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一名小儿脑瘫患者脊柱侧弯手术期间发生恶性高热危象:早期识别与成功干预一例

Malignant hyperthermia crisis during scoliosis surgery in a pediatric cerebral palsy patient: a case of early recognition and successful intervention.

作者信息

Kardm Saleh M, Alsiddiky Abdulmonem, Alamri Asim J, Reddy Ravi Shankar

机构信息

Department of Surgery, College of Medicine, Najran University, Najran, Saudi Arabia.

Department of Orthopedic, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

出版信息

Front Pediatr. 2025 Jun 16;13:1601801. doi: 10.3389/fped.2025.1601801. eCollection 2025.

Abstract

BACKGROUND

Malignant hyperthermia (MH) is a rare but life-threatening complication of general anesthesia, characterized by a hypermetabolic response that can lead to severe complications if not managed promptly. Patients with neuromuscular disorders, such as cerebral palsy and neuromuscular scoliosis, may have an increased risk of developing MH due to underlying genetic and physiological factors. Despite its rarity, early recognition and intervention are critical for patient survival.

CASE PRESENTATION

We present a case of MH in a 13-year-old girl with cerebral palsy and neuromuscular scoliosis undergoing elective scoliosis correction surgery under general anesthesia. The patient had no prior history of mental health (MH) susceptibility or a family history of the condition. After 90 min of surgery, she exhibited a rapid increase in end-tidal carbon dioxide (EtCO₂) to 60 mmHg, tachycardia (190 bpm), hypotension (70/40 mmHg), hyperthermia (41°C), and muscle rigidity, raising suspicion of MH. Sevoflurane inhalation was immediately discontinued, and the anesthesia circuit was changed to allow pure oxygen inhalation. The patient was treated with intravenous dantrolene, active cooling measures, forced alkaline diuresis, and correction of acid-base disturbances. These interventions successfully stabilized her vital signs, allowing the surgery to proceed safely. Postoperatively, she was transferred to the intensive care unit (ICU) for monitoring and was extubated once her condition stabilized. She was discharged on postoperative day 7 without further complications.

CONCLUSION

This case highlights the critical need for anesthesiologists and surgical teams to remain vigilant for MH in patients with neuromuscular disorders, even in the absence of a family history. Prompt recognition and immediate intervention with dantrolene and supportive therapies are essential for a favorable outcome. Preoperative MH risk assessment, avoidance of triggering agents, and preparedness for emergency management are crucial in high-risk populations.

摘要

背景

恶性高热(MH)是全身麻醉中一种罕见但危及生命的并发症,其特征为高代谢反应,若不及时处理可导致严重并发症。患有神经肌肉疾病(如脑瘫和神经肌肉型脊柱侧弯)的患者,由于潜在的遗传和生理因素,发生MH的风险可能会增加。尽管其罕见,但早期识别和干预对患者的生存至关重要。

病例报告

我们报告一例13岁患有脑瘫和神经肌肉型脊柱侧弯的女孩,在全身麻醉下接受择期脊柱侧弯矫正手术时发生MH的病例。该患者既往无恶性高热易感性病史或家族病史。手术90分钟后,她的呼气末二氧化碳(EtCO₂)迅速升至60 mmHg,出现心动过速(190次/分)、低血压(70/40 mmHg)、高热(41°C)和肌肉强直,这引起了对MH的怀疑。立即停止七氟烷吸入,并更换麻醉回路以允许纯氧吸入。患者接受了静脉注射丹曲林、积极的降温措施、强制碱性利尿以及酸碱紊乱的纠正。这些干预措施成功稳定了她的生命体征,使手术得以安全进行。术后,她被转入重症监护病房(ICU)进行监测,病情稳定后拔除气管插管。她于术后第7天出院,无进一步并发症。

结论

该病例突出表明,麻醉医生和手术团队即使在没有家族病史的情况下,也必须对神经肌肉疾病患者的MH保持警惕。及时识别并立即用丹曲林和支持性疗法进行干预对于取得良好预后至关重要。术前进行MH风险评估、避免触发因素以及做好应急处理准备在高危人群中至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f567/12206816/12706df86cc4/fped-13-1601801-g001.jpg

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