Infectious diseases of the central nervous system (CNS) remain common and life-threatening, especially in developing countries. Knowledge of the aetiological agents responsible for these infections is essential to guide empiric therapy and develop a rational public health policy. To date most data has come from patients admitted to tertiary referral hospitals in Asia and there is limited aetiological data at the provincial hospital level where most patients are seen.
We conducted a prospective Provincial Hospital-based descriptive surveillance study in adults and children at thirteen hospitals in central and southern Viet Nam between August 2007– April 2010. The pathogens of CNS infection were confirmed in CSF and blood samples by using classical microbiology, molecular diagnostics and serology.
We recruited 1241 patients with clinically suspected infection of the CNS. An aetiological agent was identified in 640/1241 (52%) of the patients. The most common pathogens were Streptococcus suis serotype 2 in patients older than 14 years of age (147/617, 24%) and Japanese encephalitis virus in patients less than 14 years old (142/624, 23%). Mycobacterium tuberculosis was confirmed in 34/617 (6%) adult patients and 11/624 (2%) paediatric patients. The acute case fatality rate (CFR) during hospital admission was 73/617 (12%) in adults and to 42/624 (7%) in children.
Citation: Ho Dang Trung N, Le Thi Phuong T, Wolbers M, Nguyen Van Minh H, Nguyen Thanh V, Van MP, et al. (2012) Aetiologies of Central Nervous System Infection in Viet Nam: A Prospective Provincial Hospital-Based Descriptive Surveillance Study. PLoS ONE 7(5): e37825. https://doi.org/10.1371/journal.pone.0037825
Editor: Yury E. Khudyakov, Centers for Disease Control and Prevention, United States of America
Received: December 15, 2011; Accepted: April 24, 2012; Published: May 25, 2012
Copyright: © 2012 Ho Dang Trung et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the Wellcome Trust Major Overseas Programme. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Despite advances in antibiotic treatment and resuscitation, infectious diseases of the central nervous system (CNS) remain life-threatening, especially in developing countries. According to the World Health Organization (WHO), there were approximately 700,000 episodes of meningitis in 2004 and 70% of these patients lived in Africa and South-East Asia . Every year, Japanese encephalitis virus, an important cause of encephalitis in Asia, causes 50,000 encephalitis cases and 15,000 deaths and leaves many survivors with severe neurological and psychiatric sequelae, whilst the case fatality rate in treated patients with tuberculous meningitis (TBM) is 65% in HIV-infected patients and 25% in HIV uninfected patients in Viet Nam , . To reduce the morbidity and mortality of CNS infections, studies are needed to establish the aetiology in order to design rational policies for prevention and empiric and specific treatment. The cause of CNS infection may vary over time, by geographic region, with age, co-morbidities, vaccination programs and the routes by which the pathogens are acquired –. However, the epidemiological data related to the aetiology of CNS infections in Viet Nam are limited and come from tertiary referral hospitals in major cities. The identification of the causes of CNS infections in Viet Nam is difficult for many reasons, including limited bacteriological culture facilities, lack of PCR and viral culture and the widespread use of antibiotics prior to presentation to any hospital. Hence, we conducted a prospective provincial hospital-based surveillance study to identify the causes of CNS infections in central and southern Viet Nam.
Materials and Methods
This study was approved by the Scientific and Ethics Committee of each study site (provincial hospitals), the Hospital for Tropical Diseases and the University of Oxford Tropical Research Ethics Committee (OXTREC 01–08). Informed consent was obtained or proxy consent from a relative was obtained for a patient with GCS score <15 or a patient under 15 year-old on admission. Patients were excluded if they did not provide written informed consent.
Study Design and Setting
A prospective hospital-based descriptive surveillance study was conducted at thirteen hospitals in central and southern Viet Nam, including one district hospital (Sa Dec, Dong Thap), seven provincial hospitals (Dong Thap, An Giang, Kien Giang, Ca Mau, Bac Lieu, Soc Trang, Tra Vinh) and one central referral hospital (Can Tho) in the Mekong River Delta; one provincial hospital (Binh Phuoc) in the South East; one provincial hospital (Dak Lak) in the Central Highlands; and one provincial hospital (Khanh Hoa) and one central referral hospital (Thua Thien-Hue) in central Viet Nam (Figure 1). The study was conducted between August 2007 and April 2010.
Participants and Recruitment
Patients who presented at the infectious diseases ward, intensive care unit or paediatric ward of participating hospitals, were eligible if they met all of the following inclusion criteria; at least one month of age; fever ≥ 38°C (axillary); at least one of the following symptoms or signs: headache, neck stiffness, altered consciousness and focal neurological signs; and a cerebrospinal fluid (CSF) sample taken. Patients were excluded if they or their relatives did not provide written informed consent. The attending physician examined the patients and completed a standardized clinical data form. Data collected included demographics, history and examination findings, past medical history, laboratory findings, treatment and outcome. Four milliliters of CSF were taken from each adult patient and 2 mls from children 5 years of age or older and 1 ml from children under five. Cerebrospinal fluid was sent to the hospital laboratory for cell count, biochemistry measurements and microbiology investigations according to the local standard of care. A half to one milliliter was stored at –20°C and later transferred to the Hospital for Tropical Diseases in Ho Chi Minh City (HTD) on dry ice for further investigations, including 200 µl for diagnostic PCR (bacteria and virus) and 100 µl for JE and Dengue serology. All bacterial isolates from CSF and blood cultures had identification confirmed at HTD and antimicrobial susceptibility assessment.
Adults and children.
Patients were assigned as adults if they were older than or equal to 15 years of age on the day of admission according to Vietnamese law. If they were less than 15 years of age, they were assigned as children.
Case definitions of clinical syndromes.
Clinical syndromes were defined in accordance with WHO case definitions of bacterial meningitis (BM) and viral encephalitis (VE), and using a consensus case definition of TBM , . If CSF lactate was available, it was included in the case definition of BM and viral encephalitis/meningitis (VE/M) (see Table 1). A patient was considered to not have a CNS infection if they had normal CSF parameters with no pathogen identified, and if the clinical diagnosis at discharge was non-infectious such as stroke, epilepsy, psychiatric disorder, drug or alcohol toxicity, hepatic encephalopathy, sepsis, or benign febrile convulsion.
Blood and CSF culture.
Blood and CSF cultures were performed in the microbiology laboratory of the hospitals using standard culture methods. Blood culture was performed using a BD BACTEC® 9050 blood culture system (BD Microbiology, USA) in Dong Thap and Kien Giang hospitals, and by the BacT/Alert blood culture system (bioMérieux, France) in Hue Central hospital. Manual blood culture using commercially available blood culture media purchased in Vietnam (Nam Khoa Biotek, Ho Chi Minh city, Viet Nam) were used in the remaining hospitals. CSF cultures were incubated overnight in candle jars, except in Hue Central hospital where a CO2 incubator was available. Laboratories used the locally available tools for identification of isolates from positive cultures. In addition, all bacterial isolates were sent to HTD for bacterial identification and antimicrobial susceptibility testing.
Internally controlled real-time PCR was used for the detection of Streptococcus pneumoniae, Haemophilus influenzae type b, Neisseria meningitidis, Streptococcus suis serotype 2, Herpes simplex virus 1 and 2, enteroviruses (generic) and Mycobacterium tuberculosis in CSF samples using methods published previously –. The RealAccurate™ Mycobacterium tuberculosis PCR kit (Patho Finder, Maastricht, The Netherlands), targeting the IS6110 sequence, was used to confirm the clinical diagnosis of TBM. This PCR kit is validated for use on respiratory samples. Its sensitivity, specificity, positive predictive value and negative predictive value were evaluated at the HTD laboratory using an appropriate set of CSF samples, including 24 TBM CSF samples confirmed by CSF smear (AFB) or mycobacterial growth indicator tube (MGIT) culture method, 16 BM CSF samples confirmed by culture and 2 Herpes simplex encephalitis CSF samples confirmed by PCR and were 67%, 94%, 94% and 68%, respectively (unpublished data).
(*) Other diagnosis included sinusitis (5 cases), brain tumours (9 cases), cerebral malaria (8 cases), mental disorders (7 cases), headache (7 cases), typhoid fever (5 cases), fever unknown origin (3 cases), autoimmune diseases (12 cases), diarrhoea (6 cases), lumbar disc herniation (2 cases), congenital heart diseases (2 cases), hydrocephalus (1 case), tetanus (1 case), severe anaemia (1 case) and chronic colitis (1 case).
Serological methods (CSF samples).
To confirm infection with JE virus or Dengue virus, a JEV/DENV IgM ELISA assay (Venture Technologies Sdn Bhd Malaysia), was used. This assay uses antigens from JEV and DENV1-DENV4 to demonstrate and distinguish recent infection by these two flaviviruses .
All variables were summarized by group (adult or children). Patients were assigned to confirmed or probable BM, VE/M or TBM according to the pre-specified case definitions of clinical syndromes (Table 1). Epidemiological characteristics of patients were analyzed for all patients with confirmed or probable CNS infections. Categorical variables were summarized as numbers and percentages (%). Continuous variables were summarized as median and interquartile range (IQR). Categorical baseline variables were compared between adults and children using chi-squared test or Fisher’s exact test (when one or more of the expected cell counts was less than 5). Time trends and seasonality of overall admission numbers of children and adults with CNS infections as well as seasonality of the number of S. suis meningitis cases was assessed using Poisson regression models, which modelled the monthly admission counts depending on a hospital effect, a global linear time trend and a sinusoidal shape for the seasonality effect (modelled with a sine- and a cosine-term, i.e. a cosinor model) . The log-number of days per month was used as an offset in the model to correct for unequal lengths of the month. For testing seasonality we tested whether the sine- and the cosine-term could jointly be omitted from the model using a likelihood ratio test. All analyses were performed with Stata version 10.1 (StataCorp, College Station, Texas, USA) and R version 2.11.1 (R Foundation for Statistical Computing, Vienna, Austria) software.
Number of cases: absolute number of adult patients with CNS infection enrolled in the study per month.
Number of cases: absolute number of children with CNS infection enrolled in the study per month.
Between August 2007 and April 2010, 1740 patients fulfilling the inclusion criteria were admitted to 2 central, 10 provincial and 1 district hospitals. None refused to provide consent. Clinical data were not available for 95 patients, including 52 adults and 43 children. In these 95 patients, pathogens were confirmed in 12/52 adults (eight S. suis serotype 2, one S. pneumoniae, one JE virus, one enterovirus and one co-infection with S. suis and enterovirus) and in 13/43 children (four enteroviruses, two JE viruses, two dengue viruses, two H. influenzae, one N. meningitidis and two co-infections with S. pneumoniae and JE virus). After reviewing the clinical presentation and hospital tests of 1645 patients that had complete clinical data and a CSF sample taken, we excluded 247 paediatric and 157 adult patients in the final analysis of the causative aetiology (Figure 2). These patients all had normal CSF data and a clinical history consistent with a non-infectious cause. Thus 1241 patients (617 adults, 624 children) were included in the final analysis.
Epidemiological Characteristics of CNS Infection
Over 80% of CNS infection patients lived in rural areas and belonged to the Kinh ethnic group. The proportion of ethnic minorities amongst children was higher than that in adults (23% versus 14%, p<0.001) (Table 2). The ratio of males to females was 1.92/1.00. The aetiology of CNS infection in children was different to that in adults. VE/M were responsible for 432/624 (70%) of paediatric CNS infections, compared to 209/617 (34%) of adult infections. Acute BM and TBM were more common in the adults (Table 2). The overall case fatality rate (CFR) at provincial hospitals was 73/617 (12%) in adults compared to 42/624 (7%) in children (Table 2). Of patients with TBM, 24/87 (28%) adult patients and 12/31 (39%) paediatric patients died before receiving anti-tuberculosis drugs.
The number of patients admitted to each of the participating hospitals and their distribution in time is depicted in Figure 3 and 4. Analysis of admission patterns of adult patients with CNS infections by Poisson regression revealed on overall linear decline in the incidence by −13% per year (95%CI [−23%; −1%]) and a significant seasonality effect (p<0.01) indicating peak incidence in June and a difference between the peak vs. the average incidence of +21% (95%CI [+8%; 36%]). However, the linear trend failed to reach conventional significance after adjustment for overdispersion (p = 0.06). Moreover, the seasonal pattern was driven by Hue Central hospital alone - the test for seasonality was significant there (p<0.001) but did not reach significance in all other hospitals combined (p = 0.36) (Figure 3). The seasonality at Hue Central hospital was driven by S. suis infection (Figure 5).
Laboratory confirmed aetiology per agegroup (bars) for patients meeting the case definition of bacterial meningitis. “Unknown aetiology” corresponds to patients with a diagnosis of probable bacterial meningitis.
A seasonal pattern of paediatric CNS infection admissions was also noted. Analysis of admission patterns by Poisson regression showed a significant seasonality effect (p<0.001). The admissions to hospitals peaked in June with an amplitude of difference (peak month vs. average) of +51% (95%CI [+34%; +69%]) and a linear time trend of −24% per year (95% CI [−33%; −14%], p<0.001) (Figure 4).
Aetiology of CNS Infection
An aetiological agent was identified in 640/1241 (52%) of patients (Table 3 and 4). The most common pathogens were Streptococcus suis serotype 2 in adults (147/617, 24%) and JE virus in children (142/624, 23%). Mycobacterium tuberculosis was confirmed by PCR in 34/617 (6%) of adults and 11/624 (2%) of children. Dual infection was demonstrated in 22 cases (12 adults, 10 children). Dual infection was most commonly due to dengue virus accompanying a bacterial pathogen (9/22 cases) or JE virus and a bacterial pathogen (7/22 cases).
Laboratory confirmed aetiology per agegroup (bars) for patients meeting the case definition of viral meningitis/encephalitis (excluding dual infection cases). “Unknown aetiology” corresponds to patients with a diagnosis of probable viral encephalitis/meningitis.
Aetiology of Bacterial Meningitis
Bacterial pathogens were identified in 198/302 (66%) of adult patients who fulfilled the clinical criteria of BM, by culture or real-time PCR method. S. suis serotype 2 caused meningitis in 147/302 (49%) of the adult BM group, which was four times higher than meningitis cases caused by S. pneumoniae in this population. S. suis was not isolated from paediatric patients. In children, H. influenzae type b (39/150, 26%) and S. pneumoniae (37/150, 25%) were the main pathogens causing BM (Table 5 and 6). The aetiology of BM varied by age. H. influenzae type b was the most common pathogen in children less than 1 year of age, causing 27/66 (41%) of cases. Over 90% (36/39) of H. influenzae type b cases were reported in the first five years of life. In adults, S. suis serotype 2 caused less than 6/70 (9%) of cases of BM in younger patients (<30 years of age), but was responsible for 141/232 (61%) of BM cases in patients over 30 years old. Twenty five percent of BM cases in children and young adults (56/220) were caused by S. pneumoniae but it was identified in less than 10% (16/232) of patients with BM older than 30 years (Figure 6).
Aetiology of Viral Encephalitis/Meningitis
JE virus was the most common pathogen identified in patients with clinical encephalitis and was responsible for 142/432 (33%) of paediatric VE/M cases. Dengue virus, enteroviruses and Herpes simplex virus were the most common identified viral pathogens in adults, each pathogen accounting for 10% of infections (23/209, 20/209 and 22/209, respectively). A viral pathogen was not identified in 56% (359/641) of patients (Table 7). JE virus was responsible for nearly 40% of encephalitis/meningitis cases in the age group 1–14, but was less common in patients younger than 1 year or older than 15 years (Figure 7).
TBM was responsible for 122/1241 (10%) of cases, including 87/617 (14%) of adult patients and 31/624 (5%) of pediatric patients. Forty nine cases (40%) were confirmed by commercial real-time PCR. Twelve of 122 (10%) patients were classified as probable TBM cases and 61/122 (50%) patients as possible TBM cases using the case definition (see Tables 1, 2 and 3 and 4).
This is the first prospective provincial hospital-based surveillance study on CNS infection in Viet Nam. The participating hospitals function as primary care hospitals for CNS infection patients in their catchment area and therefore the data reflect the burden of disease and associated pathogens within the population. S. suis serotype 2 was the predominant microorganism found in adult patients and was four times as common in adult patients as S. pneumoniae (49% vs. 12%), the most common cause of BM in Europe and the United States , . The results of this study strengthen the results from earlier studies carried out in tertiary referral hospitals in Viet Nam, and in some other intensive pig rearing countries in Asia, in which S. suis is the most important pathogen of BM in adult patients –. JE virus, the most common identified cause of paediatric CNS infection, was responsible for 23% (142/624) of paediatric cases. These findings clearly point at the important role of zoonotic infections in Vietnam, given that pigs, the main source of meat in Vietnam, function as the main reservoir for both pathogens.
The culture method was less sensitive than the PCR method in detection of the main pathogens of bacterial meningitis (Table 3, 4, 5 and 6). This may be related to the fact that nearly half of BM patients (236/452) had received antibiotic drugs prior to admission. Hence, the prevalence of other bacterial infections, which were not tested by PCR method, could be possibly underestimated.
We observed seasonality of CNS infections in both adults and children. In the adult population seasonality was driven by S. suis serotype 2 infections observed at Hue Central hospital. Hue is located in central Vietnam, where there is a larger fluctuation of air ambient temperature during the year, in comparison with the more stable air temperature of the southern provinces. We have previously shown that ingestion of high risk food items is an important risk factor for S. suis infection in Vietnam, in addition to occupational or direct contact due to skin lesions . Bacterial load in contaminated food items is likely to be higher when food is kept at higher ambient temperatures, and this may explain the seasonal pattern observed in Hue. In China and Thailand, more S. suis patients are also admitted during the rainy season, between June and September , . In the case of JE, epidemiological studies have shown that after the monsoon rains Culex mosquitoes, the main vector of JE, breed prolifically with consequent increased disease transmission. In addition, temperature may be an important factor as larval developmental time and extrinsic incubation period of JEV are shorter at higher temperatures .
Similar to other studies on CNS infections in Vietnam, the observed ratio between males and females was greater than 1 , , . In S. suis meningitis, male sex is a risk factor related to exposure to pork and pigs, and the ratio of male to female is about 4/1 . For other etiologies we do not have a good explanation for the male dominance.
H. influenzae type b (Hib) conjugate vaccine has just been introduced to the Vietnamese National Expanded Program on Immunization (NEPI) since June 2010. Consequently, this pathogen was still the most common cause of BM in children, causing a similar proportion of disease as found in other studies from around the world before the Hib conjugate vaccine era –. The incidence rate of Hib meningitis in Vietnamese children is likely to decrease sharply in the next few years, especially in the age group of children less than 5 years of age. In contrast, conjugate multi-valent S. pneumoniae vaccines are not included in the NEPI and JE vaccine is only introduced into NEPI for children 1–5 years of age in the high-risk districts, which are mostly in northern provinces .
VE/M offers a considerable diagnostic challenge to physicians. Previous aetiological studies have reported that at least 60% of patients hospitalized with encephalitis had no cause identified despite extensive laboratory testing , –. Though our study focused on the common viral pathogens of encephalitis/meningitis in Viet Nam, the proportion of patients with suspected VE/M with no pathogen identified was also approximately 60% of all cases –. JE virus is the most important identified cause of encephalitis in the South-East Asia, being responsible for 24% of VE/M cases with over 90% of cases reported in children aged <15 years in this study. JE rarely occurs in adults who live in endemic regions presumably because of exposure to virus during childhood and subsequent immunity . JE may be more common in the north of Viet Nam than in the central and south of Viet Nam. It caused 217/421 (50%) of acute encephalitis syndrome cases in five northern provinces . Another important arboviral infection in humans, dengue, has become the most important epidemic disease in this country. Neurological manifestations of dengue infection were reported in 0.5–6% of hospitalized dengue hemorrhagic fever patients , , . In this study, dengue virus, detected by the presence of specific IgM in CSF, was the only pathogen in 39/641 suspected VE/M cases (6.1%), including 25 adults and 14 children. Our result are similar to other studies in the dengue endemic region, where the proportion of dengue virus ranged from 4.2% to 47% of patients with encephalitis , , –. Dengue should be considered in patients who present with the clinical features of encephalitis, whether or not classical manifestations of dengue are present , .
In Europe and North America, enteroviruses are among the most common causes of viral meningitis in children , . In this study, enteroviruses were the second most common viral pathogen in both adults and children. However, 15/20 adult patients, compared to 6/36 paediatric patients, lived in Thua Thien – Hue province and 14 of these adults, compared to none of the children, were admitted to Hue Central hospital in the period from June to September 2009 (Figure 5). The adult cases observed in our study may therefore be related to an outbreak in Thua Thien – Hue province in the summer of 2009.
Rapid and early diagnosis of CNS infections is fundamental to patient outcome. Physicians face numerous difficulties in establishing a TBM diagnosis, including the often non-specific manifestations, low sensitivity of Ziehl-Neelsen staining and nucleic acid amplification and delays in classical culture methods . To diagnose TBM in this study, we applied the consensus case definition of TBM, which included clinical, CSF, and cerebral imaging information and could be used regardless of patient’s age and HIV status . A commercial real-time PCR test was used to help confirm TBM. Ranking after S. suis serotype 2 meningitis and JE, TBM, which was confirmed in 49 (40%) of suspected TBM cases, was the third most common cause of CNS infection in our study. This is the first report of TBM in a context of CNS infection in Vietnamese provincial hospitals. While TBM was the cause of 143/357 (40%) adult suspected CNS infections admitted to HTD , the overall TBM proportion and its proportion stratified for adults and children were 10% (122/1241), 15% (91/617) and 5% (31/624), respectively in this study. The proportion of TBM at HTD may be higher because HTD receives patients who fail to respond to treatment with antimicrobial agents for the treatment of BM from provincial hospitals, and these patients are often diagnosed with TBM. In addition, the HIV prevalence may be higher in Ho Chi Minh City and surrounding areas resulting in a higher incidence of TBM. The protective role of BCG vaccination against TBM in children may explain why TBM accounted for a lower proportion of cases in children than in adults , .
Dual infections in CNS infection, such as among members of herpesviruses or between a member of this group and a bacterium, have previously been reported in both immunocompetent and immunocompromised patients diagnosed using PCR methods and/or intrathecal antibody determinations –. In this study, we found 20 dual infection cases in 1241 suspected CNS infection patients. Most cases (18/20 cases) were infected with an endemic virus (JE virus, dengue virus or enteroviruses) and a bacterium. DENV and JEV are both endemic in south Vietnam and infection is often asymptomatic. Dual infection of JEV and enteroviruses or H. influenzae type b and enteroviruses was also reported in other studies in South-East Asia , . Our findings emphasize the role of these viruses as a co-infection pathogen in an endemic region and suggest that testing for other pathogens should still be considered when a single pathogen has been identified in the CSF. While the clinical relevance of these co-infections remain unclear, it is tempting to speculate about the interplay between viral and bacterial CNS infections, for example by facilitating entry of one or the other into the CNS compartment .
Cryptococcus neoformans is one of the most important HIV-related opportunistic infections in South-East Asia, where one third of CNS infection in HIV/AIDS patients are due to this pathogen –. It also causes meningitis in HIV uninfected patients in Viet Nam . Only two cases were reported in our study. This may be explained by the limitation of microbiological culture facilities at the provincial hospitals or by the fact that lumbar punctures were not performed in HIV infected patients at these hospitals. In Viet Nam, attending physicians rarely do lumbar puncture on HIV patients at remote provincial hospitals because of their poor prognosis or relative’s refusal.
CNS infections have a high morbidity and mortality. The case fatality rate (CFR) in this study was 12% in adults and 7% in children, but varied widely according to underlying pathogen, ranging from 5–10% in acute BM and VE/M to 30–40% in TBM. This CFR was likely related to deaths prior to prescription of anti-tuberculous drugs because most TBM patients in Vietnam are admitted first to an infectious diseases unit or a neurology unit in a general hospital before being transferred to a specialist tuberculosis unit or hospital where TBM specific treatment is started. This highlights the critical importance of considering TBM in the differential diagnosis of CNS infection throughout Viet Nam and the need for early diagnosis and treatment.
In conclusion, we identified a cause in 640/1241 (52%) suspected CNS infection cases using molecular diagnostic, serological and culture methods. The three most common pathogens in children were JE virus, H. influenzae type b and S. pneumoniae. Meanwhile, S. suis serotype 2 meningitis, an emerging zoonosis in intensive pig rearing countries, caused one fourth (147/617) of adult suspected CNS infection or a half (147/302) of adult purulent BM in Viet Nam. We also found that case fatality rate of TBM exceeded 30% at the provincial hospitals before TBM diagnosis was established. As patient outcome is directly related to early diagnosis and treatment, physicians should always think of TBM in the context of CNS infection in developing countries.
We thank all the patients participated in the research and all of the doctors and nurses, who cared for the patients, from 13 provincial hospitals in the VIZIONS CNS Infection Network.
The VIZIONS CNS Infection Network
Dong Thap Provincial Hospital (Tran Quoc Loi, Nguyen Truong Son, Phan Van Be Bay, Nguyen Thi Hong Tham and Le Thi Phuong).
Sa Dec District Hospital (Le Trung Tri and Nguyen Thi Nguyet Binh).
An Giang Provincial Hospital (Doan Cong Du, Nguyen Thi Phuong Thao, Truong Thi My Tien and Tran Thi Phi La).
Kien Giang Provincial Hospital (Bui Van Cong, Pham Ngoc Diep, Duong Phuoc Dong, Tran Thi Mong Lanh and Pham Van Dom).
Ca Mau Provincial Hospital (Tran Quang Dung, Phan Nhut Tri, Tang Thi Ho and Nguyen Anh Tai).
Bac Lieu Provincial Hospital (Quach Van Luc and Dinh Xuan Phuoc).
Soc Trang Provincial Hospital (Tang Vu, Huynh Thi Thu Thuy, Tran Thi Nguyet Hong, Au Huu Duc, Manh Anh Mai and Nguyen Huu Thu).
Tra Vinh Provincial Hospital (Lam Thi Kim Ngoc).
Can Tho Central Hospital (Nguyen Thi Thanh Tam, Tran Ngo Phuc My, Ngo Van Ut, Lam Tan Phuong, Le Khanh Toan and Dang Quang Tam).
Binh Phuoc Provincial Hospital (Ho Dinh Dung).
Dak Lak Provincial Hospital (Nguyen Hai, Hoang Ngoc Anh Tuan, Hoang Thi Thuy Tien and Tran Thi Ngoc Oanh).
Khanh Hoa Provincial Hospital (Nguyen Dong, Phan The Long, Nguyen Thanh Ngan, Mang Thi Phuong Mai, Pham EnGa, Luu Thi Minh Huong, Nguyen Thi Thuy Ai, Nguyen Ngoc Anh, Nguyen Van Xang and Nguyen Manh Tien).
Hue Central Hospital (Phan Trung Tien, Nguyen Thi Nam Lien, Tran Kiem Hao, Nguyen Thi Nhu Ly, Tran Duy Hoa, Bui Van Doan, Duong Thi Bich Hoa, Tran Thi Thu Anh, Nguyen Xuan Hien, Vo Kim Thanh, Duong Van Thong, Dinh Quang Tuan, Pham Thi Minh Khoa, Hoang Trong Hanh, Tran Thi Diem Lan, Nguyen Thai Thuan, Bui Manh Hung and Bui Duc Phu).
Conceived and designed the experiments: NHDT JF CS HTT MDDJ. Performed the experiments: NHDT TLTP HNVM VNT MPV NTVT TLV DTS PLT TNTP CBV VT THNA DN TPT LNTN HTK TNTT JC CNVV. Analyzed the data: NHDT MW CS JF. Wrote the paper: NHDT JF CS JD HRVD MDDJ MC HTT.
- 1. WHO (2008) The global burden of diseases: 2004 update. Geneva, Switzerland: World Health Organization. WHO2008The global burden of diseases: 2004 update.Geneva, SwitzerlandWorld Health Organization
- 2. Solomon T, Dung NM, Kneen R, Gainsborough M, Vaughn DW, et al. (2000) Japanese encephalitis. J Neurol Neurosurg Psychiatry 68: 405–415.T. SolomonNM DungR. KneenM. GainsboroughDW Vaughn2000Japanese encephalitis.J Neurol Neurosurg Psychiatry68405415
- 3. Thwaites GE, Nguyen DB, Nguyen HD, Hoang TQ, Do TT, et al. (2004) Dexamethasone for the treatment of tuberculous meningitis in adolescents and adults. N Engl J Med 351: 1741–1751.GE ThwaitesDB NguyenHD NguyenTQ HoangTT Do2004Dexamethasone for the treatment of tuberculous meningitis in adolescents and adults.N Engl J Med35117411751
- 4. Lu CH, Huang CR, Chang WN, Chang CJ, Cheng BC, et al. (2002) Community-acquired bacterial meningitis in adults: the epidemiology, timing of appropriate antimicrobial therapy, and prognostic factors. Clin Neurol Neurosurg 104: 352–358.CH LuCR HuangWN ChangCJ ChangBC Cheng2002Community-acquired bacterial meningitis in adults: the epidemiology, timing of appropriate antimicrobial therapy, and prognostic factors.Clin Neurol Neurosurg104352358
- 5. Peltola H (2000) Worldwide Haemophilus influenzae type b disease at the beginning of the 21st century: global analysis of the disease burden 25 years after the use of the polysaccharide vaccine and a decade after the advent of conjugates. Clin Microbiol Rev 13: 302–317.H. Peltola2000Worldwide Haemophilus influenzae type b disease at the beginning of the 21st century: global analysis of the disease burden 25 years after the use of the polysaccharide vaccine and a decade after the advent of conjugates.Clin Microbiol Rev13302317
- 6. Solomon T (2004) Flavivirus encephalitis. N Engl J Med 351: 370–378.T. Solomon2004Flavivirus encephalitis.N Engl J Med351370378
- 7. WHO (2003) WHO-recomended standards for surveillance of selected vaccine-preventable diseases. Geneva, Switzerland: World Health Organisation. WHO2003WHO-recomended standards for surveillance of selected vaccine-preventable diseases.Geneva, SwitzerlandWorld Health Organisation
- 8. Marais S, Thwaites G, Schoeman JF, Torok ME, Misra UK, et al. (2010) Tuberculous meningitis: a uniform case definition for use in clinical research. Lancet Infect Dis 10: 803–812.S. MaraisG. ThwaitesJF SchoemanME TorokUK Misra2010Tuberculous meningitis: a uniform case definition for use in clinical research.Lancet Infect Dis10803812
- 9. Corless CE, Guiver M, Borrow R, Edwards-Jones V, Fox AJ, et al. (2001) Simultaneous detection of Neisseria meningitidis, Haemophilus influenzae, and Streptococcus pneumoniae in suspected cases of meningitis and septicemia using real-time PCR. J Clin Microbiol 39: 1553–1558.CE CorlessM. GuiverR. BorrowV. Edwards-JonesAJ Fox2001Simultaneous detection of Neisseria meningitidis, Haemophilus influenzae, and Streptococcus pneumoniae in suspected cases of meningitis and septicemia using real-time PCR.J Clin Microbiol3915531558
- 10. Jerome KR, Huang ML, Wald A, Selke S, Corey L (2002) Quantitative stability of DNA after extended storage of clinical specimens as determined by real-time PCR. J Clin Microbiol 40: 2609–2611.KR JeromeML HuangA. WaldS. SelkeL. Corey2002Quantitative stability of DNA after extended storage of clinical specimens as determined by real-time PCR.J Clin Microbiol4026092611
- 11. Beld M, Minnaar R, Weel J, Sol C, Damen M, et al. (2004) Highly sensitive assay for detection of enterovirus in clinical specimens by reverse transcription-PCR with an armored RNA internal control. J Clin Microbiol 42: 3059–3064.M. BeldR. MinnaarJ. WeelC. SolM. Damen2004Highly sensitive assay for detection of enterovirus in clinical specimens by reverse transcription-PCR with an armored RNA internal control.J Clin Microbiol4230593064
- 12. Nga TV, Nghia HD, Tu le TP, Diep TS, Mai NT, et al. (2011) Real-time PCR for detection of Streptococcus suis serotype 2 in cerebrospinal fluid of human patients with meningitis. Diagn Microbiol Infect Dis 70: 461–467.TV NgaHD NghiaTP Tu leTS DiepNT Mai2011Real-time PCR for detection of Streptococcus suis serotype 2 in cerebrospinal fluid of human patients with meningitis.Diagn Microbiol Infect Dis70461467
- 13. Cardosa MJ, Wang SM, Sum MS, Tio PH (2002) Antibodies against prM protein distinguish between previous infection with dengue and Japanese encephalitis viruses. BMC Microbiol 2: 9.MJ CardosaSM WangMS SumPH Tio2002Antibodies against prM protein distinguish between previous infection with dengue and Japanese encephalitis viruses.BMC Microbiol29
- 14. Barnett AG, Dobson AJ (2010) Analysing Seasonal Health Data (Statistics for Biology and Health): Springer. AG BarnettAJ Dobson2010Analysing Seasonal Health Data (Statistics for Biology and Health): Springer
- 15. Gjini AB, Stuart JM, Lawlor DA, Cartwright KA, Christensen H, et al. (2006) Changing epidemiology of bacterial meningitis among adults in England and Wales 1991–2002. Epidemiol Infect 134: 567–569.AB GjiniJM StuartDA LawlorKA CartwrightH. Christensen2006Changing epidemiology of bacterial meningitis among adults in England and Wales 1991–2002.Epidemiol Infect134567569
- 16. Durand ML, Calderwood SB, Weber DJ, Miller SI, Southwick FS, et al. (1993) Acute bacterial meningitis in adults. A review of 493 episodes. N Engl J Med 328: 21–28.ML DurandSB CalderwoodDJ WeberSI MillerFS Southwick1993Acute bacterial meningitis in adults. A review of 493 episodes.N Engl J Med3282128
- 17. Yu H, Jing H, Chen Z, Zheng H, Zhu X, et al. (2006) Human Streptococcus suis outbreak, Sichuan, China. Emerg Infect Dis 12: 914–920.H. YuH. JingZ. ChenH. ZhengX. Zhu2006Human Streptococcus suis outbreak, Sichuan, China.Emerg Infect Dis12914920
- 18. Suankratay C, Intalapaporn P, Nunthapisud P, Arunyingmongkol K, Wilde H (2004) Streptococcus suis meningitis in Thailand. Southeast Asian J Trop Med Public Health 35: 868–876.C. SuankratayP. IntalapapornP. NunthapisudK. ArunyingmongkolH. Wilde2004Streptococcus suis meningitis in Thailand.Southeast Asian J Trop Med Public Health35868876
- 19. Kay R, Cheng AF, Tse CY (1995) Streptococcus suis infection in Hong Kong. Qjm 88: 39–47.R. KayAF ChengCY Tse1995Streptococcus suis infection in Hong Kong.Qjm883947
- 20. Mai NT, Hoa NT, Nga TV, Linh le D, Chau TT, et al. (2008) Streptococcus suis meningitis in adults in Vietnam. Clin Infect Dis 46: 659–667.NT MaiNT HoaTV NgaD. Linh leTT Chau2008Streptococcus suis meningitis in adults in Vietnam.Clin Infect Dis46659667
- 21. Wertheim HF, Nguyen HN, Taylor W, Lien TT, Ngo HT, et al. (2009) Streptococcus suis, an important cause of adult bacterial meningitis in northern Vietnam. PLoS One 4: e5973.HF WertheimHN NguyenW. TaylorTT LienHT Ngo2009Streptococcus suis, an important cause of adult bacterial meningitis in northern Vietnam.PLoS One4e5973
- 22. Ho DT, Le TP, Wolbers M, Cao QT, Nguyen VM, et al. (2011) Risk Factors of Streptococcus suis Infection in Vietnam. A Case-Control Study. PLoS One 6: e17604.DT HoTP LeM. WolbersQT CaoVM Nguyen2011Risk Factors of Streptococcus suis Infection in Vietnam. A Case-Control Study.PLoS One6e17604
- 23. Wangkaew S, Chaiwarith R, Tharavichitkul P, Supparatpinyo K (2006) Streptococcus suis infection: a series of 41 cases from Chiang Mai University Hospital. J Infect 52: 455–460.S. WangkaewR. ChaiwarithP. TharavichitkulK. Supparatpinyo2006Streptococcus suis infection: a series of 41 cases from Chiang Mai University Hospital.J Infect52455460
- 24. Nguyen TH, Tran TH, Thwaites G, Ly VC, Dinh XS, et al. (2007) Dexamethasone in Vietnamese adolescents and adults with bacterial meningitis. N Engl J Med 357: 2431–2440.TH NguyenTH TranG. ThwaitesVC LyXS Dinh2007Dexamethasone in Vietnamese adolescents and adults with bacterial meningitis.N Engl J Med35724312440
- 25. Le VT, Phan TQ, Do QH, Nguyen BH, Lam QB, et al. (2010) Viral etiology of encephalitis in children in southern Vietnam: results of a one-year prospective descriptive study. PLoS Negl Trop Dis 4: e854.VT LeTQ PhanQH DoBH NguyenQB Lam2010Viral etiology of encephalitis in children in southern Vietnam: results of a one-year prospective descriptive study.PLoS Negl Trop Dis4e854
- 26. Tran TT, Le QT, Tran TN, Nguyen NT, Pedersen FK, et al. (1998) The etiology of bacterial pneumonia and meningitis in Vietnam. Pediatr Infect Dis J 17: S192–194.TT TranQT LeTN TranNT NguyenFK Pedersen1998The etiology of bacterial pneumonia and meningitis in Vietnam.Pediatr Infect Dis J17S192194
- 27. Muangchana C, Chunsuttiwat S, Rerks-Ngarm S, Kunasol P (2009) Bacterial meningitis incidence in Thai children estimated by a rapid assessment tool (RAT). Southeast Asian J Trop Med Public Health 40: 553–562.C. MuangchanaS. ChunsuttiwatS. Rerks-NgarmP. Kunasol2009Bacterial meningitis incidence in Thai children estimated by a rapid assessment tool (RAT).Southeast Asian J Trop Med Public Health40553562
- 28. Al-Tawfiq JA, Abukhamsin A (2009) Burden and etiology of community-acquired bacterial meningitis in a hospital in Eastern Saudi Arabia: 1993–2005. Med Sci Monit 15: PI10–14.JA Al-TawfiqA. Abukhamsin2009Burden and etiology of community-acquired bacterial meningitis in a hospital in Eastern Saudi Arabia: 1993–2005.Med Sci Monit15PI1014
- 29. Cho HK, Lee H, Kang JH, Kim KN, Kim DS, et al. (2010) The causative organisms of bacterial meningitis in Korean children in 1996–2005. J Korean Med Sci 25: 895–899.HK ChoH. LeeJH KangKN KimDS Kim2010The causative organisms of bacterial meningitis in Korean children in 1996–2005.J Korean Med Sci25895899
- 30. Molyneux E, Riordan FA, Walsh A (2006) Acute bacterial meningitis in children presenting to the Royal Liverpool Children’s Hospital, Liverpool, UK and the Queen Elizabeth Central Hospital in Blantyre, Malawi: a world of difference. Ann Trop Paediatr 26: 29–37.E. MolyneuxFA RiordanA. Walsh2006Acute bacterial meningitis in children presenting to the Royal Liverpool Children’s Hospital, Liverpool, UK and the Queen Elizabeth Central Hospital in Blantyre, Malawi: a world of difference.Ann Trop Paediatr262937
- 31. Yen NT, Duffy MR, Hong NM, Hien NT, Fischer M, et al. (2010) Surveillance for Japanese encephalitis in Vietnam, 1998–2007. Am J Trop Med Hyg 83: 816–819.NT YenMR DuffyNM HongNT HienM. Fischer2010Surveillance for Japanese encephalitis in Vietnam, 1998–2007.Am J Trop Med Hyg83816819
- 32. Glaser CA, Honarmand S, Anderson LJ, Schnurr DP, Forghani B, et al. (2006) Beyond viruses: clinical profiles and etiologies associated with encephalitis. Clin Infect Dis 43: 1565–1577.CA GlaserS. HonarmandLJ AndersonDP SchnurrB. Forghani2006Beyond viruses: clinical profiles and etiologies associated with encephalitis.Clin Infect Dis4315651577
- 33. Granerod J, Ambrose HE, Davies NW, Clewley JP, Walsh AL, et al. (2010) Causes of encephalitis and differences in their clinical presentations in England: a multicentre, population-based prospective study. Lancet Infect Dis 10: 835–844.J. GranerodHE AmbroseNW DaviesJP ClewleyAL Walsh2010Causes of encephalitis and differences in their clinical presentations in England: a multicentre, population-based prospective study.Lancet Infect Dis10835844
- 34. Yong YK, Chong HT, Wong KT, Tan CT, Devi S (2008) Aetiology of viral central nervous system infection, a Malaysian study. Neurology Asia 13: 65–71.YK YongHT ChongKT WongCT TanS. Devi2008Aetiology of viral central nervous system infection, a Malaysian study.Neurology Asia136571
- 35. Huppatz C, Durrheim DN, Levi C, Dalton C, Williams D, et al. (2009) Etiology of encephalitis in Australia, 1990–2007. Emerg Infect Dis 15: 1359–1365.C. HuppatzDN DurrheimC. LeviC. DaltonD. Williams2009Etiology of encephalitis in Australia, 1990–2007.Emerg Infect Dis1513591365
- 36. Ha D, Huong V, Loan H, Thong D, Deubel V (1994) Current situation of Japanese encephaltis in the South of Viet Nam, 1976–1992. Trop Med. pp. 202–214.D. HaV. HuongH. LoanD. ThongV. Deubel1994Current situation of Japanese encephaltis in the South of Viet Nam, 1976–1992.Trop Med202214
- 37. Solomon T, Dung NM, Vaughn DW, Kneen R, Thao LT, et al. (2000) Neurological manifestations of dengue infection. Lancet 355: 1053–1059.T. SolomonNM DungDW VaughnR. KneenLT Thao2000Neurological manifestations of dengue infection.Lancet35510531059
- 38. Tu PV, Thao NT, Perera D, Huu TK, Tien NT, et al. (2007) Epidemiologic and virologic investigation of hand, foot, and mouth disease, southern Vietnam, 2005. Emerg Infect Dis 13: 1733–1741.PV TuNT ThaoD. PereraTK HuuNT Tien2007Epidemiologic and virologic investigation of hand, foot, and mouth disease, southern Vietnam, 2005.Emerg Infect Dis1317331741
- 39. Cam BV, Fonsmark L, Hue NB, Phuong NT, Poulsen A, et al. (2001) Prospective case-control study of encephalopathy in children with dengue hemorrhagic fever. Am J Trop Med Hyg 65: 848–851.BV CamL. FonsmarkNB HueNT PhuongA. Poulsen2001Prospective case-control study of encephalopathy in children with dengue hemorrhagic fever.Am J Trop Med Hyg65848851
- 40. Hendarto SK, Hadinegoro SR (1992) Dengue encephalopathy. Acta Paediatr Jpn 34: 350–357.SK HendartoSR Hadinegoro1992Dengue encephalopathy.Acta Paediatr Jpn34350357
- 41. Jackson S, Mullings A, Bennett F, Khan C, Gordon-Strachan G, et al. (2008) Dengue Infection in Patients Presenting with Neurological Manifestations in a Dengue Endemic Population. West Indian Med J 57: 473–476.S. JacksonA. MullingsF. BennettC. KhanG. Gordon-Strachan2008Dengue Infection in Patients Presenting with Neurological Manifestations in a Dengue Endemic Population.West Indian Med J57473476
- 42. Soares CN, Cabral-Castro MJ, Peralta JM, de Freitas MR, Zalis M, et al. (2011) Review of the etiologies of viral meningitis and encephalitis in a dengue endemic region. J Neurol Sci. CN SoaresMJ Cabral-CastroJM PeraltaMR de FreitasM. Zalis2011Review of the etiologies of viral meningitis and encephalitis in a dengue endemic region.J Neurol Sci
- 43. Srey VH, Sadones H, Ong S, Mam M, Yim C, et al. (2002) Etiology of encephalitis syndrome among hospitalized children and adults in Takeo, Cambodia, 1999–2000. Am J Trop Med Hyg 66: 200–207.VH SreyH. SadonesS. OngM. MamC. Yim2002Etiology of encephalitis syndrome among hospitalized children and adults in Takeo, Cambodia, 1999–2000.Am J Trop Med Hyg66200207
- 44. Varatharaj A (2010) Encephalitis in the clinical spectrum of dengue infection. Neurol India 58: 585–591.A. Varatharaj2010Encephalitis in the clinical spectrum of dengue infection.Neurol India58585591
- 45. Ihekwaba UK, Kudesia G, McKendrick MW (2008) Clinical features of viral meningitis in adults: significant differences in cerebrospinal fluid findings among herpes simplex virus, varicella zoster virus, and enterovirus infections. Clin Infect Dis 47: 783–789.UK IhekwabaG. KudesiaMW McKendrick2008Clinical features of viral meningitis in adults: significant differences in cerebrospinal fluid findings among herpes simplex virus, varicella zoster virus, and enterovirus infections.Clin Infect Dis47783789
- 46. Lee BE, Chawla R, Langley JM, Forgie SE, Al-Hosni M, et al. (2006) Paediatric Investigators Collaborative Network on Infections in Canada (PICNIC) study of aseptic meningitis. BMC Infect Dis 6: 68.BE LeeR. ChawlaJM LangleySE ForgieM. Al-Hosni2006Paediatric Investigators Collaborative Network on Infections in Canada (PICNIC) study of aseptic meningitis.BMC Infect Dis668
- 47. Thwaites G, Chau TT, Mai NT, Drobniewski F, McAdam K, et al. (2000) Tuberculous meningitis. J Neurol Neurosurg Psychiatry 68: 289–299.G. ThwaitesTT ChauNT MaiF. DrobniewskiK. McAdam2000Tuberculous meningitis.J Neurol Neurosurg Psychiatry68289299
- 48. Thwaites GE, Chau TT, Stepniewska K, Phu NH, Chuong LV, et al. (2002) Diagnosis of adult tuberculous meningitis by use of clinical and laboratory features. Lancet 360: 1287–1292.GE ThwaitesTT ChauK. StepniewskaNH PhuLV Chuong2002Diagnosis of adult tuberculous meningitis by use of clinical and laboratory features.Lancet36012871292
- 49. Kumar P, Kumar R, Srivastava KL, Kumar M (2005) Protective role of BCG vaccination against tuberculous meningitis in Indian children: a reappraisal. Natl Med J India 18: 7–11.P. KumarR. KumarKL SrivastavaM. Kumar2005Protective role of BCG vaccination against tuberculous meningitis in Indian children: a reappraisal.Natl Med J India18711
- 50. Trunz BB, Fine P, Dye C (2006) Effect of BCG vaccination on childhood tuberculous meningitis and miliary tuberculosis worldwide: a meta-analysis and assessment of cost-effectiveness. Lancet 367: 1173–1180.BB TrunzP. FineC. Dye2006Effect of BCG vaccination on childhood tuberculous meningitis and miliary tuberculosis worldwide: a meta-analysis and assessment of cost-effectiveness.Lancet36711731180
- 51. Vianello F, Barbaro F, Cogo P, Furlan A, Trevenzoli M, et al. (2008) Co-infection with Mycoplasma pneumoniae and human herpesvirus 6 (HHV-6) in an immunocompetent child with meningoencephalitis: a random association? Infection 36: 174–176.F. VianelloF. BarbaroP. CogoA. FurlanM. Trevenzoli2008Co-infection with Mycoplasma pneumoniae and human herpesvirus 6 (HHV-6) in an immunocompetent child with meningoencephalitis: a random association?Infection36174176
- 52. Casas I, Tenorio A, de Ory F, Lozano A, Echevarria JM (1996) Detection of both herpes simplex and varicella-zoster viruses in cerebrospinal fluid from patients with encephalitis. J Med Virol 50: 82–92.I. CasasA. TenorioF. de OryA. LozanoJM Echevarria1996Detection of both herpes simplex and varicella-zoster viruses in cerebrospinal fluid from patients with encephalitis.J Med Virol508292
- 53. Yamamoto T, Nakamura Y (2000) A single tube PCR assay for simultaneous amplification of HSV-1/−2, VZV, CMV, HHV-6A/−6B, and EBV DNAs in cerebrospinal fluid from patients with virus-related neurological diseases. J Neurovirol 6: 410–417.T. YamamotoY. Nakamura2000A single tube PCR assay for simultaneous amplification of HSV-1/−2, VZV, CMV, HHV-6A/−6B, and EBV DNAs in cerebrospinal fluid from patients with virus-related neurological diseases.J Neurovirol6410417
- 54. Tang YW, Espy MJ, Persing DH, Smith TF (1997) Molecular evidence and clinical significance of herpesvirus coinfection in the central nervous system. J Clin Microbiol 35: 2869–2872.YW TangMJ EspyDH PersingTF Smith1997Molecular evidence and clinical significance of herpesvirus coinfection in the central nervous system.J Clin Microbiol3528692872
- 55. Koskiniemi M, Piiparinen H, Mannonen L, Rantalaiho T, Vaheri A (1996) Herpes encephalitis is a disease of middle aged and elderly people: polymerase chain reaction for detection of herpes simplex virus in the CSF of 516 patients with encephalitis. The Study Group. J Neurol Neurosurg Psychiatry 60: 174–178.M. KoskiniemiH. PiiparinenL. MannonenT. RantalaihoA. Vaheri1996Herpes encephalitis is a disease of middle aged and elderly people: polymerase chain reaction for detection of herpes simplex virus in the CSF of 516 patients with encephalitis. The Study Group.J Neurol Neurosurg Psychiatry60174178
- 56. Weinberg A, Bloch KC, Li S, Tang YW, Palmer M, et al. (2005) Dual infections of the central nervous system with Epstein-Barr virus. J Infect Dis 191: 234–237.A. WeinbergKC BlochS. LiYW TangM. Palmer2005Dual infections of the central nervous system with Epstein-Barr virus.J Infect Dis191234237
- 57. Ooi MH, Wong SC, Podin Y, Akin W, del Sel S, et al. (2007) Human enterovirus 71 disease in Sarawak, Malaysia: a prospective clinical, virological, and molecular epidemiological study. Clin Infect Dis 44: 646–656.MH OoiSC WongY. PodinW. AkinS. del Sel2007Human enterovirus 71 disease in Sarawak, Malaysia: a prospective clinical, virological, and molecular epidemiological study.Clin Infect Dis44646656
- 58. Park BJ, Wannemuehler KA, Marston BJ, Govender N, Pappas PG, et al. (2009) Estimation of the current global burden of cryptococcal meningitis among persons living with HIV/AIDS. Aids 23: 525–530.BJ ParkKA WannemuehlerBJ MarstonN. GovenderPG Pappas2009Estimation of the current global burden of cryptococcal meningitis among persons living with HIV/AIDS.Aids23525530
- 59. Ganiem AR, Parwati I, Wisaksana R, van der Zanden A, van de Beek D, et al. (2009) The effect of HIV infection on adult meningitis in Indonesia: a prospective cohort study. Aids 23: 2309–2316.AR GaniemI. ParwatiR. WisaksanaA. van der ZandenD. van de Beek2009The effect of HIV infection on adult meningitis in Indonesia: a prospective cohort study.Aids2323092316
- 60. Tansuphasawadikul S, Amornkul PN, Tanchanpong C, Limpakarnjanarat K, Kaewkungwal J, et al. (1999) Clinical presentation of hospitalized adult patients with HIV infection and AIDS in Bangkok, Thailand. J Acquir Immune Defic Syndr 21: 326–332.S. TansuphasawadikulPN AmornkulC. TanchanpongK. LimpakarnjanaratJ. Kaewkungwal1999Clinical presentation of hospitalized adult patients with HIV infection and AIDS in Bangkok, Thailand.J Acquir Immune Defic Syndr21326332
- 61. Le T, Hong Chau TT, Kim Cuc NT, Si Lam P, Manh Sieu TP, et al. (2010) AIDS-associated Cryptococcus neoformans and Penicillium marneffei coinfection: a therapeutic dilemma in resource-limited settings. Clin Infect Dis 51: e65–68.T. LeTT Hong ChauNT Kim CucP. Si LamTP Manh Sieu2010AIDS-associated Cryptococcus neoformans and Penicillium marneffei coinfection: a therapeutic dilemma in resource-limited settings.Clin Infect Dis51e6568
- 62. Chau TT, Mai NH, Phu NH, Nghia HD, Chuong LV, et al. (2010) A prospective descriptive study of cryptococcal meningitis in HIV uninfected patients in Vietnam - high prevalence of Cryptococcus neoformans var grubii in the absence of underlying disease. BMC Infect Dis 10: 199.TT ChauNH MaiNH PhuHD NghiaLV Chuong2010A prospective descriptive study of cryptococcal meningitis in HIV uninfected patients in Vietnam - high prevalence of Cryptococcus neoformans var grubii in the absence of underlying disease.BMC Infect Dis10199
- 63. Lo Re V, 3rd , Gluckman SJ (2003) Eosinophilic meningitis. Am J Med 114: 217–223.V. Lo Re3rdSJ Gluckman2003Eosinophilic meningitis.Am J Med114217223