Constipation in Children Flashcards

1
Q

What is the definition of constipation in children?

A

A child that defecates less than 3 times per week
or
Significant difficulty passing stool.

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2
Q

What is chronic constipation associated with in children?

A

Hard pellet like stool that is difficult to pass.

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3
Q

How are most cases of constipation in children described?

A

Idiopathic or functional constipation

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4
Q

What is functional constipation due to?

A

Lifestyle factors

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5
Q

What are possible causes of constipation in children?

A
  • Low fibre diet
  • Dislike of using toilet
  • Pain on passing stool
  • Anal fissure
  • Not recognising sensation of needing to pass stool
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6
Q

What underlying conditions can constipation be a sign of?

A

Hirschsprung’s disease (MAIN)
Cystic fibrosis
Hypothyroidism.

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7
Q

What are features of constipation?

A
  • Hard stools that are difficult to pass
  • Rabbit dropping stools
  • Straining and painful passages of stools
  • Abdominal pain
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8
Q

What is retentive posturing?

A

Holding an abnormal posture

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9
Q

What might you be able to feel on a constipated child?

A

Hard stools may be palpable in abdomen

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10
Q

What do you need to check for in children before treating the constipation?

A

Faecal impaction

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11
Q

What is faecal impaction?

A

Inability to evacuate large hard inspissated concreted stool or bezoar lodged in the lower GI tract

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12
Q

What are symptoms of faecal impaction?

A
  • symptoms of severe constipation
  • overflow soiling
  • faecal mass palpable in the abdomen
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13
Q

What are red flag symptoms of constipation?

A
  • Not passing meconium within 48 hours of birth
  • Neurological signs or symptoms, particularly in the lower limbs
  • Vomiting
  • Ribbon stool
  • Abnormal anus
  • Abnormal lower back or buttocks
  • Failure to thrive
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14
Q

What is the first line management if faecal impaction is present?

A

Polyethylene glycol 3350 + electrolytes (Movicol Paediatric Plain) using an escalating dose regimen

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15
Q

What disease causes chronic constipation?

A

Hirchsprung’s disease

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16
Q

What is Hirschsprung’s disease due to?

A

Absence of ganglion cells from myenteric and submucosal plexuses

17
Q

How does Hirchsprung’s disease occur?

A

As the baby develops in utero, the distal colon is not innervated correctly.
The resulting aganglionic colon is shrunken and not able to distend properly.

18
Q

What does an aganglionic colon cause?

A

Back pressure of stool trapped in the more proximal colon.

19
Q

How can Hirschsprung’s disease present at birth?

A
  • a delay in passing meconium (>48 hours)
  • a distended abdomen
  • forceful evacuation of meconium after digital rectal examination
20
Q

How can Hirschsprung’s disease present later in childhood?

A

Chronic history of constipation
Poor response to movicol disimpaction regimens
Poor weight gain.

21
Q

How can the diagnosis of Hirschsprung’s disease be confirmed?

A

Full-thickness rectal biopsy

22
Q

What is the initial management of Hirschsprung’s disease?

A

Rectal washouts initially

23
Q

What is the definitive management of Hirschsprung’s disease?

A

Removal of the section of aganglionic colon- Anorectal pull through procedure