Evidence map›Paper›PMID 42714683›Full record

SynthesisEuropean journal of pediatrics2026

Understanding the gut microbiota to shape the future of intestinal failure care: a systematic review of the evidence.

Francesco Morotti, Giulia Fiore, Alessandra Mari, Federica Bona, Jonabell Dolor, Valentina Giorgio, Roberto Conti Nibali, Riccardo Coletta, Lacitignola Laura, Francesco Fascetti-Leon and 5 more

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Francesco MorottiDepartment of Mother and Child, Pediatric Unit B, Azienda Ospedaliera Universitaria Integrata Verona, Verona, Italy. fmorotti90@gmail.com.
Giulia FioreFoundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Pediatric Unit, Milan, Italy.
Alessandra MariDepartment of Paediatrics, Vittore Buzzi Children's Hospital, University of Milan, Milan, Italy.
Federica BonaDepartment of Paediatrics, Vittore Buzzi Children's Hospital, University of Milan, Milan, Italy.
Jonabell DolorDepartment of Paediatrics, Vittore Buzzi Children's Hospital, University of Milan, Milan, Italy.
Valentina GiorgioDepartment of Women and Child Health, UOSD Spina Bifida E Altre Branche Specialistiche, Fondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
Roberto Conti NibaliDepartment of Childhood and Developmental Medicine, Pediatric Gastroenterology Service, ASST Fatebenefratelli-Sacco, Milan, Italy.
Riccardo ColettaDepartment of Neurosciences, Drug Research and Child Health (NEUROFARBA), University of Florence, Florence, Italy.
Lacitignola LauraGastroenterology and Nutritional Unit, Meyer Children's Hospital IRCCS, Florence, Italy.
Francesco Fascetti-LeonPaediatric Surgery, Azienda Ospedale-Università Padova, Padua, Italy.
Elisa BorghiDepartment of Health Sciences, University of Milan, Milan, Italy.
Antonella DiamantiDigestive Diseases and Nutritional Rehabilitation Unit, Nutritional Treatments of Complex Diseases Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165, Rome, Italy.
Teresa CapriatiDigestive Diseases and Nutritional Rehabilitation Unit, Nutritional Treatments of Complex Diseases Research Unit, Bambino Gesù Children's Hospital, IRCCS, 00165, Rome, Italy.
Elvira VerduciFoundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Pediatric Unit, Milan, Italy.
Lorenzo NorsaDepartment of Paediatrics, Vittore Buzzi Children's Hospital, University of Milan, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal failure (IF) patients suffer a loss of intestinal mass or function and alterations in gut microbiota (GM) composition and function. Our objectives are to (1) characterise GM in IF, (2) explore associations between GM and IF health outcomes, and (3) analyse the effect of GM-based interventions on disease course. A systematic review was conducted in PubMed/MEDLINE, Embase, and Web of Science up to March 2026. Eligible studies included observational studies, prospective studies, and clinical trials in patients with IF, without age or date restrictions. The main outcomes identified included GM diversity indices, GM taxonomy, and IF complications. Risk of bias was assessed using CASP checklists. Twenty-eight studies including children (4 case reports, 1 case series, 19 cohort studies [14 cross-sectional, 5 prospective], 1 quasi-experimental study, 3 RCTs, for a total of 391 cases) and 19 studies including adults (2 case reports, 1 case series, 14 cohort studies [12 cross-sectional, 2 prospective], 2 quasi-experimental studies, for a total of 604 cases) were analysed. Given the heterogeneity among studies, only qualitative synthesis was performed. Reduced alpha diversity and marked phylum-level dysbiosis are consistently reported in patients with IF compared with healthy controls. Different IF aetiologies and bowel anatomy are associated with distinctive GM patterns. IF complication rate increases with the magnitude of GM alteration. GM-modifying interventions are poorly studied. Encouraging improvements in GM dysbiosis, enteral tolerance, and IF complications have been reported in observational studies using various interventions. Still, these findings are not confirmed in RCTs. A distinguishing GM dysbiosis, associated with worse clinical outcomes, clearly emerges in patients with IF. The low quality and heterogeneity of the studies analysed limit data interpretation. The need for a better definition of microbiota assessment, both as a bedside tool and as a therapeutic target, is highlighted as a prominent study topic for the future of IF rehabilitation. What is Known: • Intestinal failure yields substantial alterations in gut microbiota habitat, leading to dysbiosis. • The severity of dysbiosis influences multiple clinically relevant health outcomes. What is New: • IF aetiology, short bowel subtype, and patient age influence GM alterations in IF patients. • Limited longitudinal data suggest that some adverse outcomes are a result of specific dysbiosis pattern progression. • Therapies targeting GM are promising tools for personalised intestinal rehabilitation.

Indexed as

Gastrointestinal MicrobiomeIntestinal FailureDysbiosisHumansAdultsChildrenGut microbiomeIntestinal rehabilitationParenteral nutritionShort bowel syndrome

Identifiers

What OpenQuestion holds

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Registered trials

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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.