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. Author manuscript; available in PMC: 2015 Dec 18.
Published in final edited form as: Haemophilia. 2011 Dec 21;18(2):276–283. doi: 10.1111/j.1365-2516.2011.02713.x

Table 2.

Health care utilization and expenditures of male patients with haemophilia by risk group, 2008.

N Median Mean 95th percentile
Health care utilization
 No. of admission w ≥1 admission  95 (22%) 1.0 2.2 6.0
 No. of ED visits w ≥1 visit 224 (51%) 2.0 3.3 9.0
Health care expenditures
 All 435 46 737 142 987 547 397
 Haemophilia A 370 49 109‡‡ 148 215†† 555 314
 Haemophilia B 65 34 040 113 223 463 248
 Receiving no bypassing agents 343 46 737‡‡* 124 700††** 437 278
  Clotting factor§ 343 24 852‡‡ 106 807††** 416 158
 Receiving bypassing agents 27 194 542 446 945 1 656 753
  Clotting factor§ 27 64 768 287 245 1 068 799
 Child 278 31 067‡‡** 113 867††** 416 466
 Adult 157 73 291 194 549 667 367
*

and

**

represent a 5% and a 1% level of significance, respectively.

Statistical tests examine the null hypothesis that people with haemophilia A have the same costs of care as people with haemophilia B.

Statistical tests examine the null hypothesis that people who receive bypassing agents have the same costs of care as people who do not receive bypassing agents.

§

Statistical tests examine the null hypothesis that the costs of clotting factor for people who receive bypassing agents are the same as those for people who do not receive bypassing agents.

Statistical tests examine the null hypothesis that children have the same costs of care as adults.

††

t-test.

‡‡

Wilcoxon–Mann–Whitney test.

ED, emergency department.