>]. It states that 14% of the patients had status epilepticus because of progressive encephalopathy. This correlates with our set up because it is possible that a small percentage of our patients are at risk for status epilepticus even though the patients studied in that research were children. More importantly, the results suggest that rather than using EEG for seizure disorders our population needs a higher focus on why there is neuronal dysfunction with encephalopathy. Johnson et al. states that encephalopathy is a state of unconsciousness that can have multiple causes such as the following: metabolic toxicity, drug toxicity, structural dysfunction of the brain or infection [<xref ref-type="bibr" rid="scirp.96233-ref19">19</xref>]. Based on each patient’s history, there needs to be an effort to figure out the cause that makes this finding prevalent. In addition, the finding of neuronal dysfunction can suggest further risk factors such as Alzheimer’s disease. For example, one longitudinal study stated that after following patients with mild neuronal dysfunction for three years EEG showed that some patients developed Alzheimer’s disease with more theta/delta waves [<xref ref-type="bibr" rid="scirp.96233-ref20">20</xref>]. In this study EEG was used as a prognostic tool, therefore this means that it can be used as a prognostic tool in our setup as well.</p><p>Hypertension and diabetes are the main predisposing factors patients come with before an EEG, therefore we can expect certain changes in EEG when managing a patient. Like current study reported majority of patients were having diabetes and hypertension. There is not much known about hypertension and its effects on EEG readings. However, according to an article Inova et al. we can expect decreased alpha rhythms from patients with hypertension [<xref ref-type="bibr" rid="scirp.96233-ref21">21</xref>]. Furthermore, another study suggests that in stressed hypertensive patients there can be reduced theta waves in the readings [<xref ref-type="bibr" rid="scirp.96233-ref22">22</xref>]. As a result, these studies show what changes we can expect for a predisposing hypertensive patient. In diabetes one can consider that factor as a contributor to metabolic encephalopathy. In one case report, hypoglycaemia showed signs of theta waves in a 45 year old patient [<xref ref-type="bibr" rid="scirp.96233-ref23">23</xref>]. This is important because these are diagnostic signs you can see in certain patients with diabetes as a predisposing factor. Hypoglycaemia can be related to mild neuronal dysfunction with encephalopathy [<xref ref-type="bibr" rid="scirp.96233-ref19">19</xref>]. This fact can allow us to come up with differentials when doing an EEG study on a diabetic.</p><p>In our setup 74% of the time no provisional diagnosis is stated. Furthermore, in our study the provisional diagnoses have never been confirmed by the EEG. Therefore, doctors must ask what they are screening for. EEG is considered a great screening tool with higher specificity when it comes to epilepsy [<xref ref-type="bibr" rid="scirp.96233-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.96233-ref15">15</xref>]. However, many researchers state that doctors do not know how to use EEG. One researcher states that non specialist try to use it as a diagnostic tool when clinicians should be using it as an aid in differentials [<xref ref-type="bibr" rid="scirp.96233-ref24">24</xref>]. In one study it stated that 26% of requests from physicians for EEG were considered inappropriate [<xref ref-type="bibr" rid="scirp.96233-ref25">25</xref>]. These facts state that maybe EEG is being overused. It does not mean that we should completely abstain from EEGs, rather we should take into consideration finances, need and proficiency before ordering one.</p><p>This study conducted gives us an idea on what to focus on and what to look out for. This study shows that in our particular setup older patients, usually hospitalized, will show probable signs of neuronal dysfunction with encephalopathy. Further, studies suggest that younger patients under 30 will probably show particular signs of seizure disorders. Not every case will be perfect, but these trends are something we can expect. Furthermore, we know in our hospital setup we should expect more neuronal dysfunction with encephalopathy. As a result, we can better management and treatment by looking into what is the cause of this particular finding. We would have to do a further study and increase the sample specifically for these patients. We also know that most patients that come in for an EEG are hypertensive or diabetic. Therefore, with this study we should look into what particular signs are specific for these predisposing factors. We can use this information to further study these patients on EEG. Finally, we see that EEGs are not matching the provisional diagnosis. Studies must be conducted to see whether the EEGs that are being ordered actually aid in the management and treatment of the patient or we can do away with them while reducing the cost of healthcare for our patients.</p><p>Limitation for the current study was that data was from one particular hospital setup. Similar studies should be done in different hospitals all over Pakistan to get better and more accurate results. Another limitation was the small sample size. It should be done on a larger scale so there is more data to analyse particularly correlations amongst causes and effects. There should also be comparison studies amongst provinces to see any particular ethnic variations.</p></sec><sec id="s5"><title>5. Conclusion</title><p>EEG still plays a vital role in the diagnosis of neuropsychiatric conditions in developing countries. EEGs can further help to determine the relationship of different neuropsychiatric conditions and can help in early diagnosis and better prognosis.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Mohammad, D., Zaidi, S.S., Fawad, B., Qureshi, M.F.H., Abubaker, Z.J., Shaikh, M.Z., Shah, M., Lakhani, M. and Sadiq, S. (2019) Frequency of Neurological Disorders and Related EEG Finding in a Tertiary Care Hospital of Karachi. 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