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

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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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%]). 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引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vaccine Effectiveness Against Influenza A(H1N1), A(H3N2), and B–Associated Hospitalizations—United States, September 1, 2023–May 31, 2024
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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