Evidence map›Paper›PMID 30021636›Full record

ArticleSystematic reviews2018

Dietary interventions for managing glucose abnormalities in cystic fibrosis: a systematic review protocol.

Laura Birch, Fiona E Lithander, Simon Langton Hewer, Katie Harriman, Julian Hamilton-Shield, Rachel Perry

Open access · goldAbstract read
In one paragraph

Article in Systematic reviews, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

2 citing papers in PubMed, 16 citations in OpenAlex.

  1. Evolving Nutritional Needs in Cystic Fibrosis.Life (Basel, Switzerland) · 2023
    Review
  2. Cystic fibrosis-related diabetes: optimizing care with a multidisciplinary approach.Diabetes, metabolic syndrome and obesity : targets and therapy · 2019
    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

6 authors at 2 institutions in 1 country.

Laura BirchNIHR Bristol Biomedical Research Centre - Nutrition Theme, Level 3 University Hospitals Bristol Education Centre, Upper Maudlin Street, Bristol, BS2 8AE, UK. laura.birch@bristol.ac.uk.ORCID 0000-0003-1266-267X
Fiona E LithanderNIHR Bristol Biomedical Research Centre - Nutrition Theme, Level 3 University Hospitals Bristol Education Centre, Upper Maudlin Street, Bristol, BS2 8AE, UK.
Simon Langton HewerCF Specialist Centre, Bristol Royal Hospital for Children, Upper Maudlin Street, Bristol, BS2 8BJ, UK.
Katie HarrimanCF Specialist Centre, Bristol Royal Hospital for Children, Upper Maudlin Street, Bristol, BS2 8BJ, UK.
Julian Hamilton-ShieldNIHR Bristol Biomedical Research Centre - Nutrition Theme, Level 3 University Hospitals Bristol Education Centre, Upper Maudlin Street, Bristol, BS2 8AE, UK.
Rachel PerryNIHR Bristol Biomedical Research Centre - Nutrition Theme, Level 3 University Hospitals Bristol Education Centre, Upper Maudlin Street, Bristol, BS2 8AE, UK.
Bristol Royal Hospital for Children · GBNIHR Bristol Biomedical Research Centre · GB

Funding

Department of Health ICA-CDRF-2016-02-014Research Trainees Coordinating Centre ICA-CDRF-2016-02-014
6 · The paper itself

Abstract

backgroundGlucose abnormalities in cystic fibrosis (CF) are common, but there is limited evidence to guide their dietary management. Progressive impaired glucose tolerance eventually leads to cystic fibrosis-related diabetes (CFRD), the most prevalent complication of CF, which is associated with increased morbidity and mortality. Optimising glycaemic control improves clinical status and reduces mortality; insulin therapy is the primary means of controlling glycaemia in CFRD, but its role in managing pre-diabetes is less clear. CF dietary therapy requires a high calorie diet due to increased energy expenditure and malabsorption, but this energy-dense diet is typically high in fat and sugar, and high sugar intakes often result in hyperglycaemia in individuals who have impaired glucose handling. Current guidelines for the dietary management of glucose abnormalities in CF are based on clinical consensus rather than empirical evidence. A systematic review conducted in 2012 on the effects of low glycaemic index dietary intervention in CF concluded that there is a dearth of evidence in this area. This review will update the systematic review by Balzer et al. in 2012 and will broaden the scope of their review to include any type of dietary intervention for managing glucose abnormalities in CF.

methodsQuantitative studies of dietary interventions to manage glucose abnormalities in individuals aged over 5 years with CF and glucose abnormalities will be reviewed. No limits will be placed on language or study design. The comparator will be standard CF dietary therapy (energy dense, high-fat diet) in addition to insulin therapy for individuals with CFRD. Electronic databases will be searched for completed quantitative studies published in peer-review journals that focus on dietary interventions for managing glucose abnormalities in CF. Searches will be conducted from 2000 up to the present day to reflect the evolving improvements in CF management. No restrictions will be placed on study design or language. Duration of the dietary intervention must be a minimum of 2 months and only interventions in out-patient or community settings will be included. Studies must report on dietary intervention, glycaemic control, anthropometry and lung function. Evidence will be assessed for heterogeneity and a narrative review or meta-analysis conducted as appropriate. DISCUSSION: This systematic review will elucidate current knowledge of the effects of dietary interventions for managing glucose abnormalities in the vulnerable CF clinical population. SYSTEMATIC REVIEW REGISTRATION: PROSPERO registration number: CRD42018085569 www.crd.york.ac.uk/prospero/.

Indexed as

Cystic FibrosisGlucose IntoleranceBlood GlucoseBody WeightChildHumansHypoglycemic AgentsInsulinRespiratory Function TestsSystematic Reviews as TopicBlood GlucoseHypoglycemic AgentsInsulinAnthropometryBody weightCystic fibrosisCystic fibrosis-related diabetesDietary interventionGlycaemic controlImpaired glucose toleranceLung function

Identifiers

PMID30021636
PMCPMC6052510
OpenAlexW2883212545

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.