4.5 Editorial Material

Planning for COVID-19 vaccines safety surveillance

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VACCINE
卷 38, 期 40, 页码 6194-6198

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ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2020.07.013

关键词

Severe acute respiratory syndrome; coronavirus 2; SARS-CoV-2; Coronavirus; COVID-19; Vaccines; Epidemic; Outbreak; Pandemic; Clinical research; Safety; Surveillance Adverse event of special interest (AESI); Adverse event following immunization (AEFI); CEPI; WHO; Global Vaccine Safety Blueprint

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COVID-19 vaccines are the most important tool to stem the pandemic. They are being developed with unprecedented global collaboration and accelerated timelines to achieve WHO Emergency Use Listing, while using regulatory pathways through national regulatory authorities. Alongside preparations to ensure equitable access to the vaccines among people globally, preparations must be made within countries for COVID-19 vaccines safety surveillance on an urgent basis. Safety surveillance must be capable of investigating adverse events of special interest (AESI) and adverse events following immunization to determine a change in the benefit-risk profile of the vaccine, and to be able to anticipate coincidental events that might be attributed to the vaccine. Active surveillance systems should calculate the incidence of background rates of AESI prior to vaccine roll out. These background rates vary tremendously across regions, populations and case ascertainment methods. Active surveillance systems must be established or strengthened now, (including in LMIC), to calculate the background rates. Utilizing standardized case definitions and global standards for AESI will help in harmonization. Vaccine safety communication plans should be developed. Expanding the global vaccine safety system to meet the needs of COVID-19 and other emergency and routine use vaccines is a priority currently. (C) 2020 Elsevier Ltd All rights reserved.

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