This document provides guidance on evaluating and diagnosing the cause of vomiting in children. It discusses the various centers in the brain responsible for vomiting and the different types of vomiting. Common causes of vomiting are then reviewed based on the age of the child, including conditions affecting the gastrointestinal tract, central nervous system, and various metabolic disorders. The document emphasizes taking a thorough history and physical exam, including assessing associated symptoms, to determine the underlying etiology. A problem-oriented approach is recommended to diagnose the cause of vomiting.
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constipation in children , pediatric constipation , management of constipation in children , understanding constipation , causes of constipation in children , functional constipation in children , treatment of constipation ,approach to constipation in children ,constipation in infants
PYLORIC STENOSIS
Pyloric stenosis is a medical condition in which the pylorus, the muscular valve between the stomach and the small intestine, becomes abnormally narrowed or obstructed, leading to the obstruction of the gastric outlet. This narrowing of the pylorus prevents the proper passage of food from the stomach to the small intestine.
The exact cause of pyloric stenosis is still unknown, but it is believed to have a multifactorial etiology.
Genetic factors are thought to play a role, as there is a higher incidence of pyloric stenosis among siblings and family members.
Environmental factors may also contribute to the development of the condition, but specific triggers remain unidentified.
The hallmark symptom of pyloric stenosis is projectile vomiting, which occurs shortly after feeding.
Vomitus is often non-bilious and may resemble curdled milk.
Forceful vomiting that may project several feet away from the infant.
Signs of hunger and irritability despite frequent feeding attempts.
Weight loss or poor weight gain.
Dehydration and electrolyte imbalances due to excessive vomiting.
Palpable “olive-shaped” mass in the epigastric region.
Infants appear hungry, irritable, and unsatisfied after feeds.
Physical Examination:
Palpation of the abdomen may reveal a palpable “olive-shaped” mass in the epigastric region, which represents the hypertrophied pylorus.
The “olive” can often be felt when the infant is in a relaxed state and the stomach is empty.
Abdominal Ultrasound:
Abdominal ultrasound is the primary diagnostic tool for confirming pyloric stenosis.
Fluid and Electrolyte Management:
Prior to surgery, infants with pyloric stenosis often require fluid resuscitation and correction of electrolyte imbalances caused by excessive vomiting.
Intravenous hydration and electrolyte replacement may be necessary to restore the infant’s fluid and electrolyte balance.
Atropine Therapy:
In some cases, medical management with intravenous atropine may be attempted as a temporary measure to relieve pyloric spasm and improve the passage of food.
Surgical management of pyloric stenosis involves performing a pyloromyotomy.
This procedure is typically done under general anaesthesia and can be performed as an open surgery or laparoscopically.
Postoperative Nursing Care:
Monitor vital signs, surgical site, and signs of infection, such as fever, redness, swelling, or discharge.
Administer prescribed pain medications and antibiotics.
Observe for complications, such as bleeding or infection, and report any abnormalities to the healthcare team.
Encourage early feeding and monitor for successful feeding tolerance, ensuring the infant is retaining and digesting food properly.
Educate parents about postoperative care, including incision care, feeding techniques, and signs of potential complications, emphasizing the importance of follow-up visits and ongoing care.
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Aproach to child with vomiting
1. Aproach to child with vomiting
Dr. Riddhi Patel
Resident dept pediatrics
Sir Guru Gobindsingh Hospital -
Jamnagar
Ref : uptodate.com
practical stratagy in pediatric diagnosis 2nd ed
website of european society of radiology
schwartz handbook of pediatrics
2. Why to discuss?
• Very common complaint
• Can involve any system, associated with mild illness like
AGE to severe illness like raised ICT, DKA etc
• Diagnosis require good history , examinations supported by
lab evidence.
• Require “Problem oriented approach”
3. Vomiting in Children
• Vomiting is a symptom, presenting
complaint in multitude of disorders
– Range from gastrointestinal pathology to
disease in distant organ (otitis media or
intracranial lesion)
• In children, especially infants, must
distinguish from regurgitation –
effortless expulsion of gastric contents
• Integrated response to noxious stimuli,
coordinated by central nervous system
6. Centres responsible for vomiting
• Vomiting centre
– Nucleus solitarius and series of nuclei in
brainstem medulla
– Stimulation results in
• integrated motor responses involved in
vomiting
• associated vasomotor activity (pallor,
flushing), salivation, bulbar responses
– Afferent input arises from
• posterior pharynx, GIT, brain
7. • Chemoreceptor trigger zone
– Stimulated by humoral stimuli such as
opiates, cytotoxins, ketones, ammonia
– Lies in area postrema – floor of 4th
ventricle, outside blood-brain barrier
– Processes most of afferent input for the
vomiting centre
• Receptors and neurotransmitters
involved
– Dopamine (D2), histamine (H1), serotonin
(5-HT3), vasopressin, substance P
10. NEW BORN
• Large number of neonate vomit on first day of
life due to gastritis as a result of amniotic fluid
ingesion
• Regurgitation is normal phenomenon in
infants esp if he is gaining weight. It is due to
normal developemental phenomenon in
which there is poor lower esophageal
sphincter tone which stengthen with age. It
can also be due to aerophagy common in
bottle fed babies.
11. NEW BORN
• GIT: HPS,Congenital atresias,meconium
ileus,malrotation of gut/volvulus,hirshsprung
disease
• CNS:IVH,birth asphyxia,meningoencephalitis
• METABOLIC
DISORDERS/IEM:Galactosemia,Fructose
intolerance
• ENDOCRINE: CAH
• SEPTICEMIA
12. Older Infants & Children
• By far, the most common is gastroenteritis.
• However, GERD, gastroparesis, mechanical
obstruction, anaphylaxis, Munchausen
syndrome by proxy (factitious disorder by
proxy), intracranial masses, peptic ulcer
disease, and cyclic vomiting also may be
diagnostic considerations.
13. Infants
• GERD
• Gastroenteritis
• Gi
obstuction:intussusce
ption,malrotation,hps
• Dietary protein
intolerance
• Bartter syndrome
• Renal tubular acidosis
type 1 and type 2
• Adrenal crisis
• Uti
• Increased ICT
• Hepatobiliary
diseases
• pancreatitis
16. HPS
• MC congenital anomaly of children
• Age of presentation:2-6 week.
• First born male child
• 3 in 1000 live birth
• Non-billious vomotting, projectile, recurrant
• Pt dehydrated, FTT , wt loss
• Inspection of abdomen: shortly after infant
feeding may reveal paristaltic wave lt to rt
•
17. Ix : usg abdo - 85 to 100% sensitivity
pyloric muscle mass : thickness 4 mm
length 14mm
diagnostic of HPS
Treatment : correction of dehydration
surgical lapromyotomy (ramstead’s operation)
18. CONGENITAL ATRESIA
• At the level of duodenum or jejunum or illium
• Vomitting is billious if atresia is distal to
opening of amulla of vater
• Non billious if proximal to opening of ampulla
of vater
• In first 24 to 48 hr of life
• Associated with abdominal distention
•
19. Ix : xray abdomen standing
contrast study
Treatment : surgical resection of atresia f/b reanastamosis
21. MALROTATION WITH VOLVULUS
• Disruption of 2nd and 3rd stage of intestinal
rotation.
• Present in 1st week of life if with midgut
volvulus otherwise malrotaion will remain
undetectable for many years
• Vomitting : billious , intermittant , asso with
abdominal distention
22. Ix: xray abdomen – air fluid level & pausity of
distal bowel gas
Contrast usg : spiral configuration of jejunum
failure of contrast to pass beyond 2nd part of
duodenum
Surgical correction by LADD PROCEDURE
23. HIRSHSPRUNG’S DISEAES
Usually diagnosed in neonatal period..
• Pt presenting with symptoms of distal
intestinal obstruction:bilious
emesis,abdominal distension and failure to
pass meconium in first 24 hour of life.
• Affected children may present with
enterocolitis,a sepsis like picture with
fever,vomiting,diarrhoea,abdominal
distension progresses to toxic megacolon.
24. • Diagnosis: anorectal menometry
• barium enema
• rectal biopsy is GOLD STANDARD
• Treatment:resection of aganglionic colon and
reanastomosis
25. CONGENITAL ADRENAL
HYPERPLASIA
• MC DSD in neonatal period.
• Mc cause is 21 alfa hydroxylase deficiency
• Salt losing type.
• Virilization of female genitalia.
• Biochemical
abnormality:hyponatremia,hyperkalemia,hypo
glycaemia.
26. IEM
• Billious or non billious
• Associated with - metabolic acidosis
• hypoglycemia
• poor feeding
• FTT
• hapatospleenomegaly
• jaundice
• dysmorphic feature
• unsual odour
27. Ix : serum electroytes
serum ammonia
RFT / LFT
CBC
PT/APTT/INR
ABG
Specific test based on findins
28. GASTROESOPHAGEAL REFLUX
• MC cause of recurrent vomiting in infancy
• Retrogate movement of gastric contents into
esophagus as a result of abnormally
functioning LES.
• Present with
recurrent,postprandial,nonbilious
regurgitation of ingested milk within 30 min of
feeding.
29. •Treatment
child who are thriving and have normal physical
examination needs no treatment
•Thickening of human milk by adding serials
•Child who have FTT, feeding problems , respiratory
problems due to aspiration : PPI or H2 antagonist
•Prokinetic agenta : metoclopramide , erythromycine
•Reduces the process of GER by acting on LES
30. INTUSSUSCEPTION
• Telescoping of one portion of bowel into
another
• 3 month to 3 year
• MC terminal illium into the cecum by
lymphatic hypertrophy of peyer patches
following viral infection
• Billious vomotting , recurrant episodes of
abdominal cramps, currant jelly stool
• O/ E : P/A olive shaped mass in the right
lower quadrant
32. RAISED ICT
• D/T intracranial mass or tumour, meningitis,
encephalitis, creats pressure at area
prostrema causes vomitting
• Young child present with irritability ,sleep and
behavioural abnormality
• Older child : headache more common
• asso with neck or retroorbital
• pain
• vomitting is projectile and in
33. DIETORY PROTEIN INTOLERANCE
• Non IgE mediated food hypersensitivity
shortly after exposer to offending allergen in
1st post natal year
• Commonly proteins are cow milk protein
(lacto globulin) , egg protein, soy protein
• Recurrant vomitting asso with
diarrhoea,irritability , feeding intolerance
34. Ix :
stool for occult blood positive
stool for reducing substance positive
Treatment:
removal of allergen from diet
Symptoms resolves in 3 to 10 days of removal of allergens
Subsided by 18 to 24 months
35. CYCLIC VOMITING SYNDROME
• All of the criteria must be met for definition of
cyclic vomiting syndrome
1. Atleast 5 attacks in any interval or minimum 3
attacks in 6 months period
2. Episodic attacks of intence nausea and
vomiting lasted 1 hour to 10 days occuring
atleast one week apart
3. Stereotypical pattern and symptoms in
individual patients
4. Vomiting during the attacks occurs >=4/hour
for >=1 hour
5. Return to baseline health in between episodes
6. Not attributed to another disorder
36. Features of CVS
• Age of the onset: 2-5 year
• Episodes usually occur in early hours of
morning or on awakening
• Patients can have prodrome of nausea
pallor, intolerance of the noise or light,
lethargy, headache
• Precipitants include the infection, physical
stress, psychological stress.
38. Treatment
• Only empiric therapy at present
• 5 aspects
– Avoidance of precipitating factors
• Food and stressful events possible
• Mostly unavoidable
– Prophylactic agents
• Anti-migraine – propranolol, amitryptiline
• Anti-epileptic – phenobarbital, valproate
• Prokinetic agents – erythromycin
– Abortive agents
39. – Family support
• Crucial – unpredictable, disruptive,
unexplained illness, often misdiagnosed, few
definitive answers
40. PROPHYLAXIS
• Lifestyle changes
• Beta blockers: propranolol 0.5-2 mg/kg po bd
• Anti histaminics: cyproheptadine 0.25-0.5 mg/kg
po bd/tds
• TCA : amitryptiline 0.3-0.5 mg/kg po tds
• Antiepileptic : phenobarbiturate 2-3 mg/kg qds
41. History
• What to ask for?
a) history of diabetis in mother
b) Polyhydroamnions in mother
c) Birth asphyxia
d) Gestational age
e) Day of onset of vomit
f) Colour of vomit
g) Relationship with feeding
h) h/o meconium passage
i) On/ off feed; top feed; pre lactal feed
j) H/o seizure
k) Passage of blood in stool
42. What to look for ?
• Growth assessment
• Dysmorphic face
• Sex
• General appearance
• Fontanelle
• Jaundice
• Cataract
• Temperature
• Umbilical cord
• Exam of abdomen
• Exam of genitalia
• Per rectal exam
43. P/A
• Abd distension
– Localize to epigestrium : Upper GI Obs ( duodunal
stenosis/ atresia)
– Genrelize : ileal or jejunal atresia, meconium ilius,
hirschprung’s
– Marked distention with engorged vein : giant
cystic meconium peritonitis, meconium ileus
• Visible peristalsis
– Lt rt : pyloric stenosis
– Generalized peristalsis : normal newborn
44. • Guarding of abdominal muscles: absent in
newborn bt erythema of abdominal wall
suggest intraperitoneal infection.
• Lump:in HPS palpable olive in epigastrium or
rt hypochondrium just above and to rt of
umbilicus.
• Hepatospleenomegaly:galactosemia.
45. • Duration either
–Acute – short-term episode, abrupt
onset
–Recurrent – at least 3 episodes over
3-month period
–chronic - relatively mild episodes
that occur frequently
–cyclic – recurrent, intense episodes
separated by asymptomatic periods
46. • Age Of Child
• Characteristics of vomitus
– Smell
– Quantity
– Colour (content )
– Blood - bright red/dark
– red/coffee-ground
– Bilious
• Timing
– Onset
– Duration
– Frequency
– Time of day
– Triggers
47. Association with meal
• After any meal : peptic ulcer disease, GERD
• Specific food :
– Gluten : gluten sensitivity
– Fructose : hereditary fructosemia
– Galactose : galactosemia
– High Protein : hyper ammonemia
– Cow milk : milk protein allergy
48. Associated symptoms
•Fever: infectious etiology
• Abdominal pain/distension :
•Site of pain
•Nature of pain : colicky v/s non coliky
hepatitis , pyelonephritis, cholecystitis, intestinal
obstruction, UTI
DKA
• Anorexia : hepatitis
• failure to thrive :
•pyloric stenosis, IEM, Addison’s disease, CRF, RTA
50. Past history
• Chronic illnesses (diabetes)
• Travel history (infectious gastroenteritis)
• Sexual history (pregnancy)
– Ineffective use of birth control
– Last menstrual period
• Recent head trauma
• Toxin exposure
51. Physical examination
1. Vitals : (A) fever : sign of sepsis
(B) hypotention , tachycardia : volume loss
(C) tachypnoea / acid tic breathing : DKA
2. General examination
a) Consciousness : raised ICT, meningitis, metabolic
derangements, toxic ingestion
b) Weight loss : eating disorder, subacute intestinal
obstruction, IEM, CRF, Addison disease
c) Assess for sign of dehydration
Depressed anterion fontanalle
Loss of skin turger
Sunken eyes
Dry oral mucosa
56. • 1st x ray : coiling of tube : esophageal atresia
• 2 nd xray : double bubble sign : duodenal
atresia
57. • 3rd X ary : multiple air fluid level
( intestinal obstruction )
• 4th & 5th x ray : intra abd calcification in
meconium peritonitis
58. • (b) and (c) Lateral and AP views of contrast enema examination of the
same neonate illustrating a narrowed rectum compared to the sigmoid.
The rectum shows irregular contractions. This is the classic 'inverted cone
shape' rectum and 'saw-tooth' appearance. Rectal biopsy confirmed short
segment Hirschsprung disease.
59. • Necrotizing enterocolitis. (a) Supine AXR of a premature neonate who
developed severe NEC on 14th day of life, demonstrating multiple dilated bowel
loop with intramural gas (pneumatosis) (arrow) and portal venous gas (branching
linear lucencies in the liver extending to the periphery). (b) The same infant
developed bowel obstruction several weeks after the NEC episode. (c) Contrast
enema study demonstrates a focal stricture (curved arrow) with a localized
perforation at the site of previous NEC (short arrow).
60. Ix… cont…
• USG abd : HPS, CAH, Tumour
• Doppler USG : malrotation of Gut
• Urine benedict +ve, Glucose –ve =
galactosemia….send gas chromatography for
galactosemia
• ABG with electrolytes:
61. REMEMBER RED FLEG SIGN
• Lethargy and listlessness
• Inconsolability and bulging fontanelle in an
infant
• Nuchal rigidity, photophobia, and fever in an
older child
• Peritoneal signs or abdominal distention
(“surgical” abdomen)
• Persistent vomiting with poor growth or
development
62. Management
• Depends on specific cause
• early identification of surgical cause / life
threatening medical cause
• While investigating/ treating underlying
pathology
• replace lost fluids, maintain hydration
• If mild and child able to drink, can try
oral rehydration. Intravenous may also be
required
• Pharmacologic agents not usually
recommended
– May mask signs of serious disease
– Undesirable side-effects in children
63. Dimenhydrinate
Use: Prevention and treatment of nausea, vomiting
and vertigo associated with motion sickness.
Dosage: PO, IV, IM: Not indicated below 2 yr.
2-5 yr: 12.5-25 mg q 6-8 hr (Max: 75 mg/day).
6-12 yr: 25-50 mg q 6-8 hr (Max: 150 mg/day).
Brands: 50 mg Tab; Draminate, Gravol. 15.6 mg/5 ml
Syrup;
50 mg/ml Inj; Draminate.
• May cause excitation in young children; use with
precautions in patients with seizure disorder. May
lead to masking of signs and symptoms of ototoxicity
in patients on aminoglycosides, furosemide therapy.
.
65. Ondansetron
Use: Prevention of nausea and vomiting of various
etiology.
Dosage: PO: < 4 yr, 1-3 mg; 4-11 yr. 4 mg; >11 yr, 8 mg
q 8 hrly. IV: 0.15-0.45 mg/kg/dose q 8 hr.
Brands: 4 and 8 mg Tab; 2 mg/5 ml Syrup; 4 mg/ml
Inj;
Emeset, Ondem, Periset.
Combinations: Ondansetron + PCM and Ondansetron
+Ranitidine.
Administration: For IV dilute to 1 mg/ml and be given
over 15 minutes.
66. • Granisetron
• Use: Antiemetic in chemotherapy, radiation related
and postoperated nausea and vomiting.
• Dosage: IV: Children > 2 yr: 10-20 mcg/kg half an
hour before chemotherapy; 2-3 doses may be given.
PO:
• Adults: 1 mg BD or 2 mg OD 1 hour before
chemotherapy.
• Brands: 1 and 2 mg Tab; 1 mg/ml Inj; Granicip,
Topit. 1 mg/ml drops; Graniset.
• • May cause hypo or hypertension, arrhythmias,
agitation.
.
67. Metoclopramide
• Use: Gastroesophageal reflux, prevention of nausea and
• vomiting due to various causes, symptomatic treatment of
• diabetic gastric stasis.
• Dosage:
• • GE reflux: PO, IV, IM: 0.4-0.8 mg/kg/day divided q 6-8 hr.
• • Postoperative nausea and vomiting: IV: 0.1-0.2 mg/kg/dose.
• • Chemotherapy induced vomiting: PO, IV: 1-2 mg/kg/ dose q
2-4 hr as required.
• Brands: 100 mg Tab; 5 mg/ml Syrup; 5 mg/ml Inj;
Maxeron,Perinorm, Reglan, etc.
• • Contraindicated in GI obstruction, past history of seizures.
Causes extrapyramidal reactions and these can be prevented
and treated with diphenhydramine.
• .
68. Prochlorperazine
Use: Nausea, vomiting, vertigo, severe intractable migraine.
Dosage:
• Not indicated in < 2 yr or < 9 kg. PO: 0.4 mg/kg/day
divided q 6-8 hr. IM: 0.1-0.15 mg/kg/day divided q 8-12 hr.
Brands: 5 mg Tab; Bemetil, Stemetil, Vometil. 12.5 mg/ml Inj; Stemetil,
Steminol.
• Chances of extrapyramidal reactions are high in children so always use
lowest possible dose.
8
69. . Promethazine
Use: Allergic conditions, motion sickness, antiemetic and sedation.
Dosage: Not indicated below 2 yr of age.
• Antihistamine: PO: 0.1 mg/kg/dose q 6 hr (Max: 12.5 mg/day).
• Antiemetic: PO, IM, IV: 0.25-1 mg/kg/dose q 6 hr (Max:25 mg/dose).
• Sedation: PO, IV, IM: 0.5-1 mg/kg/dose q 6 hr (Max: 50 mg/dose).
• Motion sickness: PO: 0.5 mg/kg half an hour before journey, can be
repeated after 12 hr as needed.
Brands: 10 and 25 mg Tab; 5 mg/5 ml Elixir; Phenergan, Prometh, Promet. 5
mg/ml Inj; Phenergan.
• IM route is preferred, avoid IV use. May cause hypotension in fast IV and
hypertension in slow IV use.
Children with dehydration are prone to develop dystonic reactions.
Chlorpromazine and hydroxyzine also have antiemetic actions.
Dexamethasone and Lorazepam are used as adjunctive antiemetic.
70. CASE SCENARIO
A 5 yr old male child presented with loose stool nd
vomiting since last 2 days.. No history of fever nd
no past history of admission present.
On admission child was irritable,suncken eyeball
present,nd skin pinch goes back slowly.
Consindering some dehydration correction
started. With otherwise no significant history in
this child considered as a case of gastoenteritis..
71. • A 1 month old male child presented with
complain of vomiting since last 15 days
immediately after takind breast feeding nd
child not gaining weight since 15 days.
• on detailed history birth weight of child was
2.5 kg,vaginal delivered full term baby. On
admission child was lethargic,dehydrated,poor
feeding,weight is 2.9 kg. aftr correction of
dehydration usg abdo done s/o incresed
thickness nd length of pylorus p/o pyloric
stenosis. Child referred for further surgical
management
72. • A 4 yr old female child presented with c/o
vomiting since 2 days,abdominal pain since 2
days nd rapid breathing since 1 day.
• On detailed history child having increased
frequency of urine nd increased oral intake
since last 2-3 months.
• On admission child was lethargic,acidotic
breathing present, RBS done which was
high,urine sugar kitone 4+ nd large so
considered as diabetic ketoacidosis and
management started as protocols of DKA.
73. Take home message
• Vomiting is a vague symptom, Early
identification of serious disease needed in sick
child is key to successful mx
• Urgent medical as well as sx intervention may
needed
• History and examination with lab and
radiological support establish the diagnosis
Editor's Notes
Nausea: The unpleasant sensation of the imminent need to vomit, usually referred to the throat or epigastrium; a sensation that may or may not ultimately lead to the act of vomiting.
Vomiting:Forceful oral expulsion of gastric contents associated with contraction of the abdominal and chest wall musculature.
Regurgitation:The act by which food is brought back into the mouth without the abdominal and diaphragmatic muscular activity that characterizes vomiting.
Retching : effort to vomit, short of expulsion of gastric contains, may be considered an abortive attempt to vomit
Rumination: habit of bringing up semidigested food and chewing up again. Can be severe psyco social disorder and assosiated with failure to thrive
Mechanical : due to obstructive lesion of GIT can be partial or complete, congenital or acquired
Reflex : from irritating viscera ( labyrynth, urinary tract, etc) or from certain drugs and metabolites through chemo receptor trigger zone
Central : through irritation or stimulation of vomiting center is raised ICT/ inflammatory lesion of CNS ( meningitis, encephalitis, epilepsy, migraine, cyclical vomit)
Vater anomaly association
Atresia of upper intestine
Cerebral irritation / intestinal perforation
Premature NEC
Hypertrophic pyloric stenosis 2nd / 3rd week 1 st male, galactosemia after 2 week ; proximal v/s distal obs
Mucus : oesophageal atresis
altered milk : proximal to ampulla of vater
bile stained : beyond ….
fecal : small bowel obs ( lower GUT)
bloody : maternal blood v/s mucosal trauma
GER as soon as child returned to cot/ HPS : large non progectile, non bilious, occur even in upright /Chock and cynosed (TEF)
Meconium ileus, hirschprung
Dull stopped feed : galactosemia or sepsis
Seizure sepsis, trauma, BA, galactosemia
Blood in stool : NEC
Failure to thrive + persistant vomit : HPS, galactosemia, CAH
Dysmorphism : down synd duodenal atresia
1st male : pyloric stenosis
Septicemia, NEC : very sick, lithargic, scleromatous look
Buldging fontanalle : meningitis, intra cranial bleed, hydrocephalous
Jaundice : galactosemia, sepsis, GI obstruction
Cataract : galactosemia at 2 to 6 week of age
Temp imbalance in sepsis
Pus discharge : sepsis
Discuss in next slide
Virilization in female : CAH
For presence or absence of meconium, tight incapacious rectum in micro colon
Age : infancy : faulty feeding, GER, Infection
childhood : gastritis, gastro enteritis, GER, Extra cranial and intra cranial infection
Intussusception : the most common cause of intestinal obstruction between 3 mo and 6 yr of age and
the most common abdominal emergency in children <2 yr. More common in males
In typical cases, there is sudden onset, in a previously well child, of severe paroxysmal colicky pain that recurs at frequent intervals and is accompanied by straining efforts with legs and knees flexed and loud cries. Vomiting in beginning of symptom, may become bile stain. 60% case pass red current gelly stool. It is surgical emergency
Onset : acute onset : with fever , usually infectious etiology like AGE, UTI, pyelonephritis, hepatitis, pancreatitis, cholecystitis, appendicitis, Meningitis etc
: without fever : intestinal obstruction, ureteric stone ( A/W colicky abd pain )
Duration : longer duration and recurrent with completely normal period in between : migrain, motion sickness, cyclical vomiting, psychogenic
persistant daily vomit : IEM, Intra cranial tumour, chronic infection
NOTE ; absence of bilious vomit does not rule out intestinal obstruction
Time of day: early morning
Increased intracranial pressure :Headache, papilledema
Sinusitis : postnasal mucus, Sinus tenderness
Uremia
Frequency : expected dehydration and dys electrolytemia
Trigger : smell, Drugs, Toxin, etc…
D/D of episodic or cyclical vomiting :
Abdominal migraine, abdominal epilepsy
Pheochromocytoma
Porphyria
Familial dysautonomia
Metabolic inborn error
Familial Mediterranean fever
Malrotation and intermittent volvulus
Intermittent intussusception
Self-induced
Cyclic vomiting
Stool frequency
Diarrhea : Partial intestinal obstruction Infectious enteritis,Poison, inborn error of metabolism
Constipation : Intestinal obstruction or dysmotility (pseudoobstruction) Hypercalcemia, hypokalemia, porphyria, lead poisoning
Urinary output / color : dehydration , hepatitis
Headache : intra cranial/ extra cranial infection
Vertigo : labyrhynthitis
Lethargy : severe dehydration, intra cranial pathology, metabolic or electrolyte disturbance
Stiff neck : meningitis
Cough : post tussive
Sore throat URTI
Lethargy dis proportionate to sevearity of vomit : Hepatitis, raised ICT, DKA
Well looking child with periodic vomit : migraine
CVS :
2 gas shadow in upper abd , stomach and proximal duodenum rest abd are gas less