Evidence map›Paper›PMID 32317365›Full record

ArticleBMJ case reports2020

Microbial clues lead to a diagnosis of cystic fibrosis in late adulthood.

Colm Kerr, David Morrissy, Mary Horgan, Barry J Plant

Open access · greenAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in BMJ case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 3 institutions in 1 country.

Colm KerrSchool of Medicine, Trinity College Dublin Faculty of Health Sciences, Dublin, Ireland.ORCID http://orcid.org/0000-0001-9976-8033
David MorrissyHRB Clinical Research Facility, University College Cork, Cork, Ireland.
Mary HorganDepartment of Infectious Diseases, Cork University Hospital Group, Cork, Ireland.
Barry J PlantHRB Clinical Research Facility, University College Cork, Cork, Ireland b.plant@ucc.ie.
University College Cork · IECork University Hospital · IETrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) is the most common life-limiting autosomal recessive genetic disorder among Caucasian populations. The majority of CF cases are diagnosed in childhood; however, increasing numbers of adults are being diagnosed with the condition. We present the case of a 65-year-old Irish woman presenting with a chronic cough and a history of recurrent respiratory tract infections.

Indexed as

AgedAminophenolsBronchoalveolar Lavage FluidCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorFemaleGenetic TestingHumansMutationQuinolonesScedosporiumStaphylococcus aureusStenotrophomonas maltophiliaAminophenolsCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorivacaftorQuinolonescystic fibrosisgeneticsinfectious diseasesrespiratory medicinerespiratory system

Identifiers

PMID32317365
PMCPMC7202750
OpenAlexW3017327711

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.