Evidence map›Paper›PMID 29143200›Full record

ArticlePediatric radiology2018

Structural and perfusion magnetic resonance imaging of the lung in cystic fibrosis.

Christina Amaxopoulou, Ralph Gnannt, Kai Higashigaito, Andreas Jung, Christian J Kellenberger

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Pediatric radiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. 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

5 authors at 2 institutions in 1 country.

Christina AmaxopoulouDepartment of Diagnostic Imaging, University Children's Hospital Zürich, Steinwiesstr. 75, 8032, Zürich, CH, Switzerland. christina.amaxopoulou@gmail.com.
Ralph GnanntDepartment of Diagnostic Imaging, University Children's Hospital Zürich, Steinwiesstr. 75, 8032, Zürich, CH, Switzerland.
Kai HigashigaitoInstitute of Diagnostic and Interventional Radiology, University Hospital Zürich, Zürich, Switzerland.
Andreas JungChildren's Research Center, University Children's Hospital Zürich, Zürich, Switzerland.
Christian J KellenbergerDepartment of Diagnostic Imaging, University Children's Hospital Zürich, Steinwiesstr. 75, 8032, Zürich, CH, Switzerland.
University Children's Hospital Zurich · CHUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBecause of its absence of ionising radiation and possibility for obtaining functional information, MRI is promising for assessing lung disease in children who require repetitive imaging for long-term follow-up.

objectiveTo describe MRI findings in children with cystic fibrosis and evaluate semi-quantitative dynamic contrast-enhanced lung perfusion. MATERIALS AND

methodsWe retrospectively compared lung MRI in 25 children and young adults with cystic fibrosis (median age 3.7 years) to 12 children (median age 2 years) imaged for other pathologies. MRI at 1.5 T included respiratory-gated sequences and contrast-enhanced lung perfusion imaging. We described and graded any morphologic change. Signal enhancement and time to peak values of perfusion abnormalities were compared to those of normally enhancing lung parenchyma.

resultsFrequent findings in patients with cystic fibrosis were bronchial wall thickening (24/25, 96%), areas of consolidation (22/25, 88%), enlarged lymph nodes (20/25, 80%), bronchiectasis (5/25, 20%) and mucus plugging (3/25, 12%). Compared to normally enhancing lung, perfusion defects (21/25, 84%), characterised by decreased enhancement, showed prolonged time to peak. Areas of consolidation showed increased enhancement. While time to peak of procedure-related atelectasis was not significantly different from that of normal lung, disease-related consolidation showed prolonged time to peak (P=0.01).

conclusionLung MRI demonstrates structural and perfusion abnormalities in children and young people with cystic fibrosis. Semi-quantitative assessment of dynamic contrast-enhanced perfusion imaging might allow differentiation between procedure-related atelectasis and disease-related consolidation.

Indexed as

AdolescentChildChild, PreschoolContrast MediaCystic FibrosisFemaleHumansInfantLungMagnetic Resonance ImagingMaleMeglumineOrganometallic CompoundsRespiratory-Gated Imaging TechniquesRetrospective StudiesYoung AdultContrast Mediagadoterate meglumineMeglumineOrganometallic CompoundsAdolescentsChildrenCystic fibrosisFunctional magnetic resonance imagingLungPerfusion imaging

Identifiers

PMID29143200
OpenAlexW2768691818

What OpenQuestion holds

Textmetadata
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.