Evidence map›Paper›PMID 35807754›Full record

ArticleNutrients2022

Experiences and Perspectives of Individuals with Cystic Fibrosis and Their Families Related to Food Insecurity.

Montserrat A Corbera-Hincapie, Samar E Atteih, Olivia M Stransky, Daniel J Weiner, Iris M Yann, Traci M Kazmerski

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Socioeconomic burden of cystic fibrosis in Canada.BMJ open respiratory research · 2024
    Article
  6. Article
  7. Article
  8. Review
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.

Montserrat A Corbera-HincapieDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Samar E AtteihDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Olivia M StranskyCenter for Innovative Research on Gender Health Equity (CONVERGE), Pittsburgh, PA 15224, USA.
Daniel J WeinerDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Iris M YannDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Traci M KazmerskiDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.ORCID 0000-0002-3916-8260
University of Pittsburgh · USInnovative Research (United States) · US

Funding

Cystic Fibrosis Foundation CORBER20B0, CORBER21D0
6 · The paper itself

Abstract

Food insecurity (FI) rates among people with cystic fibrosis (CF) are significantly higher than in the general US population. This study explored the experiences and perceptions of adults and parents of children with CF surrounding FI. We recruited parents of children with CF ages 0-18 years and adults with CF ages 18 years and older from a large, accredited U.S. CF care center and the Cystic Fibrosis Foundation Community Voice to participate in a qualitative study using semi-structured telephone interviews to explore experiences and preferences related to food insecurity. Two coders independently reviewed each transcript to apply the codebook and identify any emerging codes using an ongoing, iterative process to identify central themes. We interviewed 20 participants (six adults with CF and 14 parents of children with CF) and identified five major themes: (1) FI in CF is influenced by a variety of factors, ranging from nutritional demands to competing financial barriers; (2) FI impacts CF health outcomes; (3) Open patient-provider communication around FI is vital; (4) FI screening and discussions should be normalized in CF care; (5) Comprehensive FI resources are vital. FI is an important topic that should routinely be addressed with the CF care team to destigmatize and encourage individuals to be more forthcoming about their FI status. Results from this study will inform future larger investigations on the impact of FI on CF health and aid in the design and planning of targeted interventions and advocacy efforts.

Indexed as

Cystic FibrosisAdolescentAdultChildChild, PreschoolCommunicationFood InsecurityHumansInfantInfant, NewbornParentsQualitative Researchcystic fibrosisexperiencesfood insecurity

Identifiers

PMID35807754
PMCPMC9268710
OpenAlexW4283261718

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.