Key result
Inpatient azithromycin use exposes ~76% of patients to multiple QTc-prolonging medications, linked to more abnormal ECGs.
Why the study?
Knowledge of inpatient prescribing patterns of azithromycin and associated risk factors for QTc prolongation is needed to recognize safe use following FDA warnings.
Are inpatient prescribing patterns of azithromycin aligned with safe use regarding patient risk factors for QTc prolongation and cardiac monitoring?
Cohort (n=100)
No
Are inpatient prescribing patterns of azithromycin aligned with safe use regarding patient risk factors for QTc prolongation and cardiac monitoring?
p-value: p=0.03
Azithromycin is frequently prescribed to hospitalized patients with multiple risk factors for QTc prolongation without adequate baseline ECG or telemetry monitoring, highlighting a gap in clinical vigilance.
High rates of multiple QTc-prolonging drugs with azithromycin warrant caution; leaves open whether targeted monitoring improves safety.
BACKGROUND: Azithromycin is used in the inpatient setting for a variety of conditions. In 2013, the US Food and Drug Administration released a warning regarding risk for corrected QT (QTc) prolongation and subsequent arrhythmias. Knowledge of inpatient prescribing patterns of QTc prolonging medications with respect to patient risk factors for adverse cardiovascular events can help recognize safe use in light of these new warnings. OBJECTIVE: To assess inpatient prescribing patterns, risk factors for QTc prolongation, and relationship between drug-drug interactions and cardiac monitoring in patients receiving azithromycin. DESIGN: Retrospective cohort study. PARTICIPANTS: One hundred inpatients ≥ 19 years of age were randomly selected from 1610 patient encounters between October 2012 and April 2013 who were administered at least 1 dose of azithromycin. MEASUREMENTS: Length of stay, reason for use, therapy duration, and concomitant medications were recorded. Telemetry charges and baseline electrocardiogram (ECG) prior to administration were assessed. RESULTS: Seventy-nine percent of azithromycin use was empiric. Sixty-five percent of patients received a baseline ECG prior to prescribing azithromycin, of which 60% had borderline or abnormal QTc prolongation. Seventy-six percent of patients were prescribed 2 or more QTc prolonging medications, of which there were more abnormal ECGs at baseline (P = 0.03) despite having telemetry ordered less than half of the time. CONCLUSIONS: In a cohort of hospitalized patients, azithromycin was prescribed despite risk factors for QTc prolongation and administration of interacting medications. Selection of azithromycin by providers appears to be independent from these risk factors, and education and vigilance to drug-drug interactions may be useful in limiting cardiac events with prescribing azithromycin.
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Lee et al. (2015) conducted a cohort in Inpatients receiving azithromycin (n=100). Azithromycin was evaluated on Inpatient prescribing patterns, risk factors for QTc prolongation, and relationship between drug-drug interactions and cardiac monitoring (p=0.03). Among 100 hospitalized patients receiving azithromycin, 76% were prescribed 2 or more QTc prolonging medications, which was associated with more abnormal baseline ECGs (P=0.03).
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