Vaccine Effectiveness Against Influenza A(H1N1), A(H3N2), and B–Associated Hospitalizations—United States, September 1, 2023–May 31, 2024

Nathaniel M Lewis, Elizabeth J Harker, Seana Cleary, Yuwei Zhu, Carlos G Grijalva, James D Chappell, Jillian P Rhoads, Adrienne Baughman, Jonathan D Casey, Paul W Blair, Ian D Jones, Cassandra A Johnson, Natasha B Halasa, Adam S Lauring, Emily T Martin, Manju Gaglani, Shekhar Ghamande, Cristie Columbus, Jay S Steingrub, Abhijit Duggal, Jamie R Felzer, Matthew E Prekker, Ithan D Peltan, Samuel M Brown, David N Hager, Michelle N Gong, Amira Mohamed, Matthew C Exline, Akram Khan, Samantha A N Ferguson, Jarrod Mosier, Nida Qadir, Steven Y Chang, Adit A Ginde, Anne Zepeski, Christopher Mallow, Estelle S Harris, Nicholas J Johnson, Kevin W Gibbs, Jennie H Kwon, Ivana A Vaughn, Mayur Ramesh, Basmah Safdar, Diya Surie, Fatimah S Dawood, Sascha Ellington, Wesley H Self
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Abstract

Background The 2023–2024 influenza season included sustained elevated activity from December 2023–February 2024 and continued activity through May 2024. Influenza A(H1N1), A(H3N2), and B viruses circulated during the season. Methods During September 1, 2023–May 31, 2024, a multistate sentinel surveillance network of 24 medical centers in 20 U.S. states enrolled adults aged ≥18 years hospitalized with acute respiratory illness (ARI). Consistent with a test-negative design, cases tested positive for influenza viruses by molecular or antigen test, and controls tested negative for influenza viruses and SARS-CoV-2. Vaccine effectiveness (VE) against influenza–associated hospitalization was calculated as (1 − adjusted odds ratio for vaccination) × 100%. Results Among 7690 patients, including 1170 influenza cases (33% vaccinated) and 6520 controls, VE was 40% (95% CI: 31%–48%) with varying estimates by age (18–49 years: 53% [34%–67%]; 50–64 years: 47% [31%–60%]; ≥65 years: 31% [16%–43%]). Protection was similar among immunocompetent patients (40% [30%–49%]) and immunocompromised patients (32% [7–50%]). VE was statistically significant against influenza B (67% [35%–84%]) and A(H1N1) (36% [21%–48%]) and crossed the null against A(H3N2) (19% [-8%–39%]). VE was higher for patients 14–60 days from vaccination (54% [40%–65%]) than >120 days (18% [-1%–33%]). Conclusions During 2023–2024, influenza vaccination reduced the risk of influenza A(H1N1)– and influenza B–associated hospitalizations among adults; effectiveness was lower in patients vaccinated >120 days prior to illness onset compared with those vaccinated 14–60 days prior.
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2023 年 9 月 1 日至 2024 年 5 月 31 日期间美国甲型 H1N1、甲型 H3N2 和乙型流感疫苗对相关住院治疗的有效性
2023-2024年流感季节包括2023年12月至2024年2月持续升高的活动性,并持续到2024年5月。流感A(H1N1)、A(H3N2)和B型病毒在这个季节流行。方法在2023年9月1日至2024年5月31日期间,美国20个州24个医疗中心的多州哨点监测网络招募了年龄≥18岁的急性呼吸道疾病(ARI)住院成年人。与检测阴性设计一致,病例经分子或抗原检测呈流感病毒阳性,对照组经流感病毒和SARS-CoV-2检测呈阴性。对流感相关住院的疫苗有效性(VE)计算为(接种1 -校正优势比)× 100%。结果在7690例患者中,包括1170例流感病例(33%接种疫苗)和6520例对照组,VE为40% (95% CI: 31%-48%),不同年龄的估计差异较大(18-49岁:53% [34%-67%];50-64岁:47% [31%-60%];≥65岁:31%[16%-43%])。免疫功能正常患者(40%[30%-49%])和免疫功能低下患者(32%[7-50%])的保护效果相似。VE对乙型流感(67%[35% ~ 84%])和甲型H1N1流感(36%[21% ~ 48%])的阳性率有统计学意义,对甲型H3N2流感(19%[-8% ~ 39%])的阳性率为零。接种疫苗后14-60天的VE(54%[40%-65%])高于接种疫苗后120天(18%[-1%-33%])。结论:在2023-2024年期间,流感疫苗接种降低了成人甲型H1N1流感和乙型流感相关住院的风险;与发病前14-60天接种疫苗的患者相比,在发病前120天接种疫苗的患者的有效性较低。
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