Evidence map›Paper›PMID 30347072›Full record

Trial reportJAMA2018

Decontamination Strategies and Bloodstream Infections With Antibiotic-Resistant Microorganisms in Ventilated Patients: A Randomized Clinical Trial.

Bastiaan H Wittekamp, Nienke L Plantinga, Ben S Cooper, Joaquin Lopez-Contreras, Pere Coll, Jordi Mancebo, Matt P Wise, Matt P G Morgan, Pieter Depuydt, Jerina Boelens and 23 more

2 registry-linked trialsOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 78 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 6 pooled it
12.1field-weighted citation impact, top 1% 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.

NCT02208154 phase3completednot on this map

RGNOSIS: Ecological Effects of Decolonisation Strategies in Intensive Care

TypeinterventionalSponsorMJM BontenRan2013 to 2017Enrolled8,665ConditionsICU-ecology (Multidrug Resistant Bacteria), ICU-acquired BacteraemiaArmsChlorhexidine oral care (CHX-Oro), Selective oropharyngeal decontamination (SOD), Selective Digestive Decontamination (SDD)
NCT04431934 naunknown statusnot on this mapstarted 2020, after this paper: background citation

Open-label, Randomized Study to Assess the Efficacy of a Probiotic or Fecal Microbiota Transplantation (FMT) on the Eradication of Rectal Multidrug-resistant Gram-negative Bacilli (MDR-GNB) Carriage (PROFTMDECOL)

TypeinterventionalSponsorHospital Clinic of BarcelonaRan2020 to 2023Enrolled437ConditionsCARRIER STATEArmsPROBIOTIC, FMT REGIMEN
3 · Its place in the literature

Who cites it

78 citing papers in PubMed, 6 syntheses or guidelines pooled it, 180 citations in OpenAlex.

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  13. Liver Cyst Infection Outcomes in Patients With ADPKD.Kidney international reports · 2026
    Article
  14. Optimal antibiotic use in the intensive care unit.Critical care (London, England) · 2025
    Review
  15. Effect of the implementation of a selective digestive decontamination protocol in an intensive care unit.Journal of critical care medicine (Universitatea de Medicina si Farmacie din Targu-Mures) · 2025
    Article
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18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors at 19 institutions in 9 countries.

Bastiaan H WittekampIntensive Care Center and Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.
Nienke L PlantingaMedical Microbiology and Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.
Ben S CooperCentre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, England.
Joaquin Lopez-ContrerasInfectious Diseases-Internal Medicine, Hospital de Sant Pau-Universitat Autònoma de Barcelona, Barcelona, Spain.
Pere CollDepartment of Microbiology, Hospital de Sant Pau-Universitat Autònoma de Barcelona, Barcelona, Spain.
Jordi ManceboDepartment of Intensive Care, Hospital de Sant Pau-Universitat Autònoma de Barcelona, Barcelona, Spain.
Matt P WiseAdult Critical Care, University Hospital of Wales, Cardiff, Wales.
Matt P G MorganAdult Critical Care, University Hospital of Wales, Cardiff, Wales.
Pieter DepuydtIntensive Care, Ghent University Hospital, Ghent, Belgium.
Jerina BoelensDepartment of Laboratory Medicine, Ghent University Hospital, Ghent, Belgium.
Thierry DugernierDepartment of Intensive Care Medicine, Clinique Saint Pierre, Ottignies-Louvain-la-Neuve, Belgium.
Valérie VerbelenMicrobiology Department, Clinique Saint Pierre, Ottignies-Louvain-la-Neuve, Belgium.
Philippe G JorensIntensiveCare Medicine, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
Walter VerbruggheIntensiveCare Medicine, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
Surbhi Malhotra-KumarLaboratory of Medical Microbiology, Vaccine, & Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.
Pierre DamasDepartment of Intensive Care Medicine, CHU Liège, Liege, Belgium.
Cécile MeexClinical Microbiology, CHU Liège, Liege, Belgium.
Kris LeleuAnesthesiology and Critical Care, AZ Sint Jan Bruges, Bruges, Belgium.
Anne-Marie van den AbeeleMicrobiology Laboratory, Saint-Lucas Hospital Ghent, Ghent, Belgium.
Ana Filipa Gomes Pimenta de MatosServiço de Medicina Intensiva, Centro Hospitalar de Trás-os-Montes os Montes e Alto Douro, Vila Real, Portugal.
Sara Fernández MéndezMedical Intensive Care Unit, Hospital Clinic of Barcelona, Barcelona, Spain.
Andrea Vergara GomezMicrobiology Department, Hospital Clinic of Barcelona, Barcelona, Spain.
Viktorija TomicLaboratory for Respiratory Microbiology, University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
Franc SifrerIntensive Care Unit, University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
Esther Villarreal TelloIntensive Care Unit, Hospital Universitario La Fe, Valencia, Spain.
Jesus Ruiz RamosIntensive Care Unit, Hospital Universitario La Fe, Valencia, Spain.
Irene AragaoIntensive Care (UCIP), Hospital Santo Antonio-Centro Hospitalar do Porto (CHP), Porto, Portugal.
Claudia SantosMicrobiology Laboratory, Hospital Santo Antonio-Centro Hospitalar do Porto (CHP), Porto, Portugal.
Roberta H M SperningDepartment of Microbiology, Azienda Ospedaliera San Camillo Forlanini, Rome, Italy.
Patrizia CoppadoroIntensive Care Unit, Azienda Ospedaliera San Camillo Forlanini, Rome, Italy.
Giuseppe NardiDepartment of Anesthesia and Intensive Care, Ospedale Infermi RIMINI-AUSL della Romagna, Rimini, Italy.
Christian Brun-BuissonMedical Intensive Care and Infection Control Unit, CHU Henri Mondor & University Paris Est Créteil, Paris, France.
Marc J M BontenMedical Microbiology and Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.
University Medical Center Utrecht · NLUniversity of Antwerp · BEAzienda Ospedaliera San Camillo-Forlanini · ITCentro Hospitalar do Porto · PTClinique Saint Pierre · BEGhent University Hospital · BEHospital Clínic de Barcelona · ESHospital Universitari i Politècnic La Fe · ESUniversitat Autònoma de Barcelona · ESUniversity Clinic of Pulmonary and Allergic Diseases Golnik · SIUniversity Hospital of Wales · GBUniversity of Liège · BEAngkor Hospital for Children · KHAZ Sint-Jan · BEAZ Sint-Lucas · BECentre Hospitalier Universitaire Henri-Mondor · FRCentro Hospitalar de Trás os Montes e Alto Douro · PTHospital de Sant Pau · ESOspedale Infermi di Rimini · IT

Funding

Medical Research Council MR/R004536/1
6 · The paper itself

Abstract

Importance: The effects of chlorhexidine (CHX) mouthwash, selective oropharyngeal decontamination (SOD), and selective digestive tract decontamination (SDD) on patient outcomes in ICUs with moderate to high levels of antibiotic resistance are unknown. Objective: To determine associations between CHX 2%, SOD, and SDD and the occurrence of ICU-acquired bloodstream infections with multidrug-resistant gram-negative bacteria (MDRGNB) and 28-day mortality in ICUs with moderate to high levels of antibiotic resistance. Design, Setting, and Participants: Randomized trial conducted from December 1, 2013, to May 31, 2017, in 13 European ICUs where at least 5% of bloodstream infections are caused by extended-spectrum β-lactamase-producing Enterobacteriaceae. Patients with anticipated mechanical ventilation of more than 24 hours were eligible. The final date of follow-up was September 20, 2017. Interventions: Standard care was daily CHX 2% body washings and a hand hygiene improvement program. Following a baseline period from 6 to 14 months, each ICU was assigned in random order to 3 separate 6-month intervention periods with either CHX 2% mouthwash, SOD (mouthpaste with colistin, tobramycin, and nystatin), or SDD (the same mouthpaste and gastrointestinal suspension with the same antibiotics), all applied 4 times daily. Main Outcomes and Measures: The occurrence of ICU-acquired bloodstream infection with MDRGNB (primary outcome) and 28-day mortality (secondary outcome) during each intervention period compared with the baseline period. Results: A total of 8665 patients (median age, 64.1 years; 5561 men [64.2%]) were included in the study (2251, 2108, 2224, and 2082 in the baseline, CHX, SOD, and SDD periods, respectively). ICU-acquired bloodstream infection with MDRGNB occurred among 144 patients (154 episodes) in 2.1%, 1.8%, 1.5%, and 1.2% of included patients during the baseline, CHX, SOD, and SDD periods, respectively. Absolute risk reductions were 0.3% (95% CI, -0.6% to 1.1%), 0.6% (95% CI, -0.2% to 1.4%), and 0.8% (95% CI, 0.1% to 1.6%) for CHX, SOD, and SDD, respectively, compared with baseline. Adjusted hazard ratios were 1.13 (95% CI, 0.68-1.88), 0.89 (95% CI, 0.55-1.45), and 0.70 (95% CI, 0.43-1.14) during the CHX, SOD, and SDD periods, respectively, vs baseline. Crude mortality risks on day 28 were 31.9%, 32.9%, 32.4%, and 34.1% during the baseline, CHX, SOD, and SDD periods, respectively. Adjusted odds ratios for 28-day mortality were 1.07 (95% CI, 0.86-1.32), 1.05 (95% CI, 0.85-1.29), and 1.03 (95% CI, 0.80-1.32) for CHX, SOD, and SDD, respectively, vs baseline. Conclusions and Relevance: Among patients receiving mechanical ventilation in ICUs with moderate to high antibiotic resistance prevalence, use of CHX mouthwash, SOD, or SDD was not associated with reductions in ICU-acquired bloodstream infections caused by MDRGNB compared with standard care. Trial Registration: ClinicalTrials.gov Identifier: NCT02208154.

Indexed as

Respiration, ArtificialAdultAgedAged, 80 and overAnti-Infective AgentsBacteremiaChlorhexidineCross InfectionDisinfectionDrug Resistance, BacterialFemaleGastrointestinal TractGram-Negative Bacterial InfectionsHospital MortalityHumansIntensive Care UnitsAnti-Infective AgentsChlorhexidineMouthwashes

Identifiers

PMID30347072
PMCPMC6583563
OpenAlexW2896346062

What OpenQuestion holds

Textmetadata
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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.