Impact of inhibitors on hemophilia a mortality in the United States
The previously published mortality studies are limited in hemophilia populations but suggest that there is no increased risk of mortality in factor VIII inhibitor patients. This retrospective study analyzed surveillance data collected on 7,386 males with severe hemophilia A over a 13‐year period to...
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Published in | American journal of hematology Vol. 90; no. 5; pp. 400 - 405 |
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Abstract | The previously published mortality studies are limited in hemophilia populations but suggest that there is no increased risk of mortality in factor VIII inhibitor patients. This retrospective study analyzed surveillance data collected on 7,386 males with severe hemophilia A over a 13‐year period to assess the association between a current inhibitor and death. During the study period, 432 participants died, among whom 48 were patients with an inhibitor. Clinical characteristics most strongly associated with death were increased number of reported bleeds, signs of liver disease, infection with either HIV or HCV, and the presence of inhibitor. Patients who underwent successful tolerization were not considered inhibitor patients in our analysis. In a multivariable analysis, the odds of death were 70% higher among patients with a current inhibitor compared to those without an inhibitor (P < 0.01). Deaths among patients with inhibitors were much more likely to be attributed to bleeding complications than those among patients without an inhibitor (42 vs. 12%, P < 0.0001). We conclude that males with severe hemophilia A and a current inhibitor are at increased risk of death.Am. J. Hematol. 90:400–405, 2015. © 2015 Wiley Periodicals, Inc. |
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AbstractList | The previously published mortality studies are limited in hemophilia populations but suggest that there is no increased risk of mortality in factor VIII inhibitor patients. This retrospective study analyzed surveillance data collected on 7,386 males with severe hemophilia A over a 13-year period to assess the association between a current inhibitor and death. During the study period, 432 participants died, among whom 48 were patients with an inhibitor. Clinical characteristics most strongly associated with death were increased number of reported bleeds, signs of liver disease, infection with either HIV or HCV, and the presence of inhibitor. Patients who underwent successful tolerization were not considered inhibitor patients in our analysis. In a multivariable analysis, the odds of death were 70% higher among patients with a current inhibitor compared to those without an inhibitor (P < 0.01). Deaths among patients with inhibitors were much more likely to be attributed to bleeding complications than those among patients without an inhibitor (42 vs. 12%, P < 0.0001). We conclude that males with severe hemophilia A and a current inhibitor are at increased risk of death. The previously published mortality studies are limited in hemophilia populations but suggest that there is no increased risk of mortality in factor VIII inhibitor patients. This retrospective study analyzed surveillance data collected on 7,386 males with severe hemophilia A over a 13‐year period to assess the association between a current inhibitor and death. During the study period, 432 participants died, among whom 48 were patients with an inhibitor. Clinical characteristics most strongly associated with death were increased number of reported bleeds, signs of liver disease, infection with either HIV or HCV, and the presence of inhibitor. Patients who underwent successful tolerization were not considered inhibitor patients in our analysis. In a multivariable analysis, the odds of death were 70% higher among patients with a current inhibitor compared to those without an inhibitor (P < 0.01). Deaths among patients with inhibitors were much more likely to be attributed to bleeding complications than those among patients without an inhibitor (42 vs. 12%, P < 0.0001). We conclude that males with severe hemophilia A and a current inhibitor are at increased risk of death.Am. J. Hematol. 90:400–405, 2015. © 2015 Wiley Periodicals, Inc. The previously published mortality studies are limited in hemophilia populations but suggest that there is no increased risk of mortality in factor VIII inhibitor patients. This retrospective study analyzed surveillance data collected on 7,386 males with severe hemophilia A over a 13-year period to assess the association between a current inhibitor and death. During the study period, 432 participants died, among whom 48 were patients with an inhibitor. Clinical characteristics most strongly associated with death were increased number of reported bleeds, signs of liver disease, infection with either HIV or HCV, and the presence of inhibitor. Patients who underwent successful tolerization were not considered inhibitor patients in our analysis. In a multivariable analysis, the odds of death were 70% higher among patients with a current inhibitor compared to those without an inhibitor (P < 0.01). Deaths among patients with inhibitors were much more likely to be attributed to bleeding complications than those among patients without an inhibitor (42 vs. 12%, P < 0.0001). We conclude that males with severe hemophilia A and a current inhibitor are at increased risk of death. |
Author | Soucie, J. Michael Walsh, Christopher E. Miller, Connie H. |
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Notes | Nothing to report. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention. Conflict of interest ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
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References | 1983; 214 1989; 71 1990; 76 2010; 38 1983; 286 1978; 54 1982; 52 2007; 110 2000; 96 2003; 9 2002; 8 2004; 2 2012; 159 2007; 109 2011; 365 2014; 20 |
References_xml | – volume: 71 start-page: 71 year: 1989 end-page: 76 article-title: Mortality and causes of death in Dutch haemophiliacs, 1973‐86 publication-title: Br J Haematol – volume: 76 start-page: 369 year: 1990 end-page: 371 article-title: Haemophiliacs with factor VIII inhibitors in Finland: Prevalence, incidence and outcome publication-title: Br J Haematol – volume: 2 start-page: 1047 year: 2004 end-page: 1054 article-title: The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977‐99 publication-title: J Thromb Haemost – volume: 159 start-page: 123 year: 2012 end-page: 134 article-title: Immune tolerance in haemophilia: The long journey to the fork in the road publication-title: Br J Haematol – volume: 38 start-page: S475 year: 2010 end-page: S481 article-title: The universal data collection surveillance system for rare bleeding disorders publication-title: Am J Prev Med – volume: 20 start-page: 65 year: 2014 end-page: 72 article-title: Randomized comparison of prophylaxis and on‐demand regimens with FEIBA NF in the treatment of haemophilia a and B with inhibitors publication-title: Haemophilia – volume: 110 start-page: 815 year: 2007 end-page: 825 article-title: Mortality rates, life expectancy, and causes of death in people with hemophilia a or B in the united kingdom who were not infected with HIV publication-title: Blood – volume: 96 start-page: 437 year: 2000 end-page: 442 article-title: Mortality among males with hemophilia: Relations with source of medical care. The hemophilia surveillance system project investigators publication-title: Blood – volume: 54 start-page: 1155 year: 1978 end-page: 1165 article-title: The effect of misclassification of exposure status in epidemiologic studies of air pollution health effects publication-title: Bull N Y Acad Med – volume: 365 start-page: 1684 year: 2011 end-page: 1692 article-title: Anti‐inhibitor coagulant complex prophylaxis in hemophilia with inhibitors publication-title: N Engl J Med – volume: 52 start-page: 7 year: 1982 end-page: 12 article-title: Changes in the life expectancy of patients with severe haemophilia a in Finland in 1930‐79 publication-title: Br J Haematol – volume: 109 start-page: 4648 year: 2007 end-page: 4654 article-title: Treatment‐related risk factors of inhibitor development in previously untreated patients with hemophilia A: The CANAL cohort study publication-title: Blood – volume: 9 start-page: 418 year: 2003 end-page: 435 article-title: The epidemiology of inhibitors in haemophilia a: A systematic review publication-title: Haemophilia – volume: 214 start-page: 199 year: 1983 end-page: 206 article-title: Deaths in Swedish hemophiliacs, 1957‐1980 publication-title: Acta Med Scand – volume: 8 start-page: 660 year: 2002 end-page: 667 article-title: Factors predictive of death among HIV‐uninfected persons with haemophilia and other congenital coagulation disorders publication-title: Haemophilia – volume: 286 start-page: 929 year: 1983 end-page: 933 article-title: Treatment of haemophilia and related disorders in Britain and northern Ireland during 1976‐80: Report on behalf of the directors of haemophilia centres in the United Kingdom publication-title: Br Med J – volume: 20 start-page: 230 year: 2014 end-page: 237 article-title: A study of prospective surveillance for inhibitors among persons with haemophilia in the United States publication-title: Haemophilia |
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SubjectTerms | Adolescent Adult Antibodies - blood Child Cytomegalovirus Infections - blood Cytomegalovirus Infections - complications Cytomegalovirus Infections - drug therapy Cytomegalovirus Infections - mortality Factor VIII - administration & dosage Factor VIII - antagonists & inhibitors Hematology Hemophilia A - blood Hemophilia A - complications Hemophilia A - drug therapy Hemophilia A - mortality HIV Infections - blood HIV Infections - complications HIV Infections - drug therapy HIV Infections - mortality Humans Male Middle Aged Retrospective Studies Risk Factors Survival Analysis United States |
Title | Impact of inhibitors on hemophilia a mortality in the United States |
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