Cardiac safety of multidrug-resistant tuberculosis treatment: moving towards individualised monitoring
A heart rate-corrected QT interval (QTc) of 500 ms or more increases the risk of potentially fatal ventricular arrhythmias, including torsade de pointes.2 Despite the frequent, long-term use of QT interval-prolonging drugs, including moxifloxacin, which is used as a positive control in thorough QT s...
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| Veröffentlicht in: | The Lancet infectious diseases Jg. 21; H. 7; S. 894 - 895 |
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| Hauptverfasser: | , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
United States
Elsevier Ltd
01.07.2021
Elsevier Limited New York, NY : Elsevier Science ; The Lancet Pub. Group, 2001 |
| Schlagworte: | |
| ISSN: | 1473-3099, 1474-4457, 1474-4457 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | A heart rate-corrected QT interval (QTc) of 500 ms or more increases the risk of potentially fatal ventricular arrhythmias, including torsade de pointes.2 Despite the frequent, long-term use of QT interval-prolonging drugs, including moxifloxacin, which is used as a positive control in thorough QT studies,3 ECG monitoring became routine during multidrug or rifampicin-resistant tuberculosis treatment only after the first phase 2 trials showed QT prolongation during treatment with bedaquiline and delamanid. [...]reassuring is the fact that patients with low albumin values do not appear to have clinically-relevant increases in the risk of QT prolongation, an initial concern.9 As expected, owing to bedaquiline's long half-life, QTc interval 4 weeks after treatment stop was reduced by only 25% and 26% in bedaquiline-containing groups, compared with 56% in the delamanid group. [...]these results give us the opportunity of re-establishing the correct priorities. |
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| Bibliographie: | SourceType-Scholarly Journals-1 ObjectType-Commentary-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 ObjectType-Commentary-3 content type line 23 |
| ISSN: | 1473-3099 1474-4457 1474-4457 |
| DOI: | 10.1016/S1473-3099(20)30836-7 |