Paeds GASTRO Flashcards

1
Q

What is the commonest cause of vomiting in infancy?

A

Gastro-oesophageal reflux

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2
Q

What is the cause of GOR in babies?

A

Inappropriate relaxation of the LOS (functional immaturity)
= a normal physiological process in infancy
Affects >40% infants

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3
Q

When does GOR present? By when does GOR usuallly resolve?

A

Usually develops before 8w
12 months: if persistent, may be due to GORD

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4
Q

How does GOR present?

A

Vomiting/ regurgitation: milky vomits after feeds
Vomiting may occur after being laid flat
Excessive crying, esp. while feeding

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5
Q

How is GOR diagnosed?

A

Clinical dx
24h LOS pH

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6
Q

What are 6 symptoms are considered red flags suggesting disorders other than GOR?

A

Projectile vomiting
Bilious vomiting
Onset after 6m/ persisting after 1y
Abdo distension/ mass
Chronic diarrhoea
Rapidly increasing head circumference

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7
Q

Which 3 symptoms warrant same day referral in GOR?

A

Haematemesis
Melaena
Dysphagia

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8
Q

Recall 6 factors prompting referral for paediatric assessment for GOR

A

Red flags

Faltering growth

Unexplained IDA

No improvement after 1y

Feeding aversion

Suspected Sandifer’s syndrome

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9
Q

What is Sandifers syndrome?

A

GORD
+
Paroxysmal dystonia: head, neck, back- Torticollis + Opisthotonus

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10
Q

Recall the general advice for GOR

A
  1. Reassure
  2. Review feeding hx
  3. Reduce feed volumes if excessive for infant’s weight
  4. Must sleep on back
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11
Q

For formula fed infants, what other management strategies should be used for GOR

A

Smaller more frequent feed
Offer thickened formula
Trial alginate 1-2w e.g. Gaviscon infant

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12
Q

For breastfed infants, what other management strategies should be used for GOR

A

Assess breast feeding- position, frequency

Trial Alginate 1-2w

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13
Q

What pharmacological treatment can be used if conservative management is ineffective for GOR?

A

PPI e.g. Omeprazole suspension
H2 receptor antagonists

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14
Q

What safety net should you watch out for when assessing GORD?

A

Monitor vomit: if bloody or green seek medical attention

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15
Q

What is necrotising enterocolitis?

A

Ischaemic necrosis of intestinal mucosa a/w severe inflammation, invasion of enteric gas forming organisms + dissection of gas into bowel wall

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16
Q

What is the major risk factor for necrotising enterocolitis?

A

Prematurity

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17
Q

Give 4 signs/ symptoms of necrotising enterocolitis

A

Abdo distension + erythema
Bloody stools
Bilious vomiting
Feeding intolerance

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18
Q

Give 2 complications of necrotising enterocolitis

A

Perforation + Peritonitis

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19
Q

What investigation is used to diagnose necrotising enterocolitis? What is seen?

A

Abdo XR
Intramural gas (pneumatosis intestinalis)
Pneumoperitoneum (perforation)
Air inside + outside bowel wall (Rigler sign)
Sentinel bowel loops

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20
Q

What is the treatment of necrotising enterocolitis?

A

Total bowel rest + TPN
Gastric decompression
Abx
Surgery: laparotomy for perforation

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21
Q

What causes pyloric stenosis? At what age does pyloric stenosis present?

A

hypertrophy of the circular muscles of the pylorus.
2-8w

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22
Q

Is pyloric stenosis more common in girls or boys?

A

Boys (4 x more common)

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23
Q

What is the main symptom of pyloric stenosis?

A

Projectile, non-billious vomiting
~30m after feed
Baby remains hungry
Increases in intensity until it becomes projectile

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24
Q

Recall 3 symptoms of pyloric stenosis other than vomiting

A

Weight loss + persistent hunger
Depressed fontanelle from dehydration
Constipation/ infrequent bowel movements

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25
Recall some signs of pyloric stenosis
Palpable 'olive' mass Visible peristalsis in upper abdomen
26
What will be the acid-base profile in pyloric stenosis?
Hypochloraemic, hypokalaemic metabolic alkalosis due to persistent vomiting may progress to a dehydrated lactic acidosis (opposite biochemial picture)
27
What is the best investigation for pyloric stenosis?
USS: shows target lesion of >3mm thickness Do CBG to guide management
28
How should pyloric stenosis be managed?
1. IV slow fluid resuscitation + correct any disturbances: 1.5 x maintenance rate 5% dextrose 0.9% saline 2. Laparoscopic Ramstedt pyloromyotomy
29
What are the symptoms of colic?
Inconsolable crying- worse in evening Drawing up knees + arching back Clenching fists
30
What is colic?
Repeated episodes of excessive + inconsolable crying in an infant that is otherwise healthy + thriving <5 months when Sx start + stop.
31
What is management of colic?
Reassurance: strategies to sooth baby: holding baby, gentle motion, white noise, winding Encourage parental wellbeing Encourage to continue breastfeeding
32
What should be considered if the colic is persistent?
Cow's milk protein allergy or reflux Try: 2 week trial of hydrosylate formula followed by 2 week trial of anti-reflux tx
33
In what age group is appendicitis less common, and what is a more likely cause of similar symptoms in this age group?
Rare in under 3s, then it's more likely to be faecolith (stony mass of impacted faeces)
34
Recall the management of appendicitis in children
GAME G: group + save A: Abx IV M: MRSA screen E: eat + drink NBM Then laparoscopic appendectomy
35
What is intussusception?
Invagination of proximal bowel into distant component (telescoping distally)
36
What is the most common site of intussusception?
Ileum through to caecum through ileocaecal valve
37
Recall the appearance of stool in intussusception, and the pathophysiology of how this happens
Red-currant jelly (blood + mucus) due to venous obstruction + compression --> oedema + mucosal bleeding This is a LATE sign
38
What are the causes of intussusception?
Idiopathic Physiological lead point: Peyer's patch Pathological lead point: malignancy, Meckl's diverticulum, Henoch-Schonlein purpura
39
What are the symptoms of intussusception?
Intermittent colicky pain Vomit: depending on type: may be bile-stained or not
40
What are the signs of intussusception?
Abdominal distention with sausage shaped mass in RUQ Emptiness on palpation in RLQ (Dance's sign) Red-currant jelly stool is a late sign
41
What are the appropriate investigations for intussusception?
1. Abdo USS: may show donut sign (think: intUSSusception) 2. AXR (may be normal) 3. Barium/ gastrogaffin enema if have 1 of 3 Ps: Perforation, Peritonitis, Pale complexion
42
How should intussusception be managed?
It's an emergency If stable: - Fluid resuscitation - Enema: pneumatic - forces bowel to un-telescope - take x rays throughout If unstable: - Don't mess about with contrast, go in with open surgery - Remove any non-viable bowel
43
What should be done if there is recurrent intussusception?
Investigate for a lead point
44
What is Meckel's diverticulum?
Congenital diverticulum of small intestine Remnant of the omphalomesenteric duct (vitello-intestinal duct) Contains ectopic ileal, gastric or pancreatic mucosa.
45
What is the rule used to remember all you need to know about Meckel's diverticulum?
Rule of twos 2 years old 2 x more common in boys 2 feet from ileocaecal valve 2 inches long 2 different mucosae (gastric + pancreatic)
46
What are the signs and symptoms of meckel's diverticulum?
Mostly asymptomatic Painless massive PR bleeding Abdo pain mimicking appendicitis Intestinal obstruction: billious vomiting, dehydration + intractable constipation
47
What is the most common cause of painless massive GI bleedingin in children between ages 1-2?
Meckels diverticulum
48
How should meckel's diverticulum be investigated if a child is stable?
99m Technetium pertechnetate scan indicates increased uptake by gastric mucosa
49
How should meckel's diverticulum be investigated if a child is unstable and transfusion is required?
Mesenteric arteriography
50
How should meckel's diverticulum be managed?
If asymptomatic, leave it alone! If symptomatic: Laparoscopic resection (excision of diverticulum) +/- lysis of adhesions Blood transfusion
51
How may volvulus present?
1. At any age, after lying quiescent for ages 2. In first few days of life, with obstruction + possible compromised blood supply --> abdo pain, billious vomiting, peritonism etc
52
What is the main sign of volvulus on abdo examination?
Scaphoid abdomen
53
How should volvulus be investigated?
1. Upper GI contrast study (urgently) to assess patency if billious vomiting 2. USS
54
How should volvulus be managed?
Urgent laparotomy Untwist volvulus, mobilise the duodenum, place bowel in a good position + remove any necrotic bowel
55
What is the first thing to exclude in suspected IBS?
Coeliac
56
Recall the signs and symptoms of IBS
Abdo pain: often worse before or relieved by defaecation Explosive loose or mucus stools Bloating Tenesmus Constipation
57
Recall the 3 most common causes of paediatric gastroenteritis in decreasing prevalence
1. Rotavirus 2. Campylobacter 3. Shigella/ salmonella
58
If there is bloody diarrhoea in gastroenteritis, which microbes should be considered first?
CHESS organisms: Campylobacter Hemorrhagic E coli Entamoeba histolytica Salmonella Shigella
59
What investigations should be done in a case of gastroenteritis?
AXR to exclude other causes Stool sample analysis for viruses = stool electron microscopy for bacteria = stool culture
60
How should paediatric gastroeneteritis be managed?
Rehydration Learn maintenance fluid volumes: 0-10 kg = 100mls/kg 10-20kgs = 1000mls + 50ml/kg for each kg over 10kg 20+ kgs = 1500mls + 20 mls/kg for each kg over 20kgs If <5 use IV fluids + maintain with oral rehydration solution If >5, give 200mls after each
61
What is the safety netting for how long vomiting and diarrhoea should last?
Vomiting: usually 1-2 days, must stop within 3 days Diarrhoea: 5-7 days, must stop within 2 weeks
62
What is the most accurate marker of dehydration in children?
Weight loss
63
What is the threshold marker of dehydration for clinical dehydration and shock?
5-10% weight loss = clinical dehydration >10% weight loss = shock
64
Recall the symptoms of hypernatraemia
Mnemonic: f(ull) of salt Flushing Oedema Fever Seizures Agitation Low urine output Thirst
65
Recall the symptoms of hyponatraemia
SALT LOSS Stupor Anorexia Limp tone Tendon reflexes reduced Lethargy Orthostatic hypotension Seizures Stomach cramps
66
When are IV fluids (rather than ORS) indicated?
Shock Deterioration Persistent vomiting
67
What are the bolus fluids given in shock?
20mls/kg 0.9% saline over 15 mins (most situations) 10mls/kg 0.9% saline over 60 mins (trauma, fluid overload, heart failure)
68
Recall the day 1, 2, 3, 4, and 5 fluid resucitation requirements in neonates
Day 1: 50-60mls/kg/day Day 2: 70-80mls/kg/day Day 3: 80-100mls/kg/day Day 4: 100-120mls/kg/day Day 5: 120-150mls/kg/day
69
Which type of fluid should be used in fluid resus for term neonates?
Isotonic crystalloids with 10% dextrose
70
If giving IV fluids to a hypernatraemic child, what should be the biggest caution?
Take care with cerebral oedema Rapid reduction in plasma sodium concentration + osmolality will lead to a shift of water into cerebral cells May result in seizures + cerebral oedema
71
When should Abx be used in gastroenteritis?
Not even indicated when cause is bacterial Use when: - SEPSIS - salmonella < 6 months - C difficile with pseudomembranous colitis
72
What is the post-gastroenteritis syndrome and how can it be treated?
Introduction of a normal diet results in a return of watery diarrhoea Treat with oral rehydration therapy
73
What would be seen on biopsy in Crohn's?
Non-caseating epitheloid cell granulomata
74
Recall some important investigations to do for Crohn's disease
1. FBC including iron, folate and B12 2. Faecal calprotectin 3. Colonoscopy + biopsy (cobblestones)
75
How should Crohn's be treated?
Induce remission: Nutritional management Replace diet with whole protein modular diet: excessively liquid, for 6-8 weeks. The products are easily-digested and replace lost weight Pharmacological management: steroids (prednisolone)
76
What is the classical presentation of UC?
Rectal bleeding Diarrhoea Abdo pain
77
What are the appropriate investigations to do in ulcerative colitis?
Same as Crohn's 1. FBC including iron, folate + B12 2. Faecal calprotectin 3. Colonoscopy + biopsy
78
What does histology reveal in UC?
Mucosal inflammation/ ulceration Crypt damage
79
What scores can be used to score paediatric UC?
Paediatric UC Activity Index Truelove + Witts
80
What is one coexisting condition that it's important to be aware of in ulcerative colitis?
Depression
81
How should UC be managed?
1st line = oral aminosalicylates: may also be used to maintain remission 2nd line - oral corticosteroid 3rd line = oral tacrolimus Surgery in resistant disease
82
When does UC become an emergency?
In severe fulminating disease
83
What is the usual cause of toddler diarrhoea?
Underlying maturational delay in intestinal mobility
84
Recall some signs and symptoms of toddler diarrhoea
Varying consistency stools: well-formed to explosive + loose, may have bits of undigested vegetable Child will be well + thriving
85
How is toddler diarrhoea managed?
Increase fibre + fat in diet (whole milk, yoghurts, cheese) Avoid fruit juice + squash
86
What is the first-line management of constipation?
All first line: 1. Advise behavioural interventions (eg schedueled toileting, bowel habit diary, reward system) 2. Advise diet + lifestyle (adequate fluid intake) 3. Medication: step 1 = movicol paediatric plan (dose escalates for 2 weeks) Step 2: maintain for 6 months
87
Recall some important things to remember in PACES counselling for constipation
Explain movicol takes some time to work (dose increases over 2 weeks) Encourage child sitting on loo after mealtimes to use reflex Advise a star chart to aid motivation
88
What is Hirschprung's?
An absence of ganglion cells from the myenteric (Auerbach) + submucosal (Meissner’s) plexuses Lumen is tonically contracted, causing a functional obstruction
89
Recall 2 risk factors for Hirschprung's
Down's Men2a
90
How may Hirschprung's present? (5)
Failure/ delay to pass meconium in first 24h Explosive passage of liquid + foul stools Abdo distension +/- enterocolitis Vomiting +/- bile Failure to thrive
91
If Hirschprung's doesn't present in first few days of life, what may happen?
May then present in a week or two with life-threatening Hirschprung's enterocolitis (C diff)
92
What is the gold standard investigation for Hirschsprung's?
Full-thickness rectal biopsy Showing absence of ganglion cells
93
What screening investigations may be performed in suspected Hirschprung's?
Contrast enema XR: contracted distal bowel + dilated proximal bowel (AXR: dilated colon + air-fluid levels)
94
What is the initial management of Hirschprungs?
Bowel irrigation "rectal washouts" IV fluids BS Abx if enterocolitis
95
What is the definitive management of Hirschsprung's ?
Anorectal pull through (colostomy followed by anastomosing normally innervated bowel)
96
What is meconium ileus?
bowel obstruction that occurs when meconium is even thicker + stickier than normal meconium
97
What condition do most children presenting with meconium ileus have?
Cystic fibrosis
98
How does meconium ileus present?
Delayed passage of meconium Abdo distension (viscid meconium obstructs terminal ileum) Bilious vomiting
99
What investigations are required for meconium ileus?
X-ray: No fluid level (meconium viscus) Contrast enema XR: shows blockage
100
What is management for meconium ileus?
IV fluids NG tube Enema may dislodge meconium plugs Surgery
101
Recall the principles of management for anal fissure
Ensure stools are soft + easy to pass (conservative) Increase dietary fibre + fluid intake Anal hygeine Safety net: seek further help if not healed within 2 weeks
102
Recall all the principles of management for threadworm
Single dose of an anti-helminth (mebendazole) for the whole household Advise rigorous hygeine for 2 weeks if on mebendazole, or 6 weeks if using hygeine measures alone Exclusion from school/ nursery is not required
103
What can cause a temporary lactase deficiency?
Gastroenteritis Crohn's Coeliac Alcoholism
104
What should be excluded in suspected lactose intolerance?
Gastroenteritis (stool sample) Crohn's (faecal calprotectin) Coeliac (anti-tTG/EMA)
105
How is a diagnosis of lactose intolerance made?
It's a clinical diagnosis trial a 2 week lactose-free diet + see how Sx are Breath hydrogen test: early rise in H2 following CHO ingestion
106
How is secondary lactose intolerance managed?
Cut out dairy to allow time to heal May need calcium + vit D supplements Digestive enzymes can be taken in a capsule before eating lactose until gut matures/ heals
107
Recall 2 genetic associations with Coeliac's?
HLA DQ2 (95%), DQ8 (80%)
108
Recall the symptoms of coeliac in children
Failure to thrive Abdo distention Bloating Irritability
109
When does coeliac disease first present in children?
8-24 months after introduction to wheat foods
110
How is coeliac disease diagnosed?
Most sensitive = IgA TTG Or (less sensitive) = IgA anti-EMA
111
What other investigations are useful in coeliac disease?
FBC + blood smear to look for anaemia In older children/ adults: OJD + biopsy can confirm dx In younger kids: no histopathological confirmation
112
How should coeliac disease be managed?
Cut out all wheat, rye + barley Dietician referral + annual review Support sources: Coeliac UK
113
What might be 4 consequences of non-adherence to diet in coeliac disease?
Micronutrient deficiency Osteoporosis EATL Hyposplenism (loss of lymphocytes in GIT)
114
What is mesenteric adenitis?
Swollen lymph glands that cause temporary abdo pain following infection
115
What are the signs and symptoms of mesenteric adenitis?
Abdo pain (may present similar to appendicitis: central-RIF) N + V + D: leading to reduced appetite Fever Often preceded by URTI/ viral infection
116
How should mesenteric adenitis be diagnosed?
Bloods: WCC + CRP Urine dip USS: enlarged LN Usually dx of exclusion Definitive dx= laparoscopy showing large mesenteric lymph nodes + normal appendix
117
How should mesenteric adenitis be managed?
Simple analgesia Safety net for increased pain, deterioration 1-4w Sx (up to 10w)
118
What is the pathophysiology of an indirect inguinal hernia?
Towards end of pregnancy the process vaginalis allows passage of testicles from abdomen to scrotum When this passage fails to close, abdo lining/ bowel can protrude through defect
119
Recall the signs and symptoms of hernia
Scrotal sac enlarged, contains palpable loops of bowel, fluid (does not always transilluminate) Swelling or bulge may be intermittent + can appear on crying or straining
120
How is hernia diagnosed?
Clinical diagnosis Examine supine + standing + try to reduce in order to determine type of hernia
121
Recall 3 risk factors for umbilical hernia
Afro-caribbean Down's Mucopolysaccharide diseases
122
How should hernia be managed?
Correct urgently 1. If < 6 weeks old, correct <2 days 2. If < 6 months old, correct <2 weeks 3. If <6 year old, correct <2 months
123
How does an umbilical granuloma appear?
Leaks + is watery
124
How is umbilical granuloma treated?
With salt
125
Where are femoral hernias located?
Beneath inguinal canal
126
What is femoral hernia most similar to?
Indirect inguinal hernia
127
What is gastroschisis?
Paraumbilical wall defect: abdominal contents outside body without a peritoneal covering Needs immediate surgery
128
What is omphalocele?
Bowel protruding out of the body with a peritoneal covering
129
How should omphalocele be managed?
Closure starting immediately, finishing at 6-12 months
130
What is encoparesis?
Soiling of underwear with stool in children who are past the age of toilet training
131
What is the usual cause of encoparesis?
Constipation with overflow
132
How should encopresis be managed?
Enquire about stressors, changes in medication, food intolerances etc
133
What are the 2 most likely causes of liver failure in children <2 y/o?
HSV infection Metabolic disease
134
What is the most likely cause of acute liver failure in children >2 y/o?
Paracetamol OD
135
What are the signs and symptoms of acute liver failure?
Jaundice Coagulopathy Hypoglycaemia Electrolyte disturbance Encephalopathy
136
How should Acute liver failure be managed?
Referral to a national paediatric liver centre To stabilise the child: - IV dextrose (due to hypoglycaemia) - broad spectrum Abx + anti-fungals to prevent sepsis - IV vit K + PPIs to prevent haemorrhage - Fluid restriction + mannitol
137
Recall some features of poor liver prognosis
Shrinking liver Falling transaminases Rising bilirubin Worsening coagulopathy
138
How should hepatic encephalopathy be managed?
Reduce nitrogen with lactulose
139
How should AI hepatitis be managed?
Prednisolone/ azothioprine
140
How should sclerosing cholangitis be managed?
Ursodeoxycholic acid (aids bile flow)
141
How should Wilson's disease be managed?
Zinc (blocks intestinal Cu resorption) Trientine/ penicillinamine (increases urinary Cu excretion) Pyridoxine (vit B6, prevents peripheral neuropathy) Symptomatic tx for tremor, dystonia + speech impediment
142
How is non-alcoholic fatty liver disease managed in children?
Weight loss Statins Treatment of diabetes Vit E + C Ursodeoxycholic acid to improve bile flow
143
How should paracetamol OD be managed?
<1 hour: activated charchoal, do paracetamol level 4 hours post ingestion, NAC if indicated >1 hour: do a paracetamol level, NAC if indicated
144
What is duodenal atresia?
Congenital narrowing/ absence of duodenum causing intestinal obstruction
145
What can suggest duodenal atresia pre-natally?
Polyhydramnios Baby not able to swallow amniotic fluid well Usually diagnosed at 20w scan
146
Give 3 signs/ symptoms of duodenal atresia
Premature birth Bilious vomiting Abdo distension
147
What is the management for duodenal atresia?
IV fluids + NG tube Surgery: Duodeno-duodenostomy or duodeno-jejunostomy.
148
What investigation is used for duodenal atresia? What may be seen?
Abdo X-ray/ USS Double bubble sign
149
What condition do 1/3 of children with duodenal atresia have?
Down syndrome