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:
| Domain | Milestones to Ask |
|---|
| Gross motor | Head control, sitting, standing, walking |
| Fine motor / Adaptive | Pincer grasp, drawing, writing |
| Language / Speech | Cooing, babbling, words, sentences |
| Social / Personal | Smiling, 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:
| Reason | Explanation |
|---|
| Narrows differential diagnosis | Absence 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 investigations | No contact with TB-positive person lowers pre-test probability of TB |
| Legal and documentation value | Proves the clinician actively asked and excluded |
| Monitors disease progression | A symptom absent today may appear later - baseline is documented |
| Avoids unnecessary treatment | No penicillin allergy history confirms safe prescription |
| Aids in pattern recognition | In 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:
| Meal | Food items | Approximate 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
| Age | Milestone |
|---|
| Birth | Flexion posture; head lag when pulled to sit |
| 1 month | Lifts chin off table in prone |
| 3 months | Head held in same plane as body when pulled to sit; raises chest in prone |
| 6 months | No head lag; sits with support; rolls over |
| 9 months | Sits without support (steady); creeps; pulls to stand |
| 12 months | Stands alone; walks with one hand held; cruising |
| 15 months | Walks independently (broad-based gait) |
| 18 months | Runs (stiffly); walks upstairs with hand held; throws ball |
| 24 months | Runs well; walks up and down stairs (both feet on each step); kicks ball |
Domain 2: Fine Motor / Adaptive
| Age | Milestone |
|---|
| 1 month | Hands fisted; grasp reflex present |
| 3 months | Hands unfisted; holds rattle briefly |
| 6 months | Palmar grasp; transfers objects hand to hand; reaches for objects |
| 9 months | Inferior pincer grasp (thumb + ring finger); bangs two cubes |
| 12 months | Superior pincer grasp (thumb + index finger tip); releases objects voluntarily |
| 15 months | Builds tower of 2 cubes; scribbles |
| 18 months | Builds tower of 3-4 cubes; turns pages (several at a time) |
| 24 months | Builds tower of 6-7 cubes; turns single pages; imitates vertical line |
Domain 3: Language / Speech
| Age | Milestone |
|---|
| 1 month | Startles to sound; cries |
| 2 months | Social smile (key milestone) |
| 3 months | Cooing (vowel sounds - "aah", "ooh") |
| 6 months | Babbling (consonant sounds - "baba", "dada" - non-specific) |
| 9 months | "Mama/dada" non-specifically; understands "no" |
| 12 months | 1-2 words with meaning (e.g., "mama" specifically); jargon |
| 15 months | 4-6 meaningful words |
| 18 months | 7-20 words; points to body parts (2-3); vocabulary spurt begins |
| 24 months | 50+ words; 2-word phrases ("mama come"); 50% speech intelligible to strangers |
Domain 4: Social / Personal
| Age | Milestone |
|---|
| 1 month | Regards face; quietens to voice |
| 2 months | Social smile (responds to smile) |
| 3 months | Recognises mother |
| 6 months | Laughs aloud; enjoys mirror image |
| 9 months | Stranger anxiety (key milestone); waves bye-bye; plays peek-a-boo |
| 12 months | Comes when called; cooperates with dressing |
| 15 months | Drinks from cup; imitates household activities |
| 18 months | Uses spoon; takes off shoes; tantrums begin |
| 24 months | Parallel 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
- Similar illness in siblings, parents, or other relatives
- Consanguinity - are parents related (first cousins, second cousins, etc.)?
- Hereditary / genetic diseases - thalassaemia, sickle cell, haemophilia, metabolic disorders
- Deaths in siblings - age at death, cause; any unexplained infant deaths (may suggest metabolic disease)
- Parental health - chronic illness in mother / father
- Infectious disease contacts - active TB in household, COVID, hepatitis B carrier
- Allergic conditions in family - asthma, eczema, allergic rhinitis (atopic tendency)
- Mental health disorders - intellectual disability, autism spectrum in family
- Number of siblings - birth order of child
- Pedigree / family tree - three-generation pedigree if hereditary disease is suspected
Socioeconomic History
- Father's occupation and education level
- Mother's occupation and education level
- Monthly family income (for socioeconomic classification)
- Type of house - pucca (permanent) / semi-pucca / kutcha (temporary)
- Number of rooms and persons per room (crowding index)
- Water supply - municipal piped / bore well / open well / tanker
- Sanitation - flush toilet / pit latrine / open defecation
- Electricity availability
- Cooking fuel - LPG / firewood / kerosene (indoor air pollution)
- Pets at home (zoonoses, allergy triggers)
- Area of residence - urban / semi-urban / rural / tribal / slum
- 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):
| Education | Score |
|---|
| Profession / Honours | 7 |
| Graduate / Postgraduate | 6 |
| Intermediate / Post-high school diploma | 5 |
| High school certificate | 4 |
| Middle school | 3 |
| Primary school | 2 |
| Illiterate | 1 |
Occupation score (Father):
| Occupation | Score |
|---|
| Professionals (doctor, engineer, etc.) | 10 |
| Semi-professional (teacher, nurse, etc.) | 6 |
| Clerical / shop owner / farmer | 5 |
| Skilled worker | 4 |
| Semi-skilled worker | 3 |
| Unskilled worker | 2 |
| Unemployed | 1 |
Monthly income score: Updated periodically for inflation (scored 1-12).
Total Score interpretation:
| Total Score | Class |
|---|
| 26-29 | Upper (Class I) |
| 16-25 | Upper middle (Class II) |
| 11-15 | Lower middle (Class III) |
| 5-10 | Upper lower (Class IV) |
| < 5 | Lower (Class V) |
B. BG Prasad Classification (Modified, used for both urban and rural)
Based on per capita monthly income (updated for CPI annually):
| Class | Description |
|---|
| Class I | Upper |
| Class II | Upper middle |
| Class III | Middle |
| Class IV | Lower middle |
| Class V | Lower |
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)
| Relationship | Degree | Coefficient of Relationship (r) | Inbreeding coefficient of offspring (F) |
|---|
| Parent - child | 1st degree | 1/2 (50%) | - |
| Siblings (full) | 1st degree | 1/2 (50%) | - |
| Uncle/aunt - nephew/niece | 2nd degree | 1/4 (25%) | 1/8 |
| First cousins | 3rd degree | 1/8 (12.5%) | 1/16 = 0.0625 |
| First cousins once removed | 4th degree | 1/16 (6.25%) | 1/32 |
| Second cousins | 4th degree | 1/16 (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
| Symbol | Meaning |
|---|
| ○ (circle) | Female |
| □ (square) | Male |
| ◇ (diamond) | Sex unspecified / unknown |
| ● (filled circle) | Affected female |
| ■ (filled square) | Affected male |
| ○ with dot inside | Carrier female (X-linked) |
| □ with dot inside | Carrier male |
| ○ or □ with diagonal line through | Deceased individual |
| = (horizontal line between ○ and □) | Mating / marriage |
| Vertical line downward from couple | Offspring line |
| Horizontal sibship line | Siblings |
| Double horizontal line between couple | Consanguineous union |
| Arrow pointing to individual | Proband (index case) |
| P or arrow | Proband |
| Dashed outline | Adopted individual |
| Twins - branching from one point | Twins (monozygotic = connected; dizygotic = separate lines) |
| ○ or □ with small filled area | Obligate 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:
- Autosomal Dominant: Every generation affected; both sexes equally; affected parent to affected child (vertical transmission)
- Autosomal Recessive: Skips generations; both sexes; consanguinity often present; horizontal pattern (siblings affected, parents normal)
- X-linked Recessive: Only males affected; carrier females; no male-to-male transmission; maternal uncles may be affected
- X-linked Dominant: Both sexes affected; affected father passes to ALL daughters, no sons; more females than males
- 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)
| Examples | Gene / Feature |
|---|
| Achondroplasia | FGFR3 mutation; short-limb dwarfism |
| Neurofibromatosis type 1 | NF1 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
| Examples | Gene / Feature |
|---|
| Cystic fibrosis | CFTR 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)
| Examples | Gene / Feature |
|---|
| Haemophilia A | Factor 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
| Examples | Gene / Feature |
|---|
| Vitamin D-resistant rickets (Hypophosphataemia) | PHEX gene; phosphate wasting rickets |
| Rett syndrome | MECP2 gene; progressive encephalopathy in females |
5. Y-linked (Holandric) Inheritance
- Mechanism: Gene on Y chromosome; passed from father to ALL sons, never to daughters
| Examples | Gene / Feature |
|---|
| Azoospermia factor (AZF) | AZF region deletions; male infertility |
| SRY gene mutations | Sex-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)
| Examples | Gene / Feature |
|---|
| MELAS syndrome | MT-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
| Examples | Gene / Feature |
|---|
| ABO blood group | IA 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
| Pattern | Generations | Sex bias | Carrier | Example |
|---|
| AD | Every generation | None | No | Achondroplasia |
| AR | Skips | None | Yes | CF, PKU |
| X-linked recessive | Skips | Males affected | Carrier females | Haemophilia, DMD |
| X-linked dominant | Every generation | Females > males | No | X-linked rickets |
| Y-linked | Every generation | Only males | No | AZF, SRY |
| Mitochondrial | Every generation | None | No | MELAS, LHON |
| Codominant | - | None | No | ABO, HbAS |
All 10 topics are fully covered. Let me know if you want any topic expanded further or formatted as notes for printing.