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Selective Digestive Decontamination in Mechanically Ventilated Patients

Key Points

  • Selective decontamination of the digestive tract (SDD) is a preventive infection control strategy involving the application of topical nonabsorbable antibiotics to the oropharynx and upper gastrointestinal tract (e.g., stomach), usually combined with a short course of intravenous antibiotics in mechanically ventilated intensive care unit (ICU) patients.
  • It is often compared with selective oral decontamination, which excludes gastric and systemic antimicrobials.
  • The principal aim of SDD is to prevent mortality from ventilator-associated pneumonia or bacteremia caused by pathogenic bacteria and secondary overgrowth with yeasts from the upper gastrointestinal tract.
  • The level of Evidence is moderate, and antimicrobial resistance is a concern. SDD is recommended only in ICU settings with a low prevalence of antibiotic resistance.1

Background

  • The framework emerged in the 1980s, initially applied to immunocompromised hematological disease patients and trauma patients.2
  • The intervention is aimed at preventing ventilator-associated pneumonia, and is based on the principle of colonization resistance, whereby the indigenous intestinal anaerobic flora provides protective effects against secondary colonization with aerobic gram-negative bacteria.3
  • The target is commonly pathogenic microorganisms, such as the following:
    • Streptococcus pneumoniae, Haemophilus influenzae, Staphylococcus aureus, Moraxella catarrhalis, Escherichia coli, Candida albicans, Klebsiella, Proteus, Morganella, Enterobacter, Citrobacter, Serratia, Acinetobacter, and Pseudomonas species.4
  • Nonabsorbable antimicrobial agents are used, as well as a short course of IV antibiotic to prevent early infections.

Treatment Population and Common Protocols

  • The Infectious Disease Society of America 2022 guidelines recommend considering SDD only in ICU settings with a low prevalence of antibiotic resistance.1
    • SDD is recognized as an “additional approach,” rather than “essential practice.”
  • SDD is standard care in the Netherlands but used sporadically in other settings.5
  • A sample protocol is below2:
    • Initiate SDD as soon as possible in mechanically ventilated patients.
    • Oral paste (colistin 10 mg, tobramycin 10 mg, nystatin 125,000 IU) is applied to the buccal mucosa and oropharynx every 6 hours.
    • Gastric suspension (colistin 100 mg, tobramycin 80 mg, nystatin 2×10^6 IU) is administered via gastric/post pyloric tube every 6 hours.
    • A four-day course of intravenous (IV) antibiotic (third-generation cephalosporin or ciprofloxacin) is administered, unless the patient is already receiving antibiotics with gram-negative coverage.
    • Continue topical components for the duration of mechanical ventilation via endotracheal tube or until day 90.
    • The institution must maintain a protocol for surveillance cultures for resistant organisms.

Level of Evidence

  • A 2022 meta-analysis of ~24,000 subjects reported a pooled risk ratio for mortality of 0.91 (95% credible interval, 0.82-0.99)6, indicating a modest mortality benefit.
    • SDD was associated with reduced risk of ventilator-associated pneumonia (RR 0.44, 95% CrI 0.36-0.54) and ICU-acquired bacteremia (RR 0.68, 95% CrI 0.57-0.81).
    • Notably, mortality benefit was observed only in trials that included an IV agent.
  • There are limited studies of effects within settings with high rates of antimicrobial resistance.4
  • Outbreaks of extended-spectrum β-lactamase-producing bacteria and colistin/aminoglycoside-resistant Enterobacteriaceae during SDD have been reported.7

Table 1. Notable findings from important publications on selective decontamination of the digestive tract
Abbreviations: SOD, selective oral decontamination; SDD, selective decontamination of the digestive tract; RCT, randomized controlled trials; ICU, intensive care unit; IV, intravenous

Concerns

  • SDD implementation requires a standardized protocol that includes dosing schedules, application techniques, and surveillance culture timing.
  • The generalizability of SDD remains controversial because many positive studies originate from Northern Europe, where low baseline antimicrobial resistance and strong stewardship practices are common.
  • Potential ecological effects on the gastrointestinal system remain an area of active investigation.
  • There is potential for adverse drug reactions, and concern for toxicity if agents, such as tobramycin, are absorbed systemically.

References

  1. Klompas M, Branson R, Cawcutt K, et al. Strategies to prevent ventilator-associated pneumonia, ventilator-associated events, and nonventilator hospital-acquired pneumonia in acute-care hospitals: 2022 update. Infect Control Hosp Epidemiol. 2022;43(6):687-713. PubMed
  2. Myburgh JA, Seppelt IM, Goodman F, et al. Effect of selective decontamination of the digestive tract on hospital mortality in critically ill patients receiving mechanical ventilation: a randomized clinical trial. JAMA. 2022;328(19):1911-21. PubMed
  3. Wittekamp BH, Plantinga NL, Cooper BS, et al. Decontamination strategies and bloodstream infections with antibiotic-resistant microorganisms in ventilated patients: a randomized clinical trial. JAMA. 2018;320(20):2087-98. PubMed
  4. Cavalcanti AB, Lisboa T, Gales AC. Is selective digestive decontamination useful for critically ill patients? Shock.2017;47(1 Suppl 1):52-7. Link
  5. Wittekamp BHJ, Oostdijk EAN, Cuthbertson BH, Brun-Buisson C, Bonten MJM. Selective decontamination of the digestive tract (SDD) in critically ill patients: a narrative review. Intensive Care Med. 2020;4 (2):343-9. PubMed
  6. Hammond NE, Myburgh J, Seppelt I, et al. Association between selective decontamination of the digestive tract and in-hospital mortality in intensive care unit patients receiving mechanical ventilation: a systematic review and meta-analysis. JAMA. 2022;328(19):1922-34. PubMed
  7. Oostdijk EAN, Kesecioglu J, Schultz MJ, et al. Effects of decontamination of the oropharynx and intestinal tract on antibiotic resistance in ICUs: a randomized clinical trial. JAMA. 2014;312(14):1429-37. PubMed
  8. de Smet AMGA, Kluytmans JAJW, Cooper BS, et al. Selective digestive tract decontamination and selective oropharyngeal decontamination and antibiotic resistance in patients in intensive-care units: an open-label, clustered group-randomised, crossover study. Lancet Infect Dis. 2011;11(5):372-80. PubMed
  9. Daneman N, Sarwar S, Fowler RA, Cuthbertson BH. Effect of selective decontamination on antimicrobial resistance in intensive care units: a systematic review and meta-analysis. Lancet Infect Dis. 2013;13(4):328-41. PubMed