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Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Challenges of neurodevelopmental follow-up for extremely preterm infants at two years
Jane L Orton1, Jennifer L McGinley2, Lisa M Fox1
1Neonatal Services, Royal Women's Hospital, Locked Bag 300, Parkville 3052, Australia.
Insights
Follow-up rates for extremely preterm (EP) and extremely low birthweight (ELBW) infants are low in routine care, impacting accurate assessment of developmental delay. Improving follow-up is crucial for these vulnerable children.
Area of Science:
- Neonatal care
- Developmental pediatrics
- Public health
Background:
- Extremely preterm (EP) and extremely low birthweight (ELBW) infants require specialized, long-term follow-up.
- Accurate assessment of developmental outcomes is critical for timely intervention.
Purpose of the Study:
- To examine follow-up rates for EP/ELBW infants at two years.
- To identify perinatal and geographical factors associated with follow-up.
- To determine rates of developmental delay and disability.
Main Methods:
- Retrospective review of two-year follow-up data for EP/ELBW infants.
- Neurodevelopmental assessment using Bayley Scales of Infant and Toddler Development (Bayley-III).
- Assessment of neurosensory disability and attrition rates.
Main Results:
- Only 50% of eligible infants attended follow-up; rates were 98% in research vs. 32% in clinical pathways.
- Loss of contact was the primary reason for missed follow-up.
- Higher rates of developmental delay were observed using local norms (72%) compared to Bayley-III norms (38%).
Conclusions:
- Routine clinical follow-up for EP/ELBW infants faces significant attrition challenges.
- High attrition complicates accurate determination of developmental delay rates.
- Centers need strategies to improve follow-up adherence for optimal patient care.
Aim:
This study examined the rates of follow-up for a cohort of extremely preterm (EP -<28weeks gestation) and/or extremely low birthweight (ELBW -<1000g) children at two years with related perinatal and geographical factors. The secondary aim was to determine the rates of developmental delay and disability.
Methods:
A retrospective review of two year follow-up data for all EP and/or ELBW infants born in a large tertiary neonatal hospital over a two year period was undertaken. Neurodevelopmental outcome was assessed using the Bayley Scales of Infant and Toddler Development Scale - 3rd edition (Bayley-III) and neurosensory disability was assessed by a paediatrician using a standard proforma. Rates of delay (composite score≥1SD below mean) were determined using the Bayley-III test norms and a local cohort normative group. Attrition rates and reasons for loss to follow-up were determined.
Results:
Only 50% (109/219) of eligible children participated in the follow-up. The follow-up rate for children engaged in an ongoing research project was excellent at 98% (58/59), however it was only 32% (51/160) for children following the clinical pathway. The main reason for not attending the follow-up was loss of contact. Factors associated with attendance included a lower gestation, sepsis and living in the metropolitan areas. The rates of delay in this cohort were greater with reference to local cohort normative data compared to Bayley-III test norms with an overall rate of delay of 72% (95%CI, 63% to 81%) compared to 38% (95%CI, 29% to 50%).
Conclusions:
Follow-up of EP/ELBW infants to two years is an important part of clinical care, however the high rate of attrition in routine clinical follow-up and consequent difficulty in accurately determining rates of delay highlight challenges for centres providing ongoing care.
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