A composite score combining procalcitonin, C-reactive protein and temperature has a high positive predictive value for the diagnosis of intensive care-acquired infections
© Robriquet et al.; licensee BioMed Central Ltd. 2013
Received: 13 March 2012
Accepted: 4 March 2013
Published: 2 April 2013
Nosocomial infection diagnosis in the intensive care unit (ICU) remains a challenge. We compared routine measurements of procalcitonin (PCT), C-reactive protein (CRP), white blood cell count (WBC) and temperature in the detection of ICU-acquired infections.
Prospective observational cohort study in a University hospital Medicosurgical ICU. All patients admitted to the ICU ≥ 5 days (n = 141) were included into two groups, either infected (documented infection, n = 25) or non-infected (discharged from the ICU without diagnosis of infection, n = 88).
PCT, CRP, WBC and temperature progression from day −4 (D-4) to day 0 (D0) (day of infection diagnosis or ICU discharge) was analysed. Differences (Δ) were calculated as D0 levels minus the lowest preceding value. D0 PCT and CRP were significantly increased in infected compared to non-infected patients (median, 1st and 3rd quartiles): 3.6 ng/mL (0.92-25) for PCT, 173 mg/L (126–188) for CRP versus 0.02 ng/mL (0.1-0.9) and 57 mg/mL (31–105) respectively (p < 0.0001). In multivariate analysis, D0 temperature > 38.6°C, PCT > 1.86 ng/mL, and CRP > 88 mg/L, performed well (AUCs of 0.88, 0.84, and 0.88 respectively). The sensitivity/specificity profiles of each marker (76%/94% for temperature, 68%/91% for PCT, and 92%/70% for CRP) led to a composite score (0.068 × D0 PCT + 0.005 × D0 CRP + 0.7 × temperature) more highly specific than each component (AUC of 0.90 and sensitivity/specificity of 80%/97%).
Combining CRP, PCT and temperature is an approach which may increase of nosocomial infection detection in the ICU.
KeywordsNosocomial infection Procalcitonin C-reactive protein Intensive care unit
Early identification of nosocomial infections is crucial to therapeutic decision-making, allowing both early antimicrobial therapy and source eradication which determine outcome . However, early discrimination between sepsis due to nosocomial infection (NI) and systemic inflammatory response syndrome (SIRS) is challenging in clinical practice. Indeed, in early sepsis, clinical signs related to the focus of infection may be minimal or obscured by non-specific symptoms of SIRS common to various non-infectious inflammatory conditions. Definitive diagnosis of infection is defined as the identification of pathogens in a biological sample from a normally sterile tissue or fluid . However, this definition still relies on clinical suspicion of infection since colonizing pathogens may be present without leading to the pathogen-related damage which defines infection . The reliance of diagnosis on clinical suspicion rather than identification of pathogens is particularly true for nosocomial infection which occurs in hospitalized patients, increasingly colonized by various pathogens over time. This absence of any “gold-standard” of infection (with some exceptions such as bacterial meningitis, fungemia etc.…) has resulted in a decades-long quest for biomarkers of infection capable of assisting or even redefining the diagnosis of infection.
In the ICU, early, sensitive, and specific laboratory tests would be crucial to guide clinicians in identifying infected patients who could benefit from prompt empirical antibiotic therapy and to avoid unnecessary antibiotic treatments.
The aim of our prospective cohort study was to test the hypothesis that inflammatory biomarkers procalcitonine (PCT) and C-reactive protein (CRP), in addition to routine biomarkers such as white blood-cell count (WBC) and clinical markers such as fever, could assist in the early identification of patients with ICU-acquired nosocomial infection.
Study design and inclusion criteria
This prospective observational study was conducted in a 16-bed medico-surgical university ICU from July 2007 to March 2008. Ethics committee approval was obtained from the French Society of Intensive Care Medicine (SRLF-CE-157) for our trial and written informed consent was obtained from each patient or designated surrogate. All patients who were aged > 18 years admitted the ICU for more than 4 days were eligible. Only the first admission to the ICU was recorded. Patients were excluded if they were pregnant, already included in another trial, or undergoing care limitation or withdrawal.
Clinically suspected VAP was defined as a new or persistent pulmonary infiltrate on the chest radiograph, with at least two of the following criteria: (i) temperature > 38°C or < 36°C; (ii) WBC > 10 or < 4 × 103/mm3; (iii) purulent tracheal aspirate [3, 4]. Microbiological confirmation was defined by the presence of at least one potentially pathogenic microorganism in respiratory samples according to predefined thresholds (bronchoalveolar lavage fluid samples yielding 104 CFU/mL or tracheal aspirates yielding 106 CFU/mL).
Bloodstream infection (BSI) was defined as the occurrence of infection associated with one or more positive blood culture results unrelated to an infection incubating at ICU admission. In case of coagulase-negative Staphylococci, two positive blood cultures on separate occasions within a 48-hrs period, and confirmation of clinical significance by the attending intensivist were required for diagnosis of bacteremia . All Other ICU-acquired infections were defined according to the modified Centre for Disease Control and Prevention criteria . Blood cultures were routinely performed when the patients' temperature was ≥ 38.5°C or < 36°C or when infection was suspected on clinical grounds.
SIRS was diagnosed in the presence of more than one of the following clinical findings: (i) body temperature higher than 38°C or lower than 36°C, (ii) heart rate higher than 90 beats per min, (iii) hyperventilation evidenced by respiratory rate higher than 20/min or arterial partial pressure of carbon dioxide (PaCO2) lower than 32 mmHg, (iv) WBC higher than 12 000 cells/μL or lower than 4 000 cells/μL.
Study design and data collection
We followed a previously described design and protocol for data collection . Briefly, “non-infected” patients had no bacteriological or clinical signs of nosocomial infections and “infected” patients were those with ICU-acquired, therefore nosocomial, infection. For analysis, only the first episode of nosocomial infection was considered. Day 0 (D0) was defined as the day of nosocomial infection diagnosis for infected patients or the day of ICU discharge for non-infected patients. Daily values of PCT, CRP, temperature, WBC and SOFA score from four days prior to day 0 (D-4) up to day 0 (D0) ware collected and analysed comparing infected and non-infected patients. For comparisons, daily values on D0 and D-4 were considered as well as biomarker variations over time (ΔPCT and ΔCRP) calculated as the difference between D0 value minus the lowest PCT and CRP value over the previous 4 days.
Collected data included age, gender, admission diagnosis, systemic inflammatory response syndrome (SIRS), Simplified Acute Physiology Score II (SAPS II), Sequential Organ Failure Assessment (SOFA) score, central vein catheterization and dwell time, mechanical ventilation and duration, anti-infectious treatment, ICU length of stay and patient outcome . PCT, CRP and WBC were measured at admission and daily until ICU discharge or death in all patients. Body temperature was measured every three hours and daily lowest and highest values were recorded. Patients were assessed daily for clinical evidence of infection, and appropriate samples for bacteriological cultures were collected whenever infection was suspected.
Blood samples were obtained from an arterial line upon admission and subsequently daily at 07:00. PCT was measured by time-Resolved Amplified Cryptase Emission technology in a Kryptor® analyser (Brahms Diagnostica, Berlin, Germany). The sensitivity of the assay was 0.05 ng/mL. CRP was measured by an immunoturbidimetric assay (Advia 2400, Bayer Diagnostics, Tarrytown, NY). WBC was quantified by the hospital hematology laboratory using an automated cell analyser (XE 20100, Sysmex, Japan).
All results are presented as number (percentage) for categorical variables and median and 25th/75th percentiles for quantitative variables (data non-normally distributed). The Kolmogorov-Smirnov test was used to assess sample distributions. Continuous variables were compared using the Mann–Whitney (2-group comparison) or Kruskall Wallis (multiple-group comparison) non-parametric tests. Categorical variables were compared with the χ2 or the Fisher’s exact test, as appropriate. All p values were two-tailed. Statistical significance was defined as p < 0.05. Time-dependent analysis of different variables was performed with a general linear model, univariate repeated-measures analysis using a split-plot design approach. We studied PCT, CRP, temperature, WBC at D0 and D-4, the ΔPCT and ΔCRP in a univariate analysis. Multivariate regression logistic analysis was used to determine values independently associated with ICU-acquired infection and Odds ratio (OR) with 95% confidence interval (CI) were calculated. Receiver–operating characteristic (ROC) curves and the areas under the curve (AUC) were determined for PCT, CRP, temperature, WBC at D0 and for the ΔPCT and ΔCRP. The AUC values are reported with the 95% confidence interval. In medical practice, a diagnostic test with an AUC < 0.75 would be regarded as non contributive. Sensitivities, specificities, positive predictive values and negative predictive values were calculated from cross-tabulations. A composite score was determined using the best values predicting nosocomial infection. Statistical analyses were performed using the SAS software version 8.2 (SAS Institute Inc., Cary, NC, USA).
During the study period, 267 patients were admitted to our ICU. One hundred and twenty-six patients were excluded (24 obstetrical patients, 8 patients under 18 years of age, 81 patients who stayed less than 4 days, and 4 patients who had treatment limited or withdrawn). One hundred and forty-one patients were included in the study, 116 non-infected among which 88 were non-infected and discharged alive from the ICU. Twenty-five patients were diagnosed with infections acquired in the ICU.
Characteristics of the 113 studied patients during ICU stay
Characteristics of patient population
NI - (88)
NI + (25)
SAPS II score at admission
Admission diagnosis, n (%)
Acute respiratory failure
Site of infection, n (%)
Catheter related infection
Delay of NI, days
Number of days without antibiotics before NI
Central venous catheter, n (%)
Duration of central venous catheter, days
MV, n (%)
Duration of MV, days
Length of ICU stay, days
Results of univariate analysis
NI - (88)
NI + (25)
PCT D-4 (ng/mL)
PCT D0 (ng/mL)
CRP D-4 (mg/L)
CRP D0 (mg/L)
WBC D-4 (cells/mm3)
WBC D0 (cells/mm3)
Temperature D-4 (°C)
Temperature D0 (°C)
Results of multivariable logistic regression model
95% confidence interval
PCT D0 (ng/mL)
1.03 – 1.16
Température D0 (°C)
1.53 – 6.14
1 – 1.03
Diagnosis accuracy of serum PCT, CRP, WBC, body temperature, ΔCRP and ΔPCT for diagnosis of ICU-acquired infection
Composite score D0
By studying simple and routinely used clinical and biological markers of infection in patients with confirmed nosocomial infection compared to non-infected ICU patients we determined that three parameters, temperature > 38.6°C, PCT > 1.86 ng/mL, and CRP > 88 mg/L, could perform well in discriminating infected from non-infected patients (AUCs of 0.88, 0.84, and 0.88 respectively). The complementary sensitivity/specificity profiles of each marker (76%/94% for fever, 68%/91% for PCT, and 92%/70% for CRP) allowed the construction of a composite score (score = 0.068 × D0 PCT + 0.005 × D0 CRP + 0.7 × temperature) more discriminating and highly specific than each single component (AUC of 0.90 and sensitivity of 97%).
Given the absence of any gold standard of infection we used the same methodology as Povoa et al.  and distinguished between patients with a confirmed diagnosis of noscomial infection, with all the limitations inherent to diagnosis of infection in the ICU, and patients discharged from the ICU without being treated by antimicrobials and therefore very unlikely to be infected.
Although one of the most frequently measured parameters in the ICU setting and non invasive, body temperature remains a poor indicator of infection . Temperature can be influenced by a number of non-infectious factors, such as non-infectious causes of fever and antipyretic therapy . Nevertheless, in the present study, temperature appeared to perform reasonably well for identifying nosocomial infection, with an AUC of 0.88. The best temperature cut-off value was 38.6°C, resulting in a sensitivity-specificity of 76%/94%.
Our data support the view of some authors that leucocyte count has little value in discriminating patients with nosocomial infection . In our study, AUC of WBC was 0.62, indicating that WBC was close to the line of non discrimination.
PCT is secreted as part of the systemic inflammatory response to infection and serum values are greatly based on the type and severity of infection. Interpretation of the literature is further complicated by frequent discrepancies or variations in the choice of the cut-off value of PCT, etiologies of infection, severity of infection, and study populations [11, 12]. Serum values of PCT vary greatly based on the type and severity of infection. The highest PCT concentrations have been reported in patients with septic shock, and patients with severe sepsis had significantly higher PCT levels than patients with sepsis or SIRS .
In the present study, we used an ultrasensitive assay for PCT, capable of measuring low levels to identify even “subclinical” inflammatory states before the development of clinically evident sepsis. The best cut-off value of PCT for identifying ICU-acquired infection was 1.86 ng/mL, with high specificity (91%) but low sensitivity (68%).
Few studies have analysed the behaviour of PCT in nosocomial ICU-acquired infection. In cardiac surgery patients, PCT measurement was found a reliable marker for diagnosis of infection: with a cut-off of 1 ng/mL allowing a sensitivity of 85% and a specificity of 95% . In another study, PCT was useful in the diagnosis of VAP with a cuff-off value of 3.9 ng/mL allowing a specificity of 100% at the cost of a sensitivity of 41% .
In a recent study assessing PCT monitoring in the early diagnosis of nosocomial infection, PCT at D0 was the best predictor of proven infection. A cut-off value of 0.44 ng/mL provided sensitivity and specificity of 65.2% and 83%, respectively for discriminating patients with proven nosocomial infection from clinically suspected but non-proven nosocomial infection .
Several reports suggested that PCT should replace CRP as a marker of infection in the ICU setting [17, 18]. In certain situations, especially to differentiate bacteremic from non-bacteremic infections, PCT was reported to be superior to CRP . A cut-off value of 0.4 ng/mL was associated with a negative predictive value of 98%. However, well-designed studies have shown that PCT is neither a better nor an earlier diagnostic marker of infection than CRP [20–22].
In a previous meta-analysis performed by Tang et al., PCT could not reliably differentiate sepsis from other non-infectious causes of systemic inflammatory response syndrome in critically ill adult patients . On the other hand, in another review, PCT concentration was found to be better than CRP for diagnosis of bacterial infection . However, this review included studies across a wide range of age group, clinical setting and spectrum diseases: 46% were paediatric patients and 57% did not have SIRS. Additionally, in some clinical situations of infectious origin commonly found in ICU, PCT can be normal or even undetectable early course of infections , localised infections , or subacute endocarditis [19, 26, 27].
CRP is an acute-phase protein, member of the pentraxin family of proteins, whose hepatic synthesis is triggered by cytokine release due to any cause of inflammation, infectious or not. In the present study, CRP D0 had the highest AUC (0.88) and a cut-off of 88 mg/L had a sensitivity of 92% and a specificity of 70% to identify patients with ICU-acquired infection. Povoa et al. studied the role of CRP to detect infections in critically ill patients . In that study, the combination of CRP > 87 mg/L and body temperature > 38.2°C was associated with infection diagnosis with a specificity of 100%. A study using the methodology we based our study upon, found that daily CRP monitoring could be used as a marker of infection prediction . Patients presenting maximum daily CRP variation > 4.1 mg/dL and a CRP level > 87 mg/L had an 88% risk of infection.
As all preceding studies we have confirmed that no single parameter or biomarker can reliably assist the clinician in diagnosing infection in the ICU. This is most probably due to: the lack of any possible gold standard for the diagnosis of infection and the extreme heterogeneity of infection in the ICU as to causal pathogen, underlying diseases, host-response, therapy, evolution and outcome. Facing these problems, our subsequent combination of diagnostic makers appears a useful approach to improve the accuracy in diagnosing nosocomial infection in ICU patients. Our results showed that combining PCT, CRP and temperature D0 was discriminant (highest AUC = 0.90) and highly specific (specificity of 97%). We found in our study a complementarity of CRP and PCT, with low specificity/high sensitivity for PCT and high sensitivity/low specificity for CRP. Such a combined clinical and multibiomarker approach for prediction has been proposed in another highly heterogenous complex disease in the ICU: adult respiratory distress syndrome (ARDS). Ware et al., studying the prediction of mortality in the ARDS cohort from the NHLBI studies, found that a combination of biomarkers and clinical predictors was superior to clinical predictors or biomarkers alone .
Some limitations of the present investigation should be noted. Our findings are based on a single centre study, one should be cautious in or extrapolating these data. Our findings cannot be generalised to specific diseases (pancreatitis, burns) or settings (cardiovascular surgical patients, neonatal/paediatric patients). Due to our study design, our findings might be only applicable to patients with late-onset nosocomial infection. Likewise, our focus on late-onset nosocomial infection led to a small number (17%) of documented infections which could also be a limitation.
It must also be acknowledged that CRP at D0 had a negative predictive value higher than our composite score (97% vs. 94%), showing that low CRP, under the threshold of 88 mg/L could assist clinicians in eliminating the diagnosis of nosocomial infection. However, the composite score had by far the highest positive predictive value (87% vs. 47%), suggesting that it could best be used in encouraging clinicians to initiate antimicrobial therapy when faced with a suspected diagnosis of nosocomial infection and a CRP over 88 mg/L.
The sequential measurements of serum PCT and CRP might be reliable and complementary biomarkers in early identification of ICU-acquired nosocomial infection. Combining CRP and PCT levels with temperature is an original approach which may increase diagnostic specificity. More prospective and large-scale studies are required to define the best approach.
Intensive Care Unit
Systemic inflammatory response syndrome
White blood cell count (WBC)
Sequential Organ Failure Assessment score.
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