- Research article
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Characteristics of neonates with culture-proven bloodstream infection who have low levels of C-reactive protein (≦10 mg/L)
BMC Infectious Diseases volume 15, Article number: 320 (2015)
Elevated C-reactive protein (CRP) level is widely used in clinical practice as a marker to distinguish between neonates with or without sepsis. However, some neonates with bacteremia have a CRP level within the normal range and they are not well characterized.
All episodes of neonatal culture-proven bloodstream infections (BSIs) between July 2004 and June 2012 were enrolled. Patients characteristics were compared for three CRP groups (low, ≤ 10 mg/L; intermediate, 11–100 mg/L; and high, > 100 mg/L) using the Chi-square test and one-way ANOVA. The sepsis-attributable mortality rates were compared using logistic regression analyses.
Of 986 episodes of neonatal BSI, 247 (25.1 %) had CRP ≤10 mg/L at the onset of clinical sepsis. In the low CRP group, patients had lower gestational age and birth weight, and an earlier occurrence of BSI. Patients with underlying gastrointestinal pathology, renal disorders, cholestasis, and pulmonary hypertension had a non-significant elevated CRP level at the onset of sepsis. In the blood culture of the low CRP group, coagulase-negative staphylococci (CoNS) were relatively more common (55.9 %, p < 0.001) than the other two groups, although one-fourth were infected with gram-negative bacilli (19.0 %), fungi (2.8 %), or polymicrobial pathogens (3.6 %). Of the BSIs with initial low CRP, 29.1 % were treated with inadequate antibiotics, 13.0 % progressed to septic shock, and 5.3 % had infectious complications. The sepsis-attributable mortality rate was lower in the low CRP group (4.9 %) than in the high CRP group (13.6 %).
A considerable proportion of neonatal BSIs had a normal or low initial CRP level (≤10 mg/L), which was more likely to occur in low birth weight or extremely preterm infants, those with earlier onset of sepsis, and those infected with CoNS. Plasma CRP level should not be used to rule out severe culture-proven sepsis or guide the empirical choice of antibiotics.
The incidence of culture-proven bloodstream infection (BSI) in the neonatal intensive care unit (NICU) is around 37 episodes per 10,000 neonate-hospital days [1–4]. Neonatal BSI is associated with significant morbidity, worse long-term outcomes, and a reported mortality rate of 12–20 % [1, 5–8]. Early and appropriate antibiotic treatment is the cornerstone of treatment [9, 10], which highlights the importance of a high index of suspicion based on clinical and laboratory parameters long before the blood culture results are known. However, some neonatal BSIs may present with nonspecific symptoms and several laboratory predictors have been investigated for better identification of bacteremia in the NICU [11–15].
C-reactive protein (CRP) is an acute-phase protein of hepatic origin that increases following interleukin-6 secretion from macrophages and T-cells [16, 17]. The synthesis of CRP in response to inflammation starts very rapidly, and serum concentration rises to > 5 mg/L after 6 h and peaks at 48 h [18, 19]. The CRP reference values in neonates reported in the literature are 1.5–20 mg/L and have a wide range of sensitivities and specificities [19, 20]. Although some studies have demonstrated that at least 2 CRP levels, both ≤ 10 mg/L and obtained 24 h apart, are needed to identify infants unlikely to be infected [19, 21], the high cut-off value associated with bacterial infection in neonates is still uncertain. Conversely, a small proportion of patients with bacteremia have CRP levels within the normal range [22, 23]. To date, this issue has not been well studied in the NICU. The present study was therefore conducted to characterize outcomes in neonates with culture-proven BSI and a CRP plasma level ≤ 10 mg/L.
We identified all episodes of culture-proven BSI in the NICU of Chang Gung Memorial Hospital (CGMH), a tertiary-level medical center in a university-affiliated teaching hospital in northern Taiwan, between 1 July 2004 and 30 June 2012. Only infants with late-onset sepsis, defined as clinical sepsis with a positive blood culture obtained after 3 days of life [1, 3, 24], were enrolled. The NICU has 3 units that include 49 beds equipped with mechanical ventilators and 28 beds in special-care nurseries. All babies under 34–35 weeks of completed gestation or birth weight < 2 kg or > 5 kg or those with any clinical signs of respiratory distress or cardiovascular, gastrointestinal, or neurological problems requiring surgical or intensive treatment were eligible for admission to our NICU. This study was approved by the institutional review board of Chang Gung Memorial Hospital, with a waiver of informed consent because all patient records/information was anonymized and de-identified prior to analysis.
Data retrieval and study database
Information for the NICU database was recorded by a full-time nurse specialist dedicated to following up neonates from birth (or admission if the neonate was transferred from another hospital) until discharge or death, and this nurse specialist has maintained the database every weekday for > 10 y. The NICU database contained information about basic demographic data, a summary of the patient’s hospital course, discharge diagnosis, and complications during prematurity. Medical records were reviewed to characterize the detailed courses of every episode of BSI, including the clinical manifestations, laboratory results, progression of septic conditions, concurrent infectious focus, treatment, infectious complications, and outcomes. The severity of illness was evaluated at the most severe period during the course of BSI using the neonatal therapeutic intervention scoring system (NTISS) .
An episode of BSI was defined according to the presence of clinical sepsis and identification of pathogens, which included any bacteria isolated from at least one blood culture and not pertaining to the saprophytic skin flora as significant. Growth of Corynebacterium spp., Propionibacterium spp., Penicillium spp., or Diphtheroids spp. in the blood cultures were considered contaminants and were excluded. The microbiology assay system in our hospital is a matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) system (Bruker’s flagship FLEX series). For coagulase-negative staphylococci (CoNS) BSI, the diagnosis required clinical signs of sepsis, a blood culture positive for CoNS, and administration of intravenous antibacterial therapy for at least 5 days after the blood culture or until death [1, 2, 7].
An episode of clinical sepsis was defined if a patient had a positive blood culture treated with antibiotic therapy for 5 or more days or treated for a shorter period if the patient died, and the presence of at least two of the following clinical symptoms of sepsis: fever or hypothermia, hyper- or hypoglycemia, apnea or tachypnea, frequent desaturation with an increased requirement for ventilator support, bradycardia and/or cyanosis, feeding intolerance, abdominal distension, seizure, decreased activity, skin mottling and hypotension [1, 7, 9].
All co-morbidities of prematurity, including respiratory distress syndrome (RDS), intra-ventricular hemorrhage (IVH), broncho-pulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), and peri-ventricular leukomalacia (PVL) were based on the latest updated diagnostic criteria . Congenital anomalies included all neonates with either documented or undocumented syndrome, chromosome abnormalities, and genetic or metabolic disorders, but not simple cleft palate or polydactyly. Persistent bacteremia or fungemia was defined as three or more consecutive positive blood cultures, at least 48 h apart, during a single episode of sepsis . All concurrent infectious foci, including NEC, ventilator associated pneumonia (VAP), catheter-related bloodstream infection (CRBSI), or meningitis were also recorded based on the strict diagnostic criteria of the Centers for Disease Control and Prevention and previous official publications [28, 29].
Infectious complications were defined as a new-onset infectious focus, empyema, abscess, venous thrombosis, or vegetation directly related to bacteremia or major organ dysfunction within 1 week after the onset of bacteremia. Empirical antibiotic therapy was considered inappropriate if the treatment regimen did not include at least 1 antibiotic active in vitro against the infecting microorganisms administered within 24 h of blood culture collection. For patients who died during hospitalization, the cause of death was recorded according to the clinician’s assessment. Sepsis-attributable mortality was defined as neonates who expired within 3 days after the onset of sepsis and those who died of infectious complications or clinically progressive deterioration following the onset of BSI.
Data on CRP
The CRP plasma level was measured with an immunoturbidimetric instrument (Modular P, Roche, Germany). We excluded episodes of BSI for which CRP was not measured on the date of BSI onset. If more than 1 CRP measurement was done on the date of BSI, we used the measurement conducted closest to the time when blood culture samples were drawn. In the laboratory, a CRP level ≤ 5 mg/L was considered within the normal range. The low limit of detection of CRP in our hospital is > 0.5 mg/L, and there is no upper limit of CRP detection. All BSI episodes were divided into 3 CRP groups: low (CRP ≤ 10 mg/L), intermediate (CRP 11–100 mg/L), and high (CRP > 100 mg/L).
The patient characteristics by CRP group were computed in contingency tables. Differences in categorical and continuous variables were tested by the χ2 test and one-way ANOVA, respectively. For continuous variables with large standard deviations, the nonparametric Kruskal–Wallis H test was applied. Trends in proportions of microorganisms in the 3 CRP groups were analyzed using the χ2 test for trend. Statistical significance was set at P < 0.05.
The sepsis-attributable mortality rate by CRP group was examined using a logistic regression model. Univariate and multivariate analyses, including the co-variables of sex, gestational age, underlying chronic co-morbidities, and bacterial subgroups, were performed. Because of the strong correlation between birth weight and gestational age, the risk factor of body weight at birth was excluded from the analysis. Estimates were expressed as odds ratios (ORs) with 95 % confidence intervals (CIs). All statistical analyses were performed using SPSS version 15.0 (SPSS, Chicago, IL, USA).
During the study period, 1010 episodes of BSI (late-onset sepsis) in 793 neonates from the NICU were identified. Those with incomplete medical records (n = 8), no CRP measurement at BSI onset (n = 12), or transfer to another hospital (n = 4) were excluded, leaving a total of 986 BSI episodes in 772 neonates. Among these, 247 (25.1 %) had a plasma CRP level ≤ 10 mg/L, 563 (57.1 %) had a plasma CRP level of 11–100 mg/L, and 176 (17.8 %) had a plasma CRP level > 100 mg/L.
Patients in the low CRP group had a lower birth body weight and gestational age and an earlier onset of BSI than patients in the intermediate and high CRP groups (Table 1). There were no significant differences in the perinatal history and most underlying chronic co-morbidities among the 3 CRP groups. However, patients with gastrointestinal pathology, pulmonary hypertension, renal disorders, or cholestasis were more likely to have high CRP at BSI onset. When the clinical symptoms or signs were compared, significantly more patients in the high CRP group had apnea, bradycardia with or without cyanosis, feeding intolerance, hyper- or hypoglycemia, or septic shock compared to those in the low CRP group (Table 1). These clinical symptoms were not significantly different between the low and intermediate CRP groups.
Episodes of BSI in the high CRP group had a significantly higher rate of abnormal laboratory findings, including leucopenia, anemia, thrombocytopenia, and metabolic acidosis compared to those in the low CRP group. The severity of illness, judged by NTISS score, was also significantly higher in the high CRP group than in the low CRP group. These demographics, clinical features, and laboratory findings were not significantly different between neonatal BSIs in the low and intermediate CRP groups as determined by post hoc analyses (data not shown). However, neonatal BSIs in the low CRP groups occurred significantly earlier than in both the intermediate and high CRP groups. Episodes of BSI with concurrent meningitis, ventilator-associated pneumonia, and catheter-related BSI also had elevated CRP at the onset of clinical sepsis (Table 1).
In the low CRP group, gram-positive, gram-negative, fungal, and polymicrobial pathogens accounted for 74.5, 19.0, 2.8, and 3.6 % of infections, respectively. CoNS was significantly more common in the blood cultures of the low CRP group compared to the other groups. A lower proportion of most gram-negative bacteria occurred in the low CRP group (Table 2). However, for gram-positive bacteria, there were significantly fewer patients with Group B Streptococcus BSI and comparable numbers of Staphylococcus aureus BSI in the low CRP group.
Of the 247 patients with an initial plasma CRP level ≤ 10 mg/L, 178 had at least 1 more CRP measurement during the days following BSI onset. Among these, 82 (46.1 %) developed a CRP response > 10 mg/L (median [IQR]: 35.0 mg/L [22.8–52.5 mg/L]) at a median of 2.8 days (range 1–7 days) after antibiotic treatment. Of the 138 episodes of CoNS BSI with an initial CRP plasma level ≤ 10 mg/L, 58 (42.0 %) were treated with initial antibiotics that were inadequate and had repeated positive blood cultures. Among the 96 episodes of neonatal BSIs with repeated CRP data that still had a CRP level ≤ 10 mg/L, 31 (32.3 %) had CoNS in their blood cultures.
Treatments and outcomes
Neonates who experienced BSI episodes and had higher CRP levels had significantly more invasive intubation or high-frequency oscillatory ventilator use (Table 3). The rates of inadequate antibiotic treatment were comparable among the 3 CRP groups. The overall sepsis-attributable mortality rate was 7.4 % and occurred in 4.9, 6.6, and 13.6 % in the low, intermediate, and high CRP groups, respectively. Neonates in the high CRP group had a significantly higher sepsis-attributable mortality compared with those in the intermediate and low CRP groups (P < 0.05 by log-rank test) (Fig. 1).
There was no difference in the sepsis-attributable mortality rate between those with CRP ≤ 10 mg/L and those with CRP of 11–100 mg/L. The CRP level was a predictor of sepsis-attributable mortality (OR 3.09, 95 % CI 1.50–6.37) in the high CRP group compared to the low CRP group. The difference between these 2 groups remained unchanged even after adjustments for birth weight, sex, gestational age, bacterial subgroups, and several underlying chronic morbidities (data not shown).
Approximately one-fourth of the cases of neonatal BSI—which is a surprisingly high proportion in the current cohort—had a CRP level of ≤ 10 mg/L at the onset of clinical sepsis. Low birth weight neonates, very low gestational age infants, and those in whom the occurrence of BSI episodes occurred earlier in life were more likely to have normal CRP at the onset of clinical sepsis. We found a high CRP level (>100 mg/L) was significantly associated with more severe clinical symptoms and worse outcomes. Although CoNS accounts for more than half of the episodes of BSI with normal CRP, in our cohort approximately one-fourth of those with normal CRP were infected with gram-negative bacteria, polymicrobial pathogens, or fungus. Furthermore, approximately 30 % of those with normal CRP were treated with inadequate initial antibiotics, and 13 % progressed to septic shock and 4.9 % had sepsis-attributable mortality.
It is reasonable to hypothesize that causative pathogens affect CRP level because some pathogens, especially gram-negative bacilli or Pseudomonas spp., tend to have a fulminant course [1, 7, 9], which can result in more severe tissue damage and inflammation. The findings here are consistent with a recent study conducted by Knudtzen et al., who found that CoNS BSI is more common in the low CRP group and that approximately 25–35 % of all CoNS BSI have normal CRP at the onset of clinical sepsis . Because drawing 2 sets of blood culture at the same time is not routinely done and the second blood culture may become negative if vancomycin was initially administrated, the lack of 2 positive blood cultures for documentation of CoNS BSI is a limitation of this study. Some possibly represent bacterial contaminations. To reduce the false positive cases of CoNS BSI, strict criteria for CoNS BSI have been applied, including requiring more than 2 septic symptoms or signs, as in previous studies [1, 2, 8]. Besides, more than three-fourths of the CoNS BSIs have elevated CRP or abnormal laboratory findings.
Because the initial symptoms of neonatal sepsis may be nonspecific and subtle and may become fulminant if appropriate antibiotics are not administered in time, the role of plasma CRP level in adequately predicting serious bacterial infection in neonates has recently become the topic of several studies [30–33]. Although we found that significantly more infectious complications and sepsis-attributable mortality occurred in the CRP group with > 100 mg/L, a possibly delayed elevation and inadequate sensitivity of CRP testing highlight the importance of investigating other predictors, including new laboratory markers [30–35] and clinical scores [36–38] and maintaining high alertness for the development of severe sepsis. Several studies report a sensitivity and specificity of 48–78 % and 71–88 %, respectively, for a single determination of CRP at 4–12 h after symptom onset [31–35]. Therefore, taken together, using the CRP level as a guide for empirical choice of antibiotics or to rule out serious infections or withhold antibiotic therapy is not recommended.
This study also investigated whether BSI episodes with initially low CRP levels developed a CRP response later. In contrast to a recent study in which 84 % of BSIs with initially normal CRP mounted a CRP response , the current study reveals that only 46 % have elevated subsequent CRP. This may be due to the high rate of initial effective antibiotic therapy and, possibly, the presence of CoNS as a low-level pathogenic bacterium that causes less tissue damage and inflammation. In a cohort of 60 neonates with early-onset sepsis, Ehl et al.  demonstrated that the CRP values decrease 16 h after successful antibiotic therapy. Some cases without CRP response in our cohort presented with a very fulminant course and hepatic failure, which was similar to a finding in a previous study .
The value of CRP as a predictive marker for bacterial infection in neonates has been studied with varying results [30–34, 38]. However, most of these studies focused on serious bacterial sepsis or critically ill neonates. This study aimed to characterize the NICU patients with normal or low CRP levels at the onset of sepsis and compared them with other neonates who had an elevated CRP level. We found the differences were most significant between neonatal BSIs in the low CRP group and those in the high CRP (>100 mg/L) group. The non-significant difference between the low CRP and the intermediate CRP groups by post hoc analyses (data not shown) implied that initial CRP level cannot be the sole predictor of final mortality. In this study, patients in the high CRP group treated with inappropriate antibiotics in the first 24 h were at especially higher risk of infectious complications and sepsis attributable mortality. However, those in the low CRP group had a relatively smooth clinical course even though they were initially treated with delayed effective antibiotics. Therefore, CRP still has a reference value as an indicator of severe infection.
We found that patients with lower gestational age or lower birth body weight tended to have a low CRP value at the onset of BSI. Because CRP is the end product of cytokine response after tissue injury, it is likely that extremely preterm or very low birth weight infants have less pronounced immunomodulatory or pre-inflammatory proteins after bacterial infection [41, 42]. Of interest, we found this cytokine response less severe in earlier life, but further investigation to validate these differences is required because the CRP level can also be affected by various factors, including pathogens, severity of illness, concomitant infectious focus, and some underlying chronic comorbidities.
There are some limitations in this study. Although a set of strict criteria was used to define true BSI, the lack of 2 positive blood cultures for CoNS as documentation of BSI is a weakness of this study. This was a retrospective, single-center cohort study, which inevitably restricts its generalizability compared to that of a prospective, multicenter study. The timing of blood sampling for culture and CRP also was not uniform because some septic work-up may be delayed because the initial septic symptoms were nonspecific and subtle. Furthermore, some CRP levels may have been falsely low because they were obtained too early before they started to rise around 4–6 h after sepsis onset. Lastly, a group with elevated CRP but without infection was not enrolled as controls. Thus, a prospective study is warranted to scientifically delineate the sensitivity and specificity of CRP as a predictive marker of neonatal sepsis.
Nearly one-forth of neonatal bloodstream infections had a normal or low initial CRP level (<=10 mg/L), which was more likely to occur in low birth weight or extremely preterm infants, those with earlier onset of sepsis, and those infected with coagulase-negative Staphylococcus. Although initial low CRP level was significantly with less severity of illness and better outcome, some critically ill neonates had CRP not significantly elevated at onset of sepsis. Therefore, plasma CRP level should not be used to rule out severe culture-proven sepsis or guide the empirical choice of antibiotics.
Center for disease control
Catheter-related bloodstream infection
Coagulase negative Staphylococcus
Central venous catheter
Group B streptococcus
Matrix-assisted laser desorption ionization time-of-flight
Neonatal intensive care unit
Neonatal therapeutic intervention scoring system
Respiratory distress syndrome
Total parenteral nutrition
Ventilator associated pneumonia (VAP)
Tsai MH, Hsu JF, Chu SM, Lien R, Huang HR, Chiang MC, et al. Incidence, clinical characteristics, and risk factors of adverse outcome in neonates with late-onset sepsis. Pediatr Infect Dis J. 2014;33:e7–13.
Makhoul IR, Sujov P, Smolkin T, Lusky A, Reichman B. Epidemiological, clinical, and microbiological characteristics of late-onset sepsis among very low birth weight infants in Israel: a national survey. Pediatrics. 2002;109:34–9.
Verstraete E, Boelens J, De Coen K, Claeys G, Vogelaers D, Vanhaesebrouck P, et al. Healthcare-associated bloodstream infections in a neonatal intensive care unit over a 20-year period (1992–2011): trends in incidence, pathogens, and mortality. Infect Control Hosp Epidemiol. 2014;35:511–8.
Stoll BJ, Hansen N, Fanaroff AA, Wright LL, Carlo WA, Ehrenkranz RA, et al. Late-onset sepsis in very low birth weight neonates: the experience of the NICHD Neonatal Research Network. Pediatrics. 2002;110:285–91.
Mitha A, Foix-L’Helias L, Arnaud C, Marret S, Vieux R, Aujard Y, et al. Neonatal infection and 5-year neurodevelopmental outcome of very preterm infants. Pediatrics. 2013;132:e372–80.
Stoll BJ, Hansen NI, Adams-Chapman I, Fanaroff AA, Hintz SR, Vohr B, et al. Neurodevelopmental and growth impairment among extremely low-birth-weight infants with neonatal infection. JAMA. 2004;292:2357–65.
Tsai MH, Chu SM, Lee CW, Hsu JF, Huang HR, Chiang MC, et al. Recurrent late-onset sepsis in the neonatal intensive care unit: incidence, clinical characteristics, and risk factors. Clin Microbiol Infect. 2014;20:O928–35.
Padula MA, Dewan ML, Shah SS, Padula AM, Srinivasan L, McGowan KL, et al. Risk factors associated with laboratory-confirmed bloodstream infections in a tertiary neonatal intensive care unit. Pediatr Infect Dis J. 2014;33:1027–32.
Tsai MH, Chu SM, Hsu JF, Lien R, Huang HR, Chiang MC, et al. Risk factors and outcomes for multidrug-resistant Gram-negative bacteremia in the NICU. Pediatrics. 2014;133:e322–9.
Tsai MH, Chu SM, Hsu JF, Lien R, Huang HR, Chiang MC, et al. Breakthrough bacteremia in the neonatal intensive care unit: incidence, risk factors, and attributable mortality. Am J Infect Control. 2015;43:20–5.
Escobar GJ, Puopolo KM, Wi S, Turk BJ, Kuzniewicz MW, Walsh EM, et al. Stratification of risk of early-onset sepsis in newborn ≧ 34 weeks’ gestation. Pediatrics. 2014;133:30–6.
Schlapbach LJ, Graf R, Woerner A, Fontana M, Zimmermann-Baer U, Glauser D, et al. Pancreatic stone protein as a novel marker for neonatal sepsis. Intensive Care Med. 2013;39:754–63.
Mikhael M, Brown LS, Rosenfeld CR. Serial neutrophil values facilitate predicting the absence of neonatal early-onset sepsis. J Pediatr. 2014;164:522–8.
Olaciregui I, Hernandez U, Munoz JA, Emparanza JI, Landa JJ. Markers that predict serious bacterial infection in infants under 3 months of age presenting with fever of unknown origin. Arch Dis Child. 2009;94:501–5.
Verstraete EH, Blot K, Mahieu L, Vogelaers D, Blot S. Prediction models for neonatal health care-associated sepsis: a meta-analysis. Pediatrics. 2015;135:e1002–14.
Worthmann H, Tryc AB, Dirks M, Schuppner R, Brand K, Klawonn F, et al. Lipopolysaccharide binding protein, interleukin-10, interleukin-6 and C-reactive protein blood levels in acute ischemic stroke patients with post-stroke infection. J Neuroinflammation. 2015;12:13.
Cekic C, Arabul M, Alper E, Pakoz ZB, Saritas E, Yuksel, et al. Elevation of the relationship between serum ghrelin, C-reactive protein and interleukin-6 levels, and disease activity in inflammatory bowel diseases. Hepatogastroenterology. 2014;61:1196–200.
Povoa P. C-reactive protein: a valuable marker of sepsis. Intensive Care Med. 2002;28:235–43.
Hofer N, Zacharias E, Muller W, Resch B. An update on the use of C-reactive protein in early-onset neonatal sepsis: current insights and new tasks. Neonatology. 2012;102:25–36.
Chiesa C, Panero A, Osborn JF, Simonetti AF, Pacifico L. Diagnosis of neonatal sepsis: a clinical and laboratory challenge. Clin Chem. 2004;50:279–87.
Hengst JM. The role of C-reactive protein in the evaluation and management of infants with suspected sepsis. Adv Neonatal Care. 2003;3:3–13.
Knudtzen FC, Nielsen SL, Gradel KO, Lassen AT, Kolmos HJ, Lensen TG, et al. Characteristics of patients with community-acquired bacteremia who have low levels of C-reactive protein (<=20 mg/L). J Infect. 2014;68:149–55.
Benitz WE, Han MY, Madan A, Ramachandra P. Serial serum C-reactive protein levels in the diagnosis of neonatal infection. Pediatrics. 1998;102:E41.
Berardi A, Rossi C, Guidotti I, Vellani G, Lugli L, Bacchi Reggiani ML, et al. Factors associated with intrapartum transmission of group B streptococcus. Pediatr Infect Dis J. 2014;33:1211–5.
Gray JE, Richardson DK, McCormick MC, Workman-Daniels K, Goldmann DA. Neonatal therapeutic intervention scoring system: a therapy-based severity-of-illness index. Pediatrics. 1992;90:561–7.
Gleason CA, Devaskar SU. Avery’s disease of the newborn. 9th ed. Philadelphia, PA: Elsevier Saunders; 2011.
Horan TC, Andrus M, Dudeck MA. CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting. Am J Infect Control. 2008;36:309–32.
Apisarnthanarak A, Holzmann-Pazgal G, Hamvas A, Olsen MA, Fraser VJ. Ventilator-associated pneumonia in extremely preterm neonates in a neonatal intensive care unit: characteristics, risk factors and outcomes. Pediatrics. 2003;112:1283–9.
Tsai MH, Lien R, Wang JW, Huang HR, Chiang CC, Chu SM, et al. Complication rates with percutaneously central venous catheters inserted at femoral and non-femoral sites in very low birth weight infants. Pediatr Infect Dis J. 2009;28:966–70.
Keane M, Fallon R, Riordan A, Shaw B. Markedly raised levels of C-reactive protein are associated with culture proven sepsis or necrotizing enterocolitis in extremely preterm neonates. Acta Paediatr. 2015;104:e289–e293.
Enguix A, Rey C, Concha A, Medina A, Coto D, Dieguez MA. Comparison of procalcitonin with C-reactive protein and serum amyloid for the early diagnosis of bacterial sepsis in critically ill neonates and children. Intensive Care Med. 2001;27:211–5.
Stein M, Schachter-Davidov A, Babai I, Tasher D, Somekh E. The accuracy of C-reactive protein, procalcitonin, and s-TREM-1 in the prediction of serious bacterial infection in neonates. Clin Pediatr (Phila). 2015;54:439–44.
Andreola B, Bressan S, Callegaro S, Liverani A, Plebani M, Da Dalt L. Procalcitonin and C-reactive protein as diagnostic markers of severe bacterial infections in febrile infants and children in the emergency department. Pediatr Infect Dis J. 2007;26:672–7.
Chacha F, Mirambo MM, Mushi MF, Karange N, Zuechner A, Kidenya BR, et al. Utility of qualitative C-reactive protein assay and white blood cells counts in the diagnosis of neonatal septicaemia at Bugando Medical Centre, Tanzania. BMC Pediatr. 2014;14:248.
Laborada G, Rego M, Jain A, Guliano M, Stavola J, Ballabh P, et al. Diagnostic value of cytokines and C-reactive protein in the first 24 hours of neonatal sepsis. Am J Perinatol. 2003;20:491–501.
Hsu JF, Chu SM, Huang YC, Lien R, Huang HR, Lee CW, Chiang MC, Fu RH, Tsai MH. Predictors of clinical and microbiological treatment failure in neonatal bloodstream infections. Clin Microbiol Infect. 2015;21:482.e9–482.e17.
Mahieu LM, De Muynck AO, De Dooy JJ, Laroche SM, Van Acker KJ. Prediction of nosocomial sepsis in neonates by means of a computer-weighted bedside scoring system (NOSEP score). Crit Care Med. 2000;28:2026–33.
Luzzani A, Polati E, Dorizzi R, Rungatscher A, Pavan R, Merlini A. Comparison of procalcitonin and C-reactive protein as markers of sepsis. Crit Care Med. 2003;31:1737–41.
Ehl S, Gehring B, Pohlandt F. A detailed analysis of changes in serum C-reactive protein levels in neonates treated for bacterial infection. Eur J Pediatr. 1999;158:238–42.
Amon S, Litmanovitz I, Regev R, Lis M, Shainkin-Kestenbaum R, Dolfin T. The prognostic virtue of inflammatory markers during late-onset sepsis in preterm infants. J Perinat Med. 2004;32:176–80.
Skogstrand K, Hougaard DM, Schendel DE, Bent NP, Svaerke C, Thorsen P. Assocation of preterm birth with sustained postnatal inflammatory respones. Obstet Gynecol. 2008;111:1118–28.
Dembinski J, Behrendt D, Martini R, Heep A, Bartmann P. Modulation of pro- and anti-inflammatory cytokine production in very preterm infants. Cytokine. 2003;21:2006.
All authors thank Mrs. Chiao-Ching Chiang for keeping the database of our NICU, and all nursing staff working in our NICUs for keeping extremely detailed patient records, which contributed greatly to the completion of this research. We want to thank Miss Chun-Chun Cheng and Mr. Yu-Jr Lin for statistical consultation, who was supported by grants from Biostatistical Center for Clinical Research, Chang Gung Memorial Hospital (CLRPG340599).
The authors declare that they have no competing interests.
M-YL: Dr. Lai conceptualized and designed the study, drafted the initial manuscript, and approved the final manuscript as submitted. M-HT: Dr. Tsai took care of these patients, collected and verified the data and had been involved in drafting the manuscript. C-WL: Dr. Lee designed the data collection instruments, coordinated and supervised data collection, and had been involved in drafting the manuscript. M-CC: Dr. Chiang took care of these patients, helped data verification, and had been involved in drafting the manuscript. RL: Dr. Lien took care of these patients, approved the agreement of interstitial review board, and had been involved in drafting the manuscript. R-HF: Dr. Fu took care of these patients, helped data verification, and had been involved in drafting the manuscript. H-RH: Dr. Huang took care of these patients, carried out the initial analyses, and had been involved in drafting the manuscript. S-MC: Dr. Chu took care of these patients, collected and verified the data, critically reviewed the manuscript, revised the manuscript, and approved the final manuscript as submitted J-FH: Dr. Hsu critically reviewed the manuscript, revised the manuscript, and approved the final manuscript as submitted. All authors have read and approve of the final version of the manuscript.
About this article
- Neonatal Intensive Care Unit
- Positive Blood Culture
- Chang Gung Memorial Hospital
- Clinical Sepsis
- Neonatal Intensive Care Unit Patient