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. 2019 Sep 3;21(5):e13158. doi: 10.1111/tid.13158

Table 1.

Patient characteristics

Characteristics (n = 287)
Age (y), median (range) 46 (18‐71)
Male, n (%) 167 (58)
Baseline disease, n (%)
AL/MDS/MPD 189 (66)
Lymphoid disorders 92 (32)
Others 6 (2)
Disease status at transplant, n (%)
CR 203(71)
PR 34 (12)
Refractory/active disease 50 (17)
Prior ASCT, n (%) 67 (23)
Period of transplant, n (%)
2017‐2018 89 (31)
2015‐2016 75 (26)
2013‐2014 79 (28)
2011‐2012 23 (8)
2008‐2010 21 (7)
Conditioning regimen, n (%)
RIC 135 (47)
Type of donor, n (%)
HLA‐identical sibling donor 105 (37)
Unrelated donor 69 (24)
Umbilical cord blood 52 (18)
Haplo‐identical family donor 61 (21)
PB stem cell source, n (% 228 (79)
HLA fully matched, n (%) 167 (58)
ATG as a part of the conditioning regimen, n (%) 66 (23)
GvHD prophylaxis, n (%)
Sir‐Tac 31 (11)
CsA + MTX 73 (25)
Post‐Cy 116 (40)
CsA + PDN and Others 67 (23)
Number of recipients with CARVs per seasons, n (%)
2018‐2019 13 (5)
2017‐2018 90 (31)
2016‐2017 39 (14)
2015‐2016 30 (10)
2014‐2015 59 (20)
2013‐2014 56 (20)
Number of CARV episodes 597
Number of LRTD CARV episodes 203
Median time from allo‐HSCT to CARV, days (range) 198 (−7 to 6177)
Number of recipients with IFD after CARVs, n (%) 29 (10)
Median time from CARV to IFD, days (range) 21 (0‐158)
Median time from allo‐HSCT to IFD, days (range) 211 (20‐989)
Median F‐up after CARV, days (range) 285 (1‐3106)

Abbreviations: AL, acute leukemia; allo‐HSCT, allogeneic hematopoietic stem cell transplantation; ASCT, autologous stem cell transplantation; ATG, antithymocyte globulin; CARV, community‐acquired respiratory virus; CR, complete remission; CsA, cyclosporine A; F‐up, follow‐up; IFD, invasive pulmonary infectious fungal disease; LRTD, lower respiratory tract disease; MDS, myelodysplastic syndrome; MPD, myeloproliferative disease; MTX, methotrexate; PDN, prednisone; Post‐Cy, post‐transplant cyclophosphamide; PR, partial remission; RIC, reduced intensity conditioning; Sir, sirolimus; Tac, tacrolimus.

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