Epidemiology of bacterial meningitis in children admitted to Gondar University Hospital in the post pneumococcal vaccine era
Ashenafi Tazebew Amare, Zemene Tigabu Kebede, Henry Delois Welch
Corresponding author: Ashenafi Tazebew, Department of Paediatrics, University of Gondar College of Medicine and Health Sciences, Gondar, Ethiopia
Received: 06 Jul 2016 - Accepted: 12 Nov 2018 - Published: 20 Nov 2018
Domain: Epidemiology
Keywords: Meningitis, children, resource limited, Ethiopia, pneumococcal vaccine
©Ashenafi Tazebew Amare et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Ashenafi Tazebew Amare et al. Epidemiology of bacterial meningitis in children admitted to Gondar University Hospital in the post pneumococcal vaccine era. Pan African Medical Journal. 2018;31:193. [doi: 10.11604/pamj.2018.31.193.10254]
Available online at: https://www.panafrican-med-journal.com//content/article/31/193/full
Original article
Epidemiology of bacterial meningitis in children admitted to Gondar University Hospital in the post pneumococcal vaccine era
Epidemiology of bacterial meningitis in children admitted to Gondar University Hospital in the post pneumococcal vaccine era
Ashenafi Tazebew Amare1,&, Zemene Tigabu Kebede1, Henry Delois Welch2
1Department of Paediatrics, University of Gondar College of Medicine and Health Sciences, Gondar, Ethiopia, 2Baylor College of Medicine, Houston, USA
&Corresponding author
Ashenafi Tazebew, Department of Paediatrics, University of Gondar College of Medicine and Health Sciences, Gondar, Ethiopia
Introduction: community acquired bacterial meningitis (CABM) is responsible for high mortality and disabling sequelae. Introduction of pneumococcal conjugate vaccine (PCV-10) and haemophilus influenzea type b (Hib) has changed the epidemiological and clinical features of patients presenting with CABM as it is shown in different literatures over the last decade. The aim of this study was to assess the clinical and epidemiologic features and outcomes of CABM after the introduction of PCV-10 in Gondar University Hospital (GUH).
Methods: this is a retrospective study among children between 2 months and 14 years of age discharged from Gondar University Hospital. All patient records discharged with a diagnosis of meningitis at GUH were reviewed from September 2011 - September 2013. The data was collected using a structured questionnaire from the patient record charts and analysis was done using SPSS-20.
Results: 80 cases (1.6%) of CABM out of 4996 admissions were identified. There were 60 (75%) cases of CABM using WHO criteria of cerebrospinal fluid leukocytosis (CSF) > 100cells/mm3, or 10-100cells/mm3 with either hypoglycorrhea or increased protein; and 20 (25%) with culture confirmation. S. Pneumoniae was the most frequent pathogen identified in 14 (70%) children. The most common age group were infants 2-12 month old (n = 32, 40%). Children with adverse outcomes had shown a higher frequency of being older children (p = 0.045), loss of consciousness (p = 0.046), seizure at admission (p < 0.01), and a positive CSF culture (p = 0.03).
Conclusion: introduction of PCV-10 has shown a decreased admission rate, mortality, and neurologic sequelae due to CABM.
Community acquired bacterial meningitis is a life threatening infection of the leptomeninges often related with serious complication and sequelae. Low and middle-income countries account for 98% of the estimated 5.6 million disability-adjusted life years attributed to meningitis globally. In high-income countries, bacterial meningitis ranks among the top ten causes of death in children younger than 14 years of age [1]. Primary prevention of meningitis using vaccines is paramount, since death and long-term disabling sequelae are substantial in all settings especially those with least access to health care [2]. Bacterial meningitis accounts for approximately 6-8% of hospital admissions in Ethiopia with a case fatality rate of as high as 22-28 [3]. The most common pathogens being S. pneumonia, N. meningitides and H.influenzea [4-6]. During the last several decades disease epidemiology and clinical features has changed dramatically in the countries that adapted the conjugate vaccines against H. influenza type b and S. pneumoniae [7-11]. In Ethiopia the implementation of Hib and PCV-10 started in 2007 and 2011, respectively. However, the impact of these vaccines on the disease epidemiology and clinical features are investigated in few international studies. Knowledge about the clinical and epidemiologic features will help practicing physicians to suspect and diagnose CABM as early as possible. Knowledge about factors associated with poor prognosis are valuable in selecting patients for more intensive monitoring and treatment. Especially in resource constrained settings where such equipment may be limited. The aim of this study was to assess the epidemiological and clinical features of CABM in our environment and to evaluate the short term outcome of CABM in Gondar University Hospital after the introduction of PCV-10 and Hib in our country.
This retrospective study was conducted at Gondar University Hospital (GUH). Gondar is a city located in the North West Ethiopia, which is in the sub-Saharan meningitis belt. Most of the patients come from Gondar, but also receives patients from the adjoining regions of Amhara Regional State. The Gondar University Hospital is the largest hospital in Gondar. It is a 400-bed teaching hospital associated with a medical college. The department of pediatrics and child health has 5 different wards the main pediatric main ward has 46 beds and provides inpatient care for children < 14 years of age. All admissions and discharges to the pediatric main ward were reviewed over a 2 years period from September, 2011 through September, 2013. Potential cases were identified from the admission registration books after which the clinical and laboratory data were obtained from the individual case records. The cases were chosen based on the inclusion criteria of those patients older than 2 month and younger than 15 years and who fulfill the case definition of acute bacterial meningitis and have a full documentation. After the cases were chosen the following data was obtained from the records of the individual cases: 1) relevant clinical parameters including month of admission, demographic data, clinical features, risk factors, duration of symptoms, preadmission antibiotics and duration of stay; 2) treatment characteristics like choice antibiotics, dexamethasone and duration of treatment; 3) microbiological data: Gram stain, culture, cellular profile as well as relevant biochemical data from the CSF; 4) outcome variables comprising of death, short term complications and disappearance
Operational definitions
Case definition: both probable and confirmed bacterial meningitis cases according to World Health Organization definition were included [12].
Probable meningitis: defined as culture-negative results but with the typical finding in cerebrospinal fluid: leukocytosis (polymorphonuclear leucocytes) > 100 cells/mm3 leukocytosis (polymorphonuclear leucocytes) 10-100cells/mm3and either elevated protein (> 100mg/dL) or decreased glucose (< 40mg/dL).
Confirmed meningitis: laboratory-confirmed by growing (culture) or identifying (by Gram stain or antigen detection methods) a bacterial pathogen in the CSF or from the blood in a child with clinical syndrome consistent with bacterial meningitis
Poor short term outcome: is defined as death or an adverse neurological outcome that was noted at the time of discharge from the hospital and that was attributable to the episode of meningitis
Data analysis: the clinical and epidemiologic data were analyzed using SPSS-20. The Chi square or Fisher exact test were used were used for assessing putative associations with adverse outcome. The confidence intervals relative risk and odds ratio were obtained as applicable. Significant association were presumed if P < 0.05. Binary logistic regression was used to identify the risk variables for the development of complications or death. For all the tests we considered a minimum significance level of 5%, with a power of 95%. The study was approved by the Institutional Review Board at Gondar University Hospital.
Over the past two years 80 children were discharged with the diagnosis of CABM. During this time there were 4994 admissions, giving an admission rate for CABM 1.6% during the study period. A peak admission rate was registered during the month of March (n=18, 22.5%) followed by February (n = 12, 15%) coinciding with the dry season. Bacterial meningitis was more common in children under one year (40%), and most patients were male (65%). Distribution of residence was slightly higher among urban and rural areas (53% vs 47%). Other demographic and clinical characteristics are shown in Table 1. Possible predisposing factors for meningitis were upper respiratory traction infection (25%), lack of breastfeeding (10%), previous admission (10%), lack of immunization (10%) and malnutrition of both moderate and severe in 2.5%. Of the children who werenot vaccinated or partially vaccinated, 4(50%) of them were infants and the rest are above one year of age. Only 12 (15%) of patients were admitted to our hospital within 24 hour of the onset of symptoms, the majority presented after 24 hours but within 72 hours (n = 34, 42.5%) or after 72 hours (n = 34, 42.5%). Among those admitted 22 (27.5%) received some form of antibiotics in local health centers The most common clinical manifestations for each age group are shown in Table 2. Almost all patients (n = 78, 97.5%) had CSF examination done immediately after admission, the results are shown in Table 2. Moderate pleocytosis (>1000cells/mm3) was found in 20% of children, the majority of the patients (75%) had cell count between 100-1000, cells/mm3 with a neutrophil predominance (70-98%). Hypoglycorrhea and elevated protein level was fond in 42.5%. Of 80 patients diagnosed with CABM, 20 (25%) of cases had culture confirmed ABM, S. pneumoniae was isolated in 14/20 (70%) and H. influenzea in 4/20 (20%) of the cases.
Age related clinical and laboratory features of bacterial meningitis are shown in Table 2 and Table 3. There is no specific sign or symptom which can predict culture positivity as it's shown on analysis of symptoms versus the culture positivity rate Table 4. The majority of patients (n = 50, 62.5%) were treated with ceftriaxone and the rest with a combination of penicillin and chloramphenicol (n = 30, 37.5%). Just more than half of the patients (52.5%) were treated for 10 days and 28(35%) of them were treated for 14 days. Dexamethasone was given for 56(70%) patients before the antibiotics or at the same time. Most patients (n=68, 85%) were discharged improved and the rest (n = 12, 15%) were discharged with sequelae, died or disappeared. Overall case fatality was 7.5% (6/80) and all the deaths were due to S.pneumoniae which gives a case fatality rate for this organism of 42.8%. All of the children who died were above the age of 10 years (P < 0.05). Prolonged fever is found to be more prevalent among children under five years followed by infants and older than 10 years (p = 0.36). Seizure after 72 hrs of admission was a common complication among children older than 10 years old (p = 0.283).
Different factors contributed for poor outcome in this study as it is shown on Table 5. Neurologic sequelae (focal neurologic deficit, depressed consciousness) at discharge was associated with young age < 5 years (OR = 1.2, 95% CI 0.05-1.3, p = 0.045), culture positivity (OR = 1.3, 95%CI 1.2-3, p = 0.004) and focal neurologic deficit at admission (OR = 5 95% CI 2.1-5.2, p < 0.001).Children presenting with loss of consciousness had a risk of seizure after 72 hr (OR = 7.8, 95% CI, 1.7-8.7, P < 0.001). Seizures at admission was found to be strongly associated with the development of seizure after 72 hr (OR = 12, 95% CI 1.07 - 13, p=0.04), and prolonged fever (OR = 1.2, 95% CI 0.09-2.14, p = 0.01).Culture positivity was found to have an association relation with prolonged fever (OR = 1.3, 95% CI, 0.1-1.8 p = 0.01), prolonged seizure (OR=2.1 95% CI, 1.8-4.9, p = 0.01) and death (OR = 2.4, 95% CI 0.27-3.8, p < 0.01). Choice of antibiotics was found to have a strong correlation with death. Use of penicillin with chloramphenicol was found to have a high risk of death (OR = 4.1, 95%CI, 2.5-5.4, p = 0.04).
The hot, dry seasonal increase in admission and male predominance was consistent with other studies from Bangladesh [13] and BurkinaFaso [14]; but not similar to previous studies from Gondar [4] and Addis Abeba [3]. The preponderance of the under-fives underscores the age group that bears the brunt of the disease burden. Clinical features that are found to be dominant in our study are also found in the previous studies done in the pre PVC period suggesting that there is no significant change in the clinical presentation of CABM after the introduction of the vaccine [15]. We used a retrospective analysis of clinical and epidemiological features to document a reduction in admission rate of CABM by 62.7% (from 4.3% to 1.6%) and case fatality rate of 56.1% (from 17.1% to 7.5%) when compared to previous studies which were done prior to the introduction of PCV-10 [16]. Some of the reduction in death rate could still be due to the improvement in the general pediatric care. Consistent with researches done in the pre PVC-10 era in Tikur Ambessa, Gondar and Awassa University Hospitals, S. pneumoniae is still the most common organism isolated from the culture accounting for the 70% [4, 17]. Part of this may be explained by the fact most cases of pneumococcal meningitis was seen in children older than 10 years, and those who were partially immunized or unimmunized. Finally, other strains not contained by the vaccine could be the pathogen. Literature in the pre PVC-10 period indicates that CABM is associated with a high risk of neurological complications, with a percentage of up to 38%, and mortality rates up to 18% [17-20]. In the present study, this frequency was 5% for the complication and mortality rate was 7.5%, which is significantly lower than seen in previous studies.
In previous studies loss of consciousness, focal neurologic deficit, seizure at admission, delayed presentation and S. pneumoniae were found to be risk factors for poor outcome [19-23]. In the present study, the presence of seizure at admission, loss of consciousness, culture positivity and focal neurologic deficit were associated with poor outcome which was in agreement to these previous studies. However, use of dexamethasone and delayed presentation was not found to be a predictor of poor outcome in this study. Antibiotics of choice were found to have a strong association with death in the present study. This may reflect an increase in possible resistant strains in the community but it needs a laboratory baser surveillance study for to make conclusion. While third generation cephalosporins such as ceftriaxone are the first line treatment for CABM in our setting, it may not be available due to stock outs, resulting in health care providers using older treatment recommendations from WHO such as penicillin and chloramphenicol. The study was retrospective in design and subject to the potential biases of retrospective reviews. However, we collected objective clinical and laboratory features that should be reliably recorded in the medical record. The medical records also had limited data about the study patient's PCV-10 immunization status. Although overall immunization was high in the study we cannot exclude the possibility that some of our study patients were either unimmunized or under immunized with PCV-10. The other limitation was the subjectivity of discharge conditions has created some difficulties in finding the exact outcome, especially of neurologic outcomes. Another limitation was the paucity of data regarding antibiotics susceptibility patterns, since laboratory reports were incomplete. Finally, this study had only 20% culture positive specimens, though this would result in an overestimation of CABM. The limited availability of culture reflects many resource-constrained setting, and we believe by applying WHO criteria for the definition of CABM gives us a reasonable estimate of the burden of CABM in our community.
Based on the results of this study, we can conclude that introduction of PCV-10 and Hib to the immunization schedule has decreased the admission rate, mortality, and morbidity of CABM among children under 5 years old. It is also possible to conclude from this study that loss of consciousness, seizure at admission and focal neurologic deficit at admission predictors of adverse outcomes at admission and hence these patients needs proper evaluations and meticulous follow up in the ward as well as after discharge.
What is known about this topic
- The etiology and clinical features of bacterial meningitis;
- Possible outcome of patients with bacterial meningitis.
What this study adds
- The change in the epidemiology after the introduction of pneumococcal vaccine;
- The change in clinical feature and outcome of bacterial meningitis after pneumococcal vaccine.
The authors declare no competing interests.
All the authors have participated starting from the proposal writing to the manuscript preparation. All authors have read and agreed to the final version of this manuscript.
We would like to thank Department of Paediatrics and Child Health, University of Gondar.
Table 1: baseline demographics of 80 children admitted with community-acquired bacterial meningitis to Gondar University Hospital
Table 2: age group distribution of symptoms of community-acquired bacterial meningitis at onset
Table 3: age group distribution of cerebral spinal fluid characteristics in children with community-acquired bacterial meningitis
Table 4: clinical parameters according to cerebral spinal fluid isolates in children with community-acquired bacterial meningitis
Table 5: analysis of prognostic factors for poor short-term outcome of 80 patients with community acquired bacterial meningitis
- WHO. Global burden of disease estimates. Geneva: World Health Organization. 2008. Accessed on 20 June 2016.
- Edmond K, Clark A, Korczak VS, Sanderson C, Griffiths UK, Rudan I. Global and regional risk of disabling sequelae from bacterial meningitis: a systematic review and meta-analysis. Lancet Infect Dis. 2010; 10(5): 317-28. PubMed | Google Scholar
- Hailu M, Muhe L. Childhood meningitis in tertiary hospital in Addis Abeba: clinical and epidemiologic features. Ethiop Med J. 2001 Jan; 39(1): 29-38. Google Scholar
- Ahmed, Arslan. Etiology of bacterial meningitis in Ethiopia 2007 - 2011: a retrospective Study. UIO; Duo Vitenarkiv. 2012. Accessed on 20 June 2016.
- Mengistu M, Asrat D, Woldeamanuel Y, Mengistu G. Bacterial and Fungal meningitis and antimicrobial susceptibility pattern in Tikur Ambessa Hospital, Addis Abeba, Ethiopia. Ethiop Med J. 2011; 49(4):349-59. Google Scholar
- Tagene et al. Bacterial Meningitis: a five-year retrospective study among patients who had attended at University of Gondar Teaching Hospital, Northwest Ethiopia. Biomed Res Ther. 2015; 2(5): 270-278. Google Scholar
- Gessner BD. Haemophilus influenzea type b vaccine impact in resource-poor settings in Asia and Africa. Expert Rev Vaccines. 2009; 8(1): 91-102. PubMed | Google Scholar
- von Gottberg A, Cohen C, Whitelaw A et al. Invasive disease due to Haemophilus influenzea serotype b ten years after routine vaccination, South Africa 2003-2009. Vaccine. 2012; 30 (3): 565-71. PubMed | Google Scholar
- Adegbola RA, Secka O, Lahai G et al. Elimination of Haemophilus influenzae type b (Hib) disease from The Gambia after the introduction of routine immunization with a Hib conjugate vaccine: a prospective study. Lancet. 2005; 366(9480): 144-50. PubMed | Google Scholar
- Howie SR, Antonio M, Akisanya A et al. Re-emergence of Haemophilus influenzae type b (Hib) disease in The Gambia following successful elimination with conjugate Hib vaccine. Vaccine. 2007; 25(34): 6305-09. PubMed | Google Scholar
- Mudhune S, Wamae M. Network Surveillance for Pneumococcal Disease in the East African R: report on invasive disease and meningitis due to Haemophilus influenzae and Streptococcus pneumonia from the Network for Surveillance of Pneumococcal Disease in the East African Region. Clin Infect Dis. 2009; 48 (suppl 2): S147-52. Google Scholar
- World Health Organization (WHO). WHO report of the technical review group meeting, Global program for vaccines and Immunizations. Vaccine research and Development Geneva, Switzerland. WHO; 1998. Accessed on June 2016.
- S Joardar, GK Joardar, PKMandal et al. Meningitis in Children: a Study in Medical College & Hospital, Kolkata. Bangladesh J Child Helath. 2012; 36 (1) : 20-25. Google Scholar
- Traore et al. Incidence, Seasonality, Age Distribution, and Mortality of Pneumococcal Meningitis in Burkina Faso and Togo. Clin Infect Dis. 2009;48( suppl 2):S 181-88. PubMed | Google Scholar
- Mengistu M, Asrat D, Woldeamanuel Y, Mengistu G. Bacterial and Fungal meningitis and antimicrobial susceptibility pattern in Tikur Ambessa Hospital, Addis abeba, Ethiopia. Ethiop Med J. 2011 Oct; 49 (4): 349-59. Google Scholar
- David Gordon M, Sarah F, Heather R, Mehretie K. Prevalence and burden of diseases presenting to a General Pediatrics Ward in Gondar, Ethiopia. J Trop pediatrics. 2013 Oct; 59(5):350-7. PubMed | Google Scholar
- Amsalu S, Assefa A. Meningitis in children beyond the neonatal period in Gondar University hospital. Ethiop Med J. 2005 Jul;43 (3):175-80. PubMed | Google Scholar
- Melaku A. Sensorineural hearing loss in children with epidemic meningococcal meningitis at Tikur Ambessa Hospital. Ethiop Med J. 2003 Apr; 41 41(2):113-21. PubMed | Google Scholar
- Tuula Pelkonen, Irmeli Roine, Lurdes Monteiro et al. Risk factors for death and severe neurological sequelae in childhood bacterial meningitis in Sub-Sahara Africa. Clin Infect Dis. 2009; 48 (8):1107. Google Scholar
- Antoniuk SA , Hamdar F, Ducci RD, Kira AT, Cat MN, Cruz CR. Childhood acute bacterial meningitis: risk factors for neurologic complications and neurological sequelae. J Pediatr (Rio J). 2011; 87(6):535-40. Google Scholar
- McCormic DW, Wilson ML, Mankhamabo L et al. Risk factors for death and severe sequelae in Malawian Children With bacterial meningitis 1997-2010. Ped Infec Dis J. 2013: 32 Feb; 32(2):e54-61. PubMed | Google Scholar
- Farag HF, Abdel-Fattah MM, Youssri AM. Epidemiological, clinical and prognostic profile of acute bacterial meningitis among children in Alexandria, Egypt. Indian J Med Microbiol. 2005 Apr; 23(2):95-101. PubMed | Google Scholar
- Roine I, Peltola H, Fernández J, Zavala I, González Mata A, González Ayala S et al. Influence of admission findings on death and neurological outcome from childhood bacterial meningitis. Clin Infect Dis. 2008 Apr 15; 46(8):1248-52. PubMed | Google Scholar