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Published on: December 28, 2017
Torsade de pointes induced by systemic antifungal agents: lessons from a retrospective analysis of published case
1Department of Internal Medicine D, Tel-Aviv Sourasky Medical Center, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel. justo1@bezeqint.net
Abstract:
Torsade de pointes (TdP) is a potentially fatal arrhythmia that might be associated with systemic antifungal agent (SAFAs) administration. The objective of this study was to investigate all published reports on TdP induced by SAFAs in order to characterise this association. Each original report was analysed for the presence of risk factors for TdP: female gender, structural heart disease, electrolyte imbalance, concomitant use of a QT interval prolonging agent which SAFA inhibits its liver metabolism, liver cirrhosis, renal failure and more. Naranjo probability scale for adverse drug reactions was applied for every full report. Twenty-one reports on 28 patients were analysed. All patients survived. Most patients (25/28; 89.2%) used one or more agents that might have prolonged the QT interval and their liver metabolism might have been inhibited by SAFA. Female gender was the second most common risk factor for TdP (20/28; 71.4%). All patients, including female patients, had one or more risk factors for TdP prior to SAFA administration. According to Narajno probability scale, there was no definite association between TdP and SAFA in any report. SAFA alone might seldom trigger TdP. We wish to raise the level of awareness of risk factors for TdP prior to SAFA administration and for concomitant use of other dysrhythmogenic agents in particular.
Insights
Systemic antifungal agents (SAFAs) rarely cause Torsade de pointes (TdP) arrhythmia alone. Risk factors like female gender and drug interactions increase TdP risk before SAFA use.
Area of Science:
- Pharmacology
- Cardiology
- Clinical Medicine
Background:
- Torsade de pointes (TdP) is a life-threatening arrhythmia.
- Systemic antifungal agents (SAFAs) have been implicated in TdP cases.
Purpose of the Study:
- To investigate and characterize the association between SAFAs and TdP.
- To identify risk factors contributing to TdP during SAFA administration.
Main Methods:
- Systematic review of published reports on TdP associated with SAFAs.
- Analysis of patient data for TdP risk factors.
- Application of the Naranjo probability scale for adverse drug reactions.
Main Results:
- Twenty-eight TdP cases associated with SAFAs were analyzed; all patients survived.
- Common risk factors included concomitant QT-prolonging agents (89.2%) and female gender (71.4%).
- No definite SAFA-attributable TdP cases were confirmed by the Naranjo scale.
Conclusions:
- SAFAs alone are unlikely to trigger TdP.
- Awareness of pre-existing TdP risk factors and drug interactions is crucial before SAFA administration.
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