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Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020

Hepatitis A is a vaccine-preventable, communicable disease of the liver caused by the hepatitis A virus (HAV). The infection is transmitted via the fecal-oral route, usually from direct person-to-person contact or consumption of contaminated food or water. Hepatitis A is an acute, self-limited disea...

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Autores principales: Nelson, Noele P., Weng, Mark K., Hofmeister, Megan G., Moore, Kelly L., Doshani, Mona, Kamili, Saleem, Koneru, Alaya, Haber, Penina, Hagan, Liesl, Romero, José R., Schillie, Sarah, Harris, Aaron M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631741/
https://www.ncbi.nlm.nih.gov/pubmed/32614811
http://dx.doi.org/10.15585/mmwr.rr6905a1
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author Nelson, Noele P.
Weng, Mark K.
Hofmeister, Megan G.
Moore, Kelly L.
Doshani, Mona
Kamili, Saleem
Koneru, Alaya
Haber, Penina
Hagan, Liesl
Romero, José R.
Schillie, Sarah
Harris, Aaron M.
author_facet Nelson, Noele P.
Weng, Mark K.
Hofmeister, Megan G.
Moore, Kelly L.
Doshani, Mona
Kamili, Saleem
Koneru, Alaya
Haber, Penina
Hagan, Liesl
Romero, José R.
Schillie, Sarah
Harris, Aaron M.
author_sort Nelson, Noele P.
collection PubMed
description Hepatitis A is a vaccine-preventable, communicable disease of the liver caused by the hepatitis A virus (HAV). The infection is transmitted via the fecal-oral route, usually from direct person-to-person contact or consumption of contaminated food or water. Hepatitis A is an acute, self-limited disease that does not result in chronic infection. HAV antibodies (immunoglobulin G [IgG] anti-HAV) produced in response to HAV infection persist for life and protect against reinfection; IgG anti-HAV produced after vaccination confer long-term immunity. This report supplants and summarizes previously published recommendations from the Advisory Committee on Immunization Practices (ACIP) regarding the prevention of HAV infection in the United States. ACIP recommends routine vaccination of children aged 12–23 months and catch-up vaccination for children and adolescents aged 2–18 years who have not previously received hepatitis A (HepA) vaccine at any age. ACIP recommends HepA vaccination for adults at risk for HAV infection or severe disease from HAV infection and for adults requesting protection against HAV without acknowledgment of a risk factor. These recommendations also provide guidance for vaccination before travel, for postexposure prophylaxis, in settings providing services to adults, and during outbreaks
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spelling pubmed-86317412021-12-08 Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020 Nelson, Noele P. Weng, Mark K. Hofmeister, Megan G. Moore, Kelly L. Doshani, Mona Kamili, Saleem Koneru, Alaya Haber, Penina Hagan, Liesl Romero, José R. Schillie, Sarah Harris, Aaron M. MMWR Recomm Rep Recommendations and Reports Hepatitis A is a vaccine-preventable, communicable disease of the liver caused by the hepatitis A virus (HAV). The infection is transmitted via the fecal-oral route, usually from direct person-to-person contact or consumption of contaminated food or water. Hepatitis A is an acute, self-limited disease that does not result in chronic infection. HAV antibodies (immunoglobulin G [IgG] anti-HAV) produced in response to HAV infection persist for life and protect against reinfection; IgG anti-HAV produced after vaccination confer long-term immunity. This report supplants and summarizes previously published recommendations from the Advisory Committee on Immunization Practices (ACIP) regarding the prevention of HAV infection in the United States. ACIP recommends routine vaccination of children aged 12–23 months and catch-up vaccination for children and adolescents aged 2–18 years who have not previously received hepatitis A (HepA) vaccine at any age. ACIP recommends HepA vaccination for adults at risk for HAV infection or severe disease from HAV infection and for adults requesting protection against HAV without acknowledgment of a risk factor. These recommendations also provide guidance for vaccination before travel, for postexposure prophylaxis, in settings providing services to adults, and during outbreaks Centers for Disease Control and Prevention 2020-07-03 /pmc/articles/PMC8631741/ /pubmed/32614811 http://dx.doi.org/10.15585/mmwr.rr6905a1 Text en https://creativecommons.org/licenses/by/3.0/All material in the MMWR Series is in the public domain and may be used and reprinted without permission; citation as to source, however, is appreciated.
spellingShingle Recommendations and Reports
Nelson, Noele P.
Weng, Mark K.
Hofmeister, Megan G.
Moore, Kelly L.
Doshani, Mona
Kamili, Saleem
Koneru, Alaya
Haber, Penina
Hagan, Liesl
Romero, José R.
Schillie, Sarah
Harris, Aaron M.
Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020
title Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020
title_full Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020
title_fullStr Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020
title_full_unstemmed Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020
title_short Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020
title_sort prevention of hepatitis a virus infection in the united states: recommendations of the advisory committee on immunization practices, 2020
topic Recommendations and Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631741/
https://www.ncbi.nlm.nih.gov/pubmed/32614811
http://dx.doi.org/10.15585/mmwr.rr6905a1
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