Table 1

Characteristics of HCT recipients with influenza virus respiratory tract disease

CharacteristicsVirus type
All patients (N = 161)
Influenza A (N = 103)Influenza B (N = 40)2009 H1N1 (N = 18)
Age, y, median (IQR) 42 (32-54) 41.5 (24-51) 41.5 (18-52) 42 (30-52) 
Time after transplant, d, median (IQR) 78 (40-197) 69 (41-212) 601.5 (270-977) 80 (44-294) 
Male sex 62 (60.2) 21 (52.5) 8 (44.4) 91 (56.5) 
Disease risk at transplantation     
    Nonadvanced 59 (57.3) 19 (47.5) 9 (50.0) 87 (54.0) 
    Advanced 44 (42.7) 21 (52.5) 9 (50.0) 74 (46.0) 
Transplant type     
    Autologous 15 (14.6) 11 (27.5) 5 (27.8) 31 (19.3) 
    Matched related 39 (37.9) 16 (40.0) 4 (22.2) 59 (36.6) 
    Mismatched or unrelated 49 (47.6) 13 (32.5) 9 (50.0) 71 (44.1) 
Stem cell source     
    Bone marrow or UBC 45 (43.7%) 20 (50.0%) 5 (27.8%) 70 (43.5%) 
    Peripheral blood 58 (56.3%) 20 (50.0%) 13 (72.2%) 91 (56.5%) 
Conditioning regimen     
    Myeloablative 84 (81.4%) 34 (85.0%) 15 (83.3%) 133 (82.6%) 
    Reduced intensity 19 (18.5%) 6 (15.0%) 3 (16.7%) 28 (17.4%) 
Lymphocyte count (cells/mm3)*     
    < 100 20 (20.0) 18 (45.0) 5 (29.4) 43 (27.4) 
    100-300 35 (35.0) 6 (15.0) 3 (17.6) 44 (20.0) 
    > 300 45 (45.0) 16 (40.0) 9 (52.9) 70 (44.6) 
Corticosteroid treatment     
    None 43 (41.7) 20 (50.0) 7 (38.9) 70 (43.5) 
    Low-dose 27 (26.2) 16 (40.0) 10 (55.6) 53 (32.9) 
    High-dose 33 (32.0) 4 (10.0) 1 (15.0) 38 (23.6) 
Early antiviral therapy for URD     
    Yes (≤ 48 h) 39 (38.2) 6 (15.0) 7 (38.9) 52 (32.5) 
    No (> 48 h) 11 (10.8) 2 (5.0) 6 (33.3) 19 (11.9) 
    No antiviral therapy for URD§ 52 (51.0) 32 (80.0) 5 (27.8) 89 (55.6) 
CharacteristicsVirus type
All patients (N = 161)
Influenza A (N = 103)Influenza B (N = 40)2009 H1N1 (N = 18)
Age, y, median (IQR) 42 (32-54) 41.5 (24-51) 41.5 (18-52) 42 (30-52) 
Time after transplant, d, median (IQR) 78 (40-197) 69 (41-212) 601.5 (270-977) 80 (44-294) 
Male sex 62 (60.2) 21 (52.5) 8 (44.4) 91 (56.5) 
Disease risk at transplantation     
    Nonadvanced 59 (57.3) 19 (47.5) 9 (50.0) 87 (54.0) 
    Advanced 44 (42.7) 21 (52.5) 9 (50.0) 74 (46.0) 
Transplant type     
    Autologous 15 (14.6) 11 (27.5) 5 (27.8) 31 (19.3) 
    Matched related 39 (37.9) 16 (40.0) 4 (22.2) 59 (36.6) 
    Mismatched or unrelated 49 (47.6) 13 (32.5) 9 (50.0) 71 (44.1) 
Stem cell source     
    Bone marrow or UBC 45 (43.7%) 20 (50.0%) 5 (27.8%) 70 (43.5%) 
    Peripheral blood 58 (56.3%) 20 (50.0%) 13 (72.2%) 91 (56.5%) 
Conditioning regimen     
    Myeloablative 84 (81.4%) 34 (85.0%) 15 (83.3%) 133 (82.6%) 
    Reduced intensity 19 (18.5%) 6 (15.0%) 3 (16.7%) 28 (17.4%) 
Lymphocyte count (cells/mm3)*     
    < 100 20 (20.0) 18 (45.0) 5 (29.4) 43 (27.4) 
    100-300 35 (35.0) 6 (15.0) 3 (17.6) 44 (20.0) 
    > 300 45 (45.0) 16 (40.0) 9 (52.9) 70 (44.6) 
Corticosteroid treatment     
    None 43 (41.7) 20 (50.0) 7 (38.9) 70 (43.5) 
    Low-dose 27 (26.2) 16 (40.0) 10 (55.6) 53 (32.9) 
    High-dose 33 (32.0) 4 (10.0) 1 (15.0) 38 (23.6) 
Early antiviral therapy for URD     
    Yes (≤ 48 h) 39 (38.2) 6 (15.0) 7 (38.9) 52 (32.5) 
    No (> 48 h) 11 (10.8) 2 (5.0) 6 (33.3) 19 (11.9) 
    No antiviral therapy for URD§ 52 (51.0) 32 (80.0) 5 (27.8) 89 (55.6) 

Data are no. (%) of patients, unless otherwise indicated. Influenza A and B indicate seasonal influenza in all the tables and figures. One patient had H1N1 several years after experiencing an infection; with seasonal influenza A, only the first episode was included in the analyses.

IQR indicates interquartile range; MDS, myelodysplastic syndrome; and UBC, umbilical cord blood.

*

Lymphocyte counts were not available in 4 patients.

Low-dose indicates < 1 mg/kg of prednisone or oral beclomethasone diproprionate; and High-dose, ≥ 1 mg/kg of prednisone or prednisone equivalent dose of other steroids.

Time between influenza URD diagnosis and initiation of antiviral treatment.

§

This includes patients who receive no antiviral treatment ever after influenza diagnosis and who had LRD at the presentation.

Eighteen of 32 were diagnosed as influenza B infection before the regulatory approval of the neuraminidase inhibitors.

or Create an Account

Close Modal
Close Modal