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Hirschsprung’s Disease in Africa in the 21st Century

1. Definition and background


Hirschsprung's disease (HD) is a form of functional intestinal obstruction caused by absence of ganglion cells in
the myenteric and submucosal plexuses of the intestine, which results in absent peristalsis in the affected bowel.
It is also referred to as congenital megacolon or congenital colonic aganglionosis, and occurs in 1 in 5,000-
7,200 newborns. (1-3)In Africa only 20-40% present as neonates, compared to more than 90% in developed
countries. (4-8)The male: female ratio is 4:1, but this becomes equal in long segment disease and familial cases.

Congenital megacolon was first described by Ruysch in 1691, and then more widely reported by Danish
Paediatrician Harald Hirschsprung in 1886. The pathophysiology of aganglionosis was not determined until the
middle of the 20th century following which Swenson recommended rectosigmoidectomy as the optimal
treatment in 1948. (9-10) Initially this operation was performed without colostomy, but the debilitated and
malnourished state in which many children presented caused most surgeons to adopt a multi-staged approach.
Recent advances and refinements in surgical technique have resulted in a shift towards one-stage and minimal
access procedures for the treatment of this disease. (1-2) In Africa, ignorance and poverty on the part of the
parents, late presentation with attendant complications, limited access to trained paediatric surgeons and
limitation of facilities for prompt diagnosis characterize management of this disease. Hence, multiple stages of
management still predominate in sub Saharan Africa, (7)(8) (11)

2. Embryology and aetiology


Neural crest cells originate in the vagal neural crest and then migrate craniocaudally into the embryonic
intestine reaching the rectum at the 12th week. Auerbach’s myenteric plexus layer is formed first and Meissner’s
submucosal plexus develops later, with cells maturing after arriving at their destination. (2)

Abnormalities in the microenvironment result in the neural crest cells failing to reach the distal bowel. There
are differences in extracellular matrix proteins (fibronectin, laminin), abnormal cell-cell interactions (absent
neural cell adhesion molecule) and absence of neurotrophic factors in aganglionic bowel when compared with
normal bowel. (12-13)

Other investigators suggest that neural crest cells originate in both vagal and sacral sites and migrate toward the
middle of the intestine, raising the possibility that the neural crest cells get to their destination, but then fail to
survive, proliferate, or differentiate. (14) Additionally, the observation that the smooth muscle cells of
aganglionic colon are electrically inactive points to a myogenic component in the development of HD. (15)
Abnormalities in the pacemaker Interstitial Cells of Cajal, have also been postulated as an important
contributing factor. (16)

3. Genetic Abnormalities
Sporadic occurrence accounts for 80% to 90% of cases of HD. Variable expressivity and incomplete sex-
dependent penetrance are observed, suggestive of a more complex pattern of inheritance and the involvement of
several genes.

A positive family history occurs in approximately 10% of children, especially those with longer segment
disease. Children with Down syndrome and other genetic abnormalities also have a higher incidence of HD.
HD has been associated with the RET proto-oncogene the endothelin family of genes, SOX-10 gene and SIP1.
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It is unclear exactly how these genetic abnormalities result in the phenotype of HD. Development of the disease
is a multi-genic phenomenon that can occur at any number of stages during the normal process of neural crest
cell migration, differentiation, and survival.

Animal models demonstrate that some mutations may produce early maturation or differentiation of neural crest
cells, and mutations in the RET proto-oncogene likely act by depriving the migrating neural crest cells of an
adequately supportive microenvironment. (17)
The genetic mutations associated with HD can best be understood by examining how they relate to the family of
neurocristopathies, many of which have similar genetic patterns (Table 1).

TABLE 1
Syndromes and Genetic Abnormalities Associated with Hirschsprung's Disease.

Syndrome Identified Genetic Basis


Down syndrome Trisomy 21
Neurocristopathy syndromes Endothelin and SOX-10
Waardenberg-Shah syndrome
Yemenite deaf-blind-hypopigmentation
Piebaldism
Other hypopigmentation syndromes
Goldberg-Shprintzen syndrome Possibly SIP1
Multiple Endocrine Neoplasia 2 RET
Central hypoventilation syndrome (Ondine's curse) Unknown

4. Pathology
Normal intestinal motility is primarily under the control of intrinsic neurons that control both contraction and
relaxation of smooth muscle, with relaxation predominating. Extrinsic control is mainly through the cholinergic
and adrenergic fibers (2) In HD, ganglion cells are absent, leading to a marked increase in smooth muscle tone
and an imbalance of smooth muscle contractility, uncoordinated peristalsis, and a functional obstruction.

The gross appearance of a bowel segment affected by HD is an aganglionic distal spastic and narrow segment
with a proximal hypertrophic and dilated bowel separated by a 5-10cm transition zone.

Histologically, the absence of ganglion cells in the distal intestine is the hallmark of the disease. Ganglion cells
are absent in both the submucosal (Meissner's) plexus and the myenteric (Auerbach's) plexus. There is usually a
marked hypertrophy of nerve fibers that extend into the submucosa that may be seen on routine hematoxylin-
eosin stained slides but are more easily seen using an acetylcholinesterase stain (Figure 1 and 2) Cases with
long segment or total colon HD may not have nerve hypertrophy on rectal biopsy.

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Figure 1: Normal ganglion cells in myenteric plexus

Figure 2: Staining with acetylcholinesterase shows abnormal pattern of hypertrophic nerves in HD (source
BHC)

Aganglionosis is always present in the rectum and progresses proximally and continuously for a varying
distance. Exceptions have been documented (skip lesions (18)), though these cases are so rare that the finding
of ganglion cells proximal to an aganglionic segment indicates that the biopsy was taken within the transition
zone. The transition zone has a 5-10cm progressive decrease of ganglion cells until the aganglionosis level is
reached. The transition zone may not be symmetric circumferentially, which has implications in deciding how
much bowel to remove.

5. Classification
Hirschsprung’s disease is classified based on the length of involved bowel and location of transition zone.

Length of bowel involved Proportion of HD cases


Rectosigmoid 70-80%
Long segment (above sigmoid) 10- 25%
Total colonic 3- 15%
Total intestinal 0.4- 4%
Ultrashort segment <1%

6. Clinical presentations
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There are three ways that HD characteristically presents: neonatal bowel obstruction, chronic constipation, and
enterocolitis. Most patients in the African series presented with intestinal obstruction while about 30%
presented with constipation, 11% with enterocolitis, and 2% with intestinal perforation. (5-7) (11)

In developed countries, the age at which HD is diagnosed has progressively decreased over the past century so
that 90% of patients with HD are now diagnosed in the newborn period. In Africa less than 50% of HD cases
present as neonates, and those usually present with complete intestinal obstruction or cecal perforation and
suffer high morbidity and mortality. (7) (8) (11) (19) (20) Presentation in adulthood has also been reported.
(21), (22)

6.1. Neonatal bowel obstruction


There is a history of delayed passage of meconium in about 80% of newborns with HD. A study of normal
African newborns found that 75% passed meconium within 24 hours of birth, 92% within 48 hours and 98%
within 72 hours. (23) A delay of more than 48 hours in passage of meconium should raise concern about HD.

6.2. Chronic constipation


Many children in the African settings with delayed passage of meconium or infrequent passage of stool are
managed with traditional enemas. (Figure 3 (24))

Figure 3: Congolese wooden traditional


enema cup (source BHC)

Children with HD may present later with chronic constipation, failure to thrive, gross abdominal distention and
dependence on enemas without significant encopresis. (Figures 4 and 5) The impacted sigmoid megacolon
may also undergo volvulus (Fig 6).

Figure 4

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Figures 4 and 5: Gross abdominal distension and failure to thrive in children with chronic constipation and
intestinal obstruction due to Hirschsprung’s disease (Courtesy Prof. E. A. Ameh, ABUTH, Zaria).

Figure 6a. Dilated rectosigmoid segment loaded with faeces above the transition zone, leading to a sigmoid
volvulus (arrow shows point of volvulus).

Figure 6b: Hugely dilated sigmoid above transition zone has become gangrenous. Note the viable pink bowel
adjacent to gangrenous sigmoid. (source, author LOA)

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6.3. Enterocolitis

Hirschsprung’s Enterocolitis (HEC) is characterized by fever, abdominal distention, and explosive or foul-
smelling diarrhea, and may lead to life threatening septic shock. Approximately 10% of children with HD have
diarrhea as part of the presentation, and the diagnosis may therefore be missed. (8) Suspicion of HD should be
raised if a history of failure to pass meconium and intermittent obstructive episodes is elicited.

6.4. Associated Anomalies and Syndromes

The incidence of associated congenital anomalies is approximately 20% involving the neurological,
cardiovascular, urological, or gastrointestinal system. (25) In addition, HD may be part of a large number of
recognized syndromes, some of which have an identifiable chromosomal or genetic basis (Table 1). HD should
therefore be suspected in any child with constipation or neonatal intestinal obstruction who is known to have
one of these syndromes. In addition, a diagnosis of HD should alert the clinician to the increased possibility of
these associated anomalies.

7. Diagnosis
The differential diagnosis of HD in infancy includes other causes of neonatal intestinal obstruction. (Table 2)
HD may be suspected in older children presenting with functional constipation who do not respond to usual
treatments.

Table: 2 Differential diagnoses for Hirschsprung’s disease according to age of presentation

Neonates Older children


Distal intestinal obstruction: Functional constipation
– Ileal atresia
– Meconium ileus Fecal impaction
– Meconium plug syndrome
Small left colon syndrome Abdominal tumor
Prematurity
Sepsis and electrolyte imbalance Abdominal Tuberculosis and lymphoma
Cretinism and myxedema
Metabolic abnormalities
Intestinal neuronal dysplasia
Pseudo-obstruction

The appropriate diagnostic approach varies, depending on the age of the patient and the presenting clinical
picture. After a careful history eliciting delayed passage of meconium, chronic constipation and or repeated
diarrhea and adequate physical examination including a digital rectal examination which gives a tight rectum
with absent fecal content, the diagnostic steps should include radiographic studies, and rectal biopsy.

7.1. Plain radiographs usually show dilated bowel loops with characteristic flank fullness (Figure 7a). The
colon may show stippled shadows which are evidence of large amounts of fecal stasis proximal to the
obstruction. Pneumoperitoneum may be evident in those who have developed intestinal perforation. In
newborns, a prone lateral x-ray (Figure 7b) can demonstrate that the rectum is narrower than the proximal
bowel in HD.
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Figure 7a

Prone Lateral view

Figures 7a and 7b: Grossly dilated large bowel loop on anteroposterior view. The prone lateral x-ray shows a
more dilated sigmoid compared with the rectum (arrow): a rectosigmoid index of less than 1 is abnormal and
suggests HD. (source BHC)

7.2. Contrast enema


In older children with HD, a water soluble contrast enema will demonstrate a funnel shaped transition zone
between the normal and aganglionic bowel. These features are better elicited on the lateral or oblique films
since superimposed loops of sigmoid colon make the interpretation difficult on the anteroposterior film.
(Figures 8a and 8b) The transition zone may be absent in 25% of neonates and in older children with a very
short aganglionic segment. (26) A rectosigmoid index (the ratio of rectal diameter/sigmoid diameter) less than
1.0 and retention of barium on a 24-hour post evacuation film are other findings supporting the diagnosis of
HD.

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The findings in total colonic HD may include a normal barium enema, a short colon of normal caliber, a
microcolon, or a transition zone in the ileum. There may also be an easy, extensive reflux far back into small
bowel, a pseudo-transition zone in the colon, and intraluminal small bowel calcification.

Figure 8a

Transition
zone

Figure 8a and 8b: Contrast enema demonstrating the funnel shaped transition zone (arrow) (source LOA)

Figure 9: CT scan of abdomen in a child presenting with an abdominal ‘tumor’ (source BHC)

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Although a computerised tomographic scan is not generally indicated in the diagnosis of HD, this 20 month old
infant with an abdominal ‘tumor’ has faecal loading in the grossly dilated rectosigmoid segment and was found
to have HD. (Fig 9)

7.3. Anorectal Manometry may show absence of the rectoanal inhibitory reflex. It is not widely available in
Africa and not used frequently in Canada because it is unreliable and not diagnostic.

7.4. Rectal Biopsy


The gold standard for definitive diagnosis of HD is rectal biopsy, looking for the absence of ganglion cells and
the finding of hypertrophied nerve trunks. The biopsy is taken 2-3 cm above the dentate line on the posterior
wall of the rectum. Going too distally may result in a false-positive diagnosis of HD because ganglion cells are
normally absent in the anal canal.
The most common technique used in Africa is full thickness rectal wall biopsy, which requires close
collaboration with a good pathologist. Disadvantages of full thickness biopsy include the potential for bleeding
and scarring and the need for general anesthesia. Evaluation of biopsy specimens may be enhanced by staining
of the tissue for acetylcholinesterase and immunohistochemistry with calretinin. (27) Histochemistry is also
useful in differentiating between HD and intestinal neuronal dysplasia.
A suction rectal biopsy can be used to obtain tissue for histologic examination. Rectal mucosa and submucosa
are sucked into the suction device, and a self-contained cylindrical knife cuts off the tissue (Figure 10). The
distinct advantage of the suction biopsy is that it can be easily performed at the bedside without general
anaesthesia and can be repeated several times. In experienced centres, the accuracy is 99.7%. Interpretation of
the specimen is technically more demanding for pathologists, and some will require a full thickness biopsy to
confirm the diagnosis of HD. This device is expensive and not readily available in Africa.

Figure 10: rbi2TM rectal mucosa suction device (Aus Systems PTY Ltd.)

8. Treatment
Once the diagnosis of HD has been established, the goals of initial management are 2-fold:
a. Resuscitation and treatment of complications.
b. Colonic decompression before definitive surgical correction.

8.1. Steps in resuscitation and treatment of complications

i) Rehydration and correction of electrolyte derangements.


ii) Nasogastric decompression in patients with gross abdominal distension and vomiting.
iii) Intravenous broad spectrum antibiotics to prevent progression of septicaemia.
iv) Nutritional rehabilitation through nasogastric feeding or parenteral nutrition if available.

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8.2. Colonic decompression

There are 2 options for colonic decompression.


i) Rectal irrigations using normal saline (20mls/kg per instillation) given through a large rectal tube. Care
should be taken to ensure that the tip of the tube reaches above the level of aganglionosis and perforation is
avoided by lubrication and gentle push on the catheter. The irrigation is repeated until most of the accumulated
faeces is evacuated, ensuring that no more than 20 ml/kg of fluid is retained at once (retention of enema fluid
may lead to perforation). Fecal disimpaction may be necessary before embarking on colonic irrigation, and it
must be ensured that there is no evidence of intestinal perforation. Subsequently, the irrigation is done 1-4
times daily to keep the colon decompressed until the time of definitive surgical correction.

ii) Colostomy is necessary if colonic irrigation is contraindicated or fails to achieve adequate decompression
especially in very sick babies, grossly dilated, redundant and flabby colon, hard stools feculoma and
uncooperative parents.

The desirable colostomy is one which sites the stoma just above the level of aganglionosis in normally
ganglionated colon (leveling colostomy). This can generally be identified by contrast enema and gross
appearance. (Figure 11) Biopsies should be taken from the colostomy site. If the colostomy is placed
mistakenly on or just above the Transition Zone, obstruction and Hirschsprung’s enterocolitis will persist.
(Figure 12) It may be safer to resect most of the distal colon at the time of colostomy otherwise, the large
dilated colon may take months to shrink enough for safe pull through and may be responsible for persistent
postoperative constipation.

Transition zone

Figure 11. Rectosigmoid transition zone

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Transition zone

Stoma site

Figure 12: Incorrect stoma site below the transition zone


(source LOA and Prof. E. A. Ameh, ABUTH, Zaria, Nigeria)

Some paediatric surgeons prefer using a transverse colostomy (particularly in the absence of facilities for frozen
section as it is in most centres in Africa) as it places the stoma as far as possible from the usual rectosigmoid
level of aganglionosis. However, a transverse colostomy may make it difficult to clean out the intestine distal to
the stoma before definitive correction. A high transition zone may make it necessary to take down the
transverse loop colostomy and either resect additional bowel, have a second anastomosis, or refashion a more
proximal colostomy. Loop colostomies also invariably prolapse (Figure 13a and b).
An ileostomy may be required when cecal perforation has occurred or in cases of total colonic aganglionosis

Figure 13a.

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Figures 13a and 13b: Prolapsed loop colostomies with skin escoriation in an infant (a) and older child (b)
(source LOA and Prof. E. A. Ameh, ABUTH, Zaria, Nigeria).

8.3. Bowel preparation

Formal bowel preparation is important in the African child to reduce bulk although the practice is becoming less
favoured in the developed countries. The significance of bowel preparation prior to definitive pull-through
surgery to avoid faecal contamination of the anastomosis and resultant leakage to reduce morbidity and
mortality, as emphasized by Nmadu (28) in a review of 2 decades of Hirschsprung’s disease managed in Zaria,
Nigeria.
The options for mechanical bowel preparation include:
i) A 3- day preparation comprising mechanical bowel irrigation with warm saline and use of cathartic and
antibiotics- neomycin, dulcolax and or thalazole are used in our practice in Ilorin, Nigeria.
ii) One or 2 day bowel preparation with the use of lactulose, Polyethylene glycol (PEG) or Picosalax. These are
not readily available in Africa.

8.4. Definitive surgical options

The goals of surgical management for Hirschsprung's disease are to remove the aganglionic bowel and
reconstruct the intestinal tract by bringing the normally innervated bowel down to the anus, while preserving
normal sphincter function.
We will discuss the available operations, the operative approaches, and whether or not to perform a staging
colostomy.

The most commonly performed operations are the Swenson, Soave, and Duhamel procedures (Figure 14).
Most of the evidence available reports systematic reviews of the outcome these procedures without a
comparison between them. There are no prospective trials comparing surgical treatments of Hirschsprung's
disease and surgeons will get the best results doing the operation they have been trained to do, and do with
some frequency.

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Figure 14: from previous edition of Pediatric Surgery (2)

The Swenson procedure is a low anterior resection of the rectum with an end-to-end anastomosis performed by
prolapsing the rectum and pulled-through bowel outside the anus.

The Duhamel procedure entails leaving the native rectum in situ and bringing the normally innervated colon
behind the rectum with an end-to-side anastomosis 2cm above the dentate line and joining the two lumens side
to side. Originally, this was accomplished by leaving a clamp across the common wall until it fell off, but in
more recent years most surgeons use a linear stapler. Adeniran et al (29) have devised a Hand sewn technique
for African surgeons who do not have access to the staplers. (Figure 15) This has also assisted in preventing the
complications caused by premature dislodgement of clamps. (28)

Figure 15: Hand sewn technique of Duhamel operation by Adeniran et al (29)

The Soave endorectal pull-through consists of stripping the rectal mucosa with preservation of the rectal
muscular cuff. Ganglionated colon is pulled through the muscular cuff and anastomosed just above the dentate
line. The operation was designed to avoid injury to pelvic vessels and nerves, which are theoretically at risk
with the Swenson procedure. In the original description, the pulled-through bowel was left hanging out for
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several weeks, and was then amputated and the anastomosis was completed. Boley's modification involved a
primary anastomosis with the mucosa being excised at same sitting and is the technique employed today.

8.5. Multi-stage vs. Single-stage (primary) Pull-through


Surgery can be done in 2 or 3 stages with a colostomy to protect the anastomosis. Over the years, as surgical
and magnification techniques improved, many surgeons began to do the definitive operation at an earlier age
and in one-stage. (30), (31), (32) This avoids the known morbidity of stomas in infants and is more cost
effective, but a one-stage approach is only advisable with pathologic frozen section support to confirm the
transition zone. (33), (34) Many centers in Africa use the barium enema and intra-operative findings to
determine this, however, a recent study suggests that 8-10% of children with a rectosigmoid transition zone on
contrast study actually have a more proximal pathological transition zone. (35) This may give rise to the
‘acquired Hirschsprung disease’ when an aganglionic remnant is left behind.
A single stage pull-through in Africa would be indicated if patients present early without complications and the
expertise is available to reduce morbidity of repeated surgery, cost to the parents and long waiting list time.

8.6. Laparoscopy assisted and transanal pull through


Pull-through procedures originally entailed a combination of abdominal and perineal approach but recently
laparoscopic assisted (Figures 16 and 17) or exclusively transanal dissection has been applied for all
procedures.

Figure 16: Infant positioned with legs suspended for laparoscopy assisted transanal pull-through (BHC)

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Figure 17: Laparoscopic view of rectum and pelvis. The colon can be biopsied and the rectosigmoid mobilized
laparoscopically before proceeding to the transanal pull through. (source, BHC)

The transanal Soave procedure starts with a submucosal dissection from below with or without laparoscopic
biopsy and mobilization of the intra-abdominal rectum. (32)(33) The rectal mucosa is incised circumferentially
1-2cm above the dentate line, and the dissection is continued along the rectal wall. The entire rectum and part of
the sigmoid colon can be delivered through the anus. The transition zone is identified, and the anastomosis is
performed from below. This operation has been shown to be safe and associated with a short hospital stay, early
feeding, and minimal analgesia requirements compared with the open Soave operation. (36) Options for
accessing the proximal bowel in order to do the biopsy include laparoscopy or a small umbilical incision, which
can also be used to mobilize the splenic flexure in children with higher transition zones.
The transanal approach can be used in a patient with a preexisting colostomy, either taking down the colostomy
to use for the pull-through or closing it at a third procedure.(Figures 18-21)

Figure 18: Infant positioned for a trans-anal pull through procedure (LOA).

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Figure 19: Anal retraction with sutures in the absence of an expensive ‘lone-star’ retractor (seen in Fig.20)

Figure 20: Transanal pullthrough of sigmoid colon prior to anastomosis. (BHC)


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Figure 21: After completion of colo-anal anastomosis. (BHC)

8.7. Total Colonic Hirschsprung’s disease


Laparotomy is done to take multiple biopsies including the appendix to identify the pathological transition zone,
which may differ from what the surgeon sees grossly. An ileostomy is left in the patient and a definitive
reconstructive procedure is planned for an older age (6-18 months).
The options for reconstruction are: colonic patch, straight ileoanal pull-through and J-pouch construction.
A segment of colon has been retained for water absorption (2), but the aganglionic colon gradually dilates and
some of the patients develop severe enterocolitis that requires removal of the patch. (37) Hence, the short
Duhamel small bowel-rectal patch is recommended.
Straight pull-throughs are performed using any one of the standard pullthrough techniques. The J-pouch
procedure is the same as that performed commonly for children and adults with ulcerative colitis and polyposis.
(38) Little has been written about the results of this approach in the management of HD.

8.8. Near-total intestinal aganglionosis


Children with HD involving the colon and entire small bowel usually do not survive because they do not have
adequate nutrient absorptive capacity. The surgical options available are:
a. Bowel tapering, imbrication, or bowel-lengthening procedures, such as the Bianchi or STEP (Serial Tapering
EnteroPlasty) operation for children who develop significant proximal dilatation of the normally innervated
bowel. (39)
b. Zeigler technique of myectomy-myotomy. (40)
c. Small bowel transplantation. (41)

8.9. Postoperative care

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Following the formation of a stoma, bowel function usually returns within 24-48 hours and oral feeding can be
commenced usually with breast milk in the infants and maize or sorghum-based paste in older children. The
mothers are taught about how to take care of the stoma on the wards before discharge which usually takes place
after the 7th day of operation if there are no other concerns. Because of the cost and non availability of stoma
bags, Zinc oxide in petrolatum paste (Vaseline) is used to protect the skin and local clothing materials or
napkins are used to wrap the stoma to receive the faeces (Figure 22). Mothers are advised to change the
receptacle as soon as faeces are collected on it so that contact with the skin is limited.

Figure 22: A home-made ostomy appliance from Guyana. (BHC)

After a pull-through procedure most infants begin bowel movements within 24 hours and can start liquid feeds
right away. In trans-anal pull-through with or without laparotomy oral intake in form of liquid diet is usually
commenced after 48 hours to delay fecal contact with the peri-anal wound. Adequate parenteral and enteral
analgesia is provided and a caudal block, when available, provides additional pre-emptive analgesia.
Anal dilatation is commenced after 2 weeks and mothers are taught to use their fingers, Hegar’s dilator or
trimmed candle stick 1-2 times daily for up to 3-6 months to prevent anal stricture.

9. Complications
9.1. Intra-operative and Early Postoperative Complications
The complications of surgery for HD include the general group of complications of any abdominal surgery,
including bleeding, infection, injury to adjacent organs, and the risks of anesthesia. Those children who undergo
a staged procedure with a preliminary stoma may experience stoma-specific complications such as prolapse,
skin breakdown, stricture, and retraction. (42)

Anastomotic leak and strictures occur infrequently, and can be avoided by close attention to adequate blood
supply of the pulled-through bowel. Minimizing tension on the anastomosis will help prevent ischemia and
retraction of the pull-through. The incidence of anastomotic leak in laparoscopic and transanal pull-through
appears to be lower than that reported in the older literature of open pull-throughs. The complications reported
with primary pull through are less than with staged pull through. (43)
Postoperative perineal excoriation is common and can be treated with a zinc based cream. In children with a
colostomy, the perineal skin can be toughened by applying stool to the perineum for several weeks
preoperatively to diminish postoperative excoriation.

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9.2. Late Complications

Two categories of patients have been identified that are not doing well after the pull through for HD (44) (45)
They are:
i) those that are distended with recurrent episodes of enterocolitis which may cause failure to thrive and
ii) those who are soiling or have fecal incontinence.

The incidence of postoperative enterocolitis is reported from 5-35% and partly depends on how strictly one
defines enterocolitis. (46) Enterocolitis may occur postoperatively, and it is extremely important that the
surgeon educate the family about the risk of this complication which may be life-threatening. Parents should be
urged early return to the hospital if the child should develop any concerning symptoms such as distension
associated with foul-smelling diarrhea and signs of systemic infection.

Enterocolitis and obstructive symptoms may be associated with internal anal sphincter dysfunction. This can be
treated by injection of botulinum toxin into the sphincter, anal myectomy, or topical nifedipine cream.

In some severe cases of obstructive symptoms, the child may be best served by use of a cecostomy and
administration of antegrade enemas as described by Malone, or even by the creation of a proximal stoma. (47)
Malone operation may not be acceptable in the African setting and the patient may do better with dietary
management. (Table 3)

TABLE 3: Potential causes of Late Complications following a Pull-through

Incidence 8-30% 5-35%

Causes a. Mechanical obstruction a. Abnormal sphincter a. Obstruction


function
b. Persistent or acquired b. Genetic or immunologic
aganglionosis b. Abnormal sensation predisposition

c. Colonic motility disorder c. Overflow incontinence due


c. Abnormal mucin
to constipation
d. Internal sphincter achalasia

e. Stool-holding behavior

Postoperative bowel dysfunction is evaluated by taking a detailed history noting the patient’s bowel habits, use
of anti-motility drugs or laxatives, need for dilation or irrigation, and the type of previous surgery. Patients with
an associated syndrome and those with long-segment disease have been found to have poorer outcomes. (37),
(48)
A contrast enema will provide information about the degree of megacolon, fecal impaction and presence of a
stricture or transition zone.

The digital rectal examination, preferably under general anaesthesia, should evaluate the integrity of the anal
canal, location of anastomosis in relation to the dentate line, presence of stricture, sphincter tone, and presence
of large rectal pouch or a Soave cuff. A full thickness rectal biopsy should be done to rule out persistent

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aganglionosis. Persistent aganglionosis may be due to pathologist’s error on the original specimen, or a
transition zone pull-through, and in some cases there may be ganglion cell loss after a pull-through.

Although some strictures can be managed using repeated dilations, some require revision of the pull-through.
Duhamel spurs can be resected from above or managed by extending the staple line from below, with or without
laparoscopic visualization.

It is well recognized that children with HD may have associated motility disorders, with histologic
abnormalities such as intestinal neuronal dysplasia. (49) Investigations for motility disorder may include a
radiologic shape study, colonic manometry, and laparoscopic biopsies looking for intestinal neuronal dysplasia.
(50), (51) If a focal abnormality is found, consideration should be given to resection and repeat pull-through
using normal bowel. If the abnormality is diffuse, the appropriate treatment is bowel management and the use of
prokinetic agents.

10. Outcomes
Most children with Hirschsprung's disease overcome the postoperative problems and do well. (52) Studies have
suggested that obstructive symptoms and incontinence seem to resolve with time, and that the risk of
enterocolitis, in the absence of an ongoing obstructive cause, is almost eliminated after the first 5 years of life.
Sexual function, social satisfaction, and quality of life all appear to be relatively normal in the vast majority of
patients. (53-54)
A recent large multicenter review showed no significant differences in continence or stooling patterns after
transanal versus transabdominal pull through procedure. (55)

11. African experience


Hirschsprung’s Disease management is a major problem in the practice of surgery in Africa; many patients may
default on follow up appointment and would never get to complete their scheduled procedures for various
reasons. (6-7) Reasons include: lack of funds for treatment (non-availability of health insurance), parents or
babies having an illness at the time of appointment or parents having another engagement. (56) Perhaps some
patients may have died from complications of initial intervention or the disease. There are instances when
patients are referred to colleagues for follow up and possible completion of intervention either by choice of the
parents because of reason of proximity/closeness. Feedbacks are never gotten back from these referrals which
make completion of reports difficult.

12. Recommendations
1. Public enlightenment and awareness about Hirschsprung’s Disease should be stepped up.
2. Parents and other care givers (including general practitioners) should be made aware of the classical features
of presentation and that the supposed ‘fountain sign’ (projectile flush of watery offensive stool on digital
rectal examination) in children with constipation is a feature of enterocolitis which suggest danger that
needs urgent and adequate intervention.
3. Parents should also be educated as to the signs and symptoms of enterocolitis so that they can seek medical
attention early.
4. For patients that are not doing well post pull-through, efforts should be made for proper evaluation and
expert treatment so that the quality of life of the patients is optimized.
5. There should be feedback or a form of collaboration among practitioners and surgeons so that many
questions, yet to be answered about epidemiology and pathology of Hirschsprung’s disease in Africa, are
addressed and support from developed countries is secured.

20
6. The algorithm at the end of this article summarizes our approach to diagnosis and treatment of HD (Figure
23)

Lukman O. Abdur-Rahman MPH, FWACS


Senior Lecturer and Consultant Paediatric Surgeon,
University of Ilorin and University of Ilorin Teaching Hospital,
Ilorin, Nigeria
bolarjide@yahoo.com

Brian H. Cameron, FRCSC, FACS


Professor of Pediatric Surgery,
McMaster University,
Hamilton, Canada

(Reviewed by Prof. E. Ameh, Ahmadu Bello University Teaching Hospital, Zaria, Nigeria)

21
Figure 23: Algorithm for management of patients with suspected Hirschsprung’s disease

Newborn with delayed Enterocolitis, Chronic constipation


passage of meconium suspected HD

Fluid resuscitation
Plain abdominal xrays Contrast enema
IV Antibiotics
Contrast enema
Rectal irrigations
+/- Colostomy

Full thickness or
suction rectal biopsy
confirms HD Levelling colostomy above
transition zone
con OR transverse loop colostomy

Rectal irrigations followed by


one-stage pullthrough

Trans-anal, laparoscopic or open


pullthrough procedure

Post-op anal dilation


+/- 3rd stage
Close colostomy

Postoperative incontinence,
encopresis or enterocolitis

EUA, rectal biopsy, contrast Anal dilation, anal sphincter botox or


study, motility studies myectomy, redo pullthrough or bowel
management program

22
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