Key result
Marijuana wax vaping triggers severe QTc prolongation and Torsades de pointes resolved by isoproterenol and nadolol.
Why the study?
Recent reports link tetrahydrocannabinol vaping to sudden cardiac arrest, but the underlying mechanisms remain unclear.
Case Report (n=1)
No
High-potency marijuana wax vaping (dabbing) can unmask latent genetic susceptibility to QTc prolongation and trigger life-threatening Torsades de pointes even in patients with a previously normal baseline ECG.
There are several recent reports of tetrahydrocannabinol vaping-related sudden cardiac arrest, and the mechanisms are unclear. We report a unique case of a 19-year-old female who suffered documented prolonged QTc leading to Torsades de pointes and cardiac arrest in the setting of frequent marijuana wax vaping. While she demonstrated normal baseline QTc measurements years earlier, she was found to have a genetic predisposition to QTc prolongation (genetic mutation, family history of prolonged QTc), suggesting that specific patient populations are at higher risk of these adverse events. The patient was acutely managed with isoproterenol to increase the heart rate and was discharged on nadolol after placement of an implantable cardioverter-defibrillator. Marijuana wax vaping and dabbing may cause fatal Torsades de pointes in susceptible patients, and further research is required to identify these patients a priori.
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Shah et al. (2021) conducted a case report in QTc prolongation-related ventricular fibrillation arrest and Torsades de pointes due to excessive marijuana wax vaping (n=1). Marijuana wax vaping (dabbing) exposure; managed acutely with isoproterenol and chronically with dual-chamber ICD and nadolol was evaluated on Resolution of Torsades de pointes and QTc interval normalization. Marijuana wax vaping triggered QTc prolongation to 622 msec and Torsades de pointes in a 19-year-old female, which resolved with isoproterenol (QTc 465 msec) and long-term nadolol plus ICD.
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