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Constipation in Children
Constipation in Children
Constipation in Children
CONSTIPATION IN CHILDREN
Definitions
<2 motions/wk
>1 fecal incontinence/wk
Painful hard bowel movement
Large faecal mass in rectum
Large stool obstructing toilet
2 or more of above
General practical definition
Muscular
Spinal muscular atrophy
Neurofibromatosis
Neurological
Currarino's triad (rectal
Neuronal intestinal stenosis, hemi sacrum,
dysplasia presacral mass)
Cerebral palsy (static
encephalopathy) Celiac disease
Tethered cord Cow's milk intolerance
Metabolical
Mitochondrial disorders
Imperforate Anus Hypercalcemia
Anal stenosis, Hypokalemia
Anterior displacement of Hypothyroidism
the anus Drugs
Hirschsprung disease
Hirschsprung disease or aganglionosis occurs in 1 in
5,000 births. M:F ratio is 4:1
The diagnostic lack of ganglion cells in the
myenteric and submucosal plexus of the bowel wall
extends proximally from the internal anal sphincter.
In among 80% of the involved children, the
aganglionic segment does not extend above the
sigmoid.
Hirschsprung disease
Difficulty with evacuation is present from
birth;
Meconium passage delayed > 48 hours of life
in 40% of involved infants.
Recurrent abdominal distension, emesis,
failure to thrive, and acute enterocolitis allow
diagnosis of 60% of patients by 3 months of
age.
Neuronal dysplasia
Neuronal disorders
Any damage to corticospinal pathways - lumbosacral
myelomeningocele, cerebral palsy
Muscular disorders
Anorectal dysfunction after operative pullthrough
surgery for high imperforate anus or colectomy.
Prolonged diarrhea (pelvic floor muscles fatigue)
Muscular dystrophy
Prune belly
Obstructive causes
Congenital anterior anus
Anterior ectopic anus is defined by a measurable
displacement of the anal opening based on the ratio of
the anus-to-fourchette to the coccyx-to-fourchette being
less than 0.34 in females and less than 0.46 in males.
the shift creates a broad posterior rectal shelf that
increases with distension of the ampulla.
Anal ring stenosis presents with painful constipation in
infancy.
Endocrine/metabolic
The term “pseudo-obstruction syndrome” has been
applied to all non anatomic disorders of abnormal
peristalsis.
Motility abnormalities may manifest with delayed
gastric emptying, small bowel stasis, and/or
constipation.
The primary form is familial, presenting in infancy with
FTT, distension, and progressive dysmotility with
delayed gastric emptying and constipation.
Endocrine/Metabolic causes
Endocrine: Drugs:
Hypothyroidism Antimotility drugs
Electrolytes: Anticholinergics
Hypercalcemia Antidepressants
Hypokalemia Opiates
Antacids
Phenothiazines
Methylphenidate
Encopresis
predominantly ~ 3 - 7 yrs
The child is not aware of the soiling until it is
nearly complete.
Manometry shows decreased sensitivity to
distension.
In one study 40% experienced delays in toilet
training, and 60% reported painful stools
before age of 3 years.
> 90% of chronic encopresis occurs in the
context of functional constipation.
Complications of constipation
Thyroid functions
Serum calcium, magnesium, UEC
Urine mcs
The plain abdominal Xray may be of value.
Lumbosacral spine radiographs or magnetic
resonance imaging if indicated.
Lab…
Disimpaction yes
Fecal impaction
Maintenance Rx No
Not effective
Maintenance Rx
Not effective Diet,laxative,toilet training
Re-assessment
Re-educate Effective
Diff.medication
Wean and observe
Not effective
Blood tests:
T4,TSH,Ca,Celiac serology
Approach to constipation(> 1
History
Yr) and physical examination Functional constipation
Yes
Disimpaction Fecal impaction
Maintenance Rx No
Not effective
Blood tests:
T4,TSH,Ca,Pb,Celiac serology
Management: recommendations for children
Disimpaction: oral or rectal medication,or enemas
Diet: a balanced diet,containing whole grains, fruits,
vegetables
Laxative:lactulose,sorbitol,magnesium hydroxide,
mineral oil are safe & effective
Behavioral therapy:toilet training (5-10min after meal)
Rescue therapy:short course of stimulant laxative