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. 2013 Apr 9;68(8):1872–1880. doi: 10.1093/jac/dkt111

Table 3.

Risk factor analysis for all-cause mortality in allo-HSCT recipients

Characteristic All-cause mortality (n = 44) Survival (n = 236) COR (95% CI) P value AOR (95% CI) P value
Age (years), median (range)a 50 (14–70) 47 (3–68) 1.29 (1.0, 1.66) 0.046 1.45 (1.1, 1.9) 0.008
Male sex 33 (75) 125 (53) 2.66 (1.29, 5.52) 0.008 2.76 (1.25, 6.09) 0.012
Non-white race 16 (36) 83 (35) 1.05 (0.54, 2.06) 0.879
Corticosteroidsb 28 (64) 113 (48) 1.9 (0.98, 3.7) 0.058
Myeloablative conditioning regimen 18 (41) 99 (42) 0.96 (0.49, 1.84) 0.898
Time from HSCT (days), median (range)a 91 (1–1426) 173 (1–2167) 0.94 (0.9, 0.98) 0.008 0.94 (0.9, 0.99) 0.012
Donor relationship
 matched related 27 (61) 131 (56) 1.0
 matched unrelated 14 (32) 98 (42) 0.69 (0.35, 1.39) 0.302
 mismatched 3 (7) 7 (3) 2.08 (0.51, 8.56) 0.310
Haematopoietic cell source
 marrow 12 (27) 64 (27) 1.0
 peripheral 31 (71) 159 (67) 1.04 (0.5, 2.15) 0.916
 cord 1 (2) 13 (6) 0.41 (0.05, 3.44) 0.411
GVHD at the time of diagnosis of RSV infection 27 (61) 153 (65) 0.86 (0.44, 1.67) 0.66
Neutropenia (ANC <500/μL)c 8 (18) 7 (3) 7.27 (2.48, 21.27) <0.001 3.21 (0.91, 11.33) 0.069d
Lymphocytopenia (ALC <200/μL)c 17 (39) 31 (13) 4.16 (2.04, 8.51) <0.001 3.03 (1.33, 6.91) 0.008
Pulmonary coinfectionse
 viral 3 (7) 10 (4) 2.12 (0.55, 8.14) 0.274
 bacterial 8 (18) 6 (3) 9.42 (3.06, 29.03) <0.001
 fungal 3 (7) 8 (3) 2.65 (0.67, 10.54) 0.167
Nosocomial infection 7 (16) 23 (10) 1.75 (0.7, 4.38) 0.230
LRTI at presentation 17 (39) 26 (11) 5.09 (2.45, 10.56) <0.001
Lack of antiviral therapy at the URTI stagef 27 (61) 96 (41) 2.32 (1.2, 4.48) 0.013 2.43 (1.16, 5.11) 0.019
Year of RSV diagnosis (2001 and later) 35 (80) 182 (77) 1.15 (0.52, 2.55) 0.724 1.33 (0.55, 3.24) 0.532d

COR, crude OR.

aMeasure of effect for age and time from HSCT expressed per 10 year and 30 day interval, respectively.

bWithin 1 month before RSV diagnosis.

cAt the time of first assessment of respiratory symptoms at the hospital.

dNeutropenia was retained in the model due to confounding effects and year of RSV diagnosis was included in the model to adjust for the overall advances in the clinical management of patients during recent years.

eWithin 1 month prior to and after RSV diagnosis. In cases of LRTI, coinfections occurred on the same day as RSV diagnosis or within 2 weeks prior to RSV LRTI. Viral coinfections included influenza virus (7), parainfluenza virus (3), picornavirus (2) and adenovirus (1); bacterial coinfections included Klebsiella oxytoca (1), Pseudomonas aeruginosa and Pseudomonas fluorescens (4), methicillin-resistant Staphylococcus aureus (2), Stenotrophomonas maltophilia (6) and Escherichia coli (1); and fungal coinfections included 8 Aspergillus spp. and 3 Nocardia spp. infections.

fRibavirin alone or combined with IVIG or palivizumab.