Guidance for the Conduct and Reporting of Clinical Trials of Breast Milk Substitutes.


Journal

JAMA pediatrics
ISSN: 2168-6211
Titre abrégé: JAMA Pediatr
Pays: United States
ID NLM: 101589544

Informations de publication

Date de publication:
01 09 2020
Historique:
pubmed: 12 5 2020
medline: 26 3 2021
entrez: 12 5 2020
Statut: ppublish

Résumé

Breast milk substitutes (BMS) are important nutritional products evaluated in clinical trials. Concerns have been raised about the risk of bias in BMS trials, the reliability of claims that arise from such trials, and the potential for BMS trials to undermine breastfeeding in trial participants. Existing clinical trial guidance does not fully address issues specific to BMS trials. To establish new methodological criteria to guide the design, conduct, analysis, and reporting of BMS trials and to support clinical trialists designing and undertaking BMS trials, editors and peer reviewers assessing trial reports for publication, and regulators evaluating the safety, nutritional adequacy, and efficacy of BMS products. A modified Delphi method was conducted, involving 3 rounds of anonymous questionnaires and a face-to-face consensus meeting between January 1 and October 24, 2018. Participants were 23 experts in BMS trials, BMS regulation, trial methods, breastfeeding support, infant feeding research, and medical publishing, and were affiliated with institutions across Europe, North America, and Australasia. Guidance development was supported by an industry consultation, analysis of methodological issues in a sample of published BMS trials, and consultations with BMS trial participants and a research ethics committee. An initial 73 criteria, derived from the literature, were sent to the experts. The final consensus guidance contains 54 essential criteria and 4 recommended criteria. An 18-point checklist summarizes the criteria that are specific to BMS trials. Key themes emphasized in the guidance are research integrity and transparency of reporting, supporting breastfeeding in trial participants, accurate description of trial interventions, and use of valid and meaningful outcome measures. Implementation of this guidance should enhance the quality and validity of BMS trials, protect BMS trial participants, and better inform the infant nutrition community about BMS products.

Identifiants

pubmed: 32391870
pii: 2765822
doi: 10.1001/jamapediatrics.2020.0578
pmc: PMC7215627
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

874-881

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Auteurs

Katharine Jarrold (K)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Bartosz Helfer (B)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Mona Eskander (M)

Bureau of Nutritional Sciences, Food Directorate, Health Canada, Ottawa, Ontario, Canada.

Helen Crawley (H)

First Steps Nutrition Trust, London, United Kingdom.
Scientific and Technical Advisory Group on the Inappropriate Promotion of Foods for Infants and Young Children, World Health Organization, Geneva, Switzerland.

Jillian Trabulsi (J)

Department of Behavioral Health and Nutrition, University of Delaware, Newark.

Laura E Caulfield (LE)

Center for Human Nutrition, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

Gillian Duffy (G)

Department of Public Health Nutrition Standards, Food Standards Australia New Zealand, Canberra, Australia.

Vanessa Garcia-Larsen (V)

Center for Human Nutrition, The Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

Deborah Hayward (D)

Bureau of Nutritional Sciences, Food Directorate, Health Canada, Ottawa, Ontario, Canada.

Matthew Hyde (M)

Section of Neonatal Medicine, Imperial College London, London, United Kingdom.

Suzan Jeffries (S)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.
International Board of Certified Lactation Consultant Examiners, Fairfax, Virginia.

Mikael Knip (M)

Children's Hospital, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland.

Jo Leonardi-Bee (J)

Medical Statistics, University of Nottingham, Nottingham, United Kingdom.

Elizabeth Loder (E)

Research, British Medical Journal , London, United Kingdom.
Department of Neurology, Harvard Medical School, Cambridge, Massachusetts.

Caroline J Lodge (CJ)

Allergy and Lung Health Unit, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.

Adrian J Lowe (AJ)

Allergy and Lung Health Unit, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.

William McGuire (W)

Centre for Reviews and Dissemination, University of York, York, United Kingdom.

David Osborn (D)

Division of Obstetrics, Gynaecology and Neonatology, University of Sydney, Sydney, New South Wales, Australia.

Hildegard Przyrembel (H)

Department of Food Safety, Federal Institute for Risk Assessment, Berlin, Germany.

Mary J Renfrew (MJ)

Mother and Infant Research Unit, University of Dundee School of Nursing and Health Sciences, Dundee, United Kingdom.

Paula Trumbo (P)

Nutrition Programs, Food and Drug Administration, Silver Spring, Maryland.

John Warner (J)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Barbara Schneeman (B)

Department of Nutrition, University of California, Davis, Davis.

Robert J Boyle (RJ)

National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Centre of Evidence-Based Dermatology, University of Nottingham, Nottingham, United Kingdom.

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Classifications MeSH