Evidence map›Paper›PMID 39672981›Full record

ReviewEuropean journal of pediatrics2024

Antibiotic treatment of bacterial lung infections in cystic fibrosis.

Giovanni Taccetti, Vito Terlizzi, Silvia Campana, Daniela Dolce, Novella Ravenni, Cristina Fevola, Michela Francalanci, Valeria Galici, Anna Silvia Neri

Abstract readReview
In one paragraph

Review in European journal of pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

9 authors.

Giovanni TaccettiMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy. giovanni.taccetti@meyer.it.ORCID http://orcid.org/0000-0002-9448-5381
Vito TerlizziMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.
Silvia CampanaMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.
Daniela DolceMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.
Novella RavenniMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.
Cristina FevolaMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.
Michela FrancalanciMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.
Valeria GaliciMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.
Anna Silvia NeriMeyer Children's Hospital IRCCS, Cystic Fibrosis Regional Reference Centre, 50139, Florence, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial infections of the lower airways are the main cause of mortality and morbidity in cystic fibrosis. The most frequently isolated pathogens are S. aureus and P. aeruginosa; bacterial co-infections are frequently observed. The aim of this review is to provide, in the current context, the indications regarding the best antibiotic strategy to adopt in subjects affected by CF infected with the most common pathogens. We selected relevant publications (guidelines, systematic reviews and clinical studies published so far on these topics) and we analysed the sampling methods used and antibiotic strategies adopted. Oropharyngeal sampling methods are considered less sensitive for pathogen detection than sputum. In non-expectorating people, induced sputum is considered equivalent to two-lobe bronchoalveolar lavage, which is considered invasive. Antibiotic treatment against the main pathogens can consist in eradication treatment in the early stages of infection, chronic suppressive therapy and treatment of the pulmonary exacerbations. This scheme is valid for P. aeruginosa but remains to be demonstrated for the other pathogens. For S. aureus, no evidence-based therapeutic strategies on how to treat the different stages of bacterial infection have been established with certainty. With regard to the treatment of the other classic pathogens (B. cepacia complex, A. xylosoxidans and S. maltophilia), no evidence-based indications exist and decision is left to the clinician. The recent introduction of highly effective modulators on the CFTR protein, in addition to the favourable effects described in regulatory trials, has led to a reduction in bacterial isolations; the real effect of which in clinical practice has still to be assessed on the basis of scientific data.

conclusionsThe reliability of culture examination depends on sampling methods, and expectorated sputum continues to be the best method as it is simple and non-invasive. P. aeruginosa is the pathogen for which antibiotic strategies for the various stages of infection appear best established, and the efficacy of early eradication treatment and chronic suppressive therapy have been underlined in clinical trials and systematic reviews. The recent introduction of modulators into clinical practice, despite their widely described efficacy, has not yet led to suggestions for changes in antibiotic strategies against the pathogens most frequently isolated.

Indexed as

Anti-Bacterial AgentsCystic FibrosisBacterial InfectionsHumansPseudomonas aeruginosaPseudomonas InfectionsRespiratory Tract InfectionsSputumAnti-Bacterial AgentsAntibioticCystic fibrosisLungPseudomonas aeruginosaStaphylococcus aureus

Identifiers

PMID39672981
PMCPMC11645307

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.