Idris Fadul Alaa Abdallah, Osman Mohamed Areij Awad, Mohammed Ahmed Ahmed Abdullahi Sidahmed, Elmobark Sara, Merghani Hammour Amjad Saeed, Elgaleel Khir Elsiad Nusayba Mustafa Nour, Mohammed Elhaj Ebtihal Abdalglil
Internal Medicine, Al-Zahraa University Hospital, Cairo, EGY.
Internal Medicine, Sudan Heart Center, Khartoum, SDN.
Cureus. 2025 Apr 27;17(4):e83083. doi: 10.7759/cureus.83083. eCollection 2025 Apr.
Emerging evidence suggests that coronavirus disease 2019 (COVID-19) survivors face increased risks of cardiovascular complications, but the long-term risks, underlying mechanisms, and clinical implications remain incompletely characterized. This systematic review synthesizes current evidence on post-COVID-19 cardiovascular manifestations, evaluating their incidence, pathophysiology, and outcomes. A comprehensive literature search was conducted across PubMed/MEDLINE, Embase, Scopus, Web of Science, and the Cochrane Library, following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 guidelines. Fifteen observational studies (cohort, case-control, cross-sectional) meeting predefined eligibility criteria, confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, cardiovascular outcomes assessed ≥4 weeks post-infection, sample sizes >10, and peer-reviewed publication, were included. The risk of bias was assessed using the Newcastle-Ottawa Scale. The multinational studies (United States, Europe, Asia, South America) involved diverse populations (n=80-8,126,462), with follow-up durations ranging from three to 24 months. Mechanisms such as endothelial dysfunction, myocardial inflammation, and autonomic dysregulation were consistently supported across studies via imaging (e.g., cardiac MRI) and biomarkers (e.g., troponin, C-reactive protein (CRP)). Persistent arrhythmias and subclinical myocardial injury were directly demonstrated in 40-60% of patients. Worse outcomes were associated with hospitalization during acute infection, preexisting cardiovascular disease, and metabolic syndrome. Heterogeneity in follow-up durations may limit the detection of very-late-onset complications, though risks remained elevated across all intervals. Individualized management strategies should include cardiovascular imaging (echocardiography, MRI), biomarker profiling, and tailored pharmacotherapy (anti-inflammatory agents, anticoagulants). The ethical rationale for randomized trials is now strengthened by the clear evidence of long-term risks; ongoing trials are testing targeted anti-inflammatory and anticoagulant regimens. These findings underscore the necessity of systematic cardiovascular surveillance and risk-stratified care for COVID-19 survivors. Future research should prioritize extended follow-up studies and randomized controlled trials (RCTs) to optimize interventions for this growing population.
新出现的证据表明,2019冠状病毒病(COVID-19)幸存者面临心血管并发症风险增加的情况,但长期风险、潜在机制和临床意义仍未完全明确。本系统评价综合了当前关于COVID-19后心血管表现的证据,评估其发生率、病理生理学和结局。按照系统评价和Meta分析的首选报告项目(PRISMA)2020指南,在PubMed/MEDLINE、Embase、Scopus、Web of Science和Cochrane图书馆进行了全面的文献检索。纳入了15项符合预定义纳入标准的观察性研究(队列研究、病例对照研究、横断面研究),这些研究证实了严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染,在感染后≥4周评估心血管结局,样本量>10,且为同行评审出版物。使用纽卡斯尔-渥太华量表评估偏倚风险。这些多国研究(美国、欧洲、亚洲、南美洲)涉及不同人群(n = 80 - 8,126,462),随访时间为3至24个月。通过成像(如心脏磁共振成像)和生物标志物(如肌钙蛋白、C反应蛋白(CRP)),研究一致支持内皮功能障碍、心肌炎症和自主神经调节异常等机制。40%至60%的患者直接表现出持续性心律失常和亚临床心肌损伤。更差的结局与急性感染期间住院、既往心血管疾病和代谢综合征有关。随访时间的异质性可能会限制对极晚期并发症的检测,不过在所有时间段风险仍然升高。个体化管理策略应包括心血管成像(超声心动图、磁共振成像)、生物标志物分析和针对性药物治疗(抗炎药、抗凝药)。长期风险的明确证据现在加强了随机试验的伦理依据;正在进行的试验正在测试针对性的抗炎和抗凝方案。这些发现强调了对COVID-19幸存者进行系统心血管监测和风险分层护理的必要性。未来的研究应优先进行延长随访研究和随机对照试验(RCT),以优化针对这一不断增长人群的干预措施。