2. Today
• Early problems of 25 weeks gestation baby
• Review in out patient department at one (1) year age
3. Case study
• FK, 12 months (CA: 8 months) old boy came for paediatric follow up
• He is an extreme premature baby, born at 24 weeks gestational age, FK’s mother, 46
years old, with k/c/o HPT
• Formula milk + breastfeeding (mother has not enough milk). Weaning at 6 months
old
• Birth history
• 24 weeks into pregnancy
• Mother’s blood pressure went very high and emergency lower segment caesarean
section was arranged.
• transverse lies,
• After delivery
• weight 795g
• Child admitted to NICU for 4 months
• Immunisation up to date
• Development at one year of age
• Gross Motor: sits straight without support
• Fine Motor and Vision: transfers between hands
• Speech and Language: uses finger to point at things. Peek-a-boo
• Social / Personal: strangers anxiety
5. 1 year follow up
• Major goals
• Examine the infant's motor, intellectual, and behavioural
development
• Provide an ongoing assessment of growth
• Growth rates and Head growth
• Evaluate the adequacy of nutrition
• Proper feeding and weaning
• Deliver preventive care
• Immunisation
• Follow-up on congenital disease
• Check whether disease is worsening or any new complication arises
• Referral to appropriate professional; eyes to ophthalmologist,
• Adjust treatment to suit patient and ensure compliance
6. Summary
• There are a lot of premature complications.
• Try to prolong pregnancy until at term
• Holistic approach and MDT is required
extremely preterm (<28 weeks)
very preterm (28 to <32 weeks)
moderate to late preterm (32 to <37 weeks).
Corrected age
• Low birth weight LBW <2,500 g
• Very low birth weight VLBW <1,500 g
• Extremely low birth weight ELBW <1,000 g
Growth rates to determine growth failure which maybe due to nutritional deprivation caused by underlying disease eg. chronic lung disease, congenital heart disease extreme prem babies take 2 years to catch up to peer’s rate of growth or might never
An assessment of head growth is especially important in patients with a history of a chromosomal disorder eg downs and brain insult secondary to hypoxic-ischemic encephalopathy