Journal List > J Korean Med Sci > v.30(10) > 1022748

Park, Oh, Kim, Song, Yoo, Shim, Lee, Lee, Yun, Kim, Kim, Lee, Kim, Cha, Lee, Seo, and Jung: Role of Atypical Pathogens and the Antibiotic Prescription Pattern in Acute Bronchitis: A Multicenter Study in Korea

Abstract

The role of atypical bacteria and the effect of antibiotic treatments in acute bronchitis are still not clear. This study was conducted at 22 hospitals (17 primary care clinics and 5 university hospitals) in Korea. Outpatients (aged ≥ 18 yr) who had an acute illness with a new cough and sputum (≤ 30 days) were enrolled in 2013. Multiplex real-time polymerase chain reaction (RT-PCR) was used to detect five atypical bacteria. A total of 435 patients were diagnosed as having acute bronchitis (vs. probable pneumonia, n = 75), and 1.8% (n = 8) were positive for atypical pathogens (Bordetella pertussis, n = 3; B. parapertussis, n = 0; Mycoplasma pneumoniae, n = 1; Chlamydophila pneumoniae, n = 3; Legionella pneumophila, n = 1). Among clinical symptoms and signs, only post-tussive vomiting was more frequent in patients with atypical pathogens than those without (P = 0.024). In all, 72.2% of the enrolled patients received antibiotic treatment at their first visits, and β-lactams (29.4%) and quinolones (20.5%) were the most commonly prescribed agents. In conclusion, our study demonstrates that the incidence of atypical pathogens is low in patients with acute bronchitis, and the rate of antibiotic prescriptions is high.

Graphical Abstract

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INTRODUCTION

Acute bronchitis is one of the most common illnesses in outpatient settings, and its annual incidence is about 5% among adults (1). Currently, viruses are the most common cause, and the illness is usually self-limited (2). However, the etiology is still poorly established and many patients are treated with antibiotics (3).
To date, although bacterial pathogens commonly implicated in community-acquired pneumonia (CAP) have been isolated from patients with acute bronchitis, there is no strong evidence to support their role in the pathogenesis of acute bronchitis (123). However, several atypical organisms including Bordetella pertussis have received considerable attention as important pathogens for acute bronchitis (45). In particular, Mycoplasma pneumoniae and Chlamydophila pneumoniae are associated with prolonged cough illness and outbreaks in young adults (67). Therefore, if such patients are identified and treated early, we might be able to expect some beneficial effect.
Evidence of beneficial effects of antibiotic treatments in acute bronchitis is still limited. A systematic review demonstrated that antibiotics did not influence the natural history of the symptoms, and any minor benefits were offset by their side effects (8). Macfarlane et al. (1) showed that antibiotic treatments or the presence of bacterial pathogens were not related to revisits to clinics. However, on contrary, several authors demonstrated that bacterial pathogens were more frequently isolated than viruses, and in clinical practice, more than 60%-70% of patients with acute bronchitis receive antibiotics (9).
To investigate the incidence of atypical pathogens in acute bronchitis, we performed a prospective, multi-center study in an outpatient setting. We used multiplex real-time polymerase chain reaction (RT-PCR), which facilitates the rapid and simultaneous detection of several pathogens, especially strains that are difficult to culture using standard methods (10). We also investigated the pattern of antibiotic prescription by participating physicians.

MATERIALS AND METHODS

Study population

This study was conducted during two periods (March-June and October-November 2013) at 22 hospitals (17 primary care clinics and 5 university hospitals) in Korea. Inclusion criteria were outpatients aged ≥18 yr who were previously healthy (or in a well-controlled state if the patient had a chronic lung disease), had an acute illness with a new cough and sputum, and had a duration of illness of 30 days or less. Exclusion criteria included a history of antibiotic treatment within 5 days before visiting the hospitals, a symptom duration of >30 days, a fever (>38.0℃), an acute exacerbation of chronic airway disease (e.g., bronchial asthma, chronic obstructive lung disease, or bronchiectasis), immunocompromised status (e.g., AIDS, leukemia, aplastic anemia, organ transplant, autoimmune diseases, or chemotherapy), pneumonia proven by chest radiography, or a confirmed alternative cause for cough illness (e.g., allergic rhinitis, acute pharyngitis, sinusitis, or gastro-esophageal reflux). When a patient had a focal sign (i.e., crackle) or was suspected to have pneumonia by the physician, the patient was defined as having "probable pneumonia" and was not included in the main analyses.

Data collection

Clinical information was collected by the participating investigators at outpatient departments. Data on age, sex, chronic respiratory diseases, comorbidities, history of smoking, cough (and sputum) duration, and other respiratory symptoms were collected. In addition, we investigated the nature of the cough (i.e., paroxysms, inspiratory whooping, or post-tussive vomiting) and the characteristics of sputum. We conducted multiplex RT-PCR tests for five atypical pathogens (M. pneumoniae, C. pneumoniae, Legionella pneumophila, B. pertussis, and B. parapertussis). Sputum specimens were collected and transferred at room temperature to a central laboratory (Seegene Medical Institute) and plated on culture media within 24 hr. In addition, we investigated the antibiotic prescriptions (i.e., beta-lactams, quinolones, macrolides, and others) by the participating physicians at the outpatient departments. The selection and prescription of antibiotics were at the physicians' discretion.

RT-PCR for atypical organisms

An Anyplex™ II RB5 detection kit was used to detect the five bacteria (1011). The assay was performed according to the manufacturer's instructions. PCR was performed with a CFX96™ real-time PCR detection system (Bio-Rad, Hercules, CA, USA) under the following conditions: denaturation at 95℃ for 15 min; 50 cycles at 95℃ for 30 sec; 60℃ for 1 min; and 72℃ for 30 sec. After reaction, Catcher Melting Temperature Analysis (CMTA) was performed at three PCR cyclic points (30, 40, and 50 cycles) by cooling the reaction mixture to 55℃, holding at 55℃ for 30 sec, and heating from 55℃ to 85℃. The fluorescence was measured continuously during the temperature rise. The melting peaks were derived from the initial fluorescence (F) versus temperature (T) curves by plotting the negative derivative of fluorescence over temperature versus temperature (-dF/dT vs. T). Table 1 shows the melting temperature for each target. The melting-temperature analysis was done by Seegene viewer software (11).

Data analyses

The primary outcomes were the prevalence of atypical organisms isolated from adults with acute bronchitis. Secondary outcomes were as follows: significant factors associated with positive results for atypical organisms, the frequency of antibiotic use, and factors associated with antibiotic prescription.
Data are expressed as means±standard deviations (or medians and interquartile ranges [IQRs]) for continuous variables and as percentages for categorical variables, unless otherwise indicated. Student's t-test was performed for continuous data, whereas chi-square or Fisher's exact tests were used for categorical data. A multivariate analysis by logistic regression was performed with covariates significant in univariate analysis. All reported P values were two-sided, and P<0.05 indicated statistical significance. All analyses were conducted using SPSS statistical software (IBM SPSS Statistics version 21, Standard for Medical Network).

Ethics statement

All patients provided written informed consent, and the protocol of this study was approved by the institutional review board of Hallym University Sacred Heart Hospital (IRB No. 2013-S009) and each participating hospital. The authors assert that all procedures contributing to this work comply with the Helsinki Declaration of 1975 and its later amendments.

RESULTS

Demographics and clinical symptoms

Among the 536 patients that were initially enrolled, 26 were excluded due to incomplete clinical data, and 435 were diagnosed as having acute bronchitis (vs. probable pneumonia, n=75; Fig. 1). The mean age of the patients with acute bronchitis was 48.6±16.5 yr, and 56.1% were female (Table 2). Median cough and sputum durations were 7 days (3-7 days) and 5 days (3-7 days), respectively, and among the accompanying symptoms, rhinorrhea (41.4%), and sore throat (44.1%) were the most common (Fig. 2). Hypertension was the most common co-morbidity reported, and 14.0% of patients had a chronic airway disease (i.e., bronchial asthma or chronic obstructive pulmonary disease).

Microbiologic data and clinical characteristics

Among 435 patients with acute bronchitis, a total of 8 (1.8%) were PCR positive, and of these, C. pneumoniae (3/435) and B. pertussis (3/435) were the most common pathogens (Table 3). There were no significant differences in most symptoms and signs between patients with and without atypical organisms (data not shown). Only post-tussive vomiting was more frequent in patients with a positive PCR result than those with negative results (P=0.024). Among 75 patients with probable pneumonia, only 1 patient was positive for C. pneumoniae.

Antibiotic prescription

Antibiotic agents were prescribed in 72.2% of patients with acute bronchitis (vs. 100.0% in those with probable pneumonia) at their first visits to outpatient departments. Among the antibiotics prescribed, β-lactams were the most common (29.4%), and the proportion of patients who received quinolones (20.5%) was similar to that in those with probable pneumonia (Fig. 3).
Patients with rhinorrhea, headache, chest pain, myalgia, a shorter duration of cough and/or sputum, inspiratory whooping, dark sputum, or rhonchi were more likely to receive antibiotics (Table 4); however, there were no significant differences in the prescription rate between primary care clinics and university hospitals. In multivariate analysis (Hosmer-Lemeshow test, χ2=7.128 and P=0.523), rhinorrhea, myalgia, inspiratory whooping, dark sputum, and rhonchi were independent factors for antibiotic prescription.

DISCUSSION

Our study revealed several interesting findings. First, the incidence of atypical pathogens was 1.8% in patients with acute bronchitis who presented to outpatient clinics. Second, only post-tussive vomiting was associated with atypical infection. Finally, more than 70% of patients received antibiotics at their first visits.
To date, the etiology of acute bronchitis (or acute lower respiratory tract illness) has not been well established, either due to the inadequate definition or the low microbiological yield (i.e., 20%-40%) (12). However, approximately 90% of cases of acute bronchitis are caused by viruses (e.g., rhinovirus, influenza, and parainfluenza viruses), and routine culture or serologic tests are not recommended in clinical practice (31314). Although there is no definite evidence suggesting that bacterial pathogens cause acute bronchitis in healthy adults, several atypical pathogens have received attention as causes of acute bronchitis in previous studies (215).
Atypical pathogens are a frequent cause of CAP, accounting for 6%-20% in ambulatory patients and ~40% in hospitalized patients (16). In particular, children and young adults are more likely to be infected by C. pneumoniae and M. pneumoniae (17), and elderly patients with cardiopulmonary comorbidities are at high risk for severe CAP caused by C. pneumoniae (18). L. pneumophila is also an important cause of severe CAP, with an incidence of 1.9%-7.9% (19). However, the incidence of these atypical organisms is much lower in patients with acute bronchitis. Some authors have also insisted that atypical pathogens have no role in acute bronchitis (3). When considering the results of previous studies conducted since 1990 (Table 5), although several studies showed an incidence of >10.0% for both M. pneumoniae and C. pneumoniae, other studies with only PCR tests showed a lower incidence for atypical pathogens in acute bronchitis (M. pneumoniae, 0.8%-4.1%; C. pneumoniae, 0.0%-2.3%). With regard to L. pneumophila, Lieberman et al. (2021) showed an incidence of 6.8% and 10.9%, respectively, in their two studies where serological tests were used, but other studies demonstrated an incidence of 0% (3142223). These low incidence rates of atypical pathogens are not much different from those of our study. Therefore, we can say that there is still a lack of evidence supporting the role of atypical pathogens in acute bronchitis.
Pertussis is a well-known infectious disease with a high attack rate. Although it is a vaccine-preventable disease, its incidence has increased substantially in adults since 1980, and a large outbreak occurred in the United States in 2012 (24). However, in Korea, there have been three prospective studies performed on adults in outpatient settings (42526). Among them, two multi-center studies, which used a PCR method, showed incidence rates of 0.5% and 6.9%, respectively. However, the rate can vary by the length of cough illness. Among adults with subacute or chronic cough illnesses (a duration of ≥3 weeks) (27), the incidence rate is 26%-31%, but among adults with acute cough illnesses, it is 7% (28). In the present study, most patients had an acute cough illness (cough duration, 3-7 days) but the incidence (i.e., 0.7%) might have been underestimated because we did not perform other methods of sampling. Nonetheless, physicians should acknowledge that pertussis can still be an important cause of acute bronchitis in non-epidemic settings.
With regard to clinical symptoms and signs, only post-tussive vomiting was associated with PCR positivity for atypical bacteria in the present study. Although this result can be partly due to patients with B. pertussis, it should be further clarified in future studies. However, atypical pathogens are often associated with persistent cough, headache, and pharyngitis (29), and C. pneumoniae infection is associated with wheezing or asthmatic bronchitis. Therefore, taking into consideration these clinical findings together might be helpful for suspecting atypical origin.
Currently, antibiotic treatment is not recommended for routine use in patients with acute bronchitis (2). A randomized controlled study and two meta-analyses demonstrated no significant beneficial effects of antibiotics in patients with acute bronchitis (303132). However, despite these results, more than 60%-70% of patients receive antibiotics at outpatient clinics (9). This may be partly because of patient expectations. A survey by Wilson et al. (33) showed that more than half of patients believed that antibiotic treatments were effective for upper respiratory infections. In the present study, although all of the physicians were aware of the current guidelines, 72.2% of patients received antibiotics. Among the antibiotics used, beta-lactams were the most frequently prescribed, and 20.5% of patients received quinolones, which are mostly broad-spectrum agents. As many physicians know, inappropriate antibiotic use can be associated with an increased risk of adverse effects, including Clostridium difficile infection and increasing antibiotic resistance (34). In contrast, interestingly, several studies have reported results in favor of the role of bacterial pathogens. Some authors demonstrated epithelial cell injury by atypical pathogens (15), and other authors showed an increasing hospitalization rate with a decreasing antibiotic prescription rate (35). In particular, Macfarlane et al. (123) demonstrated a higher incidence of bacterial pathogens than viruses, which contrasts with the results of other studies. Nonetheless, the evidences supporting antibiotic use are still limited and the current guidelines recommend against it in acute bronchitis. Our study also is in concordance with the current guidelines. Therefore, physicians need to refrain from injudicious use of antibiotics in patients with acute bronchitis without any evidence of pneumonia.
The present study has several limitations. First, we did not investigate viruses and other bacterial pathogens. This can limit the scope of our results. Second, there is a possibility that some patients with upper respiratory infections might have been included. Third, we did not use nasopharyngeal or throat swabs for sampling or serological or culture tests for identification. This could be associated with the low incidence of atypical pathogens. Fourth, although we used multiplex RT-PCR, which has high sensitivity, there is still no standardized PCR method for the detection of atypical pathogens. Finally, follow-up data were not available in the present study, which could have provided interesting results about the effectiveness of antibiotics. However, this is one of the few studies on the etiology of acute bronchitis in Korea, and our study was a prospective, multi-center one. In particular, we also found that many physicians are prescribing antibiotics for cough illnesses. This could be valuable information for future measures for antibiotic use.
In conclusion, our study demonstrates that the incidence of atypical pathogens is low in patients with acute bronchitis in an outpatient setting, and the frequency of post-tussive vomiting is high in patients with atypical infection. Importantly, the antibiotic prescription rate for acute bronchitis is still high. Therefore, physicians should take into account the low incidence of atypical pathogens and the currently high prescription rate of antibiotics in acute bronchitis.

Figures and Tables

Fig. 1

Flow diagram of enrolled patients.

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Fig. 2

Frequency of clinical symptoms among patients with acute bronchitis (n = 435).

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Fig. 3

Freuqency of antibiotic prescriptions by participating physicians.

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Table 1

Melting temperatures for each target

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Fluorescence Target Tm*
FAM Mycoplasma pneumoniae 65℃
Legionella pneumophila 74℃
HEX Bordetella pertussis 64℃
Bordetella parapertussis 73.5℃
Cal Red 610 Chlamydophila pneumoniae 65℃
Quasar 670 Internal control 64.5℃

*Melting temperature.

Table 2

Baseline characteristics of the participants (n = 435)

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Characteristics Values
Age (yr)* 48.6 ± 16.5
Females/males 244/191
Smoker, never/ex-/current 305/59/71
Diabetes 40 (9.2%)
Hypertension 80 (18.4%)
Bronchial asthma 41 (9.4%)
COPD 20 (4.6%)
Bronchiectasis 10 (2.3%)
Interstitial lung disease 1 (0.2%)
Heart disease 13 (3.0%)
Liver disease 14 (3.2%)
Chronic kidney disease 15 (3.4%)
Cough duration 7 days (3-7 days)
Sputum duration 5 days (3-7 days)

*Mean±SD; median (Interquartile range). COPD, chronic obstructive pulmonary disease.

Table 3

Microbiological results in patients with acute bronchitis (n = 435)

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Organisms* PCR positivity (%)
Bordetella pertussis 3 (0.7)
Bordetella parapertussis 0 (0.0)
Mycoplasma pneumoniae 1 (0.2)
Chlamydophila pneumoniae 3 (0.7)
Legionella pneumophila 1 (0.2)

*Among patients with probable pneumonia, one was PCR positive for C. pneumonia. PCR, polymerase chain reaction.

Table 4

Clinical characteristics in patients with acute bronchitis by antibiotic use (n = 435)

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Symptoms/signs Use of antibiotics P value P value§
No (n = 121) Yes (n = 314)
Rhinorrhea 37 (30.6%) 143 (45.5%) 0.005 0.001
Chest pain 8 (6.6%) 43 (13.7%) 0.040 0.095
Headache 19 (15.7%) 82 (26.1%) 0.021 0.847
Myalgia 11 (9.1%) 81 (25.8%) < 0.001 0.014
Cough duration (day)* 7.0 (3.0-10.0) 5.0 (3.0-7.0) 0.043 0.130
Inspiratory whooping 8 (6.6%) 43 (13.7%) 0.040 0.004
Sputum duration (day)* 7.0 (3.0-10.0) 5.0 (3.0-7.0) 0.008 0.104
Sputum color 78/42/0/1 109/195/4/6 < 0.001 < 0.001
Rhonchi 10 (8.3%) 94 (29.9%) < 0.001 < 0.001

*Median (Interquartile range); white/yellow/brown/green; Univariate analysis; §multivariate analysis.

Table 5

Frequencies of atypical bacteria in acute bronchitis from studies since 1990.

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Studies Reference Year N Methods M. pneumoniae (%) C. pneumoniae (%) L. pneumophila (%)
Boldy et al. (12) 1990 42 Serology 7.1 - - -
Macfarlane et al.* (23) 1993 206 Serology 0.5 - 0.0 C. burnetii (0.5)
Thom et al.* (36) 1994 743 PCR + Serology 1.9 2.8 - -
Macfarlane et al. (22) 1997 156 Serology 1.9 14.0 0.0 C.psittaci (0.6), C. burnetii (0)
Jonsson et al. (37) 1997 113 Serology 0.9 0.9 - -
Meijer et al. (38) 2000 557 PCR + Serology 1.3 1.1 - -
Macfarlane et al.* (1) 2001 316 PCR + Serology 7.3 17.4 - -
Lieberman et al.* (21) 2002 175 Serology 10.3 1.1 10.9 C. burnetii (1.7)
Wadowsky et al. (29) 2002 473 PCR + culture 0.8 0.0 - -
Lieberman et al. (20) 2003 132 Serology 11.2 2.3 6.8 -
Graffelman,et al.* (39) 2004 145 PCR + Serology 9.0 1.4 - -
Gaillat et al. (40) 2005 2,336 PCR 4.1 2.3 - -
Creer et al. (3) 2006 80 PCR 1.3 1.3 0.0 -
Holm et al. (14) 2007 316 PCR 2.2 0.6 0.0 -
The present study 2014 435 PCR 0.2 0.7 0.2 -

*Patients with pneumonia were included; Elderly patients hospitalized for non-pneumonic lower respiratory tract infection.

ACKNOWLEDGEMENTS

The authors thank Jin Ok Cheon (Cheon Clinic of Internal Medicine), Na Rae Joo (Shincheon-Yeonhap Clinic of Internal Medicine), Jun Wook Ha (Cheongchun Clinic of Internal Medicine), Ju Hyung Kim (Bon Clinic of Otolaryngology), Ji-Won Suhr (Hanaro Clinic of Internal Medicine), Tae Rim Park (Kunwoo Clinic of Internal Medicine) for their contributions to this study. The authors also thank Seegene Medical Institute for their contributions to microbiological tests.

Notes

Funding This study was supported by an academic fund from the Seegene Medical Institute.

DISCLOSURE The authors and the Seegene Medical Institute have no conflicts of interest to declare. The funder played no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

AUTHOR CONTRIBUTION Design of this study and drafting the manuscript: Jung KS, Park S. Analysis and interpretation of data: Oh KC, Lee MG, Lee JM, Yoo KH, Shim YS. Collection of data: all authors. Critical revision of the manuscript: Jung KS, Park S. Manuscript approval: all authors.

References

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ORCID iDs

Sunghoon Park
https://orcid.org/http://orcid.org/0000-0001-7004-6985

Kwang Ha Yoo
https://orcid.org/http://orcid.org/0000-0001-9969-2657

Do Il Kim
https://orcid.org/http://orcid.org/0000-0001-9046-3970

Jae-Myung Lee
https://orcid.org/http://orcid.org/0000-0002-6241-6349

Ki-Suck Jung
https://orcid.org/http://orcid.org/0000-0002-6878-6543

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