Tang Katherine B, Simpson Michael D, Burns Michele M
Department of Emergency Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Harvard Medical Toxicology, Division of Emergency Medicine, Boston Children's Hospital, Boston, MA, USA.
Clin Toxicol (Phila). 2024 Sep;62(9):574-582. doi: 10.1080/15563650.2024.2390138. Epub 2024 Aug 28.
Tricyclic antidepressants often cause drug-induced QRS complex prolongation in overdose but are now less commonly prescribed. We sought to determine, among a contemporary cohort of patients, the pharmaceuticals independently associated with QRS complex prolongation in acute overdose.
We performed secondary analysis of data from the Toxicology Investigators Consortium (ToxIC) Core Registry. We included adult patients presenting from January 2016 through March 2023 with acute or acute-on-chronic pharmaceutical exposures. The primary outcome was QRS complex prolongation >0.12 s. Secondary outcomes included cardiac arrest, death, ventricular dysrhythmia, intensive care unit admission, initiation of vasopressors, and treatment with sodium bicarbonate. We used a multivariable logistic regression model with QRS complex prolongation as the outcome and individual pharmaceuticals of interest as independent variables. We assessed yearly trends of the contribution of relevant pharmaceuticals to QRS complex prolongation since 2016.
Of 11,945 patients in the total cohort (median age 37 years, 6,652 [55.7%] female), 366 (3.1%) developed QRS complex prolongation. Of 9,417 patients included in the model, 290 (3.1%) developed QRS complex prolongation. Amitriptyline, nortriptyline, doxepin, imipramine, noxiptiline, bupropion, flecainide, carvedilol, propranolol, diphenhydramine, and lamotrigine poisonings were independent predictors of QRS complex prolongation. Flecainide poisoning conferred the greatest odds of QRS complex prolongation (OR 574.1; 95% CI: 88.3-12,747). The contribution of tricyclic antidepressants to QRS complex prolongation decreased from 38.8% to 17.6% of all patients with QRS complex prolongation from 2016 to 2022. In 2022, the proportion of QRS complex prolongation from diphenhydramine (20.6%) surpassed that of tricyclic antidepressants.
This study provides insights into contemporary pharmaceutical poisoning associated with QRS complex prolongation. Tricyclic antidepressants remain clinically relevant exposures but are no longer the most common cause of drug-induced QRS complex prolongation.
Bupropion, diphenhydramine, and antidysrhythmics are increasingly common causes of QRS complex prolongation, each associated with numerous severe outcomes in poisoning. Greater safety measures to protect patients from cardiovascular toxicity from these pharmaceuticals are warranted.
三环类抗抑郁药过量服用时常导致药物性QRS波群延长,但如今其处方量已不那么常见。我们试图在当代一组患者中确定与急性过量服用时QRS波群延长独立相关的药物。
我们对毒理学研究人员联盟(ToxIC)核心登记处的数据进行了二次分析。我们纳入了2016年1月至2023年3月出现急性或急性-on-慢性药物暴露的成年患者。主要结局是QRS波群延长>0.12秒。次要结局包括心脏骤停、死亡、室性心律失常、入住重症监护病房、开始使用血管加压药以及用碳酸氢钠治疗。我们使用以QRS波群延长为结局、感兴趣的单个药物为自变量的多变量逻辑回归模型。我们评估了自2016年以来相关药物对QRS波群延长贡献的年度趋势。
在整个队列的11945名患者中(中位年龄37岁,6652名[55.7%]为女性),366名(3.1%)出现了QRS波群延长。在纳入模型的9417名患者中,290名(3.1%)出现了QRS波群延长。阿米替林、去甲替林、多塞平、丙咪嗪、诺昔替林、安非他酮、氟卡尼、卡维地洛、普萘洛尔、苯海拉明和拉莫三嗪中毒是QRS波群延长的独立预测因素。氟卡尼中毒导致QRS波群延长的几率最大(比值比574.1;95%置信区间:88.3-12747)。从2016年到2022年,三环类抗抑郁药对QRS波群延长的贡献在所有出现QRS波群延长的患者中从38.8%降至17.6%。2022年,苯海拉明导致QRS波群延长的比例(20.6%)超过了三环类抗抑郁药。
本研究为当代与QRS波群延长相关的药物中毒提供了见解。三环类抗抑郁药在临床上仍是相关的暴露因素,但不再是药物性QRS波群延长的最常见原因。
安非他酮、苯海拉明和抗心律失常药物是QRS波群延长越来越常见的原因,每种药物在中毒时都与众多严重结局相关。有必要采取更大的安全措施来保护患者免受这些药物引起的心血管毒性。