<?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">
    wjcs
   </journal-id>
   <journal-title-group>
    <journal-title>
     World Journal of Cardiovascular Surgery
    </journal-title>
   </journal-title-group>
   <issn pub-type="epub">
    2164-3202
   </issn>
   <issn publication-format="print">
    2164-3210
   </issn>
   <publisher>
    <publisher-name>
     Scientific Research Publishing
    </publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">
    10.4236/wjcs.2025.154011
   </article-id>
   <article-id pub-id-type="publisher-id">
    wjcs-142168
   </article-id>
   <article-categories>
    <subj-group subj-group-type="heading">
     <subject>
      Articles
     </subject>
    </subj-group>
    <subj-group subj-group-type="Discipline-v2">
     <subject>
      Medicine 
     </subject>
     <subject>
       Healthcare
     </subject>
    </subj-group>
   </article-categories>
   <title-group>
    Heart Transplant at Seoul National University Hospital: Is It Reproducible in Sub-Saharan Africa?
   </title-group>
   <contrib-group>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Koutoua Eric
      </surname>
      <given-names>
       Katche
      </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>
       Ahou Sarrah
      </surname>
      <given-names>
       Assie
      </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>
       Jeanne Iris
      </surname>
      <given-names>
       Degni
      </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>
       Dominique Sarra
      </surname>
      <given-names>
       Arriko
      </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>
       Ahoua Gnita
      </surname>
      <given-names>
       Kone
      </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>
       Lucien
      </surname>
      <given-names>
       Asseke
      </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>
       Kwadjau Anderson
      </surname>
      <given-names>
       Amani
      </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>
       Patrick
      </surname>
      <given-names>
       Bogbe
      </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>
       Jean Calaire
      </surname>
      <given-names>
       Degre
      </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>
       Aimé
      </surname>
      <given-names>
       Kirioua-Kamenan
      </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>
       Junior
      </surname>
      <given-names>
       Yeo
      </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>
       Kouassi Antonin
      </surname>
      <given-names>
       Souaga
      </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>
       Woog-Han
      </surname>
      <given-names>
       Kim
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff2"> 
      <sup>2</sup>
     </xref>
    </contrib>
   </contrib-group> 
   <aff id="aff1">
    <addr-line>
     aInsitut de Cardiologie Abidjan, Université Félix Houphouët-Boigny, Abidjan, Côte d’ivoire
    </addr-line> 
   </aff> 
   <aff id="aff2">
    <addr-line>
     aChildren Hospital, Séoul National University Hospital, Seoul, Republic of Korea
    </addr-line> 
   </aff> 
   <pub-date pub-type="epub">
    <day>
     08
    </day> 
    <month>
     04
    </month>
    <year>
     2025
    </year>
   </pub-date> 
   <volume>
    15
   </volume> 
   <issue>
    04
   </issue>
   <fpage>
    122
   </fpage>
   <lpage>
    134
   </lpage>
   <history>
    <date date-type="received">
     <day>
      2,
     </day>
     <month>
      January
     </month>
     <year>
      2025
     </year>
    </date>
    <date date-type="published">
     <day>
      21,
     </day>
     <month>
      January
     </month>
     <year>
      2025
     </year> 
    </date> 
    <date date-type="accepted">
     <day>
      21,
     </day>
     <month>
      April
     </month>
     <year>
      2025
     </year> 
    </date>
   </history>
   <permissions>
    <copyright-statement>
     © 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>
    <b>Introduction</b>: Heart transplantation is used to treat heart failure. The first human-to-human heart transplant took place in South Africa in 1967. However, this surgical technique is not practiced in sub-Saharan Africa, but heart failure is clearly increasing in the young and active African populations. We report the case of 03 heart transplants successfully performed in the pediatric cardiac surgery department at Seoul National University Hospital. 
    <b>Objective</b>: To present heart transplantations for congenital heart disease in order to reproduce them technically in sub-Saharan Africa. 
    <b>Cases</b> 
    <b>series</b>
    <b>:</b> 
    <b>Case</b> 
    <b>1</b>: Male, 3 years old. Background: main pulmonary artery (MPA) banding, Ventricular Septal defect (VSD) closure, Heart failure requiring left ventricular assist device (LVAD) implantation. Echocardiography: left ventricle dysfunction (EF 28%), Heart transplantation. The immediate postoperative follow-up was simple. 
    <b>Case</b> 
    <b>2</b>: Male, 9 years old. Background: Dilated cardiomyopathy (DCMP), Left ventricular assist Device (LVAD) implantation. Echocardiography: Severe LV dysfunction, global akinesia, LV FS/EF 10.4/22.4% (PLAX). Heart transplantation. The immediate postoperative follow-up was simple. 
    <b>Case</b> 
    <b>3</b>: Male, 20 years old. Background: dilated cardiomyopathy (DCMP), Duchenne Muscular Dystrophy (DMD), Left ventricular assisted device (L-VAD) (HeartMate 3) implantation. Echocardiography: Aggravated LV dysfunction (EF 26% - 29%). Heart transplantation. The immediate postoperative follow-up was simple. 
    <b>Conclusion</b>: Heart transplantation according to the bi-caval procedure has made it possible to treat children with end-stage heart failure at Seoul National University Hospital. End-stage heart failure in Africa is clearly increasing among the young working population. Although Africa faces a range of challenges, heart transplantation is reproducible in sub-Saharan Africa.
   </abstract>
   <kwd-group> 
    <kwd>
     Heart Transplantation
    </kwd> 
    <kwd>
      Heart Failure
    </kwd> 
    <kwd>
      Ventricular Assist Device
    </kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <sec id="s1">
   <title>1. Introduction</title>
   <p>
    <xref ref-type="bibr" rid="scirp.142168-"></xref>Heart transplantation (HTx) is the final treatment for patients with advanced heart failure <xref ref-type="bibr" rid="scirp.142168-1">
     [1]
    </xref>. It is estimated that 26 million adults worldwide are living with heart failure (HF) <xref ref-type="bibr" rid="scirp.142168-2">
     [2]
    </xref>, costing roughly 1% - 2% of healthcare expenditures in Europe and North America <xref ref-type="bibr" rid="scirp.142168-3">
     [3]
    </xref>. In Korea, heart failure prevalence was estimated to be 1.53% in 2013 <xref ref-type="bibr" rid="scirp.142168-4">
     [4]
    </xref>. Heart failure is a serious and frequent pathology in Africa. It affects young and active subjects <xref ref-type="bibr" rid="scirp.142168-5">
     [5]
    </xref>. According to PIO et al. <xref ref-type="bibr" rid="scirp.142168-5">
     [5]
    </xref> in Togo, the prevalence of HFs was 28.6%. PIO found left ventricular systolic dysfunction in 213 patients (56.6%) <xref ref-type="bibr" rid="scirp.142168-5">
     [5]
    </xref>. Thiam <xref ref-type="bibr" rid="scirp.142168-6">
     [6]
    </xref> in Senegal reported a prevalence of 37.7%. In Côte d’Ivoire, according to Gnaba et al., HF accounted for 60 to 65% of hospitalized patients. The average left ventricular ejection fraction (LVEF) was 35.8 ± 13% <xref ref-type="bibr" rid="scirp.142168-7">
     [7]
    </xref>. The main identified causes of heart failure were ischemic heart disease (60%) and hypertensive heart disease (20%) <xref ref-type="bibr" rid="scirp.142168-7">
     [7]
    </xref>. Patients with end-stage heart failure and cardiomyopathies are candidates for heart transplantation. The first attempt was made 118 years ago, in 1905, by Alexis Carrel and Charles Guthrie at the University of Chicago. In 1967, Human-to-human heart transplantation, which is the replacement of a failing heart with one from a suitable donor, was first carried out by Dr Christian Barnard at the Groote Schuur Hospital in Cape Town, South Africa <xref ref-type="bibr" rid="scirp.142168-8">
     [8]
    </xref>. Since 1982, more than 14,000 heart transplants have been performed in pediatric patients worldwide <xref ref-type="bibr" rid="scirp.142168-9">
     [9]
    </xref>, which corresponds to around 10% of all heart transplants <xref ref-type="bibr" rid="scirp.142168-10">
     [10]
    </xref>. About 50% of pediatric patients received heart transplants due to CHD <xref ref-type="bibr" rid="scirp.142168-9">
     [9]
    </xref>, while this proportion is 2.2% in the adult comparison group <xref ref-type="bibr" rid="scirp.142168-11">
     [11]
    </xref> <xref ref-type="bibr" rid="scirp.142168-12">
     [12]
    </xref>. The indications (<xref ref-type="table" rid="table1">
     Table 1
    </xref>) and contraindications (<xref ref-type="table" rid="table2">
     Table 2
    </xref>) for heart transplantation according to the European Society of Cardiology (ESC) and American Heart Association (AHA) guidelines are varied. There are two surgical techniques used in cardiac transplantation: the right atrial (RA) technique and the bi-caval technique. The bi-caval anastomosis technique is currently used. This gesture is not practiced in Sub-Saharan Africa, due to the absence of laws in force and certain beliefs. Dilated cardiomyopathies with severe heart failure are on the rise in our countries.</p>
   <p>We report the cases of 3 children who underwent successful heart transplants in pediatric cardiac surgery at Seoul National University Hospital from July to October 2024.</p>
   <table-wrap id="table1">
    <label>
     <xref ref-type="table" rid="table1">
      Table 1
     </xref></label>
    <caption>
     <title>
      <xref ref-type="bibr" rid="scirp.142168-"></xref>Table 1. Main indications for heart transplantation.</title>
    </caption>
    <table class="MsoTableGrid custom-table" border="0" cellspacing="0" cellpadding="0"> 
     <tr> 
      <td class="custom-bottom-td custom-top-td acenter" width="94.01%"><p style="text-align:center">Advanced heart failure</p></td> 
     </tr> 
     <tr> 
      <td class="custom-top-td aleft" width="94.01%"><p style="text-align:left">Cardiogenic shock with the need for circulatory support with devices or the need for continuous administration of inotropes</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Use of long-term circulatory support devices</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">NYHA III-IV, despite optimally tolerated therapy and application of resynchronization therapies</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Multiple episodes of fluid retention leading to pulmonary congestion or significant peripheral edema requiring high-dose diuretics or decreased cardiac output at res requiring inotropic and/or vasoconstrictor drugs leading to &gt;1 unscheduled emergency department visit or hospitalization in a year</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Severe cardiac dysfunction with LVEF &lt; 30% or right ventricular dysfunction or inoperable valvular diseases or elevated NT-proBNP values and evidence of severe diastolic dysfunction (ultrasound, cardiac catheterization ), or structural abnormalities according to the definitions for HFrEF, HfpEF.</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Intolerance to mild exercise with peak VO2 &lt; 10 Ml/kg/min</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Recurrent life-threatening ventricular arrhythmias despite ICD use or ablation therapy</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">End-stage heart failure due to congenital defects without evidence of pulmonary hypertension</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Resistant angina without further possibility of pharmaceutical or surgical treatment</p></td> 
     </tr> 
     <tr> 
      <td class="custom-bottom-td aleft" width="94.01%"><p style="text-align:left">Abbreviations: NYHA, New York Heart Association; LVEF, Left Ventricular Ejection Fraction; HFpEF, Heart Failure with preserved Ejection Fraction; ICD, Implantable Cardioverter Defibrillator</p></td> 
     </tr> 
    </table>
   </table-wrap>
   <table-wrap id="table2">
    <label>
     <xref ref-type="table" rid="table2">
      Table 2
     </xref></label>
    <caption>
     <title>
      <xref ref-type="bibr" rid="scirp.142168-"></xref>Table 2. Main contraindications for heart transplantation.</title>
    </caption>
    <table class="MsoTableGrid custom-table" border="0" cellspacing="0" cellpadding="0"> 
     <tr> 
      <td class="custom-bottom-td custom-top-td acenter" width="94.01%"><p style="text-align:center">Active serious infection, except LVAD device infection, which is an indication</p></td> 
     </tr> 
     <tr> 
      <td class="custom-top-td aleft" width="94.01%"><p style="text-align:left">Severe peripheral vascular disease with reduced possibility of recovery and no possibility of revascularization</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Medically irreversible pulmonry hypertension (PASP &gt; 60 mmHg, PVR &gt;5 WU, TPG &gt; 15 mmHg)</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Malignancies with a poor prognosis</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Irreversible liver damage or kidney damage (eGFR &lt; 30 Ml/min/1.73 m<sup>2</sup>)</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Systemic disease involving multiple organs</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Abuse of alcohol or addictive substances</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Poor social support with inability to care in the period after surgery</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Serious neurological diseases</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Active pulmonary embolism</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Frailty (&gt;10 Ibs weight loss, fatigue, muscle cachexia</p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">BMI &gt; 35 kg/m<sup>2</sup></p></td> 
     </tr> 
     <tr> 
      <td class="aleft" width="94.01%"><p style="text-align:left">Diabetes with HbA1c &gt;7.5 % despite optimal meddication and target organ complications excluding retinopathy</p></td> 
     </tr> 
     <tr> 
      <td class="custom-bottom-td aleft" width="94.01%"><p style="text-align:left">Abbreviations: LVAD, Left Ventricular Assist Device; PASP, Pulmonary Artery Systolic Pressure; PVR, Pulmonary Vascular Resistance; TPG, Transpulmonary Pressure Gradient; eGFR, estimated Glomerular Filtration Rate; BMI, Body Mass Index; HbA1C, hemoglobin A1C</p></td> 
     </tr> 
    </table>
   </table-wrap>
  </sec><sec id="s2">
   <title>2. Case Series</title>
   <sec id="s2_1">
    <title>2.1. Case 1</title>
    <p>Male patient, 3 years old, height = 91 cm and weight = 15.3 Kg. Background: pulmonary hyper flow requiring a banding of the trunk of the pulmonary artery in July 2021. Veno-arterial extracorporeal membrane oxygenation (VA ECMO) insertion (2022/6/3). Finally, left ventricular assist device (LVAD) insertion was performed (2022/6/9). The patient was then transferred from his initial health center to Seoul National University Hospital (SNUH).</p>
    <p>
     <xref ref-type="bibr" rid="scirp.142168-"></xref>At Seoul National University Hospital, LVAD pump has been changed (2024/7/01). Ventricular Septal Defect has been closed (2022/10/24). Clinical examination had shown heart failure, Blood pressure = 109/73 mmHg, temperature = 36˚4 and saturation wSpO<sub>2</sub> = 96% - 99%. The patient had LVAD (Berlin heart, heart mate III) (CO 25 cc x 75 bpm = 1.875) in situ. The hemoglobin level was 10.7 g/dl, the platelet level was 138,000/mm<sup>3</sup>. The INR was 2.88 on warfarin.</p>
    <p>Normal Sinus Rythm, Left Atrial Dilatation, Left Ventricular Hypertrophy, prolonged QT (QTc 478 ms).</p>
    <p>1) LV dysfunction, septal thinning, paradoxal septal wall motion (+)</p>
    <p>LV EF (auto) 28% (A4C) 42% (Bip), (biplane simpson s) 43% (4CV simpson) 34.9%.</p>
    <p>(m mode PLAX) 32.6%, probably inaccurately measured d/t PSWM.</p>
    <p>2) LVAD inflow cannula in situ, peak vel 4.2 m/s at late systole</p>
    <p>In LV and LA cavity, no visible thrombus.</p>
    <p>Aortic valve opening (+) trivial AR.</p>
    <p>3) moderate-severe MR (type III large eccentric zet), MV annulus = 21.6 mm</p>
    <p>Careful preparation and perfect cooperation between the collection and transplantation teams. A complete preoperative check-up, Compatibility tests, The start of immunosuppressive treatment.</p>
    <p>GEA, full median sternotomy, pericardium -tenting, arterial cannulation-Distal ascending aorta, venous cannulation-SVC direct, IVC direct, Vent-RUPV, CPB 327 mn, ACC 191 mn, Donor ischemic time 163 mn; approach-LA, Aorta, RA, PA.</p>
    <p>Redo-sternotomy, Adhesiolysis, cannulation (distal ascending aorta, SVC, IVC, RUPV for vent); CBP on; L-VAD (Berline Heart Excor) weaning and clamping; additional dissectin and mobilization around SVC and RA and pulmonary vein; ACC. Cardiecomy.</p>
    <p>
     <xref ref-type="bibr" rid="scirp.142168-"></xref>ICD explantation, LVAD cannlae retrieval; donor heart CPS; LA anastomosis (5-0, double-layer continuous sutures, x4) (<xref ref-type="fig" rid="fig1">
      Figure 1
     </xref>); aorta anstomosis (5-0 prolene; double -layer continuous sutures, x2); ACC release; IVC-RA anastomosis (6-0 prolene, single-layer continuous sutures, x1); SVC anastomosis (6-0 prolene, single-layer continuous sutures, x1). Rewarming, root vent, CPB weaning; modified ultrafiltration; decannulation; meticulous bleeding control; chest tube insertion; pericardial coverage with seprafilm; wound closure layer-by-layer.</p>
    <p>Transfer to intensive care unit.</p>
    <fig id="fig1" position="float">
     <label>Figure 1</label>
     <caption>
      <title>Figure 1. Intraoperative view of heart transplantation, time of left atrium suture.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId14.jpeg?20250424013653" />
    </fig>
   </sec>
   <sec id="s2_2">
    <title>2.2. Case 2</title>
    <p>Male patient, 9 years old, height = 125 cm and weight = 23 Kg. Background: dilated cardiomyopathy (D-CMP); Biventricular dysfunction and dilatation.</p>
    <p>Maintenance treatment: ASA, Plavix, Dilatrend hold, Warfarin hold → heparinization, Lasilix, spironolactone, digoxin, Viagra</p>
    <p>Heart Failure, PHT d/t D-CMP s/p L-VAD (24. 01. 25)</p>
    <p>Clinical examination has shown heart failure, Blood pressure = 89/51 mmHg, heart rate = 90 - 95 per minute on Dobutamine 3 mcg/kg/min. Peripheral partial oxygen saturation wSpO2 (RA) 97% - 99%. The body temperature was 36.3˚C. Biological assessment: The haemoglobin level was 8.4, the platelet count was 222,000/mm<sup>3</sup>, the INR was 1.58.</p>
    <p>Chest X-rays were taken before and after transplantation (<xref ref-type="fig" rid="fig2">
      Figure 2
     </xref>).</p>
    <fig id="fig2" position="float">
     <label>Figure 2</label>
     <caption>
      <title>(A) (B)Figure 2. X-ray of the chest from the front. (A) Preoperative; (B) Postoperative.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="" />
    </fig>
    <fig id="fig2" position="float">
     <label>Figure 2</label>
     <caption>
      <title>(A) (B)Figure 2. X-ray of the chest from the front. (A) Preoperative; (B) Postoperative.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId15.jpeg?20250424013654" />
    </fig>
    <fig id="fig2" position="float">
     <label>Figure 2</label>
     <caption>
      <title>(A) (B)Figure 2. X-ray of the chest from the front. (A) Preoperative; (B) Postoperative.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId16.jpeg?20250424013654" />
    </fig>
    <p>The electrocardiogram showed junctional rhythm.</p>
    <p>Severe Left Ventricle dysfunction, global akinesia, LV FS/EF 10.4/22.4% (PLAX). LV apex inflow cannula and AAo outflow cannula in situ no visible thrombus below aortic valve. Mild MR. Severe RAE, RAA 19.8 cm<sup>2</sup> (Z 4.87), moderate TR, coaptation gap 13 mm, RV dilatation.</p>
    <p>
     <xref ref-type="bibr" rid="scirp.142168-"></xref>Careful preparation and perfect cooperation between the collection and transplantation teams. A complete preoperative check-up, Compatibility tests. The start of immunosuppressive treatment.</p>
    <p>GEA, full median sternotomy, pericardium-tenting, arterial cannulation-Distal ascending aorta, venous cannulation-SVC direct, IVC direct, Vent-RUPV, CPB 259 mn, ACC 157 mn, Donor ischemic time 153 mn; approach-LA, Aorta, RA, PA</p>
    <p>Redo-sternotomy, Adhesiolysis, cannulation (distal ascending aorta, SVC, IVC, RUPV for vent); CBP on; L-VAD (Berline Heart Excor) outflow graft clamping, LVAD (Berlin Heart Excor) weaning; additional dissection and mobilization around SVC and RA and pulmonary vein; ACC. Cardiecomy (<xref ref-type="fig" rid="fig3">
      Figure 3
     </xref>).</p>
    <fig id="fig3" position="float">
     <label>Figure 3</label>
     <caption>
      <title>(A) (B)Figure 3. View of the heart outside the body. (A) Pathological heart removed; (B) Donor heart ready for transplant.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="" />
    </fig>
    <fig id="fig3" position="float">
     <label>Figure 3</label>
     <caption>
      <title>(A) (B)Figure 3. View of the heart outside the body. (A) Pathological heart removed; (B) Donor heart ready for transplant.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId17.jpeg?20250424013655" />
    </fig>
    <fig id="fig3" position="float">
     <label>Figure 3</label>
     <caption>
      <title>(A) (B)Figure 3. View of the heart outside the body. (A) Pathological heart removed; (B) Donor heart ready for transplant.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId18.jpeg?20250424013655" />
    </fig>
    <fig id="fig4" position="float">
     <label>Figure 4</label>
     <caption>
      <title>Figure 4. Examination of the heart ready before transplantation.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId19.jpeg?20250424013655" />
    </fig>
    <p>ICD explantation, LVAD cannlae retrieval; donor heart examination (<xref ref-type="fig" rid="fig4">
      Figure 4
     </xref>); LA anastomosis (5-0, double-layer continuous sutures, x4); aorta anstomosis (5-0 prolene; double -layer continuous sutures, x2); ACC release; IVC-RA anastomosis (6-0 prolene, single-layer continuous sutures, x1); SVC anastomosis (6-0 prolene, single-layer continuous sutures, x1). Rewarming, root vent, CPB weaning; modified ultrafiltration; decannulation; meticulous bleeding control; chest tube insertion; pericardial coverage with seprafilm; wound closure layer-by-layer.</p>
    <p>Transfer to the intensive care unit.</p>
   </sec>
   <sec id="s2_3">
    <title>2.3. Case 3</title>
    <p>
     <xref ref-type="bibr" rid="scirp.142168-"></xref>Male patient, 20 years old, rhesus blood type AB+, height = 156 cm, weight = 54.9 Kg. Background: DMD (Duchenne Muscular Dystrophy); Hypercalciuria; dilated cardiomyopathy (DCMP); L-VAD (HeartMate 3) insertion (2022/12/13); anticoagulation: aspirin + warfarin, Heart failure medication: carvedilol 6.25 mg bid, ivabradine 5 mg bid. Clinical examination: heart failure.</p>
    <p>
     <xref ref-type="bibr" rid="scirp.142168-"></xref>Aggravated LV dysfunction: EF 26% - 29%, No visible intracardiac thrombus. LV dimension: no significant interval change.</p>
    <p>IVS flattening –; AV opening –; Mild to moderate AR; Mild to moderate MR; Trivial TR; Trivial PR; No pericardial effusion.</p>
    <p>Electrocardiogram showed normal sinus rhythm.</p>
    <p>The preoperative chest X-ray was normal and showed the left ventricular assist device (<xref ref-type="fig" rid="fig5">
      Figure 5
     </xref>).</p>
    <fig id="fig5" position="float">
     <label>Figure 5</label>
     <caption>
      <title>Figure 5. Chest x-ray from the front and side.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="" />
    </fig>
    <fig id="fig5" position="float">
     <label>Figure 5</label>
     <caption>
      <title>Figure 5. Chest x-ray from the front and side.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId20.jpeg?20250424013658" />
    </fig>
    <fig id="fig5" position="float">
     <label>Figure 5</label>
     <caption>
      <title>Figure 5. Chest x-ray from the front and side.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId21.jpeg?20250424013658" />
    </fig>
    <p>Careful preparation and perfect cooperation between the collection and transplantation teams. A complete preoperative check-up, Compatibility tests, The start of immunosuppressive treatment.</p>
    <fig id="fig6" position="float">
     <label>Figure 6</label>
     <caption>
      <title>Figure 6. CT angiography showing heart and L-VAD.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId22.jpeg?20250424013658" />
    </fig>
    <p>GEA, full median sternotomy, pericardium-tenting, arterial cannulation-Distal ascending aorta, venous cannulation-SVC direct, IVC direct, Vent-RUPV, CPB 289 mn, ACC 189 mn, Donor ischemic time 157 mn; approach-LA, Aorta, RA, PA.</p>
    <p>Redo-sternotomy, Adhesiolysis, cannulation (distal ascending aorta, SVC, IVC, RUPV for vent); CBP on; L-VAD (Berline Heart Excor) weaning and clamping; additional dissectin and mobilization around SVC and RA and pulmonary vein; ACC. Cardiecomy (<xref ref-type="fig" rid="fig7">
      Figure 7
     </xref>).</p>
    <fig id="fig7" position="float">
     <label>Figure 7</label>
     <caption>
      <title>(A) (B)Figure 7. View of a heart outside the organism, (A) Recipient’s heart; (B) Donor’s heart.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="" />
    </fig>
    <fig id="fig7" position="float">
     <label>Figure 7</label>
     <caption>
      <title>(A) (B)Figure 7. View of a heart outside the organism, (A) Recipient’s heart; (B) Donor’s heart.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId23.jpeg?20250424013659" />
    </fig>
    <fig id="fig7" position="float">
     <label>Figure 7</label>
     <caption>
      <title>(A) (B)Figure 7. View of a heart outside the organism, (A) Recipient’s heart; (B) Donor’s heart.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId24.jpeg?20250424013658" />
    </fig>
    <fig id="fig8" position="float">
     <label>Figure 8</label>
     <caption>
      <title>Figure 8. Intraoperative view of a heart transplant: beginning of anastomosis of LA.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId25.jpeg?20250424013659" />
    </fig>
    <p>ICD explantation, LVAD cannlae retrieval; donor heart CPS; Donor heart inspection: PFO primary closure (6-0 prolene, simple sure,x1); LA anastomosis (5-0, double-layer continuous sutures, x4) (<xref ref-type="fig" rid="fig8">
      Figure 8
     </xref>); aorta anstomosis (5-0 prolene; double -layer continuous sutures, x2); ACC release; IVC-RA anastomosis (6-0 prolene, single-layer continuous sutures, x1); SVC anastomosis (6-0 prolene, single-layer continuous sutures, x1). Rewarming, root vent, CPB weaning; modified ultrafiltration; decannulation; meticulous bleeding control; chest tube insertion; pericardial coverage with seprafilm; wound closure layer-by-layer.</p>
    <p>Transfer to the pediatric intensive care unit.</p>
   </sec>
  </sec><sec id="s3">
   <title>3. Discussion</title>
   <p>Heart transplantation (HTx) remains the last therapeutic resort for patients with advanced heart failure. The first clinical heart transplant was accomplished in an adult by Barnard in Cape Town, South Africa, in 1967 <xref ref-type="bibr" rid="scirp.142168-13">
     [13]
    </xref>. Thus, this first heart transplant in Africa has raised hope in the African population. But heart transplantation remains absent in sub-Saharan Africa. However, heart failure in the African working population is clearly on the rise. According to the Global Observatory of Donation and Transplantation 2017 database, Africa recorded only 14 heart transplants out of 7881 globally, representing 0.2% of the global total in 2016 <xref ref-type="bibr" rid="scirp.142168-14">
     [14]
    </xref>. Similarly, in 2022, the International Report on Organ Donation and Transplantation Activities recorded heart transplantations in only one country in Africa, Tunisia <xref ref-type="bibr" rid="scirp.142168-15">
     [15]
    </xref>.</p>
   <p>During our internship in the Department of Pediatric Cardiac Surgery at Seoul National University Hospital, 3 males children whose ages were 3, 9 and 20 years old were operated on. The majority of pediatric transplant patients are those with pre- and postoperative complex CHDs and those with cardiomyopathies. In our study, One patient had ventricular septal disease operated on and two patients had cardiomyopathy. In the pediatric population, congenital heart disease accounts for about half of the indications; these are either non-repairable malformations or malformations operated on but resulting in terminal heart failure. The 3 patients had left ventricular dysfunction with an ejection function of 28% for case 1, 22.4% for case 2 and 26% - 29% for case 3. The alteration of left ventricular function required the implementation of left ventricular support for the 3 patients. This essential ventricular support allows patients to wait until they have a donor for a heart transplant. All 3 patients had left ventricular assist device (L-VAD). These LVADs increase the difficulties and operating time during the preparation of the recipients. Recipients with congenital heart disease pose specific technical problems related to initial malformations and/or various palliative interventions. Heart transplantation in CHD patients is usually complicated by multiple previous operations, cardiac defects, abnormal situs, and collateral circulation, which should be precisely recorded before the heart transplantation. Case No. 1 had a VSD, i.e. a congenital heart disease. Case 2 had dilated cardiomyopathy of unidentified etiology. Case No. 3 had dilated cardiomyopathy, whose etiology was Duchenne Muscle Dystrophy. Though VAD has been widely used for end-stage heart failure and bridge-to-transplantation or destination therapy, VAD application in CHD patients is not extensively used <xref ref-type="bibr" rid="scirp.142168-16">
     [16]
    </xref>. VADs in pediatric and adult CHD populations are increasing due to the shortage of donor’s hearts and an increasing number of patients with heart failure <xref ref-type="bibr" rid="scirp.142168-17">
     [17]
    </xref> <xref ref-type="bibr" rid="scirp.142168-18">
     [18]
    </xref>. Previous studies found that VAD therapy can prolong survival in high-risk CHD patients who would either die or be delisted due to clinical deterioration <xref ref-type="bibr" rid="scirp.142168-19">
     [19]
    </xref>.</p>
   <p>Total heart transplantation requires careful preparation and perfect cooperation between the collection and transplantation teams. Particular attention should be paid to the condition of the pulmonary arterial bed. Accurate assessment of pulmonary vascular resistance. Several factors determine the outcome of HTx, such as ABO and HLA compatibility, graft size, ischemic time, and age. Active infection, peripheral vascular disease, malignancies, and increased BMI are frequent contraindications. The major complications of HTx include graft rejection, graft angiopathy, primary graft failure, infection, neoplasms, and retransplantation. Advances in the field of HTx encompass novel monitoring for acute cellular rejection and antibody-mediated rejection (Nikolaos) <xref ref-type="bibr" rid="scirp.142168-20">
     [20]
    </xref>.</p>
   <p>The 3 patients were operated on under general anesthesia and extracorporeal circulation, with moderate hypothermia. The heart transplant technique was the bicaval technique for the 3 patients. There are currently two surgical techniques used in cardiac transplantation: the right atrial (RA) technique and the bi-caval technique. The latter is a more recent technique and has become more popular than the former. In RA cardiac transplantation, when the native heart is explanted, the posterior walls of both atria of the recipient heart are left in place (<xref ref-type="fig" rid="fig9">
     Figure 9
    </xref>) and are anastomosed to the donor heart <xref ref-type="bibr" rid="scirp.142168-21">
     [21]
    </xref>.</p>
   <fig id="fig9" position="float">
    <label>Figure 9</label>
    <caption>
     <title>Figure 9. Right atrial technique (Backer, transplantation 2015) <xref ref-type="bibr" rid="scirp.142168-22">
       [22]
      </xref>.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="" />
   </fig>
   <fig id="fig9" position="float">
    <label>Figure 9</label>
    <caption>
     <title>Figure 9. Right atrial technique (Backer, transplantation 2015) <xref ref-type="bibr" rid="scirp.142168-22">
       [22]
      </xref>.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId26.jpeg?20250424013659" />
   </fig>
   <fig id="fig9" position="float">
    <label>Figure 9</label>
    <caption>
     <title>Figure 9. Right atrial technique (Backer, transplantation 2015) <xref ref-type="bibr" rid="scirp.142168-22">
       [22]
      </xref>.</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId27.jpeg?20250424013659" />
   </fig>
   <p>Figure 9. Right atrial technique (Backer, transplantation 2015) <xref ref-type="bibr" rid="scirp.142168-22">
     [22]
    </xref>.</p>
   <fig id="fig10" position="float">
    <label>Figure 10</label>
    <caption>
     <title>Figure 10. Bicaval technique (Backer, transplantation, 2015).</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="" />
   </fig>
   <fig id="fig10" position="float">
    <label>Figure 10</label>
    <caption>
     <title>Figure 10. Bicaval technique (Backer, transplantation, 2015).</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId28.jpeg?20250424013659" />
   </fig>
   <fig id="fig10" position="float">
    <label>Figure 10</label>
    <caption>
     <title>Figure 10. Bicaval technique (Backer, transplantation, 2015).</title>
    </caption>
    <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/1960579-rId29.jpeg?20250424013659" />
   </fig>
   <p>In the bi-caval technique (<xref ref-type="fig" rid="fig10">
     Figure 10
    </xref>), the RA is also explanted from the recipient, leaving only the posterior wall of the left atrium (LA) with four pulmonary veins attached <xref ref-type="bibr" rid="scirp.142168-21">
     [21]
    </xref>. Anastomoses are made between the LA, aorta, IVC, SVC, PA.</p>
   <p>Studies have shown that bicaval anastomosis is less likely to require a pacemaker, and patients need less time in the hospital <xref ref-type="bibr" rid="scirp.142168-23">
     [23]
    </xref>. The bicaval technique preserves normal atrial morphology, sinus node function, and valvular function <xref ref-type="bibr" rid="scirp.142168-24">
     [24]
    </xref>. As a result, it has consistently been associated with a decreased incidence of atrial arrhythmias and the need for pacemaker implantation. However, potential disadvantages include an increased ischemic time and the possibility of narrowing of the caval anastomosis.</p>
   <p>
    <xref ref-type="bibr" rid="scirp.142168-"></xref>The immediate postoperative follow-up was simple for the 3 patients.</p>
   <p>
    <xref ref-type="bibr" rid="scirp.142168-"></xref>Heart transplantation is considered one of the most effective treatments for end-stage heart failure, giving patients another chance for survival and an improved quality of life. However, this practice faces impediments in Africa due to various barriers, including inadequate infrastructure, a lack of personnel for such procedures, a shortage of organ donors, negative beliefs regarding organ donation, and economic constraints. In 2021, it was reported in Uganda that one of the major barriers to performing a heart transplant was the financial challenge it poses on the part of the patient and the medical facility due to it being an expensive procedure <xref ref-type="bibr" rid="scirp.142168-25">
     [25]
    </xref>. The infrastructure required to support heart transplantation is often unavailable in many African countries. This includes specialized cardiac centers with dedicated intensive care units, sophisticated diagnostic materials, surgical equipment, tissue typing, cross-matching, and some viral studies <xref ref-type="bibr" rid="scirp.142168-26">
     [26]
    </xref>. Although there are difficulties, heart transplantation will give patients a second chance. They will then be able to contribute to the development of Africa.</p>
  </sec><sec id="s4">
   <title>4. Conclusion</title>
   <p>Heart transplantation according to the bi-caval procedure has made it possible to treat children with end-stage heart failure in Seoul National University Hospital. End-stage heart failure in Africa is clearly increasing among the young working population. Although Africa faces a range of challenges, heart transplantation is reproducible in sub-Saharan Africa. Also, given the scarcity of donors and the morbidity and mortality of transplants, emphasis could be placed on other means of acquiring grafts, in particular xenotransplantation and cardiac tissue bioengineering.</p>
  </sec>
 </body><back>
  <ref-list>
   <title>References</title>
   <ref id="scirp.142168-ref1">
    <label>1</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Demiralp, G., Arrigo, R.T., Cassara, C. and Johnson, M.R. (2024) Heart Transplantation—Postoperative Considerations. Critical Care Clinics, 40, 137-157. &gt;https://doi.org/10.1016/j.ccc.2023.05.004
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref2">
    <label>2</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Ambrosy, A.P., Fonarow, G.C., Butler, J., Chioncel, O., Greene, S.J., Vaduganathan, M., et al. (2014) The Global Health and Economic Burden of Hospitalizations for Heart Failure: Lessons Learned from Hospitalized Heart Failure Registries. Journal of the American College of Cardiology, 63, 1123-1133. &gt;https://doi.org/10.1016/j.jacc.2013.11.053
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref3">
    <label>3</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Cowie, M.R., Anker, S.D., Cleland, J.G.F., Felker, G.M., Filippatos, G., Jaarsma, T., et al. (2014) Improving Care for Patients with Acute Heart Failure: Before, during and after Hospitalization. ESC Heart Failure, 1, 110-145. &gt;https://doi.org/10.1002/ehf2.12021
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref4">
    <label>4</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Lee, H. and Oh, B. (2017) Heart Transplantation in Asia. Circulation Journal, 81, 617-621. &gt;https://doi.org/10.1253/circj.cj-17-0162
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref5">
    <label>5</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Pio, M., Goeh-Akue, E., Afassinou, Y., Baragou, S., Atta, B., Missihoun, E., et al. (2014) Insuffisances cardiaques du sujet jeune: Aspects épidémiologiques, cliniques et étiologiques au CHU Sylvanus Olympio de Lomé. Annales de Cardiologie et d’Angéiologie, 63, 240-244. &gt;https://doi.org/10.1016/j.ancard.2014.04.008
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref6">
    <label>6</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Thiam, M. (2003) Insuffisance cardiaque en milieu cardiologique africain. Bulletin de la Societe de Pathologie Exotique, 96, 217-218.
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref7">
    <label>7</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Ambroise, G.L., Ben Justin, K.D., Florent, K., Estelle, T.M., Stéphane, K.K. and Jean-Baptiste, A.K. (2019) L’Insuffisance cardiaque (IC) à l’Institut de Cardiologie d’Abidjan: Aspects clinico-électrocardiographiques et échocardiographiques Heart failure (HF) at the Abidjan Institute of Cardiology: Clinical, Electrocardiographic and Echocardiographic Data. Revue internationale des sciences d’Abidjan, 21, 206-211.
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref8">
    <label>8</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Hassoulas, J. (2012) Transplantation of the Heart: An Overview of 40 Years’ Clinical and Research Experience at Groote Schuur Hospital and the University of Cape Town: Part I. Surgical Experience and Clinical Studies. South African Medical Journal, 102, 350-352. &gt;https://doi.org/10.7196/samj.5020
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref9">
    <label>9</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Scheld, H.H., Netz, H., Moosdorf, R., Bertram, U., Bauer, J., Stertmann, W.A., Fitz, H. and Becker, H.E. (1989) Herztransplantation Im Alter unter 2 Jahren. Die Medizinische Welt, 40, 66-69. 
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref10">
    <label>10</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Rossano, J.W., Singh, T.P., Cherikh, W.S., Chambers, D.C., Harhay, M.O., Hayes, D., et al. (2019) The International Thoracic Organ Transplant Registry of the International Society for Heart and Lung Transplantation: Twenty-Second Pediatric Heart Transplantation Report—2019; Focus Theme: Donor and Recipient Size Match. The Journal of Heart and Lung Transplantation, 38, 1028-1041. &gt;https://doi.org/10.1016/j.healun.2019.08.002
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref11">
    <label>11</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Canter, C.E., Shaddy, R.E., Bernstein, D., Hsu, D.T., Chrisant, M.R.K., Kirklin, J.K., et al. (2007) Indications for Heart Transplantation in Pediatric Heart Disease. Circulation, 115, 658-676. &gt;https://doi.org/10.1161/circulationaha.106.180449
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref12">
    <label>12</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Burchill, L.J., Edwards, L.B., Dipchand, A.I., Stehlik, J. and Ross, H.J. (2014) Impact of Adult Congenital Heart Disease on Survival and Mortality after Heart Transplantation. The Journal of Heart and Lung Transplantation, 33, 1157-1163. &gt;https://doi.org/10.1016/j.healun.2014.05.007
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref13">
    <label>13</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Barnard, C.N. (1967) The Operation. A Human Cardiac Transplant: An Interim Report of a Successful Operation Performed at Groote Schuur Hospital, Cape Town. South African Medical Journal, 41, 1271-1274.
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref14">
    <label>14</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Ulasi, I., Ijoma, C., Ifebunandu, N., Arodiwe, E., Ijoma, U., Okoye, J., et al. (2021) Organ Donation and Transplantation in Sub-Saharan Africa: Opportunities and Challenges. In: Mihaylov, V., Ed., Organ Donation and Transplantation, IntechOpen, 1-34. &gt;https://doi.org/10.5772/intechopen.94986
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref15">
    <label>15</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Global Observatory on Donation and Transplantation (2023) International Report on Organ Donation and Transplantation Activities 2022. &gt;https://www.transplant-observato-ry.org/wp-content/uploads/2023/11/2022-data-global-report_VF_2.pdf 
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref16">
    <label>16</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Santamaria, R.L., Jeewa, A., Cedars, A., Buchholz, H. and Conway, J. (2020) Mechanical Circulatory Support in Pediatric and Adult Congenital Heart Disease. Canadian Journal of Cardiology, 36, 223-233. &gt;https://doi.org/10.1016/j.cjca.2019.10.006
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref17">
    <label>17</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     VanderPluym, C.J., Cedars, A., Eghtesady, P., Maxwell, B.G., Gelow, J.M., Burchill, L.J., et al. (2018) Outcomes Following Implantation of Mechanical Circulatory Support in Adults with Congenital Heart Disease: An Analysis of the Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS). The Journal of Heart and Lung Transplantation, 37, 89-99. &gt;https://doi.org/10.1016/j.healun.2017.03.005
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref18">
    <label>18</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Villa, C.R., Khan, M.S., Zafar, F., Morales, D.L.S. and Lorts, A. (2017) United States Trends in Pediatric Ventricular Assist Implantation as Bridge to Transplantation. ASAIO Journal, 63, 470-475. &gt;https://doi.org/10.1097/mat.0000000000000524
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref19">
    <label>19</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Cedars, A., Tecson, K.M., Zaidi, A.N., Lorts, A. and McCullough, P.A. (2020) Impact of Durable Ventricular Assist Device Support on Outcomes of Patients with Congenital Heart Disease Waiting for Heart Transplant. ASAIO Journal, 66, 513-519. &gt;https://doi.org/10.1097/mat.0000000000001041
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref20">
    <label>20</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Chrysakis, N., Magouliotis, D.E., Spiliopoulos, K., Athanasiou, T., Briasoulis, A., Triposkiadis, F., et al. (2024) Heart Transplantation. Journal of Clinical Medicine, 13, Article 558. &gt;https://doi.org/10.3390/jcm13020558
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref21">
    <label>21</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Park, M.K. and Salamat, M. (2022) Park’s Pediatric Cardiology for Practitioners. 7th Edition, Elsevier, 437-443.
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref22">
    <label>22</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Mavroudis, C. and Backer, C.L. (2015) Atlas of Pediatric Cardiac Surgery. Springer.
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref23">
    <label>23</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Maning, J., Blumer, V., Hernandez, G., Acuna, E., Li, H. and Chaparro, S.V. (2020) Bicaval vs Biatrial Anastomosis Techniques in Orthotopic Heart Transplantation: An Updated Analysis of the UNOS Database. Journal of Cardiac Surgery, 35, 2242-2247. &gt;https://doi.org/10.1111/jocs.14887
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref24">
    <label>24</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Aziz, T., Burgess, M., Khafagy, R., Hann, A.W., Campbell, C., Rahman, A., et al. (1999) Bicaval and Standard Techniques in Orthotopic Heart Transplantation: Medium-Term Experience in Cardiac Performance and Survival. The Journal of Thoracic and Cardiovascular Surgery, 118, 115-122. &gt;https://doi.org/10.1016/s0022-5223(99)70150-9
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref25">
    <label>25</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     (2024) Heart Transplantation—Uganda Heart Institute. &gt;http://www.uhi.go.ug/heart-transplantation 
    </mixed-citation>
   </ref>
   <ref id="scirp.142168-ref26">
    <label>26</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Awuah, W.A., Ng, J.C., Bulut, H.I., et al. (2023) The Unmet Need of Organ Transplantation in Africa. International Journal of Surgery, 109, 519-520.
    </mixed-citation>
   </ref>
  </ref-list>
 </back>
</article>