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Antimicrobial prophylaxis in acute leukaemia: prospective randomized study comparing two methods of selective
Summary
Selective decontamination of the digestive tract using cotrimoxazole, polymyxin B, and nystatin (regimen A) showed better oropharyngeal pathogen control than regimen B in acute leukemia patients. Both regimens effectively prevented severe gram-negative infections.
Area of Science:
- Infectious Diseases
- Hematology
- Microbiology
Background:
- Patients with acute leukemia undergoing remission induction therapy are at high risk for infections.
- Selective decontamination of the digestive tract (SDD) is a strategy to prevent infections in immunocompromised patients.
Purpose of the Study:
- To compare the efficacy of two different SDD regimens in patients with acute leukemia.
- To evaluate the impact of SDD on the occurrence of gram-negative infections and colonization.
Main Methods:
- A prospective randomized study involving 78 acute leukemia patients during remission induction therapy.
- Two SDD regimens were compared: Group A (cotrimoxazole, polymyxin B, nystatin) and Group B (nalidixic acid, polymyxin B, neomycin, nystatin).
- Gastrointestinal and oropharyngeal decontamination, acquired infections, and gram-negative bacteremia were monitored.
Main Results:
- Both regimens effectively decontaminated the gastrointestinal tract from potential pathogens.
- Regimen A demonstrated significantly better oropharyngeal decontamination of Enterobacteriaceae (P < 0.01).
- Fewer than 10% of acquired infections were caused by gram-negative bacilli in both groups, with no gram-negative septicaemia.
- The median time to the first acquired infection was shorter in Group A (17 days) compared to Group B (36 days) (P < 0.05).
Conclusions:
- Regimen A may be more effective than regimen B for selective decontamination of the digestive tract in acute leukemia patients.
- Both SDD regimens reliably prevent severe gram-negative infections.
- Targeted oropharyngeal decontamination is crucial in managing infection risk during leukemia therapy.