Ayten Omer, Özdemir Cengiz, Dalar Levent, Karaci Ali Riza
Department of Pulmonary Medicine, Istinye University, Istanbul, Turkey.
Department of Pediatric Cardiovascular Surgery, Istanbul Bilim University Medical Faculty, Istanbul, Turkey.
Thorac Cardiovasc Surg. 2025 Jan;73(S 03):e39-e45. doi: 10.1055/a-2635-3320. Epub 2025 Jun 27.
Central airway stenosis following congenital heart malformation surgery is a rare but significant cause of postoperative weaning failure. In selected cases, bronchoscopic interventions are effective treatment options for managing these kind of airway obstructions and achieving successful weaning.The data of six pediatric patients who were unable to be weaned from mechanical ventilation due to central airway obstruction following congenital heart malformation surgery were retrospectively analyzed. Rigid and flexible bronchoscopies were performed under general anesthesia for six patients.Six patients (4 males and 2 females; age range: 4 months to 6 years) with an airway obstruction after surgery due to congenital heart malformations included the study. Three patients had an obstruction of the left main bronchus, two of the right main bronchus, and one of bilateral main bronchus. Balloon dilatation was applied to one patient, mechanical dilatation was applied to three patients, and airway stent was applied to two patients. Two of six patients died from nonprocedural causes (acute respiratory distress syndrome due to pneumonia and cardiac arrest due to severe heart failure) and four patients were weaned successfully from mechanical ventilation and they were still alive during the follow-up period. No procedural-related mortality was seen in the study population. In one patient, stent placement could not be performed due to desaturation and hemodynamic instability during the procedure, and in another patient, granulation tissue developed due to a covered metallic stent, and the metallic stent was removed and replaced with a biodegradable stent.In selected cases, bronchoscopic interventions offer efficient approach to managing airway obstructions due to congenital heart malformation surgery.
先天性心脏畸形手术后的中央气道狭窄是术后脱机失败的一种罕见但重要的原因。在特定病例中,支气管镜介入是处理这类气道阻塞并实现成功脱机的有效治疗选择。对6例因先天性心脏畸形手术后中央气道阻塞而无法从机械通气脱机的儿科患者的数据进行了回顾性分析。在全身麻醉下对6例患者进行了硬质和软质支气管镜检查。本研究纳入了6例(4例男性和2例女性;年龄范围:4个月至6岁)因先天性心脏畸形手术后出现气道阻塞的患者。3例患者左主支气管阻塞,2例右主支气管阻塞,1例双侧主支气管阻塞。1例患者应用了球囊扩张,3例患者应用了机械扩张,2例患者应用了气道支架。6例患者中有2例死于非手术相关原因(肺炎导致的急性呼吸窘迫综合征和严重心力衰竭导致的心脏骤停),4例患者成功从机械通气脱机,且在随访期间仍存活。研究人群中未观察到与手术相关的死亡。1例患者在手术过程中因血氧饱和度下降和血流动力学不稳定无法进行支架置入,另1例患者因带膜金属支架出现肉芽组织,金属支架被移除并更换为可生物降解支架。在特定病例中,支气管镜介入为处理先天性心脏畸形手术后的气道阻塞提供了有效的方法。