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Impact of regulatory risk communication on thrombosis with thrombocytopenia syndrome for COVID-19 adenovirus vector vaccines on European Healthcare Professionals
ID Vliet, Ella van (Avtor), ID Čebron Lipovec, Nanča (Avtor), ID van der Goot, Marloes (Avtor), ID Abtahi, Shahab (Avtor), ID Ribeiro-Vaz, Inês (Avtor), ID Poplavska, Elita (Avtor), ID Dermiki-Gkana, Foteini (Avtor), ID Oikonomou, Chara (Avtor), ID Deligianni, Elena (Avtor), ID Kos, Mitja (Avtor)

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Izvleček
Purpose: The European Medicines Agency (EMA) issued regulatory actions and communications in 2021 on thrombosis withthrombocytopenia syndrome (TTS) associated with adenovirus vector vaccines Vaxzevria or Jcovden. This study aimed to eval-uate the impact of these actions on awareness, knowledge and implementation in practises of healthcare professionals (HCP).Methods: Web-based cross-sectional surveys were conducted on HCPs engaged in the vaccination, monitoring or counsellingabout the vaccines. We measured awareness and knowledge of the risk of TTS and their implementation of recommendationsin practise. Descriptive and qualitative analyses were conducted. This study took place in Greece, Latvia, Netherlands, Portugaland Slovenia. Results: We surveyed 1659 HCPs. From these, 914 were included in the analysis. Most were aware about the reports of TTSassociated with COVID-19 adenovirus vector vaccines, with countries reporting percentages between 85% and 97%. Mainstreammedia, health authorities and peers were the main sources of TTS risk information. Most HCPs were able to identify key symptoms from TTS but were less familiar with minor symptoms. Guidelines from health authorities on COVID-19 vaccinationimpacted on professional practise of 55%–77% of HCPs. The reported use of product information across countries was moderate,with some variations. Conclusions: Awareness about and knowledge of TTS risk from COVID-19 adenoviral vector vaccines were high among HCPs.HCPs reported a clear preference for national guidelines as source of risk information and the implementation of product infor-mation remained moderate across countries.

Jezik:Angleški jezik
Ključne besede:COVID-19 vaccines, healthcare professionals, regulatory actions, risk communication, SARS- CoV-2 adenovirus vector vaccines, thrombosis with thrombocytopenia syndrome
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FFA - Fakulteta za farmacijo
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2024
Št. strani:14 str.
Številčenje:Vol. 33, iss. 12, [article e70057]
PID:20.500.12556/RUL-165843 Povezava se odpre v novem oknu
UDK:615.371:616-005.6
ISSN pri članku:1053-8569
DOI:10.1002/pds.70057 Povezava se odpre v novem oknu
COBISS.SI-ID:216692483 Povezava se odpre v novem oknu
Datum objave v RUL:12.12.2024
Število ogledov:681
Število prenosov:94
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Pharmacoepidemiology and drug safety
Skrajšan naslov:Pharmacoepidemiol. drug saf.
Založnik:Wiley
ISSN:1053-8569
COBISS.SI-ID:1515540 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:regulativni ukrepi, zdravstveni delavci, tromboza s trombocitopeničnim sindromom, tromboza, cepiva, SARS-CoV-2, COVID-19

Projekti

Financer:Drugi - Drug financer ali več financerjev
Številka projekta:EMA/2018/23/PE
Naslov:European Medicines Agency
Akronim:EMA

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