Tomita Katsuyuki, Okada Shinichi, Sugihara Shuji, Ikeuchi Tomoyuki, Touge Hirokazu, Hasegawa Junichi, Yamasaki Akira
Department of Respiratory Medicine, National Hospital Organization Yonago Medical Center, Yonago 683-0006, Japan.
Department of Pediatrics, National Hospital Organization Yonago Medical Center, Yonago 683-0006, Japan.
Yonago Acta Med. 2021 Nov 10;64(4):339-344. doi: 10.33160/yam.2021.11.003. eCollection 2021 Nov.
BNT162b2, an mRNA COVID-19 vaccine, was launched in many countries as an intramuscular vaccination for COVID-19 infection. Few studies have assessed the physical indications of pain at the immunization site. This study aimed to characterize pain at the injection site and investigate morphological attributes using ultrasound.
Forty-three of 211 healthcare workers who received a second dose of BNT162b2 between February 2021 and March 2021 were enrolled in the study. The mean age of the subjects was 40 years. We evaluated patients' pain at the injection site using the Numerical Rating Pain Scale (NRPS). We also assessed the thickness of the deltoid muscle fascia at the injection site by ultrasound. Bayesian robust correlation was employed to explore the relationship between the pain intensity scores and ultrasound measurements.
All eligible subjects complained of pain at the injection site. A median pain onset of 8 hours post-vaccination and a median peak intensity score of 4 were reported. Onset of relief occurred after 2 days. Ultrasound images demonstrated a 2.5-fold increase in fascia thickness at the injection site without intramuscular echogenicity change in all subjects. A correlation was established between the NRPS score and the non-injection-to-injection-side ratio of fascia thickness at the injection site (rho = 0.66).
A sore arm was the most prevalent side effect of BNT162b2 vaccination and could be attributed to temporal fasciitis.
BNT162b2是一种新冠病毒mRNA疫苗,在许多国家作为预防新冠病毒感染的肌肉注射疫苗推出。很少有研究评估免疫接种部位疼痛的体征。本研究旨在描述注射部位的疼痛特征,并使用超声研究其形态学特征。
在2021年2月至2021年3月期间接受第二剂BNT162b2疫苗的211名医护人员中,有43人纳入本研究。受试者的平均年龄为40岁。我们使用数字疼痛评分量表(NRPS)评估患者注射部位的疼痛情况。我们还通过超声评估注射部位三角肌筋膜的厚度。采用贝叶斯稳健相关性分析来探讨疼痛强度评分与超声测量结果之间的关系。
所有符合条件的受试者均诉说注射部位疼痛。报告的疼痛中位发作时间为接种疫苗后8小时,中位峰值强度评分为4分。2天后疼痛开始缓解。超声图像显示,所有受试者注射部位的筋膜厚度增加了2.5倍,肌肉内回声无变化。在NRPS评分与注射部位筋膜厚度的非注射侧与注射侧比值之间建立了相关性(rho = 0.66)。
手臂酸痛是BNT162b2疫苗接种最常见的副作用,可能归因于暂时性筋膜炎。