Format of paediatrics history taking all sub headings in order

Here is the standard format for paediatric history taking, with all subheadings in order:

Paediatric History Taking - Format


1. Identifying Data / Demographic Details

  • Name
  • Age / Date of birth
  • Sex
  • Address
  • Religion / Ethnicity
  • Informant (mother, father, caregiver) and reliability

2. Chief Complaint (Presenting Complaint)

  • Main symptom(s) in the informant's own words
  • Duration

3. History of Present Illness (HPI)

  • Onset (sudden / gradual)
  • Duration
  • Character / nature of complaint
  • Severity
  • Progression (improving / worsening / static)
  • Aggravating and relieving factors
  • Associated symptoms
  • Previous similar episodes
  • Treatment received so far (prior to presentation)

4. Antenatal History (Maternal History)

  • Mother's age at delivery
  • Parity (G_P_L_A_)
  • Antenatal check-ups (regular / irregular)
  • Maternal illness during pregnancy (diabetes, hypertension, infections - TORCH, thyroid disease)
  • Medications during pregnancy (folic acid, iron, teratogens)
  • Radiation exposure
  • Alcohol, smoking, drug use
  • Blood group and Rh typing; Rh incompatibility
  • Ultrasonography findings (anomalies detected)
  • Fetal movements

5. Natal / Perinatal History (Birth History)

  • Place of delivery (hospital / home)
  • Mode of delivery (normal vaginal, LSCS, forceps, vacuum)
  • Gestation at birth (term / preterm / post-term)
  • Birth weight
  • Cry at birth (immediate / delayed / absent)
  • APGAR score (if known)
  • Complications at birth (birth asphyxia, birth trauma, cord around neck, meconium-stained liquor)
  • Resuscitation required (NICU admission)

6. Postnatal / Neonatal History

  • Neonatal period (first 28 days)
    • Jaundice (onset, severity, treatment - phototherapy / exchange transfusion)
    • Cyanosis, convulsions, apnoeic spells
    • Feeding difficulties in neonatal period
    • Infections (sepsis, meningitis, umbilical sepsis)
    • Congenital anomalies detected
  • Discharge from hospital (day of discharge, any concerns)

7. Feeding History

For infants:
  • Breastfeeding: exclusive / mixed; duration; technique; frequency
  • Time of introduction of top feeds / formula
  • Weaning / complementary feeding: age of introduction, types of food introduced
For older children:
  • Current diet (vegetarian / non-vegetarian)
  • Appetite (good / poor)
  • Dietary recall (24-hour recall)
  • Vitamin / iron / calcium supplementation

8. Developmental History

Assess across four domains:
DomainMilestones to Ask
Gross motorHead control, sitting, standing, walking
Fine motor / AdaptivePincer grasp, drawing, writing
Language / SpeechCooing, babbling, words, sentences
Social / PersonalSmiling, stranger anxiety, play behaviour
  • Age at which each milestone was achieved
  • Any regression of milestones
  • School performance (for school-age children)
  • Behavioural concerns

9. Immunisation History

  • Vaccines received as per national immunisation schedule (BCG, OPV, DPT/Pentavalent, Hepatitis B, Measles/MMR, Typhoid, etc.)
  • Age-appropriate or delayed
  • Adverse reactions to any vaccine
  • Recent vaccinations (relevant to current illness)

10. Past Medical History

  • Previous illnesses (hospitalizations, surgeries, procedures)
  • Previous similar episodes
  • Known chronic diseases (asthma, epilepsy, congenital heart disease, etc.)
  • Allergies (drugs, food, environmental) - nature of reaction
  • Previous blood transfusions

11. Family History

  • Similar illness in siblings or family members
  • Consanguinity (important in paediatrics)
  • Hereditary / genetic disorders in family
  • Parental age and health
  • Deaths in siblings (age, cause)
  • Tuberculosis or other infectious disease contacts at home

12. Socioeconomic and Environmental History

  • Father's and mother's occupation and education
  • Monthly income / socioeconomic status (Kuppuswamy / BG Prasad scale)
  • Type of house (pucca / semi-pucca / kutcha)
  • Crowding (number of persons per room)
  • Water supply (safe / unsafe)
  • Sanitation (latrine facility)
  • Pets at home

13. Personal History (for older children)

  • Sleep pattern
  • Bowel and bladder habits
  • Behavioural habits (thumb sucking, nail biting, breath-holding spells)
  • School attendance and performance
  • Recreational activities / hobbies

14. Review of Systems (Systemic Enquiry)

A brief screen of each system not already covered:
  • Respiratory, cardiovascular, gastrointestinal, genitourinary, CNS, musculoskeletal, skin, ENT, eyes

15. Summary Statement

A brief 2-3 sentence summary of the key positive and relevant negative findings from the history, leading logically into the examination.

Key points unique to paediatric history:
  • The informant is usually a parent/caregiver - always note who gave the history and assess reliability.
  • Antenatal, natal, and neonatal histories are mandatory in all paediatric cases.
  • Developmental history is a core component - not optional.
  • Feeding and immunisation histories are paediatric-specific essentials.
  • Socioeconomic and family history carry more weight than in adult medicine.Here are all 9 remaining topics covered in full:

2. Importance of Negative History

A negative history refers to the deliberate recording of symptoms or findings that are absent but clinically relevant to the case.

Why it matters:

ReasonExplanation
Narrows differential diagnosisAbsence of fever rules out infective causes; no rash rules out viral exanthems
Rules out serious conditions"No convulsions" in a febrile child rules out febrile seizures
Guides investigationsNo contact with TB-positive person lowers pre-test probability of TB
Legal and documentation valueProves the clinician actively asked and excluded
Monitors disease progressionA symptom absent today may appear later - baseline is documented
Avoids unnecessary treatmentNo penicillin allergy history confirms safe prescription
Aids in pattern recognitionIn paediatrics, absence of developmental regression helps exclude neurodegenerative conditions

Examples in paediatrics:

  • Child with cough: "No blood in sputum, no night sweats, no weight loss" - excludes TB
  • Child with fever: "No seizures, no neck stiffness, no photophobia" - excludes meningitis
  • Child with jaundice: "No pale stools, no dark urine" - helps distinguish haemolytic from obstructive jaundice
  • Child with wheeze: "No foreign body aspiration history" - excludes airway foreign body

3. How to Collect Diet History

Step 1 - Establish the child's age group first

Diet history method differs for:
  • < 6 months: breastfeeding / formula details
  • 6 months - 2 years: weaning / complementary feeding
  • > 2 years: regular family diet with 24-hour recall

Step 2 - For Infants (< 6 months)

Breastfeeding:
  • Exclusive breastfeeding or mixed feeding?
  • Frequency (on demand / timed) and duration of each feed
  • Latching technique - correct or not?
  • Night feeds present or not?
  • Any breast problems (engorgement, cracked nipple, mastitis)?
  • Maternal diet and medications
Formula / Top feeds:
  • Type of formula (brand, dilution - concentrated / correct / over-diluted?)
  • Volume per feed, number of feeds per day
  • Method of preparation and sterilisation of bottles
  • Introduction of cow's milk (premature introduction is a risk)

Step 3 - For Weaning Age (6 months - 2 years)

  • Age at which complementary foods were introduced (should be 6 months)
  • Type of foods introduced - cereals, pulses, vegetables, fruits, egg, meat
  • Consistency - pureed / mashed / lumpy / family foods
  • Frequency of complementary feeds per day
  • Continued breastfeeding alongside?
  • Intake of iron-rich foods (important for anaemia prevention)

Step 4 - For Children > 2 years (24-hour Dietary Recall)

Ask the caregiver to recall everything the child ate and drank in the past 24 hours:
MealFood itemsApproximate quantity
Early morning
Breakfast
Mid-morning snack
Lunch
Evening snack
Dinner
Night feeds / beverages
Then assess:
  • Caloric adequacy (RDA for age)
  • Protein intake (animal vs. plant sources)
  • Micronutrients - iron, calcium, Vitamin A, Vitamin D, iodine
  • Junk food / fast food frequency
  • Fruit and vegetable intake
  • Fluid intake (water, juices, carbonated drinks)

Step 5 - Additional Questions Always Ask

  • Appetite - good, poor, or selective?
  • Any food allergies or intolerances?
  • Vitamin / mineral supplements given?
  • Who feeds the child - self-feeding or fed by caregiver?
  • Any feeding difficulties (dysphagia, vomiting after feeds)?
  • Socioeconomic factors affecting food availability?

4. Developmental Milestones Till 2 Years - All Domains

Domain 1: Gross Motor

AgeMilestone
BirthFlexion posture; head lag when pulled to sit
1 monthLifts chin off table in prone
3 monthsHead held in same plane as body when pulled to sit; raises chest in prone
6 monthsNo head lag; sits with support; rolls over
9 monthsSits without support (steady); creeps; pulls to stand
12 monthsStands alone; walks with one hand held; cruising
15 monthsWalks independently (broad-based gait)
18 monthsRuns (stiffly); walks upstairs with hand held; throws ball
24 monthsRuns well; walks up and down stairs (both feet on each step); kicks ball

Domain 2: Fine Motor / Adaptive

AgeMilestone
1 monthHands fisted; grasp reflex present
3 monthsHands unfisted; holds rattle briefly
6 monthsPalmar grasp; transfers objects hand to hand; reaches for objects
9 monthsInferior pincer grasp (thumb + ring finger); bangs two cubes
12 monthsSuperior pincer grasp (thumb + index finger tip); releases objects voluntarily
15 monthsBuilds tower of 2 cubes; scribbles
18 monthsBuilds tower of 3-4 cubes; turns pages (several at a time)
24 monthsBuilds tower of 6-7 cubes; turns single pages; imitates vertical line

Domain 3: Language / Speech

AgeMilestone
1 monthStartles to sound; cries
2 monthsSocial smile (key milestone)
3 monthsCooing (vowel sounds - "aah", "ooh")
6 monthsBabbling (consonant sounds - "baba", "dada" - non-specific)
9 months"Mama/dada" non-specifically; understands "no"
12 months1-2 words with meaning (e.g., "mama" specifically); jargon
15 months4-6 meaningful words
18 months7-20 words; points to body parts (2-3); vocabulary spurt begins
24 months50+ words; 2-word phrases ("mama come"); 50% speech intelligible to strangers

Domain 4: Social / Personal

AgeMilestone
1 monthRegards face; quietens to voice
2 monthsSocial smile (responds to smile)
3 monthsRecognises mother
6 monthsLaughs aloud; enjoys mirror image
9 monthsStranger anxiety (key milestone); waves bye-bye; plays peek-a-boo
12 monthsComes when called; cooperates with dressing
15 monthsDrinks from cup; imitates household activities
18 monthsUses spoon; takes off shoes; tantrums begin
24 monthsParallel play; pulls on simple clothing; bowel control achieved

Key "Warning Flags" (Red Flags)

  • No social smile by 3 months
  • No babbling by 9 months
  • No words by 18 months
  • No 2-word phrases by 24 months
  • Any loss of previously acquired milestones at any age

5. Points to Ask in Family and Socioeconomic History

Family History

  1. Similar illness in siblings, parents, or other relatives
  2. Consanguinity - are parents related (first cousins, second cousins, etc.)?
  3. Hereditary / genetic diseases - thalassaemia, sickle cell, haemophilia, metabolic disorders
  4. Deaths in siblings - age at death, cause; any unexplained infant deaths (may suggest metabolic disease)
  5. Parental health - chronic illness in mother / father
  6. Infectious disease contacts - active TB in household, COVID, hepatitis B carrier
  7. Allergic conditions in family - asthma, eczema, allergic rhinitis (atopic tendency)
  8. Mental health disorders - intellectual disability, autism spectrum in family
  9. Number of siblings - birth order of child
  10. Pedigree / family tree - three-generation pedigree if hereditary disease is suspected

Socioeconomic History

  1. Father's occupation and education level
  2. Mother's occupation and education level
  3. Monthly family income (for socioeconomic classification)
  4. Type of house - pucca (permanent) / semi-pucca / kutcha (temporary)
  5. Number of rooms and persons per room (crowding index)
  6. Water supply - municipal piped / bore well / open well / tanker
  7. Sanitation - flush toilet / pit latrine / open defecation
  8. Electricity availability
  9. Cooking fuel - LPG / firewood / kerosene (indoor air pollution)
  10. Pets at home (zoonoses, allergy triggers)
  11. Area of residence - urban / semi-urban / rural / tribal / slum
  12. Literacy of primary caregiver (impacts compliance with treatment)

6. Socioeconomic Classification

A. Kuppuswamy Scale (Urban - most widely used in India)

Based on three parameters: Education + Occupation of father + Monthly family income
Education score (Father):
EducationScore
Profession / Honours7
Graduate / Postgraduate6
Intermediate / Post-high school diploma5
High school certificate4
Middle school3
Primary school2
Illiterate1
Occupation score (Father):
OccupationScore
Professionals (doctor, engineer, etc.)10
Semi-professional (teacher, nurse, etc.)6
Clerical / shop owner / farmer5
Skilled worker4
Semi-skilled worker3
Unskilled worker2
Unemployed1
Monthly income score: Updated periodically for inflation (scored 1-12).
Total Score interpretation:
Total ScoreClass
26-29Upper (Class I)
16-25Upper middle (Class II)
11-15Lower middle (Class III)
5-10Upper lower (Class IV)
< 5Lower (Class V)

B. BG Prasad Classification (Modified, used for both urban and rural)

Based on per capita monthly income (updated for CPI annually):
ClassDescription
Class IUpper
Class IIUpper middle
Class IIIMiddle
Class IVLower middle
Class VLower

C. Pareek Scale (Rural areas)

Used in rural India - based on caste, land holding, housing, farm power, material possessions, and education.

7. Consanguinity Degrees

Consanguinity = marriage between biological relatives sharing at least one common ancestor.

Coefficient of Relationship (r) / Coefficient of Inbreeding (F)

RelationshipDegreeCoefficient of Relationship (r)Inbreeding coefficient of offspring (F)
Parent - child1st degree1/2 (50%)-
Siblings (full)1st degree1/2 (50%)-
Uncle/aunt - nephew/niece2nd degree1/4 (25%)1/8
First cousins3rd degree1/8 (12.5%)1/16 = 0.0625
First cousins once removed4th degree1/16 (6.25%)1/32
Second cousins4th degree1/16 (6.25%)1/64
Double first cousins-1/4 (25%)1/8

Clinical relevance in paediatrics:

  • First cousin marriage (most common form in India, Middle East) raises risk of autosomal recessive diseases significantly
  • The closer the consanguinity, the higher the inbreeding coefficient
  • Always ask: "Are you and your spouse related to each other?" and if yes, "How are you related?"
  • Important for diseases like: thalassaemia, sickle cell, G6PD deficiency, metabolic disorders, congenital anomalies

8. Family Pedigree Chart - Symbols and Interpretation

Standard Symbols

SymbolMeaning
○ (circle)Female
□ (square)Male
◇ (diamond)Sex unspecified / unknown
● (filled circle)Affected female
■ (filled square)Affected male
○ with dot insideCarrier female (X-linked)
□ with dot insideCarrier male
○ or □ with diagonal line throughDeceased individual
= (horizontal line between ○ and □)Mating / marriage
Vertical line downward from coupleOffspring line
Horizontal sibship lineSiblings
Double horizontal line between coupleConsanguineous union
Arrow pointing to individualProband (index case)
P or arrowProband
Dashed outlineAdopted individual
Twins - branching from one pointTwins (monozygotic = connected; dizygotic = separate lines)
○ or □ with small filled areaObligate carrier

Generations:

  • Labelled with Roman numerals (I, II, III...) from top to bottom
  • Individuals within a generation labelled 1, 2, 3... from left to right
  • Proband is identified with an arrow

How to Interpret a Pedigree:

  1. Autosomal Dominant: Every generation affected; both sexes equally; affected parent to affected child (vertical transmission)
  2. Autosomal Recessive: Skips generations; both sexes; consanguinity often present; horizontal pattern (siblings affected, parents normal)
  3. X-linked Recessive: Only males affected; carrier females; no male-to-male transmission; maternal uncles may be affected
  4. X-linked Dominant: Both sexes affected; affected father passes to ALL daughters, no sons; more females than males
  5. Mitochondrial: Transmitted only through mother; all children of affected mother are affected; father cannot pass it on

9. Tuberculosis Contact History - Points to Ask

When TB is suspected in a child, a thorough contact history is mandatory because most childhood TB is primary infection from an adult source case.

Points to Ask:

1. Identify the contact:
  • Is there any family member / household contact with TB?
  • Any visitor who stays frequently (domestic worker, relative)?
  • Any contact at school, crèche, or neighbourhood?
2. Type of TB in contact:
  • Pulmonary TB (most infectious) or extrapulmonary?
  • Is it sputum smear positive (highly infectious) or smear negative?
  • Is it drug-resistant TB (MDR/XDR)?
3. Duration and proximity of contact:
  • How long has the child been in contact?
  • Is the contact a household / close contact or casual contact?
  • Does the child share the same room / bed with the contact?
4. Treatment status of contact:
  • Is the contact on anti-TB treatment (ATT)?
  • For how long have they been on treatment?
  • Are they adherent to treatment?
  • Have they been declared cured or still under treatment?
5. Child's own TB workup:
  • Previous TB infection or treatment in the child
  • BCG vaccination status (scar present?)
  • Previous Mantoux / TST / IGRA test results
  • Previous chest X-ray done?
6. Symptoms in the child:
  • Prolonged fever (> 2 weeks)
  • Weight loss / failure to thrive
  • Cough > 2 weeks
  • Night sweats
  • Lymph node enlargement
  • Loss of appetite
7. HIV status:
  • Child's HIV status (HIV increases TB risk significantly)
  • Maternal HIV status
Note: Any child < 5 years with household TB contact should receive isoniazid preventive therapy (IPT) regardless of Mantoux result, after ruling out active TB.

10. Types of Inheritance Patterns - With 2 Examples Each

1. Autosomal Dominant (AD)

  • Mechanism: One mutated copy of gene on autosome is sufficient to cause disease
  • Pedigree pattern: Every generation affected; male = female; 50% risk to offspring
  • No carrier state (heterozygote is affected)
ExamplesGene / Feature
AchondroplasiaFGFR3 mutation; short-limb dwarfism
Neurofibromatosis type 1NF1 gene; cafe-au-lait spots, neurofibromas

2. Autosomal Recessive (AR)

  • Mechanism: Both copies of gene must be mutated to cause disease
  • Pedigree pattern: Skips generations; horizontal pattern; consanguinity common; 25% risk if both parents carriers
  • Carrier state present
ExamplesGene / Feature
Cystic fibrosisCFTR gene; chronic lung disease, malabsorption
Phenylketonuria (PKU)PAH gene; intellectual disability if untreated

3. X-linked Recessive (XLR)

  • Mechanism: Mutated gene on X chromosome; females are carriers (protected by second X); males are affected
  • Pedigree: Males affected; no male-to-male transmission; carrier females
  • Key rule: Affected father cannot pass to son; passes to all daughters (who become carriers)
ExamplesGene / Feature
Haemophilia AFactor VIII gene (F8); bleeding disorder
Duchenne Muscular Dystrophy (DMD)Dystrophin gene; progressive muscle weakness

4. X-linked Dominant (XLD)

  • Mechanism: One mutated copy on X chromosome sufficient; both sexes affected but females milder (due to lyonisation)
  • Pedigree: Both sexes; affected father passes to ALL daughters but NO sons
ExamplesGene / Feature
Vitamin D-resistant rickets (Hypophosphataemia)PHEX gene; phosphate wasting rickets
Rett syndromeMECP2 gene; progressive encephalopathy in females

5. Y-linked (Holandric) Inheritance

  • Mechanism: Gene on Y chromosome; passed from father to ALL sons, never to daughters
ExamplesGene / Feature
Azoospermia factor (AZF)AZF region deletions; male infertility
SRY gene mutationsSex-determining region; 46,XY disorders of sex development

6. Mitochondrial Inheritance

  • Mechanism: Mitochondrial DNA (mtDNA) mutations; inherited exclusively through mother; heteroplasmy may cause variable severity
  • Pedigree: All children of affected mother are affected; father cannot transmit; affects organs with high energy needs (brain, muscle, heart)
ExamplesGene / Feature
MELAS syndromeMT-TL1 gene; mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes
Leber's Hereditary Optic Neuropathy (LHON)MT-ND genes; painless bilateral visual loss in young males

7. Codominance

  • Mechanism: Both alleles expressed simultaneously in heterozygote
ExamplesGene / Feature
ABO blood groupIA and IB alleles both expressed in AB blood group
Sickle cell trait (HbAS)Both HbA and HbS expressed; not as severe as HbSS

Quick Summary Table

PatternGenerationsSex biasCarrierExample
ADEvery generationNoneNoAchondroplasia
ARSkipsNoneYesCF, PKU
X-linked recessiveSkipsMales affectedCarrier femalesHaemophilia, DMD
X-linked dominantEvery generationFemales > malesNoX-linked rickets
Y-linkedEvery generationOnly malesNoAZF, SRY
MitochondrialEvery generationNoneNoMELAS, LHON
Codominant-NoneNoABO, HbAS

All 10 topics are fully covered. Let me know if you want any topic expanded further or formatted as notes for printing.
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