Evidence map›Paper›PMID 42427916›Full record

ArticleRespirology case reports2026

Delayed Diagnosis of Cystic Fibrosis and Nontuberculous Mycobacterial Infection in Refractory CRSwNP.

Robert Greig, Philipp Suter, Rory Chan, David Connell, Brian Lipworth

Abstract read
In one paragraph

Article in Respirology case reports, 2026. 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
–field-weighted citation impact
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.

  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

5 authors.

Robert GreigScottish Centre for Respiratory Research University of Dundee Dundee UK.ORCID https://orcid.org/0000-0001-7668-286X
Philipp SuterScottish Centre for Respiratory Research University of Dundee Dundee UK.
Rory ChanScottish Centre for Respiratory Research University of Dundee Dundee UK.
David ConnellNinewells Respiratory Department NHS Tayside Dundee UK.
Brian LipworthScottish Centre for Respiratory Research University of Dundee Dundee UK.ORCID https://orcid.org/0000-0002-8140-2014

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis is a systemic disease inherited in an autosomal recessive pattern associated with multisystem pathology including increased mucus viscosity and consequently reduced clearance. Here we report a case of a 31 year old woman who experienced several years of treatment-resistant type 2 low chronic rhinosinusitis. Repeat chest imaging revealed tree-in-bud change leading to a diagnosis of

Indexed as

chronic rhinosinosituscystic fibrosismycobacterium abcessustype 2 inflammation

Identifiers

PMID42427916
PMCPMC13349531

What OpenQuestion holds

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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.