Pediatrics
Pediatrics
Pediatrics
Patient details
Name, age, sex, address :
Informant (reliable/not) :
Date of admission :
2. Presenting complaint
(In chronological order, in patient’s own words)
3. History of presenting complaint
Onset (sudden, gradual, insidious)
Progression (increasing, decreasing, static)
Quality
Relieving, aggravating factors, radiation
Severity
Timing
Associated symptoms
Diurnal variations
Present status
Negative status
Note: In a CP Child Past History and Birth History can be combined
4. Past medical history
H/o similar illness (if yes, describe)
H/o previous hospitalization
H/o any significant illness (asthma, TB, epilepsy, jaundice, diarrhea, heart disease)
H/o vaccine preventable diseases (TB, mumps, measles, hepatitis, whooping cough)
H/o any surgeries
H/o any drug intake
5. Birth history
(A) Antenatal history
Age of mother at conception
Age of father at conception
Birth order
Consanguineous / non-consanguineous marriage
H/o any abortions
d) Language milestone :
Turn head to sound 1 month
Cooing (vowels) 3 months
Laugh out loud 4 months
Monosyllables (ba,da,pa) 6 months
Bisyllables (mama,papa) 9 months
2-3 words with meaning 12 months
Vocabulary of 10-15 words 18 months
Vocabulary of 100 words, 2-3 word sentence 2 years
Asks questions, knows full name and gender 3 years
Coherent account of events, experiences, simple stories 4 years
Asks meaning of words 5 years
e) Vision :
Follow upto 45 0 at the birth
Visual fixation; follow upto 90 0 1 month
Follow upto 180 0 3 months
Adjusts position to follow objects of interest 6 months
Fixation on rapidly moving objects 1 year
f) Hearing :
Respond to sound by ery, blink, etc…. at birth
Turns head toward source of sound 3-4 months
Directly looks at the source of sound 10 months
7) Dietetic history
When put to breast?
Exclusive breast feeding upto _______ months, and breast feeding continued upto
_____ months / year.
When Complementary feeding was started? With what?
When was solid food started?
When started sharing family diet?
The child is getting ______ kCal and _____ g protein respectively against the ICMR 2010
recommendations of _______ & _______ for age.
Hence, calorie gap = _______, protein gap = ______.
Diet rich in fruits, green leafy vegetables, non- veg diets, vitamins & minerals.
Any dietary modifications due to illness?
Dietary modifications you have advised.
INDEX
Item Qty. K cal Protein (g) Item Qty. K cal Protein (g)
Groundnut 10 20 1 Beef
8) Immunization history
Whether immunization is adequate for age? If not, reason?
Bcq scar present
Last vaccine taken on?
Any optional vaccine taken? If so, mention details?
Booster doses of the vaccine taken?
Advice given to the parent, if any?
18 months ( 1 1/2 year ) DPT 1stbooster, OPV 1st booster, MMR, Measles-2 ( if MMR
not given ), Vit-A (Vit-A doses given every 6 months from
then till 5 years - total 9 doses)
**PV = DPT + Hi b
9) Family history
Draw Pedigree (3 gen)
Mother - age, healthy/not
Father - age, healthy/not
Consanguineous/non consanguineous marriage? If yes, then degree?
Siblings - age, health/not
Order of birth
Any significant illnesses in the family? (TB, asthma, epilepsy, jaundice, heart disease,
DM, HTN)
Any congenital anomalies, abortion, still birth?
10) Socioeconomic history
APL / BPL family
Joint / Nuclear family
Education ,Occupation of parents
Family income
o Housing ;
o Roof thatched/tiled/terrace (RC)
o Floor
o Ventilation
o No. of rooms
o Any overcrowding?
Sanitation
Water supply? Distance from toilet?
Drinking boiled /cooled water or not?
Environment and surroundings?
Any risk of passive smoking in the family?
Any financial supports? (RSBY, JSY, old age pension, pension for disabled)
General examination
During examination, the child is
Conscious /cooperative (mental attitude)
Active /playful/comfortable /restless/bedridden (physical attitude
Vitals (given below)
Pallor, icterus, cyanosis, clubbing, lymphadenopathy, edema
Skin, hair, nails?
Other findings if any (mantoux, IV line, nasogastric tube, catheter etc…)
Vitals:
(1) Pulse rate, rhythm, volume, character, RF delay, vessel wall thickening, all peripheral
pulsation.
Pulse rate in : NB-140/-, upto 1 year -120/-, upto 5 year-100/-, upto 10 year -90/-, >10 year – 80/-
Tachycardia : >200 in NB, >150 in infants, >120 in older children.
Cuff 2/3 rd size of arm, length; 80 % of arm circumferences, breadth; 40 % of arm circumference.
Doppler method is more accurate.
Flush method is infants (tie cuff-raise limb-massage to branch-fully inflate cuff-gradually deflate-
point of sudden flushing of distal limb
= (mean arterial pressure) ( mean BP =diastolic BP + 1/3 PP )
LL BP > UL BP (app. 10 mm of hg).
Normal BP is defined as SBP & DBP < 90 th percentile for that age & sex
HTN is average SBP or DBP> 95 th percentile for that age & sex or at least 3 occasions.
NB-60/40 mm Hg; upto 2 years-70/50 mm Hg; upto 5 years-90/50 mm of hg.
Low set ears in: trisomy 13,18,21 (patau, edward’s, turner ), down’s syndrome, cri du chat syndrome,
noonan syndrome, digeorge syndrome, apert’s syndrome, potter’s syndrome.
Method to identify: make the patient stand straight and an imaginary line is drawn from outer
canthus of eye straight back to occiput, thus parallel to the floor (normally 1/3 rd of the eye comes
above this line. When <20 % comes above this line, it is a low set ear).
Nose: DNS , polyp ?
Oral cavity: hygiene, dentition, palate, tonsils, lips. Any caries, glosittis,stomatitis.
Neck: LNs, short neck, low neckline, (below C5 spine, as in turner’s)
(normal neck:height = 1:13)
Chest: shape, wide nipples, other findings of rickets?
Limbs: UL pallor, clubbing; LL edema
Abdomen: distension, dilated veins?
External genitalia :
Spine: any deformities?
Skin: rashes, pyoderma, neurocutaneous markers, finding of PEM, others?
Nails: normal/not? Not; koilonychia, discolouration?
Anthropometry
1. Weight actual -----, expected ------, inference?
5 years 6x
1 S.D = 12.5 % of value
7 years 7x
10 years 10x
IAP classification of PEM IAP classification of PEM Welcome trust classification of PEM
Maximum circumference of head from the occipital protuberance to the supra orbital ridges
on the forehead is recorded by cross taping.
DINE’s Formula for H.C in 1st year of life
H.C = l/2 + 9.5 ± 2.5 cm (l = length of child in cm)
Age Normal H.C (cm) Age Rate of increase of H.C
At Birth 34-35 Birth – 3 mon 2 cm/ mon
2 mon 38
3 mon 40 3 – 6 mon 1 cm/ mon
4mon 41
6 mon 43 7 – 12 mon 0.5 cm/ mon
1 year 45
2 year 47 1 - 3 years 2 cm/ mon
3 year 49
4year 50 3 – 5 years 1 cm/ mon
5 year 51 1 S.D = 2.5 % of value
12 year 52 (1.25 cm approx.)
Microcephaly reduction in h.c by > 3 S.D from normal (or) less than 5 th percentile for
the age and sex.
(Down’s syndrome, Edward’s syndrome, IU infections –toxoplasmosis, rubella, fetal alcohol
syndrome, fetal hydantoin syndrome)
Macrocephaly increase in H.C by > 2 S.D from normal (or) H.C more than 95th
percentile for age.
(Hydrocephaly, rickets, achondroplasia, Noonan syndrome, hydrencephaly)
Other methods;
Shakir’s tape: plastic tape with coloured zone -->green, yellow, red
(green >13.5 cm, yellow - 12.5 to 13.5 cm, red < 12.5 cm.
Bangle test: if the bangle of inner diameter $ cm crosses the elbow, the child is
malnourished.
Quack-stick method: it consists of two set of marking - one indicating (Ht) and other
MUAC for the corresponding height. MUAC is measured and the stick is placed
behind the standing child. If the height is more than the expected height for
measured MUAC, the child is malnourished.
The distance between the tips of middle finger of both < 5 years A.S 2 cm lesser
arms when the arms are spread apart right angle to the than height
body.
5- 10 years A.S 1 cm lesser
The child is to be positioned to the wall as to measure
than height
the height.
A.S > height marsan’s syndrome, klinfelter’s 10 years A.S = height
syndrome, homocystinuria.
A.S < height achondroplasia , cretinism.
>10 years A.S 2 cm more
than the
height