Skip to main content

Cardiac events after macrolides or fluoroquinolones in patients hospitalized for community-acquired pneumonia: post-hoc analysis of a cluster-randomized trial



Guidelines recommend macrolides and fluoroquinolones in patients hospitalized with community-acquired pneumonia (CAP), but their use has been associated with cardiac events. We quantified associations between macrolide and fluoroquinolone use and cardiac events in patients hospitalized with CAP in non-ICU wards.


This was a post-hoc analysis of a cluster-randomized trial as a cohort study; including patients with a working diagnosis of CAP admitted to non-ICU wards without a cardiac event on admission. We calculated cause-specific hazard ratio’s (HR’s) for effects of time-dependent macrolide and fluoroquinolone exposure as compared to beta-lactam monotherapy on cardiac events, defined as new or worsening heart failure, arrhythmia, or myocardial ischemia during hospitalization.


Cardiac events occurred in 146 (6.9%) of 2107 patients, including heart failure (n = 101, 4.8%), arrhythmia (n = 53, 2.5%), and myocardial ischemia (n = 14, 0.7%). These occurred in 11 of 207 (5.3%), 18 of 250 (7.2%), and 31 of 277 (11.2%) patients exposed to azithromycin, clarithromycin, and erythromycin for at least one day, and in 9 of 234 (3.8%), 5 of 194 (2.6%), and 23 of 566 (4.1%) exposed to ciprofloxacin, levofloxacin, and moxifloxacin, respectively. HR’s for erythromycin, compared to beta-lactam monotherapy, on any cardiac event and heart failure were 1.60 (95% CI 1.09;2.36) and 1.89 (95% CI 1.22;2.91), respectively. HR’s for levofloxacin and moxifloxacin, compared to beta-lactam monotherapy, on any cardiac event were 0.40 (95% CI 0.18;0.87)and 0.56 (95% CI 0.36;0.87), respectively. Findings remained consistent after adjustment for confounders and/or in a sensitivity analysis of radiologically confirmed CAP (n = 1604, 76.1%).


Among patients with CAP hospitalized to non-ICU wards, erythromycin use was associated with a 68% increased risk of hospital-acquired cardiac events, mainly heart failure. Levofloxacin and moxifloxacin were associated with a lower risk of heart failure. Although our study does not fully exclude confounding bias, findings remained largely unchanged in crude, adjusted, and sensitivity analyses. These findings may caution the use of erythromycin as empirical therapy in these patients.

Trial registration

The original trial was retrospectively registered under Identifier NCT01660204 on August 8th, 2012.

Peer Review reports


The use of beta-lactam, macrolide, and fluoroquinolone antibiotics, either alone or in combination, is recommended in international guidelines for empirical treatment of patients hospitalized with community-acquired pneumonia (CAP) [1,2,3]. However, the evidence-base for the addition of atypical coverage, especially macrolides, to beta-lactam antibiotics in patients with CAP admitted to non-ICU wards has been questioned [4, 5].

Results from observational studies have suggested that the use of macrolides (azithromycin, clarithromycin, and erythromycin) is associated with the occurrence of cardiovascular events, especially in patients with increased cardiovascular risk [6,7,8,9,10]. In a Danish study the relative risk for cardiac events after receiving azithromycin was not increased in the general population [11]. In US patients hospitalized with CAP, azithromycin was associated with a lower risk of all-cause mortality and any cardiac event, although the risk for myocardial infarction up to day 90 after admission did increase (5.1% vs 4.4%; odds ratio 1.17 95% confidence interval (CI) 1.08 to 1.25) with azithromycin use [7]. In another study, clarithromycin use during admission had an increased hazard ratio for cardiovascular events of 1.68 (95% CI 1.18 to 2.38) after one year follow-up among patients hospitalized with CAP [8]. Fluoroquinolones have been associated with an increased risk of arrhythmia in the general population, thus potentially increasing cardiovascular risk when treating CAP patients [10, 12].

Naturally, residual confounding cannot be excluded in these observational studies. However, the possibility of harm caused by macrolides or fluoroquinolones is likely to change the risk-benefit evaluation for atypical coverage in the empirical antibiotic treatment of CAP patients; particularly for macrolides in the context of limited evidence of benefit.

A recent Swiss randomized clinical trial showed a non-significant increase in 30-day mortality of 1.4% (p = 0.42) for beta-lactam monotherapy compared to combination therapy with a macrolide in hospitalized CAP patients; clinical stability criteria were met earlier in the combination group (4.5 days) vs beta-lactam monotherapy (5 days) [13]. This is in line with our own cluster-randomized trial, in which we demonstrated that a strategy of beta-lactam monotherapy was non-inferior to beta-lactams combined with a macrolide or fluoroquinolone monotherapy in terms of all-cause mortality for CAP patients admitted to non- intensive care unit (non-ICU) medical wards [14]. Here we present the results of a post-hoc analysis of these data on the association between specific macrolides and fluoroquinolones and the occurrence of cardiac events during hospitalization.


Study setting

We used data from the Community-Acquired Pneumonia: Study on the initial Treatment with Antibiotics of lower Respiratory Tract infections (CAP-START) trial, a cluster-randomized cross-over trial comparing three empiric antibiotic strategies for the treatment of CAP. These strategies consisted of empirical treatment with beta-lactam monotherapy, beta-lactam/macrolide combination therapy, or fluoroquinolone monotherapy. The trial was performed in seven Dutch teaching hospitals in the Netherlands from February 2011 until October 2013, during which the strategies rotated in 4-month periods. In this study all patients who were admitted with a working diagnosis of CAP to a non-ICU ward for at least 24 h were eligible for inclusion. Details about the methods and results of the trial have been previously published [14, 15].

For the current analysis we only included patients without evidence of a cardiac event at the time of hospital admission (i.e. in the emergency room).

Patients in the CAP-START trial gave written informed consent within 72 h for data collection. Data collection for the current analysis was approved by the ethics review board of the University Medical Center Utrecht with a waiver for additional informed consent.

Data collection

Demographic data, co-morbidities, clinical parameters, laboratory data, imaging results, and outcome data were collected from the medical records as part of the CAP-START trial by trained research nurses and were anonymously recorded in case record forms. During the course of the study, four investigators (DFP, CHvW: authors; LAM and KV: see acknowledgements) systematically collected additional data on the presence of cardiac and vascular comorbidities on admission, use of cardiovascular drugs, and the occurrence of cardiac events through chart review.

Cardiac events

All patients were screened for cardiac events by the same protocol, using pre-specified criteria for new or worsening cardiac events, as described in the literature [16]. We recorded the (co)occurrence of three types of cardiac events: new or worsening arrhythmia, heart failure, and myocardial ischemia. New or worsening arrhythmia was defined as documentation in medical records or electrocardiogram (ECG) of newly recognized atrial fibrillation, flutter, supraventricular tachycardia, ventricular tachycardia or ventricular fibrillation. New or worsening heart failure was defined as clinical signs of new heart failure noted in medical records by treating physicians and a chest X-ray or CT-scan demonstrating evidence of heart failure. New or worsening myocardial ischemia was defined as documentation in medical records of at least two of three criteria: chest pain, acute electrocardiographic changes (ST segment and T wave changes without formation of Q waves, new Q waves or a clear loss of R waves), and/or elevated cardiac enzymes (CPK-MB, troponin-T). Cardiac events were considered worsening when therapeutic action (e.g. increase of diuretic dosage) was needed for already present cardiac disease.

First, admission and discharge letters were examined; if these did not contain detailed information, medical files were reviewed. In case of doubt, findings were presented in a plenary session to obtain group consensus (DFP, CHvW, and JJO: authors; LAM and KV: see acknowledgements) on the occurrence of an event.

Antibiotic exposure

In the current analyses, macrolide and fluoroquinolone exposure were defined as time-varying exposures starting at the first day of antibiotic prescription until the end of admission. Azithromycin, clarithromycin, and erythromycin were the administered macrolides, and ciprofloxacin, ofloxacin, levofloxacin, and moxifloxacin were the administered fluoroquinolones. Ofloxacin was grouped with and referred to as ciprofloxacin because of the low number of ofloxacin users (n = 1).

Data analysis

Comparisons of baseline variables between groups were analyzed using Chi-squared tests, Fischer’s exact tests, One-way ANOVA’s, and Kruskal-Wallis tests, as appropriate.We assessed the association between macrolide and fluoroquinolone exposure and cardiac events using an extended Cox proportional hazards model with time-varying covariates for exposure to these antibiotics. Antibiotic exposure was modelled as present from the starting date of the antibiotic prescription until the end of admission, as previously mentioned. This ensured that cardiac events occurring before an antibiotic was started could not be attributed to this antibiotic. Crude models included all six antibiotics (azithromycin, clarithromycin, erythromycin, ciprofloxacin, levofloxacin, and moxifloxacin) as time-dependent covariates and the different cardiac events (any cardiac event, heart failure, and arrhythmia) as outcomes. The calculated hazard ratios for time-dependent exposure to macrolides or quinolones are in comparison to patients who did not receive macrolide or fluoroquinolone antibiotics at any time during admission i.e. who received beta-lactam monotherapy. Hospital discharge, transfer or death during admission led to right censoring in the analysis.

To calculate adjusted hazard ratios, we added the following confounders to our models: PSI score, number of other cardiac comorbidities, statin use, anti-platelet use, smoking history, positive pneumococcal urinary antigen test, and serum C-reactive protein. The linearity of continuous variables was checked visually by plotting martingale residuals.

To assess the effect of the domain definition of clinical versus radiologically proven CAP, we repeated all analyses in the subgroup of patients with radiologically proven CAP.

As an additional sensitivity analysis we performed a competing risk analysis, using three competing outcomes during admission: a new or worsening cardiac event, in-hospital death, or hospital discharge. Following competing risk methodology, we set out to calculate cause-specific hazard ratios and sub-distribution hazard ratios for our exposures of interest for each outcome [17]. The cause-specific hazard ratio is an estimate of the instantaneous risk of failing from a certain outcome, given that no outcome has yet occurred. Patients failing from competing outcomes are censored in these analyses. The cause-specific hazard ratio is equal to our extended Cox proportional hazards model mentioned above. The sub-distribution hazard ratio (SDHR) is an estimate of failing from an outcome of interest when competing outcomes have or have not occurred; thus it describes the ‘net effect’ a variable has on the cumulative incidence function [18].

Missing data were imputed by multiple imputation, except for data on respiratory rate, heart rate, and confusion at admission; the values for these variables were assumed to be normal when not explicitly documented in the medical records as they are frequently not recorded if within the normal range. P-values below .05 were considered statistically significant. All analyses were performed in R software, version 3.2.0 [19].

Role of the funding source

The original trial was supported by a grant from The Netherlands Organization for Health Research and Development. This source did not have a role in the design, conduct and reporting of the study.



We included 2107 patients who were admitted to non-ICU wards with a working diagnosis of CAP and without a cardiac event on admission (Fig. 1). Baseline characteristics and outcomes, stratified by receipt of any macrolide or fluoroquinolone during admission, are displayed in Table 1. The median length of stay was 6 days (IQR 4–9 days). There were 146 (6.9%) patients with new cardiac events and 66 (3.1%) died during hospital stay (Table 1, Fig. 1). The self-reported use of antibiotics before admission occurred in just over 30% of patients, with a median length of 3 days (IQR 1 to 6 days); 5.4% of patients reported the use of macrolides and 2.5% reported fluoroquinolones before admission (Table 1). The microbial etiology, stratified by the occurrence of any cardiac event, is presented in Table 2.

Fig. 1

Inclusion of patients and cardiac event rates per population. n/w new or worsening; BL beta-lactam; BLM beta-lactam combination with macrolide; FQL fluoroquinolone. The population for the primary analysis consisted of patients with a working diagnosis of CAP; the population for the sensitivity analysis consisted of the patients that developed radiological evidence of CAP during the first 48 h of admission. Crude new or worsening cardiac event rates are presented from the original trial arms for patients only receiving the cluster-randomized antibiotic strategy (per protocol) or who were non-adherent to the strategy

Table 1 Baseline patient characteristics and outcomes stratified by use of any macrolide or fluoroquinolone during admission
Table 2 Microbial aetiology of CAP stratified by cardiac event

Six hundred fifty patients (30.8%) received at least one day of macrolide treatment, and 954 (45.3%) received at least one day of fluoroquinolones during admission. Treatment mostly started on the first day of admission (Table 3). Erythromycin was predominantly (94.9%) administered intravenously, whereas other macrolides were only used orally (as they are not available for intravenous administration in the Netherlands). Azithromycin and clarithromycin were predominantly prescribed together with ceftriaxone or amoxicillin with or without clavulanic acid, while erythromycin was predominantly prescribed with penicillin or cefuroxime. Levofloxacin and moxifloxacin were usually prescribed as monotherapy, while ciprofloxacin was administered together with beta-lactams (Table 4). The proportion of patients receiving fluoroquinolones that started with oral treatment on admission ranged from 30.4% for ciprofloxacin to 67.5% for moxifloxacin (Table 3). Patients receiving macrolides, as compared to the overall cohort, were less likely to have cardiac comorbidities (29.7% vs 34.8%, p-value 0.122), a history of diabetes (12.8% vs 16.1%, p-value 0.088), and anticoagulants (13.2% vs 16.4%, p-value 0.188). There were no obvious differences in baseline characteristics such as co-morbidities or use of cardiovascular medication for patients receiving fluoroquinolones as compared to the overall cohort. The disease severity upon admission, as represented by the PSI score or CURB-65 score, was slightly, but significantly, lower in patients using any macrolide during admission (PSI score 82 vs 85, p-value 0.007). (Table 1). The 146 patients with cardiac events developed 101 (4.8%) first episodes of heart failure, 53 (2.5%) of arrhythmia, and 14 (0.7%) of myocardial ischemia.

Table 3 Starting days and crude event rates for different macrolides and fluoroquinolones
Table 4 Administered beta-lactams at admission for patients with or without different macrolides and fluoroquinolones

Macrolide exposure and cardiac events

In the patients receiving macrolides (n = 650), 207, 250, and 277 patients were exposed to azithromycin, clarithromycin, and erythromycin for at least one day, of which 11 (5.3%), 18 (7.2%), and 31 (11.2%) developed a cardiac event, respectively. The crude hazard ratio for a cardiac event after erythromycin use was 1.60 (95% CI 1.09; 2.36), and was 1.89 (95% CI 1.22; 2.91) for heart failure specifically. After adjustment for confounders hazard ratios were 1.68 (95% CI 1.07; 2.62) for any cardiac event and 2.08 (95% CI 1.25; 3.46) for heart failure. Adjusted hazard ratios for any cardiac event were 0.89 (95% CI 0.48; 1.67) and 1.06 (95% CI 0.61; 1.83) for azithromycin and clarithromycin, respectively. The numbers of cardiac events due to arrhythmia were too low for meaningful interpretations.(Table 5).

Table 5 Hazard ratio’s for macrolides during admission

Risk estimates were similar in the subgroup analysis of patients with radiologically confirmed CAP. (Table 5) In most macrolide-exposed patients that developed cardiac events (n = 45, 78.9%), macrolides were started on the day of admission. (Fig. 2).

Fig. 2

Timing of events in macrolide users with cardiac events. Figure depicts timing of events through admission for each patient which used a macrolide and experienced a cardiac event. Individual patients are on the y-axis and time in days of admission is on the x-axis. Cardiac events occurring before prescription of a macrolide were not attributed to the antibiotic in statistical models as antibiotics were modelled time-dependently

Time-dependent exposure to fluoroquinolones

In the fluoroquinolone group (n = 954), 234, 194, and 566 patients were exposed to ciprofloxacin, levofloxacin, and moxifloxacin, of which 9 (3.8%), 5 (2.6%), and 23 (4.1%) developed a cardiac event, respectively. (Table 3) Both levofloxacin and moxifloxacin were associated with lower risks of any cardiac event in crude analyses, with a hazard ratio of 0.40 (95% CI 0.18; 0.87) for levofloxacin and 0.56 (95% CI 0.36; 0.87) for moxifloxacin. Hazard ratios for heart failure specifically were 0.25 (95% CI 0.08; 0.80) for levofloxacin and 0.48 (95% CI 0.27; 0.84) for moxifloxacin. Associations for any cardiac event remained comparable after adjustment for confounders. The association between moxifloxacin and heart failure lost statistical significance after adjustment (Table 6). The numbers of cardiac events due to arrhythmia were too low for meaningful interpretations. Ciprofloxacin was not associated with a significantly changed hazard ratio for cardiac events. (Table 6).

Table 6 Hazard ratio’s for fluoroquinolones during admission

Competing risk analysis

The calculated sub-distribution hazard ratios from our competing risk analysis were comparable to the primary analysis for all associations. (Tables 7 & 8).

Table 7 Sub-distribution hazard ratio’s for macrolides during admission
Table 8 Sub-distribution hazard ratio’s for fluoroquinolones during admission


In this study of 2107 patients hospitalized with CAP to non-ICU wards, of which 146 (6.9%) developed a cardiac event during admission, erythromycin use was associated with a 68% higher hazard of cardiac events during hospital admission. This effect almost completely resulted from episodes of new or worsening heart failure. In contrast, levofloxacin and moxifloxacin were associated with a lower risk of cardiac events, mainly because of a lower risk of heart failure during admission.

This was a post-hoc analysis of a cluster-randomized cross-over study evaluating three antibiotic treatment strategies for patients hospitalized with CAP [14]. Baseline differences between patients who did or did not receive macrolides or fluoroquinolones during admission were small. Disease severity scores (i.e. PSI and CURB-65) at baseline were slightly lower in patient who received macrolides at any time during admission, although these differences do not seem clinically significant. If anything, classical cardiovascular risk factors were less prevalent in patients that received macrolides such as erythromycin. Hence, it is possible that physicians considered these antibiotics as potential risks for cardiac events in CAP patients, which may have attenuated the crude effect estimates in this analysis [20]. Consequently, the effect estimate between macrolides and cardiac events increased after adjustment for potential confounders. The findings were largely unchanged in patients with radiologically confirmed CAP. As associations between erythromycin use and competing outcomes such as in-hospital death or hospital discharge could change the interpretation of effect estimates, we performed a competing risk analysis which did not change our results [17]. Assessing associations with the original trial arms would have diluted effect sizes too much due to protocol non-adherence, while using subgroups (per-protocol and non-adherent populations) would have led to the same loss of randomization, but with smaller groups, as our current observational cohort study approach. We have tried to optimally correct for indication bias by using time-varying effects for antibiotic exposure and adjustment for confounders.

Several biological mechanisms could explain the observed associations between erythromycin, levofloxacin, and moxifloxacin use and cardiac events, which could be attributed almost completely to occurrences of heart failure. The proposed explanation for this is the volume and sodium load associated with intravenous administration of erythromycin, compared to regimens including either other macrolides (which are only orally available) or monotherapy with levofloxacin or moxifloxacin. The latter fluoroquinolones are also frequently given as oral treatment as the bioavailability of these antibiotics is known to be high [21]. When looking at the different beta-lactams co-administered with the three types of macrolides, erythromycin was most frequently prescribed together with penicillin. Still, we assume that different beta-lactams are not cardiotoxic and that the sodium and volume load does not differ too much between beta-lactams (Table 4). Unfortunately, we did not have data on fluid balances (intravenous fluid administration) for our patients to further strengthen this hypothesis. In addition, erythromycin is a pro-arrhythmic drug, metabolized through CYP3A4 thus frequently interacting with other drugs, which can prolong the QT-interval [22, 23]. Such effects would most likely occur shortly after start of treatment, and can lead to anything from self-limiting episodes of arrhythmia to severe arrhythmia or Torsade des Pointes, and consequently to demand ischemia and/or decompensated heart failure. Yet, the current analysis might have been underpowered to identify associations between use of any macrolide and occurrence of arrhythmias, as compared to previous analyses in out-patient populations [6, 9, 10, 12]. Finally, erythromycin might have a weaker anti-inflammatory effect than other macrolides, thus leading to more heart failure if this was predominantly driven by pro-inflammatory cytokines [24, 25].

Our findings do not support previous findings of increased risks for cardiac events when using azithromycin or clarithromycin in hospitalized CAP patients [7, 8]. In these studies all hospitalized patients with CAP, including those needing ICU-admission, were included with considerable longer follow-up periods for cardiac events, ranging from 90 days after discharge to one year after admission. In both studies, cardiac events mainly involved myocardial ischemia, which was a relatively infrequent event during hospitalization in our study. Moreover, fluoroquinolones have been associated with an increased risk for arrhythmia in the general population, [10, 12] as mentioned before, our study was probably underpowered to properly assess this association.

Our post-hoc analysis has limitations. The occurrence of cardiac events during the course of the study was based on medical chart review in an open-label trial. This methodology has a risk for misclassification and observational bias. Random misclassification might have led to general underreporting of cardiac events, which would affect the precision of the effect estimates. More importantly, observational bias might have occurred if treating physicians would be more alert to report cardiac events in medical charts of erythromycin users, which would have biased the results from null. As this could also apply to registration of cardiac events by researchers, we used pre-specified criteria for recording cardiac events to reduce this bias. Unfortunately, we were not able to systematically gather information on the etiology of heart failure, e.g. true left-ventricular heart failure as compared to sepsis-induced episodes, which would have helped in identifying causal mechanisms. Another limitation could be residual confounding by indication. Although patient groups were comparable in terms of disease severity at baseline (Table 1), clinical stability during the first two to four days of admission is an important prognostic factor for adverse outcomes in CAP [26, 27]. Therefore, clinical deterioration during the first days of admission might have stimulated treating physicians to add macrolides or fluoroquinolones, creating confounding by indication. Since changes in disease severity during these first days of admission were not determined, this could not be accounted for. Still, the majority of erythromycin users with a cardiac event (n = 25, 80.6%) started with erythromycin on the day of admission. (Fig. 2) Lastly, we did not have data on concomitant use of drugs interacting with macrolides or fluoroquinolones, nor did we determine specific causes of death. The latter could have increased the efficacy of end-point detection, and might have allowed discrimination between sudden cardiac death, cardiovascular death, and death due to other causes, although cause-of-death statements are not always interpreted unequivocally [28].


In this post-hoc analysis, intravenous erythromycin use, but not oral azithromycin or clarithromycin use, increases the risk for cardiac events, especially heart failure, in patients hospitalized with CAP to non-ICU wards. Volume overload associated with intravenous administration of erythromycin in elderly could be one of the mechanisms for heart failure. Inversely, this might explain why levofloxacin and moxifloxacin were associated with a lower risk of cardiac events, mainly heart failure, during admission. Although our study does not fully exclude confounding bias, findings remained largely unchanged in crude, adjusted, and sensitivity analyses. Together with the absence of survival benefit these findings may caution the use of intravenous erythromycin for empirical treatment of CAP patients admitted to non-ICU wards.



Community-acquired pneumonia




Intensive Care Unit


  1. 1.

    Mandell LA, Wunderink RG, Anzueto A, Bartlett JG, Campbell GD, Dean NC, et al. Infectious Diseases Society of America/American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults. Clin Infect Dis. 2007;44(Supplement 2):S27–72 Available from: [cited 10 Jul 2014].

    CAS  Article  Google Scholar 

  2. 2.

    Lim WS, Baudouin SV, George RC, Hill AT, Jamieson C, Le Jeune I, et al. BTS guidelines for the management of community acquired pneumonia in adults: update 2009. Thorax. 2009;64(Suppl 3):iii1–iii55.

    Article  Google Scholar 

  3. 3.

    Wiersinga WJ, Bonten MJ, Boersma WG, Jonkers RE, Aleva RM, Kullberg BJ, et al. SWAB/NVALT (dutch working party on antibiotic policy and dutch association of chest physicians) guidelines on the management of community-acquired pneumonia in adults. Neth J Med. 2012;70(2):90–101 Available from:

    CAS  PubMed  Google Scholar 

  4. 4.

    Oosterheert JJ, Bonten MJM, Hak E, Schneider MME, Hoepelman IM. How good is the evidence for the recommended empirical antimicrobial treatment of patients hospitalized because of community-acquired pneumonia? A systematic review. J Antimicrob Chemother. 2003;52(4):555–63. Available from: [cited 23 Nov 2015].

  5. 5.

    File TM, Marrie TJ. Does empiric therapy for atypical pathogens improve outcomes for patients with CAP? Infect Dis Clin North Am. 2013;27(1):99–114 Available from: [cited 24 Nov 2015].

    Article  Google Scholar 

  6. 6.

    Ray WA, Murray KT, Hall K, Arbogast PG, Stein CM. Azithromycin and the risk of cardiovascular death. N Engl J Med. 2012;366(20):1881–90 Available from:

    CAS  Article  Google Scholar 

  7. 7.

    Mortensen EM, Halm EA, Pugh MJ, Copeland LA, Metersky M, Fine MJ, et al. Association of azithromycin with mortality and cardiovascular events among older patients hospitalized with pneumonia. JAMA. 2014;311(21):2199–208 Available from:

    Article  Google Scholar 

  8. 8.

    Schembri S, Williamson PA, Short PM, Singanayagam A, Akram A, Taylor J, et al. Cardiovascular events after clarithromycin use in lower respiratory tract infections: analysis of two prospective cohort studies. BMJ. 2013;346:f1235 Available from: [cited 14 Sep 2015].

    Article  Google Scholar 

  9. 9.

    Ray WA, Murray KT, Meredith S, Narasimhulu SS, Hall K, Stein CM. Oral erythromycin and the risk of sudden death from cardiac causes. N Engl J Med. 2004;351(11):1089–96 Available from: [cited 14 Sep 2015].

    CAS  Article  Google Scholar 

  10. 10.

    Chou H-W, Wang J-L, Chang C-H, Lai C-L, Lai M-S, Chan KA. Risks of Cardiac Arrhythmia and Mortality Among Patients Using New-Generation Macrolides, Fluoroquinolones, and β-Lactam/β-Lactamase Inhibitors: A Taiwanese Nationwide Study. Clin Infect Dis. 2015;60(4):566–77 Available from: [cited 29 Sep 2015].

    CAS  Article  Google Scholar 

  11. 11.

    Svanström H, Pasternak B, Hviid A. Use of azithromycin and death from cardiovascular causes. N Engl J Med. 2013;368(18):1704–12 Available from:

    Article  Google Scholar 

  12. 12.

    Lapi F, Wilchesky M, Kezouh A, Benisty JI, Ernst P, Suissa S. Fluoroquinolones and the risk of serious arrhythmia: a population-based study. Clin Infect Dis. 2012;55(11):1457–65 Available from: [cited 29 Sep 2015].

    CAS  Article  Google Scholar 

  13. 13.

    Garin N, Genné D, Carballo S, Chuard C, Eich G, Hugli O, et al. β-Lactam monotherapy vs β-lactam-macrolide combination treatment in moderately severe community-acquired pneumonia: a randomized noninferiority trial. JAMA Intern Med. 2014;174(12):1894–901 Available from: [cited 27 Aug 2015].

    Article  Google Scholar 

  14. 14.

    Postma DF, Van Werkhoven CH, Van Elden LJR, Thijsen SFT, Hoepelman AIM, Kluytmans JAJW, et al. Antibiotic treatment strategies for community-acquired pneumonia in adults. N Engl J Med. 2015;372(14):1312-23.

  15. 15.

    van Werkhoven CH, Postma DF, Oosterheert JJ, Bonten MJM. Antibiotic treatment of moderate-severe community-acquired pneumonia: design and rationale of a multicentre cluster-randomised cross-over trial. Neth J Med. 2014;72(3):170–8 Available from: [cited 2015 Mar 13].

    PubMed  Google Scholar 

  16. 16.

    Corrales-Medina VF, Musher DM, Wells GA, Chirinos JA, Chen L, Fine MJ. Cardiac complications in patients with community-acquired pneumonia: incidence, timing, risk factors, and association with short-term mortality. Circulation. 2012;125(6):773–81 Available from: [cited 1 Mar 2015].

    Article  Google Scholar 

  17. 17.

    Andersen PK, Geskus RB. De witte T, putter H. competing risks in epidemiology: possibilities and pitfalls. Int J Epidemiol. 2012;41(3):861–70.

    Article  Google Scholar 

  18. 18.

    Fine JP, Gray RJ. A proportional hazards model for the subdistribution of a competing risk. J Am Stat Assoc. 1999;94:496–509 Available from:

  19. 19.

    Team RDC. R: a language and environment for statistical computing, vol. 1: R Foundation for Statistical Computing; 2011. Available from:

  20. 20.

    Abo-Salem E, Fowler JC, Attari M, Cox CD, Perez-Verdia A, Panikkath R, et al. Antibiotic-induced cardiac arrhythmias. Cardiovasc Ther. 2014;32(1):19–25 Available from: [cited 30 Sep 2015].

    CAS  Article  Google Scholar 

  21. 21.

    Zhanel GG, Fontaine S, Adam H, Schurek K, Mayer M, Noreddin AM, et al. A Review of New Fluoroquinolones : Focus on their Use in Respiratory Tract Infections. Treat Respir Med. 2006;5(1176–3450 (Print)):437–65.

    CAS  Article  Google Scholar 

  22. 22.

    Goldstein EJC, Owens RC, Nolin TD. Antimicrobial-Associated QT Interval Prolongation: Pointes of Interest. Clin Infect Dis. 2006;43(12):1603–11 Available from: [cited 29 Sep 2015].

    Article  Google Scholar 

  23. 23.

    Guo D, Cai Y, Chai D, Liang B, Bai N, Wang R. The cardiotoxicity of macrolides: a systematic review. Pharmazie. 2010;65(9):631–40 Available from: [cited 29 Sep 2015].

    CAS  PubMed  Google Scholar 

  24. 24.

    Amsden GW. Anti-inflammatory effects of macrolides—an underappreciated benefit in the treatment of community-acquired respiratory tract infections and chronic inflammatory pulmonary conditions? J Antimicrob Chemother. 2005;55(1):10–21 Epub 2004 Dec 8.

    CAS  Article  Google Scholar 

  25. 25.

    Ersoy B, Aktan B, Kilic K, Sakat MS, Sipal S. The anti-inflammatory effects of erythromycin, clarithromycin, azithromycin and roxithromycin on histamine-induced otitis media with effusion in Guinea pigs. J Laryngol Otol. 2018;132(7):579–83.

    CAS  Article  Google Scholar 

  26. 26.

    Halm EA, Fine MJ, Marrie TJ, Coley CM, Kapoor WN, Obrosky DS, et al. Time to clinical stability in patients hospitalized with community-acquired pneumonia: implications for practice guidelines. JAMA. 1998;279(18):1452–7 Available from: [cited 29 Sep 2015].

    CAS  Article  Google Scholar 

  27. 27.

    Takada K, Matsumoto S, Kojima E, Iwata S, Ninomiya K, Tanaka K, et al. Predictors and impact of time to clinical stability in community-acquired pneumococcal pneumonia. Respir Med. 2014;108(5):806–12 Available from: [cited 29 Sep 2015].

    Article  Google Scholar 

  28. 28.

    Smith Sehdev AE, Hutchins GM. Problems with proper completion and accuracy of the cause-of-death statement. Arch Intern Med. 2001;161(2):277–84 Available from: [cited 29 Sep 2015].

    CAS  Article  Google Scholar 

Download references


We would like to thank all members of the CAP-START study group for securing the conduct of the study. Additional thanks go to L.A. Michielsen and K. Verbon for their help in data collection and preparation.


CAP-START was supported by a financial grant from The Netherlands Organization for Health Research and Development (ZonMw, Health care efficiency research, project id: 171202002). This organization was not involved in the design of the study or the collection, analysis, and interpretation of data, nor in writing the manuscript.

Availability of data and materials

An anonymized dataset and full statistical code are available at reasonable request from the corresponding author.

Author information




All authors have read and approved the manuscript and have agreed to be accountable for all aspects of the work for appropriate portions of the content. DFP participated in the design and conduct of the CAP-START study and the current analysis, performed the current analysis, and wrote the current manuscript. CS participated in the design of the current analysis and performed parts of the analysis, and participated in writing the manuscript. CHvW participated in the design and conduct of the CAP-START study, and revised the current manuscript. LJRvE participated in the design and conduct of the current analysis and revised the current manuscript. JJO participated in the design and supervision of the CAP-START study, and revised the current manuscript. MJMB participated in the design and supervision of the CAP-START study, and supervised writing of the current manuscript.

Corresponding author

Correspondence to Douwe F. Postma.

Ethics declarations

Ethics approval and consent to participate

Data collection for the current analysis was approved by the ethics review board of the University Medical Center Utrecht with a waiver for additional informed consent.

Consent for publication

Not applicable

Competing interests

CHvW reports consultation fees, presentation fees, and thesis print support from Pfizer. MJMB reports research grants and an educations grant from Pfizer, paid to institution. Other authors have nothing to disclose.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Postma, D.F., Spitoni, C., van Werkhoven, C.H. et al. Cardiac events after macrolides or fluoroquinolones in patients hospitalized for community-acquired pneumonia: post-hoc analysis of a cluster-randomized trial. BMC Infect Dis 19, 17 (2019).

Download citation


  • Community-acquired pneumonia
  • Antibiotics
  • Macrolides
  • Fluoroquinolones
  • Cardiac events
  • Complications