Why the study?
Many drug therapies cause QT prolongation and increase Torsades de Pointes risk, requiring guidance for clinicians managing patients at risk, exposed to QT-prolonging drugs, or with QT prolongation.
Answers are grounded in this paper and cite their sources.
Provides a practical algorithm to guide the clinical management of patients at risk for or experiencing drug-induced QT prolongation.
Many drug therapies are associated with prolongation of the QT interval. This may increase the risk of Torsades de Pointes (TdP), a potentially life-threatening cardiac arrhythmia. As the QT interval varies with a change in heart rate, various formulae can adjust for this, producing a 'corrected QT' (QTc) value. Normal QTc intervals are typically <450 ms for men and <460 ms for women. For every 10 ms increase, there is a ~5% increase in the risk of arrhythmic events. When prescribing drugs associated with QT prolongation, three key factors should be considered: patient-related risk factors (eg, female sex, age >65 years, uncorrected electrolyte disturbances); the potential risk and degree of QT prolongation associated with the proposed drug; and co-prescribed medicines that could increase the risk of QT prolongation. To support clinicians, who are likely to prescribe such medicines in their daily practice, we developed a simple algorithm to help guide clinical management in patients who are at risk of QT prolongation/TdP, those exposed to QT-prolonging medication or have QT prolongation.
No takes yet. Share an insight, caveat, or question.
Khatib et al. (2020) conducted a review in Drug-induced QT prolongation. Clinical management algorithm was evaluated.
Synapse has enriched 10 related papers. Consider them for comparative context: