<?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">AID</journal-id><journal-title-group><journal-title>Advances in Infectious Diseases</journal-title></journal-title-group><issn pub-type="epub">2164-2648</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/aid.2015.51007</article-id><article-id pub-id-type="publisher-id">AID-54930</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Central Nervous System Tuberculosis: Clinical Characteristics and Outcome. A Saudi Tertiary Care Centre Experience
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>ohammad</surname><given-names>Bo Saeed</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>Adel</surname><given-names>Alothman</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>Suleiman</surname><given-names>Kojan</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>Suliman</surname><given-names>Almahmoud</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>Ali</surname><given-names>Al Khathaami</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>Mohammed</surname><given-names>Al Ghobain</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia</addr-line></aff><aff id="aff2"><addr-line>King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia</addr-line></aff><pub-date pub-type="epub"><day>16</day><month>02</month><year>2015</year></pub-date><volume>05</volume><issue>01</issue><fpage>63</fpage><lpage>71</lpage><history><date date-type="received"><day>24</day>	<month>February</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>18</month>	<year>March</year>	</date><date date-type="accepted"><day>24</day>	<month>March</month>	<year>2015</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: Tuberculosis is an endemic problem that is of important public health concern in Saudi Arabia. Available recent prevalence of tuberculosis (pulmonary and extra-pulmonary) was estimated to be 13.7 per 100,000 people living in the Kingdom of Saudi Arabia. Methods: A retrospective chart review of all Central Nervous System tuberculosis patients (CNS-TB) treated at King Abdulaziz Medical City, Riyadh, Saudi Arabia between 1996 and 2010. CNS-TB was defined as follows: patients who had symptoms and signs of CNS-TB with radiographic, microbiologic, or histopathologic evidence of tuberculous infection and/or those with highly probable diagnosis, supported by radiographic typical features, not confirmed microbiologically but who responded to anti-TB therapy. Results: Eighty two patients (46 males) met our definition with the mean age of 50 years. Only 11 patients (13.4%) reported previous TB infection. The most common presenting symptoms were: headache (51%), fever (50%), weakness (43%), confusion (29%) and seizures (28%). The most common signs found by clinical examination were: weakness (45%) followed by sensory impairment. Positive CSF acid-fast bacilli (AFB) culture confirmed the diagnosis in 20 out of 49 tested patients (about 41%). Brain CT scan was done in 74 patients and meningeal enhancement was identified in only 6 patients (8%) but ring enhancing lesions were found in 19 patients (26%). In MRI meningeal enhancement was founded in 26 patients (37%) and ring enhanced lesions in 36 patients (51%). After receiving treatment, 45 patients (55%) had complete or good recovery and 23 patients (28%) had partial recovery. However, 15% (12 patients) had poor or no improvement. 2 patients (2%) lost their follow up. Conclusion: CNS-TB continues to be a major health issue especially in endemic areas such as Saudi Arabia. The diverse clinical presentations, lack of high yield, practical and reliable diagnosis methods and inconsistent management plans require further research and harder work in order to meet the current challenges and reach a unified case definition and evidence based management guidelines that would be a very practical step.
 
</p></abstract><kwd-group><kwd>Tuberculosis</kwd><kwd> Central Nervous System</kwd><kwd> Saudi Arabia</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Tuberculosis (TB) continues to be one of the most important communicable diseases worldwide due to significant morbidity and mortality despite modern anti-tuberculosis chemotherapy. It accounted for 1.4 Million deaths worldwide in 2012 alone [<xref ref-type="bibr" rid="scirp.54930-ref1">1</xref>] . Central nervous system tuberculosis (CNS-TB), most severe form of extra-pul- monary TB, constitutes of 1% of all newly diagnosed TB cases [<xref ref-type="bibr" rid="scirp.54930-ref2">2</xref>] and about 6% of all extra-pulmonary TB in immunocompetent individuals [<xref ref-type="bibr" rid="scirp.54930-ref3">3</xref>] .</p><p>The pathogenesis of CNS-TB is poorly understood plus there are no rapid, sensitive and reliable diagnostic tests. In addition, delaying its diagnosis and/or treatment, often, leads to increased morbidity and mortality [<xref ref-type="bibr" rid="scirp.54930-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.54930-ref5">5</xref>] making it a very challenging and serious disorder [<xref ref-type="bibr" rid="scirp.54930-ref6">6</xref>] .</p><p>There are no standardized diagnostic criteria for CNS-TB and the available published case series are heterogeneous since different case definitions had been adopted [<xref ref-type="bibr" rid="scirp.54930-ref7">7</xref>] -[<xref ref-type="bibr" rid="scirp.54930-ref14">14</xref>] . Plus there are no randomized, controlled trials to determine optimal drug combination, dosage, or duration of anti-tuberculous chemotherapy. The current principles of CNS-TB treatment are those that govern the management of pulmonary TB [<xref ref-type="bibr" rid="scirp.54930-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.54930-ref16">16</xref>] .</p><p>In Saudi Arabia, tuberculosis is an endemic illness that is of important public health concern. Available recent prevalence in 2011 of tuberculosis (pulmonary and extra-pulmonary) was estimated to be 13.7 per 100,000 populations in Saudi Arabia [<xref ref-type="bibr" rid="scirp.54930-ref17">17</xref>] . Reported CNS-TB from Saudi Arabia varied widely between hospitals and at different time periods [<xref ref-type="bibr" rid="scirp.54930-ref18">18</xref>] . In 1982, Froude et al. found that CNS TB was the most common form in 162 patients diagnosed with extra-pulmonary TB [<xref ref-type="bibr" rid="scirp.54930-ref19">19</xref>] . More recently, Al-Otaibi et al. reviewed 248 patients diagnosed with extra-pulmonary TB at King Khalid University Hospital, Riyadh and CNS-TB accounted for 4.4% of extra- pulmonary TB cases admitted between 2001 and 2007 [<xref ref-type="bibr" rid="scirp.54930-ref20">20</xref>] .</p></sec><sec id="s2"><title>2. Methods</title><p>A retrospective chart review of all CNS-TB patients treated at King Abdulaziz Medical City (KAMC), Riyadh, Saudi Arabia between 1996 and 2010 inclusive. KAMC is a distinguished healthcare provider in Saudi Arabia with a capacity of more than 700 beds and located in Riyadh city. The study included the patients who was admitted and followed up in this hospital.</p><p>CNS-TB was defined as follows: patients who had symptoms and signs of CNS Tuberculosis with radiographic, microbiologic, or histopathologic evidence of tuberculous infection and/or those with highly probable diagnosis, supported by radiographic typical features, not confirmed microbiologically but who responded to anti-TB therapy.</p><p>Patient’s demography, presenting symptoms and signs, Cerebrospinal Fluid (CSF) parameters, radiological changes, treatment regimen, and final outcome were reviewed.</p><p>Patients’ outcome was classified as: 1) full or good recovery (resumption of patient’s normal life with no or minor neurological or psychological deficits); 2) partial recovery (mild to moderate disability, but independent activities of daily living); 3) poor or no improvement (dependent for activities of daily living due to moderate to severe mental or physical disability, including persistent vegetative state and death); 4) outcome status not available.</p><p>The data were entered into a Microsoft Excel spreadsheet. Statistical Analysis System SAS was used for data analysis.</p><p>The study was approved from King Abdullah International Medical Research Center at King Saud bin Abdulaziz University for Health Sciences before starting data collection as the study does not disclose patient identity, and poses no risks to patients (Reference N. RR11/054). This approval granted a permission to conduct the study and there was no need for informed consent from patients.</p></sec><sec id="s3"><title>3. Results and Discussion</title><p>A total of 124 patients, labeled as CNS-TB, were treated at KAMC-Riyadh between 1996 and 2010. However, only 82 patients (46 males 56%) met our case definition and the remaining 42 patients were excluded.</p><p>The mean age was 50 years. Only 11 patients (13.4%) reported previous TB infection. About one quarter of patients had at least one chronic co-morbid disorder such as diabetes mellitus (23%) and hypertension (26%) (<xref ref-type="table" rid="table1">Table 1</xref>).</p><sec id="s3_1"><title>3.1. Presentation</title><p>Time to diagnosis ranged from 1 day to 10 months (mean 38 days). The most common presenting symptoms were: headache (51%), fever (50%), weakness (43%), confusion (29%) and seizures (28%). Other symptoms such as nausea and vomiting presented in 8% and 32% respectively. 18% of patients presented with coma (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>The most common signs found by clinical examination were: weakness (45%) followed by sensory impairment. 23% of the patients were reported to have encephalopathy and impaired level of consciousness. Documented fever upon presentation was found in 35% of patients but meningeal signs were uncommon and only found in 12% of them (<xref ref-type="table" rid="table2">Table 2</xref>).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Characteristics of 82 patients with CNS-TB</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characteristic</th><th align="center" valign="middle" >n = 82 (%)</th></tr></thead><tr><td align="center" valign="middle" >Age (years)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Range</td><td align="center" valign="middle" >5 - 90 years</td></tr><tr><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >50 years</td></tr><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Males</td><td align="center" valign="middle" >46 (56%)</td></tr><tr><td align="center" valign="middle" >Females</td><td align="center" valign="middle" >36 (44%)</td></tr><tr><td align="center" valign="middle" >Past history of TB</td><td align="center" valign="middle" >11 (13%)</td></tr><tr><td align="center" valign="middle" >Pulmonary</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >Spine</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Miliary</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Peritoneal</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >Lymph nodes</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >CNS</td><td align="center" valign="middle" >2</td></tr><tr><td align="center" valign="middle" >Co-morbidities</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Diabetes Mellitus</td><td align="center" valign="middle" >19 (23%)</td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >21 (26%)</td></tr><tr><td align="center" valign="middle" >Chronic kidney disease</td><td align="center" valign="middle" >9 (11%)</td></tr><tr><td align="center" valign="middle" >Chronic liver disease</td><td align="center" valign="middle" >2 (2%)</td></tr><tr><td align="center" valign="middle" >Solid organ transplant</td><td align="center" valign="middle" >2 (2%)</td></tr><tr><td align="center" valign="middle" >Date of presentation</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >1996-1999</td><td align="center" valign="middle" >18 (22%)</td></tr><tr><td align="center" valign="middle" >2000-2005</td><td align="center" valign="middle" >34 (41%)</td></tr><tr><td align="center" valign="middle" >2006-2010</td><td align="center" valign="middle" >30 (37%)</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Clinical features of CNS tuberculosis patients</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Symptoms</th><th align="center" valign="middle" >n = 82 (%)</th></tr></thead><tr><td align="center" valign="middle" >-Constitutional:</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >・ Fever</td><td align="center" valign="middle" >41 (50%)</td></tr><tr><td align="center" valign="middle" >・ Weight loss</td><td align="center" valign="middle" >13 (16%)</td></tr><tr><td align="center" valign="middle" >・ Sweating</td><td align="center" valign="middle" >10 (12%)</td></tr><tr><td align="center" valign="middle" >・ Fatigue</td><td align="center" valign="middle" >7 (8%)</td></tr><tr><td align="center" valign="middle" >-Specific:</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >・ Headache</td><td align="center" valign="middle" >42 (51%)</td></tr><tr><td align="center" valign="middle" >・ Weakness</td><td align="center" valign="middle" >35 (43%)</td></tr><tr><td align="center" valign="middle" >・ Seizure</td><td align="center" valign="middle" >23 (28%)</td></tr><tr><td align="center" valign="middle" >・ Confusion</td><td align="center" valign="middle" >25 (30%)</td></tr><tr><td align="center" valign="middle" >・ Urine incontinence</td><td align="center" valign="middle" >5 (6%)</td></tr><tr><td align="center" valign="middle" >・ Dizziness</td><td align="center" valign="middle" >6 (7%)</td></tr><tr><td align="center" valign="middle" >・ Visual disturbance</td><td align="center" valign="middle" >4 (5%)</td></tr><tr><td align="center" valign="middle" >・ Photophobia</td><td align="center" valign="middle" >3 (3%)</td></tr><tr><td align="center" valign="middle" >・ Coma</td><td align="center" valign="middle" >15 (18%)</td></tr><tr><td align="center" valign="middle" >-Others:</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >・ Vomiting</td><td align="center" valign="middle" >26 (32%)</td></tr><tr><td align="center" valign="middle" >・ Anorexia</td><td align="center" valign="middle" >15 (18%)</td></tr><tr><td align="center" valign="middle" >・ Nausea</td><td align="center" valign="middle" >7 (8%)</td></tr><tr><td align="center" valign="middle" >Signs:</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >・ Fever</td><td align="center" valign="middle" >29 (35%)</td></tr><tr><td align="center" valign="middle" >・ Lymphadenopathy</td><td align="center" valign="middle" >3 (3%)</td></tr><tr><td align="center" valign="middle" >・ Impaired conscious level</td><td align="center" valign="middle" >19 (23%)</td></tr><tr><td align="center" valign="middle" >・ Disorientation</td><td align="center" valign="middle" >8 (9%)</td></tr><tr><td align="center" valign="middle" >・ Meningeal signs</td><td align="center" valign="middle" >10 (12%)</td></tr><tr><td align="center" valign="middle" >・ Neurological deficit</td><td align="center" valign="middle" >37 (45%)</td></tr><tr><td align="center" valign="middle" >Sensory</td><td align="center" valign="middle" >7 (8%)</td></tr><tr><td align="center" valign="middle" >Motor</td><td align="center" valign="middle" >37 (45%)</td></tr><tr><td align="center" valign="middle" >・ Ataxia</td><td align="center" valign="middle" >3 (3%)</td></tr></tbody></table></table-wrap></sec><sec id="s3_2"><title>3.2. Investigations</title><p>Tuberculin skin test was not performed routinely for our patients.</p><p>Lumbar puncture (LP) was performed, on the day of admission, in 59 patients (72%) (<xref ref-type="table" rid="table3">Table 3</xref>). The remaining patients were denied LP due increased procedure risk (symptoms and/or signs of increased intra-cranial pressure) or had alternative working diagnoses during the first admission day. The CSF white cell count (WBC) was elevated in 48 out of 59 tested patients (81%) with no specific differentials. Total CSF protein was elevated</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Cerebrospinal fluid characteristics</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >CSF protein g/L</th><th align="center" valign="middle" >n = 55 (%)</th></tr></thead><tr><td align="center" valign="middle" >High (&gt;0.40)</td><td align="center" valign="middle" >46 (83%)</td></tr><tr><td align="center" valign="middle" >Normal (0.15 - 0.40)</td><td align="center" valign="middle" >7 (13%)</td></tr><tr><td align="center" valign="middle" >Low (&lt;0.15)</td><td align="center" valign="middle" >2 (4%)</td></tr><tr><td align="center" valign="middle" >CSF: serum glucose ratio</td><td align="center" valign="middle" >n = 53 (%)</td></tr><tr><td align="center" valign="middle" >Less than 0.3</td><td align="center" valign="middle" >19 36%</td></tr><tr><td align="center" valign="middle" >0.3 - 0.6</td><td align="center" valign="middle" >24 45%</td></tr><tr><td align="center" valign="middle" >More than 0.6</td><td align="center" valign="middle" >10 19%</td></tr><tr><td align="center" valign="middle" >CSF AFB</td><td align="center" valign="middle" >n = 49 (%)</td></tr><tr><td align="center" valign="middle" >Smear positive</td><td align="center" valign="middle" >2 (4%)</td></tr><tr><td align="center" valign="middle" >Culture positive</td><td align="center" valign="middle" >20 (41%)</td></tr></tbody></table></table-wrap><p>in 46 out of 55 tested patients (83%). Very high protein level (above 3 g/L) was noticed in about 25% (14 patients). 33% (18 patients) had CSF glucose below the minimum reference value. The CSF to serum glucose ratio could be calculated in a total of 53 patients. The ratio was below 0.5 in 66% of these patients.</p><p>Only 2 patients had positive AFB smear in the CSF. Positive CSF Mycobacterium Tuberculosis MTB culture confirmed the diagnosis in 20 out of 49 tested patients (about 41%). Drug susceptibility testing for first line drugs was performed for all culture positive cases. Only one isolate (5%) was resistant to first line therapy (both Rifampicin and Isoniazid).</p><p>Other non-specific laboratory features such as leukocytosis (WBC &gt; 11.0 &#215; 10<sup>9</sup>/Liter), hyponatremia (sodium level below 135 mmol/L), were found in 23% and 52% respectively. In about 30% of the patients the serum sodium was significantly reduced (less than 130 mmol/L). Chest X-ray was performed in 76 patients and was found abnormal (mostly non-specific changes) in 27 cases (36%).</p><p>18 patients underwent meningeal and/or brain biopsies, which showed “Necrotizing Caseating Granuloma” in 11 patients (61%), non-specific inflammation in 11% and normal results in 28%. Biopsy tissues AFB stains were positive in 3 samples (17%) and MTB culture in 2 samples (11%).</p><p>Majority of patients had either cranial computed tomography (CT) or Magnetic resonance imaging (MRI). 63 patients had both scans performed during the same hospital stay. Brain CT scan was done in 74 patients and meningeal enhancement was identified in only 6 patients (8%) but ring enhancing lesions were found in 19 patients (26%). Tuberculoma like lesions were reported on 9% of the patients. Other findings such as hydrocephalus and brain edema were found in 28% and 38% respectively (<xref ref-type="table" rid="table4">Table 4</xref>). CT scan was normal in 13 patients, 9 of them had brain MRI performed, that had positive, additional diagnostic value by showing meningeal enhancement and/or ring enhancing lesions.</p><p>Brain MRI was done in 71 patients. 14% of the patients had tuberculomas, 17% hydrocephalus and 35% had brain edema. Meningeal enhancement was found in 26 patients (37%) and ring-enhanced lesions in 36 patients (51%) (<xref ref-type="table" rid="table4">Table 4</xref>).</p><p>Only two patients had both CT and MR scans normal.</p></sec><sec id="s3_3"><title>3.3. Treatment</title><p>Standard treatment regimen as per the recommendations of American and British Thoracic Societies, Infectious Disease Society of America, and the U.S. Centers for Disease Control and Prevention was applied [<xref ref-type="bibr" rid="scirp.54930-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.54930-ref16">16</xref>] . Patients received an initial two month course of intensive therapy using the four first line therapies (Isoniazid, Rifampicin, Pyrazinamide, and Ethambutol) followed by a prolonged course lasting 7 - 10 months, of 2 drugs (Isoniazid and Rifampicin) based on clinical response and established drug sensitivity of the isolate.</p><p>Therefore almost all the patients received Isoniazid (INH) and Rifampicin initially but only 70% continued these 2 medications for full course therapy. Ethambutol and Pyrazinamide were used in 88% and 94% respectively. The first line therapy was stopped due to significant adverse effects (e.g. Drug induced hepatitis occurred</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Neuroradiological findings of patients where both MRI &amp; CT was performed</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="3"  >WITHOUT contrast n = 63 (%)</th></tr></thead><tr><td align="center" valign="middle" >Findings</td><td align="center" valign="middle" >CT scan</td><td align="center" valign="middle" >MRI</td></tr><tr><td align="center" valign="middle" >Tubercoloma</td><td align="center" valign="middle" >4 (6%)</td><td align="center" valign="middle" >7 (11%)</td></tr><tr><td align="center" valign="middle" >Hydrocephalus</td><td align="center" valign="middle" >18 (28%)</td><td align="center" valign="middle" >12 (19%)</td></tr><tr><td align="center" valign="middle" >Edema</td><td align="center" valign="middle" >23 (36%)</td><td align="center" valign="middle" >24 (38%)</td></tr><tr><td align="center" valign="middle" >Stroke</td><td align="center" valign="middle" >7 (11%)</td><td align="center" valign="middle" >7 (11%)</td></tr><tr><td align="center" valign="middle"  colspan="3"  >WITH contrast n = 54 (%)</td></tr><tr><td align="center" valign="middle" >Meningeal enhancement</td><td align="center" valign="middle" >6 (11%)</td><td align="center" valign="middle" >20 (37%)</td></tr><tr><td align="center" valign="middle" >Ring enhancing lesions</td><td align="center" valign="middle" >14 (26%)</td><td align="center" valign="middle" >30 (55%)</td></tr><tr><td align="center" valign="middle" >Non-ring enhancing lesions</td><td align="center" valign="middle" >17 (31%)</td><td align="center" valign="middle" >12 (22%)</td></tr></tbody></table></table-wrap><p>in 18 patients (22%)), or lack of response or resistance. Alternative medications used included Ciprofloxacin in 10 patients and Moxifloxacin in 13. Amikacin was added to the regimen used to treat the single patient with multi-drug resistant TB. Corticosteroids were used in 62 patients (76%).</p></sec><sec id="s3_4"><title>3.4. Clinical Outcome</title><p>Average hospital length of stay was 39 days. About a third of patients required Intensive Care Unit (ICU) admission with an average of 20 days spent in the ICU (<xref ref-type="table" rid="table5">Table 5</xref>).</p><p>Post discharge patients were followed in the outpatient clinics for at least 12 months. 68 patients (83%) had favorable outcome. 45 patients (55%) had complete or good recovery and 23 patients (28%) had partial recovery. However, 12 patients (15%) had poor or no improvement. 2 patients (2%) lost their follow up. 30 day mortality rate was 8.5% (7 patients had died).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Early recognition, diagnosis and treatment are essential. However, CNS TB remains a very challenging infection due to variable, often non-specific, symptoms and signs, prolonged symptoms prior to presentation (from days to months) and lack of time efficient specific testing [<xref ref-type="bibr" rid="scirp.54930-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.54930-ref22">22</xref>] . Tuberculosis of the CNS showed variable results in diagnosis measures, management response, and prognosis comparing to other sites of the infection (e.g. spine).</p><p>Our case definition of CNS TB was based on previous studies in which similar case definition was used [<xref ref-type="bibr" rid="scirp.54930-ref23">23</xref>] . Still there is no recognized international CNS TB case definition but a trial of making a consensus case definition has been done based on experts meeting few years ago [<xref ref-type="bibr" rid="scirp.54930-ref24">24</xref>] . The different case definitions used in various studies make the comparison of research findings somewhat difficult but in general our study showed different data in regarding of the disease behavior and outcome comparing to other limited local results [<xref ref-type="bibr" rid="scirp.54930-ref18">18</xref>] -[<xref ref-type="bibr" rid="scirp.54930-ref20">20</xref>] .</p><p>Available investigations, although often helpful, are time consuming plus there is no single test modality that is highly sensitive and/or specific. The gold standard diagnostic test is to culture the MTB from the CSF or the tissue that may take longer time that would significantly delay the diagnosis confirmation and starting treatment. AFB smear positivity would have saved significant amount of time and/or resources but this was rarely positive (4%) “Section 3.2”. Brain and/or meningeal biopsy, an invasive potentially harmful procedure, helped confirming the diagnosis in a number of patients. Other tests, i.e. CSF leukocyte count, total protein concentration, glucose ratio and serum sodium levels are neither highly sensitive nor specific.</p><p>Available imaging modalities are helpful to make the diagnosis and monitor therapy response. As in “Section 3.2”, MRI compared to CT scan, proved more sensitive for identifying meningeal enhancement (37% vs. 11% respectively) and ring enhancing lesions (55% vs. 26% respectively). Although some experts have suggested outcome predictor value of brain imaging at the time of diagnosis particularly with CT modality, however, these were not reliable or validated. Especially in those who develop imaging predictors particularly by CT images [<xref ref-type="bibr" rid="scirp.54930-ref25">25</xref>] -[<xref ref-type="bibr" rid="scirp.54930-ref27">27</xref>] .</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Outcome of 82 patients with CNS tuberculosis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >n = 82 (%)</th></tr></thead><tr><td align="center" valign="middle" >Hospital stay</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Range</td><td align="center" valign="middle" >4 days - 17 months</td></tr><tr><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >39 days</td></tr><tr><td align="center" valign="middle" >ICU admission</td><td align="center" valign="middle" >27 (33%)</td></tr><tr><td align="center" valign="middle" >Rang</td><td align="center" valign="middle" >1 day - 3 months</td></tr><tr><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >20 days</td></tr><tr><td align="center" valign="middle" >Response to Anti-TB</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Full recovery</td><td align="center" valign="middle" >45 (55%)</td></tr><tr><td align="center" valign="middle" >Partial recovery</td><td align="center" valign="middle" >23 (28%)</td></tr><tr><td align="center" valign="middle" >No improvement</td><td align="center" valign="middle" >12 (15%)</td></tr><tr><td align="center" valign="middle" >Lost follow up</td><td align="center" valign="middle" >2 (2%)</td></tr><tr><td align="center" valign="middle" >30-day mortality</td><td align="center" valign="middle" >7 (8.5%)</td></tr></tbody></table></table-wrap><p>Tuberculosis infection had been fatal until specific anti-TB drugs were discovered in the second half of the 20th century. However, both mortality and morbidity continue to be high reaching 60% particularly in developing countries. Complications can be seen in 25% of survivors despite five major and numerous minor drug options available [<xref ref-type="bibr" rid="scirp.54930-ref12">12</xref>] -[<xref ref-type="bibr" rid="scirp.54930-ref28">28</xref>] . A delay in starting anti-tuberculosis medications is associated with a higher rate of mortality and serious neurological complications in survivors. In the absence of a rapid and highly sensitive test, decision to initiate treatment is often made before the diagnosis is been confirmed.</p><p>In comparing of the disease outcome, the mortality rate in our cases was significantly lower than other reported case series and 83% of our patients had a favorable outcome [<xref ref-type="bibr" rid="scirp.54930-ref29">29</xref>] -[<xref ref-type="bibr" rid="scirp.54930-ref31">31</xref>] .</p><p>It should be noted that in our study has a limitation of being only descriptive of an original data. It is retrospective chart review with some limitation of reaching all the desired information. No logistic regression analysis or advanced statistical tests were done. Further prospective studies and clinical trials are required for getting closer to understand the specifics of this disease.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Central nervous system tuberculosis continues to be a major health issue especially in endemic areas such as Saudi Arabia. The diverse clinical presentations, lack of high yield, practical and reliable diagnosis methods and inconsistent management plans require further research and harder work in order to meet the current challenges and reach a unified case definition and evidence based management guidelines that would be a very practical step.</p></sec><sec id="s6"><title>Competing Interests</title><p>The authors declare that they have no competing interests.</p></sec><sec id="s7"><title>List of Abbreviations</title><p>Tuberculosis (TB)</p><p>Central nervous system tuberculosis (CNS-TB)</p><p>Cerebrospinal Fluid (CSF)</p><p>Lumbar puncture (LP)</p><p>Mycobacterium tuberculosis (MTB)</p><p>White blood cells (WBC)</p><p>Acid-fast bacilli (AFB)</p><p>Cranial computed tomography (CT)</p><p>Magnetic resonance imaging (MRI)</p><p>Isoniazid (INH)</p><p>Intensive care unit (ICU)</p></sec><sec id="s8"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.54930-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">World Health Organization (2012) Global Tuberculosis Database. www.who.int/tb/publications/global_report/en/index.html</mixed-citation></ref><ref id="scirp.54930-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Phypers, M., Harris, T. and Power, C. (2006) CNS Tuberculosis: A Longitudinal Analysis of Epidemiological and Clinical Features. International Journal of Tuberculosis and Lung Disease, 10, 99-103.</mixed-citation></ref><ref id="scirp.54930-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">CDC (2012) Reported Tuberculosis in the United States, 2011. US Department of Health and Human Services, Atlanta.</mixed-citation></ref><ref id="scirp.54930-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Al-Otaibi, F. and El Hazmi, M.M. (2010) Extra-Pulmonary Tuberculosis in Saudi Arabia. Indian Journal of Pathology and Microbiology, 53, 227-231. http://dx.doi.org/10.4103/0377-4929.64327</mixed-citation></ref><ref id="scirp.54930-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Kennedy, D.H. and Fallon, R.J. (1979) Tuberculous Meningitis. JAMA, 241, 264-268. http://dx.doi.org/10.1001/jama.1979.03290290032021</mixed-citation></ref><ref id="scirp.54930-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Thwaites, G.E., Chau, T.T.H., Stepniewska, K., Phu, N.H., Chuong, L.V., Sinh, D.X., et al. (2002) Diagnosis of Adult Tuberculous Meningitis by Use of Clinical and Laboratory Features. Lancet, 360, 1287-1292. http://dx.doi.org/10.1016/S0140-6736(02)11318-3</mixed-citation></ref><ref id="scirp.54930-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Alothman, A., Memish, Z.A., Awada, A., Al Mahmood, S., Al Sadoon, S., Rahman, M.M. and Khan, M.Y. (2001) Tuberculous Spondylitis: Analysis of 69 Cases from Saudi Arabia. Spine, 26, 565-570. http://dx.doi.org/10.1097/00007632-200112150-00020</mixed-citation></ref><ref id="scirp.54930-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Marais, S., Thwaites, G., Schoeman, J.F., Torok, M.E., Misra, U.K., Prasad, K., et al. (2010) Tuberculous Meningitis: A Uniform Case Definition for Use in Clinical Research. Lancet Infectious Diseases, 10, 803-812. http://dx.doi.org/10.1016/S1473-3099(10)70138-9</mixed-citation></ref><ref id="scirp.54930-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Toeh, R., Humphries, M.J., Hoare, R.D. and O’Mahony, G. (1989) Clinical Correlation of CT Changes in 64 Chinese Patients with Tuberculous Meningitis. Journal of Neurology, 236, 48-51. http://dx.doi.org/10.1007/BF00314218</mixed-citation></ref><ref id="scirp.54930-ref10"><label>10</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Jie</surname><given-names> L. </given-names></name>,<etal>et al</etal>. (<year>1988</year>)<article-title>Computerized Tomography in Tuberculous Meningitis</article-title><source> Chinese Medical Journal</source><volume> 101</volume>,<fpage> 388</fpage>-<lpage>390</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.54930-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Trautmann, M., Kluge, W., Otto, H.S. and Loddenkemper, R. (1986) Computed Tomography in CNS Tuberculosis. European Neurology, 25, 91-97. http://dx.doi.org/10.1159/000115993</mixed-citation></ref><ref id="scirp.54930-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Kent, S.J., Crowe, S.M., Yung, A., Lucas, C.R. and Mijch, A.M. (1993) Tuberculous Meningitis: A 30-Year Review. Clinical Infectious Diseases, 17, 987-994. http://dx.doi.org/10.1093/clinids/17.6.987</mixed-citation></ref><ref id="scirp.54930-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Sütlas, P.N., Unal, A., Forta, H., Senol, S. and Kirbas, D. (2003) Tuberculous Meningitis in Adults: Review of 61 Cases. Infection, 31, 387-391.</mixed-citation></ref><ref id="scirp.54930-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Christensen, A.S.H., Andersen, A.B., Thomsen, V.O., Andersen, P.H. and Johansen, I.S. (2011) Tuberculous Meningitis in Denmark: A Review of 50 Cases. BMC Infectious Diseases, 11, 47. http://dx.doi.org/10.1186/1471-2334-11-47</mixed-citation></ref><ref id="scirp.54930-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Anderson, N.E., Somaratne, J., Mason, D.F., Holland, D. and Thomas, M.G. (2010) A Review of Tuberculous Meningitis at Auckland City Hospital, New Zealand. Journal of Clinical Neuroscience, 17, 1018-1022. http://dx.doi.org/10.1016/j.jocn.2010.01.007</mixed-citation></ref><ref id="scirp.54930-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Froude, J.R. and Kingston, M. (1982) Extrapulmonary Tuberculosis in Saudi Arabia, a Review of 162 Cases. King Faisal Specialized Hospital Medical Journal, 2, 85-95.</mixed-citation></ref><ref id="scirp.54930-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Alrajhi, A.A. and Al-Barrak, A.M. (2002) Extrapulmonary Tuberculosis, Epidemiology and Patterns in Saudi Arabia. Saudi Medical Journal, 23, 503-508.</mixed-citation></ref><ref id="scirp.54930-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Ministry of Health KSA (2011) Health Statistical Year Book. www.moh.gov.sa</mixed-citation></ref><ref id="scirp.54930-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Blumberg, H.M., Burman, W.J., Chaisson, R.E., et al. (2003) American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America: Treatment of Tuberculosis. American Journal of Respiratory and Critical Care Medicine, 167, 603-662. http://dx.doi.org/10.1164/rccm.167.4.603</mixed-citation></ref><ref id="scirp.54930-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Joint Tuberculosis Committee of the British Thoracic Society (1998) Chemotherapy and Management of Tuberculosis in the United Kingdom: Recommendations 1998. Thorax, 53, 536-548.</mixed-citation></ref><ref id="scirp.54930-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Torok, M.E., Chau, T.T., Mai, P.P., Duy Phong, N., Thi Dung, N., Van Chuong, L., et al. (2008) Clinical and Microbiological Features of HIV-Associated Tuberculous Meningitis in Vietnamese Adults. PLoS ONE, 3, e1772.</mixed-citation></ref><ref id="scirp.54930-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">van der Weert, E.M., Hartgers, N.M., Schaaf, H.S., Eley, B.S., Pitcher, R.D., Wieselthaler, N.A., et al. (2006) Comparison of Diagnostic Criteria of Tuberculous Meningitis in Human Immunodeficiency Virus-Infected and Uninfected Children. Pediatric Infectious Disease Journal, 25, 65-69. http://dx.doi.org/10.1097/01.inf.0000183751.75880.f8</mixed-citation></ref><ref id="scirp.54930-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Thwaites, G.E., Bang, N.D., Dung, N.H., Thi Quy, H., Oanh, D.T.T., Cam Thoa, N.T., et al. (2004) Dexamethasone for the Treatment of Tuberculous Meningitis in Adolescents and Adults. New England Journal of Medicine, 351, 1741-1751. http://dx.doi.org/10.1056/NEJMoa040573</mixed-citation></ref><ref id="scirp.54930-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Kalita, J., Misra, U.K. and Ranjan, P. (2007) Predictors of Long-Term Neurological Sequelae of Tuberculous Meningitis: A Multivariate Analysis. European Journal of Neurology, 14, 33-37. http://dx.doi.org/10.1111/j.1468-1331.2006.01534.x</mixed-citation></ref><ref id="scirp.54930-ref25"><label>25</label><mixed-citation publication-type="other" xlink:type="simple">Saitoh, A., Pong, A., Waecker Jr., N.J., Leake, J.A., Nespeca, M.P. and Bradley, J.S. (2005) Prediction of Neurologic Sequelae in Childhood Tuberculous Meningitis: A Review of 20 Cases and Proposal of a Novel Scoring System. The Pediatric Infectious Disease Journal, 24, 207-212. http://dx.doi.org/10.1097/01.inf.0000154321.61866.2d</mixed-citation></ref><ref id="scirp.54930-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Karande, S., Gupta, V., Kulkarni, M. and Joshi, A. (2005) Prognostic Clinical Variables in Childhood Tuberculous Meningitis: An Experience from Mumbai, India. Neurology India, 53, 191-195. http://dx.doi.org/10.4103/0028-3886.16407</mixed-citation></ref><ref id="scirp.54930-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">van Well, G.T., Paes, B.F., Terwee, C.B., et al. (2009) Twenty Years of Pediatric Tuberculous Meningitis: A Retrospective Cohort Study in the Western Cape of South Africa. Pediatrics, 123, e1-e8. http://dx.doi.org/10.1542/peds.2008-1353</mixed-citation></ref><ref id="scirp.54930-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Marais, S., Thwaites, G., Schoeman, J.F., Torok, M.E., Misra, U.K., et al. (2010) Tuberculous Meningitis: A Uniform Case Definition for Use in Clinical Research. The Lancet Infectious Diseases, 10, 803-812. http://dx.doi.org/10.1016/S1473-3099(10)70138-9</mixed-citation></ref><ref id="scirp.54930-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Thwaites, G.E. and Tran, T.H. (2005) Tuberculous Meningitis: Many Questions, Too Few Answers. Lancet Neurology, 4, 160-170. http://dx.doi.org/10.1016/S1474-4422(05)70019-3</mixed-citation></ref><ref id="scirp.54930-ref30"><label>30</label><mixed-citation publication-type="other" xlink:type="simple">Thwaites, G., Chau, T.T.H., Mai, N.T.H., et al. (2000) Tuberculous Meningitis. Journal of Neurology, Neurosurgery &amp; Psychiatry, 68, 289-299. http://dx.doi.org/10.1136/jnnp.68.3.289</mixed-citation></ref><ref id="scirp.54930-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Hosoglu, S., Geyik, M.F., Balik, I., et al. (2002) Predictors of Outcome in Patients with Tuberculous Meningitis. International Journal of Tuberculosis and Lung Disease, 6, 64-70.</mixed-citation></ref></ref-list></back></article>