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带状疱疹重组疫苗的有效性和安全性:真实世界证据的综述。

Effectiveness and safety of recombinant zoster vaccine: A review of real-world evidence.

机构信息

Global Medical Affairs, GSK, Wavre, Belgium.

US Health Outcomes and Epidemiology, GSK, Philadelphia, PA, USA.

出版信息

Hum Vaccin Immunother. 2023 Dec 15;19(3):2263979. doi: 10.1080/21645515.2023.2263979. Epub 2023 Nov 15.

Abstract

The recombinant zoster vaccine (RZV) was licensed in the US for prevention of herpes zoster (HZ) in 2017. We conducted a literature search (January 1, 2017-August 1, 2023) using PubMed, Embase, and Scopus to consolidate the real-world evidence related to RZV. Overall, RZV effectiveness against HZ was high across the studied populations in real-world settings, including adults aged ≥ 50 years and patients aged ≥ 18 years with immunodeficiency or immunosuppression. Effectiveness was higher with two doses versus one dose, especially in elderly people and immunocompromised individuals. The safety profile of RZV was broadly consistent with that established in clinical trials. RZV does not appear to increase the risk of disease flares in patients with immune-mediated diseases. Approximately two-thirds of individuals received a second RZV dose within 2-6 months after the first dose. Collectively, RZV effectiveness against HZ was high, and these real-world studies reaffirm its favorable benefit-risk profile.

摘要

重组带状疱疹疫苗(RZV)于 2017 年在美国获得许可,用于预防带状疱疹(HZ)。我们使用 PubMed、Embase 和 Scopus 进行了文献检索(2017 年 1 月 1 日至 2023 年 8 月 1 日),以整合与 RZV 相关的真实世界证据。总体而言,在真实世界环境中,研究人群包括≥50 岁的成年人和≥18 岁有免疫缺陷或免疫抑制的患者,RZV 对 HZ 的有效性较高。两剂接种的有效性高于一剂接种,尤其是在老年人和免疫功能低下的个体中。RZV 的安全性概况与临床试验中确立的一致。RZV 似乎不会增加免疫介导性疾病患者疾病加重的风险。大约三分之二的个体在第一剂后 2-6 个月内接受了第二剂 RZV。总的来说,RZV 对 HZ 的有效性较高,这些真实世界研究再次证实了其良好的获益风险状况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5568/10653743/bdb99498564c/KHVI_A_2263979_UF0001_OC.jpg

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