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. 2014 Oct 22;124(23):3389–3397. doi: 10.1182/blood-2014-07-580498

Table 5.

Comparison of patients enrolled in RODIN and the remainder of the cohort

UK-RODIN subjects (n = 88) Non-RODIN subjects (n = 319) P
Inhibitors reported, n (%)
 All 33 (37.5) 85 (26.7) .05
 High titer 17 (19.3) 43 (13.5) .17
 Low titer 16 (18.2) 42 (13.2) .23
Age at first treatment, mo
 Median 8 9
 IQR 2-12 4-14 .14
 Range 0-52 0-95
Ethnicity
 White 73 (83) 281 (88) .21
 Nonwhite 15 (17) 38 (12)
FVIII mutation
 High risk 54 (61.4) 190 (59.6)
 Low risk 31 (35.2) 102 (32) .79
 Not known 3 (3.4) 27 (8)
Intensive treatment at first exposure, n (%)
 Yes 19 (21.6) 37 (11.6) .02
 No 69 (78.4) 274 (85.9)
 Not known 0 (0.0) 8 (2.5)
Intensive treatment during first 50 EDs (excluding first exposure), n (%)
 Yes 40 (45.5) 135 (42.3) .82
 No 48 (54.5) 171 (53.6)
 Not known 0 (0.0) 13 (4.1)
 FH of a FVIII inhibitor 15 (17.05) 26 (8.15) .03
Peak inhibitor titer
 Median 5 5
 IQR 2. 0-29.2 1.13-17.9 .86
 Range 0.07-222 0.3-1562
EDs to inhibitor formation
 Median 16.5 15
 IQR 8.75-31.75 (9-29) .93
 Range 3-358 [1-442]
Follow up for patients not developing an inhibitor, mo
 Median 48.0 44.3
 IQR 30.0-69.0 24.0-60.0 .58
 Range 6.0-142.5 1.6-154.5