<?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">OJU</journal-id><journal-title-group><journal-title>Open Journal of Urology</journal-title></journal-title-group><issn pub-type="epub">2160-5440</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oju.2022.122010</article-id><article-id pub-id-type="publisher-id">OJU-115092</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>
 
 
  Prediction of Acute Renal Failure in Dengue Fever Patients
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Salwa</surname><given-names>Abd Almoneim Mohammed Ali</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>Omer Abaker Gibreel</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>Nazik</surname><given-names>Sir El Khatim Bakhit Suliman</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>Khider Ali Mohammed</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bakri</surname><given-names>Yousif Mohamed Nour</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff4"><addr-line>Department of Clinical Chemistry, Faculty of Medical Laboratory Sciences, University of Gezira, Wad Medani, Sudan</addr-line></aff><aff id="aff3"><addr-line>Department of Microbiology, Eastern Sudan College of Medical Science and Technology, Port Sudan, Sudan</addr-line></aff><aff id="aff2"><addr-line>Department of Hematology and Immunohematology, Port Sudan Ahlia College, Port Sudan, Sudan</addr-line></aff><aff id="aff1"><addr-line>Department of Clinical Chemistry, Eastern Sudan College of Medical Science and Technology, Port Sudan, Sudan</addr-line></aff><pub-date pub-type="epub"><day>09</day><month>02</month><year>2022</year></pub-date><volume>12</volume><issue>02</issue><fpage>99</fpage><lpage>106</lpage><history><date date-type="received"><day>13,</day>	<month>December</month>	<year>2021</year></date><date date-type="rev-recd"><day>7,</day>	<month>February</month>	<year>2022</year>	</date><date date-type="accepted"><day>10,</day>	<month>February</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>
 
 
  Background: Dengue virus (DENV) infection is caused by an arboviral strain and is transmitted by the mosquito Aedes aegypti which is found in Sudan especially Red Sea and Kassala states in the east. The disease is known to cause renal disturbances and a thorough understanding of that will potentially help in the prediction, diagnosis and treatment of the disease. 
  Methods: This study is a prospective observational cross sectional study conducted in the Eastern Sudan College of Medical Science and Technology and Port Sudan Teaching Hospital. 200 confirmed Dengue virus infected patients along with 200 healthy appearing adults (control) were enrolled for the study. Statistical analysis was carried out after the collection of patients’ demographic, clinical, and investigational data including serum urea and creatinine values. Ethical approval was obtained from the ministry of health, Red Sea state and informed written consent was obtained from each participant. 
  Results: The highest incidence of DENV infection was observed in individuals of the middle age group (29%). Elevated blood urea levels were detected in 10 (5%) patients while elevated creatinine levels were seen in 17 (8.5%) patients. Although fallen within reference ranges found in the literature, mean blood urea and creatinine values differed significantly between patients and controls and between different categories of the disease. Mean blood urea concentration showed a statistically significant difference between the control (22.3 mg/dl) and the test (28.4 mg/dl) (P value &lt; 0.001). Similarly, mean serum creatinine in the control (0.70 mg/dl) differed significantly (P value &lt; 0.001) from test (0.94 mg/dl). Clinically, fever was present in 97.5% of patients, headache in 95.5%, joints pain in 71%, lethargy in 67%, vomiting in 49%, skin rash in 40%, abdominal pain in 24% and bleeding in 17.5%. 
  Conclusion: We strongly conclude that renal involvement is not uncommon in Dengue fever and that blood urea and creatinine evaluation should be considered in the counseling of DENV infection patients. Patients need to be subjected to necessary laboratory investigations associated with acute kidney injury to decrease the rate of morbidity and mortality associated with the disease.
 
</p></abstract><kwd-group><kwd>Dengue Virus</kwd><kwd> Acute Kidney Injury</kwd><kwd> Hemorrhagic Fever</kwd><kwd> Shock Syndrome</kwd><kwd> Eastern Sudan</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Dengue fever is a mosquito borne viral infection that constitutes a major health problem in tropical and sub-tropical regions of the world. Urbanization and air travel are among the factors associated with the increased trend of infection in recent years. Over 2.5 billion people of the world’s population are now at risk for Dengue. The consequence of Dengue virus (DENV) infection ranges from the asymptomatic condition (Dengue fever (DF), to more severe forms, such as Dengue hemorrhagic fever (DHF) and Dengue shock syndrome (DSS). Severe Dengue is characterized either by plasma leakage, fluid accumulation, respiratory distress, severe bleeding, or organ impairment. Clinical manifestations offer the earliest markers in predicting severe Dengue Disease [<xref ref-type="bibr" rid="scirp.115092-ref1">1</xref>].</p><p>Patients with Dengue fever are clustered into two groups: one with warning signs including abdominal pain, mucosal bleeding and hepatomegaly that warrant ICU admission and the other without those signs. Early prediction of severe Dengue infection in patients without any warning signs who may later develop severe DHF is very important to give the best supportive care since approved vaccines for immunization are yet to be commercialized. An ideal biomarker should be able to identify individuals who are at risk of developing severe Dengue infection [<xref ref-type="bibr" rid="scirp.115092-ref2">2</xref>]. Dengue patients show fever symptoms during peak of viraemia while DHF/DSS appears during the time when the virus has been cleared from the circulation suggesting that severe Dengue disease is most likely associated with immunopathology [<xref ref-type="bibr" rid="scirp.115092-ref2">2</xref>].</p><p>Dengue infection has been associated with a variety of renal disorders. Acute renal failure is a potential complication of severe Dengue infection and is typically associated with hypotension, rhabdomyolysis, or hemolysis. Acute renal failure occasionally complicates severe Dengue infection and carries a high mortality rate. Transient proteinuria has been detected in most patients with severe Dengue infection. Hematuria has been reported in a significant subset of patients with severe forms of the infection. Various types of glomerulonephritis have been reported during or shortly after Dengue infection in humans and mouse models. Meningeal proliferation and immune complex deposition are the dominant histologic features. On a rare occasion, Dengue infection is associated with systemic autoimmune disorders involving the kidneys. In the vast majority of cases, Dengue infection and associated renal disorders are self-limited [<xref ref-type="bibr" rid="scirp.115092-ref3">3</xref>].</p><p>Dengue infection evolving into systemic lupus erythematosus and lupus nephritis has been reported with antibodies directed against nuclear antigens including ANA and double-stranded DNA [<xref ref-type="bibr" rid="scirp.115092-ref3">3</xref>].</p><p>In Sudan, Dengue fever (DF) is considered a major public health issue in the Eastern region of the country, where it has been reported since 1908 with endemicity and frequent outbreaks in the coastal and sub-coastal areas of the Red Sea and Kassala states. Dengue fever reported in the Sudanese population is associated with serious presentations including DHF and DSS with an increased rates of morbidity and mortality. Acute kidney injury (AKI) is a serious and potentially lethal complication of this disease. It is obvious that Dengue Fever is becoming a serious problem and this needs specific investigation and diagnosis to avoid complications of the disease. Approximately 2.5 billion individuals from more than 110 countries are in danger of DENV infection each year due to the lack of an efficient vaccine and a specific treatment [<xref ref-type="bibr" rid="scirp.115092-ref4">4</xref>]. Dengue fever is transmitted by Aedes aegypti with other species of Aedes mosquito involved [<xref ref-type="bibr" rid="scirp.115092-ref5">5</xref>]. There are 4 serotypes of dengue viruses known as DENV-1, DENV-2, DENV-3, and DENV-4 [<xref ref-type="bibr" rid="scirp.115092-ref6">6</xref>].</p><p>Renal function is routinely assessed by a profile that includes the determination of serum urea, creatinine, creatinine clearance and electrolytes. An elevated concentration of urea in the blood is called azotemia. Very high plasma urea concentration accompanied by renal failure is called uremia, or the uremic syndrome. This condition is eventually fatal if not treated by dialysis or transplantation [<xref ref-type="bibr" rid="scirp.115092-ref7">7</xref>]. Decreased renal function causes an increase in plasma urea concentration as a result of compromised urea excretion. Renal causes of elevated urea include acute and chronic renal failure, glomerular nephritis, tubular necrosis, and other intrinsic renal diseases. Measurement of creatinine concentration is used to determine sufficiency of kidney function and the severity of kidney damage and to monitor the progression of kidney disease. The amount of creatinine in the bloodstream is reasonably stable, although the protein content of the diet does influence the plasma concentration because of the constancy of endogenous production [<xref ref-type="bibr" rid="scirp.115092-ref8">8</xref>].</p><p>Acute kidney injury (AKI) is a condition where kidneys suddenly stop working properly. It can range from minor loss of kidney function to complete kidney failure. AKI normally happens as a complication of another serious illness. It is not the result of a physical blow to the kidneys, as the name might suggest. This type of kidney damage is usually seen in older people who are unwell with other conditions and the kidneys are also affected. It is essential that AKI is detected early and treated promptly. Without quick treatment, abnormal levels of salts and chemicals can build up in the body, which affects the ability of other organs to work properly. If the kidneys shut down completely, this may require temporary support from a dialysis machine, or lead to death [<xref ref-type="bibr" rid="scirp.115092-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.115092-ref10">10</xref>]. This study is designed to incorporate the prediction of acute renal injury as a routine check in approaching Dengue fever patients.</p></sec><sec id="s2"><title>2. Methods</title><p>This was an hospital-based cross sectional descriptive study conducted at Port Sudan Teaching Hospital in the period from June 2018 to September 2021 to evaluate the involvement of acute kidney injury (where kidney suddenly stops working properly) in confirmed Dengue fever patients. Enrolled in the study are 200 diagnosed Dengue fever patients (fixed number) and other 200 healthy appearing people as a control group. Patients with a past history of renal or liver disease before diagnoses of Dengue fever and patients who have lupus erythromatosis were excluded. Ethical approval was achieved from the research committee in the ministry of health, Red Sea state and an informed written consent was obtained from each participant.</p><p>Venous blood samples were collected from each patient, one in heparinized containers, and another in plain containers then refrigerated at 2˚C - 8˚C till analyzed. The diagnosis of Dengue fever was established by the detection of DENV IgG/IgM antibodies by ELISA Technique.</p><p>Blood urea and creatinine were measured photometrically by the enzymatic method using the PT350 Bio system spectrophotometer and reagent kits from Biosystems Company. Data were statistically analyzed by the SPSS software and frequencies, concentrations and correlations were illustrated.</p></sec><sec id="s3"><title>3. Results</title><p>The higher percentage of patients of DENV infection was from individuals of middle age (40 - 49 years old) representing 29% of cases (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>Out of the 200 confirmed DENV positive patients included in this study, 126 (63%) were males and 74 (37%) were females along with other 200 healthy appearing adults of whom 100 (50%) were males and 100 (50%) were females as a control group, 160 (80%) were found to suffer from mild Dengue fever, 35 (17.5%) suffered from Dengue hemorrhage fever, 5 (2.5%) suffered from Dengue shock syndrome. Eight patients (4%) showed signs of acute kidney injury (1 patient with acute kidney injury the result of ANA, anti-dsDNA were significantly increased).</p><p><xref ref-type="table" rid="table1">Table 1</xref> shows a statistically significant difference between Dengue fever patients and the control group in the concentration of serum urea and creatinine.</p><p>Bio chemical findings in the different categories of Dengue virus infection showed statistically significant differences. <xref ref-type="table" rid="table2">Table 2</xref> illustrates the difference between Dengue fever and Dengue hemorrhagic fever.</p><p>Similarly, <xref ref-type="table" rid="table3">Table 3</xref> shows a significant difference in biochemical finding between Dengue fever and Dengue shock syndrome especially in urea concentration.</p><p>In contrast, <xref ref-type="table" rid="table4">Table 4</xref> illustrates an insignificant difference in biochemical finding between Dengue hemorrhagic fever and Dengue shock syndrome.</p><p>Insignificant differences were also seen in biochemical findings according to gender in Dengue virus infected patients in different categories of the disease in urea and creatinine concentration apart from creatinine in males and females of Dengue fever (Tables 5-7).</p></sec><sec id="s4"><title>4. Discussion</title><p>Dengue fever can be presented with a variety of clinical presentations associated</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Comparison between test and control in biochemical findings</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parameter</th><th align="center" valign="middle" >Reference Range</th><th align="center" valign="middle" >Test (Mean &#177; 1 SD) N = 200</th><th align="center" valign="middle" >Control (Mean &#177; 1 SD) N = 200</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Urea (mg/dl)</td><td align="center" valign="middle" >15 - 50</td><td align="center" valign="middle" >28.40 &#177; 25.7</td><td align="center" valign="middle" >22.30 &#177; 6.30</td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >Creatinine (mg/dl)</td><td align="center" valign="middle" >Up to 1</td><td align="center" valign="middle" >0.94 &#177; 0.08</td><td align="center" valign="middle" >0.70 &#177; 0.15</td><td align="center" valign="middle" >&lt;0.001</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Comparison between DF and DHF in biochemical findings</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parameter</th><th align="center" valign="middle" >DF (Mean &#177; 1 SD) N = 160</th><th align="center" valign="middle" >DHF (Mean &#177; 1 SD) N = 35</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Urea (mg/dl)</td><td align="center" valign="middle" >22.3 &#177; 6.005</td><td align="center" valign="middle" >44.88 &#177; 39.80</td><td align="center" valign="middle" >0.020</td></tr><tr><td align="center" valign="middle" >Creatinine (mg/dl)</td><td align="center" valign="middle" >0.75 &#177; 0.18</td><td align="center" valign="middle" >1.44 &#177; 1.45</td><td align="center" valign="middle" >&lt;0.001</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Comparison between DF and DSS in biochemical findings</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parameter</th><th align="center" valign="middle" >DF (Mean &#177; 1 SD) N = 160</th><th align="center" valign="middle" >DSS (Mean &#177; 1 SD) N = 5</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Urea (mg/dl)</td><td align="center" valign="middle" >22.3 &#177; 6.005</td><td align="center" valign="middle" >109.30 &#177; 76.50</td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >Creatinine (mg/dl)</td><td align="center" valign="middle" >0.75 &#177; 0.18</td><td align="center" valign="middle" >3.54 &#177; 1.10</td><td align="center" valign="middle" >0.050</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Comparison between DHF and DSS in biochemical findings</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parameter</th><th align="center" valign="middle" >DHF (Mean &#177; 1 SD) N = 35</th><th align="center" valign="middle" >DSS (Mean &#177; 1 SD) N = 5</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Urea (mg/dl)</td><td align="center" valign="middle" >44.88 &#177; 39.80</td><td align="center" valign="middle" >109.3 &#177; 76.5</td><td align="center" valign="middle" >0.500</td></tr><tr><td align="center" valign="middle" >Creatinine (mg/dl)</td><td align="center" valign="middle" >1.44 &#177; 1.45</td><td align="center" valign="middle" >3.54 &#177; 1.10</td><td align="center" valign="middle" >0.100</td></tr></tbody></table></table-wrap><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Comparison between dengue fever male and female patients in biochemical findings</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parameter</th><th align="center" valign="middle" >Males (Mean &#177; 1 SD) N = 103</th><th align="center" valign="middle" >Females (Mean &#177; 1 SD) N = 57</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Urea (mg/dl)</td><td align="center" valign="middle" >22.92 &#177; 6.20</td><td align="center" valign="middle" >21.21 &#177; 5.60</td><td align="center" valign="middle" >0.080</td></tr><tr><td align="center" valign="middle" >Creatinine (mg/dl)</td><td align="center" valign="middle" >0.77 &#177; 0.19</td><td align="center" valign="middle" >0.70 &#177; 0.11</td><td align="center" valign="middle" >0.040</td></tr></tbody></table></table-wrap><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Biochemical findings in patients of dengue hemorrhagic fever based on gender</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parameter</th><th align="center" valign="middle" >Males (Mean &#177; 1 SD) N = 20</th><th align="center" valign="middle" >Females (Mean &#177; 1 SD) N = 15</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Urea (mg/dl)</td><td align="center" valign="middle" >53.5 &#177; 49.70</td><td align="center" valign="middle" >33.4 &#177; 15.70</td><td align="center" valign="middle" >0.100</td></tr><tr><td align="center" valign="middle" >Creatinine (mg/dl)</td><td align="center" valign="middle" >1.70 &#177; 1.85</td><td align="center" valign="middle" >1.05 &#177; 0.45</td><td align="center" valign="middle" >0.200</td></tr></tbody></table></table-wrap><table-wrap id="table7" ><label><xref ref-type="table" rid="table7">Table 7</xref></label><caption><title> Biochemical findings in patients of dengue shock syndrome based on gender</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Parameter</th><th align="center" valign="middle" >Males (Mean &#177; 1 SD) N = 3</th><th align="center" valign="middle" >Females (Mean &#177; 1 SD) N = 2</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Urea (mg/dl)</td><td align="center" valign="middle" >156.0 &#177; 52.40</td><td align="center" valign="middle" >39.25 &#177; 39.24</td><td align="center" valign="middle" >0.070</td></tr><tr><td align="center" valign="middle" >Creatinine (mg/dl)</td><td align="center" valign="middle" >3.90 &#177; 0.18</td><td align="center" valign="middle" >3.10 &#177; 0.21</td><td align="center" valign="middle" >0.400</td></tr></tbody></table></table-wrap><p>with unpredictable progression and outcomes. They range from asymptomatic illness to severe shocks eventually resulting in death [<xref ref-type="bibr" rid="scirp.115092-ref11">11</xref>]. Dengue is considered a major health threat by the World Health Organization. An increase in infection has been seen in recent years due to many factors including urbanization and air travel. Approximately over 2.5 billion people of the words population are now at risk for Dengue [<xref ref-type="bibr" rid="scirp.115092-ref12">12</xref>]. The purpose why only a few DENV disease cases get worse is poorly understood but the host immune response has been considered as the major factor responsible for Dengue pathogenesis [<xref ref-type="bibr" rid="scirp.115092-ref13">13</xref>]. Dengue infection is associated with multiple organ dysfunction involving liver, muscles, heart, brain and kidney [<xref ref-type="bibr" rid="scirp.115092-ref14">14</xref>]. Dengue fever has been associated with various types of renal disorders such as proteinuria, hematuria, glomerulonephritis, and acute kidney injury [<xref ref-type="bibr" rid="scirp.115092-ref15">15</xref>].</p><p>In this study, out of the confirmed two hundred Dengue patients, eight patients (4%) had Acute Kidney Injury (AKI). Results that are similar to those of s study done by Warappa ES. et al. who reported that the prevalence of renal manifestation in Dengue fever patients was (9.02%) [<xref ref-type="bibr" rid="scirp.115092-ref16">16</xref>]. The fact that the prevalence of DF in males was higher than females in our study along with the clinical presentation that fever was detected in (97.5%) of patients, is similar to the results of a study done by Relwani P. R. et al. who found that fever was one of the common features associated with Dengue infection (98.66%) [<xref ref-type="bibr" rid="scirp.115092-ref17">17</xref>].</p><p>In our study the (mean &#177; 1 SD) of serum urea levels of (22.3 &#177; 6.01 mg/dl) for Dengue fever patients, (44.88 &#177; 39.8 mg/dl) for Dengue hemorrhagic fever patients, and (109.3 &#177; 76.5 mg/dl) for Dengue shock syndrome patients, was similar to what was seen by Guzman MG. and Halsted SB. [<xref ref-type="bibr" rid="scirp.115092-ref18">18</xref>] who showed increased urea levels in all categories of the disease.</p><p>Similarly, the (mean &#177;1SD) of creatinine levels in Dengue fever patients was (0.75 &#177; 0.18 mg/dl), in Dengue Hemorrhagic fever patients was (1.44 &#177; 1.45 mg/dl), and in Dengue shock syndrome was (3.5 &#177; 1.10 mg/dl), is agreed to the results of a study by Taurqeer H. and Amer K. [<xref ref-type="bibr" rid="scirp.115092-ref19">19</xref>] who reported an increase in creatinine levels in all the categories of Dengue infection.</p><p>The present study found that only one patient with acute kidney injury had increased levels of anti-dsDNA, and ANA which is similar to the findings of a study by Rajadhyaksha A. and Mehra S. in a case report [<xref ref-type="bibr" rid="scirp.115092-ref20">20</xref>] showing an increase in anti-dsDNA and ANA.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Renal involvement is frequent in patients with Dengue fever especially in those exhibiting complications of the disease. Routine assessment of these patients should include the determination of blood urea and creatinine as a check marker for the prediction of acute kidney injury.</p></sec><sec id="s6"><title>Acknowledgements</title><p>We would like to thank many people without the help of whom this work would have not seen light. Thanks are for our families for valuable support. Especial thanks are for Dr. Monammed Haroun Mohammed Ali the head manager of the department of training, Red Sea state for his unlimited encouragement and support.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors have no conflicts of interest to disclose.</p></sec><sec id="s8"><title>Cite this paper</title><p>Ali, S.A.A.M., Gibreel, M.O.A., Suliman, N.S. El K.B., Mohammed, A.K.A. and Nour, B.Y.M. (2022) Prediction of Acute Renal Failure in Dengue Fever Patients. Open Journal of Urology, 12, 99-106. https://doi.org/10.4236/oju.2022.122010</p></sec></body><back><ref-list><title>References</title><ref id="scirp.115092-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">John Wiley and Sons Ltd. (2017) Regulatory T-Cells in Acute Dengue Viral Infection. 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