164. Effectiveness of Adjuvanted Inactivated Influenza Vaccine versus High-Dose Inactivated Influenza Vaccine Against PCR-Confirmed Influenza among Adults ≥65 years: A Pragmatic Randomized Study

医学 流感疫苗 病毒学 灭活疫苗 接种疫苗 免疫学
作者
Amber Hsiao,Arnold Yee,Thomas Leong,Ousseny Zerbo,Bruce Fireman,Karen B. Jacobson,John Hansen,Evan Layefsky,Mendel Haag,Ian McGovern,Bin Zhang,Juliet Dang,Nicola P. Klein
出处
期刊:Open Forum Infectious Diseases [Oxford University Press]
卷期号:12 (Supplement_1) 被引量:1
标识
DOI:10.1093/ofid/ofae631.001
摘要

Abstract Background In the US, adults aged ≥65 years are recommended to receive an adjuvanted or higher dose influenza vaccine. Adjuvanted (aIIV) and high-dose (HD-IIV) inactivated influenza vaccines were similarly effective against influenza in several studies based on diagnostic codes. However, less is known about their relative vaccine effectiveness (rVE) against laboratory-confirmed influenza and they have never been compared in a randomized study. We assessed the rVE of adjuvanted vs. high-dose vaccines against PCR-confirmed influenza in adults aged ≥65 years at Kaiser Permanente Northern California (KPNC). Methods During the 2023-2024 influenza season, we randomized all KPNC facilities to administer aIIV vs. HD-IIV in alternating weeks to achieve balance between the two vaccine groups. Individuals received either aIIV or HD-IIV depending on which facility and week they sought vaccination. The primary outcome was PCR-confirmed influenza in any clinical setting. Secondary outcomes were hospitalizations or emergency department (ED) visits for PCR-confirmed influenza and hospitalizations for community-acquired pneumonia (CAP). Using Cox regression on a calendar timeline, we estimated the relative vaccine effectiveness (rVE) of aIIV vs. HD-IIV as 1 minus the adjusted hazard ratio, adjusted for age, sex, race/ethnicity, and other covariates. Results The study population included 429,600 individuals; 212,887 (49.6%) received aIIV and 216,723 (50.4%) received HD-IIV. Baseline characteristics were well balanced between the two groups (Table 1). There were 836 cases of PCR-confirmed influenza (3.9 per 1000 persons) after aIIV and 867 cases (4.0 per 1000 persons) after HD-IIV. Comparing aIIV with HD-IIV, the rVE against PCR-confirmed influenza was 1.5% (95% CI: -8.4%, 10.5%; Table 2). AIIV and HD-IIV also did not differ in effectiveness against PCR-confirmed influenza hospitalizations/ED visits (rVE: 9.1%; CI: -3.9%, 20.4%) and CAP hospitalizations (rVE: 1.0%; CI: -11.4%, 12.0%). Conclusion In this large, pragmatic randomized study in adults aged ≥65 years during the 2023-2024 influenza season, adjuvanted and high-dose influenza vaccines did not differ in effectiveness against laboratory-confirmed influenza. Disclosures Mendel Haag, PhD, PharmD, CSL Seqirus: Employee|CSL Seqirus: Stocks/Bonds (Public Company) Ian McGovern, MPH, CSL Seqirus: employee|CSL Seqirus: Stocks/Bonds (Public Company) Bin Zhang, ScD, MA, CSL Seqirus: Employee|CSL Seqirus: Stocks/Bonds (Public Company) Juliet Dang, PhD, MS, CSL Seqirus: Employee|CSL Seqirus: Stocks/Bonds (Public Company) Nicola P. Klein, MD, PhD, GlaxoSmithKline: Grant/Research Support|Merck: Grant/Research Support|Pfizer: Grant/Research Support|Sanofi Pasteur: Grant/Research Support|Seqirus: Grant/Research Support
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