Wen Li and Fang Yuan contributed equally to this work.
Abkürzungen
BM
Bacterial meningitis
CRP
C-reactive protein
CSF
Cerebrospinal fluid
N-ICU
Neurological intensive care unit
PCT
Procalcitonin
Dear Editor,
The identification of pathogenic bacteria facilitates better targeted treatments for bacterial meningitis (BM). However, early differentiation of Gram-positive and Gram-negative BM is a persisting challenge, especially in patients with empiric antibiotic pretreatment. Serum procalcitonin (PCT) was reported to be associated with Gram-negative bacterium in bloodstream infections [1]. Our previous study demonstrated that CSF-PCT was a superior diagnostic biomarker for BM even in patients who had received empiric antibiotic pretreatment [2]. In this study, we aimed to evaluate the discriminative power of CSF-PCT for Gram-negative BM.
Anzeige
Consecutive patients with BM [3] admitted to neurological intensive care unit (N-ICU) at Xijing Hospital between October 2013 and April 2018 were included in this study. A total of 225 patients with suspected meningitis/encephalitis were screened. One hundred fourteen patients with tuberculous meningitis or viral meningitis/encephalitis or autoimmune encephalitis and 21 patients with unknown etiology were excluded. Ninety patients were diagnosed with BM, among them, 59 had definite pathogenic bacteria identified by CSF culture and Gram stain: 33 (56%) patients were Gram-positive, and 26 (44%) patients were Gram-negative (Additional file 1: Figure S1). Of these 59 patients, 25 (42%) cases were community-acquired and 34 (58%) cases were nosocomial BM (Additional file 1: Table S1). Bacterial etiologies were presented in Additional file 1: Table S2. All the participants had empiric antibiotic pretreatments before admission to our N-ICU. Demographics, severity, clinical characteristics, treatments, and the time from CSF-PCT test to onset of BM were balanced in Gram-positive group and Gram-negative group (Additional file 1: Table S3). The CSF-PCT level of Gram-negative patients was significantly higher than that of Gram-positive patients (0.5 [0.2–1.6] versus 0.1 [0.1–0.3] ng/ml, p < 0.001) (Table 1, Fig. 1). There were no significant differences of other biomarkers between Gram-positive and Gram-negative group (Additional file 1: Figure S2). CSF-PCT yielded an area under the curve (AUC) of 0.85 (95% CI, 0.73 to 0.93), which was superior to serum PCT, CSF/serum C-reactive protein (CRP) (Fig. 1).
Table 1
CSF and serum data
Total (n = 59)
Gram-positive (n = 33)
Gram-negative (n = 26)
P value
CSF
PCT, ng/mL
0.2 (0.1–0.5)
0.1 (0.1–0.3)
0.5 (0.2–1.6)
< 0.001
Leukocyte, cells/mm3
230.0 (99.0–1790.0)
214.0 (105.5–1970.0)
237.5 (56.0–1870.0)
0.54
Neutrophils, cells/mm3
154.1 (13.2–1432.0)
147.6 (7.0–1726.5)
165.0 (23.0–1768.9)
0.91
Lymphocyte, cells/mm3
50.4 (20.1–114.7)
52.1 (17.4–150.6)
44.3 (23.3–100.5)
0.71
Protein, g/L
1.6 (0.7–2.9)
1.6 (0.8–2.9)
1.6 (0.7–3.0)
0.95
Glucose, mg/dL
53.3 (37.3–72.0)
54.0 (38.9–74.7)
48.9 (34.7–69.4)
0.29
CRP, mg/L
0.3 (0.2–0.9)
0.3 (0.2–1.0)
0.3 (0.2–0.8)
0.82
First pressure, cmH2O
157.5 (130.0–230.0)
150.0 (127.5–205.0)
180.0 (142.5–285.0)
0.12
Last pressure, cmH2O
95.0 (70.0–130.0)
90.0 (70.0–128.8)
100.0 (72.5–167.5)
0.26
Serum
PCT, ng/mL
0.6 (0.1–3.1)
0.4 (0.1–4.3)
0.8 (0.1–2.7)
0.61
Leukocyte, cells/mm3
11.8 (7.8–14.9)
10.5 (7.0–14.6)
13.2 (9.4–15.0)
0.16
Glucose, mg/dL
144.5 (120.6–173.8)
142.2 (117.9–175.1)
147.6 (128.5–169.7)
0.34
CRP, mg/L
9.9 (2.2–59.3)
9.5 (2.0–52.9)
14.6 (2.3–68.0)
0.71
Albumin, g/L
33.9 ± 4.4
33.1 ± 4.7
34.9 ± 4.0
0.13
CSF/serum ratio
CSF/serum PCT ratio
0.7 (0.2–1.4)
0.7 (0.2–1.4)
0.7 (0.1–1.4)
0.75
CSF/serum glucose ratio
0.4 (0.3–0.5)
0.4 (0.3–0.5)
0.3 (0.2–0.4)
0.08
The CSF and serum samples were collected on the same day. Continuous variables were expressed as mean ± standard deviation (normally distributed), as medians and interquartile ranges (IQR, not normally distributed), which were compared using the Student t test or Mann-Whitney U test. The CSF and serum samples were collected on the same day
CSF cerebrospinal fluid, PCT procalcitonin, CRP C-reactive protein
Fig. 1
Diagnostic value of CSF-PCT for Gram-negative BM. a Levels of CSF-PCT in Gram-negative and Gram-positive BM. The red lines and blue squares correspond to the group interquartile ranges and averages, respectively. **P < 0.001. b ROC curves of CSF/serum PCT, CSF/serum CRP for predicting Gram-negative BM. CSF-PCT: AUC = 0.85 (95% CI, 0.73 to 0.93); serum PCT: AUC = 0.56 (95% CI, 0.42 to 0.69); CSF-CRP: AUC = 0.56 (95% CI, 0.42 to 0.70); serum CRP: AUC = 0.53 (95% CI, 0.39 to 0.67). Comparisons of AUC: CSF-PCT vs serum PCT, P < 0.0001; CSF-PCT vs CSF-CRP, P = 0.0034; CSF-PCT vs serum CRP, P = 0.0005
×
The early identification for the pathogenic bacteria of BM is of great importance to the rational use of antibiotics. However, meningitis with a negative Gram stain poses a diagnostic and therapeutic dilemma, especially in developing countries like China [4]. CSF and serum CRP were previously indicated to be associated with Gram-negative BM [5], but in patients with empiric antibiotic pretreatment, they were not informative any more. Our study indicated that CSF-PCT was a more robust and superior diagnostic biomarker for Gram-negative BM, even in patients who had received empiric antibiotic pretreatment.
Acknowledgements
None.
Funding
Wen Jiang obtained funding from the National Natural Science Foundation of China (grant 81771406) and Wen Li obtained funding from the Science and Technology Development Project of Shaanxi Province (grant 2016SF-084) for this work.
Anzeige
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
This study was based on a prospective non-interventional research on BM that registered in ClinicalTrials.gov (NCT02278016) and was approved by the ethics committee of Xijing Hospital (KY20140916-3). All procedures involving the patients complied with the ethical standards of the institutional and national research committees and with the 1975 Declaration of Helsinki and its later amendments.
Consent for publication
Yes.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
