Professional Documents
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AGE ACTIVITY
CHECKUP
•Physical examination
•Examination by MO at 1 month old
0-6 month Monthly •Evaluation of development and growth
•Immunisation
•Breast Feeding counselling
•Physical examination
•Dental check up 0-9month
•Evaluation of development and growth
6-12 month 2 monthly
•Immunisation
•Breast Feeding and weaning counselling
•Physical examination
•Examination by Mo at 18month
•Dental check up 10-23month
•Evaluation of development and growth
1-2years 3 monthly
•M-chart
•Additional immunisation
•Diet counselling
•Physical examination by Mo at 2-4 years
•Visual Check up
•Dental check up 2-4 years
2-4 years 6monthly •Evaluation of development and growth
•M-chart
•Diet counselling
•Physical examination
5-6 years once yearly •Evaluation of development and growth
•Diet counselling
• Head circumference:
– Average : 35cm at birth
– Increases 12cm for the first year (6cm in 1st three
months, 3cm in 2nd three months and 3cm in last
three months )
How to interpret a growth chart?
• Obtain accurate measurement
• Select appropriate growth chart
– Birth up to 2 years of age
– Aged 2 through 19 years
• Record data
– Patient’s name
– Date of birth
– Birth weight and length
• Calculate BMI when a child is aged 2 to 20 years
old
• Plot measurements
– The WHO growth standard charts use the 2nd and the
98th percentiles as the outer most percentile cutoff
values indicating abnormal growth
– The CDC growth reference charts use the 5th and 95th
percentile as the outer most percentile cutoff values
indicating abnormal growth
Developmental milestones
• Development can be monitored by documenting
achievement of age-appropriate milestones for
intellectual, motor and social skills.
• Early identification of developmental delays allows
timely implementation of appropriate interventions.
• There are 4 fields of developmental skills to consider
whenever a young child is seen:
Gross motor
Vision and fine motor
Hearing, speech and language
Social, emotional and behavioral
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Gross motor
Vision
Social
Language
Gross motor
Fine Motor
Hearing
Gross motor
Fine Motor
Social
Hearing
Language
Umur 9 Bulan
Gross motor
Fine motor
Social
Language
Fine motor
Gross motor
Fine motor
Language
Social
Gross motor
IMMUNIZATION FOR CHILDREN
BY AGE
Immunisations
• Immunity – Ability of the body to fight infection
• Immunity can be obtained:
Active – Antibodies production from disease or
vaccine.
Passive – Antibodies obtained from transfusion eg:
from mother to baby or from infusion of
immunoglobulin.
• Immunization – method of protecting children in a
safe, effective and simple method by vaccination, thus
producing antibodies against diseases.
• Vaccine can be weakened or dead virus/bacteria given
by injection or by orally.
Classification of vaccines
Live Attenuated Inactivated/ whole
killed
BCG, MMR Poliomyelitis (IPV)
Varicella, Rotavirus, oral Diphtheria
typhoid vaccine Pertussis
Tetanus
Hepatitis A, B
Hib
Some influenza vaccines
(H1N1)
Rotavirus
At least 4-week-gap before the next dose of live vaccine given
Herd Immunity
• Aim of vaccine– to
protect children who
have taken the vaccine.
• These group of children
rarely have the disease.
• Provide ‘indirect’
protection to children
who have yet to be
vaccinated.
Primary Oral Healthcare
The EARLY CHILDHOOD ORAL HEALTHCARE
PROGRAMME is an extension of the antenatal
programme and targets postnatal mothers and
parents/carers of children aged 4 years and below who
are seen under the Child Health Services of the
Ministry of Health (MOH). The main objective of the
early childhood oral healthcare programme is to
promote and maintain good oral health of toddlers
towards achieving their optimum growth and
development.
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Causes to consider
• Inadequate caloric intake/retention – Diabetes mellitus
(most common) – Hyperthyroidism
– Inadequate amount of food provided • Other medical causes
– Breastfeeding issues – Genetic disorders
– Physical reasons baby can’t feed well (e.g. – Inborn errors of metabolism
cleft palate)
• Psychosocial factors
– Persistent vomiting
– Parental depression
– Chronic disease causing anorexia
– Coercive feeding (feeding becomes a
• Inadequate absorption battle)
– Coeliac disease – Distractions at meal times
– Chronic liver disease – Poverty (the single biggest risk factor in
– Pancreatic insufficiency (e.g. CF) both developed and developing countries)
– Chronic diarrhoea (e.g. protein-losing – Behavioural disorders
enteropathy) – Poor social support
• Excessive caloric utilisation – Neglect and abuse (risk of child abuse is
– UTIs 4x higher in children with FTT)
– Chronic respiratory disease (e.g. severe
asthma, bronchiectasis)
– Congenital heart disease
History
• Antenatal/birth/postnatal history—including growth parameters
• Feeding history (most important aspect)
– Infants—BF/attachment, formula feeding, timing, volumes (e.g. weigh
infant before and after, mother expressing and measuring breast milk),
vomiting?, solids introduction
– Toddlers—types and amounts of foods/ liquids, especially iron
containing foods, food intake inside and outside home, mealtime
battles, distractions, food refusal, milk volume, parental food attitudes
• Medical history
• Developmental history (e.g. regression, syndromes)
• Family history (e.g. mid-parental height, parents’or siblings’
childhood weight gain)
• Social history (e.g. finance, supports)
• For a girl, midparental height is calculated as
follows:
(Paternal height (cm)-13) + Maternal height (cm)
2
• For a boy, midparental height is calculated as
follows:
Paternal height (cm) + (Maternal height (cm) + 13)
2
Examination
• Growth charts
• General appearance (does the child look sick/ irritable/lethargic? dehydration?
loss of subcutaneous fat? pallor? inappropriate bruising or affect)
• Observation of infant feeding and child–parent interaction (a home visit, or
assessment by a lactation consultant/early childhood nurse may be useful here)
• Dysmorphic features
• Developmental assessment
• Jaundice/bruising/scratches
• Skin, hair and nails
• ENT
• Cardiac/respiratory
• Abdomen (e.g. distention, organomegaly)
• Endocrine (e.g. goitre, urinalysis, finger prick glucose)
• Lymphadenopathy
• Clinical signs of malnutrition
• Observation of feeding
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Clinical signs of malnutrition
Angular stomatitis
Sparse hair
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Investigations
• In a healthy infant with no concerns found on history and examination, no
investigations are required, and reassuring the family and further monitoring is
appropriate.
• If concerns are found, targeted investigation for these should be done. Simple first
line investigations may include:
• FBC – IDA, megaloblastic anemia
• RFT – signs of dehydration
• LFT – chronic liver failure [hypoalbuminemia]
• FERRITIN – to confirm IDA
• ESR/CRP – infection / inflammation
• TFT – thyroid level
• Depends on the clinical suspicion
• Barium swallowing in GERD
• Karyotyping in syndrome
Failure to thrive (FTT)
• defined
• as children whose weight <3rd percentile on ≥
2 occasions,
• or whose weight crosses two centile line over
time.
Short stature
• Short stature is considered to be below the 3rd percentile.
In general, it is important to differentiate between normal
physiological variants of growth and pathological causes.
• Causes
• Familial short stature—this follows the family trend of a
genetically small family.
• Constitutional delay in maturation—a common and normal
variant in which the growth spurt is later than average.
Bone age is delayed.
• Pathological causes—of the many causes, some are rare
but serious conditions, such as coeliac disease, Crohn
disease and chronic kidney failure. These may present with
slow growth as the only abnormal sign.
Stunting/short stature
• Linear growth faltering
Example
• The growth pattern of a child with low weight,
length, and head circumference is commonly
associated with familial short stature. These
children are genetically normal but are smaller
than most children.
• A child who, by age, is preadolescent or
adolescent and who starts puberty later than
others may have the normal variant called
constitutional short stature; careful examination
for abnormalities of pubertal development
should be done, although most are normal.
Tall stature
• Tall stature is considered to be above the 97th percentile. It is not a
common presenting childhood problem in general practice.
• Causes
• familial (predicted final height should roughly match mid-parental
height)
• precocious puberty
• growth hormone excess (pituitary gigantism)
• hyperthyroidism
• syndromic: Marfan, Klinefelter, homocystinuria
• Management
• As tall stature is generally socially acceptable, reassurance,
counselling and education may alleviate the family’s concerns. If
treatment is considered appropriate, the management should be
undertaken by endocrinologists.
Tall stature
• Hgt > 97th centile
• Less common
Management
• Intervention need to be taken as soon as FTT
detected
• Challenging and complicated
• Multidisciplinary approach
• Aims:
To provide sufficient nutrition
To treat underlying condition
To provide long-term social support
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Organic Failure to Thrive
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Non-organic Failure to Thrive
Nursery placement
Clinical psychologist & social
- Alleviate stress at home
services
- Assist feeding
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