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Longchain polyunsaturated fatty acid supplementation in preterm infants
1Neonatal Clinical Care Unit, King Edward Memorial Hospital for Women and Princess Margaret Hospital for Children, Bagot Road, Subiaco, WA, Australia.
The Cochrane Database of Systematic Reviews
|February 20, 2004
Summary
Supplementing preterm infant formula with long-chain polyunsaturated fatty acids (LCPUFA) showed no long-term benefits for visual acuity or development. LCPUFA supplementation did not impair growth in preterm infants.
Area of Science:
- Neonatal Nutrition
- Developmental Pediatrics
- Essential Fatty Acids
Background:
- Preterm infants may have insufficient capacity to synthesize long-chain polyunsaturated fatty acids (LCPUFA).
- LCPUFA are crucial for developing brain and retina, leading to debate on their essentiality for preterm infants.
Purpose of the Study:
- To evaluate the safety and efficacy of supplementing preterm infant formula with LCPUFA.
- To determine if LCPUFA supplementation offers benefits to preterm infants.
Main Methods:
- Systematic review of eleven randomized trials assessing clinical endpoints.
- Searches included MEDLINE, Oxford Database of Perinatal Trials, and Cochrane Central Register of Controlled Trials.
- Data collection involved reviewing trials with clinical outcomes and assessing study quality.
Main Results:
- Most studies found no significant differences in visual acuity (measured by Teller acuity cards, VEP, ERG) between supplemented and control infants.
- Meta-analysis of Bayley Scales of Infant Development (BSID) showed no significant effect on development; some studies indicated potential impacts on novelty preference.
- Growth outcomes were generally not significantly affected, though some trials reported decreased growth while others showed increased weight and length.
Conclusions:
- No long-term benefits were demonstrated for preterm infants receiving formula supplemented with LCPUFA.
- Supplementation with n-3 and n-6 LCPUFA did not impair the growth of preterm infants.
- Variations in trial methodology, dosage, and formula composition limit definitive conclusions.