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老年人(≥60 岁)使用呼吸道合胞病毒疫苗:免疫实践咨询委员会更新的建议-美国,2024 年。

Use of Respiratory Syncytial Virus Vaccines in Adults Aged ≥60 Years: Updated Recommendations of the Advisory Committee on Immunization Practices - United States, 2024.

出版信息

MMWR Morb Mortal Wkly Rep. 2024 Aug 15;73(32):696-702. doi: 10.15585/mmwr.mm7332e1.

DOI:10.15585/mmwr.mm7332e1
PMID:39146277
Abstract

Respiratory syncytial virus (RSV) is a major cause of respiratory illness and hospitalization in older adults during fall and winter in the United States. The 2023-2024 RSV season was the first during which RSV vaccination was recommended for U.S. adults aged ≥60 years, using shared clinical decision-making. On June 26, 2024, the Advisory Committee on Immunization Practices voted to update this recommendation as follows: a single dose of any Food and Drug Administration-approved RSV vaccine (Arexvy [GSK]; Abrysvo [Pfizer]; or mResvia [Moderna]) is now recommended for all adults aged ≥75 years and for adults aged 60-74 years who are at increased risk for severe RSV disease. Adults who have previously received RSV vaccine should not receive another dose. This report summarizes the evidence considered for these updated recommendations, including postlicensure data on vaccine effectiveness and safety, and provides clinical guidance for the use of RSV vaccines in adults aged ≥60 years. These updated recommendations are intended to maximize RSV vaccination coverage among persons most likely to benefit, by clarifying who is at highest risk and by reducing implementation barriers associated with the previous shared clinical decision-making recommendation. Continued postlicensure monitoring will guide future recommendations.

摘要

呼吸道合胞病毒(RSV)是美国秋冬季节导致老年人呼吸道疾病和住院的主要原因。2023-2024 年 RSV 季节是首次推荐使用共享临床决策为美国≥60 岁成年人接种 RSV 疫苗。2024 年 6 月 26 日,免疫实践咨询委员会投票决定更新以下建议:所有≥75 岁的成年人以及 60-74 岁有严重 RSV 疾病风险的成年人都推荐接种任何经食品和药物管理局批准的 RSV 疫苗(Arexvy[葛兰素史克];Abrysvo[辉瑞];或 mResvia[莫德纳])一剂。以前接种过 RSV 疫苗的成年人不应再接种一剂。本报告总结了考虑这些更新建议的证据,包括疫苗有效性和安全性的上市后数据,并为≥60 岁成年人使用 RSV 疫苗提供了临床指导。这些更新的建议旨在通过明确高危人群并减少与先前共享临床决策建议相关的实施障碍,最大限度地提高最有可能受益人群的 RSV 疫苗接种覆盖率。持续的上市后监测将指导未来的建议。

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