Evidence map›Paper›PMID 29314745›Full record

ArticlePediatric pulmonology2018

Stenotrophomonas maltophilia: A marker of lung disease severity.

Laura Berdah, Jessica Taytard, Sophie Leyronnas, Annick Clement, Pierre-Yves Boelle, Harriet Corvol

Open access · bronzeAbstract read
In one paragraph

Article in Pediatric pulmonology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Stenotrophomonas maltophilia in people with Cystic Fibrosis: a systematic review of prevalence, risk factors and management.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2023
    Pooled it
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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

6 authors at 2 institutions in 1 country.

Laura BerdahAPHP, Hôpital Trousseau, Cystic Fibrosis Center, Paris, France.
Jessica TaytardAPHP, Hôpital Trousseau, Cystic Fibrosis Center, Paris, France.ORCID 0000-0002-7552-3880
Sophie LeyronnasAPHP, Hôpital Trousseau, Cystic Fibrosis Center, Paris, France.
Annick ClementAPHP, Hôpital Trousseau, Cystic Fibrosis Center, Paris, France.
Pierre-Yves BoelleSorbonne Universités, UPMC University Paris 06, INSERM, Institut Pierre Louis d'épidémiologie et de Santé Publique (IPLESP UMRS 1136), Paris, France.
Harriet CorvolAPHP, Hôpital Trousseau, Cystic Fibrosis Center, Paris, France.ORCID 0000-0002-7026-7523
Inserm · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile the prevalence of Stenotrophomonas maltophilia lung infection in cystic fibrosis (CF) patients has increased in the last decades, its pathogenicity remains controversial. The aim of this study was to investigate the effects of S. maltophilia initial infection on the progression of lung disease in CF children.

methodsThis case-control retrospective study took place in a pediatric CF center. A total of 23 cases defined by at least one sputum culture positive for S. maltophilia, were matched for age, sex, and CFTR mutations to 23 never infected CF controls. The clinical data were collected for 2 years before and after S. maltophilia initial infection and comprised lung function analyses, rates of exacerbations and of antibiotic courses.

resultsCompared with controls, cases had lower lung function (P = 0.05), more frequent pulmonary exacerbations (P = 0.01), hospitalizations (P = 0.02), and intravenous antibiotic courses (P = 0.04) before S. maltophilia acquisition. In the year following S. maltophilia initial infection, lung function decline was similar in cases and controls but cases remained more severe, with more frequent pulmonary exacerbations (P = 0.01), hospitalizations (P = 0.02) and intravenous antibiotic courses (P = 0.02).

conclusionsS. maltophilia seems to be a marker of CF lung disease severity and international recommendations to reduce lung infection by this pathogen should rapidly emerge.

Indexed as

Cystic FibrosisGram-Negative Bacterial InfectionsRespiratory Tract InfectionsStenotrophomonas maltophiliaAdolescentAnti-Bacterial AgentsCase-Control StudiesChildChild, PreschoolDisease ProgressionFemaleHumansMalePrevalenceRespiratory Function TestsRetrospective StudiesAnti-Bacterial Agentschildrencystic fibrosislung functionpulmonary exacerbation Stenotrophomonas maltophilia

Identifiers

PMID29314745
PMCPMC5900908
OpenAlexW2782259167

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.