一名患有左侧波氏大疝并伴有二氧化碳麻醉的成年患者的围手术期挑战与处理:病例报告

IF 2.3 4区 医学 Q2 ANESTHESIOLOGY Journal of cardiothoracic and vascular anesthesia Pub Date : 2024-10-25 DOI:10.1053/j.jvca.2024.09.070
Arupratan Maiti , Amrita Guha , Ranjeeta Kumari , Tamasish Mukherjee , Arpan Chakraborty
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引用次数: 0

摘要

目的成人伯氏疝可能多年无症状,也可能急性出现呼吸道或胃肠道并发症。设计与方法 一位 57 岁的男性患者因 2 型呼吸衰竭(PCO2>100 mmHg)和昏迷出现在急诊室。他患有儿童脊髓灰质炎并伴有后遗症(坐轮椅)、严重的胸腰椎脊柱侧凸、肥胖伴有阻塞性睡眠呼吸暂停、糖尿病、高血压和甲状腺功能减退。胸部 X 光片显示左胸有巨大的半透明区,鼻胃管尖端在原位。HRCT 证实左侧有巨大的 Bochdalek 疝。患者在重症监护室完全依赖 NIV(无创通气),但仍处于高碳酸血症(PCO2 70+ mmHg)和缺氧状态(70%FiO2 条件下 PO2 70mmHg),因此计划进行手术修复。他预计气道困难(Mallampati 3,短颈,喉前),功能极差。术前超声心动图显示左右心室功能正常。血液常规检查正常。手术室安装了标准的 ASA 监护仪。在清醒状态下进行有创置管(在超声实时成像引导下,在局麻状态下进行左侧20G桡动脉置管和右侧颈内7.5Fr 5腔中心静脉置管)后,通过NIV以100%氧气进行预吸氧。通过 NIV 以 100% Fio2 获得的最大 SPO2 为 96%。在诱导全身麻醉(丙泊酚、芬太尼、顺阿曲库铵,然后是七氟醚、空气、氧气)后,使用视频喉镜为他一次性插管。然后插入单腔支气管阻断器以隔离左肺。进行了左侧开胸手术和巨大膈疝的网片修补术。疝内容物包括网膜、胃、肠系膜和左结肠。发现左下肺部分发育不良,进行了楔形切除。进行了肋间区域阻滞和皮肤切口局部浸润。病人第二天拔管,但拔管后出现中度高碳酸血症,术后第 3 天出现肺炎。他在重症监护室再次插管,最终需要进行气管切开术才能脱离呼吸机。气管造口术于第 41 天关闭。结果和结论Bochdalek疝是位于后插入部的膈肌发育不良导致的先天性缺陷。与右侧(13%)和双侧(2%)相比,左侧后外侧疝更为常见(85%)。无症状的波赫达雷克疝在成人中非常罕见(占成人总数的 0.17%),多发于女性(77%),主要出现在右侧(68%)。CT 扫描是准确评估患者解剖结构的金标准方法。成人 Bochdalek 疝通常表现为肺发育不全或胃肠道绞窄,但我们的病例比较特殊,表现为二氧化碳中毒。由于患有多种严重的并发症,术中面临着严峻的挑战,包括困难的气道、肥胖、脊柱侧凸导致的患者体位、维持单肺通气和术后止痛。在危及生命的急性病例中,手术修复是一种选择,但麻醉方面的挑战也是巨大的。在正确的时间进行正确的干预和管理是非常有益的。
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PERIOPERATIVE CHALLENGES AND MANAGEMENT OF AN ADULT PATIENT WITH LARGE LEFT SIDED BOCHDALEK HERNIA PRESENTING WITH CO2 NARCOSIS: A CASE REPORT

Objective

Bochdalek hernia in adults may remain asymptomatic for years and may present acutely with respiratory or gastro-intestinal complications. Our patient with multiple comorbidities presented with CO2 narcosis and posed serious challenges in perioperative period.

Design and method

A 57-year-old gentleman presented with Type 2 respiratory failure (PCO2>100 mmHg) and obtundation in Emergency Room. He was known case of childhood Poliomyelitis with residual weakness (wheelchair bound), severe thoracolumbar kyphoscoliosis, obesity with obstructive sleep apnoea, diabetic, hypertensive, hypothyroid. Chest X-ray showed huge translucent area in left chest and tip of nasogastric tube in-situ. The HRCT confirmed large Bochdalek hernia(left). Patient was completely NIV (non invasive ventilation) dependent in ITU but still was hypercarbic (PCO2 70+ mmHg) and hypoxic(PO2 70mmHg in 70%FiO2) and hence surgical repair was planned. He had anticipated difficult airway (Mallampati 3, short neck, anterior larynx) with very poor functional capacity. Pre operative Echocardiography showed normal left and right ventricular function. Routine blood investigations were normal .Proper patient consent was obtained. In operation theatre standard ASA monitors were attached. After awake invasive lines (left20G radial line and right internal jugular 7.5Fr 5 lumen central venous line under local anaesthesia guided by live ultrasonography),he was preoxygenated with 100% O2 via NIV. Maximum SPO2 acquired with 100% Fio2 on NIV was 96%. After induction of general anaesthesia(Propofol,Fentanyl,Cisatracurium followed by Sevoflurane, Air, Oxygen) he was intubated electively with video-laryngoscope at single attempt. Then single lumen bronchial blocker was inserted to isolate left lung. Left thoracotomy and mesh repair of the huge diaphragmatic hernia was performed. Contents of the hernia were omentum ,stomach,mesentry and left colon.Part of left lower lung was found to be hypoplastic and wedge resection was done. Intercostal regional block and local infiltration to skin incision were administered. Patient got extubated next day but after extubation he had moderate hypercarbia and developed a pneumonia on day3 of post operative period. He was intubated again in ITU and eventually needing a tracheostomy to wean off ventilator. Tracheostomy was closed on day41. Eventually he was discharged on day 49.

Results and conclusions

Bochdalek hernia is congenital defect resulting from developmental failure of diaphragm located in the posterior insertion. Left posterolateral hernias are more frequent (85%) as compared to the right side (13%) and bilateral are (2%).Mostly Bochdalek hernia is diagnosed in children and in neonates and present clinical symptoms caused by associated pulmonary insufficiency. In adults asymptomatic Bochdalek hernia is rare (0.17% of the adult population).It tends to affect women(77%) mostly and predominantly appears on the right side(68%). A CT scan is the gold standard method providing an accurate assessment of the patients anatomy. Adult Bochdalek hernia usually presents as lung hypoplasia or gastrointestinal strangulation but our case was unique that it presented with CO2 narcosis. With multiple serious comorbidities, intraoperative challenges were steep including difficult airway, obesity, patient positioning due to kyphoscoliosis and maintaining one lung ventilation and post operative pain relief . Surgical repair is the option and anaesthetic challenges can be enormous in acute life-threatening presentations. Right intervention and management at right time is rewarding.
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来源期刊
CiteScore
4.80
自引率
17.90%
发文量
606
审稿时长
37 days
期刊介绍: The Journal of Cardiothoracic and Vascular Anesthesia is primarily aimed at anesthesiologists who deal with patients undergoing cardiac, thoracic or vascular surgical procedures. JCVA features a multidisciplinary approach, with contributions from cardiac, vascular and thoracic surgeons, cardiologists, and other related specialists. Emphasis is placed on rapid publication of clinically relevant material.
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