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流感疫苗接种改善急性心力衰竭患者预后(PANDA II):一项在中国进行的多地区、季节性、基于医院的整群随机对照试验。

Influenza vaccination to improve outcomes for patients with acute heart failure (PANDA II): a multiregional, seasonal, hospital-based, cluster-randomised, controlled trial in China.

作者信息

Anderson Craig S, Hua Chang, Wang Zhiyan, Wang Chi, Jiang Chao, Liu Rong, Han Rong, Li Qiang, Shan Sana, Billot Laurent, Macintyre C Raina, Patel Anushka, Zhang Hongjia, Ma Changsheng, Dong Jianzeng, Du Xin

机构信息

The Institute of Science and Technology for Brain-inspired Intelligence, Fudan University, Shanghai, China; The George Institute for Global Health, University of New South Wales, Sydney, NSW, Australia; Neurology Department, Royal Prince Alfred Hospital, Sydney, NSW, Australia; Heart Health Research Center, Beijing, China.

Beijing Anzhen Hospital, Capital Medical University, Beijing, China.

出版信息

Lancet. 2025 Sep 6;406(10507):1020-1031. doi: 10.1016/S0140-6736(25)01485-0. Epub 2025 Aug 30.

Abstract

BACKGROUND

Influenza vaccination is widely recommended to prevent death and serious illness in vulnerable people, including those with heart failure. However, the randomised evidence to support this practice is limited and few people are vaccinated in many parts of the world. We aimed to determine whether influenza vaccination can improve the outcome of patients after an episode of acute heart failure requiring admission to hospital in China.

METHODS

We undertook a pragmatic, multiregional, parallel-group, cluster (hospital)-randomised, controlled, superiority trial over three winter seasons in China. Participating hospitals were located in the counties of 12 provinces with the capability of establishing a point-of-care service to provide free influenza vaccination to a sufficient number of patients before their discharge, if allocated to the intervention group. No such service was used in hospitals allocated to usual care (control) but patients were informed of fee-for-service influenza vaccination being available at local community medical centres, as per usual standard of care. Hospitals were randomised (1:1) in each year, stratified by province and up to three times (ie, new randomisation for each season), to include eligible adult (aged ≥18 years) patients with moderate to severe heart failure (New York Heart Association class III or IV) and no contraindication to influenza vaccination. Patient enrolment was conducted over three consecutive winter seasons, from October in each year to March of the following year, between 2021 and 2024. All patients received usual standard of care and were followed up at 1, 3, 6, and 12 months after their hospital discharge by trained study personnel using a standardised protocol. The primary outcome was a composite of all-cause mortality or any hospital readmission over 12 months, excluding events that occurred within 30 days after hospital discharge at all sites and in the summer season only for sites in northern China. The effect of the intervention was assessed at an individual level in the modified intention-to-treat population (all randomly assigned patients with available information until the time of last follow-up, excluding censored events) with a two-level hierarchical logistic regression model that included study period (year) as a fixed effect, and hospital and hospital-period as random effects, with the censored events excluded. The trial is registered at the Chinese Clinical Trial Registry (ChiCTR2100053264).

FINDINGS

Of 252 hospitals assessed for eligibility, 196 hospitals agreed to join and were randomised in three batches at the beginning of each winter season from October, 2021, but 32 hospitals subsequently withdrew before any patients were included. Overall, 7771 participants were enrolled at 164 hospitals in each winter season between Dec 3, 2021, and Feb 14, 2024, with 3570 assigned to the influenza vaccination group and 4201 to the usual care (control) group. The primary outcome occurred in 1378 (41·2%) of 3342 patients in the vaccination group and in 1843 (47·0%) of 3919 patients in the usual care group (odds ratio 0·83 [95% CI 0·72-0·97]; p=0·019). The result was consistent in the sensitivity analysis. The number of participants with a serious adverse event was significantly lower in the vaccination group (1809 [52·5%] of 3444) than the usual care group (2426 [59·0%] of 4110; odds ratio 0·82 [0·70-0·96]; p=0·013).

INTERPRETATION

Influenza vaccination during a hospital admission in patients with acute heart failure can improve their survival and reduce likelihood of readmission to hospital over the subsequent 12 months. The integration of influenza vaccination into inpatient care could offer a widely applicable strategy for an underserved high-risk patient group, that is relevant to resource-limited and possibly resource-rich settings.

FUNDING

Sanofi and the Chinese Society of Cardiology.

摘要

背景

广泛推荐流感疫苗接种以预防包括心力衰竭患者在内的易感人群死亡和严重疾病。然而,支持这种做法的随机证据有限,并且在世界许多地区,接种流感疫苗的人很少。我们旨在确定在中国,流感疫苗接种能否改善因急性心力衰竭发作而需住院治疗的患者的预后。

方法

我们在中国三个冬季开展了一项务实的、多地区、平行组、整群(医院)随机、对照、优效性试验。参与的医院位于12个省份的县,具备建立即时护理服务的能力,以便在出院前为足够数量的患者免费接种流感疫苗(如果分配到干预组)。分配到常规护理(对照)组的医院不提供此类服务,但按照常规护理标准,告知患者当地社区医疗中心提供收费的流感疫苗接种服务。每年医院按1:1随机分组,按省份分层,最多随机三次(即每个季节重新随机分组),纳入符合条件的成年(≥18岁)中重度心力衰竭患者(纽约心脏病协会III或IV级)且无流感疫苗接种禁忌证。患者入组在2021年至2024年期间每年10月至次年3月的三个连续冬季进行。所有患者均接受常规护理标准,并在出院后1、3、6和12个月由经过培训的研究人员使用标准化方案进行随访。主要结局是12个月内全因死亡或任何再入院的复合结局,不包括所有研究点出院后30天内发生的事件以及仅中国北方研究点夏季发生的事件。在改良意向性分析人群(所有随机分配且有可用信息直至末次随访的患者,不包括删失事件)中,采用两级分层逻辑回归模型在个体水平评估干预效果,该模型将研究期间(年份)作为固定效应,医院和医院-时期作为随机效应,删失事件除外。该试验已在中国临床试验注册中心注册(ChiCTR2100053264)。

结果

在评估符合条件的252家医院中,196家医院同意加入,并在2021年10月开始的每个冬季分三批进行随机分组,但随后有32家医院在纳入任何患者之前退出。总体而言,在2021年12月3日至2024年2月14日期间的每个冬季,164家医院共纳入7771名参与者,其中3570名分配到流感疫苗接种组,4201名分配到常规护理(对照)组。接种组3342例患者中有1378例(41.2%)发生主要结局,常规护理组3919例患者中有1843例(47.0%)发生主要结局(比值比0.83 [95%CI 0.72 - 0.97];p = 0.019)。敏感性分析结果一致。接种组发生严重不良事件的参与者数量(3444例中的1809例[52.5%])显著低于常规护理组(4110例中的2426例[59.0%];比值比0.82 [0.70 - 0.96];p = 0.013)。

解读

急性心力衰竭患者住院期间接种流感疫苗可提高其生存率,并降低随后12个月内再次入院的可能性。将流感疫苗接种纳入住院护理可为服务不足的高危患者群体提供一种广泛适用的策略,这与资源有限和可能资源丰富的环境都相关。

资助

赛诺菲和中国心脏学会。

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