Abstract
Background:
Intracranial complications of bacterial meningitis can arise at any stage and may necessitate neurosurgical intervention. This study evaluates clinical, laboratory, and imaging findings predictive of surgical need in these cases.
Methods:
Between 2013 and 2023, 52 pediatric patients with severe neurological symptoms due to bacterial meningitis were admitted to PICU at Van Training and Research Hospital. Patients were classified into two groups: those with intracranial complications (Group 1, nā=ā36) and those without (Group 2, nā=ā16). Group 1 was further divided into those requiring surgery (Group 1B, nā=ā9) and those not (Group 1A, nā=ā27). Statistical analyses were conducted.
Results:
Among 52 patients (67.3% male, mean age 76.7ā±ā72.0 months), 36 (69.2%) developed intracranial complications, and 9 (17.3%) required surgery. CRP levels were significantly higher in Group 1B (226ā mg/dl) than in Group 1A (63ā mg/dl) (pā<ā0.001). Significant differences were also found in CSF protein/glucose ratio (pā=ā0.011) and CSF glucose levels (pā=ā0.049). Subdural empyema (SDE) developed in 25 cases, with single-area involvement significantly more frequent in surgical cases (77.8% vs. 12.5%, pā=ā0.012). ROC analysis was performed for CSF protein/glucose, CSF glucose, and serum CRP values.
Conclusion:
CRP >150ā mg/dl, CSF glucose <6.75ā mg/dl, and protein/glucose ratio >18.9 indicate high surgical risk. MRI is recommended for localization, with early neurosurgical consultation and multidisciplinary management for cases with single-area empyema.
1 Introduction
Bacterial meningitis (BM) in children is a common and destructive disease of the central nervous system, caused by various pathogens leading to inflammation of the meninges. The main clinical features of the disease include fever, increased intracranial pressure, meningeal irritation, and purulent changes in the cerebrospinal fluid (CSF) (, ).
Achieving favorable neurological outcomes in BM relies on early diagnosis, rapid medical treatment, and timely detection of the need for surgical intervention to commence drainage (ā). A multidisciplinary approach involving a pediatric intensive care specialist, neurosurgeon, neurologist, and physical medicine and rehabilitation specialist is recommended for managing potential neurological complications and surgical needs under intensive care conditions (, ).
Throughout the literature, various scoring systems and predictive models have been developed to foresee mortality and sequels in BM prognosis from ancient times to the present (ā). However, there are no scoring and predictive models specifically designed to identify cases of BM that might require surgical intervention.
The primary objective of this study is to identify early predictive markersāspecifically laboratory and CSF parameters obtained at initial admissionāthat may help clinicians recognize the presence of intracranial complications (ICCs) and estimate their potential severity, including the likelihood of requiring surgical intervention. By highlighting these parameters, we aim to assist physicians in making timely decisions regarding neuroimaging, treatment planning, and intensive monitoring in a pediatric critical care setting.
2 Methods
Our study retrospectively examined the records of 52 patients aged 1 month to 18 years, who were diagnosed with meningitis based on clinical, laboratory, and MRI findings between January 2013 and January 2023 at the pediatric intensive care unit.
Patients were included in the study in accordance with WHO meningitis diagnostic criteria (). The study included patients who were previously healthy without any underlying conditions predisposing to meningitis. Patients were excluded based on the following criteria: (i) patients born prematurely, those with congenital intracranial anomalies, those with ventriculoperitoneal (VP) shunts, patients with immunodeficiency diagnoses, patients with syndromic conditions, cases of meningitis following head trauma, and postoperative brain surgery meningitis cases were excluded. (ii) Additionally, patients for whom CSF findings were not available, those without accessible MRI records or only had CT reports, patients who could not be reached for a physical examination one year after diagnosis, and those with incomplete data were also excluded. Patients whose families refused imaging and lumbar puncture, and all known cases of traumatic lumbar puncture were also excluded from the study.
2.1 Patient grouping and definitions
To ensure clarity in our cohort classification, the 52 pediatric patients diagnosed with bacterial meningitis (BM) were categorized based on the presence of intracranial complications (ICC) and surgical intervention status as follows:
- ā¢Group 1
: Patients with one or more intracranial complications (
nā=ā36).
- ā¢
Group 1A: Patients with ICC who did not require surgery (nā=ā27).
- ā¢
Group 1B: Patients with ICC who required neurosurgical intervention (nā=ā9).
- ā¢
- ā¢
Group 2: Patients without any identified intracranial complications (nā=ā16).
2.2 Definition of intracranial complications (ICC)
Intracranial complications were defined as the development of one or more of the following conditions confirmed through MRI imaging and clinical evaluation: Subdural empyema (SDE), Hydrocephalus, Cerebral thrombosis and/or infarction, Brain abscess, Ventriculitis and Parenchymal shift due to space-occupying lesions. A detailed breakdown of complications and their combinations is presented in TableĀ 1.
Table 1
| Complication | All group 1 patients (nā=ā36) | Group 1A (nā=ā9) | Group 1B (nā=ā27) |
|---|---|---|---|
| Empyema | 25 (69%) | 9 (100%) | 16 (59%) |
| Isolated Empyema | 8 (32%) | 1 (11%) | 7 (26%) |
| Empyema+Thrombosis | 6 (24%) | 1 (11%) | 5 (29%) |
| Empyema+Hydrocephalus | 3 (12%) | 2 (22%) | 1 (4%) |
| Empyema+Ventriculitis | 2 (8%) | 0 (0%) | 2 (7%) |
| Empyema+Thrombosis+Abscess+Infarct | 2 (8%) | 1 (11%) | 1 (4%) |
| Empyema+Abscess+Shift | 1 (4%) | 1 (11%) | 0 (0%) |
| Empyema+Ventriculitis+Thrombosis | 1 (4%) | 1 (11%) | 0 (0%) |
| Empyema+Thrombosis+Hydrocephalus+Infarct | 1 (4%) | 1 (11%) | 0 (0%) |
| Empyema+Thrombosis+Hydrocephalus+Abscess+Shift | 1 (4%) | 1 (11%) | 0 (0%) |
| Hydrocephalus | 4 (11%) | 0 (0%) | 4 (15%) |
| Thrombosis | 3 (8%) | 0 (0%) | 3 (11%) |
| Thrombosisā+āInfarct | 2 (7%) | 0 (0%) | 2 (7%) |
| Ventriculitis | 1 (3%) | 0 (0%) | 1 (4%) |
| Hydrocephalusā+āVentriculitis | 1 (3%) | 0 (0%) | 1 (4%) |
Detailed evaluation of intracranial complications in group 1 patients.
ICC, intracranial complications.
2.3 Surgical indications and procedures performed
Surgical intervention decisions were made by the pediatric neurosurgery team based on a combination of clinical and radiological findings. Objective criteria included the presence of intracranial complications such as subdural empyema, brain abscess, or significant effusion associated with midline shift, cerebral edema, or elevated intracranial pressure. Clinical deterioration despite medical treatmentāmanifested by altered consciousness, focal neurological deficits, or signs of raised intracranial pressureāalso guided surgical decision-making. These criteria were consistently applied across cases to ensure appropriate and timely intervention.
Surgical interventions performed in our study included:
- ā¢
Decompressive craniotomy (nā=ā4)
- ā¢
Burr hole drainage (nā=ā3)
- ā¢
Craniotomy with ventriculoperitoneal (VP) shunt placement (nā=ā2)
Additional procedures such as external ventricular drain (EVD) placement and repeated lumbar punctures were also implemented as part of individualized patient management.
This classification enabled a focused analysis of both the presence of complications and the clinical thresholds necessitating surgical treatment. A visual representation of the grouping is also provided in FigureĀ 1, which includes laboratory markers associated with each subgroup.
Figure 1
2.4 Statistical analysis
Data were analyzed using SPSS version 29.0. The statistical parameters analyzed included descriptive statistics (mean, standard deviation) for continuous variables and frequencies and percentages for categorical variables. Comparative analyses were performed using Chi-square tests for categorical variables and independent t-tests or MannāWhitney U tests for continuous variables, depending on the data distribution. Logistic regression was employed to determine the factors significantly associated with the need for surgical intervention. Receiver operating characteristic (ROC) curves were used to evaluate the diagnostic performance of the significant variables in predicting surgical necessity. Statistical significance was set at pā<ā0.05 for all tests.
3 Results
3.1 Sociodemographic characteristics of patients
Over a 10-year period, 298 children were admitted to our pediatric intensive care unit with a diagnosis of meningitis. Among them, 52 patients who met the inclusion criteria and had complete records were included in the analysis.
The ages of the patients ranged from 1 month to 18 years, with an average age of 77ā±ā72 months. 67% (35/52) of the patients were male, and 33% (17/52) were female.
Intracranial complications developed in 36 of the 52 patients (69%), and emergency neurosurgical interventions were required in 9 of these cases (17%). Neurological deficits were recorded in 44% (23/52) of our patients, with 89% patients (8/9) in the operated group having severe neurological sequelae.
3.1.1 Initial imaging
Among patients diagnosed with intracranial complication (ICC) (Group 1, nā=ā36), 16 patients (44%) had normal cranial CT scans within the first 24ā h of admission. These initially unremarkable imaging findings were associated with a delay in obtaining gadolinium-enhanced MRI and initiating appropriate treatment. Of these 16 patients, 14 (87%) subsequently developed neurological sequelae, and 5 (31%) ultimately required surgical intervention. Representative MRI images from four of these patients, along with explanatory annotations, are presented in FigureĀ 2 to illustrate the radiological progression and clinical relevance of delayed diagnosis.
Figure 2
3.1.2 Intracranial complications
The study detailed the complications of the 36 patients who developed intracranial complications. Subdural empyema (SDE) was the most common complication, occurring in 25 of the 36 patients (69%). Of these 25 patients, 8 developed isolated empyema, while 17 developed additional complications alongside the empyema (see TableĀ 1 for details).
3.1.3 Neurosurgical interventions
Among the 9 patients who underwent surgery, a total of 9 procedures were performed: 4 decompressive craniotomies (DC), 3 burr hole surgeries, and 2 craniotomies with ventriculoperitoneal (VP) shunt placements. Each patient underwent a single neurosurgical intervention; no patient received more than one type of surgery. In addition to the operated group, some patients in the non-surgical group required less invasive procedures to manage elevated intracranial pressure. These included repeated lumbar punctures (for CSF drainage) in 2 patients, external ventricular drain (EVD) placement followed by VP shunt in 1 patient, and VP shunt placement alone in another patient.
3.1.4 Mortality
Two patients with intracranial complications were evaluated for surgery and found to have definitive surgical indications. However, both patients experienced severe hemodynamic instability and septic shock, which precluded surgical intervention. Despite maximal medical support, they died before surgery could be initiated. To maintain analytical consistency, these patients were excluded from subgroup analyses.
Detailed descriptions of the complications developed in patients who underwent surgery are presented in TableĀ 1.
3.2 Patient grouping
In our study, the 52 patients diagnosed with bacterial meningitis (BM) were divided into two main groups based on the development of intracranial complications (ICC): those who developed complications (36 patients) and those who did not (16 patients). Further, the 36 patients who developed intracranial complications were subdivided into two groups: those who underwent surgery (9 patients) and those who did not require surgical intervention (27 patients). This grouping is illustrated in the flowchart provided in the study documentation.
This classification allowed for a structured analysis of outcomes and interventions based on the presence of intracranial complications and the necessity of surgical procedures, facilitating a clearer understanding of the diseaseās impact and the effectiveness of the treatment approaches used.
3.3 Characteristics of age groups among the groups
According to the classification above, there was no significant difference in the average ages of children in Group 1 (76ā±ā77 months) compared to those in Group 2 (79ā±ā61 months) (pā=ā0.699). When children were divided into two age groups, those under 2 years old and those older than 2 years, the proportion of children under 2 years in Group 1 was significantly higher (pā=ā0.041), indicating that the incidence of intracranial complications (ICC) is significantly higher in children between 0 and 2 years old (TableĀ 2). The average ages and age group distributions for children in Groups 1A and 1B were found to be similar (pā=ā0.909 and pā=ā0.847, respectively). However, it was determined that 5 of the 9 patients requiring surgery were between 1 and 6 months old.
Table 2
| Parameter | Group 1 (Patients with ICC, nā=ā36) | Group 2 (Patients without ICC, nā=ā16) | P value |
|---|---|---|---|
| Average age, months | 76ā±ā77 (1ā204) | 79ā±ā61 (2ā192) | 0.699a |
| 0ā2 years, n (%) | 20 (56%) | 4 (25%) | 0.041b |
| >2 years, n (%) | 16 (44%) | 12 (75%) | |
| Elevated WBC (>12,000ā /mm3) | 18 (50%) | 2 (13%) | 0.010b |
| CRP, mg/dl | 104ā±ā124 | 58ā±ā75 | 0.172a |
| CSF protein, mg/dl | 427ā±ā785 | 165ā±ā330 | 0.279a |
| CSF glucose, mg/dl | 34ā±ā26 | 46ā±ā25 | 0.189a |
| CSF protein/glucose ratio | 63ā±ā130 | 62ā±ā148 | 0.490a |
| Time from symptom to PICU transfer, hours | 156ā±ā158 | 28ā±ā20 | <0.001a |
| Neurological sequelae at 1 year, n (%) | 20 (56%) | 2 (13%) | 0.004b |
Basic characteristics and laboratory values of patients in groups 1 and 2.
ICC, intracranial complications; WBC, white blood count; CRP, C-reactive protein; CSF, cerebro-spinal fluid; PICU, pediatric intensive care unit.
Independent samples t test.
Pearson chi-square test, significant p values are bold.
3.4 Differences in laboratory parameters between the groups
When comparing laboratory parameters between Group 1 and Group 2, only the elevation of white blood cells (WBC) defined as >12,000ā /mm3 was found to be significantly higher in Group 1 (50% vs. 13%, pā=ā0.010). Serum CRP levels (pā=ā0.172), CSF protein (pā=ā0.279), CSF glucose (pā=ā0.189), and CSF protein/glucose ratio (pā=ā0.490) did not show significant differences between the groups.
When comparing laboratory parameters between Groups 1A and 1B, similar levels of WBC elevation were found (pā=ā0.248), however, serum CRP levels were significantly higher in Group 1B (226ā±ā94 vs. 63ā±ā105, pā<ā0.001). Regarding CSF values, while CSF protein levels were similar between the two groups (pā=ā0.110), CSF glucose levels were significantly lower in Group 1B (pā=ā0.049). The CSF protein/glucose ratio was also significantly higher in Group 1B (pā=ā0.011) (TableĀ 3).
Table 3
| Parameter | Group 1A (ICC and NOT requiring surgery, nā=ā27) | Group 1B (ICC and required surgery, nā=ā9) | P value |
|---|---|---|---|
| Average age, months | 77ā±ā77 | 73ā±ā82 | 0.909a |
| 0ā2 years, n (%) | 14 (52%) | 5 (56%) | 0.847b |
| >2 years, n (%) | 13 (48%) | 4 (44%) | |
| Elevated WBC (>12,000ā /mm3) | 12 (44%) | 6 (67%) | 0.248b |
| CRP, mg/dl | 63ā±ā105 | 226ā±ā94 | <0.001a |
| CSF protein level, mg/dl | 289ā±ā427 | 925ā±ā1,489 | 0.110a |
| CSF glucose level, mg/dl | 39ā±ā26 | 16ā±ā18 | 0.049a |
| CSF protein/glucose ratio | 28ā±ā62 | 189ā±ā228 | 0.011a |
| Time from symptom to PICU transfer, hours | 133ā±ā160 | 224ā±ā136 | 0.134a |
| Neurological sequelae at 6 months, n (%) | 12 (44%) | 8 (89%) | 0.020b |
Basic characteristics and laboratory values of patients in groups 1A and 1B.
ICC, intracranial complications; WBC, white blood count; CRP, C-reactive protein; CSF, cerebro-spinal fluid; PICU, pediatric intensive care unit.
Independent samples t test.
Pearson chi-square test, significant p values are bold.
3.5 ROC analysis for CSF and Serum parametersārelationship to surgical necessity
ROC analyses were conducted to evaluate the predictive power of key CSF and serum parameters for surgical intervention among patients with intracranial complications (
nā=ā36).
- ā¢
CSF glucose levels below 6.75ā mg/dl were significantly associated with the need for surgery, with an AUC of 0.789 (pā=ā0.016), 60% sensitivity, and 94% specificity.
- ā¢
A CSF protein/glucose ratio >18.9 also showed strong predictive value (AUC: 0.811, pā=ā0.011), with 80% sensitivity and 78% specificity.
- ā¢
Serum CRP levels >150.3ā mg/dl demonstrated the highest predictive accuracy (AUC: 0.840, pā<ā0.001), with both sensitivity and specificity at 89%.
- ā¢
In contrast, CSF protein alone was not a statistically significant predictor (AUC: 0.644, pā=ā0.312), though a cut-off of 304.5ā mg/dl yielded moderate sensitivity (60%) and specificity (72%).
These findings suggest that CRP, CSF glucose, and the CSF protein/glucose ratio may serve as reliable early markers for identifying patients who may require neurosurgical intervention (
FigureĀ 3).
Figure 3
Since these three parameters showed significant differences between patients with and without surgical indication in descriptive analysesāand also demonstrated statistically significant predictive value in the ROC analysisāpatients who tested positive for all three parameters were further evaluated under the criterion of ā3ā+āparameter positivity.ā Accordingly, six patients were identified with simultaneous positivity for CRP, CSF glucose, and the CSF protein/glucose ratio. All of these patients belonged to the group requiring surgical intervention. The presence of 3ā+āpositive parameters was found to have a highly significant predictive power in determining surgical necessity (pā<ā0.001).
3.6 Definition of SDE areas and risk of surgery based on involvement
Among the 36 patients with intracranial complications (ICC), subdural empyema (SDE) was detected in 25. Of these 25 patients, 16 did not undergo surgery, and 9 underwent surgical procedures. Patients with SDE were divided into two groups based on the presence of surgery and evaluated based on the anatomical location of the empyema, which was divided into 5 quadrants. It was found that the involvement of empyema in a single quadrant showed a significant difference between those who underwent surgery and those who did not (p: 0.012). Details are shown in the TableĀ 4; FiguresĀ 4,5.
Table 4
| Quadrant Involvement | Operated patients (nā=ā9) | Non-operated patients (nā=ā16) | P-value |
|---|---|---|---|
| Single quadrant | 7/9 (78%)** | 2/16 (13%) | 0.012a |
| Two quadrants | 1/9 (11%) | 6/16 (38%)** | |
| Four quadrants | 1/9 (11%) | 3/16 (19%) | |
| Five quadrants | 0/9 (0%) | 3/16 (19%) | |
| Isolated fifth area | 0/9 (0%) | 2/16 (13%) |
Surgical interventions based on quadrant involvement.
Bold values and ** indicate parameters with statistically significant differences between operated and non-operated patients (pāÆ<āÆ0.05).
Pearson chi-square test was used, and significant difference was found between groups.
Figure 4
Figure 5
Upon reviewing the 25 patients with SDE, 5 were infratentorial, and 20 were supratentorial. Of the 5 infratentorial cases, 2 were exclusively infratentorial, and 3 were both infra- and supratentorial. None of the 5 patients with infratentorial empyema underwent surgery.
This analysis provides insights into how the extent of anatomical involvement may influence the decision for surgical intervention in patients with intracranial complications (ICC). The significant difference observed in single quadrant involvement suggests a higher tendency for surgery when SDE is localized, as indicated by the marked difference in surgery rates between the groups (78% vs. 13%).
4 Discussion
Prompt diagnosis and immediate treatment of acute bacterial meningitis (ABM) are critical for patient survival. In particular, early detection and surgical management of subdural empyema (SDE)āa neurosurgical emergency that can arise secondary to bacterial meningitisāare essential to reduce morbidity and mortality (, ā). Delays in surgical intervention are associated with mortality rates exceeding 90% (), whereas intervention within 72ā h of symptom onset lowers the risk of disability to 10%, compared to 70% when delayed beyond 72ā h ().
Yılmaz et al. reported that all 28 children with SDE secondary to meningitis underwent decompressive craniotomy or burr hole procedures, while Kanu et al. performed surgery on 17 infants with complicated meningitis (, ). The average time to surgery was one to two months in these studies, with late presentations leading to 100% surgical intervention and severe neurological sequelae. These findings highlight the devastating impact of delayed recognition and treatment, particularly in resource-limited settings ().
To improve early identification, several studies have proposed scoring systems to predict poor outcomes and identify patients at high risk for intracranial complications (ICCs), including SDE (, ). These efforts support closer monitoring in neurocritical care units for selected pediatric patients (, ).
Young age, particularly under one year, is a well-established risk factor for ICCs such as hydrocephalus, subdural effusion, SDE, seizures, and hearing loss (). Subdural effusion occurs in approximately 40%ā60% of infants with bacterial meningitis and may progress to SDE through secondary infection (, ). Immature immune responses and the vulnerability of the developing brain may contribute to the severity of outcomes (). Additionally, male sex has been associated with an increased risk of SDE ().
In our study, consistent with previous findings, ICCs were significantly more frequent in children under two years of age (pā=ā0.041). Notably, 5 of the 9 operated patients (55.5%) were younger than six months, emphasizing the need for heightened clinical vigilance and early intervention in this age group.
Previous studies have shown that high cerebrospinal fluid (CSF) protein and low glucose levels are associated with a greater risk of neurological sequelae, including hearing loss, epilepsy, and death (, , ). For example, CSF glucose below 1.5ā mmol/L () or 40ā mg/dl () has been linked to a 41.7% risk of sequelae. While these parameters have been used to predict complications, they do not differentiate which patients with ICCs will ultimately require surgery (). Our study aims to fill this gap by evaluating CSF and serum markers alongside imaging findings to better predict the need for surgical intervention.
Elevated CSF protein levels have been associated with an intensified inflammatory response and are considered a risk factor for neurological sequelae (, ). Similarly, decreased CSF glucose reflects both the virulence of pathogens and the extent of brain damage, correlating with poorer prognosis (). Several authors suggest that abnormalities in CSF protein and glucose not only indicate risk for neurological complications but may also signal the development of intracranial complications (e.g., SDE) in bacterial meningitis (, , ).
Previous studies have reported significantly abnormal CSF protein and glucose levels in patients who required surgical treatment for SDE (, ). Notably, YalƧınkaya et al. () proposed the CSF protein/glucose ratio as a screening tool, identifying a cut-off of 4.65 with 100% sensitivityābelow which no patients developed SDE. In our study, a much higher ratio of 18.9āapproximately four to five times that thresholdāwas strongly associated with surgical intervention, warranting serious clinical attention.
We found a significant difference in the CSF protein/glucose ratio between the non-operated (Group 1A; nā=ā27, mean 28ā±ā62) and operated (Group 1B; nā=ā9, mean 189ā±ā227) groups (pā=ā0.011). CSF glucose levels were also significantly lower in Group 1B (pā=ā0.049). While CSF protein levels did not reach statistical significance (pā=ā0.11), the near threefold increase observed in operated patients is notable and may be attributed to the limited sample size.
To further explore predictive performance, we conducted ROC analysis. A protein/glucose ratio cut-off of 18.9 yielded 77.8% specificity for identifying patients needing surgical intervention. A CSF glucose cut-off of 6.75ā mg/dl provided 94.4% specificity, and a CSF protein cut-off of 304.5ā mg/dl was associated with ICC development in 72.2% of patients.
Serum inflammatory markers such as CRP and WBC were also examined, as previous studies have linked them to the development of SDE (, ). While a WBC count >12,000 was significantly associated with ICC development (pā=ā0.010), it did not distinguish between operated and non-operated groups. Sequential measurements (day 3 and 4 CRP) can predict significant neurological sequelae, highlighting its importance in prognosis and clinical outcomes (, ). In contrast to WBC, CRP levels were significantly higher in Group 1B (226ā±ā94) compared to Group 1A (63ā±ā105) (pā<ā0.001). A CRP cut-off of 150.3ā mg/dl was predictive of surgical need, with a specificity of 88.9%.
Our findings suggest that while WBC count >12,000 may indicate risk for ICCs, CRP levels are more reliable in predicting surgical necessity. These results underscore the importance of early LP and communication with families, particularly when lumbar puncture is delayed or refused. In such cases, CRP levels >150.3ā mg/dl should prompt urgent neuroimaging, ideally with gadolinium-enhanced MRI, and immediate evaluation of CSF parameters to guide early intervention.
A CRP level above 150.3ā mg/dl, a CSF protein/glucose ratio of 18.9, and a CSF glucose level of 6.75ā mg/dl collectively indicate a high bacterial load and extensive infectionāstrong predictors of the need for surgical intervention. When all three parameters are present, they should be evaluated jointly as critical red flags in the management of complicated meningitis. Such cases warrant urgent surgical assessment.
In subdural empyema (SDE), particularly among neonates and young infants, clinical signs are often vague and nonspecific (), complicating early diagnosis. Imaging thus becomes essential (, , , ). However, conventional CT scans may fail to detect relevant abnormalities. Studies report that up to 63% of CT scans in bacterial meningitis patients can appear normal, and CT is often inadequate in identifying cerebral herniation or localized fluid collections (). In suspected cases of SDE, gadolinium-enhanced MRI remains the gold standard, as it is more sensitive in detecting small or localized collections (, , ). When venous sinus thrombosis is also suspected, MR venography may be required for comprehensive assessment ().
In our cohort with ICC (Group 1, nā=ā36), 44% (16/36) had normal CT scans within the first 24ā h. These unremarkable imaging results led to delays in obtaining gadolinium-enhanced MRI and initiating timely intervention. Among these 16 patients, 14 (87%) developed neurological sequelae, and 5 eventually required surgery. It appears that normal initial CT findings, coupled with high initial GCS scores (e.g., GCS 15) and subtle clinical presentations, may have contributed to underestimation of disease severity. Therefore, we emphasize that physicians should remain highly vigilant and pursue early MRI in the presence of abnormal CRP and CSF markersāespecially when the ā3ā+āparametersā are observedāeven if initial imaging or clinical findings appear benign.
In resource-limited settings, late hospital admissions and normal or delayed CT reports often result in underestimating the severity of bacterial meningitis. Additionally, refusal of lumbar puncture by families leads to both misdiagnosis and inadequate treatment. These patients often experience prolonged hospital stays and eventually require surgical intervention due to worsening neurological complications. Our findings highlight that delayed recognition and intensive care interventionsārather than late presentation aloneāare critical contributors to adverse outcomes. As previously reported, outcomes following delayed surgical treatment are typically poor (, ). Thus, when all three parameters (CRP >150ā mg/dl, CSF glucose <6.75ā mg/dl, and protein/glucose ratio >18.9) are present, urgent surgical evaluation, early neurosurgical consultation, and timely admission to pediatric intensive care are essential.
Elevated intracranial pressure (ICP) is most pronounced during the first 72ā h of meningitis. If not controlled through aggressive medical treatment by days 3ā5, it may lead to irreversible neurological damage or death (, ). Therefore, many experts recommend admitting high-risk patients to neurocritical care units during this early window for intensive monitoring (, , ), repeat imaging, and multidisciplinary decision-making to prevent poor outcomes (, , , ). Such patients should be managed by a coordinated team including pediatric intensivists, neurosurgeons, neurologists, infectious disease specialists, and rehabilitation experts ().
In our study, we aimed to identify patients at surgical risk regardless of their clinical conditionāincluding GCS scores, sepsis, shock, respiratory or cardiac arrest, intubation, or seizures. The presence of three or more positive parameters (3+) was found to significantly predict the need for surgical intervention. Based on this, we propose that all patients meeting this threshold should be admitted to the Pediatric Intensive Care Unit (PICU) for the first five days, even if they appear clinically stable. Only in this setting can aggressive treatment, close neuroimaging surveillance, and continuous monitoring be ensured to reduce ICP, surgical risk, and neurological sequelae.
In our cohort, nine patients required surgery between days 6 and 19 following diagnosis. This delay was primarily due to reassuring GCS scores, subtle clinical signs in infants, normal CT findings, and earlier misdiagnoses, which led to suboptimal antibiotic use. These factors likely masked the true severity of disease and prevented timely intervention. In patients meeting the 3+ criteria, regular and early imaging is vitalāparticularly as SDE-related complications such as sinus venous thrombosis, infarction, hydrocephalus, and ventriculitis can further elevate ICP (, , ). Notably, all nine patients who underwent surgery also had one or more of these complications.
To enhance early recognition of high-risk cases, we analyzed the anatomic distribution of empyema in patients undergoing initial MRI. Brain regions were divided into five quadrants, and in the surgical group (Group 1B), empyema were localized to a single quadrant in 7 of 9 cases (77.8%). In contrast, among the non-operated group (nā=ā16), only 2 cases (12.5%) had single-quadrant involvementāa statistically significant difference (pā=ā0.012). Although the literature associates intracranial mass lesions such as tumors and abscesses with elevated ICP, the effect of empyema size and distribution on ICP is less clearly defined. Our findings suggest that even small-volume empyema may exert considerable pressure when confined to a single anatomical region. This may be explained by the physical principle that pressure (P) equals force (F) divided by area (A). Given the same mass (force), a smaller area leads to higher pressure:[Pressure is defined as force per unit area. It is expressed as \(P\) for pressure in pascals, \(F\) as the force in newtons, and \(A\) as the area in square meters.]
Thus, an empyema localized to a smaller surface may exert greater mechanical pressure on adjacent brain tissue than a more diffusely distributed one. While this remains hypothetical, our results support the notion that both the biochemical severity (3+ parameters) and anatomic concentration of the empyema contribute to surgical risk and worse neurological outcomes. Further studies are warranted to validate this model and improve surgical risk stratification.
4.1 Limitations
This study has several limitations. First, its retrospective design restricts the ability to control for confounding variables and may introduce information bias. Second, as it was conducted at a single tertiary care center, the findings may not be generalizable to other institutions or populations. Third, despite covering a 10-year period, the overall sample sizeāparticularly within the surgical subgroup (nā=ā9)āwas relatively small, limiting statistical power and external validity. Additionally, variability in treatment initiation timing, antibiotic regimens, and imaging practices may have influenced clinical management and outcomes. Furthermore, although surgical decisions were made based on consistent clinical and radiological criteria, such as the presence of empyema, abscess, midline shift, or signs of elevated intracranial pressure, the absence of a universally standardized surgical risk assessment tool introduces a degree of subjectivity that is inherent to retrospective neurosurgical evaluations. Nonetheless, the primary aim of our study was to identify early laboratory parametersābased on initial blood and CSF findingsāthat could assist clinicians in recognizing pediatric patients at risk for severe intracranial complications. We believe our findings offer valuable insights, but future prospective, multicenter studies using standardized clinical protocols and objective surgical criteria are needed to validate and expand upon these results.
5 Conclusion
Our findings suggest that the presence of three specific parametersāCRP >150ā mg/dl, CSF glucose <6.75ā mg/dl, and a CSF protein/glucose ratio >18.9āstrongly indicates the need for surgical intervention in complicated bacterial meningitis. In such cases, immediate MRI is recommended to evaluate for intracranial complications, particularly subdural empyema (SDE). If the empyema is localized to a single quadrant, early neurosurgical consultation is essential. These high-risk patients should be managed in a pediatric intensive care unit (PICU) under multidisciplinary supervision to ensure timely diagnosis, appropriate intervention, and improved outcomes.
Statements
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving humans were approved by Van Yüzüncü Yıl University Ethics Committee for Clinical Research (date: 20.12.2024, decision no: 2024/14-18). The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants' legal guardians/next of kin.
Author contributions
MB: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing ā original draft, Writing ā review & editing. SY: Conceptualization, Formal analysis, Investigation, Methodology, Resources, Software, Validation, Writing ā original draft, Writing ā review & editing. AĆ: Investigation, Resources, Supervision, Writing ā original draft, Writing ā review & editing. MĆ: Investigation, Resources, Software, Writing ā original draft, Writing ā review & editing. SA: Project administration, Resources, Validation, Writing ā original draft, Writing ā review & editing. ÅK: Validation, Writing ā original draft, Writing ā review & editing. EB: Conceptualization, Formal analysis, Project administration, Resources, Supervision, Writing ā original draft, Writing ā review & editing.
Funding
The author(s) declare that no financial support was received for the research and/or publication of this article.
Acknowledgments
We would like to express our gratitude to Prof. Dr. Remzi Kiziltan for his invaluable mentorship throughout this study.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declare that no Generative AI was used in the creation of this manuscript.
Publisherās note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Summary
Keywords
meningitis, surgical intervention, empyema, intracranial complications (ICC), cerebrospinal fluid (CSF), pediatric intensive care unit (PICU)
Citation
Boyraz M, Yüce S, Ćzel A, Ćrmeci MT, Akkaya S, Kƶksal AtiÅ Å and Botan E (2025) Identifying the need for surgical intervention in pediatric bacterial meningitis: single-center experience. Front. Pediatr. 13:1631570. doi: 10.3389/fped.2025.1631570
Received
19 May 2025
Accepted
01 July 2025
Published
16 July 2025
Volume
13 - 2025
Edited by
Tanıl Kendirli, Ankara University, Türkiye
Reviewed by
Faruk Ekinci, Ćukurova University, Türkiye
Daniela Teixeira, Federal University of Minas Gerais, Brazil
Updates
Copyright
Ā© 2025 Boyraz, Yüce, Ćzel, Ćrmeci, Akkaya, Kƶksal AtiÅ and Botan.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Servet Yüce servetyuce@istanbul.edu.tr
ORCID Servet Yüce orcid.org/0000-0002-5264-3038
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.