Costa Fábio, Valentim Maria, Ferreira Carla, Santos Maria
Anesthesiology, Hospital de Braga, Braga, PRT.
Cureus. 2024 Sep 6;16(9):e68797. doi: 10.7759/cureus.68797. eCollection 2024 Sep.
Vertebral defects, anorectal anomalies, cardiac anomalies, tracheoesophageal fistula (TEF)/esophageal atresia, renal anomalies, and limb abnormalities (VACTERL) association is a rare congenital disorder presenting with a constellation of birth defects. The diagnosis is primarily clinical, and patients exhibit at least three of these anomalies. These patients' management involves a multidisciplinary approach tailored to the individual's condition. Anesthetic management is particularly challenging due to the diverse and complex anomalies. This article discusses the anesthetic management of a term newborn male (39 weeks, six days gestation, 3340 g) diagnosed with VACTERL association. The newborn was admitted to the neonatal intensive care unit (NICU) and scheduled for the surgical repair of TEF and derivative colostomy on the second day of life. To mitigate the risk of air leak and abdominal distension from positive pressure ventilation, a derivative colostomy was performed first under regional anesthesia preserving spontaneous ventilation. To achieve that, the patient was sedated with ketamine and dexmedetomidine, and an ultrasound-guided single-shot caudal block with ropivacaine was performed. Post-abdominal decompression, general anesthesia was induced, and intubation was managed via videolaryngoscopy. Thoracoscopic TEF repair required several pauses for ventilation and hemodynamic optimization. Dopamine was administered intraoperatively for blood pressure support. The newborn was extubated and started on enteral feeding by the seventh postoperative day, progressing well by the time of discharge. In this case, a derivative colostomy before TEF repair avoided positive pressure ventilation complications. Ultrasound-guided caudal block provided effective regional anesthesia with high success rates. Ketamine and dexmedetomidine offered balanced sedation with minimal respiratory compromise. Dopamine was used effectively to maintain adequate perfusion, monitored with invasive blood pressure and cerebral oximetry. Anesthetic management of newborns with VACTERL association undergoing simultaneous repair of TEF and anal atresia demands meticulous and tailored planning to address the specific needs and minimize associated risks. This case highlights the importance of comprehensive anesthetic management and its impact on the patient's outcome.
脊柱缺陷、肛门直肠畸形、心脏畸形、气管食管瘘(TEF)/食管闭锁、肾脏畸形和肢体异常(VACTERL)综合征是一种罕见的先天性疾病,表现为一系列出生缺陷。诊断主要依靠临床症状,患者至少出现其中三种异常。这些患者的治疗需要采取针对个体情况的多学科方法。由于异常情况多样且复杂,麻醉管理极具挑战性。本文讨论了一名足月新生儿男性(孕39周零6天,体重3340克)诊断为VACTERL综合征的麻醉管理。该新生儿入住新生儿重症监护病房(NICU),计划在出生后第二天进行TEF手术修复和衍生结肠造口术。为降低正压通气导致漏气和腹胀的风险,首先在区域麻醉下进行衍生结肠造口术,保留自主通气。为实现这一点,患者使用氯胺酮和右美托咪定镇静,并进行超声引导下的单次骶管阻滞,使用罗哌卡因。腹部减压后,诱导全身麻醉,并通过视频喉镜进行插管。胸腔镜下TEF修复需要多次暂停通气和优化血流动力学。术中使用多巴胺支持血压。新生儿在术后第七天拔管并开始肠内喂养,出院时情况良好。在本病例中,TEF修复前进行衍生结肠造口术避免了正压通气并发症。超声引导下的骶管阻滞提供了有效且成功率高的区域麻醉。氯胺酮和右美托咪定提供了平衡的镇静,对呼吸的影响最小。多巴胺有效地用于维持充足灌注,通过有创血压和脑氧饱和度监测。对患有VACTERL综合征同时进行TEF和肛门闭锁修复的新生儿进行麻醉管理需要精心且量身定制的计划,以满足特定需求并将相关风险降至最低。本病例突出了全面麻醉管理的重要性及其对患者预后的影响。