Bamgbade Olumuyiwa A, Alfa John A, Khalaf Wael M, Zuokumor Andrew P
J Med Case Rep. 2009 Jun 23;3:7293. doi: 10.4076/1752-1947-3-7293.
Perioperative spinal myoclonus is extremely rare. Many anaesthetists and perioperative practitioners may not diagnose or manage this complication appropriately when it occurs. This case report of unusual acute spinal myoclonus following regional anaesthesia highlights certain aspects of this rare complication that have not previously been published.
A series of four consecutive patients who developed acute lower-limb myoclonus following spinal or epidural anaesthesia are described. The case series occurred at three different hospitals and involved four anaesthetists over a 3-year period. Two Caucasian men, aged 90-years-old and 67-years-old, manifested unilateral myoclonus. Two Caucasian women, aged 64-years-old and 53-years-old, developed bilateral myoclonus. Myoclonus was self-limiting in one patient, treated with further regional anaesthesia in one patient and treated with intravenous midazolam in two patients. The overall outcome was good in all patients, with no recurrence or sequelae in any of the patients.
This case series emphasizes that spinal myoclonus following regional anaesthesia is rare, has diverse pathophysiology and can have diverse presentations. The treatment of perioperative spinal myoclonus should be directed at the aetiology. Anaesthetists and perioperative practitioners who are unfamiliar with this rare complication should be reassured that it may be treated successfully with midazolam.
围手术期脊髓肌阵挛极为罕见。许多麻醉医生和围手术期从业者在其发生时可能无法正确诊断或处理这一并发症。本例关于区域麻醉后罕见急性脊髓肌阵挛的病例报告突出了这一罕见并发症以前未发表过的某些方面。
描述了一系列连续的4例患者,他们在脊髓或硬膜外麻醉后出现急性下肢肌阵挛。该病例系列发生在3家不同的医院,在3年期间涉及4名麻醉医生。两名白人男性,年龄分别为90岁和67岁,表现为单侧肌阵挛。两名白人女性,年龄分别为64岁和53岁,出现双侧肌阵挛。1例患者的肌阵挛为自限性,1例患者接受了进一步的区域麻醉治疗,2例患者接受了静脉注射咪达唑仑治疗。所有患者的总体预后良好,无一例复发或出现后遗症。
该病例系列强调区域麻醉后脊髓肌阵挛罕见,具有多种病理生理学机制,表现形式多样。围手术期脊髓肌阵挛的治疗应针对病因。不熟悉这一罕见并发症的麻醉医生和围手术期从业者应放心,咪达唑仑可能成功治疗该疾病。