Nutrient-enriched formula versus standard formula for preterm infants.
Journal
The Cochrane database of systematic reviews
ISSN: 1469-493X
Titre abrégé: Cochrane Database Syst Rev
Pays: England
ID NLM: 100909747
Informations de publication
Date de publication:
17 07 2019
17 07 2019
Historique:
pubmed:
18
7
2019
medline:
29
9
2019
entrez:
18
7
2019
Statut:
epublish
Résumé
Preterm infants may accumulate nutrient deficits leading to extrauterine growth restriction. Feeding preterm infants with nutrient-enriched rather than standard formula might increase nutrient accretion and growth rates and might improve neurodevelopmental outcomes. To compare the effects of feeding with nutrient-enriched formula versus standard formula on growth and development of preterm infants. We used the Cochrane Neonatal standard search strategy. This included electronic searches of the Cochrane Central Register of Controlled Trials (CENTRAL; 2018, Issue 11), MEDLINE, Embase, and the Cumulative Index to Nursing and Allied Health Literature (until November 2018), as well as conference proceedings, previous reviews, and clinical trials databases. Randomised and quasi-randomised controlled trials that compared feeding preterm infants with nutrient-enriched formula (protein and energy plus minerals, vitamins, or other nutrients) versus standard formula. We extracted data using the Cochrane Neonatal standard methods. Two review authors separately evaluated trial quality and extracted and synthesised data using risk ratios (RRs), risk differences, and mean differences (MDs). We assessed certainty of evidence at the outcome level using Grading of Recommendations Assessment, Development and Evaluation (GRADE) methods. We identified seven trials in which a total of 590 preterm infants participated. Most participants were clinically stable preterm infants of birth weight less than 1850 g. Few participants were extremely preterm, extremely low birth weight, or growth restricted at birth. Trials were conducted more than 30 years ago, were formula industry funded, and were small with methodological weaknesses (including lack of masking) that might bias effect estimates. Meta-analyses of in-hospital growth parameters were limited by statistical heterogeneity. There is no evidence of an effect on time to regain birth weight (MD -1.48 days, 95% confidence interval (CI) -4.73 to 1.77) and low-certainty evidence suggests that feeding with nutrient-enriched formula increases in-hospital rates of weight gain (MD 2.43 g/kg/d, 95% CI 1.60 to 3.26) and head circumference growth (MD 1.04 mm/week, 95% CI 0.18 to 1.89). Meta-analysis did not show an effect on the average rate of length gain (MD 0.22 mm/week, 95% CI -0.70 to 1.13). Fewer data are available for growth and developmental outcomes assessed beyond infancy, and these do not show consistent effects of nutrient-enriched formula feeding. Data from two trials did not show an effect on Bayley Mental Development Index scores at 18 months post term (MD 2.87, 95% CI -1.38 to 7.12; moderate-certainty evidence). Infants who received nutrient-enriched formula had higher Bayley Psychomotor Development Index scores at 18 months post term (MD 6.56. 95% CI 2.87 to 10.26; low-certainty evidence), but no evidence suggested an effect on cerebral palsy (typical RR 0.79, 95% CI 0.30 to 2.07; 2 studies, 377 infants). Available data did not indicate any other benefits or harms and provided low-certainty evidence about the effect of nutrient-enriched formula feeding on the risk of necrotising enterocolitis in preterm infants (typical RR 0.72, 95% CI 0.41 to 1.25; 3 studies, 489 infants). Available trial data show that feeding preterm infants nutrient-enriched (compared with standard) formulas has only modest effects on growth rates during their initial hospital admission. No evidence suggests effects on long-term growth or development. The GRADE assessment indicates that the certainty of this evidence is low, and that these findings should be interpreted and applied with caution. Further randomised trials would be needed to resolve this uncertainty.
Sections du résumé
BACKGROUND
Preterm infants may accumulate nutrient deficits leading to extrauterine growth restriction. Feeding preterm infants with nutrient-enriched rather than standard formula might increase nutrient accretion and growth rates and might improve neurodevelopmental outcomes.
OBJECTIVES
To compare the effects of feeding with nutrient-enriched formula versus standard formula on growth and development of preterm infants.
SEARCH METHODS
We used the Cochrane Neonatal standard search strategy. This included electronic searches of the Cochrane Central Register of Controlled Trials (CENTRAL; 2018, Issue 11), MEDLINE, Embase, and the Cumulative Index to Nursing and Allied Health Literature (until November 2018), as well as conference proceedings, previous reviews, and clinical trials databases.
SELECTION CRITERIA
Randomised and quasi-randomised controlled trials that compared feeding preterm infants with nutrient-enriched formula (protein and energy plus minerals, vitamins, or other nutrients) versus standard formula.
DATA COLLECTION AND ANALYSIS
We extracted data using the Cochrane Neonatal standard methods. Two review authors separately evaluated trial quality and extracted and synthesised data using risk ratios (RRs), risk differences, and mean differences (MDs). We assessed certainty of evidence at the outcome level using Grading of Recommendations Assessment, Development and Evaluation (GRADE) methods.
MAIN RESULTS
We identified seven trials in which a total of 590 preterm infants participated. Most participants were clinically stable preterm infants of birth weight less than 1850 g. Few participants were extremely preterm, extremely low birth weight, or growth restricted at birth. Trials were conducted more than 30 years ago, were formula industry funded, and were small with methodological weaknesses (including lack of masking) that might bias effect estimates. Meta-analyses of in-hospital growth parameters were limited by statistical heterogeneity. There is no evidence of an effect on time to regain birth weight (MD -1.48 days, 95% confidence interval (CI) -4.73 to 1.77) and low-certainty evidence suggests that feeding with nutrient-enriched formula increases in-hospital rates of weight gain (MD 2.43 g/kg/d, 95% CI 1.60 to 3.26) and head circumference growth (MD 1.04 mm/week, 95% CI 0.18 to 1.89). Meta-analysis did not show an effect on the average rate of length gain (MD 0.22 mm/week, 95% CI -0.70 to 1.13). Fewer data are available for growth and developmental outcomes assessed beyond infancy, and these do not show consistent effects of nutrient-enriched formula feeding. Data from two trials did not show an effect on Bayley Mental Development Index scores at 18 months post term (MD 2.87, 95% CI -1.38 to 7.12; moderate-certainty evidence). Infants who received nutrient-enriched formula had higher Bayley Psychomotor Development Index scores at 18 months post term (MD 6.56. 95% CI 2.87 to 10.26; low-certainty evidence), but no evidence suggested an effect on cerebral palsy (typical RR 0.79, 95% CI 0.30 to 2.07; 2 studies, 377 infants). Available data did not indicate any other benefits or harms and provided low-certainty evidence about the effect of nutrient-enriched formula feeding on the risk of necrotising enterocolitis in preterm infants (typical RR 0.72, 95% CI 0.41 to 1.25; 3 studies, 489 infants).
AUTHORS' CONCLUSIONS
Available trial data show that feeding preterm infants nutrient-enriched (compared with standard) formulas has only modest effects on growth rates during their initial hospital admission. No evidence suggests effects on long-term growth or development. The GRADE assessment indicates that the certainty of this evidence is low, and that these findings should be interpreted and applied with caution. Further randomised trials would be needed to resolve this uncertainty.
Identifiants
pubmed: 31314903
doi: 10.1002/14651858.CD004204.pub3
pmc: PMC6636703
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
CD004204Subventions
Organisme : Department of Health
ID : SRP/16/114/03
Pays : United Kingdom
Références
Pediatr Res. 2007 Aug;62(2):209-14
pubmed: 17597641
Lancet. 1990 Jun 23;335(8704):1477-81
pubmed: 1972430
Pediatrics. 2014 Jan;133(1):63-70
pubmed: 24344103
Curr Probl Pediatr. 1987 Apr;17(4):213-88
pubmed: 3556038
World Rev Nutr Diet. 2013;106:26-32
pubmed: 23428677
J Pediatr. 2009 Aug;155(2):229-34
pubmed: 19446846
Arch Dis Child. 2003 Jun;88(6):482-7
pubmed: 12765911
J Pediatr. 2013 Mar;162(3 Suppl):S107-14
pubmed: 23445841
Am J Clin Nutr. 2005 Feb;81(2):480-7
pubmed: 15699238
Arch Dis Child Fetal Neonatal Ed. 2015 Mar;100(2):F173-8
pubmed: 25293712
Clin Perinatol. 2013 Mar;40(1):1-10
pubmed: 23415260
Pediatrics. 2012 Mar;129(3):e827-41
pubmed: 22371471
S Afr Med J. 1984 Jan 28;65(4):125-7
pubmed: 6364395
Pediatrics. 2003 May;111(5 Pt 1):986-90
pubmed: 12728076
J Pediatr. 1986 Jun;108(6):955-63
pubmed: 3712165
Lancet. 2001 Feb 10;357(9254):413-9
pubmed: 11273059
Arch Dis Child Fetal Neonatal Ed. 2012 Jan;97(1):F56-61
pubmed: 21856644
Pediatrics. 2015 Jul;136(1):e84-92
pubmed: 26101360
Early Hum Dev. 2013 Jul;89(7):487-96
pubmed: 23597678
Arch Dis Child. 2004 Apr;89(4):347-50
pubmed: 15033844
Curr Opin Clin Nutr Metab Care. 2011 May;14(3):297-301
pubmed: 21378555
J Bone Miner Res. 1999 May;14(5):810-20
pubmed: 10320530
Cochrane Database Syst Rev. 2016 May 08;(5):CD000343
pubmed: 27155888
J Med Libr Assoc. 2016 Oct;104(4):309-312
pubmed: 27822154
Nurs Res. 1999 Mar-Apr;48(2):86-93
pubmed: 10190835
Pediatrics. 2001 Feb;107(2):270-3
pubmed: 11158457
Turk J Pediatr. 1992 Jan-Mar;34(1):31-6
pubmed: 1509527
BMJ. 1998 Nov 28;317(7171):1481-7
pubmed: 9831573
Turk J Pediatr. 2000 Apr-Jun;42(2):138-44
pubmed: 10936980
Arch Dis Child. 1989 Nov;64(11):1570-8
pubmed: 2690739
J Pediatr. 2013 Mar;162(3 Suppl):S7-16
pubmed: 23445851
Lancet. 1990 Dec 22-29;336(8730):1519-23
pubmed: 1979363
South Med J. 1984 Jan;77(1):13-6, 20
pubmed: 6364370
Adv Nutr. 2017 Jan 17;8(1):80-91
pubmed: 28096129
Am J Clin Nutr. 2000 Mar;71(3):822-8
pubmed: 10702179
Semin Fetal Neonatal Med. 2017 Feb;22(1):15-22
pubmed: 27595621
J Pediatr Gastroenterol Nutr. 2010 Jan;50(1):85-91
pubmed: 19881390
Bone. 2009 Jul;45(1):142-9
pubmed: 19306955
Arch Dis Child Fetal Neonatal Ed. 2008 Mar;93(2):F108-14
pubmed: 17660214
J Med Assoc Thai. 1989 Jan;72 Suppl 1:61-5
pubmed: 2659718
Pediatrics. 2006 Nov;118(5):e1452-65
pubmed: 17079546
Semin Perinatol. 2003 Aug;27(4):302-10
pubmed: 14510321
Syst Rev. 2016 Dec 5;5(1):210
pubmed: 27919275
Acta Paediatr. 1996 Feb;85(2):230-6
pubmed: 8640056
Lancet. 2003 Mar 29;361(9363):1089-97
pubmed: 12672313
N Engl J Med. 1991 Jul 25;325(4):231-7
pubmed: 2057024
J Pediatr. 1981 Oct;99(4):617-24
pubmed: 7277107
Cochrane Database Syst Rev. 2016 Dec 13;12:CD004696
pubmed: 27958643
Horm Res. 2008;70(6):319-28
pubmed: 18953169
J Pediatr. 1984 Jan;104(1):118-22
pubmed: 6690656
Arch Pediatr Adolesc Med. 2000 Aug;154(8):778-84
pubmed: 10922273
Rev Chil Pediatr. 1987 May-Jun;58(3):197-202
pubmed: 3454457
J Nutr. 2002 Jun;132(6 Suppl 1):1395S-577S
pubmed: 12042465
Front Nutr. 2017 May 08;4:14
pubmed: 28534028
J Pediatr Gastroenterol Nutr. 1984 Nov;3(5):696-9
pubmed: 6502369