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Trivalent and quadrivalent influenza vaccination effectiveness in Australia and South Africa: results from a modelling study.
Milne, George J; Halder, Nilimesh; Kelso, Joel K; Barr, Ian G; Moyes, Jocelyn; Kahn, Kathleen; Twine, Rhian; Cohen, Cheryl.
Affiliation
  • Milne GJ; School of Computer Science and Software Engineering, University of Western Australia, Perth, WA, Australia.
  • Halder N; School of Computer Science and Software Engineering, University of Western Australia, Perth, WA, Australia.
  • Kelso JK; School of Computer Science and Software Engineering, University of Western Australia, Perth, WA, Australia.
  • Barr IG; World Health Organization (WHO) Collaborating Centre for Reference and Research on Influenza, Melbourne, Vic., Australia.
  • Moyes J; Centre for Respiratory Disease and Meningitis, National Institute for Communicable Diseases, Johannesburg, South Africa.
  • Kahn K; MRC/Wits Rural Public Health and Health Transitions Research Unit (Agincourt), Faculty of Health Science, School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.
  • Twine R; MRC/Wits Rural Public Health and Health Transitions Research Unit (Agincourt), Faculty of Health Science, School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.
  • Cohen C; Centre for Respiratory Disease and Meningitis, National Institute for Communicable Diseases, Johannesburg, South Africa.
Influenza Other Respir Viruses ; 10(4): 324-32, 2016 07.
Article in En | MEDLINE | ID: mdl-26663701
BACKGROUND: A modelling study was conducted to determine the effectiveness of trivalent (TIV) and quadrivalent (QIV) vaccination in South Africa and Australia. OBJECTIVES: This study aimed to determine the potential benefits of alternative vaccination strategies which may depend on community-specific demographic and health characteristics. METHODS: Two influenza A and two influenza B strains were simulated using individual-based simulation models representing specific communities in South Africa and Australia over 11 years. Scenarios using TIV or QIV, with alternative prioritisation strategies and vaccine coverage levels, were evaluated using a country-specific health outcomes process. RESULTS: In South Africa, approximately 18% fewer deaths and hospitalisations would be expected to result from the use of QIV compared to TIV over the 11 modelled years (P = 0·031). In Australia, only 2% (P = 0·30) fewer deaths and hospitalisations would result. Vaccinating 2%, 5%, 15% or 20% of the population with TIV using a strategy of prioritising vulnerable age groups, including HIV-positive individuals, resulted in reductions in hospitalisations and mortality of at least 7%, 18%, 57% and 66%, respectively, in both communities. CONCLUSIONS: The degree to which QIV can reduce health burden compared to TIV is strongly dependent on the number of years in which the influenza B lineage in the TIV matches the circulating B lineages. Assuming a moderate level of B cross-strain protection, TIV may be as effective as QIV. The choice of vaccination prioritisation has a greater impact than the QIV/TIV choice, with strategies targeting those most responsible for transmission being most effective.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Influenza A virus / Influenza B virus / Influenza Vaccines / Influenza, Human Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Africa / Oceania Language: En Journal: Influenza Other Respir Viruses Journal subject: VIROLOGIA Year: 2016 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Influenza A virus / Influenza B virus / Influenza Vaccines / Influenza, Human Type of study: Prognostic_studies Limits: Female / Humans / Male Country/Region as subject: Africa / Oceania Language: En Journal: Influenza Other Respir Viruses Journal subject: VIROLOGIA Year: 2016 Type: Article Affiliation country: Australia