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与免疫介导的炎症性疾病患者接种 SARS-CoV-2 疫苗后短期不良事件相关的风险因素。

Risk factors associated with short-term adverse events after SARS-CoV-2 vaccination in patients with immune-mediated inflammatory diseases.

机构信息

Department of Neurology and Neurophysiology, Amsterdam Neuroscience, Amsterdam UMC, Location Academic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.

Department of Clinical Neurophysiology, St Antonius Hospital, Nieuwegein, The Netherlands.

出版信息

BMC Med. 2022 Mar 2;20(1):100. doi: 10.1186/s12916-022-02310-7.

Abstract

BACKGROUND

Studies have suggested incremental short-term adverse events (AE) after repeated vaccination. In this report, we assessed occurrence and risk factors for short-term AEs following repeated SARS-CoV-2 vaccination in patients with various immune-mediated inflammatory diseases (IMIDs).

METHODS

Self-reported daily questionnaires on AEs during the first 7 days after vaccination were obtained of 2259 individuals (2081 patients and 178 controls) participating in an ongoing prospective multicenter cohort study on SARS-CoV-2 vaccination in patients with various IMIDs in the Netherlands (T2B-COVID). Relative risks were calculated for potential risk factors associated with clinically relevant AE (rAE), defined as AE lasting longer than 2 days or impacting daily life.

RESULTS

In total, 5454 vaccinations were recorded (1737 first, 1992 second and 1478 third vaccinations). Multiple sclerosis, Crohn's disease and rheumatoid arthritis were the largest disease groups. rAEs were reported by 57.3% (95% CI 54.8-59.8) of patients after the first vaccination, 61.5% (95% CI 59.2-63.7) after the second vaccination and 58% (95% CI 55.3-60.6) after the third vaccination. At day 7 after the first, second and third vaccination, respectively, 7.6% (95% CI 6.3-9.1), 7.4% (95% CI 6.2-8.7) and 6.8% (95% CI 5.4-8.3) of patients still reported AEs impacting daily life. Hospital admissions and allergic reactions were uncommon (<0.7%). Female sex (aRR 1.43, 95% CI 1.32-1.56), age below 50 (aRR 1.14, 95% CI 1.06-1.23), a preceding SARS-CoV-2 infection (aRR 1.14, 95% CI 1.01-1.29) and having an IMID (aRR 1.16, 95% CI 1.01-1.34) were associated with increased risk of rAEs following a vaccination. Compared to the second vaccination, the first vaccination was associated with a lower risk of rAEs (aRR 0.92, 95% CI 0.84-0.99) while a third vaccination was not associated with increased risk on rAEs (aRR 0.93, 95% CI 0.84-1.02). BNT162b2 vaccines were associated with lower risk on rAEs compared to CX-024414 (aRR 0.86, 95% CI 0.80-0.93).

CONCLUSIONS

A third SARS-CoV-2 vaccination was not associated with increased risk of rAEs in IMID patients compared to the second vaccination. Patients with an IMID have a modestly increased risk of rAEs after vaccination when compared to controls. Most AEs are resolved within 7 days; hospital admissions and allergic reactions were uncommon.

TRIAL REGISTRATION

NL74974.018.20 , Trial ID: NL8900. Registered on 9 September 2020.

摘要

背景

研究表明,多次接种后会出现短期的不良事件(AE)。在本报告中,我们评估了在荷兰进行的一项正在进行的多中心前瞻性队列研究中,各种免疫介导的炎症性疾病(IMID)患者接受多次 SARS-CoV-2 疫苗接种后 7 天内短期 AE 的发生和危险因素。

方法

从正在进行的荷兰各种 IMID 患者接受 SARS-CoV-2 疫苗接种的前瞻性多中心队列研究(T2B-COVID)中,获得了 2259 名个体(2081 名患者和 178 名对照)在接种后第 1 天至第 7 天内每日报告的 AE 情况。计算了与临床相关 AE(rAE)相关的潜在危险因素的相对风险,定义为持续时间超过 2 天或影响日常生活的 AE。

结果

共记录了 5454 次疫苗接种(第 1 次 1737 次,第 2 次 1992 次,第 3 次 1478 次)。多发性硬化症、克罗恩病和类风湿关节炎是最大的疾病群体。第 1 次、第 2 次和第 3 次接种后,患者的 rAE 分别为 57.3%(95%CI 54.8-59.8)、61.5%(95%CI 59.2-63.7)和 58%(95%CI 55.3-60.6)。在第 1 次、第 2 次和第 3 次接种后第 7 天,分别有 7.6%(95%CI 6.3-9.1)、7.4%(95%CI 6.2-8.7)和 6.8%(95%CI 5.4-8.3)的患者仍报告影响日常生活的 AE。住院和过敏反应少见(<0.7%)。女性(aRR 1.43,95%CI 1.32-1.56)、年龄<50 岁(aRR 1.14,95%CI 1.06-1.23)、先前 SARS-CoV-2 感染(aRR 1.14,95%CI 1.01-1.29)和患有 IMID(aRR 1.16,95%CI 1.01-1.34)与接种后 rAE 的风险增加相关。与第 2 次接种相比,第 1 次接种 rAE 的风险较低(aRR 0.92,95%CI 0.84-0.99),而第 3 次接种 rAE 的风险无显著增加(aRR 0.93,95%CI 0.84-1.02)。与 CX-024414 相比,BNT162b2 疫苗接种与 rAE 风险降低相关(aRR 0.86,95%CI 0.80-0.93)。

结论

与第 2 次接种相比,第 3 次 SARS-CoV-2 疫苗接种在 IMID 患者中并未增加 rAE 的风险。与对照组相比,IMID 患者接种疫苗后发生 rAE 的风险略有增加。大多数 AE 在 7 天内得到解决;住院和过敏反应少见。

试验注册

NL74974.018.20,试验 ID:NL8900。于 2020 年 9 月 9 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc7e/8889784/2d1458f700ee/12916_2022_2310_Fig1_HTML.jpg

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