Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018

Epidemiologic data regarding the risk of Guillain-Barré syndrome (GBS) following herpes zoster (HZ) are limited. We conducted a self-controlled case series analysis using two large national data sources to evaluate the risk of GBS following HZ among U.S. adults. We analyzed medical claims from the I...

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Main Authors: Tara C. Anderson, Jessica W. Leung, Rafael Harpaz, Kathleen L. Dooling
Format: Article
Language:English
Published: Taylor & Francis Group 2021-12-01
Series:Human Vaccines & Immunotherapeutics
Subjects:
Online Access:http://dx.doi.org/10.1080/21645515.2021.1985890
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author Tara C. Anderson
Jessica W. Leung
Rafael Harpaz
Kathleen L. Dooling
author_facet Tara C. Anderson
Jessica W. Leung
Rafael Harpaz
Kathleen L. Dooling
author_sort Tara C. Anderson
collection DOAJ
description Epidemiologic data regarding the risk of Guillain-Barré syndrome (GBS) following herpes zoster (HZ) are limited. We conducted a self-controlled case series analysis using two large national data sources to evaluate the risk of GBS following HZ among U.S. adults. We analyzed medical claims from the IBM® MarketScan® Commercial Claims and Encounters (persons 18–64 years during 2010–2018) and Centers for Medicare and Medicaid Services Medicare (persons ≥65 years during 2014–2018) databases. HZ cases were defined as persons with an outpatient claim with a primary or secondary ICD-9 or ICD-10 diagnostic code for HZ. GBS cases were defined as persons with an inpatient claim with a principle diagnostic code for GBS and an associated procedural code. We compared the rates of GBS following HZ in the 1–42-day risk window versus primary (100–365-day) or secondary (43–99-day) control windows. We identified 489,516 persons 18–64 years of age and 650,229 persons ≥65 years of age with HZ, among whom 11 and 41, respectively, developed GBS 1–365 days following HZ. The risk of GBS following HZ was increased during the risk window as compared to the primary control window for both groups, with a rate ratio of 6.3 (95% CI, 1.8–21.9) for those 18–64 years and 4.1 (95% CI, 1.9–8.7) for those ≥65 years. This study provides new and methodologically rigorous epidemiologic support for an association between HZ and GBS, and useful context regarding the benefits versus potential risks of zoster vaccination.
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spelling doaj.art-61a324f1c28d4030a4e086dc1828c4b92023-09-26T12:43:42ZengTaylor & Francis GroupHuman Vaccines & Immunotherapeutics2164-55152164-554X2021-12-0117125304531010.1080/21645515.2021.19858901985890Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018Tara C. Anderson0Jessica W. Leung1Rafael Harpaz2Kathleen L. Dooling3Centers for Disease Control and PreventionCenters for Disease Control and PreventionHarpaz Herman Consultants, LLCCenters for Disease Control and PreventionEpidemiologic data regarding the risk of Guillain-Barré syndrome (GBS) following herpes zoster (HZ) are limited. We conducted a self-controlled case series analysis using two large national data sources to evaluate the risk of GBS following HZ among U.S. adults. We analyzed medical claims from the IBM® MarketScan® Commercial Claims and Encounters (persons 18–64 years during 2010–2018) and Centers for Medicare and Medicaid Services Medicare (persons ≥65 years during 2014–2018) databases. HZ cases were defined as persons with an outpatient claim with a primary or secondary ICD-9 or ICD-10 diagnostic code for HZ. GBS cases were defined as persons with an inpatient claim with a principle diagnostic code for GBS and an associated procedural code. We compared the rates of GBS following HZ in the 1–42-day risk window versus primary (100–365-day) or secondary (43–99-day) control windows. We identified 489,516 persons 18–64 years of age and 650,229 persons ≥65 years of age with HZ, among whom 11 and 41, respectively, developed GBS 1–365 days following HZ. The risk of GBS following HZ was increased during the risk window as compared to the primary control window for both groups, with a rate ratio of 6.3 (95% CI, 1.8–21.9) for those 18–64 years and 4.1 (95% CI, 1.9–8.7) for those ≥65 years. This study provides new and methodologically rigorous epidemiologic support for an association between HZ and GBS, and useful context regarding the benefits versus potential risks of zoster vaccination.http://dx.doi.org/10.1080/21645515.2021.1985890zostershinglesguillain-barré syndromerecombinant zoster vaccineshingrixmarketscanmedicare
spellingShingle Tara C. Anderson
Jessica W. Leung
Rafael Harpaz
Kathleen L. Dooling
Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018
Human Vaccines & Immunotherapeutics
zoster
shingles
guillain-barré syndrome
recombinant zoster vaccine
shingrix
marketscan
medicare
title Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018
title_full Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018
title_fullStr Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018
title_full_unstemmed Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018
title_short Risk of Guillain-Barré syndrome following herpes zoster, United States, 2010–2018
title_sort risk of guillain barre syndrome following herpes zoster united states 2010 2018
topic zoster
shingles
guillain-barré syndrome
recombinant zoster vaccine
shingrix
marketscan
medicare
url http://dx.doi.org/10.1080/21645515.2021.1985890
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