<?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">OJOG</journal-id><journal-title-group><journal-title>Open Journal of Obstetrics and Gynecology</journal-title></journal-title-group><issn pub-type="epub">2160-8792</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojog.2020.1060074</article-id><article-id pub-id-type="publisher-id">OJOG-100866</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>
 
 
  The HIV’s Transmission from the Mother to the Child at the Community Hospital Center of Bangui (Central African Republic)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>N.</surname><given-names>R. Ngbale</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>C.</surname><given-names>E. Gaunefet</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>A.</surname><given-names>Koïrokpi</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>G.</surname><given-names>D. Kossa-ko-Ouakoua</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>S.</surname><given-names>Matoulou-Mbala-Wa-Ngogbe</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>S.</surname><given-names>Ouapou</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>A.</surname><given-names>Manirakiza</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>L.</surname><given-names>Kobangue</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>A.</surname><given-names>Sepou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Public Health of the University of Bangui, Bangui, Central African Republic</addr-line></aff><aff id="aff1"><addr-line>Gynaecology-Obstetrics Service of the Bangui Community Hospital, Bangui, Central African Republic</addr-line></aff><aff id="aff3"><addr-line>Dermatology-Venerology Service of the CNHU of Bangui, Bangui, Central African Republic</addr-line></aff><pub-date pub-type="epub"><day>10</day><month>06</month><year>2020</year></pub-date><volume>10</volume><issue>06</issue><fpage>802</fpage><lpage>808</lpage><history><date date-type="received"><day>6,</day>	<month>May</month>	<year>2020</year></date><date date-type="rev-recd"><day>9,</day>	<month>June</month>	<year>2020</year>	</date><date date-type="accepted"><day>12,</day>	<month>June</month>	<year>2020</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>
 
 
  Objective:
   Assess the impact of B + option on mother-to-child HIV’s transmission at the community university hospital center after 4 years of use.
   
  <b>Patients and methods:</b>
   This was a retrospective and analytical study from January 1st 2015 to December 31st 2018 i.e. 4 years. The population’s study was on HIV-positive mothers and their infants care
   
  in the service.
   
  <b>Results:</b>
   A total of 323 files of infants born from HIV-positive mothers were selected and having performed the PCR. 9 of them were HIV positive representing a rate of 2.79% mother-to-child HIV’s transmission.
   
  This prevalence was 1.1% for women who started ART before and during pregnancy. The average age of newborns was 29 years. Mothers were literally rating in 24.15% during the period of starting antiretroviral therapy, 63% during pregnancy and 19% before pregnancy. For the delivery’s way 295 delivered vaginally; they represented 91.33%. Cesarean delivery was 8.67%. Exclusive breastfeeding represented 87.31% of the diet. Mothers who started ARV therapy during the labor and after delivery were more likely to transmit HIV to their infants than mothers who started ART before and during pregnancy (p = 0.01). The other risk factors were represented by premature rupture of the membranes (p = 0.0001), hours of labor (p = 0.0001), use of suction cup (p = 0.0005), birth weight less than 2500
   
  g (p = 0.00).
   
  <b>Conclusion:</b>
   Mother-to-child HIV’s transmission still remains a public health problem at the Community University Hospital.
 
</p></abstract><kwd-group><kwd>Transmission</kwd><kwd> HIV</kwd><kwd> Community Hospital</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>For several years, the fight against the human immunodeficiency virus (HIV) has been a public health issue. A woman infected with HIV can transmit the virus to her baby during pregnancy, labor, delivery or breastfeeding. In the absence of any intervention, the risk of mother to child transmission (MTCT) of HIV is 15% to 30%. The World Health Organization (WHO) estimates that 3.3 million children living with HIV in 2012 were infected mainly vertically, and 90% of these infections had occurred in sub-Saharan Africa. In developed countries, the risk of MTCT for HIV has been reduced to less than 1% [<xref ref-type="bibr" rid="scirp.100866-ref1">1</xref>] . For more than 10 years, the Central African Republic has been developing a program to prevent mother-to-child transmission of HIV that covers the whole country, based on Niverapine prophylaxis to pregnant women and infants. Despite these interventions, the number of children infected with HIV remains high at 8%. That’s why in 2015 the B + option was adopted, which consists of systematic administration for life of the anti-retroviral triple therapy to pregnant or lactating women regardless of the CD4 count. In order to achieve the objectives of eliminating mother-to-child transmission of HIV [<xref ref-type="bibr" rid="scirp.100866-ref2">2</xref>] , our study therefore proposes to assess the impact of the B + option on the transmission after 4 years of use.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>It was a retrospective and analytical study from January 1st 2015 to December 31st 2018, 4 years. The study’s population was on HIV-positive mothers and their infants care in the service. The study included all HIV-positive women who started HAART with combination therapy (Efavirenz 600 mg, Emtricilabine 200 mg and Tenofovir 245 mg) before or during the pregnancy, as well as those who started ART during the labor. after their screening The newborns were followed up in the service: In the case of exclusive breastfeeding the newborn received Nevirapine 4 mg/Kg once a day up to a week after complete cessation of breastfeeding. In the case of replacement feeding newborns received Nevirapine 2 mg/Kg/day as a single dose for 6 weeks or Zidovudine 2 mg/Kg twice a day for 6 weeks. A first Polymerase Chain Reaction (PCR) screening was carried out at six weeks of life. If the test result (PCR1) is positive, the infant was referred to Pediatrics to start antiretroviral therapy (ART). If the test is negative and the infant is on exclusive breastfeeding, a second test (PCR2) was performed six weeks after stopping breast milk. Data’s input and analysis were carried out using Word 2013, Excel 2013 and Epi-info software version 7.1.3.3. The statistical test used for the compare was ch-2 with a significance level p &lt; 0.05. The Fisher test was used when the workforce used was less than 5.</p><p>RESULTS: In total, out of 323 files of infants born from HIV-positive mothers selected and having carried out the PCR, 9 were HIV positive, representing a rate of 2.79% mother-to-child HIV’s transmission This rate was 1.1% for women who started ART before and during pregnancy. The average age of newborns was 29 with extremes 15 to 45. The mothers were literally rate in 24.15% and the primary level in 44.58%. The majority of mothers were pauciparous during the period of starting antiretroviral therapy 63% during pregnancy and 19% before pregnancy. The 233 women who achieved CD4 counts, 49.3% had a CD4 count below 350. Hours of labor were normal in 86.07 parturients. Pregnant women who gave birth after a premature rupture of the membranes represented 4.33%. For the delivery’s way 295 delivered vaginally; they represented 91.33%. Cesarean delivery was 8.67%. Out of 323 registered infants, 117 (36.22%) were boys and 206 (63.78%) were girls. Exclusive breastfeeding represented 87.31% of the diet. Mothers who started ARV therapy during labor and after delivery were more likely to transmit HIV to their infants than mothers who started ART before and during pregnancy (p &lt; 0.01). The other risk factors were represented by premature rupture of the membranes (p &lt; 0.0001), hours of work (p &lt; 0.0001), use of suction cup (p &lt; 0.0005), birth weight less 2500 g (p &lt; 0.00), and episiotomy (p &lt; 0.0009) (<xref ref-type="fig" rid="fig1">Figure 1</xref> and Tables 1-4).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of pregnant women according to the state of the membranes, working time, use of suction cup</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Number</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >Premature rupture of membranes</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >No Yes</td><td align="center" valign="middle" >309 14</td><td align="center" valign="middle" >95.6 4.33</td></tr><tr><td align="center" valign="middle" >Duration of labor</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Undetermined Extended Normal</td><td align="center" valign="middle" >15 30 278</td><td align="center" valign="middle" >4.64 9.29 86.07</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >323</td><td align="center" valign="middle" >100.00</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 infants according to whether the mother was delivered by episiotomy and use of suction cup</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Number</th><th align="center" valign="middle" >Pourcentage</th></tr></thead><tr><td align="center" valign="middle" >Episiotomy</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >No Yes Undetermined</td><td align="center" valign="middle" >270 29 24</td><td align="center" valign="middle" >83.59 8.98 7.43</td></tr><tr><td align="center" valign="middle" >Suction cup</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >No Yes</td><td align="center" valign="middle" >289 34</td><td align="center" valign="middle" >89.4 10.6</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >323</td><td align="center" valign="middle" >100.00</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Distribution of infants according to feeding method</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Infant feeding</th><th align="center" valign="middle" >Number</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >Mixed breastfeeding</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >3.71</td></tr><tr><td align="center" valign="middle" >Exclusive breastfeeding</td><td align="center" valign="middle" >282</td><td align="center" valign="middle" >87.31</td></tr><tr><td align="center" valign="middle" >Artificial breastfeeding</td><td align="center" valign="middle" >29</td><td align="center" valign="middle" >8.98</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >323</td><td align="center" valign="middle" >100.00</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Distribution of children according to HIV virological status and factors influencing HIV transmission</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="4"  >Treatment start period</th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >HIV positive</td><td align="center" valign="middle" >HIV negative</td><td align="center" valign="middle" >p</td></tr><tr><td align="center" valign="middle" >During labor and after childbirth</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >52</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Before and during pregnancy</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >262</td><td align="center" valign="middle" >0.01</td></tr><tr><td align="center" valign="middle" >Premature rupture of membranes</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >0.0001</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >306</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Duration of labor</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >extended</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >22</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Normal</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >277</td><td align="center" valign="middle" >0.0001</td></tr><tr><td align="center" valign="middle" >Birth weight</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;2500 g</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >107</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >≥2500 g</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >214</td><td align="center" valign="middle" >0.0096</td></tr></tbody></table></table-wrap></sec><sec id="s3"><title>3. Discussion</title><p>The diagnosis of HIV/AIDS in infants before the age of 3 months is made by polymerase chain reaction (PCR). PCR detects the virus itself in the blood (or blood cells). In our study, the transmission rate was 2.79% at PCR1 over the entire population studied, this rate is close to those achieved in Mali and Ivory Cost which were respectively 1.98% and 3.28% [<xref ref-type="bibr" rid="scirp.100866-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.100866-ref4">4</xref>] ; different from that one of Ngeumbi in 2004 which was 17.4% [<xref ref-type="bibr" rid="scirp.100866-ref5">5</xref>] , of Ngbal&#233; in 2013 carried out in the same service had a rate of 8.3% [<xref ref-type="bibr" rid="scirp.100866-ref6">6</xref>] . This difference is justified by the protocol used at the time which was A + option that consisted in administering a monotherapy based on nevirapine alone whereas in our series 82% of women before and during pregnancy were already on antiretroviral triple therapy for their own health by reducing the viral load and the risk of mother-to-child transmission. The average age was 29 with extremes of 15 to 45. This average age is practically the same as that one found by SANON in Senegal [<xref ref-type="bibr" rid="scirp.100866-ref7">7</xref>] . The average age varying from one country to another can be explained by the weight of culture and lifestyle on sexual behavior. In the Central African Republic, women enter sex early, as SEPOU noted during a study on sexual parameters among Central African women in urban areas [<xref ref-type="bibr" rid="scirp.100866-ref8">8</xref>] . Understanding and assimilating the messages given by health education services are easier for women with a certain level of education. Several studies have shown that uneducated women have more health problems than those with less education [<xref ref-type="bibr" rid="scirp.100866-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.100866-ref10">10</xref>] .</p><p>Screening is the gateway to prevention and care [<xref ref-type="bibr" rid="scirp.100866-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.100866-ref12">12</xref>] . For example, mothers who were screened before or during pregnancy have had the privilege of receiving interventions to reduce the risk of mother-to-child HIV’s transmission. Administering ARVs during pregnancy and childbirth effectively reduces mother-to-child transmission of the virus. These treatments reduce the risk of MTCT by decreasing the replication of the virus in the mother on the one hand, and on the other hand by ensuring prophylaxis in the infant during and after his exposure to the virus [<xref ref-type="bibr" rid="scirp.100866-ref7">7</xref>] . In our study, the mother-to-child transmission rate among women who were screened and put on treatment before and during pregnancy was 1.1%, similar to studies done in France and Thailand which have proven their effectiveness with ARV treatment during pregnancy with a transmission rate that had gone from 15% to 1% after 10 years. A low CD4 count is an indicator of high viral load; more immunosuppression is advanced the higher the rate of transmission [<xref ref-type="bibr" rid="scirp.100866-ref7">7</xref>] . Ngwende’s Zimbabwe study found that children born to mothers with low CD4 counts showed more risk to have HIV infection [<xref ref-type="bibr" rid="scirp.100866-ref13">13</xref>] . Other studies have found similar results reporting that women with a CD4 count &lt; 200 cells/ml were 5 times more likely to transmit HIV [<xref ref-type="bibr" rid="scirp.100866-ref14">14</xref>] . In our series, 49.30% of women had a CD4 ≤ 350/mm<sup>3</sup>. These women therefore had a high risk of transmitting HIV to their children; even if it’s not statistically significant. Our result could be explained by the fact that most mothers with CD4 ≤ 350/mm<sup>3</sup> during pregnancy were already receiving antiretroviral therapy. This could reduce the viral load and therefore the risk of mother-to-child HIV’s transmission. Obstetric factors have been shown to influence the HIV’s transmission between mother and child. In our cohort, obstetric factors such as prolonged labor, and premature rupture of the membranes were significantly associated. This observation is close to that one Landesman made during a prospective study by observing 522 deliveries he discovered that the duration of labor after rupture of the membranes represented a preponderant factor in the risk of perinatal HIV’s transmission [<xref ref-type="bibr" rid="scirp.100866-ref15">15</xref>] . Generally, the use of a suction cup is according to the rule of art causes less trauma which reduces the risk of MTCT. In our series on 30 pregnant women who gave birth after applying a suction cup, four significantly transmitted HIV to their child. Our result corroborates that one of Tebeu in Cameroon [<xref ref-type="bibr" rid="scirp.100866-ref16">16</xref>] . Finally among the 82.04% of our patients who had started their treatment before and during pregnancy; 14% or 53.84% had been delivered by episiotomy. The MTCT of HIV among these was less than 1%. It can be said that despite the use of episiotomy, the ARV treatment started early probably reduced the viral load thus reducing the risk of MTCT of HIV in a way significant. Children born with birth weight &lt; 2500 grams had a significantly increased risk of MTCT compared to those born with a weight ≥ 2500 grams. This could be justified by the method of delivery of a low birth weight fetus which is made into a cannonball causing microtrauma for the AIDS virus to easily enter.</p></sec><sec id="s4"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s5"><title>Cite this paper</title><p>Ngbale, N.R., Gaunefet, C.E., Ko&#239;rokpi, A., Kossa-ko-Ouakoua, G.D., Matoulou-Mbala-Wa-Ngogbe, S., Ouapou, S., Manirakiza, A., Kobangue, L. and Sepou, A. (2020) The HIV’s Transmission from the Mother to the Child at the Community Hospital Center of Bangui (Central African Republic). Open Journal of Obstetrics and Gynecology, 10, 802-808. https://doi.org/10.4236/ojog.2020.1060074</p></sec></body><back><ref-list><title>References</title><ref id="scirp.100866-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">OMS (2012) Utilisation des Antirétroviraux pour traiter la femme enceinte et prévenir l’infection à VIH chez le nourrisson: Mise à jour pragmatique. 10.  
http://www.who.int/about/licensing/copyright_form/en/index.html</mixed-citation></ref><ref id="scirp.100866-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">OMS. Organisation mondiale de la Santé. Département de lutte contre le VIH/sida. 20, Avenue Appia CH-1211 Genève 27 Transmission du VIH de la mère à l’enfant SUISSE Courriel: hiv-aids@who.int. http://www.who.int/hiv/fr</mixed-citation></ref><ref id="scirp.100866-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Traore, Y., Dicko Traore, F. and Teguete, I. (2011) Prévention de la transmission mère enfant du VIH en milieu hospitalier africain, Bamako. Mali Medical, 1, 18-22.</mixed-citation></ref><ref id="scirp.100866-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Lasme-Guillao, B.E., Sissoko, G.P. and Amon-Tanoh-Dick, F. (2011) Transmission mère enfant du VIH à Abidjan: Surmonter les obstacles socioculturels. Cote d’Ivoire. Médecine d’Afrique Noire, 58, 395-403.</mixed-citation></ref><ref id="scirp.100866-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Ngembi, E., Yanza, M.C., Sepou, A., Ndoide, Y.M. and Gresenguet, G. (2004) Performance du projet de prévention de la transmission du VIH de la mère à l’enfant en République Centrafricaine. Bulletin Médical d’Owendo, 24, 170-172.</mixed-citation></ref><ref id="scirp.100866-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Ngbale, R.N., Komangoya, N.D., Diemer, H., Goddot-Nangouma, M.J.C., Gaunefet, C.E., Songo-Kette, K., Koirokpi, A., Akilimali, P.Z. and Sepou, A. (2013) Difficultés de la prévention de la transmission du VIH de la mère à l’enfant dans les maternités au Sud du Sahara. Cas de l’Hopital Communautaire de Bangui. Annals of African Medicine, 2, 1345-1351.</mixed-citation></ref><ref id="scirp.100866-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Sanon, D.A. (2006) Evaluation du statut séro-immunologique des enfants nés de Mères séropositives au VIH suivies au centre de traitement Ambulatoire du service des maladies infectieuses Ibrahima Diop du CHU de Fann de Dakar. Thèse DEA en Population, Développement et Santé de la Reproduction, Dakar, 63 p.</mixed-citation></ref><ref id="scirp.100866-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Sepou, A., Yanza, M.C., Domande-Modanga, Z. and Nguembi, E. (2002) Paramètres sexuels chez les femmes Centrafricaines en milieu urbain. Médecine d’Afrique Noire, 49, 87-91.</mixed-citation></ref><ref id="scirp.100866-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Sepou, A., Enza, J. and Nali, M.N. (2000) Les difficultés à l’expansion de la contraception en zones urbaine et semi-urbaine de la République Centrafricaine. Médecine d’Afrique Noire, 47, 73-78.</mixed-citation></ref><ref id="scirp.100866-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Desclaux, A., Sow, K., Mbaye, N. and Signate, S.Y.H. (2014) Passer de la prévention de la transmission mère-enfant du VIH à son élimination avant 2015: Un objectif irréaliste? Enjeux sociaux au Sénégal Médecine et Sante Tropical.</mixed-citation></ref><ref id="scirp.100866-ref11"><label>11</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Meda</surname><given-names> N. </given-names></name>,<etal>et al</etal>. (<year>2010</year>)<article-title>Prévention de la transmission mère-enfant du VIH: état de lieux et nouvelles stratégies</article-title><source> Transcriptases</source><volume> 143</volume>,<fpage> 1</fpage>-<lpage>6</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.100866-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">ONUSIDA (2003) Conseil et test VIH volontaires: Une voie d’accès à la prévention et aux soins. Genève, 104 p.</mixed-citation></ref><ref id="scirp.100866-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Ngwende, S., Gombe, N.T., Midzi, S., Tshimanga, M., Shambira, G. and Chadambuk, A.A. (2013) Factors Associated with HIV Infection among Children Born to Mothers on the Prevention of Mother to Child Programme at Chitungwiza Hospital Zimbabwe 2008. BMC Public Health, 13, Article No. 1181.  
https://doi.org/10.1186/1471-2458-13-1181</mixed-citation></ref><ref id="scirp.100866-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Iiff, P.J., Piwoz, E.G. and Tavengwa, N.V. (2005) Early Exclusive Breast Feeding Reduces the Risk of Post Natal HIV 1 Transmission and Increases HIV Free Survival. AIDS, 19, 699-708. https://doi.org/10.1097/01.aids.0000166093.16446.c9</mixed-citation></ref><ref id="scirp.100866-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Landesman, S.H., Kalish, L.A. and Burns, D.N. (1996) Obstétrical Factor and the Transmission of Human Immunodeficiency Virus Type 1 from Mother to Child. The New England Journal of Medicine, 334, 1617-1623.  
https://doi.org/10.1056/NEJM199606203342501</mixed-citation></ref><ref id="scirp.100866-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Tebeu, P.M., Kouam, L. and Obama Abena, M.T. (2004) Facteurs de transmission verticale du VIH: Augmentation potentielle chez l’adolescente; Cameroun. Médecine d’Afrique Noire, 51, 407-408.</mixed-citation></ref></ref-list></back></article>