University Health, Pharmacotherapy and Pharmacy Services, San Antonio, TX, USA.
UT Health San Antonio, Pharmacotherapy Education and Research Center, San Antonio, TX, USA.
J Pharm Pract. 2024 Apr;37(2):513-516. doi: 10.1177/08971900221137389. Epub 2022 Oct 31.
Calcium channel blockers (CCB) are a leading cause of ingestion-associated fatality. Angiotensin-converting enzyme inhibitor (ACEi) overdose as part of co-ingestion is common and associated with refractory shock. Treatment options to manage this profound vasoplegia are limited. We describe the first case of use of newly formulated Angiotensin II for treatment of severe ACEi and CCB poisoning. A 57-year-old man presented after suicide attempt by ingesting 20 tablets each of amlodipine 10 mg and benazepril 20 mg. His hypotension was initially managed with 35 mL/kg of crystalloid, norepinephrine, and hyperinsulinemic euglycemic therapy (HIET). His hemodynamics further deteriorated, and he developed lactic acidosis, electrolyte derangements, and renal dysfunction. Further complications of his ingestion included cardiac arrest, subsequent requirement for emergency cricothyrotomy, and renal replacement therapy. Maximal hemodynamic support with HIET therapy insulin drip 4.4 units/kg/hour, norepinephrine 2 mcg/kg/min, epinephrine 1 mcg/kg/min, vasopressin .06 units/hour, and intravenous lipid emulsion was unsuccessful. Ang II was started and titrated to maximal doses with dramatic improvement in hemodynamics. Within hours of starting Ang II, epinephrine was stopped and norepinephrine decreased by 50%. He was downgraded from the intensive care unit without any ongoing end-organ dysfunction. Isolated CCB overdoses have high complication rates and well-established treatments. Therefore, management of CCB and ACEi co-ingestion is typically driven by CCB poisoning algorithm. There are multiple reports of CCB and ACEi co-ingestions causing treatment-refractory shock. Therapeutic options are limited by toxicities and availability of salvage therapies. Ang II is a safe and highly effective option to manage these patients.
钙通道阻滞剂(CCB)是摄入相关死亡的主要原因。血管紧张素转换酶抑制剂(ACEi)作为共摄入的一部分过量很常见,并且与难治性休克有关。管理这种严重血管扩张的治疗选择有限。我们描述了首例使用新配方血管紧张素 II 治疗严重 ACEi 和 CCB 中毒的病例。 一名 57 岁男子因企图自杀而摄入 20 片 10mg 氨氯地平片和 20mg 贝那普利片。他的低血压最初通过输注 35ml/kg 的晶体液、去甲肾上腺素和高血糖胰岛素治疗(HIET)进行管理。他的血液动力学进一步恶化,出现乳酸酸中毒、电解质紊乱和肾功能障碍。他摄入的其他并发症包括心脏骤停、随后需要紧急环甲膜切开术和肾脏替代治疗。使用 HIET 治疗胰岛素滴注 4.4 单位/公斤/小时、去甲肾上腺素 2 微克/公斤/分钟、肾上腺素 1 微克/公斤/分钟、血管加压素 0.06 单位/小时和静脉内脂肪乳剂的最大血液动力学支持均不成功。开始使用血管紧张素 II 并滴定至最大剂量,血液动力学显著改善。在开始使用血管紧张素 II 的几个小时内,停止使用肾上腺素,去甲肾上腺素减少 50%。他从重症监护病房降级,没有任何持续的终末器官功能障碍。 单独的 CCB 过量有很高的并发症发生率和既定的治疗方法。因此,CCB 和 ACEi 共摄入的管理通常由 CCB 中毒算法驱动。有多个关于 CCB 和 ACEi 共摄入导致治疗抵抗性休克的报告。治疗选择受到毒性和可获得的挽救治疗的限制。血管紧张素 II 是管理这些患者的安全且非常有效的选择。