Marchetta Michele, Lopez Rocio I, Golino Michele, Thomas Georgia, Abbate Antonio
Berne Cardiovascular Research Center and Division of Cardiology, University of Virginia, Charlottesville, VA, USA.
Berne Cardiovascular Research Center and Division of Cardiology, University of Virginia, Charlottesville, VA, USA; Department of Internal Medicine and Pauley Heart Center, Virginia Commonwealth University, Richmond, VA, USA.
Int J Cardiol. 2025 Oct 15;437:133516. doi: 10.1016/j.ijcard.2025.133516. Epub 2025 Jun 14.
Pericarditis is a recognized but rare complication of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) vaccination. While most cases are self-limited, some develop recurrent, difficult-to-treat pericarditis, requiring prolonged management. The exact pathophysiology remains unclear, but vaccine-related immune activation and inflammasome-mediated responses have been implicated.
We reported eight cases of difficult-to-treat pericarditis temporally associated with SARS-CoV-2 vaccination, seen at a single center between October 2021 and January 2025. Diagnosis followed ESC 2015 guidelines, and all patients tested negative for acute SARS-CoV-2 infection.
The median age was 56 years, with six receiving Pfizer-BioNTech BNT162b2 and two Moderna mRNA-1273. For six individuals, this was their first episode of pericarditis, whereas two had a prior history of pericarditis. The median time to symptom onset was 14 days. Chest pain was reported by all patients, requiring emergency visits in six cases. Pericardial effusion was present in six patients, with one progressing to tamponade. Cardiac magnetic resonance revealed pericardial late gadolinium enhancement in three of seven patients. All patients received nonsteroidal anti-inflammatory drugs and seven were treated with colchicine. Due to inadequate response to first-line therapies, corticosteroids were administered in all eight cases. Due to persistent symptoms, six patients initiated rilonacept therapy, which led to complete symptom resolution.
Pericarditis following SARS-CoV-2 vaccination can evolve into a recurrent, difficult-to-manage inflammatory condition. Effective treatment may require IL-1 blockade to disrupt the autoinflammatory cycle. Prompt recognition and early escalation of therapy are essential to reduce morbidity and prevent complications.
心包炎是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗接种一种已被认识但罕见的并发症。虽然大多数病例为自限性,但有些会发展为复发性、难以治疗的心包炎,需要长期管理。确切的病理生理学仍不清楚,但疫苗相关的免疫激活和炎性小体介导的反应被认为与之有关。
我们报告了8例与SARS-CoV-2疫苗接种在时间上相关的难以治疗的心包炎病例,这些病例于2021年10月至2025年1月在单一中心就诊。诊断遵循欧洲心脏病学会(ESC)2015年指南,所有患者急性SARS-CoV-2感染检测均为阴性。
中位年龄为56岁,6人接种辉瑞-生物科技公司的BNT162b2疫苗,2人接种莫德纳公司的mRNA-1273疫苗。6人是首次发生心包炎,而2人有过心包炎病史。症状出现的中位时间为14天。所有患者均报告有胸痛,6例需要急诊就诊。6例患者存在心包积液,1例进展为心脏压塞。心脏磁共振成像显示7例患者中有3例心包延迟钆增强。所有患者均接受了非甾体抗炎药治疗,7例接受了秋水仙碱治疗。由于对一线治疗反应不足,所有8例患者均使用了皮质类固醇。由于症状持续存在,6例患者开始使用利罗西普治疗,症状完全缓解。
SARS-CoV-2疫苗接种后的心包炎可演变为复发性、难以管理的炎症状态。有效的治疗可能需要抑制白细胞介素-1以中断自身炎症循环。及时识别和早期加强治疗对于降低发病率和预防并发症至关重要。