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CHAPTER 61

                Neonatal Intestinal Obstruction



                                                       Daniel Sidler
                                                      Miliard Debrew
                                                      Kokila Lakhoo



                           Introduction                          The  midgut  comprises  the  jejunum  and  ileum  as  well  as  the
        Neonatal  intestinal  obstruction  (NIO)  is  one  of  the  most  common   ascending and proximal transverse colon. These are supplied by the
        emergency conditions a paediatric surgeon is called upon to assess   superior mesenteric vessels.
        during the neonatal period. Successful management of NIO depends   The hindgut comprises the distal colon, which is supplied by the
        on timely diagnosis and referral for therapy. The diagnosis is based   inferior mesenteric vessels, and the rectum, which is supplied by the
        on history (symptoms) and physical examination (signs) confirmed by   internal iliac vessels.
        some investigations such as radiographic and histopathological stud-  Aberrations of foregut formation include duodenal stenosis, duodenal
        ies. Catastrophic events such as volvulus, ischaemic loop of bowel,   atresia, and annular pancreas. Maldevelopment of the midgut includes
        pneumoperitoneum, and/or pneumonia from aspiration and malnutri-  malrotation as well as jejunal and ileal atresia. Meconium ileus involves
        tion could be overcome through efficient and timely resuscitation and   the  distal  ileum.  Hirschsprung’s  disease  (aganglionic  megacolon),
        urgent transport to a specialised unit.                meconium plug syndrome, and imperforate anus involve the hindgut.
           The  desired  goal  of  healthy  survival  of  neonatal  intestinal   Enteric duplications occur in all three locations.
        obstruction  requires  a  coordinated  interaction  of  medical,  nursing,   Jejunoileal atresia  is a condition acquired during foetal development
        and  rehabilitative  specialties  in  an  organised  team.  Early  surgical   due to disruption of the mesenteric blood supply. In their classic work on
        intervention is paramount and may mean all the difference between   foetal dogs in 1955, Louw and Barnard from Cape Town, South Africa,
        intestinal salvage and crippling short gut syndrome. The typical case   clarified  the  pathophysiology  of  jejunoileal  atresia.   Other  abdominal
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        of  neonatal  bowel  obstruction  is  generally  straightforward,  and  the   conditions occurring in utero, such as gastroschisis, volvulus, or intus-
        outcome is potentially excellent. Only very preterm babies and those   susception,  may  be  associated  with  intestinal  atresia  due  to  kinking,
        of extremely low birth weight may succumb. However, in Africa, late   stretching, or otherwise disrupting the blood flow to the foetal bowel.
        presentations and poor resources lend to a mortality of up to 50%.    Chromosomal anomalies are rare (<1%) in babies with jejunoileal atresia.
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        Few dedicated paediatric hospitals exist in developing countries. 2
           Intestinal  obstruction  can  be  complete  (atresia,  anorectal   Meconium ileus  is the earliest manifestation of cystic fibrosis (CF),
        malformation  (ARM))  or  incomplete  (stenosis,  web).  Obstruction   an autosomal recessive condition characterised by abnormalities in cel-
        may  be  intraluminal  (meconium  ileus  or  meconium  plug  syndrome)   lular membrane physiology and chloride ion transport that contribute to
        or  functional  (Hirschsprung’s  disease  (HD)).  Proximal  obstruction   progressive respiratory failure, derangements in cellular secretory pat-
        presents with earlier vomiting and less abdominal distention, whereas   terns, and diminished mucosal motility. In developed countries, 10–20%
        distal bowel obstruction lends itself to late emesis and greater abdominal   of newborns with CF present with meconium ileus, an association first
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        distention.  This  chapter  provides  an  overview  on  neonatal  bowel   described by Landsteiner in 1905.  A cystic fibrosis gene that is different
        obstruction. Each specific condition is covered in chapters elsewhere   from that in the caucasian population has been identified in the black
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        in  this  book,  specifically,  Chapter  58  (inguinal  and  femoral  hernias   African population;  however, the incidence in Africa is much reduced,
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        and hydroceles), Chapter 62 (duodenal atresia and stenosis), Chapter   and in many sub-Saharan countries, the disease is not reported.
        63 (intestinal atresia and stenosis), Chapter 65 (intestinal malrotation   Abnormalities  in  the  cystic  fibrosis  transmembrane  regulator
        and  midgut  volvulus),  Chapter  67  (meconium  disease),  Chapter  76   (CFTR)  disrupt  transmembrane  flux  of  the  chloride  ion,  which
        (Hirschsprung’s disease), and Chapter 77 (anorectal anomalies).  subsequently  affects  sodium  transport  as  well.  The  meconium  of
                                                               affected babies is thick and sticky; this, coupled with the poor motility
                          Demographics                         of  an  immature  intestine,  leads  to  intraluminal  obstruction  of  the
        The incidence of NIO is approximately 1 in 5,000 live births. The true   terminal ileum. A contrast enema might reveal the characteristic finding
        incidence in Africa is unknown, but a recent report from Tanzania has   of a microcolon. It is essential to push the contrast up to the level of
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        shown that it is still the most common neonatal surgical emergency.    obstruction, namely, the distal ileum to be therapeutic by flushing out
        Many cases still die undiagnosed and untreated.        the meconium plugs (Figures 61.1 to 61.4).
                   Aetiology/Pathophysiology                   Meconium plug  syndrome refers to inspissated meconium obstruct-
        Neonatal  intestinal  obstruction  has  varied  aetiology,  so  the  patho-  ing the colon; it may denote HD but not CF. Conditions that predispose
        physiology is diverse.                                 to  dysmotility  of  the  neonatal  bowel  (e.g.,  maternal  pre-eclampsia,
           The  gastrointestinal  tract  (GIT)  arises  from  the  yolk  sac.  At  3   diabetes  mellitus,  administration  of  magnesium  sulfate,  prematurity,
        to  4  weeks’  gestation,  it  becomes  a  distinct  entity.  A  connection,   sepsis, and hypothyroidism) may be responsible for the formation of the
        the  vitelline  (omphalomesenteric)  duct,  may  persist  as  a  Meckel’s   meconium plug. A water-soluble contrast enema can be both diagnostic
        diverticulum. The alimentary tube is divided according to its blood   and therapeutic for this condition.
        supply into the foregut, midgut, and hindgut.          Hirschsprung’s disease  is a disorder of the neuroenteric pathways
           The foregut comprises the oesophagus, stomach, and duodenum.   in the distal colon that results in a bowel that is tonically contracted.
        These  are  vascularised  by  multiple  sources—the  thyrocervical,   Bowel peristalsis is controlled by neuroenteric ganglion cells, which
        intercostal, celiac axis, and superior mesenteric vessels.
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