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心肌梗死后的流感疫苗接种:一项随机、双盲、安慰剂对照、多中心试验。

Influenza Vaccination After Myocardial Infarction: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Trial.

机构信息

Örebro University, Faculty of Health, Department of Cardiology, Sweden (O.F., F.C.).

Department of Cardiology, Skane University Hospital, Clinical Sciences, Lund University, Sweden (M.G., D.E., A.M.).

出版信息

Circulation. 2021 Nov 2;144(18):1476-1484. doi: 10.1161/CIRCULATIONAHA.121.057042. Epub 2021 Aug 30.

Abstract

BACKGROUND

Observational and small, randomized studies suggest that influenza vaccine may reduce future cardiovascular events in patients with cardiovascular disease.

METHODS

We conducted an investigator-initiated, randomized, double-blind trial to compare inactivated influenza vaccine with saline placebo administered shortly after myocardial infarction (MI; 99.7% of patients) or high-risk stable coronary heart disease (0.3%). The primary end point was the composite of all-cause death, MI, or stent thrombosis at 12 months. A hierarchical testing strategy was used for the key secondary end points: all-cause death, cardiovascular death, MI, and stent thrombosis.

RESULTS

Because of the COVID-19 pandemic, the data safety and monitoring board recommended to halt the trial before attaining the prespecified sample size. Between October 1, 2016, and March 1, 2020, 2571 participants were randomized at 30 centers across 8 countries. Participants assigned to influenza vaccine totaled 1290 and individuals assigned to placebo equaled 1281; of these, 2532 received the study treatment (1272 influenza vaccine and 1260 placebo) and were included in the modified intention to treat analysis. Over the 12-month follow-up, the primary outcome occurred in 67 participants (5.3%) assigned influenza vaccine and 91 participants (7.2%) assigned placebo (hazard ratio, 0.72 [95% CI, 0.52-0.99]; =0.040). Rates of all-cause death were 2.9% and 4.9% (hazard ratio, 0.59 [95% CI, 0.39-0.89]; =0.010), rates of cardiovascular death were 2.7% and 4.5%, (hazard ratio, 0.59 [95% CI, 0.39-0.90]; =0.014), and rates of MI were 2.0% and 2.4% (hazard ratio, 0.86 [95% CI, 0.50-1.46]; =0.57) in the influenza vaccine and placebo groups, respectively.

CONCLUSIONS

Influenza vaccination early after an MI or in high-risk coronary heart disease resulted in a lower risk of a composite of all-cause death, MI, or stent thrombosis, and a lower risk of all-cause death and cardiovascular death, as well, at 12 months compared with placebo. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02831608.

摘要

背景

观察性研究和小型随机研究表明,流感疫苗可能会降低心血管疾病患者未来发生心血管事件的风险。

方法

我们进行了一项由研究者发起的、随机的、双盲试验,比较了在心肌梗死(MI;99.7%的患者)或高危稳定型冠心病后不久给予灭活流感疫苗与生理盐水安慰剂。主要终点是 12 个月时的全因死亡、MI 或支架血栓形成的复合终点。采用分层检验策略对次要关键终点进行检验:全因死亡、心血管死亡、MI 和支架血栓形成。

结果

由于 COVID-19 大流行,数据安全和监测委员会建议在达到预定样本量之前停止试验。2016 年 10 月 1 日至 2020 年 3 月 1 日,在 8 个国家的 30 个中心随机分配了 2571 名参与者。1290 名参与者被分配到流感疫苗组,1281 名参与者被分配到安慰剂组;其中,2532 名参与者接受了研究治疗(1272 名接受流感疫苗,1260 名接受安慰剂),并纳入了改良意向治疗分析。在 12 个月的随访中,67 名(5.3%)接受流感疫苗治疗的参与者和 91 名(7.2%)接受安慰剂治疗的参与者发生了主要结局(风险比,0.72 [95%CI,0.52-0.99];=0.040)。全因死亡率分别为 2.9%和 4.9%(风险比,0.59 [95%CI,0.39-0.89];=0.010),心血管死亡率分别为 2.7%和 4.5%(风险比,0.59 [95%CI,0.39-0.90];=0.014),MI 发生率分别为 2.0%和 2.4%(风险比,0.86 [95%CI,0.50-1.46];=0.57)。

结论

与安慰剂相比,心肌梗死后或高危冠心病患者早期接种流感疫苗可降低 12 个月时全因死亡、MI 或支架血栓形成的复合风险,以及全因死亡和心血管死亡的风险。

注册信息

网址:https://www.clinicaltrials.gov;唯一标识符:NCT02831608。

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