Evidence map›Paper›PMID 30901344›Full record

Trial reportPloS one2019

Methicillin-resistant Staphylococcus aureus eradication in cystic fibrosis patients: A randomized multicenter study.

Daniela Dolce, Stella Neri, Laura Grisotto, Silvia Campana, Novella Ravenni, Francesca Miselli, Erica Camera, Lucia Zavataro, Cesare Braggion, Ersilia V Fiscarelli and 16 more

Registry-linked trialOpen access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04176328 (An Open-label, Dose-escalation Study to Evaluate the Pharmacokinetics of Inhaled Teicoplanin in Cystic Fibrosis Patients), which is not on this map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
3.0field-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.

NCT04176328 phase1completednot on this map

An Open-label, Dose-escalation Study to Evaluate the Pharmacokinetics of Inhaled Teicoplanin in Cystic Fibrosis Patients

TypeinterventionalSponsorNeupharma SrlRan2019 to 2020Enrolled12ConditionsCystic FibrosisArmsTeicoplanin Sandoz 200 mg powder and solvent for solution for injection or infusion or oral solution.
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Article
  7. Drugs, Drugs, Drugs: Current Treatment Paradigms in Cystic Fibrosis Airway Infections.Journal of the Pediatric Infectious Diseases Society · 2022
    Review
  8. Review
  9. Review
  10. Molecular characterisation of methicillin-resistantEpidemiology and infection · 2020
    Article
  11. Article
  12. Antimicrobial Treatment ofFrontiers in pharmacology · 2019
    Review
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

26 authors at 8 institutions in 1 country.

Daniela DolceCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Stella NeriCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Laura GrisottoDepartment of Statistics, Computer Science and Applications "G. Parenti", University of Florence, Florence, Italy.
Silvia CampanaCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Novella RavenniCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Francesca MiselliCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Erica CameraCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Lucia ZavataroCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Cesare BraggionCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.
Ersilia V FiscarelliCystic Fibrosis Microbiology and Cystic Fibrosis Center, Children's Hospital and Research Institute Bambino Gesù, Rome, Italy.
Vincenzina LucidiCystic Fibrosis Microbiology and Cystic Fibrosis Center, Children's Hospital and Research Institute Bambino Gesù, Rome, Italy.
Lisa CarianiLaboratory for Cystic Fibrosis Microbiology, Fondazione IRCCS, Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.
Daniela GirelliLaboratory for Cystic Fibrosis Microbiology, Fondazione IRCCS, Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.
Nadia FaelliCystic Fibrosis Center, University of Milan, Fondazione IRCCS, Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.
Carla ColomboCystic Fibrosis Center, University of Milan, Fondazione IRCCS, Ca' Granda-Ospedale Maggiore Policlinico, Milan, Italy.
Cristina LucantoCystic Fibrosis and Pediatric Gastroenterology Unit, University of Messina, Messina, Italy.
Mariangela LombardoCystic Fibrosis and Pediatric Gastroenterology Unit, University of Messina, Messina, Italy.
Giuseppe MagazzùCystic Fibrosis and Pediatric Gastroenterology Unit, University of Messina, Messina, Italy.
Antonella ToscoDepartment of Translational Medical Sciences, Pediatric Cystic Fibrosis Center, Federico II University, Naples, Italy.
Valeria RaiaDepartment of Translational Medical Sciences, Pediatric Cystic Fibrosis Center, Federico II University, Naples, Italy.
Serena ManaraCenter for Integrative Biology, University of Trento, Trento, Italy.
Edoardo PasolliCenter for Integrative Biology, University of Trento, Trento, Italy.
Federica ArmaniniCenter for Integrative Biology, University of Trento, Trento, Italy.
Nicola SegataCenter for Integrative Biology, University of Trento, Trento, Italy.ORCID 0000-0002-1583-5794
Annibale BiggeriDepartment of Statistics, Computer Science and Applications "G. Parenti", University of Florence, Florence, Italy.
Giovanni TaccettiCystic Fibrosis Center, Anna Meyer Children's University Hospital, University of Florence, Florence, Italy.ORCID 0000-0002-9448-5381
Meyer Children's Hospital · ITUniversity of Trento · ITUniversity of Messina · ITBambino Gesù Children's Hospital · ITFederico II University Hospital · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUniversity of Florence · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFew studies, based on a limited number of patients using non-uniform therapeutic protocols, have analyzed Methicillin-resistant Staphylococcus aureus (MRSA) eradication.

methodsIn a randomized multicenter trial conducted on patients with new-onset MRSA infection we evaluated the efficacy of an early eradication treatment (arm A) compared with an observational group (B). Arm A received oral rifampicin and trimethoprim/sulfamethoxazole (21 days). Patients' microbiological status, FEV1, BMI, pulmonary exacerbations and use of antibiotics were assessed.

resultsSixty-one patients were randomized. Twenty-nine (47.5%) patients were assigned to active arm A and 32 (52.5%) patients to observational arm B. Twenty-nine (47.5%) patients, 10 patients in arm A and 19 in arm B, dropped out of the study. At 6 months MRSA was eradicated in 12 (63.2%) out of 19 patients in arm A while spontaneous clearance was observed in 5 (38.5%) out of 13 patients in arm B. A per-protocol analysis showed a 24.7% difference in the proportion of MRSA clearance between the two groups (z = 1.37, P(Z>z) = 0.08). Twenty-seven patients, 15 (78.9%) out of 19 in arm A and 12 (92.3%) out of 13 in arm B, were able to perform spirometry. The mean (±SD) FEV1 change from baseline was 7.13% (±14.92) in arm A and -1.16% (±5.25) in arm B (p = 0.08). In the same period the BMI change (mean ±SD) from baseline was 0.54 (±1.33) kg/m2 in arm A and -0.38 (±1.56) kg/m2 in arm B (p = 0.08). At 6 months no statistically significant differences regarding the number of pulmonary exacerbations, days spent in hospital and use of antibiotics were observed between the two arms.

conclusionsAlthough the statistical power of the study is limited, we found a 24.7% higher clearance of MRSA in the active arm than in the observational arm at 6 months. Patients in the active arm A also had favorable FEV1 and BMI tendencies.

Indexed as

Anti-Bacterial AgentsCystic FibrosisMethicillin-Resistant Staphylococcus aureusRifampinStaphylococcal InfectionsTrimethoprim, Sulfamethoxazole Drug CombinationAdolescentAdultChildChild, PreschoolFemaleHumansMaleMiddle AgedTime FactorsAnti-Bacterial AgentsRifampinTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID30901344
PMCPMC6430412
OpenAlexW2923386324

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Registered trials

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.