<?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">OJIM</journal-id><journal-title-group><journal-title>Open Journal of Internal Medicine</journal-title></journal-title-group><issn pub-type="epub">2162-5972</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojim.2019.92003</article-id><article-id pub-id-type="publisher-id">OJIM-93275</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>
 
 
  Factors Associated to the Acute Metabolic Decompensation of Diabetes in Lome
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abago</surname><given-names>Balaka</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>Toyi</surname><given-names>Tchamdja</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>Kodjo</surname><given-names>Agb&amp;#233;ko Djagadou</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>Komi</surname><given-names>Dzidzonu N&amp;#233;mi</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>Mohaman</surname><given-names>Awalou Djibril</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>Datouda</surname><given-names>Redah</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Health Science Faculty, Universit&amp;amp;#233; de Kara, Kara, Togo</addr-line></aff><aff id="aff1"><addr-line>Internal Medicine Unit, Lom&amp;amp;#233; &amp;amp; Kara, Togo</addr-line></aff><aff id="aff3"><addr-line>Health Science Faculty, Universit&amp;amp;#233; de Lom&amp;amp;#233;, Lom&amp;amp;#233;, Togo</addr-line></aff><pub-date pub-type="epub"><day>26</day><month>06</month><year>2019</year></pub-date><volume>09</volume><issue>02</issue><fpage>12</fpage><lpage>18</lpage><history><date date-type="received"><day>10,</day>	<month>April</month>	<year>2019</year></date><date date-type="rev-recd"><day>24,</day>	<month>June</month>	<year>2019</year>	</date><date date-type="accepted"><day>27,</day>	<month>June</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The purpose of the study was to define basic factors of the acute metabolic decompensations of diabetes mellitus at the medical emergency units at the CHU-SO of Lom&#233;. The question is about a prospective study carried on along 12 months from 1
  <sup>st</sup> January, to December 31, 2013. It implicated 83 diabetes patients known or unknown admitted at the casualty department for an acute metabolic complication. In total the frequency of acute metabolic complications of diabetes mellitus that have been essentially done through the ketoacidosis model (73.49%) and hypoglycaemic (26.5%) is of 23.38%. Majority of diabetes patients were of type 2 (68.66%) and aged 50 and over with a sex-ratio of 0.76. The ketoacidosis revealed the disease in 43.37% cases. The main factors of ketoacidosis decompensations were infections, treatment termination and myocarditis ischaemia. Hypoglycemia decompensation factors were due to the absence or deficiency of food, the overdosage. Metabolic complications of diabetes then remain frequent. Infection and treatment termination are the major factors of ketoacidosis decompensation whereas those of the absence or deficiency of food are that of hypoglycemia. The prevention is compulsory through early screening of the disease and high treatment awareness of diabetes patients.
 
</p></abstract><kwd-group><kwd>Diabetes</kwd><kwd> Ketoacidosis Hypoglycemia</kwd><kwd> Cause</kwd><kwd> Prevention</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Diabetes is a chronic disease that affects a great number of people worldwide. [<xref ref-type="bibr" rid="scirp.93275-ref1">1</xref>] . If in the past diabetes caused the death of people in developed countries, developing countries today are not in safety [<xref ref-type="bibr" rid="scirp.93275-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref2">2</xref>] . Its evolution is speckled with complications namely acute metabolic complications which caused the admission of a great number of people at the emergency services and intensive care unit at a mortality rate estimated at 30.8% [<xref ref-type="bibr" rid="scirp.93275-ref3">3</xref>] in Morocco and at 28.1% in Mali [<xref ref-type="bibr" rid="scirp.93275-ref4">4</xref>] . The gravity of these complications leads to the recognition of its factors leading to their right treatment and their prevention. Hence the interest of our study aims to study the factors profile at the origin of the acute metabolic complications of the disease in Lom&#233;.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>It was a prospective transversal and descriptive study over twelve months, from 1<sup>st</sup> January to December 31, 2013. It took place in the medical emergency department of Sylvanus Olympio Teaching Hospital of Lom&#233;. Our study concerned all known and unknown diabetic patients who were admitted to medical emergencies for acute metabolic complications (ketoacidosis, hyperosmolar hyperglycemia syndrome, hypoglycemia). The diagnosis of ketoacidosis was based on a hyperglycemia superior or equal to 2.5 g/l, glycosuria and ketonuria. The diagnosis of hyperglycemia-hyperosmolar syndrome was based on dehydration, hyperglycemia superior or equal to 6 g/l, an absence of ketonuria, and hyperosmolarity above 350 mmol/l. The diagnosis of hypoglycemia was based on a glicemia inferior to 0.6 g/l. Were not included patients who don’t agree to participate to this study.</p><p>Parameters studied for each patient are as follow: epidemiological factors (age, sex, socio-professional status), type of diabetes, clinical manifestations at admission, type of acute metabolic decompensation, decompensation factors (at clinical and paraclinical examination). The systematic paraclinical check-up of all patients was glycemia, urinary test strip (glycosuria, ketonuria, albuminuria, nitrites, PH); hemogram, blood ionogram, uremia, serum creatinine, thick blood (looking for plasmodium), cytobacteriological study of urine, and electrocardiogram. Other assessments were as a result of the symptomatology and the progressive modalities under treatment. The Khi-2 test was used to assess the significance while associated with p &lt; 0.05.</p></sec><sec id="s3"><title>3. Results</title><sec id="s3_1"><title>3.1. Epidemiological Aspects</title><p>During our period of listening, 83 had suffered acute metabolic complications out of 355 diabetics admitted to the unit that is 23.83% of rate. The frequency of metabolic complications increased to 60 years old people and regresses beyond. The females were the most concerned with a sex ratio of 0.76 (36 men versus 47 women). In most cases housewives were represented at a rate of 45.78%. Noninsulin-dependent diabetes was represented in 68.66% compared to 31.34% for insulin-dependent diabetes. If 43.37% of diabetes patients are unaware of their disease, 56.62% were known and were under treatment of which 33 under an oral antidiabetic and 14 under insulin.</p></sec><sec id="s3_2"><title>3.2. Clinical Aspects</title><p>The most frequent clinical manifestations at polypnee admission (N = 35), coma (N = 29), fever (N = 25), deterioration of general state of health (N = 23), dehydration (N = 18), polyuria-polydipsia (N = 17).</p><p>The types of metabolic decompensation were ketoacidosis (73.49%) and hypoglycemia (26.51%).</p></sec><sec id="s3_3"><title>3.3. Decompensation Factors</title><p>The most common ketoacidosis decompensation factors were infection (52.46%) and treatment termination (23%) as shown in <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>These different factors of decompensation were statistically connected to the ketoacidosis with a Khi2 to 127.89 and a p &lt; 0.01.</p><p>The most frequent found infections were those insoft tissues (28.12%), malaria (25%) and urinary infections (12.5%) as shown in <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> Distribution of patients according to decompensation factors</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Decompensation factors acidocetosique (ketoacidosis)</th><th align="center" valign="middle" >Number</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >Infection</td><td align="center" valign="middle" >32</td><td align="center" valign="middle" >52.46</td></tr><tr><td align="center" valign="middle" >Treatment termination</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >23</td></tr><tr><td align="center" valign="middle" >Myocardic ischemia</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >6.56</td></tr><tr><td align="center" valign="middle" >Corticotherapy</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3.28</td></tr><tr><td align="center" valign="middle" >Pregnancy</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.64</td></tr><tr><td align="center" valign="middle" >Thrombophlebitis</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.64</td></tr><tr><td align="center" valign="middle" >Traditional medicine</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3.28</td></tr><tr><td align="center" valign="middle" >Unspecified factors</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >23</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Distribution of patients regarding infection</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Infection</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >Infection of the skin and soft part</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >28.12</td></tr><tr><td align="center" valign="middle" >Malaria</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >25</td></tr><tr><td align="center" valign="middle" >urinary infections</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >12.5</td></tr><tr><td align="center" valign="middle" >General infection</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >9.37</td></tr><tr><td align="center" valign="middle" >Pulmonary Tuberculosis</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >9.37</td></tr><tr><td align="center" valign="middle" >Lung disease of trivial germ</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >6.25</td></tr><tr><td align="center" valign="middle" >Feverish acute gastroenteritis</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >6.25</td></tr><tr><td align="center" valign="middle" >Viral B Hepatitis</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >3.12</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >32</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>Concerning hypoglycemia, factors associated with the hypoglycemic decompensation were respectively due to the absence or deficiency of food after taking antidiabetic medicines (81.81%) and the overdosage of antidiabetic medicines (9.09%) with a test of khi2 a p to 0.0029.</p></sec></sec><sec id="s4"><title>4. Discussion</title><sec id="s4_1"><title>4.1. Epidemiological Aspects</title><p>We recorded 83 cases of acute metabolic complications of diabetes out of 355 diabetics admitted at the unit, that is to say a frequency of 23.38%, similar to those reported by Sow [<xref ref-type="bibr" rid="scirp.93275-ref5">5</xref>] in Dakar and by Ou&#233;draogo [<xref ref-type="bibr" rid="scirp.93275-ref6">6</xref>] in Ouagadougou respectively 23% and 22.86%. But one should note that the frequency of these complications is differently appreciated by African authors [<xref ref-type="bibr" rid="scirp.93275-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref8">8</xref>] .</p><p>Our study observed a frequent growth of metabolic complications of people getting to 60 years of age and a regression after this age. This gradual decrease in these complications could be explained by the short life expectancy in our countries. This same observation was made by Diakit&#233; [<xref ref-type="bibr" rid="scirp.93275-ref4">4</xref>] in Mali in 2010, but its peak was 70 years, coping with the European data especially the French ones which estimate that the increase is observed up to 75 years and strongly decreases beyond due to the excess of diabetic mortality [<xref ref-type="bibr" rid="scirp.93275-ref9">9</xref>] . As we consider sex, the sex ratio is differently reported according to sets of studies [<xref ref-type="bibr" rid="scirp.93275-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref10">10</xref>] .</p><p>Acute metabolic complications have more affected low-income groups in our study. This same observation was made by Wright [<xref ref-type="bibr" rid="scirp.93275-ref11">11</xref>] in England in 2009 whom study reported nearly 32% of decompensation patients being unemployed. The predominance of metabolic complications in this socio-economic level may be explained not only by the lack of therapeutic respect but also by that of medical follow-up due to limited financial means.</p></sec><sec id="s4_2"><title>4.2. Clinical Aspects</title><p>Clinical manifestations at admission are dominated by coma (34.91%), fever (30.12%), impairment of general health (27.71%), digestive disorders (3132%) and dehydration (20.48%). This clinical profile remains classic. But it is reported at various frequencies according to sets of studies [<xref ref-type="bibr" rid="scirp.93275-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref10">10</xref>] .</p></sec><sec id="s4_3"><title>4.3. Hyperglycemia Decompensation Factors</title><sec id="s4_3_1"><title>4.3.1. Infections</title><p>They were the main mode of hyperglycemic decompensation. Infections are one of the most frequent and serious of recurrent complications of diabetes. [<xref ref-type="bibr" rid="scirp.93275-ref12">12</xref>] . On the one hand diabetes favours immunodepression for infections and on the other hand, infections favour the decompensation of diabetes. It results in a vicious circle hard to separate [<xref ref-type="bibr" rid="scirp.93275-ref13">13</xref>] . The infectious sites remain the same with a distribution, reported in various ways in the study [<xref ref-type="bibr" rid="scirp.93275-ref10">10</xref>] . Infections of the skin and soft tissues (leg erysipelas, boil, diabetes at the foot, over-infected bedsore) mostly drew our attention as well as in [<xref ref-type="bibr" rid="scirp.93275-ref14">14</xref>] series opposed to some studies which consider them in the second place [<xref ref-type="bibr" rid="scirp.93275-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref15">15</xref>] . This difference of opinion could be explained by the particularity of the bacterial area, climate or lifestyle (poor corporal hygiene) with regard to the regions where the works are carried out. Regarding the 5 cases of pulmonary infections, lung tuberculosis has been noted with three patients. Indeed, the incidence of tuberculosis remains two to three times greater in diabetes patients than in non-diabetics. Radi reported two cases in his sets of study (6.6%) of pleuropneumonia infections including one Fendi tuberculosis [<xref ref-type="bibr" rid="scirp.93275-ref16">16</xref>] and Mbadinga-Mupangu [<xref ref-type="bibr" rid="scirp.93275-ref17">17</xref>] got respectively in their series 15% and 5.2% of respiratory infections. Urogenital infections caused the ketoacidosis decompensation in 7 patients. Indeed, most of the time, urinary infection in the diabetes patient is asymptomatic and therefore develop silently and can be complicated by pyelonephritis in patients already at a risk, some of nephropathy diabetes.</p></sec><sec id="s4_3_2"><title>4.3.2. Termination of Treatment</title><p>It is preceded by infection in second position. The reasons for this treatment termination were: weariness of treatment, financial issues and religious beliefs. Indeed, the quality of treatment observance remains a major problem in the caring of chronic diseases, and the financial problem as well as religious beliefs constitute the major obstacles to access to treatment in developing countries [<xref ref-type="bibr" rid="scirp.93275-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.93275-ref19">19</xref>] . A national policy of free antidiabetic drugs must be considered in our countries. Moreover, ethno-cultural approach of the disease has to be taken into account in therapy education so as to optimize the caring of patients.</p></sec><sec id="s4_3_3"><title>4.3.3. Myocardial Ischemia</title><p>We dealt with four of our patients. In his set Sarr [<xref ref-type="bibr" rid="scirp.93275-ref10">10</xref>] also reported myocardial ischemia as a factor of ketoacidosis decompensation. Painless ischemia occurrence and an acute myocardial infarct in a diabetes patient is much higher compared to non-diabetics [<xref ref-type="bibr" rid="scirp.93275-ref20">20</xref>] . These patients with myocardial infarction have a poor prognosis and hyperglycemia on admission and is as a result a predictive hospital mortality factor.</p></sec><sec id="s4_3_4"><title>4.3.4. Corticotherapy</title><p>Two of our patients have decompensated because of corticosteroid treatment. Corticosteroids induce insulin resistance. They reduce the effect of insulin by increasing gluconeogenesis and lowering the collecting and use of possibilities of glucose by peripheral tissues [<xref ref-type="bibr" rid="scirp.93275-ref21">21</xref>] . However, diabetes imbalance is higher if the level of glyceric hemoglobin exceeds 8% and when age and body mass index are high [<xref ref-type="bibr" rid="scirp.93275-ref21">21</xref>] .</p></sec><sec id="s4_3_5"><title>4.3.5. The Pregnancy</title><p>Pregnancy originated the inaugural ketoacidosis decompensation in one of our patients. It was a question of an extra-uterine pregnancy. One must note that the retention of dead egg has been reported as a cause of ketoacidosis decompensation by Sarr [<xref ref-type="bibr" rid="scirp.93275-ref10">10</xref>] . So one must insist more on diabetes screening of our people and on treatment awareness because a pregnancy does with metabolic preparation and the conception must be conceived by controlling glycaemia and consider a perfect normalized glycemic hemoglobin.</p></sec><sec id="s4_3_6"><title>4.3.6. Undefined Factors</title><p>In our sets, it was not possible to find the active factor in 16.87%. In the Fendi sets [<xref ref-type="bibr" rid="scirp.93275-ref16">16</xref>] , ketosis remains unclear in two cases. In Sarr’s [<xref ref-type="bibr" rid="scirp.93275-ref10">10</xref>] , no etiological factor was found in 6.84% cases. As for Mbadinga-Mupangu [<xref ref-type="bibr" rid="scirp.93275-ref17">17</xref>] , he reported 12.3% of undefined factors.</p></sec></sec><sec id="s4_4"><title>4.4. Hypoglycemic Decompensation Factors</title><p>The absence or deficiency of meals after taking antidiabetic medicine has been the most frequent cause of hypoglycemia in our study. This result matches with that of Sihem’s [<xref ref-type="bibr" rid="scirp.93275-ref22">22</xref>] which requires a good education of diabetes treatment. The overdose of antidiabetic drugs reported in our sets has also been reported by Sihem [<xref ref-type="bibr" rid="scirp.93275-ref22">22</xref>] .</p></sec></sec><sec id="s5"><title>5. Conclusion</title><p>Despite the improvement of diabetes patients’ caretaking, the acute metabolic complications of diabetes mellitus remain relatively frequent still with a little and unclear prognosis. Prevention of these decompensations necessarily is possible not only by an early screening of the disease but also by quality of treatment awareness of any diabetic patient and people around him.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Balaka, A., Tchamdja, T., Djagadou, K.A., N&#233;mi, K.D., Djibril, M.A. and Redah, D. (2019) Factors Associated to the Acute Metabolic Decompensation of Diabetes in Lome. Open Journal of Internal Medicine, 9, 12-18. https://doi.org/10.4236/ojim.2019.92003</p></sec></body><back><ref-list><title>References</title><ref id="scirp.93275-ref1"><label>1</label><mixed-citation publication-type="book" xlink:type="simple">Papoz, I. and Delcourt, C. (1996) Le diabète et ses complications dans la population Francaise. MASSON. Ed. Inserm, Paris, 106.</mixed-citation></ref><ref id="scirp.93275-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Nebi&amp;#233;, L.V.A. (1993) Les complications du diabète sucr&amp;#233; en milieu hospitalier en C&amp;#244;te d’Ivoire: Etude transversale d’une population homog&amp;#232;ne de 120 patients au CHU de Treichville. Facult&amp;#233; de M&amp;#233;decine de l’Universit&amp;#233; de Cocody. Th&amp;#232;se de M&amp;#233;decine, Abidjan, No. 25.</mixed-citation></ref><ref id="scirp.93275-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Mohamadi, M., El-Idrissi, F., Belkadir, J., El Idrissi-Langhari, A. and Benabed, K. (1999) Mortalit&amp;#233; diab&amp;#233;tique dans un service de m&amp;#233;decine &amp;#224; propos de 117 cas. M&amp;#233;decine du Maghreb &amp;#233;lectronique, 58, 5-9.</mixed-citation></ref><ref id="scirp.93275-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Diakit&amp;#233;n, Y. (2010) Prise en charge des complications m&amp;#233;taboliques aigues du diab&amp;#232;te sucr&amp;#233; dans le service d’anesth&amp;#233;sie et r&amp;#233;animation du CHU Gabriel Tour&amp;#233;. Th&amp;#232;se de m&amp;#233;decine. Facult&amp;#233; de m&amp;#233;decine, pharmacie et d’odonto-stomatologie de l’universit&amp;#233; de Bamako, No. 17.</mixed-citation></ref><ref id="scirp.93275-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Sow, A.M., Sankal&amp;#233;, M. and Ndiaye, M. (1979) Le coma diab&amp;#233;tique et le coma chez les diab&amp;#233;tiques au S&amp;#233;n&amp;#233;gal. M&amp;#233;decine d’Afrique noire &amp;#233;lectronique, 26, 731-737.</mixed-citation></ref><ref id="scirp.93275-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Ou&amp;#233;draogo, S.M. (1998) Motifs de consultation, complications et facteur de d&amp;#233;compensation des diab&amp;#233;tiques en urgences au centre hospitalier National Yalgado Ou&amp;#233;draogo (Apropos de 85 cas). Th&amp;#232;se de m&amp;#233;decine, Facult&amp;#233; des sciences de la sant&amp;#233; de Ouagadougou, No. 25, 125p.</mixed-citation></ref><ref id="scirp.93275-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Orban, J.C. and Ichai, C. (2008) Complications m&amp;#233;taboliques aigu&amp;#235;s du diab&amp;#232;te sucr&amp;#233;. R&amp;#233;animation, 17, 761-767. https://doi.org/10.1016/j.reaurg.2008.09.006</mixed-citation></ref><ref id="scirp.93275-ref8"><label>8</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>El Hassane</surname><given-names> S. </given-names></name>,<etal>et al</etal>. (<year>2000</year>)<article-title>Complications majeures du diab&amp;#232;te sucr&amp;#233; en Afrique</article-title><source> Annales de M&amp;#233;decine Interne</source><volume> 151</volume>,<fpage> 673</fpage>-<lpage>678</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.93275-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Blickl&amp;#233;, J.F., Attali, J.R., Barrou, Z., Brocker, P., De Rekeneire, N., et al. (1999) Le diab&amp;#232;te du sujet ag&amp;#233;. Diabetes and Metabolism, 25, 84-93.</mixed-citation></ref><ref id="scirp.93275-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Sarr, A., Diedhiou, D., N’dour-Mbaye, N.M., L&amp;#233;ye, Y.M., KA-Ciss&amp;#233;, M.S., L&amp;#233;ye, A., et al. (2011) Acidoc&amp;#233;tose chez le sujet diab&amp;#233;tique de Type 1: A propos de 73 cas collig&amp;#233;s &amp;#224; Dakar. Mali m&amp;#233;dical, 26, 50-54.</mixed-citation></ref><ref id="scirp.93275-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Wright, J., Ruck, K., Rabbitts, R., Charlton, M., et al. (2009) Diabetes Ketoacidosis in Birmingham, UK; 2000-2009, and Evaluation of Risk Factors for Recurrence and Mortality. British Journal of Diabetes and Vascular Disease, 9, 278-282.https://doi.org/10.1177/1474651409353248</mixed-citation></ref><ref id="scirp.93275-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Drabo, Y.J., Kabore, J., Lengani, A. and Ilboudo, P.D. (1996) Diab&amp;#232;te sucr&amp;#233; au Centre hospitalier National de Ouagadougou: Epid&amp;#233;miologie, types et manifestations cliniques. Bulletin de la Soci&amp;#233;t&amp;#233; de pathologie exotique, 89, 185-190.</mixed-citation></ref><ref id="scirp.93275-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Raherison, R.E. (2013) Infections communautaires chez les diab&amp;#233;tiques hospitalis&amp;#233;s au service d’endocrinologie de l’h&amp;#244;pital Universitaire Joseph Rasetabefelatanana. M&amp;#233;moire de M&amp;#233;decine Interne, Facult&amp;#233; de m&amp;#233;decine de l’Universit&amp;#233; d’Antananarivo, No. 274.</mixed-citation></ref><ref id="scirp.93275-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Radi, L., Chadli, A., El Ghimari, H. and Tarouqi, A. (2009) Les complications infectieuses r&amp;#233;v&amp;#233;lant le diab&amp;#232;te de type 2. Diabetes and Metabolism, 35, A89.https://doi.org/10.1016/S1262-3636(09)72062-2</mixed-citation></ref><ref id="scirp.93275-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Belouidhnine, M., Zouaoui, C., Jaidarie, A., Ouertani, H. and Borni, Z. (2013) Diab&amp;#232;te et complications infectieuses: aspects &amp;#233;pid&amp;#233;miologiques et cliniques. Diab&amp;#232;te et M&amp;#233;tabolisme, 39, A117. https://doi.org/10.1016/S1262-3636(13)72127-X</mixed-citation></ref><ref id="scirp.93275-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Fendi, O., Gaigi, I., Khadhtaoui, E., Falfoul, A., Ben Mami, F., Trabelsi, N., et al. (2011) La c&amp;#233;tose diab&amp;#233;tique: Facteurs de d&amp;#233;compensation. Diabetes and Meabolism, 37, A81. https://doi.org/10.1016/S1262-3636(11)70826-6</mixed-citation></ref><ref id="scirp.93275-ref17"><label>17</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Mbadinga-Mupangu</surname><given-names> N. </given-names></name>,<etal>et al</etal>. (<year>1991</year>)<article-title>Les facteurs de d&amp;#233;compensation du diab&amp;#232;te sucr&amp;#233; au Congo</article-title><source> M&amp;#233;decine d’Afrique noire &amp;#233;lectronique</source><volume> 38</volume>,<fpage> 764</fpage>-<lpage>66</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.93275-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Tieno, H., Bouda, M., Ouedraogo, S.M., Traore, R., Ouedraogo, C. and Drabo, Y.J. (2010) Observance du traitement antidiab&amp;#233;tique dans un pays en d&amp;#233;veloppement: Le cas du Burkina Faso. M&amp;#233;decine des Maladies M&amp;#233;taboliques, 2, 207-211.https://doi.org/10.1016/S1957-2557(10)70046-8</mixed-citation></ref><ref id="scirp.93275-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Carmoi, T., Verret, C., Debonne, J.M. and Klotz, F. (2007) Prise en charge du diab&amp;#232;te de type 2 en Afrique subsaharienne: Constats actuels et perspectives. M&amp;#233;decine Tropicale, 67, 601-606.</mixed-citation></ref><ref id="scirp.93275-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Brandle, M., Lehmann, R. and Spinas, G.A. (2001) Epid&amp;#233;miologie, diagnostic et prophylaxie de la maladie coronarienne en pr&amp;#233;sence du diab&amp;#232;te sucr&amp;#233; de type 2. Forum m&amp;#233;d. Suisse, 1, 545-549. https://doi.org/10.4414/fms.2001.04154</mixed-citation></ref><ref id="scirp.93275-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Garcia, C., Banal, F., Bordoir, L., Leberre, J.P., Mayaudon, H., et al. (2008) Diab&amp;#232;te et corticoth&amp;#233;rapie. M&amp;#233;decine des Maladies M&amp;#233;taboliques, 2, 587-592.https://doi.org/10.1016/S1957-2557(08)74922-8</mixed-citation></ref><ref id="scirp.93275-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Sihem, T., Leila, S., Molka, C., Amel, M., Maha, K., et al. (2001) Les hypoglyc&amp;#233;mies graves chez les diab&amp;#233;tiques. Diab&amp;#232;te et m&amp;#233;tabolisme, 37, A50.https://doi.org/10.1016/S1262-3636(11)70690-5</mixed-citation></ref></ref-list></back></article>