Cited by 813Nosocomial Infections in ICUSepsis Diagnosis and TreatmentAntifungal resistance and susceptibility

Decontamination of the digestive tract and oropharynx in ICU patients

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de Smet, A.M.G.A., Kluytmans, J.A.J.W., Cooper, B.S., Mascini, E.M., Benus, R.F.J., van der Werf, T.S., van der Hoeven, J.G., Pickkers, P. +33 more·2009·New England Journal of Medicine

Abstract

BACKGROUND: Selective digestive tract decontamination (SDD) and selective oropharyngeal decontamination (SOD) are infection-prevention measures used in the treatment of some patients in intensive care, but reported effects on patient outcome are conflicting. METHODS: We evaluated the effectiveness of SDD and SOD in a crossover study using cluster randomization in 13 intensive care units (ICUs), all in The Netherlands. Patients with an expected duration of intubation of more than 48 hours or an expected ICU stay of more than 72 hours were eligible. In each ICU, three regimens (SDD, SOD, and standard care) were applied in random order over the course of 6 months. Mortality at day 28 was the primary end point. SDD consisted of 4 days of intravenous cefotaxime and topical application of tobramycin, colistin, and amphotericin B in the oropharynx and stomach. SOD consisted of oropharyngeal application only of the same antibiotics. Monthly point-prevalence studies were performed to analyze antibiotic resistance. RESULTS: A total of 5939 patients were enrolled in the study, with 1990 assigned to standard care, 1904 to SOD, and 2045 to SDD; crude mortality in the groups at day 28 was 27.5%, 26.6%, and 26.9%, respectively. In a random-effects logistic-regression model with age, sex, Acute Physiology and Chronic Health Evaluation (APACHE II) score, intubation status, and medical specialty used as covariates, odds ratios for death at day 28 in the SOD and SDD groups, as compared with the standard-care group, were 0.86 (95% confidence interval [CI], 0.74 to 0.99) and 0.83 (95% CI, 0.72 to 0.97), respectively. CONCLUSIONS: In an ICU population in which the mortality rate associated with standard care was 27.5% at day 28, the rate was reduced by an estimated 3.5 percentage points with SDD and by 2.9 percentage points with SOD. (Controlled Clinical Trials number, ISRCTN35176830.)

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Crossref · 10.1056/nejmoa0800394

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Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Gut dysbiosis amplifies organ dysfunction through gut-brain, gut-lung, gut-liver, gut-kidney, and gut-heart/spleen axes.

    “Dysbiosis in turn amplifies organ dysfunction through gut-brain, gut-lung, gut-liver, gut-kidney, and gut-heart/spleen axes.”

    From Progress on the correlation between sepsis and gut microbiota: a narrative review (2026) · cites this paper as de Smet et al., 2009

    The Adverse Events section reports effects of digestive-tract and oropharyngeal decontamination on bacterial carriage and antibiotic resistance. Neither those passages nor searches for dysbiosis and the named gut–organ axes address a mechanism by which dysbiosis amplifies organ dysfunction. Page numbers were not supplied in our copy. (LLM, conf=0.76)

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Research works printed but not linked: 2

  1. Bootsma M, Hoes A. Selective decontami- nation of digestive tract in intensive care. Lancet 2003;362:2118-9.
  2. Kerver AJH, Rommes JH, Mevissen- 25. Verhage EAE, et al. Prevention of coloni- zation and infection in critically ill pa- tients: a prospective randomized study. Crit Care Med 1988;16:1087-93.

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Authors
de Smet, A. M. G. A., Kluytmans, J. A. J. W., Cooper, B. S., Mascini, E. M., Benus, R. F. J., van der Werf, T. S., van der Hoeven, J. G., Pickkers, P., Bogaers-Hofman, D., van der Meer, N. J. M., Bernards, A. T., Kuijper, E. J., Joore, J. C. A., Leverstein-van Hall, M. A., Bindels, A. J. G. H., Jansz, A. R., Wesselink, R. M. J., de Jongh, B. M., Dennesen, P. J. W., van Asselt, G. J., te Velde, L. F., Frenay, I. H. M. E., Kaasjager, K., Bosch, F. H., van Iterson, M., Thijsen, S. F. T., Kluge, G. H., Pauw, W., de Vries, J. W., Kaan, J. A., Arends, J. P., Aarts, L. P. H. J., Sturm, P. D. J., Harinck, H. I. J., Voss, A., Uijtendaal, E. V., Blok, H. E. M., Thieme Groen, E. S., Pouw, M. E., Kalkman, C. J., & Bonten, M. J. M.
Affiliations
  • Amphia Ziekenhuis (NL)
  • Rijnstate Hospital (NL)
  • Utrecht University (NL)
  • Leiden University Medical Center (NL)
  • Diakonessenhuis hospital (NL)
  • Catharina Ziekenhuis (NL)
  • University Medical Center Utrecht (NL)
Venue
New England Journal of Medicine
Published
2009-01
Volume
360
Issue
1
Pages
20-31
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2065088137
Cited by
813
References
34
Citations by year
2026: 12 · 2025: 22 · 2024: 16 · 2023: 30 · 2022: 32 · 2021: 39 · 2020: 36 · 2019: 29 · 2018: 39 · 2017: 48 · 2016: 45 · 2015: 61 · 2014: 52 · 2013: 62 · 2012: 68
FWCI
59.40
Type
journal article
Language
en
Open access
Locations
  • New England Journal of Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
  • University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion)
  • Radboud Repository (Radboud University) (submittedVersion, other-oa)
  • Pure Amsterdam UMC (submittedVersion)
  • Radboud Repository (Radboud University) (submittedVersion)
  • University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
Topics
  • Health Sciences › Medicine › Critical Care and Intensive Care Medicine › Nosocomial Infections in ICU
  • Health Sciences › Medicine › Epidemiology › Sepsis Diagnosis and Treatment
  • Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
Keywords
selective decontamination of the digestive tract, selective oropharyngeal decontamination, intensive care unit patients, nosocomial infection prevention, 28-day mortality, cefotaxime, tobramycin, colistin, amphotericin B, antibiotic resistance, intubation, critically ill patients
MeSH terms
Aged, Anti-Bacterial Agents, Cross Infection, Decontamination, Female, Gram-Negative Bacteria, Humans, Intensive Care Units, Male, Middle Aged, Oropharynx, Respiration, Artificial, Logistic Models, Bacteremia, Critical Illness, Infection Control, Cross-Over Studies, APACHE, Gastrointestinal Tract

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