Pediatrics 1
Pediatrics 1
:Physiological hyperbilirubinemia
Timing……3rd day
Prevention of jaundice
:Pathological jaundice
:Causes
:Hemolytic disease of the newly born -1
Cause…..Rh (-) mom and Rh(+) baby
Most common cause of sensitization of the mom…..hidden
feta-maternal hge bleeding
How to prevent…….anti-D after any maternal bleeding
:ABO incomptability-2
If mom is O and the baby is A, B or AB
Can occur if first baby born
Mild hemolysis
:Sepsis-3
Fever, bad general condition and jaundice
When to do phototherapy????
bilirubin >270micromol/L
Phenobarbital-3
:N:B
When to say direct hyperbilirubinemia……..when direct is
more than 20% of the total
Direct hyperbilirubinemia after 1st week………biliary atresia
:Congenital hypothyrodism
Most common cause…….thyroid dysgenesis
Cp…..prolonged jaundice, constipation, hypotonia, enlarged
tongue, umbilical or inguinal hernia, mental retardation
:prevention
Screening……..2nd and 7th day of life
Technique………blood sample from the heel
TTT…..thyroxine
:Gilbert syndrome
Most common cause of hyperbilirubinemia
Genetics…..AD
Cause….low glucuronyl transferase
Cp…..jaundice
Type…..indirect hyperbilirubinemia
TTT…..none
:Crilger Najar
Same as Gilbert
But more severe ….needs ttt
:Dubin Johonson and Rotor syndrome
Conjugated hyperbilirubinemia
No ttt
With Dubin Johonson…..green colored liver biopsy
:Neonatal seizures
:TTT
:Neonatal hypoglycemia
:TTT
IV glucose….if hypoglycemia persist give IM Glucagon…vvv imp
:Neonatal hypothermia
…choanal atresia:
:Cp
RDS
:TTT
Surgery
:Cytomegalovirus in neonate
Most common cause of congenital neonatal infection
Most common cause of birth defect
:Cp
Hearing loss
Vision loss…..pigmented
retina
Mental disability
Small head size………microcephaly
Seizures
Death
Inv of choice……urine antigen
TTT…….ganicyclovir
:Oral candidiasis
,Cp….difficult suckling
Exam….whitish lesion removed easily
TTT…..oral nystatin
:Innocent murmur
:Characteristics
Decreases by sitting up
:Umbilical Granuloma
Complication…….infection
: Omphalitis
Fever
Omphalocele vs Gastroschisis
Omphalocele……….there is a sac
Gastroschiasis……….nooooo sac
:TTT
Gastroschisis…….emergency surgery
:Omphalocele
:Tongue tie
:Timing of repair
months or 3-4
years 1-2
Usually unilateral
affect feeding -1
affect speech-2
aspiration pneumonia-4
:Timing of surgery
:Metatarsus adductus
Cp…..adducted foot
Resolution…..usually by 3 years
Usually NO ttt
CORRECTIVE SHOES
SERIAL CASTING
IF NOT…..SURGERY
AGE…….toddler
:TTT
OBSERVE
Site …..femur
:TTT
Resolution….by 8-9 ys
:Pediatrics infections
:maculopapular-1
Measles
Mumps
Roseola infantum
Scarlet fever
Infectious mononucleosis
SLE
Sweat rash
:Roseola infantum
Complications……febrile convulsions
TTT…….symptomatic
:Rubella
Cp….fever
:Measles
IT IS A NOTIFIABLE DISEASE
:Cp
Koplik's spots
Cause……….parvovirus B19
:Cp
Slapped cheek
Maculopapular rash
School exclusion…….none
TTT……symptomatic
:Scarlet fever
Cause…..group A streptococcus
:Cp
Strawberry tongue
Circumoral pallor
Complication…….glomerulonephritis
TTT……penicillin
:Cp
Mouth………ulcer
Hands and foot …..maculopapular rash then vesicles
:herpangina
Organism…… coxsackie
Both of them………vesicles
:Bronchiolitis
Cause……RSV
X-ray……hyperinflation
No antibiotics
:Cp
fever
Harsh voice
Barking cough
……TTT
Epiglottitis
Cause…….hemophilus influenza
:Cp
Toxic look
DROLLLLLLLLING of saliva
:/Management
First step……admission
Intubation
If cannot intubate…….cricothyrodectomy
Antibiotics
:KAWAZAKI disease
Inv…..ECHO….VVVVVVVIMP
:Signs
:TTT
If no response……….amox
If still no response,………amox-clav
Most imp test to be done to the baby after recovery……hearing
assessment vvvvvvvvvvvvvvvv imp
Mastoiditis :2
Inv……CT
:MENINGITIS-3
Organism……strep.pneumoniae
:Worm infections
:Ascaris lumbricoides
Most common worm …..very long worm
Complications….intestinal obstruction, lung affection
TTT….albendazole
Hook worm( ankylostoma)
Abdominal pain and diarrhea
Most common worm causing iron deficiency anemia in
kids
Hypoalbuminemia
Inv….stool analysis
TTT…..albendazole and iron
Enterobius vermicularis…vvvvv imp
Most common cp…….itchy anus
Inv of choice…….adhesive tape at night
TTT….single dose albendazole and repeat after 2 wks
:Trichinella spiralis
Undercooked meat
Most common cp…….muscle pain
Inv of choice……larva in muscle biopsy
TTT….mebendazole
:Trichuris trichura
Most common complication….rectal prolapsed
Cp….periumbilical pain
TTT….albendazole
:Cp
Fever
Vaccine….live attenuated-1
:MUMPS
Cp….fever, fatigue
TTT….supportive
:Infectivity period
:Stages
:Complications
CNS…..convulsions
Serology…..low value
Prevention….DTP vaccine
:TTT
:Down syndrome
Cause…..Triosomy 21
:CP
upward slanting palbebral fissure
inner epicanthal fold
open mouth with tongue protrusion
hypotonia
Hearing loss
Simian crease
Gonadal deficiency
Hypothyroidism
Antanto-axial instability
:Very important tips for down
Most common genetic disorder…..non-dysjunction
Most common risk factor……maternal age
Most common cause of death…..leukemia (acute
lymphoblastic)
Mentally…..early onset alzeheimer
Most common CVS abnormality….endocardial cushion
defect followed by VSD
Most common GIT abnormality……duodenal atresia
Most common endocrine abnormality…..hypothyrosim
Most common spine abnormality….. Antanto-axial
instability
Recurrence rate with Down…..1%
risk of down syndrome by age chart Australia: vvvimp
1/870……20
1/500.……30
1/200.……35
1/100.……40
1/25……45
1/10……49
:Klienfelter syndrome
Genetics…..47XXY
:Cp
Tall man
Long limbs
Slim
Hypogonadism….small testis
Decreased testosterone hormone
gynecomastia
Low IQ
Behavioural problems
:Marfan syndrome
Genetics….AD
Mutation in fibrillin gene
Tall stature
Long slim limbs
Decreased U:L limb ratio
Arachnodactyly
Joint laxity and subluxation
Eye…..upward subluxation of the lens
Heart….AR
Aortic dissection
Spine…..scoliosis
Pectus excavatum
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:ndrome
Genetics….AD
Hyperextensible skin
Easily fragile
Joint laxity
MVP
AR
Aortic dissection
Blue sclera
:Osteogenesis imperfecta
Genetics….AD
Blue conjunctiva
Scoliosis
Recurrent multiple fracture
DD….child abuse
:
: .…Peutz-jeghers syndrome
VVVVVVVV IMP
Genetics……AD
Lips……pigmentation
Colon…..polyps
:Risk
intussception-1
colon cancer….SCREEN-2
Albinism
Blue eyes
Premature graying
:Pediatric oncology
% Recurrence rate……2-5
Asymptomatic……..no ttt
:Meningocele
Herniation…..meninges but not the spinal cord
Covered by skin
Do ct ……exclude hydrocephalus
TTT……surgery
:Meningomyelocele
Inv….CT….exclude hydrocephalus
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:Wilms tumour
Age……2-5 ys
Usually unilateral
:Association
Hemi hypertrophy
Aniridia
:TTT
Then chemotherapy
Prognosis…..excellent
:Neuroblastoma
Origin……neural cells
Periorbital ecchymosis
:Inv
Vanillymanillic acid……increased
The best inv…………..CT
:N:B
:Craniopharyngioma
:Cp
Increased ICP
Panhypopituitarism
The best…..MRI
x-ray……calcification
TTT…..surgery
:Infratentorial tumours
Astrocyroma:…….most common
Medulloblastoma…….midline infratentorial
:Pediatrics toxicology
:Lead poisoning
:Cp
TTT……chelation
:Acetaminophen
RUQ pain
:Labs
TTT:……. N- acetylcystine
How is it given……..iv
First symptom……hyperventilation
:Cp
Vomiting
TINNITUS
:ABG
Then…..metabolic acidosis
TTT…….alkalinization of urine
:Carbon monoxide
Complications…..rhabdomyelosis……renal failure
TTT……..high flow O2
Organophosphorus:……….PESTICIDES
Diarrhea
Urination
Bradycardia
Miosis
imp
Atropine…….ttt the symptoms
:Iron
:Cp
Liver dysfunction
:Inv
TTT……deferoxamine
:TCA
WHITE TABLETS