Literature DB >> 11274587

Risk factors for infection with HBV and HCV in a largecohort of hemophiliac males.

J M Soucie1, L C Richardson, B L Evatt, J V Linden, B M Ewenstein, S F Stein, C Leissinger, M Manco-Johnson, C L Sexauer.   

Abstract

BACKGROUND: Before the implementation of donor screening and the development of effective virus-inactivation procedures, persons with hemophilia (PWHs) were at risk of infection with HBV and HCV transmitted through clotting factor concentrates. STUDY DESIGN AND METHODS: Data collected from the medical records of a cohort of 2,772 males with hemophilia who resided in six states of the United States were used to examine relations between demographic and clinical characteristics and laboratory markers of past or present infection with HBV and HCV using logistic regression.
RESULTS: Test results were available for 60 percent of the cohort. Among those tested, 30 percent were positive for markers of HBV infection and 64 percent for HCV infection. Factors associated with increased odds of positive HBV markers and HCV infection were greater severity of hemophilia, larger amounts of factor use, and HIV infection. Markers of HBV infection persisted in birth cohorts as late as 1992 and those of HCV infections in birth cohorts through 1991. Compared to same-age US males, PWHs born between 1987 and 1989 were more likely to have markers of HBV and HCV infection.
CONCLUSION: PWHs who received clotting factor concentrates before 1990 may be at risk for infection with hepatitis B or hepatitis C and should be tested.

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Year:  2001        PMID: 11274587     DOI: 10.1046/j.1537-2995.2001.41030338.x

Source DB:  PubMed          Journal:  Transfusion        ISSN: 0041-1132            Impact factor:   3.157


  14 in total

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Authors:  J Michael Soucie
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Authors:  Ann-Marie Nazzaro; Sally Owens; W Keith Hoots; Kelly L Larson
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3.  Correlates of spontaneous clearance of hepatitis C virus among people with hemophilia.

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Review 4.  Some reflections on the Code of Ethics of the International Society of Blood Transfusion.

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Review 5.  Gene therapy in an era of emerging treatment options for hemophilia B.

Authors:  P E Monahan
Journal:  J Thromb Haemost       Date:  2015-06       Impact factor: 5.824

6.  Evidence for the transmission of parvovirus B19 in patients with bleeding disorders treated with plasma-derived factor concentrates in the era of nucleic acid test screening.

Authors:  J Michael Soucie; Christine De Staercke; Paul E Monahan; Michael Recht; Meera B Chitlur; Ralph Gruppo; W Craig Hooper; Craig Kessler; Roshni Kulkarni; Marilyn J Manco-Johnson; Jerry Powell; Meredith Pyle; Brenda Riske; Hernan Sabio; Sean Trimble
Journal:  Transfusion       Date:  2012-09-24       Impact factor: 3.157

7.  Healthcare expenditures for males with haemophilia and employer-sponsored insurance in the United States, 2008.

Authors:  S Guh; S D Grosse; S McAlister; C M Kessler; J M Soucie
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8.  A model for a regional system of care to promote the health and well-being of people with rare chronic genetic disorders.

Authors:  Judith R Baker; Sally O Crudder; Brenda Riske; Val Bias; Ann Forsberg
Journal:  Am J Public Health       Date:  2005-09-29       Impact factor: 9.308

9.  Inhibitors and mortality in persons with nonsevere hemophilia A in the United States.

Authors:  Ming Y Lim; Dunlei Cheng; Michael Recht; Christine L Kempton; Nigel S Key
Journal:  Blood Adv       Date:  2020-10-13

10.  Antihemophilic factor (recombinant) plasma/albumin-free method for the management and prevention of bleeding episodes in patients with hemophilia A.

Authors:  Steven Pipe
Journal:  Biologics       Date:  2009-07-13
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