Evidence map›Paper›PMID 32662862›Full record

Trial reportJAMA2020

Effect of Maternal Docosahexaenoic Acid Supplementation on Bronchopulmonary Dysplasia-Free Survival in Breastfed Preterm Infants: A Randomized Clinical Trial.

Isabelle Marc, Bruno Piedboeuf, Thierry Lacaze-Masmonteil, William Fraser, Benoît Mâsse, Ibrahim Mohamed, Mosarrat Qureshi, Jehier Afifi, Brigitte Lemyre, Georges Caouette and 16 more

Registry-linked trialOpen access · bronzeAbstract readEquivalence TrialMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02371460 (Maternal Omega-3 Supplementation to Reduce BronchopulmonarY Dysplasia in Very Preterm Infants), which is not on this map. Cited by 36 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 4 pooled it
5.2field-weighted citation impact, top 3% 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.

NCT02371460 phase3terminatednot on this map

Maternal Omega-3 Supplementation to Reduce BronchopulmonarY Dysplasia in Very Preterm Infants (MOBYDIck Trial)

TypeinterventionalSponsorCHU de Quebec-Universite LavalRan2015 to 2023Enrolled461ConditionsBronchopulmonary Dysplasia, Child Development, Neonatal and Perinatal ConditionsArmsDHA-rich algal oil, Placebo
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 4 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Effect of enteral supplementation of DHA with or without ARA in preterm infants: a meta-analysis.Archives of disease in childhood. Fetal and neonatal edition · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 18 institutions in 1 country.

Isabelle MarcDepartment of Pediatrics, Faculty of Medicine, Centre Hospitalier Universitaire de Québec-Université Laval, Quebec City, Quebec, Canada.
Bruno PiedboeufDepartment of Pediatrics, Faculty of Medicine, Centre Hospitalier Universitaire de Québec-Université Laval, Quebec City, Quebec, Canada.
Thierry Lacaze-MasmonteilDepartment of Pediatrics, Cumming School of Medicine, University of Calgary, Foothills Medical Centre, Calgary, Alberta, Canada.
William FraserDepartment of Obstetrics and Gynecology, Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.
Benoît MâsseSchool of Public Health, Université de Montréal, Montreal, Quebec, Canada.
Ibrahim MohamedDepartment of Pediatrics, Université de Montréal, Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada.
Mosarrat QureshiDivision of Neonatology, Royal Alexandra Hospital, Edmonton, Alberta, Canada.
Jehier AfifiDepartment of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada.
Brigitte LemyreDivision of Neonatology, Children's Hospital of Eastern Ontario, Ottawa, Canada.
Georges CaouetteDepartment of Pediatrics, Faculty of Medicine, Centre Hospitalier Universitaire de Québec-Université Laval, Quebec City, Quebec, Canada.
Julie BartholomewDepartment of Neonatology, Jewish General Hospital, McGill University, Montreal, Quebec, Canada.
Anne Monique NuytDepartment of Pediatrics, Université de Montréal, Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada.
Pierre JulienDepartment of Endocrinology and Nephrology, Centre Hospitalier Universitaire de Québec-Université Laval, Quebec City, Quebec, Canada.
Anne SynnesDepartment of Pediatrics, Division of Neonatology, University of British Columbia, Vancouver, Canada.
Michel LucasDepartment of Social and Preventive Medicine, Centre Hospitalier Universitaire de Québec-Université Laval, Hôpital du Saint-Sacrement, Quebec City, Quebec, Canada.
Thérèse PerreaultDivision of Neonatology, Montréal Children's Hospital, McGill University, Montreal, Quebec, Canada.
Lannae StruebyDepartment of Pediatrics, University of Saskatchewan, Saskatoon, Canada.
Zenon CieslakDepartment of Pediatrics, Royal Columbian Hospital, New Westminster, British Columbia, Canada.
Kamran YusufDepartment of Pediatrics, Section of Neonatology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Gustavo PelligraDepartment of Maternity Care and Pediatrics, Victoria General Hospital, Island Health, Victoria, British Columbia, Canada.
Edith MasséDepartment of Pediatrics, Université de Sherbrooke, Hôpital Fleurimont, Sherbrooke, Quebec, Canada.
Bodil LarsenFaculty of Agricultural, Life, and Environmental Sciences, University of Alberta, Edmonton, Canada.
Cecilia de CaboDepartment of Pediatrics and Child Health, Max Rady School of Medicine, University of Manitoba, Winnipeg, Canada.
Chelsea RuthDepartment of Pediatrics and Child Health, Max Rady School of Medicine, University of Manitoba, Winnipeg, Canada.
Faiza KhurshidDepartment of Pediatrics, Queen's University, Kingston, Ontario, Canada.
Pascal M LavoieDepartment of Pediatrics, Division of Neonatology, University of British Columbia, Vancouver, Canada.
Centre hospitalier universitaire de Québec · CACentre Hospitalier Universitaire Sainte-Justine · CAMcGill University · CAUniversité Laval · CAUniversity of British Columbia · CAUniversity of Calgary · CAUniversity of Manitoba · CACentre Hospitalier Universitaire de Sherbrooke · CAChildren's Hospital of Eastern Ontario · CADalhousie University · CAQueen's University · CARoyal Alexandra Hospital · CARoyal Columbian Hospital · CAUniversité de Montréal · CAUniversité de Sherbrooke · CAUniversity of Alberta · CAUniversity of Saskatchewan · CAVictoria General Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Maternal docosahexaenoic acid (DHA) supplementation may prevent bronchopulmonary dysplasia, but evidence remains inconclusive. Objective: To determine whether maternal DHA supplementation during the neonatal period improves bronchopulmonary dysplasia-free survival in breastfed infants born before 29 weeks of gestation. Design, Setting, and Participants: Superiority, placebo-controlled randomized clinical trial at 16 Canadian neonatal intensive care units (June 2015-April 2018 with last infant follow-up in July 2018). Lactating women who delivered before 29 weeks of gestation were enrolled within 72 hours of delivery. The trial intended to enroll 800 mothers, but was stopped earlier. Interventions: There were 232 mothers (273 infants) assigned to oral capsules providing 1.2 g/d of DHA from randomization to 36 weeks' postmenstrual age and 229 mothers (255 infants) assigned to placebo capsules. Main Outcomes and Measures: The primary outcome was bronchopulmonary dysplasia-free survival in infants at 36 weeks' postmenstrual age. There were 22 secondary outcomes, including mortality and bronchopulmonary dysplasia. Results: Enrollment was stopped early due to concern for harm based on interim data from this trial and from another trial that was published during the course of this study. Among 461 mothers and their 528 infants (mean gestational age, 26.6 weeks [SD, 1.6 weeks]; 253 [47.9%] females), 375 mothers (81.3%) and 523 infants (99.1%) completed the trial. Overall, 147 of 268 infants (54.9%) in the DHA group vs 157 of 255 infants (61.6%) in the placebo group survived without bronchopulmonary dysplasia (absolute difference, -5.0% [95% CI, -11.6% to 2.6%]; relative risk, 0.91 [95% CI, 0.80 to 1.04], P = .18). Mortality occurred in 6.0% of infants in the DHA group vs 10.2% of infants in the placebo group (absolute difference, -3.9% [95% CI, -6.8% to 1.4%]; relative risk, 0.61 [95% CI, 0.33 to 1.13], P = .12). Bronchopulmonary dysplasia occurred in 41.7% of surviving infants in the DHA group vs 31.4% in the placebo group (absolute difference, 11.5% [95% CI, 2.3% to 23.2%]; relative risk, 1.36 [95% CI, 1.07 to 1.73], P = .01). Of 22 prespecified secondary outcomes, 19 were not significantly different. Conclusions and Relevance: Among breastfed preterm infants born before 29 weeks of gestation, maternal docosahexaenoic acid supplementation during the neonatal period did not significantly improve bronchopulmonary dysplasia-free survival at 36 weeks' postmenstrual age compared with placebo. Study interpretation is limited by early trial termination. Trial Registration: ClinicalTrials.gov Identifier: NCT02371460.

Indexed as

Dietary SupplementsAdultBronchopulmonary DysplasiaDocosahexaenoic AcidsEquivalence Trials as TopicFemaleGestational AgeHumansInfant, Extremely PrematureInfant, NewbornLactationPatient ComplianceSample SizeDocosahexaenoic Acids

Identifiers

PMID32662862
PMCPMC7361648
OpenAlexW3042629957

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.