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Vaccination of the Immunocompromised Host

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Table 7. Vaccination of Persons With Asplenia or a Sickle Cell Disease, Cochlear Implants, or CSF Leak Recommendation (Strength, Evidence Quality) Vaccine Asplenia or a Sickle Cell Disease Cochlear Implants a or CSF Leak H influenzae type b conjugate U: age <5 y (SR-M) R: age ≥5 y (WR-L) U (SR-M) Hepatitis A U (SR-M) U (SR-M) Hepatitis B U (SR-M) U (SR-M) DTaP, Td, Tdap U (SR-M) U (SR-M) HPV U (SR-M) U (SR-M) Influenza, inactivated U (SR-M) U (SR-M) Influenza, live attenuated X (WR-VL) U (SR-M) MMR, live U (SR-M) U (SR-M) MMRV, live U (SR-M) U (SR-M) Meningococcal conjugate R: age 2-55 y b (SR-L) U (SR-M) Meningococcal polysaccharide R: age >55 y b (SR-L) U (SR-M) Pneumococcal conjugate (PCV13) U: age <6 y c (SR-M) R: age ≥6 y d (SR-VL) U: age <6 y c (SR-M) R: age ≥6 y d (SR-L) Pneumococcal polysaccharide (PPSV23) R: age ≥2 y e (SR-L) R: age ≥2 y e (SR-M) Poliovirus, inactivated U (SR-M) U (SR-M) Rotavirus, live U (SR-M) U (SR-M) Varicella, live U (SR-M) U (SR-M) Zoster, live U (SR-M) U (SR-M) R, recommended—administer if not previously administered or not current; such patients may be at increased risk for this vaccine-preventable infection; U, usual—administer if patient not current with recommendations for dose(s) of vaccine for immunocompetent persons in risk and age categories; X, contraindicated. a Includes patients with profound hearing loss who are scheduled to receive a cochlear implant or have inner ear-cerebrospinal fluid communication. b A 2-dose primary series should be administered and an additional dose every 5 years. c Two doses of PCV13 for children 2 through 5 years of age who have not previously received doses of PCV or received <3 doses of PCV7. d If PCV13 has not previously been administered. For patients ≥19 years who have previously received PPSV23, PCV13 should be administered aer an interval of ≥1 year aer the last PPSV23 dose (WR-L). e Administer 8 or more weeks aer indicated dose(s) of PCV13 and a single revaccination with PPSV23 5 years aer the initial dose (SR-M). 29

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