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慢性阻塞性肺疾病和哮喘患者接种新冠病毒灭活疫苗和mRNA疫苗后的有效性及呼吸道不良事件:一项基于中国人群的研究

Effectiveness and Respiratory Adverse Events Following Inactivated and mRNA COVID-19 Vaccines in Patients with COPD and Asthma: A Chinese Population-Based Study.

作者信息

Qin Simon Xiwen, Cheng Franco Wing Tak, Kwok Wang Chun, Fung Lydia W Y, Ma Tian Tian, Yiu Hei Hang Edmund, Bloom Chloe, McDonald Christine F, Cheung Ching-Lung, Lai Francisco Tsz Tsun, Chui Celine Sze Ling, Li Xue, Wong Carlos King Ho, Wan Eric Yuk Fai, Wong Ian Chi Kei, Chan Esther Wai Yin

机构信息

Centre for Safe Medicine Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, L2-57, Laboratory Block, 21 Sassoon Road, Pokfulam, Hong Kong SAR, China.

Laboratory of Data Discovery for Health (D24H), Hong Kong Science and Technology Park, Sha Tin, Hong Kong SAR, China.

出版信息

Drug Saf. 2024 Feb;47(2):135-146. doi: 10.1007/s40264-023-01364-7. Epub 2023 Dec 12.

Abstract

INTRODUCTION

Effectiveness and respiratory adverse events following coronavirus disease-2019 (COVID-19) vaccines have not been well investigated in Chinese patients with chronic obstructive pulmonary disease (COPD) and asthma.

METHODS

Using electronic health care records in Hong Kong, we included adults with COPD or asthma or both and hospitalised for severe respiratory exacerbation in a self-controlled case series (SCCS) study between 23/02/2021 and 30/11/2022. Conditional Poisson regression models were used to estimate the incidence of outcomes within exposure periods (28 days after each dose) compared with baseline periods. Cox proportional hazard models evaluated vaccine effectiveness (VE) against COVID-related mortality, hospitalisation, and severe complications, including admission to intensive care units or ventilatory support. The VE assessment was based on vaccine types and the number of doses.

RESULTS

In the SCCS, 343 CoronaVac recipients and 212 BNT162b2 recipients were included. No increased risk of outcomes was observed within the exposure periods. In the cohort study, 108,423 and 83,323 patients received ≥ 2 doses of CoronaVac and BNT162b2, respectively. The VE (95% CI) against COVID-related mortality, hospitalisation, and severe complications after two-dose CoronaVac was 77% (74-80%), 18% (6-23%), and 29% (12-43%), respectively, while for the two-dose regimen of BNT162b2, it was 92% (91-94%), 33% (30-37%), and 57% (45-66%), respectively. Higher VE against COVID-related mortality, hospitalisation, and severe complications was found for the three-dose regimen of CoronaVac (94%, 40%, and 71%) and BNT162b2 (98%, 65%, and 83%). Administering a fourth dose of either vaccine showed additional reductions in COVID-related outcomes.

CONCLUSIONS

Among people with COPD and asthma, the COVID-19 vaccines CoronaVac and BNT162b2 did not increase severe exacerbations and achieved moderate-to-high effectiveness against COVID-related outcomes. COVID-19 vaccination remains essential and should be encouraged to protect this vulnerable population in future epidemic waves.

摘要

引言

2019冠状病毒病(COVID-19)疫苗对中国慢性阻塞性肺疾病(COPD)和哮喘患者的有效性及呼吸道不良事件尚未得到充分研究。

方法

利用香港的电子医疗记录,我们纳入了患有COPD或哮喘或两者皆有的成年人,他们于2021年2月23日至2022年11月30日期间因严重呼吸道加重而住院,进行自我对照病例系列(SCCS)研究。使用条件泊松回归模型估计暴露期(每剂接种后28天)内与基线期相比的结局发生率。Cox比例风险模型评估疫苗对COVID相关死亡率、住院率和严重并发症(包括入住重症监护病房或接受通气支持)的有效性(VE)。VE评估基于疫苗类型和接种剂量数。

结果

在SCCS中,纳入了343名科兴疫苗接种者和212名BNT162b2疫苗接种者。在暴露期内未观察到结局风险增加。在队列研究中,分别有108,423名和83,323名患者接种了≥2剂科兴疫苗和BNT162b2疫苗。两剂科兴疫苗接种后对COVID相关死亡率、住院率和严重并发症的VE(95%CI)分别为77%(74-80%)、18%(6-23%)和29%(12-43%),而两剂BNT162b2疫苗接种方案的相应VE分别为92%(91-94%)、33%(30-37%)和57%(45-66%)。科兴疫苗和BNT162b2疫苗的三剂接种方案对COVID相关死亡率、住院率和严重并发症的VE更高(分别为94%、40%和71%以及98%、65%和83%)。接种第四剂任何一种疫苗均显示与COVID相关结局进一步降低。

结论

在COPD和哮喘患者中,COVID-19疫苗科兴疫苗和BNT162b2疫苗不会增加严重加重情况,并且对COVID相关结局具有中到高有效性。COVID-19疫苗接种仍然至关重要,应鼓励在未来疫情浪潮中保护这一脆弱人群。

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