Cluster-randomized Trial of Adjuvanted Versus Nonadjuvanted Trivalent Influenza Vaccine in 823 US Nursing Homes

Author:

McConeghy Kevin W12ORCID,Davidson H Edward3,Canaday David H456,Han Lisa3,Saade Elie456,Mor Vince1278,Gravenstein Stefan1278

Affiliation:

1. Center on Innovation in Long-Term Services and Supports, Veterans Administration Medical Center, Providence, Rhode Island, USA

2. School of Public Health, Brown University, Providence, Rhode Island, USA

3. Insight Therapeutics, LLC, Norfolk, Virginia, USA

4. Louis Stokes Veterans Administration Center, Cleveland, Ohio, USA

5. Department of Medicine, Case Western Reserve University, Cleveland, Ohio, USA

6. University Hospitals Cleveland Medical Center, Cleveland, Ohio, USA

7. Center for Gerontology and Healthcare Research, Brown University, Providence, Rhode Island, USA

8. Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA

Abstract

Abstract Background Influenza leads in preventable infection-related hospitalization in nursing home (NH) residents. The adjuvanted trivalent influenza vaccine (aTIV) is more immunogenic than similarly dosed nonadjuvanted trivalent influenza vaccine (TIV), and observational studies suggest aTIV better prevents hospitalizations in older adults. We prospectively tested this in an NH setting. Methods NHs with ≥50 long-stay residents aged ≥65 years were randomized to offer aTIV or TIV for residents for the 2016–2017 influenza season. Using intent-to-treat resident-level analysis with Cox proportional hazards regression models adjusted for clustering by facility and a priori baseline covariates (eg, age, heart failure, and facility-level characteristics), we assessed relative aTIV:TIV effectiveness for hospitalization (ie, all-cause, respiratory, and pneumonia and influenza [P&I]). Results We randomized 823 NHs, housing 50 012 eligible residents, to aTIV or TIV. Residents were similar between groups by age (mean, ~79 years), heart failure, lung disease, and influenza and pneumococcal vaccine uptake, except aTIV homes housed fewer Black residents (14.5 vs 18.9%). Staff vaccine uptake was similar (~55%). P&I and all-cause resident hospitalization rates were lower (adjusted HR [aHR], .80 [95% CI, .66–.98; P = .03] and .94 [.89–.99; P = .02], respectively) for aTIV versus TIV, while the respiratory hospitalization rate was similar, in a season where vaccine effectiveness was considered poor. Conclusions aTIV was more effective than TIV in preventing all-cause and P&I hospitalization from NHs during an A/H3N2-predominant season when TIV was relatively ineffective. Clinical Trials Registration NCT02882100.

Funder

Seqirus Pharmaceuticals

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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