Prophylaxis versus Episodic Treatment to Prevent Joint Disease in Boys with Severe Hemophilia
Marilyn J. Manco-Johnson, M.D., Thomas C. Abshire, M.D., Amy D. Shapiro, M.D., Brenda Riske, M.S., M.B.A., M.P.A., Michele R. Hacker, Sc.D., Ray Kilcoyne, M.D., J. David Ingram, M.D., Michael L. Manco-Johnson, M.D., Sharon Funk, B.Sc., P.T., Linda Jacobson, B.S., Leonard A. Valentino, M.D., W. Keith Hoots, M.D., George R. Buchanan, M.D., Donna DiMichele, M.D., Michael Recht, M.D., Ph.D., Deborah Brown, M.D., Cindy Leissinger, M.D., Shirley Bleak, M.S.N., Alan Cohen, M.D., Prasad Mathew, M.D., Alison Matsunaga, M.D., Desiree Medeiros, M.D., Diane Nugent, M.D., Gregory A. Thomas, M.D., Alexis A. Thompson, M.D., Kevin McRedmond, M.D., J. Michael Soucie, Ph.D., Harlan Austin, Ph.D., and Bruce L. Evatt, M.D.
Background Effective ways to prevent arthropathy in severe hemophiliaare unknown.
Methods We randomly assigned young boys with severe hemophiliaA to regular infusions of recombinant factor VIII (prophylaxis)or to an enhanced episodic infusion schedule of at least threedoses totaling a minimum of 80 IU of factor VIII per kilogramof body weight at the time of a joint hemorrhage. The primaryoutcome was the incidence of bone or cartilage damage as detectedin index joints (ankles, knees, and elbows) by radiography ormagnetic resonance imaging (MRI).
Results Sixty-five boys younger than 30 months of age were randomlyassigned to prophylaxis (32 boys) or enhanced episodic therapy(33 boys). When the boys reached 6 years of age, 93% of thosein the prophylaxis group and 55% of those in the episodic-therapygroup were considered to have normal index-joint structure onMRI (P=0.006). The relative risk of MRI-detected joint damagewith episodic therapy as compared with prophylaxis was 6.1 (95%confidence interval, 1.5 to 24.4). The mean annual numbers ofjoint and total hemorrhages were higher at study exit in theepisodic-therapy group than in the prophylaxis group (P<0.001for both comparisons). High titers of inhibitors of factor VIIIdeveloped in two boys who received prophylaxis; three boys inthe episodic-therapy group had a life-threatening hemorrhage.Hospitalizations and infections associated with central-catheterplacement did not differ significantly between the two groups.
Conclusions Prophylaxis with recombinant factor VIII can preventjoint damage and decrease the frequency of joint and other hemorrhagesin young boys with severe hemophilia A. (ClinicalTrials.govnumber, NCT00207597
[ClinicalTrials.gov]
.)
Source Information
Authors' affiliations are listed in the Appendix.
Address reprint requests to Dr. M.J. Manco-Johnson, Mountain States Regional Hemophilia and Thrombosis Center, MS F-416, PO Box 6507, Aurora, CO 80045, or at marilyn.manco-johnson{at}uchsc.edu.
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