Our Lady of Lourdes Hospital, Drogheda, Ireland.
BMC Anesthesiol. 2024 May 10;24(1):173. doi: 10.1186/s12871-024-02539-0.
Bethlem Myopathy is a collagen VI-related myopathy presenting as a rare hereditary muscular disorder with progressive muscular weakness and joint contractures. Despite its milder clinical course relative to other myopathies, anaesthetic management can be challenging. High arched palates and fixed flexion deformities may contribute to a difficult airway. A progressive decline in pulmonary function can present later into adulthood. This respiratory decline can carry secondary cardiovascular consequences due to the progressive nature of restrictive lung disease, including right sided heart disease and pulmonary hypertension. We describe a case of a male patient with Bethlem Myopathy undergoing anaesthesia, to contribute to the limited body of literature on this condition and enhance awareness and guidance amongst anaesthesiologists on approaching patients with this condition. This is the first case report within the literature of its kind.
This case details a 33-year-old male with Bethlem Myopathy undergoing tonsillectomy. Diagnosed in childhood following developmental delays, the patient had no prior anaesthetic exposure and no family history of anaesthetic complications. Anaesthetic induction was achieved without complications, avoiding depolarizing muscle relaxants and careful airway management. Extreme care was taken in patient positioning to prevent complications. The surgery proceeded without incident and muscle paralysis was reversed with Suggammadex, resulting in no adverse post-operative respiratory complications. The patient was discharged on the first post-operative day without any respiratory or cardiovascular compromise.
Bethlem Myopathy, while often exhibiting a mild clinical course, can present anaesthetic challenges. Awareness of potential complications including a difficult airway, cardiovascular and respiratory implications as well as the need for specialised monitoring and positioning is crucial to ensure a safe peri-operative course.
Bethlem 肌病是一种与六型胶原相关的肌病,表现为一种罕见的遗传性肌肉疾病,伴有进行性肌肉无力和关节挛缩。尽管与其他肌病相比,其临床病程较轻,但麻醉管理可能具有挑战性。高拱形腭和固定的屈曲畸形可能导致气道困难。肺功能的逐渐下降可能在成年后出现。由于限制性肺病的进行性性质,包括右侧心脏病和肺动脉高压,这种呼吸下降可能会带来继发性心血管后果。我们描述了一例 Bethlem 肌病男性患者的麻醉情况,旨在为该疾病的有限文献做出贡献,并提高麻醉师对该疾病患者的处理方法的认识和指导。这是文献中首例此类病例报告。
本病例详细介绍了一名 33 岁男性患者,患有 Bethlem 肌病,行扁桃体切除术。该患者在儿童时期因发育迟缓被诊断出患有 Bethlem 肌病,此前从未接受过麻醉,也没有麻醉并发症的家族史。麻醉诱导无并发症,避免使用去极化肌松药和小心的气道管理。在患者体位方面非常小心,以防止并发症。手术过程顺利,肌肉松弛剂用 Suggammadex 逆转,术后无呼吸并发症。患者在术后第一天出院,无呼吸或心血管并发症。
Bethlem 肌病虽然常表现为较轻的临床病程,但可能会出现麻醉挑战。了解潜在的并发症,包括气道困难、心血管和呼吸影响,以及需要专门的监测和体位的必要性,对于确保围手术期的安全至关重要。