<?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">OJNeph</journal-id><journal-title-group><journal-title>Open Journal of Nephrology</journal-title></journal-title-group><issn pub-type="epub">2164-2842</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojneph.2022.121011</article-id><article-id pub-id-type="publisher-id">OJNeph-115735</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>
 
 
  Spectrum of Neurological Disorders amongst Patients on Maintenance Haemodialysis in Douala, Cameroon: A Cross-Sectional Study
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Halle</surname><given-names>Marie Patrice</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>Tchouamou</surname><given-names>Tchouamou Eric Gildas</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Fouda</surname><given-names>Hermine</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Gams</surname><given-names>Massi Daniel</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ngamby</surname><given-names>Vincent Ebenezer</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tewafeu</surname><given-names>Denis</given-names></name><xref ref-type="aff" rid="aff6"><sup>6</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Kaze</surname><given-names>Folefack Francois</given-names></name><xref ref-type="aff" rid="aff7"><sup>7</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mapoure</surname><given-names>Njankouo Yacouba</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Internal Medicine, Douala General Hospital, Douala, Cameroon</addr-line></aff><aff id="aff7"><addr-line>Yaounde Teaching Hospital, Yaounde, Cameroon</addr-line></aff><aff id="aff6"><addr-line>Department of Internal Medicine, Regional Hospital of Buea, Buea, Cameroon</addr-line></aff><aff id="aff4"><addr-line>Faculty of Health Sciences, University of Buea, Buea, Cameroon</addr-line></aff><aff id="aff2"><addr-line>Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon</addr-line></aff><aff id="aff5"><addr-line>Department of Internal Medicine, Douala Laquintinie Hospital, Douala, Cameroon</addr-line></aff><aff id="aff3"><addr-line>Faculty of Medicine and Biomedical Sciences, University of Yaounde I, Yaounde, Cameroon</addr-line></aff><pub-date pub-type="epub"><day>12</day><month>01</month><year>2022</year></pub-date><volume>12</volume><issue>01</issue><fpage>112</fpage><lpage>123</lpage><history><date date-type="received"><day>5,</day>	<month>February</month>	<year>2022</year></date><date date-type="rev-recd"><day>6,</day>	<month>March</month>	<year>2022</year>	</date><date date-type="accepted"><day>9,</day>	<month>March</month>	<year>2022</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>
 
 
  Context: Neurologic disorders are common in patients on maintenance haemodialysis (MHD). Data in Sub-Saharan Africa are scarce. 
  Aim: To determine the prevalence and associated factors of neurological disorders amongst patients on MHD in Cameroon. 
  Settings and Design: This was a four-month cross-sectional study carried out at the Douala General Hospital (DGH) a tertiary referral hospital in Cameroon. 
  Methods: The diagnosis of neuropathy was made using the Michigan Neuropathy Screening Instrument (MNSI), neuropathic pain with the DN4 score, Restless Legs Syndrome (RLS) with the International Restless Legs Syndrome Study Group questionnaire (IRLSSG) and cognitive disorders with the Mini-Mental State Examination test (MMS). Student T and Chi-square tests were used to compare qualitative and quantitative variables. The level of significance was set at p &lt; 0.05. 
  Results: A total of 157 patients were included with 65% being males. The mean age was 48.8 &#177; 13.7 years. The main comorbidities were hypertension (90.4%), diabetes (19.1%), hepatitis C (10.5%) and HIV infection (10.8%). The median dialysis vintage was 36 (1 - 178) months. The overall prevalence of neurological disorders was 85.4%. The leading type was sensory polyneuropathy (57.3%), cognitive dysfunction (52.9%), neuropathic pain (23%), and restless legs syndrome (17.8%). Male gender was statistically associated with neuropathic pain, while age ≥ 40 years and diabetes were associated with sensory neuropathy and RLS. 
  Conclusions: The burden of neurological disorders is high among patients on MHD as up to 4/5 of them had neurological involvement dominated by sensory polyneuropathy and cognitive dysfunction.
 
</p></abstract><kwd-group><kwd>Neurological Disorder</kwd><kwd> Haemodialysis</kwd><kwd> Prevalence</kwd><kwd> Cameroon</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Chronic kidney disease (CKD) is a worldwide public health problem with an 8% to 10% prevalence in the adult population [<xref ref-type="bibr" rid="scirp.115735-ref1">1</xref>]. Data in Africa are rare but the hospital-based prevalence in sub-Saharan Africa is estimated between 2% and 12% [<xref ref-type="bibr" rid="scirp.115735-ref2">2</xref>]. CKD accounted for 1% - 5% of global deaths in 2017 and was the 12th leading cause of death globally [<xref ref-type="bibr" rid="scirp.115735-ref3">3</xref>]. CKD progress in five stages and at end-stage, renal replacement therapy (RRT) either dialysis or renal transplantation is necessary for survival [<xref ref-type="bibr" rid="scirp.115735-ref4">4</xref>].</p><p>Haemodialysis (HD) is the main modality of RRT [<xref ref-type="bibr" rid="scirp.115735-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref6">6</xref>]. The outcome of patients on HD is characterized by a high morbidity and mortality rate [<xref ref-type="bibr" rid="scirp.115735-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref9">9</xref>] mainly due to comorbidities and HD complications [<xref ref-type="bibr" rid="scirp.115735-ref10">10</xref>]. These complications affect all body systems, especially the cardiovascular and nervous systems [<xref ref-type="bibr" rid="scirp.115735-ref11">11</xref>]. Neurological complications affect both the central nervous system such as stroke, cognitive dysfunction, and encephalopathy, and the peripheral nervous systems such as autonomic and peripheral neuropathies [<xref ref-type="bibr" rid="scirp.115735-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref13">13</xref>]. These complications are mainly related to uremic toxins, dialysate type, water quality and HD follow-up [<xref ref-type="bibr" rid="scirp.115735-ref13">13</xref>]. They are found in almost 60% of patients with kidney failure (KF) patients [<xref ref-type="bibr" rid="scirp.115735-ref14">14</xref>]. These complications are generally underdiagnosed and consequently less treated, contributing to the morbidity and mortality of affected patients [<xref ref-type="bibr" rid="scirp.115735-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref13">13</xref>]. In Cameroon, HD is the only RRT available and has been expanded considerably in the last decade with an increasing number of patients undergoing this treatment. The mortality rate is high and estimated at 26.8% [<xref ref-type="bibr" rid="scirp.115735-ref15">15</xref>]. Data on neurological disorders amongst KF patients in Sub Sahara Africa are rare. This study aimed to determine the prevalence and factors associated with neurological disorders amongst patients on maintenance HD in a tertiary hospital in Cameroon.</p></sec><sec id="s2"><title>2. Subjects and Methods</title><sec id="s2_1"><title>2.1. Study Setting and Participants</title><p>This was a cross-sectional study carried out from January 1<sup>srt</sup> to 3<sup>rd</sup> April 2018 in the haemodialysis and neurology units of the Douala General Hospital. At the time of the study, the center was equipped with 25 Fresenius 4008S generators (Fresenius Medical Care, Hamburg, Germany), synthetic polysulfone dialysis membrane; and bicarbonate dialysate. The center had 2 nephrologists, 1 general practitioner, and 12 nursing staff, and opens from Monday to Saturday, runs 3 dialysis shifts a day and offers to registered patients two 4-hour dialysis sessions per week. All consenting patients with KF on maintenance haemodialysis (MHD) were included. For each patient, socio-demographic characteristics (age, gender, occupation, matrimonial status, residence, educational level, existence of health insurance), comorbidities such as diabetes, hypertension, HIV infection, hepatitis B and C, systemic diseases (lupus), gout, neurological pathologies (Stroke, Dementia). Presumed cause of KF, duration on dialysis, and current treatment were obtained from patient’s files. Neurological disorders detected after dialysis initiation were also recorded.</p><p>A complete neurologic examination was done by a neurologist The Mini-Mental Status (MMS) was used to diagnose cognitive impairment [<xref ref-type="bibr" rid="scirp.115735-ref16">16</xref>] and for neuropathy the Michigan Neuropathy Screening Instrument (MNSI) was used [<xref ref-type="bibr" rid="scirp.115735-ref17">17</xref>], the International Restless Legs Syndrome Study Group questionnaire for the restless legs syndrome (IRLSSG) [<xref ref-type="bibr" rid="scirp.115735-ref18">18</xref>], and the DN4 score for neuropathic pain [<xref ref-type="bibr" rid="scirp.115735-ref19">19</xref>]. Tinel and Phalen’s manoeuvres were used to diagnose carpal tunnel syndrome. Assessment of the autonomic nervous system was based on the patient’s history and the Valsalva manoeuvre used to assess orthostatic hypotension. Co-morbidity evaluation was done using Charlson’s score [<xref ref-type="bibr" rid="scirp.115735-ref20">20</xref>].</p></sec><sec id="s2_2"><title>2.2. Statistical Analysis</title><p>Data were analyzed using the Statistical Package for Social Sciences (SPSS) Standard version, Release 20.0 (IBM Inc. 2012, Armonk, NY). Quantitative variables were expressed as means with standard deviation. The Student’s T-test was used to compare means and the Chi-Square test to compare qualitative variables. Statistical significance was set at a p &lt; 0.05.</p></sec><sec id="s2_3"><title>2.3. Operational Definition of Terms</title><p>- Neuropathic pain was defined by a DN4 score ≥ 4.</p><p>- Orthostatic hypotension was defined, as a decrease of systolic blood pressure of more than 20 mmHg and/or a decrease of diastolic blood pressure of more than 10 mm Hg within 3 minutes of standing without modification of the heart rate.</p><p>- Carpal tunnel syndrome was considered in every patient with a positive Phalen and/or Tinel sign associated with acroparesthesia on the sensory distribution of the median nerve associated or not with atrophy of the thumb muscles.</p><p>- Restless legs syndrome was considered in every patient with an IRLSSG score &gt; 4 for obligatory diagnostic criteria.</p><p>- Neuropathy was considered in every patient with an MNSI Score &gt; 3 on clinical examinations and/or greater than 7 on the questionnaire.</p><p>- Cognitive impairment was considered in all patients with a mini-mental state examination (MMS) score less than that recommended for his/her level of education. The threshold values for normality were 19 for patients who benefited from 0 to 4 years of education, 23 for those with 5 to 8 years of education, 27 for patients with 9 to 12 years of education, 29 for patients who graduated from high school. Based on the score, cognitive impairment was classified as followed: absent if score between 29 to 26, mild (25 to 20), moderate (19 to 16) and dementia (≤15).</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Baseline Characteristics of the Study Population</title><p>We included 157 patients with KF on MHD, of whom 107 (68.15%) were males. The mean age was 48.8 (13.7) years. A total of 66/157 (42%) patients were unemployed, and only 11/157 (7%) had a health insurance. Half (50.3%) of the participants had a secondary level of education. Hypertension (142/157; 90.2%) was the most frequent co-morbidity, followed by diabetes 30/157 (19.1%) (<xref ref-type="table" rid="table1">Table 1</xref>). The main past neurological history was stroke (8.9%) with 50% of cases occurring after dialysis initiation. The mean comorbidity score was 4.25 &#177; 2.31, with 26.1% of patients having scores ranging from high to very high. The median duration on dialysis was 36 (1 - 178) months.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Baseline characteristics of the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Variable</th><th align="center" valign="middle" >Frequency n N = 157</th><th align="center" valign="middle" >Percentage (%) 100</th></tr></thead><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >107</td><td align="center" valign="middle" >68.15</td></tr><tr><td align="center" valign="middle" >Health insurance</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >07</td></tr><tr><td align="center" valign="middle" >Unemployed</td><td align="center" valign="middle" >66</td><td align="center" valign="middle" >42</td></tr><tr><td align="center" valign="middle" >Secondary level of education</td><td align="center" valign="middle" >79</td><td align="center" valign="middle" >50.3</td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >142</td><td align="center" valign="middle" >90.4</td></tr><tr><td align="center" valign="middle" >Diabetes mellitus</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >19.1</td></tr><tr><td align="center" valign="middle" >Hepatitis C</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >10.8</td></tr><tr><td align="center" valign="middle" >HIV infection</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >10.8</td></tr><tr><td align="center" valign="middle" >Gout</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >9.6</td></tr><tr><td align="center" valign="middle" >Hepatitis B</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >5.1</td></tr><tr><td align="center" valign="middle" >Past neurological illness</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >11.5</td></tr><tr><td align="center" valign="middle" >Stroke</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >8.9</td></tr><tr><td align="center" valign="middle" >Facial palsy</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.6</td></tr><tr><td align="center" valign="middle" >Paraparesis</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.6</td></tr><tr><td align="center" valign="middle" >Parkinsonian syndrome</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.6</td></tr><tr><td align="center" valign="middle" >Meningioma</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.6</td></tr></tbody></table></table-wrap></sec><sec id="s3_2"><title>3.2. Prevalence of Neurological Disorders and Associated Factors</title><p>After clinical evaluation, tremors account was present in 24.8% of patients followed by myoclonus (9%). Plastic hypertonia was present in 2.5% of patients and hyporeflexia/areflexia was the most reflex jerk abnormality encountered (48.4%). Cranial nerve VIII was the main involved nerve (8.9%) and orthostatic hypotension was found in 15.9% of case (<xref ref-type="table" rid="table2">Table 2</xref>).</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Neurological signs amongst study participants</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Signs</th><th align="center" valign="middle" >Frequency (n)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Motor signs</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Myoclonus</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >9</td></tr><tr><td align="center" valign="middle" >Tremor</td><td align="center" valign="middle" >39</td><td align="center" valign="middle" >24.8</td></tr><tr><td align="center" valign="middle" >Asterixis</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle" >Fasciculations</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >1.9</td></tr><tr><td align="center" valign="middle" >Muscle tone abnormalities</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Spastic hypertonia</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.3</td></tr><tr><td align="center" valign="middle" >Plastic hypertonia</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >2.5</td></tr><tr><td align="center" valign="middle" >Hypotonia</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.3</td></tr><tr><td align="center" valign="middle" >Reflex jerk of the lower limbs</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Hyporeflexia/areflexia</td><td align="center" valign="middle" >76</td><td align="center" valign="middle" >48.4</td></tr><tr><td align="center" valign="middle" >Hyperreflexia</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >3.2</td></tr><tr><td align="center" valign="middle" >Sensitivity abnormality</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Monofilament perception</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Reduced</td><td align="center" valign="middle" >46</td><td align="center" valign="middle" >44.58</td></tr><tr><td align="center" valign="middle" >Absent</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >11.94</td></tr><tr><td align="center" valign="middle" >Perception test on diapason</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Reduced</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >43.3</td></tr><tr><td align="center" valign="middle" >Absent</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >12.69</td></tr><tr><td align="center" valign="middle" >Cranial nerve involvement</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Nerve I</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >3.2</td></tr><tr><td align="center" valign="middle" >Nerve VII</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Nerve VIII</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >8.9</td></tr><tr><td align="center" valign="middle" >Orthostatic disturbances</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Orthostatic hypotension</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >15.9</td></tr><tr><td align="center" valign="middle" >Orthostatic vertigo</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >13.4</td></tr><tr><td align="center" valign="middle" >Other syndromes</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Pyramidal syndrome</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >6.4</td></tr><tr><td align="center" valign="middle" >Cerebellar syndrome</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >2.5</td></tr><tr><td align="center" valign="middle" >Spinal cord compression</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.6</td></tr></tbody></table></table-wrap><p>Neurological disorders were found in 134/157 patients (85.4%), of which 64/157 (40.8%) had mixed disorders involving the central and peripheral nervous systems. Reported symptoms were headache with 76/157 (48.9%), sleep disorders with 69/157 (45.1%) and seizures 8/157 (5.1%). The main central nervous disorders were cognitive impairment 83/157 (52.9%) (<xref ref-type="table" rid="table3">Table 3</xref>) and it was mild in 42.2% of patients, moderate in 2.4% and dementia was present in 4.8% of patients. All patients with stroke were on dialysis for less than 6 months. The main peripheral nervous disorder was sensory polyneuropathy 90/157 (57.3%) while neuropathic pain was found in 34/157 (21.7%) patients and restless legs syndrome in 28 (17.8%). Among the cases of sensory polyneuropathy, 26 were diabetic, 11 had hepatitis C and 9 patients were HIV positive. Diabetes mellitus was associated with the occurrence of sensory polyneuropathy and neuropathic pain (p &lt; 0.05), while age greater than 40 years was associated with both sensory polyneuropathy (p = 0.001) and restless legs syndrome (p = 0.02). Duration on HD, presence of HIV, hepatitis B and C and gout were not associated to neurological disorders (<xref ref-type="table" rid="table4">Table 4</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>This study aimed to determine the prevalence of neurological disorders and their associated factors in patients on MHD. The prevalence of neurological manifestations was high (85.4%). Cognitive impairment was the most common central nervous system manifestation while sensory polyneuropathy was the leading presentation of neuropathy. Male gender was associated with neuropathic pain while age ≥ 40 years, diabetes was associated with sensory neuropathy and restless legs syndrome.</p><p>Few studies exist on the spectrum of neurological disorders in patients on MHD. Most of them assessed specific aspects. Rizzo et al. in a review estimate the prevalence of neurological disorders in these patients at 60% [<xref ref-type="bibr" rid="scirp.115735-ref14">14</xref>]. Our prevalence (85.4%) was higher without the use of electrophysiology study (subclinical screening). An explanation could be the fact that patients in our setting received only 2 sessions of dialysis of 4 hours duration per week, instead of 3 sessions as</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Neurological disorders in the study population</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Neurological disorders</th><th align="center" valign="middle" >Frequency (n)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Sensitive polyneuropathy</td><td align="center" valign="middle" >90</td><td align="center" valign="middle" >57.3</td></tr><tr><td align="center" valign="middle" >Cognitive dysfunction</td><td align="center" valign="middle" >83</td><td align="center" valign="middle" >52.9</td></tr><tr><td align="center" valign="middle" >Neuropathic pain</td><td align="center" valign="middle" >34</td><td align="center" valign="middle" >21.7</td></tr><tr><td align="center" valign="middle" >Restless legs syndrome</td><td align="center" valign="middle" >28</td><td align="center" valign="middle" >17.8</td></tr><tr><td align="center" valign="middle" >Orthostatic hypotension</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >15.9</td></tr><tr><td align="center" valign="middle" >Orthostatic Vertigo</td><td align="center" valign="middle" >22</td><td align="center" valign="middle" >14.0</td></tr><tr><td align="center" valign="middle" >Carpal Tunel syndrome</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >8.9</td></tr><tr><td align="center" valign="middle" >Stroke</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >2.5</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Factors associated with neurological disorders among patients on MHD</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Factors</th><th align="center" valign="middle" >CD n (%) p</th><th align="center" valign="middle" >PN n (%) p</th><th align="center" valign="middle" >NP n (%) p</th><th align="center" valign="middle" >RLS* n (%) p</th><th align="center" valign="middle" >OD n (%) p</th></tr></thead><tr><td align="center" valign="middle" >Sex Female Male</td><td align="center" valign="middle" >23 (46.9) 60 (57.1) 0.27</td><td align="center" valign="middle" >22 (68.8) 68 (84) 0.07</td><td align="center" valign="middle" >3 (9.4) 33 (40.7) 0.001</td><td align="center" valign="middle" >9 (28.1) 15 (18.5) 0.26</td><td align="center" valign="middle" >9 (19.l4) 16 (16) 0.56</td></tr><tr><td align="center" valign="middle" >Age (years) &lt;40 40 - 60 ≥60</td><td align="center" valign="middle" >20 (54.1) 34 (44.2) 0.32 29 (72.5) 0.09</td><td align="center" valign="middle" >9 (47.4) 45 (83.3) 0.003 38 (90) 0.001</td><td align="center" valign="middle" >0 14 (25.9) 0.99 22 (55) 0.99</td><td align="center" valign="middle" >8 (42.1) 11 (20.4) 0.07 5 (12.5) 0.02</td><td align="center" valign="middle" >6 (16.2) 14 (18.7) 0.75 5 (13.9) 0.78</td></tr><tr><td align="center" valign="middle" >Duration on HD &lt;5 years ≥5 years</td><td align="center" valign="middle" >65 (54.2) 18 (48.2) 0.68</td><td align="center" valign="middle" >70 (83.3) 20 (69) 0.09</td><td align="center" valign="middle" >24 (28.6) 12 (40) 0.28</td><td align="center" valign="middle" >18 (21.4) 6 (20) 0.88</td><td align="center" valign="middle" >18 (21.4) 7 (20) 0.88</td></tr><tr><td align="center" valign="middle" >Hypertension No Yes</td><td align="center" valign="middle" >7 (46.7) 76 (54.7) 0.55</td><td align="center" valign="middle" >9 (100) 81 (77.9) 0.20</td><td align="center" valign="middle" >3 (100) 33 (77.9) 0.91</td><td align="center" valign="middle" >3 (33.3) 21 (20.2) 0.40</td><td align="center" valign="middle" >4 (33.33) 21 (20.2) 0.40</td></tr><tr><td align="center" valign="middle" >Diabetes Non Oui</td><td align="center" valign="middle" >66 (52.8) 17 (58.6) 0.57</td><td align="center" valign="middle" >64 (73.3) 26 (100) 0.003</td><td align="center" valign="middle" >23 (26.4) 13 (50) 0.02</td><td align="center" valign="middle" >20 (23) 4 (15.4) 0.41</td><td align="center" valign="middle" >20 (23) 5 (15.4) 0.41</td></tr><tr><td align="center" valign="middle" >Hepatitis B No Yes</td><td align="center" valign="middle" >78 (53.1) 5 (71.4) 0.45</td><td align="center" valign="middle" >85 (80.2) 5 (71.4) 0.71</td><td align="center" valign="middle" >34 (80.2) 2 (71.4) 0.85</td><td align="center" valign="middle" >22 (20.8) 2 (28.6) 0.64</td><td align="center" valign="middle" >22 (20.8) 3 (28.6) 0.64</td></tr><tr><td align="center" valign="middle" >Hepatitis C No Yes</td><td align="center" valign="middle" >74 (53.6) 9 (56.9) 0.84</td><td align="center" valign="middle" >79 (79.8) 11 (78.6) 1.00</td><td align="center" valign="middle" >28 (28.3) 8 (57.1) 0.06</td><td align="center" valign="middle" >20 (20.2) 4 (15.4) 0.49</td><td align="center" valign="middle" >20 (20.2) 5 (28.6) 0.72</td></tr><tr><td align="center" valign="middle" >HIV No Yes</td><td align="center" valign="middle" >74 (69.8) 9 (52.4) 0.41</td><td align="center" valign="middle" >81 (80.2) 9 (75.0) 0. 71</td><td align="center" valign="middle" >35 (34.7) 1 (8.3) 0.10</td><td align="center" valign="middle" >21 (20.8) 3 (25) 0.72</td><td align="center" valign="middle" >21 (20.8) 4 (25) 0..72</td></tr><tr><td align="center" valign="middle" >Gout No Yes</td><td align="center" valign="middle" >74 (52.9) 9 (64.3) 0.41</td><td align="center" valign="middle" >60 (82.2) 20 (75.0) 0.36</td><td align="center" valign="middle" >29 (52.9) 9 (64.3) 0.14</td><td align="center" valign="middle" >21 (21.2) 3 (11.4) 1.00</td><td align="center" valign="middle" >21 (21.2) 4 (11.4) 1.00</td></tr></tbody></table></table-wrap><p>CD: Cognitive Dysfunction; PN: Polyneuropathy; NP: Neuropathic Pain; OD: Orthostatic dysfunction; HIV: Human Immunodeficiency Virus; RLS: Restless Legs Syndrome; HD: Hemodialysis.</p><p>recommended and also the shortage of dialysis consumables that lead to irregular dialysis sessions. These are factors that contribute to poor dialysis and the accumulation of uremic toxins that are known to be toxic for nerves.</p><p>Sensory polyneuropathy was the most present disorder (17.3%) using the MNSI which is a validated score for the diagnosis of peripheral neuropathy [<xref ref-type="bibr" rid="scirp.115735-ref17">17</xref>]. Among these patients, more than half (51%) had other diseases susceptible to induce polyneuropathy such as diabetes, HIV, hepatitis B and C. Mambelli et al. in Italy, and Tiki et al. in Turkishreported respectively a prevalence of 61.3% and 97% for polyneuropathy amongst patients on MHD [<xref ref-type="bibr" rid="scirp.115735-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref19">19</xref>]. These high prevalence in their studies could be due to the fact that they used electromyoneurography, which enables infra clinical diagnosis of neuropathies, and also the rate of patients with risk factors (comorbidities) of neuropathy in their studies was higher.</p><p>A decrease in the amplitude of sensory potential was remarkable on the median, ulnar and sural nerves. Whereas the motor conduction velocity was reduced on the peroneal nerve associated to an increased latence interval. As for non-uremic polyneuropathies, excluding diabetes and viral infections that are common in Cameroon [<xref ref-type="bibr" rid="scirp.115735-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref23">23</xref>], another study reported in 20 patients on MHD with neuropathy, four cases of non uremic neuropathy notably one Guillain Barre syndrome, one chronic polyradiculoneuritis, one progressive spinal amyothrophy and a case associated to transplantation [<xref ref-type="bibr" rid="scirp.115735-ref24">24</xref>]. These findings suggest the multifactorial origin of polyneuropathy in our context.</p><p>Similar to Mambelli et al., increased age was associated to polyneuropathy as well as type 2 diabetes [<xref ref-type="bibr" rid="scirp.115735-ref18">18</xref>], which generally occurs with age justifying their coexistence as associated factors in our study. Cognitive impairment was present in 52.9% of which 4.8% of cases were recognized dementia. Our results were similar to those of Pereira et al. in Brazil who reported 40% of case [<xref ref-type="bibr" rid="scirp.115735-ref25">25</xref>]. These increased proportions can be explained by the presence of several major cerebrovascular risk factors such as hypertension, diabetes and HIV; and also, by the episodes of cerebral hypo perfusion occurring during dialysis sessions resulting in transient ischemia enhancing nerve cell damage in these patients. In 2012, Kurella et al. in the USA [<xref ref-type="bibr" rid="scirp.115735-ref26">26</xref>], in a series of 80 patients found that 38% of patients had severe dementia. This proportion is far greater than the 4.8% in our study. The mean age of their patients estimated at 61 years (versus 48 years in our study), could have contributed to an increase in the proportion of dementia.</p><p>Headache was the main symptom with a prevalence of 48% compared to 44% found by Aladlouni et al. in Morocco [<xref ref-type="bibr" rid="scirp.115735-ref27">27</xref>] and 40% reported by Goksan et al. in Turkey [<xref ref-type="bibr" rid="scirp.115735-ref28">28</xref>]. In Brazil, Antoniazzi et al. then Feitosa et al. respectively had 70 and 76% cases of headache [<xref ref-type="bibr" rid="scirp.115735-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref30">30</xref>]. The main clinical presentations were migraine (48%), tension-type headache (19%) and associated forms (migraine and tension-type headache) in 8% of patients [<xref ref-type="bibr" rid="scirp.115735-ref28">28</xref>]. Sleep disorders were found in 44.4% of patients. These results are similar to the prevalence (44%) of sleep disorders reported in the study Giovanni et al. [<xref ref-type="bibr" rid="scirp.115735-ref31">31</xref>] but about much lower than those reported by Sabry et al. in Egypt (79.5%) and Merlino et al. in Italy (80%) [<xref ref-type="bibr" rid="scirp.115735-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref33">33</xref>]. This difference could be linked to the study method used; in our study, the diagnosis was mainly clinical in contrast with these two studies that used well defined scores in addition to polysomnography.</p><p>In our study, the prevalence of restless legs syndrome was 17.8% using IRLSSG criteria. This result is in the range with those of Araujo et al. (21.5%) on a population of 400 patients and Salman et al. in Saudi Arabia (20.3%) on 123 patients using the same questionnaire [<xref ref-type="bibr" rid="scirp.115735-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref35">35</xref>]. Age greater than 60 years was associated with restless legs syndrome, similar to the report of Araujo et al. [<xref ref-type="bibr" rid="scirp.115735-ref34">34</xref>]. This association could be justified by the fact that increased age enhances the degenerescence of descending dopaminergic pathways which could cause restless legs syndrome [<xref ref-type="bibr" rid="scirp.115735-ref35">35</xref>]. Finally, no association was found between restless legs syndrome and comorbidities, nor duration of dialysis, similar to other studies in the literature [<xref ref-type="bibr" rid="scirp.115735-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref35">35</xref>].</p><p>Autonomic dysfunctions were frequent in chronic haemodialysis patients. Orthostatic hypotension was found in 15.9%. In our study, diabetes was the second comorbidity (19.1%) inducing severe neuropathies with autonomic dysfunction responsible for orthostatic hypotension. Sasaki et al. in Japan reported a prevalence three times ours (42%) [<xref ref-type="bibr" rid="scirp.115735-ref36">36</xref>]. The mean duration of dialysis in this Japanese study could explain the difference (14 years against 3 years in our study). The mechanism remains yet unknown.</p><p>Carpal tunnel syndrome was found in 8.9% of our patients who had a common characteristic of dialysis duration greater than 5 years. In fact, carpal tunnel syndrome is due to the accumulation of Beta-2 microglobulin, in particular and juxta-articular structures. Whereas Beta-2-microglobulin is a uremic toxin mildly eliminated via HD hence the correlation with the duration of dialysis. Using clinical criteria, our result is closed to that reported by Kopec et al. and Mbarki et al. in Tunisia which found respectively 10.4% and 8.3% [<xref ref-type="bibr" rid="scirp.115735-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.115735-ref38">38</xref>]. However, our finding was low compared to that of Namazi et al. (30.5%) [<xref ref-type="bibr" rid="scirp.115735-ref39">39</xref>]. This could be due to the fact that in their study, an electromyoneurography was performed and the duration on dialysis was much longer (10 years) [<xref ref-type="bibr" rid="scirp.115735-ref39">39</xref>].</p><p>This study has shortcomings which include mainly the absence of electrophysiological assessment for diagnostic confirmation and better appreciation of subclinical involvement. But the nature of this study, using validated tools for diagnosis purposes gives an idea of preliminary data and should serve as a baseline for further studies to improve the management of these disorders and comorbidities.</p></sec><sec id="s5"><title>5. Conclusion</title><p>The prevalence of neurological disorders was high among patients on MHD in the DGH affecting up to 4/5 of them. Neurological involvement was numerous and dominated by sensory polyneuropathy and cognitive dysfunction. There is a need to put in place measures to manage these complications and improve the quality of life of affected patients.</p></sec><sec id="s6"><title>Declarations</title>Ethical Considerations and Consent to Participate<p>Ethical approval was obtained from the institutional review board of the University of Douala, Cameroon. All participants and/or their relatives provided written consent. Patients with neurological disorders were addressed to the neurology unit for further management.</p>Authors’ Contribution<p>HMP, MNY, TTEG: Study conception and design;</p><p>TTEG, FH, GM, NV: data collection and supervision;</p><p>TTEG, GM, KFF, TD, HMP: data and analysis and interpretation;</p><p>HMP, MNY: drafting of the manuscript;</p><p>TTEG, NV, TD, KFF: critical revision of the manuscript;</p><p>All authors read and approved the final manuscript.</p>Acknowledgements<p>We are grateful all the patients who agreed to participate in this study</p>Conflicts of Interest<p>The authors declare that they have no competing interests</p></sec><sec id="s7"><title>Cite this paper</title><p>Patrice, H.M., Gildas, T.T.E., Hermine, F., Daniel, G.M., Ebenezer, N.V., Denis, T., Francois, K.F. and Yacouba, M.N. (2022) Spectrum of Neurological Disorders amongst Patients on Maintenance Haemodialysis in Douala, Cameroon: A Cross-Sectional Study. 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