Clinical predictors for Legionella in patients presenting with community-acquired pneumonia to the emergency department
- Rico Fiumefreddo†1,
- Roya Zaborsky†1,
- Jeannine Haeuptle†1,
- Mirjam Christ-Crain1,
- Andrej Trampuz2,
- Ingrid Steffen3,
- Reno Frei2,
- Beat Müller4Email author and
- Philipp Schuetz1
© Fiumefreddo et al; licensee BioMed Central Ltd. 2009
Received: 17 October 2008
Accepted: 19 January 2009
Published: 19 January 2009
Legionella species cause severe forms of pneumonia with high mortality and complication rates. Accurate clinical predictors to assess the likelihood of Legionella community-acquired pneumonia (CAP) in patients presenting to the emergency department are lacking.
We retrospectively compared clinical and laboratory data of 82 consecutive patients with Legionella CAP with 368 consecutive patients with non-Legionella CAP included in two studies at the same institution.
In multivariate logistic regression analysis we identified six parameters, namely high body temperature (OR 1.67, p < 0.0001), absence of sputum production (OR 3.67, p < 0.0001), low serum sodium concentrations (OR 0.89, p = 0.011), high levels of lactate dehydrogenase (OR 1.003, p = 0.007) and C-reactive protein (OR 1.006, p < 0.0001) and low platelet counts (OR 0.991, p < 0.0001), as independent predictors of Legionella CAP. Using optimal cut off values of these six parameters, we calculated a diagnostic score for Legionella CAP. The median score was significantly higher in Legionella CAP as compared to patients without Legionella (4 (IQR 3–4) vs 2 (IQR 1–2), p < 0.0001) with a respective odds ratio of 3.34 (95%CI 2.57–4.33, p < 0.0001). Receiver operating characteristics showed a high diagnostic accuracy of this diagnostic score (AUC 0.86 (95%CI 0.81–0.90), which was better as compared to each parameter alone. Of the 191 patients (42%) with a score of 0 or 1 point, only 3% had Legionella pneumonia. Conversely, of the 73 patients (16%) with ≥4 points, 66% of patients had Legionella CAP.
Six clinical and laboratory parameters embedded in a simple diagnostic score accurately identified patients with Legionella CAP. If validated in future studies, this score might aid in the management of suspected Legionella CAP.
Legionella species (spp.) causes a severe form of community-acquired pneumonia (CAP) with a high incidence of adverse medical outcomes including progression of infiltrates, respiratory failure and need for intensive care unit (ICU) admission [1, 2]. In addition, Legionella CAP has a high mortality rate of about 10 percent, which may increase up to 27 percent in patients not receiving adequate antibiotics as part of the empiric treatment on admission . Early identification of Legionella spp. in patients presenting with respiratory symptoms and suspicion of CAP to the emergency department is thus of utmost importance because it affects the timing and choice of empirical antibiotic therapy and reduces the risk for adverse outcome. Currently available diagnostic tests include detection of Legionella spp. by culture or polymerase chain-reaction (PCR) in respiratory samples and Legionella pneumophila antigen testing in urine. These tests lack sensitivity, in addition the urine antigen test only identifies Legionella pneumophila serogroup 1 [3, 4]. Previous studies comparing clinical, radiological and laboratory findings in Legionella CAP and non-Legionella CAP have produced controversial results [1, 5–12]. Two previous attempts to construct a diagnostic score that identifies Legionella in patients with CAP have been disappointing [1, 5–11]. As a limitation, these studies compared Legionella pneumophila CAP with selected cases of pneumococcal CAP [5, 6, 8]. When applied in unselected patients, these scores lack sensitivity and/or specificity. Because of this diagnostic dilemma consensus guidelines on empiric antibiotic therapy for patients with CAP to extend antibiotic coverage to Legionella in all patients with severe CAP contributing to antibiotic overuse and emergence of multi-resistant strains [13–16]. However more recent findings suggest, that severity of CAP is not an appropriate screening criterion for Legionella CAP, which further complicates the choice of empiric antibiotic treatment .
The aim of this study was to compare initial clinical and laboratory parameters of consecutive patients with Legionella CAP who were hospitalized in our institution during the last 10 years with patients with non-Legionella CAP included in two studies at the same institution [17, 18] and thereby to identify reliable diagnostic predictors of Legionella CAP.
Setting and Study population
We retrospectively evaluated all consecutive patients who were admitted to the University Hospital in Basel, Switzerland from 1997 to 2007, with a diagnosis of Legionella CAP. The diagnosis of Legionella was considered definite if Legionella was either isolated by culture or PCR of a respiratory sample or detected by urinary antigen testing. Patient records were reviewed with a standardized data-collection form to retrieve all demographic, clinical, microbiological, radiographic, laboratory and therapeutical data. To achieve a reasonable comparison, we used clinical and laboratory data on admission to the emergency department.
For comparison we used data on admission of a consecutive cohort of 368 patients with non-Legionella CAP who were admitted between December 2002 through February 2005 to the same institution and enrolled in two studies [17, 18]. The design of the two studies was similar and has been reported in detail elsewhere [17, 18]. In brief, a total of 373 consecutive patients with radiologically proven CAP were randomly assigned to be treated either with a procalcitonin (PCT)-based algorithm or standard practice. The primary endpoint of the two studies was to evaluate antibiotic exposure of a PCT-guided treatment algorithm as compared to standard recommended guidelines . Both studies excluded patients with cystic fibrosis or active pulmonary tuberculosis, hospital-acquired pneumonia and severely immunocompromized patients. In both studies, testing for Legionella with the use of the urine antigen test was recommended in all CAP patients as part of the hospital work up for CAP and part of the study protocols. Investigation for other atypical bacterial pathogens namely Mycoplasma spp. and Chlamydia spp. were only tested in suspected cases upon the decision of to the treating physicians. For the purpose of this study, the five enrolled patients with Legionella CAP were analyzed in the Legionella CAP group.
The two intervention studies were previously approved by the local Ethical Committee (EKBB, Ethikkommission beider Basel) and registered in the current controlled trials databases. The Institutional Review Board classified this retrospective analysis as a quality control study and waived the need for informed consent.
CAP was defined as the presence of an infiltrate on chest radiograph and at least one of the following signs and symptoms (cough, sputum production, dyspnea, core body temperature >38.0°C, auscultatory findings of abnormal breath sounds and rales . In all patients the Pneumonia Severity Index (PSI) and the CURB65 were calculated based on patients unique set of variables as described in detail elsewhere [20, 21]. The goldstandard for diagnosis of Legionella CAP was the clinical diagnosis of a community-acquired pneumonia with an infiltrate on chest X-ray and at least one positive microbiological test for Legionella (urinary antigen testing, culture results from respiratory specimen or PCR from respiratory specimen).
For our analysis, we used laboratory results including markers of infection (white blood count (WBC) and C-reactive protein (CRP)), liver enzymes (ALAT, ASAT, γ-glutamyltranspeptidase, alkaline phosphatase, bilirubin), markers of renal function (creatinine, urea), electrolytes (sodium, potassium), urinary testing for proteinuria and hemoglobinuria and results from arterial blood gas analysis (pH, PaO2) from the routinely collected blood analysis of all patients on admission. In our hospital, CRP concentrations are determined by an enzyme immunoassay having a detection limit of <5 mg/dl (EMIT, Merck Diagnostica, Zurich, Switzerland).
In the group of Legionella CAP Legionella spp. was diagnosed either by antigen in urine detection (Legionella pneumophila serogroup 1) using an immunoenzymetric commercial method (Legionella Urinary Antigen; Binax), by PCR from respiratory samples using an in-house PCR technique from the Institute for Medical Microbiology (IMM) in Zurich, Switzerland, or by culture [22, 23].
Discrete variables are expressed as counts (percentage) and continuous variables as medians and interquartile ranges (IQR). Frequency comparison was done by chi-square test. Two-group comparison of normally distributed data was performed by Students t-test. For data not normally distributed, the Mann-Whitney-U test was used. To estimate the potential clinical relevance of laboratory and clinical parameters to diagnose Legionella CAP, we used likelihood-ratio tests and univariate and multivariate logistic regression models. Thereby, outcomes were either Legionella CAP or non-Legionella CAP. For all independent variables in multivariate analysis, we calculated receiver-operating-characteristics (ROC) with the area under the ROC curve (AUC) being an overall diagnostic measure. For all calculations we used STATA 9.2 statistical software (Stata Corp, College Station, Tex). All testing was two-tailed and P-values less than 0.05 were considered to indicate statistical significance.
Baseline Characteristics of the 450 Patients with CAP separated by Legionella CAP (n = 82) and non-Legionella CAP (n = 368).
(n = 82)
(n = 368)
- Age (years)*
- Sex (male) – no. (%)
Coexisting illnesses – no. (%)
- Congestive heart disease
- Cerebrovascular disease
- Renal dysfunction
- Neoplastic disease
Clinical History – no. (%)
- Antibiotic pretreatment
- increase in sputum production
Clinical and laboratory findings
- Confusion – no. (%)
- Respiratory rate (breaths/minute)*
- Systolic blood pressure (mmHg)*
- Heart rate (beats/minute)*
- Body temperature (°C)*
- C-reactive protein (mg/L)*
- Procalcitonin (μg/L)*
- Hematocrit (%)*
- Leucocyte counts (×109/L)*
- Platelet counts (×109/L)*
- Sodium (mmol/L)*
< 131 mmol/L – no. (%)
- Creatinine (umol/L)*
- Urea (mmol/L)*
- Elevated liver enzymesb – no. (%)
- Creatinine kinase (U/L)*
- Lactate dehydrogenase (U/L)*
- Glucose (mmol/L)*
- Oxygen saturation (%)*
- PaO2 (kPa)*
- Hemoglobinuria – no. (%)
- Proteinuria – no. (%)
- PSIc Points*
Outcome – no. (%)
- Admission to ICUd
- Length of hospital stay (days)*
Results of microbiological tests (n = 164) in all patients with Legionella CAP (n = 82).
Established by \Etiologic Diagnosis
(n = 57)
L. pnb& L.
(n = 13)
(n = 12)
Urinary antigen testing (n = 72)
Positive (n = 59)
Negative (n = 13)
culture (n = 54)
Positive (n = 23)
Negative (n = 31)
PCRd (n = 38)
Positive (n = 34)
Negative (n = 4)
Diagnostic reliability of clinical and laboratory parameters
Prediction of Legionella CAP (n = 82) in univariate (a) and multivariate (b) logistic regression analysis
Elevated liver enzymes1
C-reactive protein (CRP)
C-reactive protein (CRP)
Area under the curve (AUC) of receiver operating curve (ROC) characteristic plot analysis.
Optimal cut off
Diagnostic accuracy of the diagnostic score at different cut off points.
The timely identification of Legionella in patients presenting with CAP to the emergency department is challenging because single clinical and laboratory parameters have shown low sensitivity and/or specificity. A reliable diagnostic score integrating different parameters is lacking . The results of this study indicate that six clinical and laboratory parameters, namely high body temperature, absence of sputum production, low serum sodium and platelet counts, and high LDH and CRP concentrations combined in a diagnostic score reliably estimate the likelihood of Legionella in patients who present with CAP to the emergency department.
Current guidelines on the management of patients with CAP recommend that empirical antibiotic coverage should be extended to Legionella in "suspicious cases", although no single parameter can reliably identify or rule out patients at risk for Legionella [8, 13]. Previous studies have addressed this dilemma and assessed potential predictors of Legionella CAP in different settings [1, 5–12]. A Spanish study found that Legionella should be suspected in middle-aged, alcohol drinking, healthy male patients, if patients lack response to previous beta-lactamic drugs, if headache, diarrhea, severe hyponatremia, and elevation in serum CK levels were present, or if no cough, expectoration, and thoracic pain were found . A recent critical review included 13 different studies that reported clinical details for the evaluation of Legionella CAP, however, concluded that using a syndromic approach cannot be recommended and, thus, an empiric antibiotic therapy covering for Legionella for all patients with CAP requiring hospitalization should be recommended . This, however, results in indiscriminate use of, mostly unnecessary, dual antibiotic therapy and thus, increased antibiotic exposure and emergence of resistance. Two previous studies have proposed a clinical prediction rule to identify Legionella CAP [5, 6]. The CBPIS score has been proposed with a maximum of 17 points based on the evaluation of temperature, serum creatinine, sodium and LDH concentrations, headache, vomiting and smoking. However, in a prospective validation study, this scoring system had a low sensitivity and/or specificity to diagnose or exclude Legionella CAP . Guidance of antibiotic therapy using this score would have left half of the patients with Legionella CAP without specific coverage and would have led to the administration of an unnecessarily broad antibiotic regimen in 14% of patients without Legionella. In addition, the model was unable to distinguish between Legionella pneumophila and Streptococcus pneumoniae, because the majority of patients were categorized into the "intermediate-probability" group. Similarly, the clinical criteria proposed by the Winthrop-University Hospital (WUH) for the identification of Legionellosis showed an inadequately low sensitivity and specificity of 78% . In addition, the WUH study included clinical data collected throughout the first 7 days of hospitalization limiting its use as a screening tool in an emergency department setting. Importantly, both studies based their scoring system on the comparison of Legionella CAP with pneumococcal CAP, which does not reflect the clinical situation in the emergency department, where the decision about empirical antibiotic therapy must be taken in all patients with CAP. In this study, a thorough and comprehensive 10 year retrospective data collection was conducted and data from two prospective studies presenting to the emergency department of the same institution were used to compare clinical and laboratory parameters. Thus we believe the proposed score reflects the clinical situation more realistically.
Simplicity of a diagnostic score is a major determinant for its future usefulness in daily practice. The WUH scale consists of 23 different criteria, which increases its complexity and may correlate with non-adherence as observed in clinical severity prediction scores [6, 24]. The herein proposed scoring system composes of only 6 routinely measured clinical and laboratory parameters that showed an independent predictive value in multivariate logistic regression analysis and a high overall diagnostic performance as demonstrated in ROC analysis.
As with any diagnostic score, the "optimal" cut off should be chosen based on the pretest probability and the clinical context, particularly the risk for adverse medical outcomes of patients. Supported by recent guidelines, treatment decision on the empirical antibiotic therapy should be based on both, the diagnostic probability and the risk of patients based on a prognostic assessment. Importantly, the PSI – but not the CURB65 score – showed a high prognostic accuracy to predict adverse medical outcomes in patients with Legionella CAP in this study. This finding is reassuring because prognostic CAP scores mainly depend on age and Legionella CAP patients tend to be younger. Thus, taking the diagnostic limitations of urinary antigen testing into account, empirical antibiotic therapy covering for atypical pathogens in patients with negative urinary antigen testing but high diagnostic probability (diagnostic score ≥ 4) may be advisable. Conversely, in low risk patients with low diagnostic probability (diagnostic score ≤ 1) and no clinical or diagnostic evidence of CAP caused by other atypical pathogens, macrolides may initially be withheld until the results of the urinary antigen tests become available.
Some limitations should be considered in interpreting our results. With a retrospective design, our results are preliminary and prospective validation is needed prior to a widespread use in clinical practice. The diagnosis of Legionella spp. in non-Legionella CAP patients was performed routinely by urinary antigen testing without PCR, culture or serology and we may have classified some patients incorrectly. Moreover there was no further routinely investigation for other atypical bacterial pathogens. We chose the 10 year retrospective design to provide the necessary number of Legionella cases to calculate multivariate analysis with adequate power. The proposed score consists of mainly objectively measurable parameters, which may robustly be ascertained in retrospect. Still, anamnestic parameters (i.e. absence of sputum production), even if highly available, may not be accurately assessed in retrospect and are thus underestimated in favour of laboratory parameters and clinical data.
In conclusion, the results of this study suggest that six clinical and laboratory signs embedded in a simple diagnostic score allow better differentiation of Legionella from unselected patients with non-Legionella CAP presenting to the emergency department. If confirmed in prospective studies, this score might improve the timing and choice of empirical antibiotic therapy and thus reduce the associated morbidity and mortality and the emergence of bacterial resistance.
We thank the staff of the clinics of emergency medicine, internal medicine and endocrinology and the department of clinical chemistry, notably Fausta Chiaverio, Martina-Barbara Bingisser, Maya Kunz, Vreni Wyss and Ursula Schild, for most helpful support during the study.
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