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Mitigating the Risk of QTc Prolongation When Using Haloperidol for Acute Treatment of Cannabinoid Hyperemesis
Sandra Merino1, Lissette Tordera1, Allison Jun1
1Department of Pharmacy, CHOC Children's Hospital, Orange, CA 92868, USA.
Insights
Cannabinoid Hyperemesis Syndrome (CHS) patients face increased QTc prolongation risk from cannabis and antiemetics like haloperidol. Vigilant EKG monitoring is crucial, with alternative treatments available for high-risk individuals.
Area of Science:
- Cardiology
- Toxicology
- Adolescent Medicine
Background:
- Cannabinoid Hyperemesis Syndrome (CHS) is increasingly prevalent due to marijuana legalization.
- Acute CHS management involves antiemetics, but these and CHS itself can prolong QTc.
- QTc prolongation and Torsades de Pointes (TdP) are serious cardiac risks.
Purpose of the Study:
- To report adolescent cases of CHS with QTc prolongation.
- To review literature on QTc prolongation/TdP in young CHS patients.
- To highlight risks and alternative management strategies.
Main Methods:
- Case reports of two adolescent females with CHS treated with haloperidol.
- Literature review of QTc prolongation/TdP in adolescents and young adults.
- Analysis of risk factors including cannabis use, electrolyte imbalance, and antiemetics.
Main Results:
- One patient presented with significant QTc prolongation (528 msec) and tachycardia, improving after haloperidol discontinuation.
- A second patient had borderline QTc prolongation (476 msec) and improved with fosaprepitant.
- Literature search revealed five severe, life-threatening QTc prolongation/TdP cases in this demographic.
Conclusions:
- Adolescents with CHS are at elevated risk for QTc prolongation.
- Haloperidol and other antiemetics, alongside cannabis use and electrolyte disturbances, contribute to this risk.
- Vigilant EKG monitoring and consideration of alternative antiemetics like topical capsaicin or olanzapine are recommended for high-risk patients.
Abstract:
Background/Objectives: Cannabinoid Hyperemesis Syndrome (CHS), associated with long-term cannabinoid use, has been increasingly observed in emergency room visits as more states in the U.S. have legislatively permitted medical and recreational marijuana use. The acute management of CHS primarily focuses on antiemetic treatment and supportive care. However, both the condition itself and the antiemetic drugs, such as haloperidol, may cause QTc prolongation. Methods: We reported two adolescent cases admitted to the emergency department for acute antiemesis management of CHS who received haloperidol treatment. A literature review was performed through October 2024 for previously published cases of QTc prolongation and/or Torsades de Pointes (TdP) in adolescents and young adults. Results: A 15-year-old female presented with hypokalemia and hypomagnesemia upon admission. She complained of chest pain and tachycardia, and the electrocardiogram (EKG) showed prolonged QTc (528 msec). The haloperidol infusion was discontinued. She recovered well post-discharge without complaints. A 17-year-old female had a borderline prolonged QT interval (476 msec). Her nausea and vomiting improved with a three-dose course of intravenous fosaprepitant before discharge. Our literature search identified five severe cases with life-threatening episodes of QTc prolongation and/or TdP in adolescents and young adults. Conclusions: Patients with CHS are at higher risk of QTc prolongation due to cannabis use, electrolyte imbalance, and antiemetic medications. We recommend vigilant EKG monitoring, particularly before initiating and throughout haloperidol treatment. If the patient presents with an increased risk of QTc prolongation, consider using topical capsaicin, lorazepam, aprepitant/fosaprepitant, and olanzapine as alternatives.
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