A prospective study of acute propranolol overdose defining dose thresholds of severe toxicity (ATOM - 9).

IF 3 3区 医学 Q2 TOXICOLOGY
Clinical Toxicology Pub Date : 2025-01-01 Epub Date: 2024-12-10 DOI:10.1080/15563650.2024.2435397
Katherine Z Isoardi, Angela L Chiew, Cuong Do, Michael Humphreys, Ahmead Mustafa, Michael S Roberts, Geoffrey K Isbister
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Abstract

Introduction: Propranolol is a beta-adrenoceptor blocking drug with sodium channel-blocking properties that can cause life-threatening toxicity in overdose. Limited research defines dose thresholds of toxicity. We aimed to investigate propranolol overdose and dose thresholds for severe toxicity.

Material and methods: This is a prospective series of patients with acute propranolol overdose ≥360 mg from August 2014 to December 2023 enrolled through the Australian TOxicology Monitoring (ATOM) collaboration. Severe toxicity was defined as seizure, coma, inotrope therapy, electrocardiographic evidence of sodium channel blockade, or cardiac arrest.

Results: There were 209 presentations in 165 patients (median age 30 years [range 15-80 years]; 117 females, 71%). The median reported dose ingested was 1,000 mg (IQR: 600-2,000 mg; range 360-16,000 mg). Co-ingestion occurred in 155 (74%) patients, most commonly involving benzodiazepines (n = 52). Bradycardia (heart rate <50 beats/min) occurred in 41 (20%), and hypotension (systolic blood pressure <90 mmHg) in 88 (42%). Severe toxicity occurred in 51 patients (24%), with 17 (8%) having a seizure and 29 (14%) developing coma. Forty-one (20%) received inotropes, including 31(15%) who were given epinephrine and 20 (10%) high-dose insulin. Electrocardiographic evidence of sodium channel blockade occurred in 16 (8%). Seven (3%) had a cardiac arrest (reported dose range 2,400-16,000 mg), with two deaths following the ingestion of propranolol 4,000 mg and 16,000 mg. The median length of stay was 17 h (IQR: 11-32 h). In 79 patients who ingested only propranolol, the lowest reported propranolol dose for hypotension was 400 mg and for bradycardia, 800 mg. The lowest reported dose for severe toxicity was propranolol 2,000 mg. In those ingesting propranolol only, 17 of 32 (53%) patients who ingested ≥2,000 mg had severe toxicity.

Discussion: Severe toxicity was common, occurring in a quarter of all propranolol overdoses and half of the isolated propranolol ingestions (≥2,000 mg). The outcome was usually favourable with good supportive care, even in severe toxicity.

Conclusion: The dose threshold for severe toxicity in isolated propranolol overdose appeared to be 2,000 mg.

急性心得安过量确定严重毒性剂量阈值(ATOM - 9)的前瞻性研究。
心得安是一种β -肾上腺素能受体阻断药物,具有钠通道阻断特性,过量可导致危及生命的毒性。有限的研究确定了毒性的剂量阈值。我们的目的是研究心得安过量和严重毒性的剂量阈值。材料和方法:本研究是通过澳大利亚毒理学监测(ATOM)合作项目纳入的2014年8月至2023年12月急性心得安过量≥360 mg患者的前瞻性研究。严重毒性被定义为癫痫发作、昏迷、肌力疗法、钠通道阻断的心电图证据或心脏骤停。结果:165例患者有209例表现(中位年龄30岁[范围15-80岁];117名女性,占71%)。报告的中位摄入剂量为1,000 mg (IQR: 600-2,000 mg;范围360- 16000毫克)。共摄入155例(74%)患者,最常见的是苯二氮卓类药物(n = 52)。心动过缓(心率讨论:严重毒性很常见,发生在四分之一的普萘洛尔过量和一半的孤立普萘洛尔摄入(≥2,000 mg)。结果通常是良好的支持护理,即使在严重的毒性。结论:普萘洛尔分离用药过量出现严重毒性的剂量阈值为2000 mg。
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来源期刊
Clinical Toxicology
Clinical Toxicology 医学-毒理学
CiteScore
5.70
自引率
12.10%
发文量
148
审稿时长
4-8 weeks
期刊介绍: clinical Toxicology publishes peer-reviewed scientific research and clinical advances in clinical toxicology. The journal reflects the professional concerns and best scientific judgment of its sponsors, the American Academy of Clinical Toxicology, the European Association of Poisons Centres and Clinical Toxicologists, the American Association of Poison Control Centers and the Asia Pacific Association of Medical Toxicology and, as such, is the leading international journal in the specialty.
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