Evidence map›Paper›PMID 34844966›Full record

ArticleBMJ case reports2021

Cystic fibrosis: a diagnosis in an adolescent.

Monica Bennett, Andreia Filipa Nogueira, Maria Manuel Flores, Teresa Reis Silva

Abstract readCase Reports
In one paragraph

Article in BMJ case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Monica BennettPediatric, Centro Hospitalar e Universitario de Coimbra EPE, Coimbra, Portugal acinomaicila@gmail.com.ORCID http://orcid.org/0000-0001-9674-0879
Andreia Filipa NogueiraPediatric, Centro Hospitalar e Universitario de Coimbra EPE, Coimbra, Portugal.
Maria Manuel FloresPediatric, Centro Hospitalar do Baixo Vouga EPE, Aveiro, Aveiro, Portugal.
Teresa Reis SilvaPediatric, Centro Hospitalar e Universitario de Coimbra EPE, Coimbra, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most patients with cystic fibrosis (CF) develop multisystemic clinical manifestations, the minority having mild or atypical symptoms. We describe an adolescent with chronic cough and purulent rhinorrhoea since the first year of life, with diagnoses of asthma, allergic rhinitis and chronic rhinosinusitis. Under therapy with long-acting bronchodilators, antihistamines, inhaled corticosteroids, antileukotrienes and several courses of empirical oral antibiotic therapy, there was no clinical improvement. There was no reference to gastrointestinal symptoms. Due to clinical worsening, extended investigations were initiated, which revealed

Indexed as

Cystic FibrosisAdolescentCystic Fibrosis Transmembrane Conductance RegulatorHumansMutationPseudomonas aeruginosaRespiratory SystemCystic Fibrosis Transmembrane Conductance Regulatorcystic fibrosispneumonia (respiratory medicine)

Identifiers

PMID34844966
PMCPMC8634203

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.