ABSTRACT
To describe the clinical characteristics and the risk factors associated with mortality in patients with meningitis. This is a retrospective review of patients diagnosed to have meningitis with positive culture of the cerebrospinal fluid (CSF) specimen. All cases aged 19 > years who were admitted to Hospital USM between January 2004 and December 2011 were included in the study. The CSF results database were obtained from the Department of Medical Microbiology and Parasitology, Hospital USM, Kelantan. A checklist was used to record the clinical characteristics. A total of 125 cases met the inclusion criteria. The age of patients ranged between newborn and 19 years old (Mean±SD, 74.5±80.6 months). The majority of them were males (65.6%). Fever was the most common presentation (73.6%) followed by poor oral intake (48.0%), seizure (36.0%) and headache (24.8%). The mortality rate was 31.2%. Coagulase negative staphylococcus was the most frequent pathogens isolated (21.6%), followed by Acinetobacter spp. (17.6%), Staphylococcus aureus (13.6%), Streptococcus spp. (11.2%) and Klebsiella pneumoniae (6.4%). There were significant association of in-hospital death with age (p=0.020) and conscious level (p=0.001). Infectious meningitis is a big health concern, especially among children. We found that coagulase negative staphylococcus, Acinetobacter species, S. aureus, Streptococcus spp and K. pneumoniae were prevalent in our hospital. These microorganisms were hospital associated pathogens. The 31% mortality linked to hospital acquired meningitis specifies the need for focused physician attention especially among younger aged patients.
Key Words: Bacterial meningitis, children, CSF, Mortality
INTRODUCTION
Meningitis is a devastating and deadly disease that kills patients within hours. Despite many new antibacterial agents, bacterial meningitis fatality rates still remain high. It is the cause of mortality in about 1,000 people around the world every day; many of them children and young adults. Survivors can be left with severe disabilities.
Infectious meningitis could be typed on the bases of several markers. The markers include pathogen: bacterial, viral, fungal, or parasitic; and host age: neonatal, young or mature adult. Individual health status is also a marker which includes normal or deficient immunity, and symptoms duration: acute or chronic.
Pediatric bacterial meningitis is most common in children younger than four years, with a peak incidence in those aged 3–8 months. The most common bacterial causes of acute meningitis in young children are Streptococcus agalactiae and Escherichia coli. These bacterium commonly infect neonates and infants up to age three months and were acquired during birth when the infant passes through the vaginal canal.
What is known is that Haemophilus influenzae infects unvaccinated children between the age of 3–6 months and 6 years; Neisseria meningitides infects children and young adults1) and it is the only organism that causes meningitis epidemics.2) Evidence suggests that Streptococcus pneumoniae occasionally infects children and increases in incidence with age. Listeria monocytogenes appears to be food-borne (dairy products, processed meat, uncooked vegetables) and affected immunocompromised patients.1)
The early symptoms of meningitis are headache, fever, and chills.3) A combination of neck stiffness, seizure and altered mental status has also been found in bacterial meningitis patients. Shock, coagulation disorders, endocarditis, pyogenic arthritis, and prolonged fever are the most common bacterial meningitis complications.1) Death occurs from shock and other serious complications within hours of the appearance of symptoms.3) Among survivors, the outcomes of meningitis include deafness, mental retardation, spasticity and/or paresis, and seizure disorder.
Published studies on meningitis are very few in the Southeast Asian region. There were only 20 research articles that clinically evaluated meningitis over a period of ten years (1990–2000).4) Similarly, there has been very few studies on meningitis among Malaysian children or adolescents in the last two decades. Thus, we hope this study will add information to the existing data and fill in the gaps of information for the purpose of reducing mortality rates. The aim of this study was to describe the clinical features, laboratory profile and the mortality rate of meningitis among children and adolescent in our hospital setting.
METHODOLOGY
Hospital Universiti Sains Malaysia (Hospital USM) is a tertiary teaching hospital which receives referrals from several district hospitals in Kelantan. The Hospital is also a referral center for neurosurgery within East Coast Malaysia. This hospital has a 15-bed neurosurgical ICU and is one of the training hospitals for neurosurgical subspecialty in Malaysia.
This study is a retrospective review of patients diagnosed to have bacterial meningitis with positive culture of the cerebrospinal fluid (CSF) specimen. The CSF results database were obtained from the Department of Medical Microbiology and Parasitology, Hospital USM, Kelantan, Malaysia and patients’ records were obtained from the record office of Hospital USM with permission. All cases aged 19 > years who were admitted to Hospital USM between January 2004 and December 2011 were included in the study. A checklist was used to record the clinical characteristics, accompanying symptoms and signs, results of relevant blood investigations and the patient’s outcome.
CSF specimens received from the ward were processed according to the standard laboratory protocol adopted from the Clinical and Laboratory Standards Institute (CLSI). The gross appearances of the CSF specimens were recorded. Microscopic examination of the CSF specimens were performed which included total cell count, Gram staining and India ink preparation followed by culture and susceptibility testing. Latex agglutination examination for five primary pathogens namely Streptococcus pneumoniae, Escherichia coli, Haemophillus influenzae, Neisseria meningitides and group B streptococcus was performed using WellcogenTM Bacterial Antigen Kit (Remel, United Kingdom). The CSF specimens were also analyzed biochemically for glucose, protein and globulin levels. In some cases, the plasma glucose was also taken at the time of lumbar puncture to determine the CSF/plasma glucose ratio.
The data were statistically analyzed using SPSS version 20 (Chicago, USA). Descriptive statistics, Mann-Whitney test and the Pearson chi-squared test were used to investigate different indicators of meningitis. P-values less than 0.05 were considered to be statistically significant.
RESULTS
We obtained a total of 141 CSF specimens for bacterial culture during the study period. The CSF specimens of 16 patients did not meet the laboratory diagnostic criteria. As such, 125 cases were included in the final analysis.
Table 1 shows the socio-demographic characteristics of the 125 cases. The age ranged from newborn to 19 years old, with 43.2% aged less than 1 year, 13.6% aged 1 to 5 and 43.2% aged above 5 years old. The mean (SD) age was 74.5 (80.6) months. The majority of cases were males (65.6%). In this study, patients originated from Terengganu (27%), Kota Bharu (28%), and other districts of Kelantan (37.6%).
Table 1.
Frequency (%) n=125 |
|
---|---|
Age | |
>5–19 year | 54 (43.2) |
>one – 5 year | 17 (13.6) |
≤one year | 54 (43.2) |
Sex | |
Male | 82 (65.6) |
Female | 43 (34.4) |
District | |
Kota Bharu | 35 (28.0) |
Terengganu | 34 (27.2) |
Other districts | 47 (37.6) |
Missing | 9 (7.2) |
Diagnosis | |
Congenital hydrocephalus | 35 (43%) |
Motor vehicle accident | 16 (20%) |
Brain tumor | 4 (4%) |
Hydrocephalus | 25 (29%) |
Brain abscess | 2 (2%) |
Spine bifida 1 | 1 (1%) |
Aterio venous malformation | 1 (1%) |
Clinical features | |
Fever | 92 (73.6) |
Poor oral intake | 60 (48.0) |
Seizure | 45 (36.0) |
Headache | 31 (24.8) |
Altered conscious level | 19 (15.2) |
Neck stiffness | 19 (15.2) |
Confusion | 14 (11.2) |
Blurred vision | 14 (11.2) |
Hydrocephalus | 13 (10.4) |
Bulging fontanelle | 6 (4.8) |
Pneumonia | 5 (4.0) |
Complication | |
Nerve palsy | 5 (4.0) |
Paralyze | 5 (4.0) |
Increased muscle tone | 4 (3.2) |
Skin rashes | 3 (2.4) |
Diarrhea | 3 (2.4) |
Outcome | |
Death | 39 (31.2) |
Alive | 86 (68.8) |
The clinical presentations of the meningitis were also shown in Table 1. Fever was the most common presentation (73.6%) followed by poor oral intake (48.0%), seizure (36.0%) and headache (24.8%). It is noted here that headache was noted by those above five year olds. The incidence of postoperative nosocomial meningitis was 67% (84 patients out of 125 patients). The distribution of underlying diseases of the patients were: congenital hydrocephalus 43% (35 patients), motor vehicle accident 20% (16 patients), brain tumor 4% (four patients), hydrocephalus 29% (25 patients), brain abscess 2% (two patients), spine bifida 1% (one patient), and aterio venous malformation 1% (one patient).
Post-operative meningeal infection mainly EVD shunt infection; was highly significant as indicated by Pearson chi square test (.000). Out of 125 cases of meningitis between 2004 and 2011, 31.2% died while in hospital due to meningitis and its related complications. The remaining 33% was community acquired (41 patients out of 125 patients) survived as were determined as bacterial meningitis cases.
Table 2 shows results of CSF examinations. Positive latex agglutination test were seen in 6.4% cases. Further examinations showed 28% had clear CSF and the rest were either blood stain, cloudy, turbid or xanthochromic.
Table 2.
Cerebrospinal fluid | n | Frequency (%) | Mean (SD) |
Median (IQR) |
---|---|---|---|---|
Latex agglutination Positive negative Cell count (cells/mm3) TWBC Polymorph Leucocyte TRBC |
125 88 83 57 73 |
8 (6.4) 117 (93.6) |
990.7 (2344.2) 922.9 (2303.7) 185.1 (618.8) 3857.2 (15348.0) |
125 (772) 100 (823) 34 (82) 150 (1366) |
Macroscopic appearance | ||||
Clear | 35 (28.0) | |||
Blood stain | 25 (20.0) | |||
Cloudy | 3 (2.4) | |||
Turbid | 13 (10.4) | |||
Xanthochromic | 14 (11.2) | |||
Aetiological agents | ||||
Coagulase negative staphylococcus | 27 (21.6) | |||
Acinetobacter species | 22 (17.6) | |||
Staphylococcus aureus | 17 (13.6) | |||
Streptococcus species | 14 (11.2) | |||
Klebsiella pneumonia | 8 (6.4) | |||
Others# | 37 (29.6) | |||
Gram Stain | ||||
Gram negative bacteria | 20 (16.0) | |||
Gram positive bacteria | 24 (19.2) | |||
No organism seen | 81 (64.8) | |||
Positive India ink | 0 (0.0) | |||
Biochemical test: Globulin | ||||
Positive | 46 (36.8) | |||
Negative | 22 (17.6) | |||
Trace | 3 (2.4) | |||
Not done | 54 (43.2) | |||
Protein (g/dL)* [0.15–0.45] | 113 | 47.34 (471.88) | ||
Glucose (mmol/L)* [2.2–4.4] | 112 | 1.40 (1.20) | ||
CSF/Plasma glucose ratio* | 48 | 0.29 (0.29) |
*skewed data
Total cell counts by microscopic examination revealed that the mean total white blood cells was 990.7 (2344.2) cells/mm3. It was found that mean polymorph counts were higher than lymphocytes mean counts. TRBC was found to be a little elevated in CSF due to traumatic tap.
Microscopic examinations showed that 20 (16.0%) were Gram negative bacteria, 24 (19.2%) were Gram positive bacteria and 81 (64.8%) were undetermined. The microorganisms isolated from the CSF cultures in descending order were: coagulase negative staphylococcus (21.6%), Acinetobacter spp (17.6%), Staphylococcus aureus (13.6%), Streptococcus spp (11.2%) and Klebsiella pneumoniae (6.4 %). The mean (SD) of CSF protein was 47.34 (471.88) mmol/l and mean (SD) of CSF glucose was 1.40 (1.20) mmol/l.
Based on our results, Positive Gram stain, high CSF WBC count, and high CSF protein count determines in bacterial meningitis. In this study 36% of patients were positive for globulin. It is mentioned here that CSF gamma globulin may help to determine the amount of protein in CSF. Increase in gamma protein level is a diagnostic criterion for neurological diseases.
From the hospital records, mortality from bacterial meningitis was 31.2% (39/125). Table 3 shows the associated factors for death from bacterial meningitis using Chi square test. There were significant associations between mortality with age (p=0.020) and conscious level (p=0.001). There were no significant associations between death and gender, fever, seizure, poor feeding, neck stiffness, headache, latex positive, level of CRP and level of protein, glucose and CSF/plasma glucose ratio.
Table 3.
Frequency (%) | P value | ||
---|---|---|---|
Death N=39 |
Alive N=86 |
||
Age | 0.020c | ||
≤ one year | 11 (28.2) | 43 (50.0) | |
>one – 5 year | 4 (10.3) | 13 (15.1) | |
>5–19 year | 24 (61.5) | 30 (34.9) | |
Sex | 0.812 c | ||
Male | 25 (64.1) | 57 (66.3) | |
Female | 14 (35.9) | 29 (33.7) | |
Fever | 0.897 c | ||
Yes | 29 (74.4) | 63 (73.3) | |
No | 10 (25.6) | 23 (26.4) | |
Altered conscious level | 0.001 c | ||
Yes | 12 (30.8) | 7 (8.1) | |
No | 27 (69.2) | 79 (91.9) | |
Seizure | 0.111 c | ||
Yes | 18 (46.2) | 27 (31.4) | |
No | 21 (53.8) | 59 (68.6) | |
Poor feeding | 0.781 c | ||
Yes | 18 (46.2) | 42 (48.8) | |
No | 21 (53.8) | 44 (51.2) | |
Neck stiffness | 0.618 c | ||
Yes | 5 (12.8) | 14 (16.3) | |
No | 34 (87.2) | 72 (83.7) | |
Headache | 0.053 c | ||
Yes | 14 (35.9) | 17 (19.8) | |
No | 25 (64.1) | 69 (80.2) | |
Latex | 1.000 c | ||
Negative | 37 (94.9) | 80 (93.0) | |
Positive | 2 (5.1) | 6 (7.0) | |
CRP | 114.5 (126.0) | 69.5 (137.0) | 0.165 c |
CSF Proteina g/dl | 1.25 (5.72) | 1.56 (3.58) | 0.752 b |
CSF Glucosea (mmol/L) | 1.00 (1.66) | 1.15 (1.66) | 0.479 b |
CSF/Plasma glucose ratioa | 0.22 (0.41) | 0.21 (0.29) | 0.412 b |
amedian (interquartile range)
bMann Whitney test
cChi square test
For logistic regression analysis, the independent variables of mortality were age and level of consciousness (GCS <10). Table 4 shows results of multiple logistic regressions between patients’ age and conscious level. Infants with bacterial meningitis were significantly three times more vulnerable to risk of death compared to children older than five years (p=0.013). Patients who presented altered conscious levels had significantly five times more likely to die compared to those who were conscious.
Table 4.
Crude OR (95% CI) | Adjusted OR (95% CI) | P value | |
---|---|---|---|
Age | |||
>5–19 year | 1.00 | 1.00 | |
>one – 5 year | 2.60 (0.75, 9.01) | 3.35 (0.87, 12.83) | 0.078 |
≤ one year | 3.13 (1.33, 7.34) | 3.11 (1.28, 7.56) | 0.013 |
Altered conscious level | |||
No | 1.00 | 1.00 | |
Yes | 5.02 (1.79, 14.04) | 5.41 (1.82, 16.07) | 0.002 |
OR = Odds Ratio
CI = Confidence Interval
DISCUSSION
A study done by Erleena Nur et al. (2008) found that the majority of bacterial meningitis admitted to a tertiary hospital in the West Coast of Malaysia were children less than five years old and the most common organisms were S. pneumoniae (23%), H. influenzae (15%), E. coli (8.5%), N. meningitides (4%) and Streptococcus spp (2%). Studies done before 1998 showed that Haemophilus influenzae type b (Hib) were the most common aetiological agent.6,7) In comparison to our study, even though the most frequent age diagnosed with bacterial meningitis remained similar; the trend of microorganisms isolated differed. In this study, we found that coagulase negative staphylococcus, Acinetobacter species, S. aureus, Streptococcus spp and K. pneumoniae were prevalent in our hospital site according to their clinical background and underlying diseases of the patient. These microorganisms were hospital associated pathogens. Other authors had noted that Gram-negative bacteria, most commonly Acinetobacter spp and P. aeruginosa; have gained importance as hospital pathogens.8-11)
This also explains why most of the latex agglutination gave negative results. Latex agglutination tests are mainly used to determine specific community acquired meningitis but not to determine hospital acquired meningitis. The cases in our study were a mixture of hospital and community acquired meningitis which was expected as our hospital was the referral centre for neurosurgery. Most of the hospital acquired bacterial meningitis cases in our study were found in patients with congenital hydrocephalus who had undergone ventriculo-peritoneal shunt.
The clinical symptoms and signs of bacterial meningitis in children vary. It depends on the age of the child and duration of disease. Nonspecific signs include abnormal vital signs such as tachycardia and fever, poor feeding, irritability, lethargy, and vomiting.12) Classical signs of meningitis include nuchal rigidity, bulging fontanelle, photophobia, and a positive Kernig’s or Brudzinski’s sign.13) Seizures are present in 20% to 30% of children with bacterial meningitis.15) Other signs like shock, disseminated intravascular coagulation (DIC), purpuric rash, and coma are more common in meningococcal meningitis.14) In this study we also found that a specific triad comprising of fever, poor oral intake and seizures were the most common presentations.
Gram stain has helped clinicians to decide on the choice of empirical antimicrobials. Recently, Diederik, reported that bacterial pathogen can be detected on a CSF Gram stain.15) In our study, we found that although the microorganism was not seen during microscopic examination; the culures were positive. Among the Gram positive bacteria, the coagulase negative staphylococcus, S. aureus and Streptococcus spp were common. If present, they are easily visible between the neutrophils.
Meningitis most commonly presents with a negative Gram stain and it is often considered an enteroviral meningitis with a benign clinical outcome. As such, used alone; the Gram stain could be an insensitive method to diagnose bacterial meningitis.
Therefore, in this study, the clinicians also replied on clinical presentations and several laboratory parameters such as gross appearance of the CSF, TWBC and the result of latex agglutination test. In this study, the organisms were isolated from CSF samples. In our hospital site, positive culture and sensitivity test was 11.1%.
Nonetheless a positive Gram stain result helps clinicians to choose suitable antimicrobial treatment for either Gram negative or Gram positive bacteria while waiting for the relevant culture result. The standard approach to the treatment of meningitis caused by Staphylococcus aureus occurs mainly after neurosurgical procedures or placement of CSF shunts. Antistaphylococcal penicillins are more effective than vancomycin for the treatment of severe S aureus disease, but empirical vancomycin can be used until susceptibility testing results are ready.16-17)
From Malaysia, Hussain et al. (1998) noted that bacterial meningitis patients who were below the age of five years, had a mortality rate of 12.5% and 21 patients (30%) suffered neurologic sequelae. In our study, we found higher mortality rate (31.2%) than the previous study done by Hussain et al. (1998), which was probably due to the differences in the aetiological agent and underlying illness. In this study, twenty patients had suffered from neurological deficient: five had nerve palsy, five had paralysis, four had increase muscle tone, four had skin rash and three had diarrhea (table 3). Evidence indicates that mortality of meningitis among children aged less than 15 years old ranged from 19.6% to 34%.18-19) Mortality is frequently seen among patients with pneumococcal meningitis.19, 20)
There are several prognostic factors involved in the outcome of meningitis. Aetiological agent, primary brain disease, initial consciousness level, very low CSF glucose concentration, presence of bacteremia, and inappropriate antibiotic use have been reported as important risk factors of mortality.21-24) Unlike other studies, we found that young age and altered consciousness were the only two significant factors associated with mortality.
This study was limited to one tertiary centre hospital. The patients in this study do not represent the population of meningitis cases within Malaysia. Further research is needed to obtain more understanding of hospital bacterial meningitis, especially in comparing between types of hospitals, patients’ risk factors, and outcomes among survivors.
CONCLUSION
Infectious meningitis is a big health concern, especially among children. The clinical presentation has not changed in hospital acquired bacterial meningitis compare with community acquired bacterial meningitis. The causative microorganisms in this study focused on hospital associated pathogens in keeping with our hospital setting and attention in neurosurgical management. Clinicians should be alert for changes in presenting symptoms and modify their choice of empirical antimicrobial therapy accordingly. Since high mortality is linked to hospital acquired meningitis, there is a need for physicians to focus attention on patients presenting significant prognostic factors, especially among younger aged patients.
Conflicts of interest
None declared
REFERENCES
- 1).Lee Goldman and Dennis Ausiello. Cecil medicine. Edited by Lee Goldman and Dennis Ausiello. 437–439, 2008, Elsevier Health Sciences, Philadelphia.
- 2).Brigham Narins. Meningitis, bacterial and viral meningitis, World of microbiology and immunology. Edited by Mark Springer. 374–375, 2003, Gale and Design and Thomson Learning, Farmington Hills, USA.
- 3).Jacquelyn G Black. Microbiology principles and explorations. Edited by Anna Melhorn. 680–681, 2002, Von Hoffmann, USA.
- 4).Lolekha S. A Review of Hib epidemiology in asia. Southeast Asian J Trop Med Public Health, 2000; 31(4): 650–657. [PubMed]
- 5).Erleena Nur H, Jamaiah I, Rohela M, Nissapatorn V. Bacterial meningitis: A five year (2001–2005) retrospective study at university malaya medical center (UMMC), kuala lumpur, Malaysia. Southeast Asian J Trop Med Public Health, 2008; 39: 73–77.
- 6).Choo KE, Ariffin WA, Ahmad T, Lim WL, Gururaj AK. Pyogenic meningitis in hospitalized children in Kelantan, Malaysia. Ann Trop Paediatr, 1990; 10: 89–98. [DOI] [PubMed]
- 7).Hussain IH, Sofiah A, Ong LC, Choo KE, Musa MN, Teh KH, Ng HP. Haemophilus influenzae meningitis in Malaysia. Pediatr Infect Dis J, 1998; 17 (9 suppl): 189–190. [DOI] [PubMed]
- 8).Krcmery V, Paradisi F. Pediatric Nosocomial Meningitis Study Group. Nosocomial bacterial and fungal meningitis in children: An eight year national survey reporting 101 cases. Int J Antimicrob Agents, 2000; 15: 143–147. [DOI] [PubMed]
- 9).Gulati S, Kapil A, Das B, Dwivedi SN, Mahapatra AK. Nosocomial infections due to Acinetobacter baumannii in a neurosurgery ICU. Neurol India, 2001; 49: 134–137. [PubMed]
- 10).O’Neill E, Humphreys H, Phillips J, Smyth EG. Third-generation cephalosporin resistance among Gram-negative bacilli causing meningitis in neurosurgical patients: Significant challenges in ensuring effective antibiotic therapy. J Antimicrob Chemother, 2006; 57: 356–359. [DOI] [PubMed]
- 11).Huang CR, Lu CH, Chuang YC, Tsai NW, Chang CC, Chen SF, et al. Adult Pseudomonas aeruginosa meningitis: High incidence of underlying medical and/or postneurosurgical conditions and high mortality rate. Jpn J Infect Dis, 2007; 60: 397–399. [PubMed]
- 12).Matthijs C. Brouwer, Allan R. Tunkel, and Diederik van de Beek. Epidemiology, diagnosis, and antimicrobial treatment of acute bacterial meningitis. Clinical Microbiology Reviews, 2010; 23(3): 467–492. [DOI] [PMC free article] [PubMed]
- 13).Saez-Llorens XM, GH XM. Acute bacterial meningitis beyond the neonatal period. Long: Principles and Practice of Pediatric Infectious Diseases, 2008; 3: 284–291.
- 14).Novelli VP, Peters M, Dobson S. "Infectious diseases," in Care of the Critically Ill Child, edited by Macnab AJ, Macrae DJ, Henning R. 281–298,1999, Churchill Livingstone, London, UK.
- 15).Nabil T. Khoury, Md Monir Hossain, Susan H. Wootton, Lucrecia Salazar, Rodrigo Hasbun, Meningitis with a negative cerebrospinal fluid gram stain in adults: Risk classification for an adverse clinical outcome. Mayo Clin Proc, 2012; 87: 1181–1188. [DOI] [PMC free article] [PubMed]
- 16).Andes DR, Craig WA. Pharmacokinetics and pharmacodynamics of antibiotics in meningitis. Infect Dis Clin North Am, 1999; 13: 595–618. [DOI] [PubMed]
- 17).DeLeo FR, Otto M, Kreiswirth BN, Chambers HF. Communityassociated meticillin-resistant Staphylococcus aureus. Lancet, 2010; 375: 1557–68. [DOI] [PMC free article] [PubMed]
- 18).Khowaja AR, Mohiuddin S, Cohen AL, Khalid A, Mehmood U, Naqvi F, Asad N, Pardhan K, Mulholland K, Hajjeh R, Zaidi AK, Shafqat S. Mortality and neurodevelopmental outcomes of acute bacterial meningitis in children aged <5 years in Pakistan. J Pediatr, 2013; 163 (1 Suppl): S86–S91. [DOI] [PubMed]
- 19).Lovera D, Arbo A. Risk factors for mortality in Paraguayan children with pneumococcal bacterial meningitis. Trop Med Int Health, 2005; 10 (12): 1235–1241. [DOI] [PubMed]
- 20).Odetola FO, Tilford JM, Davis MM. Variation in the use of intracranial-pressure monitoring and mortality in critically ill children with meningitis in the United States. Pediatrics, 2006; 117(6): 1893–1900. [DOI] [PubMed]
- 21).Mombelli G, Klastersky J, Coppens L, Daneau D, Nubourgh Y. Gram negative bacillary meningitis in neurosurgical patients. J Neurosurg, 1983; 58: 634–641. [DOI] [PubMed]
- 22).Lu CH, Chang WN, Chuang YC, Chang HW. Gram-negative bacillary meningitis in adult Post-neurosurgical patients. Surg Neurol, 1999; 52: 438–443. [DOI] [PubMed]
- 23).Federico G, Tumbarello M, Spanu T, Rosell R, Iacoangeli M, Scerrati M, Tacconelli E. Risk factors and prognostic indicators of bacterial meningitis in a cohort of 3580 postneurosurgical patients. Scand J Infect Dis, 2001; 33: 533–537. [DOI] [PubMed]
- 24).Wang KW, Chang WN, Huang CR, Tsai NW, Tsui HW, Wang HC, Su TM, Rau CS, Cheng BC, Chang CS, Chuang YC, Liliang PC, Tsai YD, Lu CH. Post-neurosurgical nosocomial bacterial meningitis in adults: Microbiology, clinical features, and outcomes. J Clin Neurosci, 2005; 12: 647–655. [DOI] [PubMed]