<?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">OALibJ</journal-id><journal-title-group><journal-title>Open Access Library Journal</journal-title></journal-title-group><issn pub-type="epub">2333-9705</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oalib.1109319</article-id><article-id pub-id-type="publisher-id">OALibJ-122275</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Business&amp;Economics</subject><subject> Chemistry&amp;Materials Science</subject><subject> Computer Science&amp;Communications</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Engineering</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject><subject> Social Sciences&amp;Humanities</subject></subj-group></article-categories><title-group><article-title>
 
 
  Diabetic Ketoacidosis in Children at the Mother and Child Academic Hospital, N’djamena Chad
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Silé</surname><given-names>Nguele Souam</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>Joséphine</surname><given-names>Toralta</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>Youssouf</surname><given-names>Hagré Djidita</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>Dadjia</surname><given-names>Djaury</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>Adrienne</surname><given-names>Ngaringuem</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>Daouya</surname><given-names>Granda</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>Ousmane</surname><given-names>Kadalla Ildjima</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>Dionadji</surname><given-names>Mbainguinam</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>Ouchemi</surname><given-names>Choua</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>Georges</surname><given-names>Moyen</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>University Hospital of Mother and Child, N’Djamena, Chad</addr-line></aff><aff id="aff2"><addr-line>University Hospital of National Reference, N’Djamena, Chad</addr-line></aff><aff id="aff3"><addr-line>Marien Ngouabi University Brazzaville (Congo), Brazzaville, Republic of the Congo</addr-line></aff><pub-date pub-type="epub"><day>01</day><month>12</month><year>2022</year></pub-date><volume>09</volume><issue>12</issue><fpage>1</fpage><lpage>8</lpage><history><date date-type="received"><day>14,</day>	<month>September</month>	<year>2022</year></date><date date-type="rev-recd"><day>27,</day>	<month>December</month>	<year>2022</year>	</date><date date-type="accepted"><day>30,</day>	<month>December</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>
 
 
  Introduction: Diabetic ketoacidosis is the most common acute complication of diabetic children. Objective: To determine the frequency of diabetic ketoacidosis in children, describe the evolutionary profile, and identify factors associated with death. 
  Patients and Method: A retrospective, descriptive, analytical study was conducted between January 2018 and November 2019. Children aged 5 to 15 years with a discharge diagnosis of diabetic ketoacidosis were included. Variables studied were age, sex, history of diabetes, clinical signs on admission, precipitating factors, blood glucose level, and outcome. The statistical test used was chi2. 
  Results: a total of 35 patients were admitted for ketoacidosis or 0.14%. They were boys n = 20 (57.1%) and girls n = 15 (42.9%) with a median age of 10.9 years. Children aged 10 to 15 years n = 26 (74%) were the most represented. The main clinical manifestations were kussmaul breathing n = 33 (94.5%), dehydration n = 27 (77%), and digestive disorders n = 26 (74%). Malaria 25 (71.4%) and urinary tract infection n = 15 (42.8%) were the triggering factors. Death was noted in 14 (40%) patients. Malaria (p: 0.03), children aged 10 - 14 years (p: 0.01), inaugural nature (p: 0.04) were associated with death. 
  Conclusion: Diabetic ketoacidosis in children is relatively frequent, and the relative mortality is high. Its reduction requires early diagnosis. Also, communication for behaviour change and improving socio-economic and cultural conditions are the axes of prevention.
 
</p></abstract><kwd-group><kwd>Ketoacidosis</kwd><kwd> Diabetes</kwd><kwd> Children</kwd><kwd> Death</kwd><kwd> CHU-ME</kwd><kwd> N’Djamena</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Diabetes, the first endocrinopathy in children, has a constantly increasing incidence worldwide. Diabetic ketoacidosis, the most frequent and dreaded acute complication of diabetes, is the consequence of a profound insulin deficiency. It reveals diabetes in 15% to 70% of cases and complicates it in 1% to 10% [<xref ref-type="bibr" rid="scirp.122275-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref3">3</xref>]. It is Africa’s leading cause of hospitalisation, morbidity, and mortality of diabetic children. It is a significant public health problem with a mortality of 1% - 2% [<xref ref-type="bibr" rid="scirp.122275-ref4">4</xref>]. In Congo, ketoacidosis reveals diabetes in 57.1% and complicates it in 42.8% with lethality of 18.2% [<xref ref-type="bibr" rid="scirp.122275-ref5">5</xref>]. In Chad, 98% of diabetic children hospitalised in 2017 were for ketoacidosis [<xref ref-type="bibr" rid="scirp.122275-ref6">6</xref>]. Having been an Academic Hospital in N’Djamena for more than eight years, this work was carried out to improve the management of childhood diabetes and ketoacidosis, the most frequent complication. The objectives were: to determine the frequency of diabetic ketoacidosis, to describe the sociodemographic and clinical characteristics of the study population, as well as the outcome and to identify the factors associated with death.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>It was a retrospective, descriptive and analytical study conducted in the paediatric emergency department of the Mother and Child Academic Hospital between January 2018 and November 2019. The study population consisted of children hospitalised in the paediatric emergency department. For those aged 5 to 15 years whose discharge diagnosis included the item “diabetic ketoacidosis”, children whose records were usable were included. Children hospitalised for a complication of diabetes other than DKA were omitted.</p><sec id="s2_1"><title>2.1. Study Sampling</title><p>It was a comprehensive sample. The inclusion criteria were for all records of patients admitted with a final diagnosis of Diabetic Ketoacidosis.</p></sec><sec id="s2_2"><title>2.2. Study Method</title><p>The data sources were the medical records and hospitalisation register of the department. All data were collected in a predefined form.</p></sec><sec id="s2_3"><title>2.3. Study Variables</title><p>The variables studied were age, sex, origin, age of diabetes, clinical signs, precipitating factors, urine dipstick data, blood count data, thick blood drop, blood ionogram, c-reactive protein, urea, creatinine, and evolutionary profile.</p></sec><sec id="s2_4"><title>2.4. Operational Definitions</title><p>The definition of ketoacidosis used is that of the ISPAD [<xref ref-type="bibr" rid="scirp.122275-ref7">7</xref>], i.e., a blood glucose level of 2 g/l (11 mmol/l) with glycosuria++, ketonuria++ and a PH 7.3 or alkaline reserve of 15 mmol/l (in the absence of blood gas analysis) associated with at least one of the following clinical signs: vomiting, abdominal pain, Kussmaul breathing, signs of dehydration and disturbances in consciousness.</p></sec><sec id="s2_5"><title>2.5. Statistical Analysis</title><p>Data were entered and analysed using SPSS software 18. The statistical test used was chi<sup>2</sup> with a significant threshold of 5%.</p></sec></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Descriptive Study</title><sec id="s3_1_1"><title>3.1.1. Epidemiological Aspects: Frequency, Age, and Sex</title><p>Of 24,750 children hospitalised during the study period, 35 were hospitalised for diabetic ketoacidosis, i.e., a hospital frequency of 0.14%. They had a mean age of 10.9 years, with extremes of 5 and 15 years. They were 5 to 9 years old, n = 9 (26%), 10 to 15 years old, and n = 26 (74%). They were boys n = 20 (57.1%) and girls n = 15 (42.8%), i.e., a sex ratio of 1.33.</p></sec><sec id="s3_1_2"><title>3.1.2. Clinical and Para-Clinical Aspects</title><p>It was an inaugural ketoacidosis of diabetes 65.7% (n = 23), the age of diabetes was one year 14.3% (n = 5), two years 8.6% (n = 3), three years 2.8% (n = 1), four years 8.6% (n = 3) (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>Clinical signs were: kussmaul breathing 94.3% (n = 33), acetone breath 82% (n = 29), dehydration 77% (n = 27), coma 62.8% (n = 22), fever 51.4% (n = 18) and hemodynamic disorder 40% (n = 14) (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>The precipitating factor identified was infectious, including malaria 71.4% (n = 25), urinary tract infection 42.8% (n = 15), pneumonia 5.7% (n = 2), skin infection 5.7% (n = 2) and interruption of treatment 5.7% (n = 2) (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Biologically, the average blood glucose level was 4.47 g/l, with extremes of 2.56 and 6 g/l. Ketonuria was two crosses 40% (n = 14), three crosses 48.6% (n = 17), four crosses 11.4% (n = 4) and glucosuria two crosses 2.8% (n = 1), three crosses 62.8% (n = 22) and four crosses 34.3% (n = 12). The outcome was favourable for 24 (60%) and 14 (40%) children died (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution by clinical manifestation</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >CLINICAL SIGNS</th><th align="center" valign="middle" >CASES</th><th align="center" valign="middle" >PERCENTAGE</th></tr></thead><tr><td align="center" valign="middle" >Coma</td><td align="center" valign="middle" >22</td><td align="center" valign="middle" >62.7%</td></tr><tr><td align="center" valign="middle" >Dehydration</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >77.1%</td></tr><tr><td align="center" valign="middle" >Hemodynamic disorders</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >40%</td></tr><tr><td align="center" valign="middle" >Digestive disorders</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >74.3%</td></tr><tr><td align="center" valign="middle" >Kussmaul breathing</td><td align="center" valign="middle" >33</td><td align="center" valign="middle" >94.3%</td></tr><tr><td align="center" valign="middle" >acetonic breath</td><td align="center" valign="middle" >29</td><td align="center" valign="middle" >82.5%</td></tr><tr><td align="center" valign="middle" >Fever</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >51.4%</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Distribution according to factors triggering diabetic ketoacidosis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >TRIGGERING FACTORS</th><th align="center" valign="middle" >CASES</th><th align="center" valign="middle" >PERCENTAGE</th></tr></thead><tr><td align="center" valign="middle" >Malaria</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >71.4%</td></tr><tr><td align="center" valign="middle" >Urinary tract infection</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >42.8%</td></tr><tr><td align="center" valign="middle" >Pneumonia</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >5.7%</td></tr><tr><td align="center" valign="middle" >Insulin interruption</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >5.7%</td></tr><tr><td align="center" valign="middle" >Skin infection</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >5.7%</td></tr><tr><td align="center" valign="middle" >Infection au foyer non determine</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >34.28%</td></tr></tbody></table></table-wrap><p>Therapeutically, 35 patients were hydrated with saline then glucose serum, insulin therapy at 0.1 IU/kg/h was started 1 hour after hydration for each patient. According to the triggering factors, 25 (71.4%) patients were treated with injectable artesunate and 17 (48.5%) patients had received Ceftriaxone IV and Gentamycin IV.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Distribution according to clinical manifestations and death</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Manifestations cliniques</th><th align="center" valign="middle"  colspan="2"  >D&#233;c&#232;s</th><th align="center" valign="middle"  rowspan="2"  >P</th></tr></thead><tr><td align="center" valign="middle" >oui</td><td align="center" valign="middle" >Non</td></tr><tr><td align="center" valign="middle" >kussmaul breathing</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >0.23</td></tr><tr><td align="center" valign="middle" >Dehydration</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >0.009</td></tr><tr><td align="center" valign="middle" >Coma</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >0.02</td></tr><tr><td align="center" valign="middle" >Hemodynamic disorders</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >0.02</td></tr><tr><td align="center" valign="middle" >Digestive disorders</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >0.63</td></tr></tbody></table></table-wrap></sec></sec><sec id="s3_2"><title>3.2. Analytical Study</title><p>Death-related factors were age between 10 and 15 years, comorbidity with malaria, undetermined infectious focus, and urinary tract infection. Other associated factors were Kussmaul breathing, coma, dehydration, and hemodynamic disorders (<xref ref-type="table" rid="table3">Table 3</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Diabetic ketoacidosis, an absolute medical emergency, is frequent in children in N’Djamena. The hospital frequency of diabetic ketoacidosis in children, estimated at 0.14%, is worrying but relatively low compared to the data in the literature, whose reported frequencies are 0.7% and 6.49% [<xref ref-type="bibr" rid="scirp.122275-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref8">8</xref>].</p><p>These disparities are explained by the sample size and the characteristics of the study population. As already reported, ketoacidosis is often observed in children between 8 and 10 years of age, as in this study, where the mean age was 10.9 years [<xref ref-type="bibr" rid="scirp.122275-ref9">9</xref>]. Some authors report higher frequencies in children under 10 years of age [<xref ref-type="bibr" rid="scirp.122275-ref10">10</xref>]. In this study, those aged 5 to 10 years represented 25.7% and those aged 10 to 15 years 74.3% of the study population. Our results differ from those of Fikaden BH et al. [<xref ref-type="bibr" rid="scirp.122275-ref10">10</xref>], who reported 34% for the 5 - 9-year-old age group and 40% for the 10 - 15-year-old age group, respectively. The difference is since in this study, only children aged 5 to 15 years were included, unlike the study by A. N. Onyiriuka et al., which included infants and children aged 0 to 15 years [<xref ref-type="bibr" rid="scirp.122275-ref11">11</xref>]. Diabetic ketoacidosis is more common in boys [<xref ref-type="bibr" rid="scirp.122275-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref12">12</xref>], representing 57.1% of our study population―Oko et al. in Congo Brazzaville report data contrary to ours concerning sex [<xref ref-type="bibr" rid="scirp.122275-ref3">3</xref>]. Ketoacidosis often reveals diabetes, as was the case in this study where it was inaugural in 65% of cases, and in the work of Oko and Henri GM with 67% and 79.3% [<xref ref-type="bibr" rid="scirp.122275-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref5">5</xref>].</p><p>The symptomatology of diabetic ketoacidosis classically includes signs related to hyperglycaemia associated with nausea and vomiting and, especially in children, abdominal pain [<xref ref-type="bibr" rid="scirp.122275-ref1">1</xref>]. In our study, the signs noted, all related to a more severe decompensation, are the same as elsewhere [<xref ref-type="bibr" rid="scirp.122275-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref14">14</xref>]. They are Kussmaul breathing, acetone breath, dehydration, and coma. All these signs have as a common denominator the delay in the decision to consult and transfer to specialised structures. The corollary of the delay in consultation is the high blood glucose level [<xref ref-type="bibr" rid="scirp.122275-ref3">3</xref>]. As in this study, the median level on admission was 4.47 g/l with transient electrolyte disturbances, including hyponatraemia and hypokalaemia during diabetic ketoacidosis, which is well known [<xref ref-type="bibr" rid="scirp.122275-ref15">15</xref>].</p><p>The triggers of diabetic ketoacidosis in Sub-Saharan Africa, the same as those reported in this study, are dominated by bacterial infections, malaria, and non-adherence to insulin therapy [<xref ref-type="bibr" rid="scirp.122275-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.122275-ref17">17</xref>].</p><p>Therapeutically, 35 patients were hydrated with saline then glucose serum, insulin therapy at 0.1 IU/kg/h was started 1 hour after hydration for each patient [<xref ref-type="bibr" rid="scirp.122275-ref7">7</xref>].</p><p>The treatment of triggering factors, 25 (71.4%) patients were treated with injectable artesunate [<xref ref-type="bibr" rid="scirp.122275-ref18">18</xref>] and 17 (48.5%) patients had received Ceftriaxone IV and Gentamycin IV.</p><p>The average length of hospital stays, evaluated at 7.6 days, is similar to that reported by Sarr A. [<xref ref-type="bibr" rid="scirp.122275-ref19">19</xref>] and Mohamed A. Life-threatening condition due to diabetic ketoacidosis varies from country to country and according to the state of the health system. It is 1 to 2% in the West [<xref ref-type="bibr" rid="scirp.122275-ref20">20</xref>], 18% in Congo according to OKO [<xref ref-type="bibr" rid="scirp.122275-ref5">5</xref>], 25% by Neal Ramesh P. in India [<xref ref-type="bibr" rid="scirp.122275-ref21">21</xref>] and 40% for us. Death-related factors were in our study as those found in the African literature. They are depth of coma (p = 0.02), infection (p = 0.000), dehydration (0.009) and the probable inefficiency in the correction of hydro-electrolytic disorders [<xref ref-type="bibr" rid="scirp.122275-ref5">5</xref>].</p><p>Our study is the first devoted specifically to diabetic ketoacidosis in children in N’Djamena. The precariousness of the parents of the patients, no ECG to screen for hypokalaemia, the ionogram was not carried out systematically because of financial difficulties. The high mortality rate is explained by the limits in the quality of care.</p><p>We note that there were no conflicts of interest in this study.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Diabetic ketoacidosis in children is frequent and severe in N’Djamena because of the high case fatality rate. It is more frequent in older children and often inaugurates diabetes. Bacterial infections, especially urinary tract infections and malaria, are the primary triggers. Coma, dehydration, hemodynamic disorders, children aged 10 to 15 years, malaria and infections of unspecified sites are associated with death. The challenge is to decrease the frequency of DKA in children by making the diagnosis earlier in the course of the disease.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest.</p></sec><sec id="s7"><title>Cite this paper</title><p>Souam, S.N., Toralta, J., Djidita, Y.H., Djaury, D., Ngaringuem, A., Granda, D., Ildjima, O.K., Mbainguinam, D., Choua, O. and Moyen, G. (2022) Diabetic Ketoacidosis in Children at the Mother and Child Academic Hospital, N’djamena Chad. Open Access Library Journal, 9: e9319. https://doi.org/10.4236/oalib.1109319</p></sec><sec id="s8"><title>Appendix. Data Collection Sheet</title><p>I. Epidemiological aspects</p><p>- Sex, age, place of origin (province or N’Djamena);</p><p>- Duration of diabetes</p><p>II. Clinical manifestations</p><p>- Fever: - Digestive disorders:</p><p>- Coma: - Hemodynamic disorders:</p><p>- Kusmaul’s dyspnoea: - Acetone breath:</p><p>- Signs of dehydration: - Triggering factors:</p><p>- Dipstick:</p><p>III. Paraclinical manifestations</p><p>- NFS; - malaria test, - Blood ionogram - Urea: - Creatinine</p><p>IV. medical care</p><p>- Rehydration; - Insulin therapy - Treatment of the risk factor</p><p>V. 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