Restarting propofol following successful management of propofol infusion syndrome: a case report

K. Durr, Brent Herritt, Naomi Niznick, J. Hooper, K. Kyeremanteng, G. D’Egidio
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Abstract

: Propofol infusion syndrome (PRIS) is a rare and potentially fatal complication seen in high-dose (>5 mg/kg/h) or prolonged (>48 h) propofol infusions. PRIS presents as a constellation of symptoms, including anion-gap metabolic acidosis, elevated lactate, cardiogenic shock, rhabdomyolysis, arrhythmia, among other biochemical abnormalities. The current standard of care focuses on early recognition, propofol cessation, and supportive management. Case reports have shown evidence for several novel therapeutic interventions, including plasmapheresis, dialysis, and extracorporeal membrane oxygenation. There has yet to be a documented case demonstrating a trial of reinitiating propofol following successful PRIS management. We present the case of a previously healthy 20-year-old male that presented to the emergency department with new-onset refractory status epilepticus, secondary to suspected autoimmune encephalitis. Despite multiple immunomodulators, anesthetic therapies, and anti-epileptic agents, he exhibited ongoing refractory seizure activity on continuous electroencephalogram monitoring. Propofol boluses were the only therapy to offer seizure burst suppression, prompting uptitration of the infusion. The patient subsequently developed hemodynamic instability and multiple biochemical abnormalities consistent with PRIS. He was managed with one round of plasmapheresis, later followed by a session of sustained-low efficiency dialysis (SLED). This therapeutic combination was successful in managing PRIS and restoring hemodynamic stability. After stopping the propofol infusion, he developed near constant electrographic seizures, with breakthrough clinical seizures despite multiple other therapeutic interventions. Propofol was later restarted for seizure control, with no further recurrence of PRIS. This case provides support for novel therapeutic modalities, plasmapheresis and SLED, when managing PRIS. This case also marks the first successful attempt at restarting propofol following PRIS.
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异丙酚输注综合征成功治疗后重新开始使用异丙酚:1例报告
:丙泊酚输注综合征(PRIS)是一种罕见且可能致命的并发症,见于高剂量(>5 mg/kg/小时)或长时间(>48小时)丙泊酚输注。PRIS表现为一系列症状,包括阴离子间隙代谢性酸中毒、乳酸升高、心源性休克、横纹肌溶解症、心律失常以及其他生化异常。目前的护理标准侧重于早期识别、停用丙泊酚和支持性管理。病例报告显示了几种新型治疗干预措施的证据,包括血浆置换、透析和体外膜肺氧合。目前还没有一个记录在案的案例证明在成功的PRIS管理后重新启动丙泊酚的试验。我们报告了一例先前健康的20岁男性,他因疑似自身免疫性脑炎继发的新发难治性癫痫持续状态而到急诊科就诊。尽管有多种免疫调节剂、麻醉疗法和抗癫痫药物,他在持续的脑电图监测中仍表现出持续的难治性癫痫发作活动。异丙酚推注是唯一能抑制癫痫发作的疗法,促使输液量增加。患者随后出现血液动力学不稳定和多种与PRIS一致的生化异常。他接受了一轮血浆置换,随后进行了持续低效透析(SLED)。这种治疗组合在治疗PRIS和恢复血液动力学稳定性方面取得了成功。在停止输注丙泊酚后,他出现了近乎持续的脑电图癫痫发作,尽管有多种其他治疗干预措施,但仍有突破性的临床癫痫发作。随后重新启动丙泊酚以控制癫痫发作,PRIS不再复发。该病例在治疗PRIS时为新的治疗方式,血浆置换和SLED提供了支持。该病例也标志着首次成功尝试在PRIS后重新启动丙泊酚。
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