Smith Silas W, Ferguson Kathy L, Hoffman Robert S, Nelson Lewis S, Greller Howard A
New York City Poison Control Center, New York, New York 10016, USA.
Clin Toxicol (Phila). 2008 Jun;46(5):470-4. doi: 10.1080/15563650701779695.
Compared to other calcium channel blockers (CCBs), overdose with dihydropyridine CCBs are considered relatively benign due to their vascular selectivity. Although not a sustained-release preparation, amlodipine's prolonged duration of effect is concerning following overdose. In addition, angiotensin II receptor blocker blunting of vasoconstrictive and sympathetic compensatory responses could exacerbate calcium channel blocker toxicity. We describe severe toxicity associated with an overdose of amlodipine and valsartan.
A 75-year-old woman presented to the ED 45 minutes after a witnessed suicidal ingestion of a "handful" of amlodipine and valsartan tablets. Hypotension, which appeared two hours after ingestion, was refractory to crystalloids and colloids, calcium gluconate, epinephrine, norepinephrine, phenylephrine, and vasopressin infusions. High-dose insulin euglycemia (HIE) therapy, and treatment with glucagon and naloxone were successful in improving her hemodynamic status. In this combined overdose, right heart catheterization demonstrated both negative inotropic effects and decreased systemic vascular resistance.
Co-ingestion of amlodipine with valsartan produced profound toxicity. Early institution of HIE therapy may be beneficial to reverse these effects.
与其他钙通道阻滞剂(CCB)相比,二氢吡啶类CCB过量服用因其血管选择性被认为相对无害。尽管氨氯地平不是缓释制剂,但过量服用后其作用持续时间延长令人担忧。此外,血管紧张素II受体阻滞剂对血管收缩和交感神经代偿反应的抑制可能会加重钙通道阻滞剂的毒性。我们描述了一例因过量服用氨氯地平和缬沙坦导致的严重毒性反应。
一名75岁女性在目睹其自杀性吞服“一把”氨氯地平和缬沙坦片剂45分钟后被送往急诊科。服药两小时后出现的低血压对晶体液、胶体液、葡萄糖酸钙、肾上腺素、去甲肾上腺素、去氧肾上腺素和血管加压素输注均无反应。高剂量胰岛素正常血糖疗法(HIE)以及胰高血糖素和纳洛酮治疗成功改善了她的血流动力学状态。在这种联合过量服用的情况下,右心导管检查显示既有负性肌力作用,又有全身血管阻力降低。
氨氯地平和缬沙坦共同服用产生了严重毒性。早期采用HIE疗法可能有助于逆转这些效应。