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Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins

BACKGROUND: Varicella zoster virus (VZV) exposure seriously threatens immunocompromised hosts. Postexposure prophylaxis (PEP) using immune globulins is considered the standard of care; however, the available literature is mainly based on its use in pediatric patients. Here, we describe a widespread...

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Autores principales: Gelman, Daniel, Zektser, Miri, Nesher, Lior
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226185/
https://www.ncbi.nlm.nih.gov/pubmed/37256153
http://dx.doi.org/10.1017/ash.2023.167
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author Gelman, Daniel
Zektser, Miri
Nesher, Lior
author_facet Gelman, Daniel
Zektser, Miri
Nesher, Lior
author_sort Gelman, Daniel
collection PubMed
description BACKGROUND: Varicella zoster virus (VZV) exposure seriously threatens immunocompromised hosts. Postexposure prophylaxis (PEP) using immune globulins is considered the standard of care; however, the available literature is mainly based on its use in pediatric patients. Here, we describe a widespread VZV exposure among immunocompromised adults treated with VZV-specific immunoglobulins (VZVSIG), and we discuss management and outcomes. METHODS: We conducted a retrospective study to describe the exposure of immunocompromised patients to a single healthcare worker with primary VZV in 2019. Patients were grouped by their overall risk for infection, and those at risk received a single intramuscular dose of 625 IU of VZVSIG and were followed for 1 year. RESULTS: In total, 83 patients received PEP at <96 hours of exposure: 14 were hospitalized, 68 were outpatients, and 1 was an immunocompromised staff member. The median age was 69 years (range, 21–92), and 49.4% were male. In addition, 30% of the patients were deemed high risk, 42% were intermediate risk, and 28% were considered low risk, although they were given PEP. Varicella infection was not diagnosed in any patient in the first weeks of follow-up. However, during the year of follow-up, 4 patients developed symptoms suspicious of VZV, all >3 months after exposure, thus were probably unrelated to the event. Adverse events related to VZVSIG (pyrexia) were reported in 2 patients (2.4%). CONCLUSIONS: Our findings demonstrate the utility of VZVSIG as PEP in one of the largest cohorts of immunocompromised adults to date. No early varicella infection was found following exposure, supporting the current recommendations of the VZVSIG administration.
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spelling pubmed-102261852023-05-30 Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins Gelman, Daniel Zektser, Miri Nesher, Lior Antimicrob Steward Healthc Epidemiol Original Article BACKGROUND: Varicella zoster virus (VZV) exposure seriously threatens immunocompromised hosts. Postexposure prophylaxis (PEP) using immune globulins is considered the standard of care; however, the available literature is mainly based on its use in pediatric patients. Here, we describe a widespread VZV exposure among immunocompromised adults treated with VZV-specific immunoglobulins (VZVSIG), and we discuss management and outcomes. METHODS: We conducted a retrospective study to describe the exposure of immunocompromised patients to a single healthcare worker with primary VZV in 2019. Patients were grouped by their overall risk for infection, and those at risk received a single intramuscular dose of 625 IU of VZVSIG and were followed for 1 year. RESULTS: In total, 83 patients received PEP at <96 hours of exposure: 14 were hospitalized, 68 were outpatients, and 1 was an immunocompromised staff member. The median age was 69 years (range, 21–92), and 49.4% were male. In addition, 30% of the patients were deemed high risk, 42% were intermediate risk, and 28% were considered low risk, although they were given PEP. Varicella infection was not diagnosed in any patient in the first weeks of follow-up. However, during the year of follow-up, 4 patients developed symptoms suspicious of VZV, all >3 months after exposure, thus were probably unrelated to the event. Adverse events related to VZVSIG (pyrexia) were reported in 2 patients (2.4%). CONCLUSIONS: Our findings demonstrate the utility of VZVSIG as PEP in one of the largest cohorts of immunocompromised adults to date. No early varicella infection was found following exposure, supporting the current recommendations of the VZVSIG administration. Cambridge University Press 2023-05-26 /pmc/articles/PMC10226185/ /pubmed/37256153 http://dx.doi.org/10.1017/ash.2023.167 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Article
Gelman, Daniel
Zektser, Miri
Nesher, Lior
Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins
title Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins
title_full Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins
title_fullStr Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins
title_full_unstemmed Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins
title_short Preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins
title_sort preventing varicella zoster infection in immunocompromised adults with varicella zoster–specific immunoglobulins
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226185/
https://www.ncbi.nlm.nih.gov/pubmed/37256153
http://dx.doi.org/10.1017/ash.2023.167
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