| DS-specific AML protocol (N = 59) | Non-DS AML protocol (N = 98) |
---|---|---|
Course characteristics | Â | Â |
Number with neutropenia (ANC <0.5 x109) at start of course (%) | 5 (8.4) | 12 (12.5)a |
Median days with neutropenia (IQR) | 11.0 (3.0, 21.0) | 16.0 (7.0, 25.0) |
Median days receiving steroids (IQR) | 0.0 (0.0, 2.0) | 2.0 (0.0, 5.0) |
Supportive care | Â | Â |
Co-trimoxazole prophylaxis (%) | 41 (69.5) | 66 (67.4) |
Fluconazole prophylaxis (%) | 28 (47.5) | 39 (39.8) |
Infection outcomes b | Â | Â |
Microbiologically documented sterile site infection (%) | 7 (11.9) | 14 (14.3) |
Bacteremia (%) | 6 (10.2) | 10 (10.2) |
  Sterile site Gram-positive bacteria (%) | 5 (8.5) | 9 (9.2) |
  Sterile site Gram-negative bacteria (%) | 2 (3.4) | 6 (6.1) |
  Sterile site fungus (%) | 0 (0.0) | 1 (1.0) |
Clinically documented infection (%) | 7 (11.9) | 29 (29.6) |
Sepsis (%) | 1 (1.7) | 3 (3.1) |
Infectious death (%) | 0 (0.0) | 0 (0.0) |