Key result
Among 21 case reports of clarithromycin-associated QTc prolongation, the major risk factors were female sex, old age, and heart disease, with no significant relationship between drug dose and QTc duration.
Why the study?
Does clarithromycin increase the risk of QTc interval prolongation and torsades de pointes in patients with specific risk factors?
Systematic Review (n=21)
Does clarithromycin increase the risk of QTc interval prolongation and torsades de pointes in patients with specific risk factors?
Effect estimate: Pearson's r -0.086
p-value: p=0.744
Major risk factors for clarithromycin-induced QTc prolongation and torsades de pointes include female sex, older age, and underlying heart disease, highlighting the need for caution when prescribing to these populations.
Female sex, older age, and heart disease may associate with clarithromycin QTc prolongation in case reports; hypothesis-generating, needs prospective confirmation.
BACKGROUND: The manufacturers of clarithromycin sought a drug similar in efficacy to erythromycin but with a superior side-effect profile. They generally achieved this outcome, but postmarketing findings identified a series of reports linking clarithromycin to QTc interval prolongation and torsades de pointes (TdP) ultimately leading to a Black Box Warning. We sought to clarify risk factors associated with TdP among case reports of patients receiving clarithromycin linked to QTc interval prolongation and TdP. METHODS AND RESULTS: In a detailed literature search, we found 15 women, five men, and one boy meeting our search criteria. Among the 17 adults with reported clarithromycin dose and concurrent QTc interval measurement, we found no statistically significant relationship between clarithromycin dose and QTc interval duration. This did not change for the adults who developed TdP. Among adults, major risk factors were female sex (15), old age (11) and heart disease (17). A total of eight adult subjects had all three major risk factors and 14 of the 20 adults had at least two major risk factors. All adult subjects had at least two risk factors besides clarithromycin. A total of four of the 20 adults received cisapride and three received disopyramide. Three adults were considered to suffer from some aspect of the congenital long QT syndrome. CONCLUSIONS: We believe that the risk factor description for this drug should be refined to emphasize the major risk factors of (1) female sex, (2) old age and (3) heart disease.
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Vieweg et al. (2013) conducted a systematic review in Clarithromycin-induced QTc interval prolongation and torsades de pointes (n=21). Clarithromycin was evaluated on Relationship between clarithromycin dose and QTc interval duration (Pearson's r -0.086, p=0.744). Among 21 case reports of clarithromycin-associated QTc prolongation, the major risk factors were female sex, old age, and heart disease, with no significant relationship between drug dose and QTc duration.
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