Rare Factor Deficiencies

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Table 4. HTC Population Profile Patient Characteristics, Rare Factor Deficiencies (excluding Factor VIII and Factor IX), Data Reported from 1/1/2012 through 3/31/2022

HTC Population Profile Patient Characteristics, Rare Factor Deficiencies (excluding Factor VIII and Factor IX)
FI FII FV Factors
V & VIII,
combined
FVII FX FXI FXIII Alpha-2
Antiplasmin
Deficiency
PAI-1
Deficiency
# (%) # (%) # (%) # (%) # (%) # (%) # (%) # (%) # (%) # (%)
# of patients 493 (100) 132 (100) 669 (100) 26 (100) 3188 (100) 348 (100) 1921 (100) 298 (100) 13 (100) 399 (100)
Age (years) <2 36 (7) * * 16 (2) * * 55 (2) * * 86 (4) 23 (8) * * 8 (2)
2–10 115 (23) 18 (14) 87 (13) * * 747 (23) 65 (19) 268 (14) 49 (16) * * 51 (13)
11–19 136 (28) 56 (42) 235 (35) * * 1356 (43) 112 (32) 475 (25) 65 (22) * * 149 (37)
20–44 126 (26) 35 (27) 211 (32) 11 (42) 734 (23) 89 (26) 589 (31) 111 (37) * * 126 (32)
45–64 49 (10) 15 (11) 83 (12) * * 179 (6) 51 (15) 245 (13) 29 (10) * * 39 (10)
65+ 31 (6) * * 37 (6) * * 117 (4) * * 258 (13) 21 (7) * * 26 (7)
Sex† Male 213 (43) 43 (33) 251 (38) 12 (46) 1560 (49) 144 (41) 847 (44) 147 (49) * * 118 (30)
Female 280 (57) 89 (67) 418 (62) 14 (54) 1628 (51) 204 (59) 1074 (56) 151 (51) * * 281 (70)
Ethnicity Hispanic, Latino/a, or Spanish origin 60 (12) * * 106 (16) * * 705 (22) 83 (24) 232 (12) 70 (23) * * 72 (18)
Not Hispanic, Latino/a, or Spanish origin 410 (83) 90 (68) 532 (80) * * 2325 (73) 251 (72) 1613 (84) 218 (73) * * 318 (80)
Unknown 23 (5) * * 31 (5) * * 158 (5) 14 (4) 76 (4) 10 (3) * * 9 (2)
Race American Indian/Alaska Native * * * * * * * * 19 (1) * * * * * * * * * *
Asian 22 (4) * * 19 (3) * * 104 (3) * * 73 (4) 28 (9) * * * *
Black or African American 30 (6) * * 22 (3) * * 562 (18) 36 (10) 81 (4) 28 (9) * * 34 (9)
Native Hawaiian or other Pacific Islander * * * * * * * * 10 (0) * * * * * * * * * *
White 385 (78) 107 (81) 571 (85) 16 (62) 2112 (66) 255 (73) 1612 (84) 206 (69) * * 321 (80)
More than one of these * * 6 (5) * * * * 55 (2) * * 14 (1) * * * * 7 (2)
Unknown 48 (10) 13 (10) 48 (7) * * 326 (10) 34 (10) 136 (7) 31 (10) * * 27 (7)
Insurance Status Insured 475 (96) 125 (95) 655 (98) * * 3116 (98) 342 (98) 1880 (98) 289 (97) * * 381 (95)
Uninsured * * * * 8 (1) * * 32 (1) * * 17 (1) * * * * * *
Unknown * * * * 6 (1) * * 40 (1) * * 24 (1) * * * * * *
History of HCV infection Yes 13 (3) 6 (5) 11 (2) * * 29 (1) 9 (3) 34 (2) 12 (4) * * * *
No 345 (70) 78 (59) 502 (75) 18 (69) 2443 (77) 260 (75) 1442 (75) 246 (83) * * 239 (60)
Unknown 135 (27) 48 (36) 156 (23) * * 716 (22) 79 (23) 445 (23) 40 (13) * * * *
History of HIV infection Yes * * * * * * * * * * * * 9 (0) * * * * * *
No 357 (72) 84 (64) 510 (76) 19 (73) 2455 (77) 270 (78) 1480 (77) 258 (87) * * 240 (60)
Unknown * * * * * * * * * * * * 432 (22) * * * * * *

Note. This table excludes individuals with Factor VIII deficiency (hemophilia A) and Factor IX deficiency (hemophilia B). “Factors V & VIII, combined” refers to an autosomal condition, which occurs when there is a defect in a gene on one of the first 22 pairs of chromosomes called autosomes. Hemophilia A and B are X-linked conditions, which occur when there is a defect on the 23rd pair of chromosomes which determine one’s sex.

† The HTC Population Profile contains 41 transgender individuals. For confidentiality purposes, the number of transgender patients is too small to report by year or other characteristics. Transgender patients have been included in the counts of male and female according to the sex assigned to them at birth since hemophilia and von Willebrand disease, the most common congenital bleeding disorders, affect the sexes differently.

* Counts greater than zero but less than five have been suppressed to protect patient confidentiality. Additional cells may be suppressed to prevent derivation of these counts by subtraction.