Ando Makoto, Nishino Takako
Department of Pediatric Cardiovascular Surgery, Kanazawa Medical University, Ishikawaken, Japan.
Ann Thorac Surg Short Rep. 2024 Apr 2;2(3):369-373. doi: 10.1016/j.atssr.2024.03.008. eCollection 2024 Sep.
The study focuses on vascular compression of the main bronchus in the aortopulmonary space, examining potential contributors within the same axial plane. Its goal is to uncover mechanisms of bronchial compression in patients with intracardiac anomalies and review surgical outcomes, aiming to enhance future results.
The morphology and topology of structures within the axial plane of the aortopulmonary space were objectively analyzed, including the sternum, ascending aorta, heart, pulmonary artery, descending aorta, and other relevant elements. Identified deviations from the normal configuration were systematically identified. Operative procedures included mobilizing and removing the compressing vessel, followed by suspending the airway wall to a rigid prosthesis (external stenting), vertebra, or ascending aorta.
Computed tomography revealed potential factors contributing to bronchial stenosis, including anteriorly deviated descending aorta (20 patients), dilated pulmonary artery (6), cardiomegaly (12), flat chest (7), funnel chest (3), posteriorly deviated ascending aorta after arterial switch operation (3), low aortic arch (3), and aberrant subclavian artery (2). Kaplan-Meier analysis demonstrated operative survival rates of 96% at 1 year, 87% at 5 years, and 80% at 8-15 years. Ten-year follow-up computed tomography after external stenting procedure revealed the narrowest diameter of the stented bronchus as 94.4% of the reference.
Consistent long-term airway patency was observed post-surgery. While the pulmonary artery and descending aorta exert direct compressive effects in most cases, various other potential mechanisms may contribute to bronchial compression. Identifying and addressing these factors through a multidisciplinary approach is crucial for sustaining bronchial patency and preventing complications.
本研究聚焦于主支气管在主动脉肺间隙的血管压迫情况,在同一轴平面内检查潜在的影响因素。其目的是揭示心内异常患者支气管受压的机制,并回顾手术结果,以期改善未来疗效。
客观分析主动脉肺间隙轴平面内结构的形态和拓扑结构,包括胸骨、升主动脉、心脏、肺动脉、降主动脉及其他相关结构。系统识别与正常结构的偏差。手术操作包括游离并移除压迫血管,随后将气道壁悬吊于刚性假体(外部支架)、椎体或升主动脉。
计算机断层扫描显示导致支气管狭窄的潜在因素,包括降主动脉向前移位(20例患者)、肺动脉扩张(6例)、心脏扩大(12例)、扁平胸(7例)、漏斗胸(3例)、动脉调转手术后升主动脉向后移位(3例)、主动脉弓低位(3例)和锁骨下动脉异常(2例)。Kaplan-Meier分析显示1年手术生存率为96%,5年为87%,8至15年为80%。外部支架置入术后10年的计算机断层扫描显示,支架置入支气管的最窄直径为参考值的94.4%。
术后观察到长期气道通畅情况良好。虽然在大多数情况下肺动脉和降主动脉会产生直接压迫作用,但其他各种潜在机制也可能导致支气管受压。通过多学科方法识别并处理这些因素对于维持支气管通畅和预防并发症至关重要。