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Decontamination Strategies and Bloodstream Infections With Antibiotic-Resistant Microorganisms in Ventilated Patients: A Randomized Clinical Trial.
Wittekamp, Bastiaan H; Plantinga, Nienke L; Cooper, Ben S; Lopez-Contreras, Joaquin; Coll, Pere; Mancebo, Jordi; Wise, Matt P; Morgan, Matt P G; Depuydt, Pieter; Boelens, Jerina; Dugernier, Thierry; Verbelen, Valérie; Jorens, Philippe G; Verbrugghe, Walter; Malhotra-Kumar, Surbhi; Damas, Pierre; Meex, Cécile; Leleu, Kris; van den Abeele, Anne-Marie; Gomes Pimenta de Matos, Ana Filipa; Fernández Méndez, Sara; Vergara Gomez, Andrea; Tomic, Viktorija; Sifrer, Franc; Villarreal Tello, Esther; Ruiz Ramos, Jesus; Aragao, Irene; Santos, Claudia; Sperning, Roberta H M; Coppadoro, Patrizia; Nardi, Giuseppe; Brun-Buisson, Christian; Bonten, Marc J M.
Afiliação
  • Wittekamp BH; Intensive Care Center and Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.
  • Plantinga NL; Medical Microbiology and Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.
  • Cooper BS; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, England.
  • Lopez-Contreras J; Infectious Diseases-Internal Medicine, Hospital de Sant Pau-Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Coll P; Department of Microbiology, Hospital de Sant Pau-Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Mancebo J; Department of Intensive Care, Hospital de Sant Pau-Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Wise MP; Adult Critical Care, University Hospital of Wales, Cardiff, Wales.
  • Morgan MPG; Adult Critical Care, University Hospital of Wales, Cardiff, Wales.
  • Depuydt P; Intensive Care, Ghent University Hospital, Ghent, Belgium.
  • Boelens J; Department of Laboratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • Dugernier T; Department of Intensive Care Medicine, Clinique Saint Pierre, Ottignies-Louvain-la-Neuve, Belgium.
  • Verbelen V; Microbiology Department, Clinique Saint Pierre, Ottignies-Louvain-la-Neuve, Belgium.
  • Jorens PG; IntensiveCare Medicine, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
  • Verbrugghe W; IntensiveCare Medicine, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.
  • Malhotra-Kumar S; Laboratory of Medical Microbiology, Vaccine, & Infectious Disease Institute, University of Antwerp, Antwerp, Belgium.
  • Damas P; Department of Intensive Care Medicine, CHU Liège, Liege, Belgium.
  • Meex C; Clinical Microbiology, CHU Liège, Liege, Belgium.
  • Leleu K; Anesthesiology and Critical Care, AZ Sint Jan Bruges, Bruges, Belgium.
  • van den Abeele AM; Microbiology Laboratory, Saint-Lucas Hospital Ghent, Ghent, Belgium.
  • Gomes Pimenta de Matos AF; Serviço de Medicina Intensiva, Centro Hospitalar de Trás-os-Montes os Montes e Alto Douro, Vila Real, Portugal.
  • Fernández Méndez S; Medical Intensive Care Unit, Hospital Clinic of Barcelona, Barcelona, Spain.
  • Vergara Gomez A; Microbiology Department, Hospital Clinic of Barcelona, Barcelona, Spain.
  • Tomic V; Laboratory for Respiratory Microbiology, University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
  • Sifrer F; Intensive Care Unit, University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia.
  • Villarreal Tello E; Intensive Care Unit, Hospital Universitario La Fe, Valencia, Spain.
  • Ruiz Ramos J; Intensive Care Unit, Hospital Universitario La Fe, Valencia, Spain.
  • Aragao I; Intensive Care (UCIP), Hospital Santo Antonio-Centro Hospitalar do Porto (CHP), Porto, Portugal.
  • Santos C; Microbiology Laboratory, Hospital Santo Antonio-Centro Hospitalar do Porto (CHP), Porto, Portugal.
  • Sperning RHM; Department of Microbiology, Azienda Ospedaliera San Camillo Forlanini, Rome, Italy.
  • Coppadoro P; Intensive Care Unit, Azienda Ospedaliera San Camillo Forlanini, Rome, Italy.
  • Nardi G; Department of Anesthesia and Intensive Care, Ospedale Infermi RIMINI-AUSL della Romagna, Rimini, Italy.
  • Brun-Buisson C; Medical Intensive Care and Infection Control Unit, CHU Henri Mondor & University Paris Est Créteil, Paris, France.
  • Bonten MJM; Medical Microbiology and Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, Netherlands.
JAMA ; 320(20): 2087-2098, 2018 11 27.
Article em En | MEDLINE | ID: mdl-30347072
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 ß-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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Respiração Artificial / Clorexidina / Desinfecção / Infecções por Bactérias Gram-Negativas / Bacteriemia / Anti-Infecciosos / Antissépticos Bucais Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Respiração Artificial / Clorexidina / Desinfecção / Infecções por Bactérias Gram-Negativas / Bacteriemia / Anti-Infecciosos / Antissépticos Bucais Tipo de estudo: Clinical_trials / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda