Forensic science, medicine, and pathology · 2026
Suicide by flecainide: a case report and review of the literature.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Ошибки и ограничения
История · было → стало
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Montana Angelo, Faro Fabrizio Lo, Turchi Chiara, Alessandrini Federica, Giorgetti Arianna
Аннотация
PURPOSE: Flecainide is a prescription drug used to treat or prevent various types of arrhythmias by decreasing conduction velocity. Despite its therapeutic utility, flecainide has a narrow safety margin and potential for fatal toxicity. This study presents a forensic case of fatal flecainide intoxication and investigates the role of pharmacogenetics in drug metabolism and toxicity.
METHODS: A 27-year-old medical doctor, prescribed flecainide, was found deceased. Postmortem examination included histological and toxicological analyses of blood and urine samples, with flecainide quantification by a validated method. CYP2D6 and CYP3A5 were genotyped to check for variants of the respective drug-metabolizing enzymes. A literature review of fatal and non-fatal flecainide intoxication is also presented.
RESULTS: Flecainide concentrations measured 3.411 mg/l and 2.962 mg/l in central and peripheral blood, respectively. Pharmacogenetic analysis identified a CYP3A5 *3/*3 poor metabolizer genotype, likely contributing to reduced drug clearance and increased toxicity. Histology revealed mild coronary stenosis and signs consistent with cardiogenic shock. The death was deemed a suicide, possibly facilitated by abnormal metabolic phenotype in a mildly compromised cardiac substrate.
CONCLUSIONS: This case highlights the complexities in diagnosing lethal flecainide intoxication, particularly considering postmortem concentration variability and individual metabolic differences. Integrating pharmacogenetic data enhances interpretation of toxicological findings and may guide personalized therapeutic strategies to mitigate risk. Further research is warranted to clarify genetic influences on flecainide toxicity.
METHODS: A 27-year-old medical doctor, prescribed flecainide, was found deceased. Postmortem examination included histological and toxicological analyses of blood and urine samples, with flecainide quantification by a validated method. CYP2D6 and CYP3A5 were genotyped to check for variants of the respective drug-metabolizing enzymes. A literature review of fatal and non-fatal flecainide intoxication is also presented.
RESULTS: Flecainide concentrations measured 3.411 mg/l and 2.962 mg/l in central and peripheral blood, respectively. Pharmacogenetic analysis identified a CYP3A5 *3/*3 poor metabolizer genotype, likely contributing to reduced drug clearance and increased toxicity. Histology revealed mild coronary stenosis and signs consistent with cardiogenic shock. The death was deemed a suicide, possibly facilitated by abnormal metabolic phenotype in a mildly compromised cardiac substrate.
CONCLUSIONS: This case highlights the complexities in diagnosing lethal flecainide intoxication, particularly considering postmortem concentration variability and individual metabolic differences. Integrating pharmacogenetic data enhances interpretation of toxicological findings and may guide personalized therapeutic strategies to mitigate risk. Further research is warranted to clarify genetic influences on flecainide toxicity.