Ishihara Taiga, Ito Nobuko, Uchida Kanji
Department of Anesthesiology and Pain Relief Center, University of Tokyo Hospital, Tokyo, Japan.
Medicine (Baltimore). 2025 May 23;104(21):e42614. doi: 10.1097/MD.0000000000042614.
Sugammadex is a synthetic cyclodextrin derivative that reverses the effects of nondepolarizing neuromuscular blockers through selective encapsulation. Residual neuromuscular blockade (NMB) after extubation can lead to adverse events such as hypoxia and cardiac arrest. We encountered a case of residual NMB, despite the appropriate use of NMB monitoring and sugammadex, as recommended by the American Society of Anesthesiologists.
A 27-year-old female underwent balloon dilatation under general anesthesia for left bronchial stenosis after lung transplantation. Rocuronium (50 mg) was administered for intubation, with 10 mg intermittently administered to maintain a train-of-four (TOF) count of <2. At the conclusion of the procedure, sugammadex (150 mg) was administered at a TOF count of 3. The patient was extubated with a TOF ratio of 100%. Fifteen minutes after transfer to the ward and 30 minutes after sugammadex administration, the patient developed respiratory distress and erythema on her trunk and upper limbs, exhibiting possible symptoms of anaphylaxis. The emergency team administered adrenaline via intramuscular injection. Despite this, the respiratory symptoms worsened.
Difficulty in breathing was possibly due to recurrent NMB caused by residual muscle relaxants that were not fully reversed.
The patient was reintubated and transferred to the intensive care unit. Bronchoscopy performed after reintubation did not reveal signs of anaphylactic airway swelling.
The patient's respiratory condition improved, and she was extubated the following morning. After extubation, she recalled being unable to breathe or move during the follow-up bronchoscopy. Plasma histamine and serum tryptase levels were measured 2 and 24 hours after the suspected anaphylactic episode, showing no increase in the levels.
This case highlights that neuromuscular monitoring and adherence to sugammadex dosing guidelines do not entirely eliminate the risk of recurarization, which may present with anaphylaxis-like symptoms, complicating the diagnosis.
舒更葡糖钠是一种合成环糊精衍生物,通过选择性包封来逆转非去极化神经肌肉阻滞剂的作用。拔管后残余神经肌肉阻滞(NMB)可导致诸如缺氧和心脏骤停等不良事件。尽管按照美国麻醉医师协会的建议适当使用了NMB监测和舒更葡糖钠,我们仍遇到了一例残余NMB的病例。
一名27岁女性在肺移植后因左支气管狭窄接受全身麻醉下的球囊扩张术。插管时给予罗库溴铵(50mg),并间歇性给予10mg以维持四个成串刺激(TOF)计数<2。手术结束时,在TOF计数为3时给予舒更葡糖钠(150mg)。患者以100%的TOF比值拔管。转入病房15分钟后且给予舒更葡糖钠30分钟后,患者出现呼吸窘迫,躯干和上肢出现红斑,表现出可能的过敏症状。急救团队通过肌肉注射给予肾上腺素。尽管如此,呼吸症状仍恶化。
呼吸困难可能是由于未完全逆转的残余肌肉松弛剂导致复发性NMB所致。
患者重新插管并转入重症监护病房。重新插管后进行的支气管镜检查未发现过敏性气道肿胀的迹象。
患者的呼吸状况改善,次日早晨拔管。拔管后她回忆起在后续支气管镜检查期间无法呼吸或移动。在疑似过敏发作后2小时和24小时测量血浆组胺和血清类胰蛋白酶水平,结果显示水平未升高。
该病例强调,神经肌肉监测和遵循舒更葡糖钠给药指南并不能完全消除再次出现肌松作用的风险,这种情况可能表现为类似过敏的症状,使诊断复杂化。