Evidence map›Paper›PMID 34579139›Full record

SynthesisNutrients2021

Breastfeeding in Cystic Fibrosis: A Systematic Review on Prevalence and Potential Benefits.

Carla Colombo, Gianfranco Alicandro, Valeria Daccò, Alessandra Consales, Fabio Mosca, Carlo Agostoni, Maria Lorella Giannì

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in Nutrients, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Breastfeeding, growth, and lung disease in the first 3 years of life in children with cystic fibrosis.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2025
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Carla ColomboFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Cystic Fibrosis Center, 20122 Milan, Italy.ORCID 0000-0002-8975-695X
Gianfranco AlicandroFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Cystic Fibrosis Center, 20122 Milan, Italy.ORCID 0000-0002-0430-2714
Valeria DaccòFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Cystic Fibrosis Center, 20122 Milan, Italy.
Alessandra ConsalesFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, NICU, 20122 Milan, Italy.
Fabio MoscaFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, NICU, 20122 Milan, Italy.
Carlo AgostoniDepartment of Clinical Sciences and Community Health, Università degli Studi di Milano, 20122 Milan, Italy.ORCID 0000-0002-5006-0832
Maria Lorella GiannìFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, NICU, 20122 Milan, Italy.ORCID 0000-0003-3901-9131
University of Milan · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breastfeeding (BF) is considered the normative standard of feeding for all infants. However, the impact of BF in patients with cystic fibrosis (CF) is not completely defined. Therefore, we conducted a systematic review to evaluate BF prevalence in the CF population and its impact on anthropometric and pulmonary outcomes. We searched MEDLINE, Embase and the Cochrane Library for original articles published in English up to 4 December 2020 that report the prevalence of BF and/or any measure of association between BF and anthropometric or pulmonary outcomes. Nine observational studies were identified (six retrospective cohort studies, one prospective cohort study, one survey and one case-control study within a retrospective cohort). The BF rate in CF patients is lower than that of the healthy population (approximately 50-60% of infants were breastfed at any time). The benefits in anthropometric outcomes of BF for >2 months in this at-risk population are unclear. A few relatively small studies suggest a potential benefit of BF in reducing lung infections, although data are inconsistent. The currently available data are insufficient to draw definite conclusions on the benefits of exclusive BF in anthropometric and pulmonary outcomes in CF. Clinical trials evaluating well-defined BF promotion interventions are needed.

Indexed as

Cystic FibrosisBody WeightBreast FeedingCase-Control StudiesCohort StudiesFemaleFollow-Up StudiesHumansInfantInfant, NewbornLungLung DiseasesRespiratory Tract Infectionsbreastfeedingcystic fibrosisgrowthinfant feedinginfectionspulmonary outcomes

Identifiers

PMID34579139
PMCPMC8469582
OpenAlexW3201413487

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.