Outcomes of Short Antibiotic Courses for Gram-Negative Bloodstream Infections in Solid Organ Transplant Recipients-A

Muath Alotaibi1,2, Abdulellah Almohaya3,4,5, Roni Bitterman2

  • 1Department of Medicine, King Faisal Specialist Hospital and Research Centre, Madinah, Saudi Arabia.

Abstract

Insights

Short antibiotic courses for gram-negative bloodstream infections (GN-BSIs) in solid organ transplant (SOT) recipients showed no significant difference in mortality or clinical failure. More research is needed due to limited sample sizes.

Area of Science:

  • Infectious Diseases
  • Transplant Medicine
  • Pharmacology

Background:

  • Gram-negative bloodstream infections (GN-BSIs) are a significant cause of mortality.
  • Optimizing antibiotic duration is crucial, especially for immunocompromised patients like solid organ transplant (SOT) recipients.
  • Limited data exist on optimal antibiotic durations for GN-BSIs in SOT recipients.

Purpose of the Study:

  • To evaluate the effectiveness of short versus long antibiotic courses for treating GN-BSIs in SOT recipients.
  • To synthesize evidence from existing randomized controlled trials (RCTs) and observational studies.

Main Methods:

  • Systematic review adhering to PRISMA guidelines.
  • Searched four databases for RCTs and observational studies up to June 2025.
  • Conducted random-effects meta-analyses assessing 90-day mortality and clinical failure, with risk of bias assessment.

Main Results:

  • Seven studies (2 RCTs, 5 cohorts) with 249 SOT patients were analyzed.
  • In RCTs, short-course antibiotics showed trends towards lower mortality and clinical failure, but not statistically significant.
  • Cohort studies indicated lower mortality with short courses, but higher clinical failure; evidence certainty was moderate to very low.

Conclusions:

  • No statistically significant differences in outcomes were found between short and long antibiotic courses for GN-BSIs in SOT recipients.
  • The limited sample size of current studies prevents definitive conclusions.
  • Larger, high-quality trials are necessary to guide antibiotic duration in this vulnerable population.

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