key: cord-0698516-5e44agay
authors: Jang, Jong Geol; Ahn, June Hong; Jin, Hyun Jung
title: Incidence and Prognostic Factors of Respiratory Viral Infections in Severe Acute Exacerbation of Chronic Obstructive Pulmonary Disease
date: 2021-05-07
journal: Int J Chron Obstruct Pulmon Dis
DOI: 10.2147/copd.s306916
sha: 59a6a86536f8195b97954c4fb409721d0448c51a
doc_id: 698516
cord_uid: 5e44agay

PURPOSE: Severe acute exacerbations of chronic obstructive pulmonary disease (AECOPD) that require hospitalization and emergency department visits are associated with considerable morbidity and mortality. Respiratory viral infection is an important cause of severe AECOPD. We evaluated the incidence and prognostic factors of viral infection in severe AECOPD. PATIENTS AND METHODS: We performed a retrospective study of 262 cases of severe AECOPD in 192 patients who required hospitalization and emergency department visits at a tertiary teaching hospital in Daegu, Korea. A multiplex polymerase chain reaction panel using a nasopharyngeal swab sample was performed to detect viral infection. RESULTS: Viral infection was detected in 108 events (41.2%) from 96 patients. The most common virus was rhinovirus/enterovirus (27.5%), followed by influenza virus (22.5%), respiratory syncytial virus (13.3%), parainfluenza virus (12.5%), coronavirus (12.5%), metapneumovirus (7.5%), and adenovirus (4.2%). Virus-positive exacerbations, compared to virus-negative exacerbations, had a higher frequency of symptoms of rhinopharyngitis, higher neutrophil count and C-reactive protein (CRP) level, and lower eosinophil count. Multivariate analysis demonstrated that elevated CRP levels (odds ratio [OR], 2.76; 95% confidence interval [CI], 1.24–6.15), symptoms of rhinopharyngitis (OR, 1.98; 95% CI, 1.03–3.78), low eosinophil count (OR, 1.74; 95% CI, 1.03–2.92), and inhaled corticosteroid (ICS) use (OR, 1.70; 95% CI 1.04–2.80) were associated with viral infection in severe AECOPD. CONCLUSION: The incidence of viral infection in severe AECOPD was 41.2%, and the most commonly detected virus was rhinovirus/enterovirus. Increased CRP level, symptoms of rhinopharyngitis, low eosinophil count, and use of ICS were associated with viral infection in severe AECOPD.

Chronic obstructive pulmonary disease (COPD) is a common, progressive disease with persistent respiratory symptoms and airflow limitation. 1 COPD is a major cause of morbidity and mortality worldwide and is expected to be the third leading cause of death in 2030. 2 Acute exacerbations of chronic obstructive pulmonary disease (AECOPD) are related to increased hospital admission, morbidity, and mortality 3 and cause accelerated lung function decline. 4 Respiratory infections, including bacterial and viral infections, are known to be important triggers of AECOPD. 5 As detection of viral infection using serology and culture has low sensitivity, 6 the role of viral infection in AECOPD has been underestimated compared to that of bacterial infection. However, with recent advances in polymerase chain reaction (PCR) techniques, the viral detection rate has reached 56%. 7 As the detection rate of virus increases, interest in the effect of viral infection on AECOPD has also increased. Rhinovirus, influenza virus, and respiratory syncytial virus (RSV) are the most commonly identified viruses in AECOPD. 8 Although there have been several studies on respiratory viruses causing AECOPD, 8, 9 they could not sufficiently demonstrate the overall prevalence since viral infection has geographic and seasonal variation.

A previous study showed that CRP level and body temperature were associated with viral detection. 10 Kwak et al reported female sex was related with high risk of viral infection. 11 But few studies have evaluated the risk factors of viral infection in patients with AECOPD. But Few studies have evaluated the risk factors of viral infection in patients with AECOPD.

Therefore, this study aimed to evaluate the prevalence of respiratory viral infection using a highly sensitive PCR method and investigate the risk factors for viral infection in patients with severe AECOPD requiring hospital admission.

We performed a retrospective study of patients with AECOPD who were hospitalized at Yeungnam University Medical Center (a 930-bed, universityaffiliated, tertiary referral hospital in Daegu, South Korea) between January 2017 and December 2018. During the study period, all COPD patients (>40 years) admitted to the hospital who had multiplex PCR results for viral identification were eligible for inclusion.

Exclusion criteria were as follows: (1) patients without a multiplex PCR test performed within 24 hour of hospitalization and (2) patients admitted with bronchial asthma or dyspnea of other origin (heart failure, pulmonary edema, or pulmonary embolism).

The primary outcome was the prevalence of respiratory viral infection in AECOPD. The secondary outcome was the risk factors of viral infection.

This study was conducted in accordance with the tenets of the Declaration of Helsinki and was reviewed and approved by the Institutional Review Board of Yeungnam University Hospital (YUH IRB 2021-01-008). Written informed consent was waived because of the retrospective study design, which is in compliance with the institutional and national policies concerning research approvals. Patient's records were anonymized before analysis to maintain their confidentiality.

According to the definition of AECOPD mentioned above, three pulmonologists (JHA, JHJ, and JGJ) made the diagnosis of COPD exacerbation. Patient electronic medical records were reviewed by all authors, and demographic, clinical, and spirometric data were collected.

Laboratory findings, including complete blood counts with differentials, blood chemistry, inflammation markers such as C-reactive protein (CRP) and procalcitonin levels, and multiplex PCR for respiratory virus results, were reviewed. Nasopharyngeal swabs were obtained at admission (within 24 hour). A multiplex PCR panel (FilmArray Respiratory Panel; BioFire Diagnostics, Inc., Salt Lake City, UT, USA), which target 17 viruses, including adenovirus, coronaviruses (OC43, 229E, NL63, and HKU1), human metapneumovirus (hMPV), human rhinovirus and enterovirus, influenza A (including subtypes H1N1, H3N2, and the 2009-H1N1) and B viruses, parainfluenza viruses (1,2,3, and 4), and RSV, was used to detect respiratory viral infections.

The diagnosis and severity of COPD was made according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria, which defines COPD as a post-bronchodilator forced expiratory volume in one second (FEV 1 ) to forced vital capacity ratio of <0.7. 1 AECOPD was defined according to the GOLD guidelines as an acute worsening of respiratory symptoms (dyspnea, increased sputum volume, and purulence) that was beyond daily variation and needed additional treatment. 12 Frequent exacerbations were defined if acute exacerbation occurred twice or more for 1 year. Respiratory viral detection was defined as detection of any respiratory virus in nasopharyngeal swab samples by multiplex PCR. Nasopharyngeal symptoms included the presence of increased rhinorrhea, nasal congestion, or sore throat. Use of inhaled corticosteroid (ICS) was defined as having been prescribed ICS for at least 3 months. 

Continuous variables are expressed as means ± standard deviation (SD), and these were compared using a Student''s s t-test or Mann-Whitney U-test. Categorical variables were compared using chi-squared test or Fisher's exact test. Continuous data were categorized using logistic regression analysis. Multivariable logistic regression analyses were performed to identify independent risk factors for viral detection in patients with severe AECOPD, as measured by the odds ratios (ORs) with 95% confidence intervals (CIs). In all analyses, a p-value <0.05 was considered statistically significant. All statistical analyses were performed using the SPSS software (ver. 24.0; SPSS Inc., Chicago, IL, USA).

During the study period, 420 patients with AECOPD were hospitalized. After application of the exclusion criteria, 262 cases from 192 patients were included ( Figure 1 ). Table 1 shows the baseline characteristics of the study population. The mean patient age was 76.5±7.9 years, and 155 (80.7%) were males. Most patients had a smoking history (92.7%). The mean FEV 1 after bronchodilator was 69.1%, and 56 (29.7%) patients had a history of severe AECOPD in the previous year.

In total, 108 (41.2%) out of 262 cases tested positive for respiratory viruses, cases with multiple viral detection were 11. The most common viruses were rhinovirus/ enterovirus (30.1%), followed by influenza virus (25.0%), RSV (14.8%), parainfluenza virus (13.9%), coronavirus (13.9%), hMPV (8.3%), and adenovirus (4.6%) ( Table 2 ).

Comparison between the two groups showed no difference in age, sex, smoking status, vital signs on admission, FEV 1 , severity of COPD, and clinical outcome (Table 3) . Nasopharyngeal symptoms were more prevalent in the virus-positive exacerbation group than in the virusnegative group. The use of ICS was more common in the virus-positive exacerbation group than in the virusnegative exacerbation group. In laboratory tests, mean neutrophil counts and CRP levels were significantly higher and eosinophil count was significantly lower in the viruspositive exacerbation group than those in the virusnegative exacerbation group (Table 4 ). 

To clarify the factors associated with viral detection in severe AECOPD cases, we investigated several variables including age, sex, nasopharyngeal symptoms, use of ICS, eosinophil count, CRP level, and absolute neutrophil count ( Table 5) . The univariable analysis revealed that nasopharyngeal symptoms, use of ICS, eosinophil count <100/uL, and CRP level >0.5mg/dL were significantly associated with viral detection. In the multivariable logistic analysis, nasopharyngeal symptoms (OR, 1.98; 95% CI, 1.03-3.78; p = 0.019), use of ICS (OR, 1.69; 95% CI, 1.01-2.84; p = 0.036), eosinophil count <100/uL (OR, 1.74; 95% CI, 1.03-2.92; p = 0.018), and CRP level >0.5 (OR, 2.76; 95% CI, 1.24-6.15; p = 0.009) were found to be associated with viral detection in severe AECOPD. This association was consistently maintained after adjusting for COPD severity and frequent exacerbation (Supplementary Table 1 ).

In our study, we analyzed the prevalence of viral infections and risk factors associated with viral infection in a large number of patients with severe AECOPD who required hospitalization. The main findings of this study were as follows: (1) The overall prevalence of viral infection was 41.2%; (2) the most commonly detected viral pathogen was rhinovirus/enterovirus; (3) the nasopharyngeal symptoms, use of ICS, low eosinophil count, and elevated CRP levels were associated with viral detection.

The prevalence of viral infection was 41.2% in our study. The rate of viral detection varies depending on the Note: Data are presented as means ± standard deviations or numbers (percentages). Abbreviations: COPD, chronic obstructive pulmonary disease; FEV, forced expiratory volume in one second; FVC, forced vital capacity; LAMA, long-acting muscarinic antagonist; LABA, long-acting β 2 agonist; ICS, inhaled corticosteroid. 13 The rates influenza virus, RSV, and coronaviruses were the most commonly detected viruses, 18 which was consistent with our results, except for parainfluenza virus. In our study, rhinovirus/enterovirus was the most commonly detected virus, which was consistent with the previous result. 11, 13, 15, 19 In the case of influenza virus, our result showed a higher detection rate compared to that in previous studies 11, 19, 20 but was consistent with those of several studies. 17, 21 As the influenza virus detection rate could be related to seasonal variation and vaccine usage, differences between studies in the detection rate of this virus is inevitable. The incidence of RSV infection was consistent with those of several studies. 19, 22 RSV is an important pathogen of respiratory infection in elderly and high-risk adults 23 and is commonly detected in patients with AECOPD. 16 hMPV is a virus that is not commonly associated with AECOPD. 16 However, Hamelin et al reported that hMPV is associated with COPD exacerbation. 24 Our results also support the role of hMPV in AECOPD. Symptoms and inflammatory markers can be used to predict viral infection. Nasopharyngeal symptoms (such as nasal congestion, increased rhinorrhea, sore throat) and fever are frequently present in patients with viral infection leading to COPD exacerbation. 10, 13, 19, 20, 22, 25 In our study, patients with viral infection had a higher frequency of nasopharyngeal symptoms than those without viral infection, indicating that nasopharyngeal symptoms might have a predictive value for viral infection.

CRP is an acute-phase systemic inflammatory biomarker that is associated with AECOPD. 26 The relationship between CRP level and viral infection remains unclear. Some studies did not show an association between CRP levels and viral infection. 11, 13, 21 However, Clark et al studied the relationship between serum CRP level and the rate of detection of virus and bacteria, and reported that CRP level was associated with viral detection, 10 which was consistent with our results.

The interesting points of this present study were the association of viral detection with use of ICS and eosinophil count. The GOLD guideline recommend the use of ICS in combination with bronchodilators for patients with a history of asthma, blood eosinophil count >300 cells/µL, and severe or frequent AECOPD despite long-acting bronchodilator therapy. 27 However, the ICS use is associated with an increased risk of pneumonia and pulmonary tuberculosis infection. [28] [29] [30] Until now, the relationship between the use of ICS and risk of viral infection remains unclear. The "Toward a Revolution in COPD Health (TORCH)" study showed that the ICS use increased the risk of upper respiratory tract infection as well as pneumonia. 31 Thomas et al reported that usage of glucocorticosteroids increases viral replication in the respiratory tract in vitro and in vivo. 32 In our data, the use of ICS increased the risk of severe COPD exacerbation, suggesting that ICS use is associated with viral infection. Further prospective studies should be performed to evaluate the association between ICS use and viral infection.

Previous studies reported that blood eosinophilia was associated with an increased risk of AECOPD 33, 34 and is a predictive biomarker of response to inhaled or systemic corticosteroid. 35 Until now, no clear relationship between eosinophil count and respiratory viral infection has been established. MacDonald et al reported that low eosinophil counts were associated with infection. 36 Drake et al showed the antiviral effects of eosinophils in vivo and in vitro, and their results suggested that eosinophils enhance viral clearance and contribute to innate immune responses. 37 However, there is no clear evidence of an association between eosinophil count and viral infection in a clinical study. Although our results showed that low eosinophil count was associated with viral infection, a prospective randomized controlled study will be required to confirm this.

Poor prognosis of AECOPD includes readmission to hospital and in-hospital mortality. Recent study reported comorbidities (heart failure, renal failure, depression, and alcohol use), previous exacerbation and hospitalization, and longer duration of admission were associated with risk factors for readmission. 38 Although one study showed frequency of AECOPD is related to the frequency of the common cold, 39 the relationship between the viral infection and poor prognosis in AECOPD is unclear. Previous studies showed that there was no difference in hospital days, in hospital death, and readmission, 11, 13, 40 which is consistent with our result. Further evaluation about impact of viral infection on poor prognosis of AECOPD will be warranted.

Our study has some limitations. First, it was a retrospective and single-center study; thus, our data were not representative of the Korean population. Furthermore, we enrolled only patients who underwent PCR test among severe AECOPD patients requiring hospitalization, so there may be some selection bias. Second, influenza virus infection is associated with vaccination, but we did not evaluate the vaccination status because of our retrospective study design. Third, bacterial infection is DovePress a potential confounding factor in this study because CRP levels can be elevated in bacterial infection associated AECOPD. However, since there was no difference in bacterial infection rate between the virus positive exacerbation group and the virus negative exacerbation group, we carefully speculate the effect of bacterial infection on CRP level in our study could be insignificant. Finally, because the PCR method cannot discriminate between active and latent viral infections, viral detection did not confirm whether AECOPD was due to an active viral infection.

Viral infection was common among patients with severe AECOPD. The commonly detected viruses were rhinovirus and influenza. Our study showed the risk factors associated with viral detection in patients with severe AECOPD. To confirm these findings, further studies are needed.

AECOPD, acute exacerbations of chronic obstructive pulmonary disease; CI, confidence interval; COPD, chronic obstructive pulmonary disease; CRP, C-reactive protein; FEV 1 , forced expiratory volume in one second; GOLD, Global Initiative for Chronic Obstructive Lung Disease; hMPV, human metapneumovirus; ICS, inhaled corticosteroid; OR, odds ratio; PCR polymerase chain reaction; RSV, respiratory syncytial virus; SD, standard deviation.

This study was conducted in accordance with all relevant tenets of the Declaration of Helsinki. The protocol was reviewed and approved by the institutional review board of our hospital (no. YUH IRB 2021-01-008). Written informed consent was waived because of the retrospective study design, which is in compliance with the institutional and national policies concerning research approvals. Patient's records were anonymized before analysis to maintain their confidentiality.

This work was supported by the Yeungnam University Research Fund (2020).

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The authors declare no competing interests.