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2.
World J Gastroenterol ; 19(9): 1354-8, 2013 Mar 07.
Article in English | MEDLINE | ID: mdl-23538680

ABSTRACT

The patient with inflammatory bowel disease will be predisposed to numerous infections due their immune status. It is therefore important to understand the immune and serologic status at diagnosis and to put the patient into an adapted vaccination program. This program would be applied differently according to two patient groups: the immunocompromised and the non-immunocompromised. In general, the first group would avoid the use of live-virus vaccines, and in all cases, inflammatory bowel disease treatment would take precedence over vaccine risk. It is important to individualize vaccination schedules according to the type of patient, the treatment used and the disease pattern.In addition, patient with inflammatory bowel disease should be considered for the following vaccines: varicella vaccine, human papilloma virus, influenza, pneumococcal polysaccharide vaccine and hepatitis B vaccine.


Subject(s)
Bacterial Infections/prevention & control , Bacterial Vaccines/administration & dosage , Immunocompromised Host , Immunosuppressive Agents/adverse effects , Inflammatory Bowel Diseases/drug therapy , Vaccination , Viral Vaccines/administration & dosage , Virus Diseases/prevention & control , Bacterial Infections/immunology , Bacterial Infections/microbiology , Bacterial Vaccines/adverse effects , Humans , Inflammatory Bowel Diseases/epidemiology , Inflammatory Bowel Diseases/immunology , Patient Selection , Practice Guidelines as Topic , Risk Factors , Treatment Outcome , Vaccination/adverse effects , Viral Vaccines/adverse effects , Virus Diseases/immunology , Virus Diseases/virology
3.
World J Gastroenterol ; 19(9): 1342-8, 2013 Mar 07.
Article in English | MEDLINE | ID: mdl-23538480

ABSTRACT

Hepatitis B virus (HBV) is a very common infection worldwide. Its reactivation in patients receiving immunosuppression has been widely described as being associated with significant morbidity and mortality unless anti-viral prophylaxis is administered. Treatment in inflammatory bowel disease (IBD) patients has changed in recent years and immunosuppression and biological therapies are now used more frequently than before. Although current studies have reported an incidence of hepatitis B in inflammatory bowel disease patients similar to that in the general population, associated liver damage remains an important concern in this setting. Liver dysfunction may manifest in several ways, from a subtle change in serum aminotransferase levels to fulminant liver failure and death. Patients undergoing double immunosuppression are at a higher risk, and reactivation usually occurs after more than one year of treatment. As preventive measures, all IBD patients should be screened for HBV markers at diagnosis and those who are positive for the hepatitis B surface antigen should receive antiviral prophylaxis before undergoing immunosuppression in order to avoid HBV reactivation. Tenofovir/entecavir are preferred to lamivudine as nucleos(t)ide analogues due to their better resistance profile. In patients with occult or resolved HBV, viral reactivation does not appear to be a relevant issue and regular DNA determination is recommended during immunosuppression therapy. Consensus guidelines on this topic have been published in recent years. The prevention and management of HBV infection in IBD patients is addressed in this review in order to address practical recommendations.


Subject(s)
Antiviral Agents/administration & dosage , Hepatitis B virus/drug effects , Hepatitis B/prevention & control , Immunocompromised Host , Immunosuppressive Agents/adverse effects , Inflammatory Bowel Diseases/drug therapy , Drug Administration Schedule , Hepatitis B/diagnosis , Hepatitis B/epidemiology , Hepatitis B/immunology , Hepatitis B virus/growth & development , Hepatitis B virus/immunology , Humans , Inflammatory Bowel Diseases/epidemiology , Inflammatory Bowel Diseases/immunology , Practice Guidelines as Topic , Predictive Value of Tests , Prevalence , Risk Factors , Treatment Outcome , Virus Activation/drug effects
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