Amir Gabriel, Frenkel Georgy, Rotstein Amichay, Nachum Elchanan, Bruckheimer Elchanan, Lowenthal Alexander, Einbinder Tom, Birk Einat
Department of Pediatric Cardiac Surgery, Schneider Children's Medical Center of Israel, 14 Kaplan st., Petach Tikva, Israel.
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Pediatr Cardiol. 2019 Mar;40(3):580-584. doi: 10.1007/s00246-018-2030-5. Epub 2019 Jan 2.
Infective endocarditis (IE) in the pediatric population can present as a life-threatening condition. Optimal timing for surgical intervention should consider surgical risks versus the risk of neurologic complications. We herein report our experience with this group of critically ill children. Retrospective analysis of patient charts of all patients who underwent urgent surgical treatment of aortic IE from 1994 to 2014 was performed. Nine patients with acute storming IE of the aortic valve or the ascending aorta were urgently operated (eight normal heart, one congenital aortic stenosis), age ranged from 8 weeks to 4.2 years. Causative organisms were Staphylococcus aureus (2), Staphylococcus coagulase negative (1), Kingella kingae (2), Streptococcus pneumoniae (2), or culture negative (2). Presenting symptoms other than hemodynamic instability were neurologic decompensation (5) coronary embolization (1) and cardiogenic shock due to scalded skin syndrome (1). CT and MRI demonstrated significant brain infarcts in four patients. Operations performed were the Ross operation (7) and ascending aortic reconstruction (2). There were no operative deaths. At a median follow-up of 6 years (range 2-196 months), all patients are alive and well. Re-intervention included homograft replacement (2) and transcatheter Melody valve implantation (1). At their last follow-up, the neo-aortic valve was functional in all patients with minimal regurgitation and all had full resolution of the neurological deficits. Urgent surgical treatment for aortic valve IE in infants is challenging. Although surgery is complex and pre-disposing conditions such as sepsis, neurologic and cardiac decompensations are prevalent, operative results are excellent and gradual and significant neurologic improvement was noted over time.
儿童感染性心内膜炎(IE)可表现为危及生命的疾病。手术干预的最佳时机应综合考虑手术风险与神经并发症风险。我们在此报告我们对这组危重症儿童的治疗经验。对1994年至2014年期间接受主动脉IE紧急手术治疗的所有患者的病历进行回顾性分析。9例患有主动脉瓣或升主动脉急性暴发性IE的患者接受了紧急手术(8例心脏正常,1例先天性主动脉狭窄),年龄范围为8周龄至4.2岁。致病微生物为金黄色葡萄球菌(2例)、凝固酶阴性葡萄球菌(1例)、金氏杆菌(2例)、肺炎链球菌(2例)或培养阴性(2例)。除血流动力学不稳定外,其他表现症状为神经功能失代偿(5例)、冠状动脉栓塞(1例)和烫伤皮肤综合征导致的心源性休克(1例)。CT和MRI显示4例患者有明显脑梗死。实施的手术包括Ross手术(7例)和升主动脉重建(2例)。无手术死亡病例。中位随访6年(范围2 - 196个月),所有患者均存活且情况良好。再次干预包括同种异体移植置换(2例)和经导管Melody瓣膜植入(1例)。在最后一次随访时,所有患者的新主动脉瓣功能良好,反流轻微,神经功能缺损均完全恢复。婴儿主动脉瓣IE的紧急手术治疗具有挑战性。尽管手术复杂,且败血症、神经和心脏失代偿等易感情况普遍存在,但手术效果极佳,且随着时间推移神经功能有逐渐且显著的改善。