Evidence map›Paper›PMID 35096701›Full record

ArticleFrontiers in pediatrics2021

Assessing the Utility of an Outpatient Exercise Program for Children With Cystic Fibrosis: A Quality Improvement Project.

Dionne Adair, Ahmad Hider, Amy G Filbrun, Chris Tapley, Sandra Bouma, Courtney Iwanicki, Samya Z Nasr

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 38% 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, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. 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 1 institution in 1 country.

Dionne AdairDepartment of Pediatrics, Division of Pediatric Pulmonology, University of Michigan, Ann Arbor, MI, United States.
Ahmad HiderUniversity of Michigan Medical School, Ann Arbor, MI, United States.
Amy G FilbrunDepartment of Pediatrics, Division of Pediatric Pulmonology, University of Michigan, Ann Arbor, MI, United States.
Chris TapleyDepartment of Pediatrics, Division of Pediatric Pulmonology, University of Michigan, Ann Arbor, MI, United States.
Sandra BoumaDepartment of Pediatrics, Division of Pediatric Pulmonology, University of Michigan, Ann Arbor, MI, United States.
Courtney IwanickiDepartment of Pediatrics, Division of Pediatric Pulmonology, University of Michigan, Ann Arbor, MI, United States.
Samya Z NasrDepartment of Pediatrics, Division of Pediatric Pulmonology, University of Michigan, Ann Arbor, MI, United States.
University of Michigan–Ann Arbor · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Children with cystic fibrosis (CF) (cwCF) suffer from inadequate weight gain, failure to thrive, and muscle weakness. The latter may be secondary to disuse atrophy (muscle wasting or reduction in muscle size associated with reduced physical activity and inflammation). Handgrip strength (HGS) is a reliable surrogate for muscle strength and lean body mass. Data from our CF center have shown an association between low HGS and forced expiratory volume in 1 s (FEV

Indexed as

CFexerciseFEV1grip strengthpediatrics-children

Identifiers

PMID35096701
PMCPMC8793844
OpenAlexW4205349599

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.