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急性心力衰竭患者的流感疫苗接种(PANDA II):在中国基于医院的、平行组、群组随机对照试验的研究方案。

Influenza vaccination in patients with acute heart failure (PANDA II): study protocol for a hospital-based, parallel-group, cluster randomized controlled trial in China.

机构信息

Heart Health Research Center (HHRC), Beijing, China.

The George Institute for Global Health, UNSW, Sydney, Australia.

出版信息

Trials. 2024 Nov 25;25(1):792. doi: 10.1186/s13063-024-08452-8.

Abstract

BACKGROUND

Influenza vaccination confers broad benefits in the elderly and certain high-risk populations, but its effectiveness in patients with acute heart failure (HF) is uncertain. Rates of influenza vaccination are low in China due to poor awareness, cultural misunderstandings, and cost.

AIMS

To determine the effectiveness of influenza vaccination in patients with acute HF admitted to hospitals in China.

METHODS

The second Population Assessment of Influenza and Disease Activity (PANDA II) study is a two-arm, parallel-group, county-level hospital-based, cluster randomized controlled trial to determine the benefits and risks of full access to routine free influenza vaccination before hospital discharge, compared to routine limited use of influenza vaccination, on the primary endpoint of death or hospital readmission. Consecutive hospitalized patients at each site are enrolled to a target of 50 participants in each autumn-winter influenza outbreak period (October to March) over 3 consecutive years to reach the required sample size. Patients are centrally followed up at 1, 3, 6, and 12 months after hospital discharge (or death if earlier). Site numbers varied across year according to predicted influenza activity and logistical reasons.

CONCLUSIONS

This study offers a unique chance to clarify uncertainties surrounding the effectiveness of influenza vaccination in patients with HF and to lay the groundwork for future prevention strategies.

TRIAL REGISTRATION

This trial was registered with the acronym PANDA II (Population Assessment of Influenza and Disease Activity) at ChiCTR.org.cn (ChiCTR2100053264). Registered on 17 November 2021.

摘要

背景

流感疫苗为老年人和某些高危人群带来了广泛的益处,但在急性心力衰竭(HF)患者中的有效性尚不确定。由于缺乏意识、文化误解和费用等原因,中国的流感疫苗接种率很低。

目的

确定在中国住院的急性 HF 患者中流感疫苗接种的效果。

方法

第二项人群评估流感和疾病活动(PANDA II)研究是一项两臂、平行组、县级医院为基础的集群随机对照试验,旨在确定在出院前全面获得常规免费流感疫苗接种的益处和风险,与常规有限使用流感疫苗接种相比,主要终点为死亡或医院再入院。每个地点的连续住院患者在每个秋季至冬季流感爆发期间(10 月至 3 月)按目标纳入 50 名参与者,连续 3 年达到所需样本量。患者在出院后(或更早死亡)的 1、3、6 和 12 个月进行中心随访。根据预计的流感活动和后勤原因,各年的地点数量有所不同。

结论

这项研究为澄清 HF 患者流感疫苗接种效果的不确定性提供了一个独特的机会,并为未来的预防策略奠定了基础。

试验注册

这项试验在中国临床试验注册中心(ChiCTR.org.cn)以 PANDA II(人群评估流感和疾病活动)的首字母缩写注册(ChiCTR2100053264)。于 2021 年 11 月 17 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d8b/11587674/1e1d6e8e56bf/13063_2024_8452_Fig1_HTML.jpg

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