<?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">OJPed</journal-id><journal-title-group><journal-title>Open Journal of Pediatrics</journal-title></journal-title-group><issn pub-type="epub">2160-8741</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojped.2022.121002</article-id><article-id pub-id-type="publisher-id">OJPed-114593</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>
 
 
  Become Immediate of Newborns Operated in the Neonatology Department of the Hospital and University Center Gabriel Toure of Bamako (Mali)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Oumar</surname><given-names>Coulibaly</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>Hawa</surname><given-names>Gouro Diall</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>Pierre</surname><given-names>Togo</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>Hawa</surname><given-names>Camara</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>Fatoumata</surname><given-names>Léonie Françoise Diakité</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>Lala</surname><given-names>Ndrayni Sidibé</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>Leyla</surname><given-names>Maiga</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>Ibrahima</surname><given-names>Ahamadou</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>Abdoul</surname><given-names>Karim Doumbia</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>Adama</surname><given-names>Dembelé</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>Belco</surname><given-names>Maiga</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>Karamoko</surname><given-names>Sacko</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>Mohamed</surname><given-names>Elmouloud Cissé</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>Djeneba</surname><given-names>Konaté</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>Fousseyni</surname><given-names>Traoré</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>Yacouba</surname><given-names>Aba Coulibaly</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>Issa</surname><given-names>Amadou Touré</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>Hamadi</surname><given-names>Sissoko</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>Mariam</surname><given-names>Maiga</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Alou</surname><given-names>Samake</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bourama</surname><given-names>Kané</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>Guédiouma</surname><given-names>Dembelé</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>Abdoul</surname><given-names>Aziz Diakité</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>Fatoumata</surname><given-names>Dicko Traoré</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>Mariam</surname><given-names>Sylla</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>Boubacar</surname><given-names>Togo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Reference Health Center of the Municipality III, Bamako, Mali</addr-line></aff><aff id="aff4"><addr-line>Reference Health Center of the Municipality VI, Bamako, Mali</addr-line></aff><aff id="aff2"><addr-line>Pediatric Surgery Department of the Gabriel Touré CHU, Bamako, Mali</addr-line></aff><aff id="aff1"><addr-line>Neonatology Department of the Gabriel Touré CHU, Bamako, Mali</addr-line></aff><aff id="aff5"><addr-line>Mali Hospital, Bamako, Mali</addr-line></aff><pub-date pub-type="epub"><day>06</day><month>01</month><year>2022</year></pub-date><volume>12</volume><issue>01</issue><fpage>12</fpage><lpage>18</lpage><history><date date-type="received"><day>22,</day>	<month>November</month>	<year>2021</year></date><date date-type="rev-recd"><day>11,</day>	<month>January</month>	<year>2022</year>	</date><date date-type="accepted"><day>14,</day>	<month>January</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>
 
 
  Neonatal surgical pathologies in developing countries are characterized by high mortality. The aim of this work was to describe the characteristics of the newborn and its surgical pathologies treated in the neonatal department of the Gabriel Tour&#233; University Hospital in Bamako (Mali). 
  <b>Patients and method:</b>
   This is a retrospective study of 626 files of newborns hospitalized over a period of 3 years (January 2016 to December 2018) for a surgical pathology, whether operated on or not. We have studied the etiological, therapeutic and evolutionary aspects. 
  <b>Results:</b>
   During the study period, we collected 626 patients who had surgical pathology, i
  .
  e
  .
   a frequency of 5.35%. The average therapeutic consultation time was 2 days with extremes (1 and 30 days). Pathologies of the abdominal wall and digestive tract represented 57.9% (n = 84) followed by pathologies of the spine 26.9% (n = 39). The mean treatment time was 4.5 days. Twenty-three point sixteen (23.16%) newborns could be operated on. The neonatal mortality rate was 12.4% (n = 18). Mortality was postoperative (100%) with a mean time to onset of 5 days. Abdominal wall pathologies were responsible for 8.7% (n = 13) of deaths. <b>Conclusion:</b> Surgical pathologies of the newborn are characterized by delayed treatment with high mortality. Improving their prognosis requires early diagnosis (prenatal diagnosis) and adequate management.
 
</p></abstract><kwd-group><kwd>Newborn</kwd><kwd> Surgical Pathologies</kwd><kwd> Mortality</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Neonatal surgical pathologies are frequent causes of neonatal morbidity and mortality [<xref ref-type="bibr" rid="scirp.114593-ref1">1</xref>]. Neonatal surgical pathologies are structural anomalies or abnormal functions that appear from birth to the end of the first month of life and require urgent surgical treatment [<xref ref-type="bibr" rid="scirp.114593-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref2">2</xref>]. It is most often a surgical emergency involving the vital and/or functional prognosis. While in industrialized countries life expectancy has improved thanks to prenatal diagnosis, in developing countries there are several difficulties in managing it [<xref ref-type="bibr" rid="scirp.114593-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref3">3</xref>]. In Africa, they are thought to be the reason for around 10% of surgical interventions in the various pediatric surgical services [<xref ref-type="bibr" rid="scirp.114593-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref4">4</xref>]. Neonatal surgical emergencies represented 19.8% of admissions to the pediatric surgery department of the Yopougon University Hospital in Abidjan, C&#244;te d'Ivoire [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] and 12.8% of those to the Pediatric Surgery department of the Lamord&#233; National Hospital in Niamey in Niger [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>]. In some contexts, newborns are cared for in general surgery departments. This is the case in Bukavu in the Democratic Republic of Congo, where surgical pathology of the newborn represents 1.31% of surgical pathology [<xref ref-type="bibr" rid="scirp.114593-ref7">7</xref>]. In Bamako in Mali, the neonatal and pediatric surgery services, the last level of national reference structures, provide synergistic management of neonatal surgical pathologies. The aim of this study was to identify neonatal surgical pathologies and to analyze their prognosis in our environment.</p></sec><sec id="s2"><title>2. Patients and Method</title><p>This was a retrospective study to aim for descriptive carried out in the neonatology department of the Gabriel Tour&#233; Hospital and University Center in Bamako, between January 2016 and December 2018, i.e. in 3 years. All newborns aged 0 to 28 days hospitalized for a life-threatening or non-life-threatening surgical pathology and whose records were usable constituted our study population. For each patient, the parameters studied were: age at admission, place of origin, means of evacuation, consultation time, weight on admission, diagnostic time, different pathologies, time therapeutic (defined as the time between indication and surgery) and mortality. Data were entered and analyzed using Epi info software version 7.2.</p></sec><sec id="s3"><title>3. Results</title><p>Of the 11,697 hospitalizations during the study period, 626 cases of surgical pathology were retained and 145 received surgery. The frequency of neonatal surgical pathologies was 5.35%. These were 85 boys and 60 girls (sex ratio: 1.4). The mean age at admission was an extreme 2.9 days (0 and 26 days). Thirty-five cases (24.2%) came from a primary structure, 57 cases (39.3%) from a secondary structure, 35 cases (24.2%) from a tertiary structure and 18 cases (12, 4%) from home. The average weight at admission was extreme 2281 g (1300 and 4100g). The reasons for consultation were dominated by spina bifida (26.9%) followed by anal imperforation (25.5%), <xref ref-type="table" rid="table1">Table 1</xref>. The mean time to consultation was extreme 1.7 days (0 and 30 days). The diagnosis of the various pathologies was made either from the referent structure or in our department with an average diagnostic delay of 3 extreme days (24 hours and 6 days). Antenatal diagnosis was made in 2 cases (1.4%). Pathologies of the digestive tract and abdominal wall accounted for 57.9% (n = 84) followed by pathologies of the spine 26.9% (n = 39). These different pathologies were summarized in <xref ref-type="fig" rid="fig1">Figure 1</xref>. Surgical management involved 145 newborns (23.16%). The mean treatment time was 4.5 days with extremes (1 and 26 days). The associated malformations were dominated by microcephaly (10.3%) followed by poly-malformation syndrome (6.9%) (<xref ref-type="fig" rid="fig2">Figure 2</xref>). Intraoperative complications were 6.2% (n = 9) dominated by hemorrhage (3.4%), cardiopulmonary arrest (2.1%) and respiratory distress (0.7%). The overall mortality in our series was 18 cases (12.4%), all postoperatively. These deaths had an average delay of 12.4 extreme days (D1 to D48). Deaths occurred in a picture of severe infection and/or sepsis in 66.7% (n = 12) and</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of newborns according to the reason for consultation</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Reason for consultation</th><th align="center" valign="middle" >effective</th><th align="center" valign="middle" >percentage</th></tr></thead><tr><td align="center" valign="middle" >Spina bifida</td><td align="center" valign="middle" >39</td><td align="center" valign="middle" >26.9</td></tr><tr><td align="center" valign="middle" >Omphalocele</td><td align="center" valign="middle" >37</td><td align="center" valign="middle" >25.5</td></tr><tr><td align="center" valign="middle" >Anal imperforation</td><td align="center" valign="middle" >28</td><td align="center" valign="middle" >19.3</td></tr><tr><td align="center" valign="middle" >Abdominal distension</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >6.9</td></tr><tr><td align="center" valign="middle" >Abdominal distension + INN</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >4.8</td></tr><tr><td align="center" valign="middle" >Malformation syndrome</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >3.4</td></tr><tr><td align="center" valign="middle" >Hydrocephalus</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >4.1</td></tr><tr><td align="center" valign="middle" >Bladder extrophy</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >2.8</td></tr><tr><td align="center" valign="middle" >Congenital malformation</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1.4</td></tr><tr><td align="center" valign="middle" >Laparoschisis</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >2.8</td></tr><tr><td align="center" valign="middle" >Macrocephaly</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >Strangulated inguinal hernia</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >Abdominal malformation</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.7</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >145</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>Spina Bifida, omphalocele and anal imperforation were the main reasons for consultation.</p><p>hemodynamic shock in 33.3% (n = 8). The distribution of mortality by pathology was summarized in <xref ref-type="fig" rid="fig3">Figure 3</xref>.</p></sec><sec id="s4"><title>4. Discussion</title><p>The aim of this work was to describe the characteristics of the newborn and its surgical pathologies treated in the neonatal department of the CHU Gabriel Tour&#233; in Bamako.</p><p>The limitations of this study are inherent in its retrospective nature. However, this study allows us to have an overview of this pathology in the absence of related data. Neonatal surgical pathologies represented 5.35% of admissions to our department with an annual incidence of 48.3 newborns. Our frequency is close to that of Natacha B in Libreville, higher than that of Fabrice C. G in Congo [<xref ref-type="bibr" rid="scirp.114593-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref8">8</xref>]. In African series, neonatal surgical pathologies represented 9.7% to 61% of admissions [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>]. In Indian and British series this incidence was higher than ours, 60 to 301 newborns per year [<xref ref-type="bibr" rid="scirp.114593-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref11">11</xref>]. The demographic characteristics of the populations and the specificities of the pediatric surgical services which cover them are variable and determine the hospital incidence. The mean age in our study was 2.9 days. In African and Indian series, we found average ages greater than ours ranging from 5 to 8 days [<xref ref-type="bibr" rid="scirp.114593-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>]. The majority of newborns were 0 to 7 days old on admission to our study (89.7%). In the studies by Badrinath et al. in Uganda, and Omid col. in Niger, the majority of patients were also admitted during the first week of life with 63.5% and 60.2% of cases, respectively parents to see their child early and urgently [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>]. In our series, as in the literature, we note a male predominance: respectively 58.5% of boys and between 56% and 75% of male newborns [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref12">12</xref>]. On the other hand, in the series of Mieret J. C, in Yopougon and Natacha B in Libreville, [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref8">8</xref>], the female sex was predominant. There is no clear consensus on the predominance of a genre.</p><p>The most common diagnosis in our study was anorectal malformations, 37.9% (n = 55), followed by myelomeningocele, 26.9% (n = 39) and anterior abdominal wall defects: omphalocele and laparoschisis, 22.1% (n = 32). In other African studies [<xref ref-type="bibr" rid="scirp.114593-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>], anorectal malformations were the most frequently found pathology: varying between 9.5% and 39% of cases. In a meta-analysis of neonatal surgery in Africa (51 studies) intestinal atresia was observed in 54.9% of the work, anterior abdominal wall defect in 52.9% of studies and anorectal malformations in 47.1% of the Ekenze series, in 2016 [<xref ref-type="bibr" rid="scirp.114593-ref3">3</xref>]. As a result, Natacha et al. in Libreville found a predominance of digestive disorders, 47.6% followed by anomalies of the anterior wall of the abdomen, 26.2% [<xref ref-type="bibr" rid="scirp.114593-ref8">8</xref>]. The spectrum of neonatal surgical admissions may vary from hospital to hospital depending on the availability of prenatal diagnostic facilities, transport facilities and presentation time.</p><p>The newborns in our series were operated less frequently (23.16%) than in other studies: from 28.3% to 67.7% of operated newborns [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref12">12</xref>]. Variations in the proportions between pathologies requiring emergency surgery (colostomy for anaorectal malformation for example) and those for which conservative treatment is possible (such as omphalocele) could explain such a difference.</p><p>Mortality is in most studies higher than ours (12.4%) varying from 25.8% to 61.1%) [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref8">8</xref>]. Advances in diagnostic techniques and perioperative care have greatly improved the therapeutic results of neonatal surgery. Despite everything, there are disparities in terms of the results of neonatal surgery between countries with high income and those with average or low income [<xref ref-type="bibr" rid="scirp.114593-ref3">3</xref>]. According to a meta-analysis this is due to late presentation and inadequate facilities in 39 studies (76.5%), lack of trained support staff in 32 series (62.7%) and lack of intensive care neonates in 29 studies (56.9%) (Ekenze, 2016) [<xref ref-type="bibr" rid="scirp.114593-ref3">3</xref>].</p><p>The morbidity and mortality factors identified in various studies were: delay in diagnosis (which could be explained by the lack of antenatal diagnosis) and management, prematurity and low birth weight, impairment of digestive system, unsafe transport, cultural factors (beliefs and customs), anesthetic complications and the presence of multiple congenital anomalies) [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref13">13</xref>].</p><p>The intraoperative complications in our study were managed by filling, transfusion, and respiratory support. Postoperative mortality in our study was 100% (n = 18). In developing countries, postoperative mortality is still very high, varying from 8.7% to 62.3% [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref14">14</xref>]. This variation in mortality could be linked, among other things, to the size of the samples and the type of structure where the study was carried out. Mortality in our patients was mostly early mortality: 38.9% of deaths (7 cases). Many other African authors have found this predominance of deaths during the first week with respectively 43.5%, 58.2%, 68% and 70% of cases [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref14">14</xref>].</p><p>Deaths occurred primarily in cases of anorectal malformations (33.3%) in our series. This observation is valid in the series by Ralahy in 2010 (28%) [<xref ref-type="bibr" rid="scirp.114593-ref15">15</xref>]. On the other hand, Mieret in Ivory Coast and Omid in Niger found a predominance of omphaloceles for deaths (34.21% and 26%) [<xref ref-type="bibr" rid="scirp.114593-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.114593-ref6">6</xref>].</p></sec><sec id="s5"><title>5. Conclusion</title><p>Neonatal surgical emergencies are relatively frequent in our study. They are characterized by a delay in diagnosis and treatment, burdened by high mortality in developing countries. Improving the prognosis of newborn surgical emergencies requires diagnosis (antenatal diagnosis) and early management, the appropriate technical platform and the creation of a neonatal intensive care unit would reduce this mortality rate.</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>Coulibaly, O., Diall, H.G., Togo, P., Camara, H., Diakit&#233;, F.L.F., Sidib&#233;, L.N., Maiga, L., Ahamadou, I., Doumbia, A.K., Dembel&#233;, A., Maiga, B., Sacko, K., Ciss&#233;, M.E., Konat&#233;, D., Traor&#233;, F., Coulibaly, Y.A., Tour&#233;, I.A., Sissoko, H., Maiga, M., Samake, A., Kan&#233;, B., Dembel&#233;, G., Diakit&#233;, A.A., Traor&#233;, F.D., Sylla, M. and Togo, B. 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