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2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022

BACKGROUND: COVID-19 vaccines are safe and effective. Rapid rollout of vaccines reduced COVID-19 morbidity and mortality globally. Pharmacovigilance systems have ensured safety of these vaccines. Well-functioning vaccine safety surveillance builds public confidence in vaccine programs, but these sys...

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Autores principales: Tursinov, Yunis, Kurbanov, Botirjon, Denebayeva, Alfiya, Horth, Roberta, Nabirova, Dilyara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677335/
http://dx.doi.org/10.1093/ofid/ofad500.2009
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author Tursinov, Yunis
Kurbanov, Botirjon
Denebayeva, Alfiya
Horth, Roberta
Nabirova, Dilyara
author_facet Tursinov, Yunis
Kurbanov, Botirjon
Denebayeva, Alfiya
Horth, Roberta
Nabirova, Dilyara
author_sort Tursinov, Yunis
collection PubMed
description BACKGROUND: COVID-19 vaccines are safe and effective. Rapid rollout of vaccines reduced COVID-19 morbidity and mortality globally. Pharmacovigilance systems have ensured safety of these vaccines. Well-functioning vaccine safety surveillance builds public confidence in vaccine programs, but these systems may be lacking in limited-resource settings. To identify gaps in pharmacovigilance surveillance, we conducted an evaluation in Khojaly District, Uzbekistan, with population of 120 thousand people. METHODS: We reviewed regulatory documents related to COVID-19 vaccination and registration of side effects after immunization. We also conducted a survey in April 2022 of 30 healthcare providers in 5 of 10 polyclinics in Khojaly districts whose responsibilities included vaccination of the population. The survey asked about their knowledge and practices related to adverse events following immunization (AEFI). AEFI was defined as any health condition that occurs after immunization and does not necessarily have a causal relationship with vaccination. RESULTS: From April 2021 to March 2022, 78,453 doses of COVID-19 vaccines were given in Khojaly district. Of these, 70% of doses were from ZF-UZ-VAC-2001 (Zifivax) vaccine doses, an adjuvanted protein produced in Uzbekistan (Table 1), 9% Pfizer–BioNTech vaccine doses and 7% Moderna vaccine doses. All AEFIs are mandatorily reported by providers (Figure 1). Of 2,464 reported AEFI, majority (75%) were procedural errors, 1% were mild allergic reactions, and only 2 cases of anaphylactic shock. Among healthcare providers surveyed (Table 2), 33% did not know where to report the AEFI and 10% reported large patient load as a barrier to reporting. Half (50%) of providers had encountered a case of AEFI following COVID-19 vaccination, 10% encountered a severe AEFI, and 43% submitted an AEFI report. In record review, we identified cases of AEFI that had only been registered in patient medical charts, and not reported into the AEFI surveillance system. Diagram of AEFI surveillance for COVID-19 vaccines in Uzbekistan [Figure: see text] COVID-19 vaccine doses and reported AEFI, Khojaly district, Uzbekistan, 2021-22 [Figure: see text] Knowledge of AEFI and AEFI reporting among COVID-19 vaccine providers, Khojaly district, Uzbekistan, 2021-22 [Figure: see text] CONCLUSION: Important considerations were identified in COVID-19 pharmacovigilance surveillance. The system can be strengthened through increased training of healthcare providers in standard operating procedures for identifying, reporting and investigation AEFI cases associated with COVID-19 vaccines. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106773352023-11-27 2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022 Tursinov, Yunis Kurbanov, Botirjon Denebayeva, Alfiya Horth, Roberta Nabirova, Dilyara Open Forum Infect Dis Abstract BACKGROUND: COVID-19 vaccines are safe and effective. Rapid rollout of vaccines reduced COVID-19 morbidity and mortality globally. Pharmacovigilance systems have ensured safety of these vaccines. Well-functioning vaccine safety surveillance builds public confidence in vaccine programs, but these systems may be lacking in limited-resource settings. To identify gaps in pharmacovigilance surveillance, we conducted an evaluation in Khojaly District, Uzbekistan, with population of 120 thousand people. METHODS: We reviewed regulatory documents related to COVID-19 vaccination and registration of side effects after immunization. We also conducted a survey in April 2022 of 30 healthcare providers in 5 of 10 polyclinics in Khojaly districts whose responsibilities included vaccination of the population. The survey asked about their knowledge and practices related to adverse events following immunization (AEFI). AEFI was defined as any health condition that occurs after immunization and does not necessarily have a causal relationship with vaccination. RESULTS: From April 2021 to March 2022, 78,453 doses of COVID-19 vaccines were given in Khojaly district. Of these, 70% of doses were from ZF-UZ-VAC-2001 (Zifivax) vaccine doses, an adjuvanted protein produced in Uzbekistan (Table 1), 9% Pfizer–BioNTech vaccine doses and 7% Moderna vaccine doses. All AEFIs are mandatorily reported by providers (Figure 1). Of 2,464 reported AEFI, majority (75%) were procedural errors, 1% were mild allergic reactions, and only 2 cases of anaphylactic shock. Among healthcare providers surveyed (Table 2), 33% did not know where to report the AEFI and 10% reported large patient load as a barrier to reporting. Half (50%) of providers had encountered a case of AEFI following COVID-19 vaccination, 10% encountered a severe AEFI, and 43% submitted an AEFI report. In record review, we identified cases of AEFI that had only been registered in patient medical charts, and not reported into the AEFI surveillance system. Diagram of AEFI surveillance for COVID-19 vaccines in Uzbekistan [Figure: see text] COVID-19 vaccine doses and reported AEFI, Khojaly district, Uzbekistan, 2021-22 [Figure: see text] Knowledge of AEFI and AEFI reporting among COVID-19 vaccine providers, Khojaly district, Uzbekistan, 2021-22 [Figure: see text] CONCLUSION: Important considerations were identified in COVID-19 pharmacovigilance surveillance. The system can be strengthened through increased training of healthcare providers in standard operating procedures for identifying, reporting and investigation AEFI cases associated with COVID-19 vaccines. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677335/ http://dx.doi.org/10.1093/ofid/ofad500.2009 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Tursinov, Yunis
Kurbanov, Botirjon
Denebayeva, Alfiya
Horth, Roberta
Nabirova, Dilyara
2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022
title 2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022
title_full 2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022
title_fullStr 2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022
title_full_unstemmed 2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022
title_short 2389. Surveillance evaluation of COVID-19 pharmacovigilance—Karakalpakstan, Uzbekistan, 2022
title_sort 2389. surveillance evaluation of covid-19 pharmacovigilance—karakalpakstan, uzbekistan, 2022
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677335/
http://dx.doi.org/10.1093/ofid/ofad500.2009
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