Background The distribution of the microbial aetiology and mortality of community-acquired pneumonia (CAP) was investigated in relation to the clinical setting and severity scores (pneumonia severity index (PSI) and confusion, blood urea nitrogen, respiratory rate, blood pressure, age (CURB-65)).
Methods 3523 patients with CAP were included (15% outpatients, 85% inpatients). The distribution of the microbial aetiology in relation to the clinical setting and severity scores (PSI, CURB-65) and the relative mortality of different aetiologies across the severity scores were analysed.
Results The aetiology was established in 1463 patients (42%), of whom 257 died (7%). The ranking of aetiologies varied according to site of care, with increasing frequency of Streptococcus pneumoniae and mixed aetiologies and decreasing frequency of atypical pathogens in hospitalised patients and those in ICUs. The distribution of aetiologies according to severity scores showed corresponding patterns; however, the severity scores were more sensitive to Gram-negative enteric bacilli (GNEB) and Pseudomonas aeruginosa and less sensitive in identifying mixed aetiologies as moderate- and high-risk conditions. Mortality rates according to aetiology and severity scoring showed increasing mortality rates for all pathogens except atypical pathogens. S pneumoniae had the highest number of deaths while GNEB, P aeruginosa, Staphylococcus aureus and mixed aetiologies had the highest mortality rates. Legionella pneumophila was similarly distributed according to site of care and prognostic scores.
Conclusions CAP due to atypical bacterial pathogens is recognised both clinically and by severity scoring as a low-risk condition. Severity scores are more sensitive in identifying patients with GNEB and P aeruginosa as moderate- and high-risk aetiologies whereas mixed aetiologies may be underestimated.
- Community-acquired pneumonia
- microbial aetiology
- severity assessment
- bacterial infection
- clinical epidemiology
- respiratory infection
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- Community-acquired pneumonia
- microbial aetiology
- severity assessment
- bacterial infection
- clinical epidemiology
- respiratory infection
Despite the use of many microbiological techniques, in nearly 50% of cases of community-acquired pneumonia (CAP) the aetiology is unknown.1 Most studies show that Streptococcus pneumoniae is the most common pathogen in CAP, and in hospitalised patients it accounts for two-thirds of the mortality.2 Other bacterial agents including Haemophilus influenzae and atypical pathogens (Mycoplasma pneumoniae, Chlamydophila pneumoniae, Coxiella burnetii and Legionella pneumophila) are described in up to 35% of CAP episodes. In addition, viral pathogens are recognised as causes of CAP, with influenza virus the leading viral pathogen.1 3
Since an aetiological diagnosis of CAP is usually unavailable, the initial empirical treatment is usually guided by microbial patterns described for the risk categories.4 5 In general, the guidelines for CAP management advocate empirical antibiotic selection on the basis of the age of the patient, comorbidities and initial severity of the illness.6–8
Recommendations of initial antimicrobial treatment according to pneumonia severity are mainly based on the notion that the risk of adverse outcomes including excess mortality in patients receiving inadequate initial antimicrobial treatment increases with pneumonia severity. However, few studies have assessed the independent effect of the microbial aetiology on severity scores (pneumonia severity index (PSI) and confusion, blood urea nitrogen, respiratory rate, blood pressure, age (CURB-65)).9 10 This study therefore aimed to investigate the distribution of the aetiology according to clinical setting and severity scores (PSI and CURB-65) and the relative mortality rates in a large series of patients with CAP.
Study setting and design
All consecutive adult patients attending the Hospital Clinic in Barcelona with CAP were prospectively studied between November 1996 and July 2008. CAP was defined as the presence of a new infiltrate on chest radiography together with clinical symptoms suggestive of lower respiratory tract infection. Exclusion criteria included: (1) severe immunosuppression (AIDS, chemotherapy, immunosuppressive drugs); (2) active tuberculosis; (3) healthcare-associated pneumonia; and (4) cases with a confirmed alternative diagnosis. Non-hospitalised patients were visited 1–7 days after attending the outpatient clinic.
Patient characteristics and CAP scoring systems
The following data were recorded on admission to hospital: age, gender, current smoking, comorbid illnesses and antimicrobial treatment prior to hospital admission, duration of symptoms prior to visit, clinical symptoms, physical examination, chest x-ray pattern, blood analysis and antimicrobial treatment at admission. All surviving patients were visited 30–40 days after discharge. PSI and CURB-65 score classes were assigned according to the authors' original designations. Patients were stratified into low-risk, intermediate-risk and high-risk classes as follows: PSI score: low risk=classes I–III, intermediate risk=class IV, high risk=class V; CURB-65: low risk=classes 0–1, intermediate risk=class 2, high risk=classes 3–5.
Microbiological examination was performed in sputum, urine, two samples of blood and nasopharyngeal swabs. Pleural puncture, tracheobronchial aspirates (TBAS) and bronchoalveolar lavage (BAL) fluid, when available, were collected for Gram and Ziehl–Nielsen stains and for cultures for bacterial, fungal and mycobacterial pathogens.
The aetiology was considered definite if one of the following criteria was met: (1) positive blood culture (in the absence of an apparent extrapulmonary focus); (2) positive bacterial culture of pleural fluid or transthoracic needle aspiration samples; (3) elevated serum levels of IgM against C pneumoniae (≥1:64), C burnetii (≥1:80) and M pneumoniae (any positive titre); (4) positive urinary antigen for L pneumophila (Binax Now L pneumophila urinary antigen test; Trinity Biotech, Bray, Ireland); (5) positive urinary antigen for S pneumoniae (Binax Now S pneumoniae urinary antigen test; Emergo Europe, The Netherlands); (6) bacterial growth in cultures of TBAS (≥105 cfu/ml), protected specimen brushing (PSB) (≥103 cfu/ml) and BAL fluid (≥104 cfu/ml); (7) seroconversion (ie, a fourfold increase in IgG titres) for C pneumoniae and L pneumophila >1:128, C burnetii >1:80 and respiratory viruses (influenza viruses A and B, parainfluenza viruses 1–3, respiratory syncytial virus, adenovirus); (8) detection of antigens by immunofluorescence assay plus virus isolation or detection by reverse transcriptase (RT)-PCR testing for respiratory viruses (influenza viruses A and B, parainfluenza viruses 1–3, respiratory syncytial virus, adenovirus).
The aetiology of pneumonia was classified as presumptive when a predominant microorganism was isolated from a purulent sample (leucocytes >25 per high power microscopic field and few epithelial cells <10 per high power microscopic field) and the findings of Gram staining were compatible. For the purpose of this study, presumptive and definitive diagnoses were analysed together.
Categorical variables were described with counts and percentages. Data for continuous variables were presented as mean (SD) or median (IQR) where appropriate. The proportions of individuals in each of the sites of care and PSI and CURB-65 groups diagnosed with each pathogen of interest were compared using χ2 tests. χ2 tests were also used to compare the proportions of individuals with each pathogen of interest between each pair of site of care, PSI and CURB-65 groups, with p values adjusted using the Bonferroni method. The κ concordance coefficient was calculated to determine agreement with risk class assignment. The interpretation of the κ index value was based on the Altman scale (<0.20, poor; 0.21–0.40, fair; 0.41–0.60, moderate; 0.61–0.80, good; and 0.81–1.00, very good).11 All analyses were performed with SPSS software Version 16; a two-sided p value of <0.05 was considered statistically significant.
Patient characteristics and outcomes
A total of 3523 adult patients with CAP were studied, of whom 514 (14.6%) were outpatients. The mean (SD) age was 65.5 (18.7) years (range 18–102); 2166 patients (62%) were aged ≥65 years. The main clinical characteristics and radiological findings of the study population are shown in table 1.
A total of 769 patients (22.4%) had received antimicrobial treatment prior to hospital admission. One-month mortality was 7% (n=257).
The distribution of groups by severity scores (PSI, CURB-65) and by site of care is shown in table 2. On admission, both scores placed the majority of patients in the low-risk group (PSI 46%; CURB-65 51%). Similarly, both scores classified similar proportions in the high-risk group (PSI, 20%; CURB-65, 21%). Nevertheless, the accordance of risk class assignment was moderate (κ=0.54, p<0.001): PSI classes I–III and CURB-65 classes 0–1 (n=1404 patients), PSI class IV and CURB-65 class 2 (n=606) and PSI class V and CURB-65 classes 3–5 (n=479). Predictions of death were similar for both risk scores (risk group 1, 1.2% and 1.8%; risk group 2, 6.8% and 7.9%; risk group 3, 21.5% and 19.2%). However, the accordance of predictions was low (κ=0.37, p<0.001): PSI classes I–III and CURB-65 classes 0–1 (n=10), PSI class IV and CURB-65 class 2 (n=41) and PSI class V and CURB-65 classes 3–5 (n=114).
Diagnostic yield of applied techniques
Aetiological diagnoses were established in 1463 cases (42%). Overall, 1463 pathogens were identified, of which 490 (34%) were detected by sputum examination (presumptively diagnostic) and 973 (66%) by other techniques (definitively diagnostic). A single pathogen was identified in 1255 patients (86%) and two pathogens were identified in 208 (14%). Additional details of all applied techniques (number of performed tests and diagnostic rates) are provided in the online supplement.
Microbial aetiology of patients with CAP
The five most frequently isolated pathogens were S pneumoniae (613 patients, 42%), atypical pathogens (C pneumoniae, M pneumoniae, L pneumophila and C burnetii) (263 patients, 18%), viruses (148 patients, 10%), H influenzae (70 patients, 5%) and Pseudomonas aeruginosa (50 patients, 3%).
More than one causative agent was found in 208 patients (14%); S pneumoniae was the most prevalent microorganism involved in mixed infections (136/208, 65%). The most frequent combinations among mixed infections were: two bacteria in 67 (32%), a bacterium plus a virus in 61 (29%) and a bacterium plus an atypical pathogen in 37 (18%) (see online supplement).
Figure 1 in the online supplement illustrates the rate of pathogen isolation during the 12-year period, showing a homogeneous incidence of all pathogens over time except for an increase in S pneumoniae in 2000 and in respiratory viruses in 2004 as a result of the introduction of the pneumococcal urinary antigen test and RT-PCR for viruses, respectively.
Overall, 333 patients had bacteraemia (S pneumoniae in 265 patients, GNEB in 14, Staphylococcus aureus in 13, H influenzae in 7, P aeruginosa in 2 and other streptococci in 32 patients). The mortality rate associated with bacteraemic pneumococcal pneumonia was 11%.
Microbial aetiology by site of care
The microbial aetiology was known in 32% of outpatients (514 isolates) and in 44% of inpatients (1302 isolates). The yield was 1042 of 2521 (41%) in patients treated on the ward and 260 of 488 (53%) in those treated in the ICU (table 3). The most frequent aetiology among outpatients was the atypical pathogen group (36%) followed by S pneumoniae (35%), viruses and mixed aetiologies (both 9%). In patients treated on the ward, S pneumoniae was the most common aetiology (43%) followed by atypical pathogens (16%), mixed aetiologies (13%) and viruses (12%). L pneumophila was identified in 10 patients (6%). In patients treated in the ICU the most common aetiologies were S pneumoniae (42%), mixed aetiologies (22%) and atypical pathogens (14%).
Microbial aetiology according to severity scores
When we analysed the aetiology by severity score groups (tables 4 and 5), the most common pathogen was S pneumoniae in all risk groups. In patients with low-risk scores, atypical pathogens were second (25%) and mixed aetiologies third (13%). The frequency of atypical pathogens decreased with severity (15% and 8%, respectively), whereas that of mixed aetiologies increased (15% and 17%, respectively). The frequencies of P aeruginosa and GNEB increased in higher risk classes (3% and 8%, and 2% and 4%). Corresponding trends were found in the distributions according to the CURB-65 severity score.
Mortality according to severity scores and microbial aetiology
Mortality rates of specific aetiologies per PSI score revealed increasing mortality rates with increasing severity scores for most pathogens. S pneumoniae had the highest number of deaths. High mortality rates were observed for S aureus and GNEB (11% and 14%, respectively) in low-risk classes. The highest mortality rates in the group treated on the ward had GNEB (26%), Moraxella catarrhalis (25%), S aureus (11%) and P aeruginosa (11%). In patients treated in the ICU, S aureus (67%), GNEB (67%), P aeruginosa (33%) and mixed aetiologies (24%) had the highest mortalities. Again, similar patterns were found for the CURB-65 score (tables 6 and 7).
The main findings of this study are: (1) according to the site of care, the ranking of aetiologies varies with an increase in mixed aetiologies and decreasing frequency of atypical pathogens from ward to ICU; (2) the distribution of aetiologies according to both severity scores PSI and CURB-65 revealed corresponding patterns; (3) mortality rates by aetiology and severity scoring showed increasing mortality rates for all pathogens except atypical pathogens. S pneumoniae had the highest number of deaths, whereas GNEB, P aeruginosa, S aureus, mixed aetiologies and others had the highest mortality rates.
Several recent studies have shown that PSI and CURB-65 (and its modification CRB-65) yield similar predictions of in-hospital mortality in patients with CAP.12–14 Our data support this finding, clearly showing a pattern of three risk classes of low-, moderate- and high-risk with mortality rates of approximately 1–2%, 7–8% and 19–22%, respectively. The last figure has been reported to be higher (30–35%) when nursing home and bedridden patients are included.15 16 However, the severity scores do not measure the same factors since accordance rates are only moderate. Furthermore, it is unclear what these severity scores truly reflect, so it seems highly relevant to study the relation between aetiology and severity.
This study is novel in that it includes three dimensions of analysis: the relation of aetiology to site of care as a reflection of clinical judgement of severity and other considerations; its relation to risk classes according to both scores; and its relation to mortality according to risk classes.
When analysing the relation of aetiology to site of care, patients with the two atypical bacterial pathogens M pneumoniae and C burnetii were significantly more frequently treated as outpatients. This is an expected finding since CAP due to M pneumoniae and C pneumoniae are usually encountered in younger patients without comorbidity and has a mild clinical course.3 17 18 The severity scores equally showed that M pneumoniae and C burnetii were found more frequently in low-risk patients (and a similar trend for C pneumoniae). Accordingly, mortality was minimal in this group, regardless of the risk class.
L pneumophila was equally distributed across all sites of care and all risk classes, with the exception of a significantly higher frequency of patients in the moderate-risk group according to the PSI. Since the association with severity was not obvious in the high-risk group, this finding cannot be considered as a consistent trend. These findings do not support those of previous studies from the same region9 10 which show low rates of Legionella spp. in patients with less severe disease. The equal distribution may be partly explained by an unexpected low overall mortality in patients with this pathogen. Indeed, the mortality of Legionella pneumonia has decreased over the years since the implementation of urinary antigen detection.19 However, in a population with high mortality in the high-risk group, the distribution of severity and, accordingly, of outpatients and inpatients was similar.20
Patients infected with viruses were treated less frequently in the ICU and had a very low mortality, although they were placed equally frequently across all risk classes for both severity scores. Since this is a somewhat heterogeneous group it should be regarded with caution, although it agrees with previous findings.21
As expected, all pathogens except atypical pathogens showed increasing mortality with increasing disease severity. S pneumoniae had the highest number of deaths, although the relative mortality rates were higher for S aureus, GNEB, P aeruginosa and mixed aetiologies. It therefore seems particularly important to identify these patients.
CAP caused by GNEB and P aeruginosa has been reported to be associated with excess mortality.22 23 Our data confirm this finding. Both severity scores reflected the adverse prognostic potential of these pathogens since they occur more frequently in moderate- and high-risk groups. Interestingly, no such association could be found in the analysis by site of care and a corresponding trend was only obvious for P aeruginosa. This finding may reflect an underestimation of these pathogens or possibly that some elderly and severely disabled patients were not admitted to the ICU due to prognostic considerations despite a moderate to high risk (PSI, CURB-65) and/or the presence of such aetiologies.23
Mixed aetiologies had a high mortality. Importantly, in 32.2% of our mixed cases, bacteria were associated with other bacteria and bacteria and viruses were found in 29.3%. In fact, de Roux et al found a higher percentage of shock (18%) when two pyogenic bacteria were associated.24 In patients with CAP due to mixed infections, the attending clinicians correctly recognised this aetiology as a moderate- to high-risk condition whereas both severity scores were less sensitive in this regard. Only PSI showed some trend in this direction. Since severity scoring was always present in clinical decision making, clinicians possibly overruled the predictions made by the scores. However, it remains unclear on what basis they did so. This issue may require separate analysis.
Only two previous studies have tried to assess the association of severity score and aetiology. In a limited number of patients (n=533) Roson et al found only S pneumoniae, GNEB, aspiration and unknown aetiologies to be associated with increased severity (PSI class V) and mortality. However, the analysis is limited by small numbers with a definite aetiology (n=283). Dambrava et al assessed the related aetiology according to American Thoracic Society risk stratification and found Legionella spp., viruses and mixed infections to be more frequent in high-risk groups and atypical bacterial pathogens other than Legionella spp. in low-risk groups. Interestingly, with the exception of the very low-risk group (previously healthy, no risk factors) in which pneumococci were somewhat less frequently encountered, S pneumoniae was found to an equal extent in all risk groups. Again, the number of patients studied (n=829) and aetiologies defined (39%) was limited. Nevertheless, several of these preliminary findings, although not expressively interpreted in the context of our approach, are supported by this analysis.
Our results do not provide further clues into the intriguing observation that both severity scores—albeit of overall equal predictive potential—obviously perform different individual classifications. All that can be said from our analysis is that both scores reflect the aetiology to a very similar extent, and that the aetiology does not seem to be a factor behind the observed divergent individual predictions. Since CURB-65 is far easier to apply, our findings support the use of this score as recommended in the most recent British Thoracic Society (BTS) guideline update.8
Our results also complement the CAP aetiological data review recently provided by the BTS guideline update8 in two respects: (1) they support the importance and similar frequency of L pneumophila in any clinical setting (ambulatory, ward and ICU); and (2) they confirm the relatively high frequency of severe CAP mixed pneumonias, a finding of potential importance for new empirical antibiotic recommendations.
An important limitation of our study is that the microbiological assessment was not homogeneous over time, which limits the validity of the microbial aetiology patterns found. This is particularly true for antigen testing. However, in studies which include long study periods such changes may be inevitable.
In conclusion, CAP due to atypical bacterial pathogens is recognised both clinically and by severity scoring as a low-risk condition and L pneumophila may be correctly identified as less severe than was thought in the past in the era of antigen testing. GNEB (in our study mainly Escherichia coli) and P aeruginosa are correctly identified as moderate- and high-risk pathogens, although prognostic considerations in patients with these aetiologies might lead to different treatment allocation. Mixed aetiologies are conditions that may be underestimated by severity scores.
The criteria behind the clinical recognition of severity in patients with mixed aetiologies remain unclear but, if identified, mixed aetiologies should probably be added as an independent risk factor. The excess mortality of mixed aetiologies supports initial empirical antimicrobial combination treatment, at least in patients with severe CAP.
Review history and Supplementary material
Funding CibeRes (CB06/06/0028)-ISCiii, 2009 SGR 911 and IDIBAPS.
Competing interests None.
Ethics approval It was not considered necessary to obtain ethical approval as this is a non-interventional study based on an epidemiological database of prospectively and routinely collected data.
Provenance and peer review Not commissioned; externally peer reviewed.
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