Evidence map›Paper›PMID 27825008›Full record

ArticleJAMA2016

Effect of Supplemental Donor Human Milk Compared With Preterm Formula on Neurodevelopment of Very Low-Birth-Weight Infants at 18 Months: A Randomized Clinical Trial.

Deborah L O'Connor, Sharyn Gibbins, Alex Kiss, Nicole Bando, Joan Brennan-Donnan, Eugene Ng, Douglas M Campbell, Simone Vaz, Christoph Fusch, Elizabeth Asztalos and 6 more

Registry-linked trialAbstract readComment
PubMed Publisher
In one paragraph

Article in JAMA, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06870981 (Improving Growth and Neurodevelopment of Very Low Birth Weight Infants Through Precision Nutrition), which is not on this map. Cited by 114 papers, 15 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 15 pooled it
18.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06870981 recruitingnot on this map

Improving Growth and Neurodevelopment of Very Low Birth Weight Infants Through Precision Nutrition: The Optimizing Nutrition and Milk (Opti-NuM) Project

TypeobservationalSponsorThe Hospital for Sick ChildrenRan2010 to 2027Enrolled1,100ConditionsVery Low Birth Weight Baby, Early Nutrition and the Preterm Infant, Nutritional Requirements, Human Milk FortificationArmsOpti-NuM is an observational secondary use of data/samples study, the investigators will analyze information and specimens from the MaxiMoM platform RCTs. No interventions form part of this study.
3 · Its place in the literature

Who cites it

114 citing papers in PubMed, 15 syntheses or guidelines pooled it, 238 citations in OpenAlex.

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54 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 1 country.

Deborah L O'ConnorPhysiology and Experimental Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada2Department of Nutritional Sciences, University of Toronto, Toronto, Ontario, Canada.
Sharyn GibbinsTrillium Health Partners, Mississauga, Ontario, Canada.
Alex KissEvaluative and Clinical Sciences, Sunnybrook Research Institute, Toronto, Ontario, Canada5Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Nicole BandoPhysiology and Experimental Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.
Joan Brennan-DonnanPhysiology and Experimental Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada2Department of Nutritional Sciences, University of Toronto, Toronto, Ontario, Canada6Department of Clinical Dietetics, The Hospital for Sick Children, Toronto, Ontario, Canada.
Eugene NgDepartment of Pediatrics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada8Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Douglas M CampbellDepartment of Pediatrics, University of Toronto, Toronto, Ontario, Canada9St. Michael's Hospital and Li Ka Shing Knowledge Institute, Toronto, Ontario, Canada10Department of Neonatology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Simone VazDepartment of Pediatrics, William Osler Health System, Brampton, Ontario, Canada.
Christoph FuschDepartment of Pediatrics, McMaster Children's Hospital and McMaster University, Hamilton, Ontario, Canada.
Elizabeth AsztalosDepartment of Pediatrics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada8Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Paige ChurchDepartment of Pediatrics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada8Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Edmond KellyDepartment of Pediatrics, University of Toronto, Toronto, Ontario, Canada13Department of Pediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Linh LyDepartment of Pediatrics, University of Toronto, Toronto, Ontario, Canada10Department of Neonatology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Alan DanemanDepartment of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada15Department of Medical Imaging, University of Toronto, Toronto, Ontario, Canada.
Sharon UngerDepartment of Pediatrics, University of Toronto, Toronto, Ontario, Canada10Department of Neonatology, The Hospital for Sick Children, Toronto, Ontario, Canada13Department of Pediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
GTA DoMINO Feeding Group
Sunnybrook Health Science Centre · CAUniversity of Toronto · CAMount Sinai Hospital · CAHospital for Sick Children · CAMcMaster Children's Hospital · CASt. Michael's Hospital · CATrillium Health Centre · CAWilliam Osler Health System · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: For many very low-birth-weight (VLBW) infants, there is insufficient mother's milk, and a supplement of pasteurized donor human milk or preterm formula is required. Awareness of the benefits of mother's milk has led to an increase in use of donor milk, despite limited data evaluating its efficacy. Objective: To determine if nutrient-enriched donor milk compared with formula, as a supplement to mother's milk, reduces neonatal morbidity, supports growth, and improves neurodevelopment in VLBW infants. Design, Setting, and Participants: In this pragmatic, double-blind, randomized trial, VLBW infants were recruited from 4 neonatal units in Ontario, Canada, within 96 hours of birth between October 2010 and December 2012. Follow-up was completed in July 2015. Interventions: Infants were fed either donor milk or formula for 90 days or to discharge when mother's milk was unavailable. Main Outcomes and Measures: The primary outcome was the cognitive composite score on the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III) at 18 months' corrected age (standardized mean, 100 [SD, 15]; minimal clinically important difference, 5 points). Secondary outcomes included Bayley-III language and motor composite scores, growth, and a dichotomous mortality and morbidity index. Results: Of 840 eligible infants, 363 (43.2%) were randomized (181 to donor milk and 182 to preterm formula); of survivors, 299 (92%) had neurodevelopment assessed. Mean birth weight and gestational age of infants was 996 (SD, 272) g and 27.7 (2.6) weeks, respectively, and 195 (53.7%) were male. No statistically significant differences in mean Bayley-III cognitive composite score (adjusted scores, 92.9 in donor milk group vs 94.5 in formula group; fully adjusted mean difference, -2.0 [95% CI, -5.8 to 1.8]), language composite score (adjusted scores, 87.3 in donor milk group vs 90.3 in formula group; fully adjusted mean difference, -3.1 [95% CI, -7.5 to 1.3]), or motor composite score (adjusted scores, 91.8 in donor milk group vs 94.0 in formula group; fully adjusted mean difference, -3.7 [95% CI, -7.4 to 0.09]) were observed between groups. There was no statistically significant difference in infants positive for the mortality and morbidity index (43% in donor milk group, 40% in formula group) or changes in growth z scores. Conclusions and Relevance: Among VLBW infants, use of supplemental donor milk compared with formula did not improve neurodevelopment at 18 months' corrected age. If donor milk is used in settings with high provision of mother's milk, this outcome should not be considered a treatment goal. Trial Registration: isrctn.org Identifier: ISRCTN35317141.

Indexed as

Double-Blind MethodMilk, HumanCanadaGestational AgeHumansInfantInfant FormulaInfant, NewbornInfant, PrematureInfant, Very Low Birth Weight

Identifiers

PMID27825008
OpenAlexW2549063171

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.