Feuchtenberger Martin, Kovacs Magdolna Szilvia, Eder Anna, Nigg Axel, Almanzar Giovanni, Prelog Martina, Schäfer Arne
Medizinische Klinik und Poliklinik II, University Hospital Würzburg, Würzburg, Germany.
Rheumatologie, MVZ MED BAYERN OST, Burghausen, Germany.
Rheumatol Adv Pract. 2024 Sep 5;8(4):rkae111. doi: 10.1093/rap/rkae111. eCollection 2024.
To assess tolerability of COVID-19 vaccination in patients with RA and controls based on patient-reported outcomes (PROs).
In total, 266 study participants were included at 6 ± 1 weeks after their second vaccination (BioNTech/Pfizer (72.2%), AstraZeneca (18.8%) and Moderna (9.0%)). In a cross-sectional, observational study design, PRO data were recorded regarding both total and symptom-level tolerability.
Overall tolerability was very high according to the patients' self-assessment scores (1.71 for the first and 1.72 for the second vaccination, 6-point Likert scale [1 (very good) to 6 (very poor)]) and did not differ significantly between patients with RA ( = 204) and controls ( = 62). Self-rated overall tolerability regarding first vaccination was significantly better ( = 0.002) in patients receiving mRNA vaccines ( = 193, mean tolerability 1.59) as compared with vector-vaccinated patients ( = 73, mean tolerability 2.04). Homologous or heterologous vaccination regimens had no statistically significant effect on vaccine tolerability ( = 0.131). Reservations about the vaccination were rare (6.4% for the first and 6.0% for the second vaccination) but significantly associated with poorer overall tolerability ( < 0.001) and significantly reduced willingness to recommend vaccination to others ( < 0.001 for the first and = 0.004 for the second vaccination).
Based on these real-world data, tolerability of COVID-19 vaccination was very good in both RA patients and controls. Reservations against COVID-19 vaccination were rare overall, but if present, associated with a significantly worse tolerability and a significantly lower degree of recommendation.
基于患者报告结局(PROs)评估类风湿关节炎(RA)患者和对照组中新型冠状病毒肺炎(COVID-19)疫苗的耐受性。
在第二次接种疫苗后6±1周,共纳入266名研究参与者(辉瑞/BioNTech疫苗占72.2%,阿斯利康疫苗占18.8%,莫德纳疫苗占9.0%)。在一项横断面观察性研究设计中,记录了关于总体和症状水平耐受性的PRO数据。
根据患者的自我评估分数,总体耐受性非常高(第一次接种评分为1.71,第二次接种评分为1.72,采用6分李克特量表[1(非常好)至6(非常差)]),RA患者(n = 204)和对照组(n = 62)之间无显著差异。与接种载体疫苗的患者(n = 73,平均耐受性2.04)相比,接受mRNA疫苗的患者(n = 193,平均耐受性1.59)对第一次接种的自我评定总体耐受性显著更好(P = 0.002)。同源或异源疫苗接种方案对疫苗耐受性无统计学显著影响(P = 0.131)。对疫苗接种的顾虑很少见(第一次接种为6.4%,第二次接种为6.0%),但与总体耐受性较差显著相关(P < 0.001),并显著降低向他人推荐接种疫苗的意愿(第一次接种P < 0.001,第二次接种P = 0.004)。
基于这些真实世界数据,COVID-19疫苗在RA患者和对照组中的耐受性都非常好。总体而言,对COVID-19疫苗接种的顾虑很少见,但如果存在,则与显著更差的耐受性和显著更低的推荐程度相关。