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Diabetes and Obesity Journal Club Carina Signori Endocrinology Fellow http://www.hepcni.net/userfiles/image/hepatitis-b.gif
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Causes acute and chronic infection of the liver. Leads to substantial morbidity and mortality. Since 1996, 29 outbreaks of HBV were reported in long-term care facilities (LTC) in the U.S. 25 of the 29 were adults with diabetes receiving assisted blood glucose monitoring. Therdfore, ACIP (Advisory Committee on Immunization Practices) evaluated risk for HBV in diabetic adults. Based on their finding, they revised the recommendations for HBV vaccination.
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Discuss HBV Risk Morbidity/mortality Infection control Vaccine Cost-effectiveness Discuss new ACIP HBV recommendations for DM
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Population risk for HBV infection in adults with DM compared to nondiabetics – (estimated from confirmed cases 2009-2010) Aged 23-50 yo DM 2.1 x (95% CI=1.6-2.8). Aged ≥ 60 yo DM 1.5x (CI 0.9-2.5). Annual incidence of reported cases in DM: 1.8 per 100,000 (CI=1.5-2.2). NHANES data from 1999-2010: 60% (p<0.001) higher HBV antibody (HB core Ag) among persons ≥18yo with DM compared to those without diabetes. Prevalence ratios: 1.7 (CI=1.3-2.2) aged 18-50 yo. 1.3 (CI=1.0-1.6) aged ≥60yo.
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National surveillance data: 3371 acute HBV reported in 2009 47% of 2126 infections which info was available for were hospitalized. 1% of 1900 infections that info was available were fatal. In other analysis, high case-fatality rate among acute HBV-infected diabetes compared to those without diabetes. Chronic HBV infection is associated with higher M and M Leads to cirrhosis and cancer in ≥15% of affected adults. Chronic HBV is a reservoir for continuing HBV transmission. Diabetics have 2x risk for chronic NAFLD and HCC than those w/o DM.
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HBV is highly infectious and enviromentally stable. Can be transmitted by medical equipment that is contaminated with blood not visible to eye. Percutaneous exposure to HBV results from assisted monitoring of blood glucose in diabetics. Transmission occurred from multipatient use of finger stick devices designed for single patient use and inadequate disinfection and cleaning of blood glucose monitors between patients. Infection control guidelines targeting safe blood glucose monitoring for LTC settings were published in 2005.
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In the U.S. 2 single antigen recombinant hep B vaccines Recombivax HB (Merck) Engerix-B (GSK) 1 combination hep A and hep B vaccines: Twinrix (GSK) Vaccine consists of 3 doses of vaccine administered IM at 0, 1, and 6 months Seroprotection from vaccine: Decreases with age, obesity, smoking, immunosuppresion and comorbid conditions (including diabetes). Revaccination with 1-3 additional doses safely increases proportion of adults who achieve a protective level of anti-HBs (≥10 mIU/mL)
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The Hepatitis Vaccines Work Group developed economic models that yielded age-stratified calculations of incremental cost per quality- adjusted life year (QALY) saved based on vaccinating adults with diabetes again HBV. Estimated cost per QALY saved= $75,1000 (persons aged 20-50yo) Cost Increased with age. 1 time vaccination covering 10% of unvaccinated U.S. adults with DM age 20-59 yo (~529,047 people) would prevent 4271 HBV infections, 467 hospitalizations, 256 chronic cases, 33 HCC, 13 liver transplants, 130 deaths. Postvaccination serologic testing and revaccination would add considerable cost with limited increase in disease protection.
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Hep B vaccination should be administered to unvaccinated adults with diabetes mellitus aged 19-59 yo (recommendations category A). Hep B vaccination may be administered at the discretion of the treating clinician to unvaccinated adults with DM aged ≥60 yo (recommendation category B).
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Shared use of blood-contaminated equipment increases risk of HBV. Continued efforts are needed to increase adherence to good infection control practice. HBV vaccine should be given as soon as diabetes is diagnosed. There is no particular vaccine that is recommended. No serologic testing or additional HBV vaccination is recommended for adults who complete a series of hep B vaccine.
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HBV vaccine can be given safely at any age but less efficacious and less cost-effective for older adults. Decisions to vaccinate adults with DM ≥60yo should consider the likelihood of acquiring HBV. Vaccine may be administered during health care visits scheduled for other purposes. As long as minimum intervals between doses are observed. There is no maximum interval between doses that makes the vaccine series ineffective.
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