The Tisdale-score achieved a sensitivity of 100% for identifying patients at risk of QTc prolongation among those prescribed systemic azole antifungal therapy, with relevant QTc prolongations occurring in only 4.7% of cases.
Retrospective cohort
No
Does the Tisdale-score accurately predict QTc prolongation in hospitalized adult patients receiving systemic azole antifungal therapy?
259 adult inpatients (≥18 years) across all medical specialties receiving 319 systemic azole antifungal prescriptions (cases), median age 61, 45% female, at a single university hospital in Germany.
Calculation of the Tisdale-score for risk stratification of QTc prolongation during systemic azole antifungal therapy
Sensitivity and specificity of the Tisdale-score with regard to detected QTc prolongations (defined as QTc ≥500 ms or ΔQTc ≥60 ms in follow-up ECG within 10 days)surrogate
The Tisdale-score demonstrated excellent sensitivity but low specificity for predicting QTc prolongation in hospitalized patients receiving systemic azole antifungals, making it a useful but potentially over-alerting screening tool.
Background QTc prolongation can trigger potentially lethal arrhythmias. Almost all azole antifungals, which are used in vulnerable patients, prolong the QTc interval and thus, may increase arrhythmia risk. The Tisdale-risk-score allows to identify patients at risk for drug-induced QTc prolongation but has not yet been investigated in this patient population. Objective To evaluate the sensitivity and specificity of the Tisdale-score with regard to detected QTc prolongations in patients prescribed systemic azole antifungals. Methods For six months (12/23-05/24), prescriptions of systemic azole antifungals were retrospectively recorded in adult inpatients of all medical specialties of a university hospital. Risk factors for QTc prolongation, including concomitant drugs and ECGs, were documented and the Tisdale-score and its sensitivity and specificity were calculated. Results In the study period, 319 systemic azole prescriptions (cases) were recorded for 259 patients. The median age of all cases was 61 years, 45% (143) were female. Including the systemic azole, a prescription of ≥2 QT-drugs was present in 283 (89%) cases. The median Tisdale-score was 7 (moderate risk). ECGs after azole initiation were available in 149 cases. Out of these, relevant QTc prolongations occurred in 7 cases (4.7%). Sensitivity of the Tisdale-score was 100%, specificity 30%. Conclusion Patients prescribed systemic azole antifungals are at risk of QTc prolongation due to regular use of multiple QT-drugs. However, relevant QTc prolongations were rare in the patient population studied. The Tisdale-score achieved a good sensitivity for the identification of patients at risk for QTc prolongation.
Building similarity graph...
Analyzing shared references across papers
Loading...
Julian Steinbrech
Ute Amann
Michael Irlbeck
Frontiers in Cardiovascular Medicine
SHILAP Revista de lepidopterología
University of Colorado Denver
German Centre for Cardiovascular Research
LMU Klinikum
Building similarity graph...
Analyzing shared references across papers
Loading...
Steinbrech et al. (Mon,) conducted a retrospective cohort in QTc prolongation due to azole antifungal therapy (n=319). Systemic Azole Antifungal Therapy was evaluated on QTc prolongation after azole initiation. The Tisdale-score achieved a sensitivity of 100% for identifying patients at risk of QTc prolongation among those prescribed systemic azole antifungal therapy, with relevant QTc prolongations occurring in only 4.7% of cases.
www.synapsesocial.com/papers/69b3aaa802a1e69014ccb69d — DOI: https://doi.org/10.3389/fcvm.2026.1685152
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: