Keck School of Medicine, University of Southern California (USC), Los Angeles, CA, USA.
Division of Cardiology, Department of Medicine, UC Davis Medical Center, Sacramento, CA, USA.
Am J Case Rep. 2023 Mar 1;24:e937955. doi: 10.12659/AJCR.937955.
BACKGROUND Cardiac allograft vasculopathy (CAV) is a post-orthotopic heart transplant (OHT) complication driven by intimal smooth muscle proliferation and immune hyperactivity to donor heart tissue. Accelerated CAV leads to allograft failure within 1 year after receiving a normal angiogram result. Viruses can contribute to CAV development, but CAV after SARS-CoV-2 infection has not been reported to date. CASE REPORT A 48-year-old man, 5 years after OHT for non-ischemic cardiomyopathy, was admitted to the Cardiac Care Unit with 3 days of abdominal pain, dyspnea, and palpitations. His medical history included hyperlipidemia and insulin-dependent diabetes. He was compliant with all medications. Two months prior, he had a mild COVID-19 case. An echocardiogram and coronary angiogram 6 and 9 months prior, respectively, were unremarkable. Right and left heart catheterization demonstrated increased filling pressures, a cardiac index of 1.7 L/ml/m², and diffuse vasculopathy most severe in the LAD artery. Flow could not be restored despite repeated ballooning and intra-catheter adenosine. Empiric ionotropic support, daily high-dose methylprednisolone, and plasmapheresis were started. A few days later, the patient had cardiac arrest requiring venoarterial extracorporeal membranous oxygenation. Given CAV's irreversibility, re-transplantation was considered, but the patient had an episode of large-volume hemoptysis and remained clinically unstable for transplant. The patient died while on palliative care. CONCLUSIONS Our patient developed accelerated CAV 2 months after having COVID-19. While CAV has known associations with certain viruses, its incidence after SARS-CoV-2 infection is unknown. Further research is needed to determine if prior SARS-CoV-2 infection is a risk factor for development of CAV in OHT recipients.
心脏同种异体移植血管病(CAV)是一种心脏同种异体移植(OHT)后并发症,由内膜平滑肌增殖和对供体心脏组织的免疫过度活跃引起。加速性 CAV 在接受正常血管造影结果后 1 年内导致移植物衰竭。病毒可导致 CAV 发展,但迄今为止尚未报告 SARS-CoV-2 感染后的 CAV。
一名 48 岁男性,因非缺血性心肌病进行 OHT 后 5 年,因腹痛、呼吸困难和心悸入院心脏监护病房。他的病史包括高血脂和胰岛素依赖型糖尿病。他一直遵守所有药物治疗。两个月前,他患有轻度 COVID-19 病例。分别在 6 个月和 9 个月前进行的超声心动图和冠状动脉造影均无异常。右心和左心导管检查显示充盈压升高,心指数为 1.7 L/ml/m²,弥漫性血管病变在 LAD 动脉最严重。尽管反复进行球囊扩张和导管内腺苷治疗,但仍无法恢复血流。开始经验性离子型支持、每日大剂量甲基强的松龙和血浆置换。几天后,患者发生心脏骤停,需要静脉动脉体外膜氧合。鉴于 CAV 的不可逆性,考虑进行再次移植,但患者出现大量咯血,移植前仍处于临床不稳定状态。患者在姑息治疗中死亡。
我们的患者在 COVID-19 后 2 个月发生加速性 CAV。虽然 CAV 与某些病毒有关,但 SARS-CoV-2 感染后其发生率尚不清楚。需要进一步研究以确定先前的 SARS-CoV-2 感染是否是 OHT 受者发生 CAV 的危险因素。