Skip to main content
letter
. 2020 Dec 22;4(24):6364–6367. doi: 10.1182/bloodadvances.2020003277

Table 1.

Probability of CMV infection, mortality, and GVHD

Variable aHR 95% CI P
CMV (any viremia)
 Vancomycin* 1.225 0.626-2.397 .55
 Cefepime* 0.799 0.425-1.501 .48
 Anaerobic antibiotics* 1.427 0.929-2.192 .10
 Mismatch/unrelated donor 1.356 0.861-2.135 .19
 CMV seronegative donor 1.015 0.682-1.510 .94
 GVHD 3-4 0.759 0.360-1.603 .47
 Lymphoid malignancy 1.276 0.836-1.946 .26
Clinically significant CMV infection
 Vancomycin* 0.961 0.422-2.193 .93
 Cefepime* 0.936 0.433-2.026 .87
 Anaerobic antibiotics* 1.937 1.176-3.193 .01
 Mismatch/unrelated donor 2.698 1.478-4.924 .001
 CMV seronegative donor 1.309 0.824-2.079 .25
 GVHD 3-4 0.743 0.328-1.681 .47
 Lymphoid malignancy 2.184 1.339-3.560 .002
All-cause mortality
 Vancomycin* 0.94 0.32-2.78 .91
 Cefepime* 1.53 0.58-4.08 .39
 Anaerobic antibiotics* 3.11 1.60-6.04 .0008
 Age 1.02 0.99-1.05 .06
 Mismatch/unrelated donor 1.29 0.56-2.97 .55
 Comorbidity score ≥2 0.84 0.33-2.15 .71
 GVHD 3-4 1.92 0.81-4.56 .14
 Acute leukemia 0.92 0.49-1.74 .80
 cs-CMVi 1.21 0.64-2.28 .55
 Bacteremia as indication for antibiotics 0.83 0.33-2.08 .69
Nonrelapse mortality
 Vancomycin* 1.28 0.27-6.07 .75
 Cefepime* 2.65 0.68-10.4 .16
 Anaerobic antibiotics* 4.23 1.81-9.86 .0008
 Age 1.03 1.00-1.01 .051
 Mismatch/unrelated donor 1.26 0.42-3.78 .68
 Comorbidity score 0.41 0.15-1.10 .08
 GVHD 3-4 1.79 0.66-4.87 .26
 Acute leukemia 1.37 0.64-2.95 .42
 cs-CMVi 1.31 0.58-2.98 .52
 Bacteremia as indication for antibiotics 0.93 0.33-2.62 .89
GVHD 3-4 aOR 95% CI P
 Vancomycin* 8.91 0.73-109 .09
 Cefepime* 0.49 0.10-2.44 .38
 Anaerobic antibiotics* 5.46 1.24-24.0 .02
 Mismatch/unrelated donor 0.55 0.11-2.64 .46
 Age 0.99 0.95-1.04 .83
 Graft source (PBSC) 0.36 0.06-2.27 .27

Cox proportional hazards regression model was used for CMV and mortality. Logistic regression analysis was used to examine the risk factors for development of GVHD.

aHR, adjusted hazard ratio; aOR, adjusted odds ratio; CI, confidence interval; PBCS, peripheral blood stem cell.

*

Compared with reference (ie, no corresponding antibiotic).

Includes acute myeloid leukemia, acute lymphoid leukemia, and acute leukemia of ambiguous lineage.

Compared with reference (ie, antibiotics for prophylaxis, culture negative fever, and other).