Table 2.
Disease | Type of Immunogen | General Recommendation(s) for Vaccination in Patients With IBD | Concerns With IBD Patients on Immunosuppressive Therapy |
---|---|---|---|
HBV | Recombinant protein | An accelerated double-dose regimen is recommended in all HBV anti-HBc–seronegative patients with IBD. | None |
Influenza | Inactivated virus | 1 dose annually | None |
Pneumococcus | Polysaccharides, conjugated or not to a protein carrier | Patients should receive 1 dose of PCV13 followed by PPSV23 after 8 weeks if immunocompromised or after 1 year if immunocompetent, followed by PPSV23 dose every 5 years. | None |
Tetanus | Inactivated toxoid | If a patient was previously vaccinated, administer 1 dose every 10 years. If a patient was not previously vaccinated or if his or her vaccination status is unknown, administer 3 doses. The first 2 doses should be administered 4 weeks apart, with the third dose administered 6-12 months following the second dose. |
None |
Varicella zoster virus | Live attenuated virus | Check titers and vaccinate if not immune 3 months prior to biologic/immunosuppression initiation. If a patient is nonimmunized, administer 2 doses (0 and 1-2 months). |
Risks and benefits should be evaluated on an individual basis. |
Herpes zoster virus | Live attenuated virus | ECCO guidelines: patients >60 years should follow the standard schedule. ACG guidelines: patients >50 years, including those on low levels of immunosuppression (methotrexate, <0.4 mg/kg/week; azathioprine, <3.0 mg/kg/day; 6-mercaptopurine, <1.5 mg/kg/ day), should follow the standard schedule. |
Risks and benefits should be evaluated on an individual basis. |
ACG, American College of Gastroenterology; anti-HBc, hepatitis B core antibody; ECCO, European Crohn’s and Colitis Organisation; HBV, hepatitis B virus; IBD, inflammatory bowel disease; PCV13, 13-valent pneumococcal conjugate vaccine; PPSV23, 23-valent pneumococcal polysaccharide vaccine. | |||
Adapted from Mir FA and Kane SV.91 |