Department of Anaesthesiology and Intensive Care Medicine, Suez Canal University, Ismailia, 41522, Egypt.
BMC Anesthesiol. 2023 May 20;23(1):172. doi: 10.1186/s12871-023-02140-x.
Bochdalek congenital diaphragmatic hernia (CDH) is a developmental defect in the posterolateral diaphragm, allowing herniation of abdominal contents into the thorax causing mechanical compression of the developing lung parenchyma and lung hypoplasia. We describe a case of an adult patient with a Bochdalek hernia who underwent minimally invasive right thoracotomy Perceval bioprosthetic aortic valve replacement (AVR) requiring one-lung ventilation (OLV) on the side of the hernia. This is a complex and challenging case that brings up numerous thought-provoking anesthetic implications. To the best of our knowledge, a Pubmed search did not reveal any publication to date of difficult airway management in an adult patient with CDH.
The first major problem encountered was patient's crus habitus anatomical condition (exceedingly ventrally displaced trachea) Mallampati Class IV and Cormack-Lehane grade IV extremely difficult endotracheal intubation. Neither glottis nor epiglottis was visible on laryngoscopy; resulting in failed placement of the double-lumen endobronchial tube (DLT) following numerous attempts. The DLT was eventually placed via GlideScope videolaryngoscopy. Whereas the endobroncheal right lung block for left OLV was successfully placed using fiberopticscopy. The crus habitus encroached on OLV tidal volume by the cranially displaced ascending colon and left kidney. Anesthesia was maintained with remifentanil /sevoflurane; adjusted to maintain bispectral index (BIS) at 40-60. Digitally recorded BIS was 38-62 except when BIS precipitously declined to 14-38 (SR, suppression ratio < 10) for 25 min after termination of the cardiopulmonary bypass.
We report a case essentially dealing with an anatomically distorted difficult airway in a patient with left Bochdalek CDH undergoing a complex AVR. We describe anesthetic difficulties and unforeseen issues encountered; such as an extremely difficult DLT placement.
Bochdalek 先天性膈疝 (CDH) 是一种后外侧膈的发育缺陷,导致腹部内容物疝入胸腔,对发育中的肺实质造成机械性压迫,导致肺发育不全。我们描述了一例成人 Bochdalek 疝患者,该患者行微创右侧开胸经 Perceval 生物瓣主动脉瓣置换术 (AVR),疝侧需要单肺通气 (OLV)。这是一个复杂而具有挑战性的病例,提出了许多发人深省的麻醉问题。据我们所知,在 PubMed 搜索中,目前尚未发现任何关于成人 CDH 患者困难气道管理的出版物。
首先遇到的主要问题是患者的胸廓习惯体位解剖条件(气管异常向下移位)、Mallampati 分级 IV 和 Cormack-Lehane 分级 IV,极难进行气管内插管。喉镜下既看不见声门也看不见会厌;多次尝试后未能成功放置双腔支气管内导管 (DLT)。最终通过 GlideScope 视频喉镜放置了 DLT。而纤维支气管镜成功地放置了右侧支气管阻塞以实现左侧 OLV。胸廓习惯体位使颅侧移位的升结肠和左肾侵占了 OLV 潮气量。麻醉采用瑞芬太尼/七氟醚维持,调整至双频谱指数 (BIS) 维持在 40-60。数字化记录的 BIS 为 38-62,除了在体外循环结束后 25 分钟 BIS 急剧下降至 14-38(SR,抑制比 < 10)外。
我们报告了一例在左 Bochdalek CDH 患者中进行复杂 AVR 手术的病例,该患者存在解剖学上扭曲的困难气道。我们描述了麻醉困难和遇到的意外问题,例如极难放置 DLT。