Department of Anesthesiology, Brussels University Hospital (H.U.B.) Erasme, Brussels, Belgium.
Department of Intensive Care, Brussels University Hospital (H.U.B.) Erasme, Brussels, Belgium.
Am J Case Rep. 2024 Nov 5;25:e944942. doi: 10.12659/AJCR.944942.
BACKGROUND Takotsubo syndrome, or stress-induced cardiomyopathy, is a rare but serious condition that mimics myocardial infarction and can cause temporary cardiac dysfunction in the absence of coronary artery disease. General anesthesia can make diagnosis more challenging. Although it has already been described in a context of solid organ transplantation, takotsubo syndrome remains under-reported in lung transplantation, necessitating awareness to avoid diagnostic and management delays. CASE REPORT We report a case of takotsubo syndrome in a 54-year-old woman undergoing pulmonary transplantation for end-stage chronic obstructive pulmonary disease. Preoperative evaluations showed no cardiac pathology. During surgery, she developed severe left ventricular failure with ST-segment elevations and diffuse hypokinesia, leading to cardiogenic shock and multiorgan dysfunction. Delayed diagnosis of takotsubo syndrome and late initiation of veno-arterial extracorporeal membrane oxygenation worsened her condition. Postoperatively, she developed lung abscesses, broncho-cutaneous fistula, and hemorrhagic shock, resulting in a prolonged intensive care unit stay. Two years after the transplant, left ventricular dysfunction was persistent, significantly affecting her quality of life. CONCLUSIONS This case report highlights the importance of awareness of takotsubo syndrome associated with lung transplantation, particularly in at-risk patients. Indeed, early diagnosis and management of this cardiomyopathy are crucial for improving outcomes. Multimodal monitoring, including transesophageal echocardiography and continuous ST-segment monitoring, is essential for timely diagnosis. Although rare, this complex clinical condition should be considered in lung transplant recipients with sudden heart failure to ensure prompt and effective treatment. Further research is needed to understand this stress cardiomyopathy in this specific setting and to develop effective management strategies.
应激性心肌病,又称心尖球囊综合征,是一种罕见但严重的疾病,它模仿心肌梗死,并可在无冠状动脉疾病的情况下导致暂时性心脏功能障碍。全身麻醉会使诊断更具挑战性。尽管它已经在实体器官移植的背景下被描述过,但在肺移植中,心尖球囊综合征的报道仍然较少,因此需要提高认识,以避免诊断和治疗延误。
我们报告了一例 54 岁女性在因终末期慢性阻塞性肺疾病行肺移植时发生应激性心肌病的病例。术前评估未发现心脏病变。手术过程中,她出现严重的左心室衰竭,伴有 ST 段抬高和弥漫性运动障碍,导致心源性休克和多器官功能障碍。应激性心肌病的延迟诊断和血管外膜氧合的延迟启动使她的病情恶化。术后,她发生了肺脓肿、支气管皮肤瘘和出血性休克,导致重症监护病房的住院时间延长。移植后两年,左心室功能仍然存在障碍,严重影响了她的生活质量。
本病例报告强调了在肺移植中意识到与应激性心肌病相关的重要性,特别是对高危患者。实际上,早期诊断和治疗这种心肌病对于改善预后至关重要。多模式监测,包括经食管超声心动图和连续 ST 段监测,对于及时诊断至关重要。尽管罕见,但在发生急性心力衰竭的肺移植受者中,应考虑到这种复杂的临床情况,以确保及时有效的治疗。需要进一步研究来了解这种应激性心肌病在特定环境中的情况,并制定有效的管理策略。