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. Author manuscript; available in PMC: 2020 Oct 1.
Published in final edited form as: J Clin Immunol. 2019 Aug 2;39(7):653–667. doi: 10.1007/s10875-019-00659-8

Table 3.

Incidence of upper and lower gastrointestinal acute GVHD in evaluable patients with and without IBD prior to allogeneic HCT (A) and in patients with controlled or uncontrolled IBD at the time of allogeneic HCT (B).

Table 3A: Baseline IBD
Variables Total
N (%)
No
N (%)
Yes
N (%)
P Value

Acute GVHD Upper Intestinal Tract (Nausea/Vomiting)
 No 125 (94.7) 82 (96.5) 43 (91.5)
 Yes 7 (5.3) 3 (3.5) 4 (8.5) 0.246
Acute GVHD Lower Intestinal Tract (Stage 1–4)
 No 117 (88.6) 75 (88.2) 42 (89.4)
 Yes 15 (11.4) 10 (11.8) 5 (10.6) 0.845
Table 3B: IBD Status (Controlled or Not)
Variables Total
N (%)
IBD
Controlled
with Meds
N* (%)
IBD Not
Controlled
with Meds
N* (%)
No IBD
N (%)
P Value
Acute GVHD Upper Intestinal Tract (Nausea/Vomiting)
 No 124 (94.7) 29 (93.5) 13 (86.7) 82 (96.5)
 Yes 7 (5.3) 2 (6.5) 2 (13.3) 3 (3.5) 0.220
Acute GVHD Lower Intestinal Tract (Stage 1–4)
 No 117 (89.3) 27 (87.1) 15 (100.0) 75 (88.2)
 Yes 14 (10.7) 4 (12.9) 0 (0.0) 10 (11.8) 0.405
*

One IBD patient was reported to have unknown status of control at the time of allogeneic HCT, and so was excluded from analyses