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Waning effectiveness against COVID-19-related hospitalization, severe complications, and mortality with two to three doses of CoronaVac and BNT162b2: a case-control study.
Yan, Vincent Ka Chun; Wan, Eric Yuk Fai; Ye, Xuxiao; Mok, Anna Hoi Ying; Lai, Francisco Tsz Tsun; Chui, Celine Sze Ling; Li, Xue; Wong, Carlos King Ho; Li, Philip Hei; Ma, Tiantian; Qin, Simon; Lau, Chak Sing; Wong, Ian Chi Kei; Chan, Esther Wai Yin.
  • Yan VKC; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, Centre for Safe Medication Practice and Research, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Wan EYF; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, Centre for Safe Medication Practice and Research, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Ye X; Laboratory of Data Discovery for Health (D24H), Hong Kong Science and Technology Park, Hong Kong, People's Republic of China.
  • Mok AHY; Department of Family Medicine and Primary Care, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Lai FTT; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, Centre for Safe Medication Practice and Research, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Chui CSL; Department of Family Medicine and Primary Care, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Li X; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, Centre for Safe Medication Practice and Research, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Wong CKH; Laboratory of Data Discovery for Health (D4H), Hong Kong Science and Technology Park, Hong Kong, People's Republic of China.
  • Li PH; Laboratory of Data Discovery for Health (D4H), Hong Kong Science and Technology Park, Hong Kong, People's Republic of China.
  • Ma T; School of Nursing, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Qin S; School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Lau CS; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, Centre for Safe Medication Practice and Research, The University of Hong Kong, Hong Kong, People's Republic of China.
  • Wong ICK; Laboratory of Data Discovery for Health (D4H), Hong Kong Science and Technology Park, Hong Kong, People's Republic of China.
  • Chan EWY; Department of Medicine, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
Emerg Microbes Infect ; 12(1): 2209201, 2023 Dec.
Artículo en Inglés | MEDLINE | ID: covidwho-2320605
ABSTRACT

BACKGROUND:

This study aims to evaluate waning effectiveness against severe and fatal COVID-19 with two to three doses of CoronaVac/BNT162b2, where data are limited.

METHODS:

A case-control study included individuals aged ≥18 years, unvaccinated or received two to three doses of CoronaVac/BNT162b2, using electronic healthcare databases in Hong Kong. Those with first COVID-19-related hospitalization, severe complications, or mortality between 1 January and 15 August 2022 were defined as cases and matched with up-to-10 controls by age, sex, index date, and Charlson Comorbidity Index. Vaccine effectiveness (VE) against COVID-19-related outcomes was estimated at different time intervals from second and third-dose vaccination (0-13 up-to 210-240 days) using conditional logistic regression adjusted for comorbidities and medications.

RESULTS:

By 211-240 days after second dose, VE against COVID-19-related hospitalization reduced to 46.6% (40.7-51.8%) for BNT162b2 and 36.2% (28.0-43.4%) for CoronaVac, and VE against COVID-19-related mortality were 73.8% (55.9-84.4%) and 76.6% (60.8-86.0%). After third dose, VE against COVID-19-related hospitalization decreased from 91.2% (89.5-92.6%) for BNT162b2 and 76.7% (73.7-79.4%) for CoronaVac at 0-13 days, to 67.1% (60.4-72.6%) and 51.3% (44.2-57.5%) at 91-120 days. VE against COVID-19-related mortality for BNT162b2 remained high from 0-13 days [98.2% (95.0-99.3%)] to 91-120 days [94.6% (77.7-98.7%)], and for CoronaVac reduced from 0-13 days [96.7% (93.2-98.4%)] to 91-120 days [86.4% (73.3-93.1%)].

CONCLUSIONS:

Significant risk reduction against COVID-19-related hospitalization and mortality after CoronaVac or BNT162b2 vaccination was observed for >240 and >120 days after second and third doses compared to unvaccinated, despite significant waning over time. Timely administration of booster doses could provide higher levels of protection.
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: COVID-19 / Vacuna BNT162 Tipo de estudio: Estudio experimental / Estudio observacional / Estudio pronóstico Tópicos: Vacunas Límite: Adolescente / Adulto / Humanos Idioma: Inglés Revista: Emerg Microbes Infect Año: 2023 Tipo del documento: Artículo

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Asunto principal: COVID-19 / Vacuna BNT162 Tipo de estudio: Estudio experimental / Estudio observacional / Estudio pronóstico Tópicos: Vacunas Límite: Adolescente / Adulto / Humanos Idioma: Inglés Revista: Emerg Microbes Infect Año: 2023 Tipo del documento: Artículo