» Articles » PMID: 22591294

Azithromycin and the Risk of Cardiovascular Death

Overview
Journal N Engl J Med
Specialty General Medicine
Date 2012 May 18
PMID 22591294
Citations 349
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Although several macrolide antibiotics are proarrhythmic and associated with an increased risk of sudden cardiac death, azithromycin is thought to have minimal cardiotoxicity. However, published reports of arrhythmias suggest that azithromycin may increase the risk of cardiovascular death.

Methods: We studied a Tennessee Medicaid cohort designed to detect an increased risk of death related to short-term cardiac effects of medication, excluding patients with serious noncardiovascular illness and person-time during and shortly after hospitalization. The cohort included patients who took azithromycin (347,795 prescriptions), propensity-score-matched persons who took no antibiotics (1,391,180 control periods), and patients who took amoxicillin (1,348,672 prescriptions), ciprofloxacin (264,626 prescriptions), or levofloxacin (193,906 prescriptions).

Results: During 5 days of therapy, patients taking azithromycin, as compared with those who took no antibiotics, had an increased risk of cardiovascular death (hazard ratio, 2.88; 95% confidence interval [CI], 1.79 to 4.63; P<0.001) and death from any cause (hazard ratio, 1.85; 95% CI, 1.25 to 2.75; P=0.002). Patients who took amoxicillin had no increase in the risk of death during this period. Relative to amoxicillin, azithromycin was associated with an increased risk of cardiovascular death (hazard ratio, 2.49; 95% CI, 1.38 to 4.50; P=0.002) and death from any cause (hazard ratio, 2.02; 95% CI, 1.24 to 3.30; P=0.005), with an estimated 47 additional cardiovascular deaths per 1 million courses; patients in the highest decile of risk for cardiovascular disease had an estimated 245 additional cardiovascular deaths per 1 million courses. The risk of cardiovascular death was significantly greater with azithromycin than with ciprofloxacin but did not differ significantly from that with levofloxacin.

Conclusions: During 5 days of azithromycin therapy, there was a small absolute increase in cardiovascular deaths, which was most pronounced among patients with a high baseline risk of cardiovascular disease. (Funded by the National Heart, Lung, and Blood Institute and the Agency for Healthcare Quality and Research Centers for Education and Research on Therapeutics.).

Citing Articles

Cardiovascular Toxicity Profile of Macrolides Investigated Using VigiBase Data: A Pharmacovigilance Study.

Kono Y, Niimura T, Goda M, Ueta S, Kawada K, Miyata K Cardiovasc Toxicol. 2025; 25(3):498-506.

PMID: 39971867 PMC: 11885371. DOI: 10.1007/s12012-025-09970-w.


Pulmonary Delivery of Antibiotics to the Lungs: Current State and Future Prospects.

Dallal Bashi Y, Mairs R, Murtadha R, Kett V Pharmaceutics. 2025; 17(1).

PMID: 39861758 PMC: 11768398. DOI: 10.3390/pharmaceutics17010111.


The role of empiric atypical antibiotic coverage in non-severe community-acquired pneumonia.

Hartlage W, Imlay H, Spivak E Antimicrob Steward Healthc Epidemiol. 2025; 4(1):e214.

PMID: 39758879 PMC: 11696604. DOI: 10.1017/ash.2024.453.


Assessment of azithromycin-induced toxicity in : Effects on morphology, behavior, and lipid metabolism.

Kalugendo E, Nazir A, Agarwal R Toxicol Rep. 2024; 13:101832.

PMID: 39717856 PMC: 11664063. DOI: 10.1016/j.toxrep.2024.101832.


Emerging Anti-Inflammatory COPD Treatments: Potential Cardiovascular Impacts.

Cazzola M, Calzetta L, Rogliani P, Matera M Int J Chron Obstruct Pulmon Dis. 2024; 19:2481-2495.

PMID: 39606712 PMC: 11600434. DOI: 10.2147/COPD.S498255.


References
1.
Landry J, Smyer M, Tubman J, Lago D, Roberts J, Simonson W . Validation of two methods of data collection of self-reported medicine use among the elderly. Gerontologist. 1988; 28(5):672-6. DOI: 10.1093/geront/28.5.672. View

2.
Sturmer T, Schneeweiss S, Brookhart M, Rothman K, Avorn J, Glynn R . Analytic strategies to adjust confounding using exposure propensity scores and disease risk scores: nonsteroidal antiinflammatory drugs and short-term mortality in the elderly. Am J Epidemiol. 2005; 161(9):891-8. PMC: 1407370. DOI: 10.1093/aje/kwi106. View

3.
De Ponti F, Poluzzi E, Montanaro N . QT-interval prolongation by non-cardiac drugs: lessons to be learned from recent experience. Eur J Clin Pharmacol. 2000; 56(1):1-18. DOI: 10.1007/s002280050714. View

4.
Poluzzi E, Raschi E, Moretti U, De Ponti F . Drug-induced torsades de pointes: data mining of the public version of the FDA Adverse Event Reporting System (AERS). Pharmacoepidemiol Drug Saf. 2009; 18(6):512-8. DOI: 10.1002/pds.1746. View

5.
Matsunaga N, Oki Y, Prigollini A . A case of QT-interval prolongation precipitated by azithromycin. N Z Med J. 2003; 116(1185):U666. View