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. 2020 Oct 16;4(2):rkaa056. doi: 10.1093/rap/rkaa056

Table 2.

Treatment at the time of inclusion or at venous thromboembolism development

Parameter All patients (n = 187) VTE group (n = 24) Non-VTE group (n = 163) P-value
Treatment at inclusion or onset of VTE
Prednisolone, n (%) 148 (79.1) 23 (95.8) 125 (76.7) 0.031
Prednisolone dose, mg/day, median (range) 10 (0–80) 15 (0–60) 8.25 (0–80) 0.3
DMARD, n (%) 91 (48.7) 12 (50) 79 (48.5) 0.89
MTX, n (%) 32 (17.1) 3 (12.5) 29 (17.8) 0.77
AZA, n (%) 35 (18.7) 4 (16.7) 31 (18.6) 1.0
MMF, n (%) 24 (12.8) 5 (20.8) 19 (11.7) 0.2
CYC, n (%) 50 (26.7) 9 (3.8) 41 (25.2) 0.2
Rituximab (within 3 months), n (%) 6 (3.2) 4 (16.7) 2 (1.2) 0.003
Warfarin, n (%) 6 (3.2) 0 0 6 (3.7) 1.0
ASA, n (%) 24 (12.8) 4 (16.7) 20 (12.3) 0.52
Statins, n (%) 32 (17.1) 3 (20.8) 29 (17.8) 0.77
RAS blockade, any (ACEi, ARB or both), n (%) 75 (40.1) 7 (29.2) 68 (41.7) 0.27
ACEi, n (%) 50 (26.7) 4 (16.7) 46 (28.2) 0.32
ARB, n (%) 30 (16.0) 4 (16.7) 26 (16) 1.0
Diuretics, n (%) 41 (21.9) 7 (29.2) 34 (20.9) 0.43
β-Blockers, n (%) 52 (27.8) 4 (16.7) 48 (29.4) 0.23
Calcium blockers, n (%) 34 (18.2) 1 (4.2) 33 (20.2) 0.08

Data are on the total cohort and the two patient subgroups (with or without VTE). Data on VTE patients were obtained at the time of VTE. P-values were calculated by comparing the two patient subgroups. Figures within parentheses are percentages unless stated otherwise. None remain significant after Bonferroni correction for multiple testing. ACEi: angiotensin-converting enzyme inhibitor; ARB: angiotensin II receptor blocker; RAS blockade: renin–angiotensin system blockade; VTE: venous thromboembolism.