Home | Volume 46 | Article number 123

Short communication

A cross-sectional study of clinical features of bacterial meningitis among neonates presumed to have sepsis in a tertiary hospital, Dar es Salaam, Tanzania

A cross-sectional study of clinical features of bacterial meningitis among neonates presumed to have sepsis in a tertiary hospital, Dar es Salaam, Tanzania

Taher Pishori1, Francis Fredrick Furia2,&, Karim Manji2

 

1Department of Pediatrics, TMJ Hospital, Dar es Salaam, Tanzania, 2Department of Pediatrics and Child Health, School of Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania

 

 

&Corresponding author
Francis Fredrick Furia, Department of Pediatrics and Child Health, School of Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania

 

 

Abstract

Identifying meningitis among neonates is usually challenging given the non-specific presentation and overlap with neonatal sepsis. This study was aimed at determining the pertinent clinical features that would suggest bacterial meningitis among infants with signs of possible serious bacterial infection and their outcomes. This hospital-based cross-sectional study was conducted among neonates presenting with clinical features of sepsis admitted at Muhimbili National Hospital (MNH) between May and December 2015. Detailed clinical features, blood cultures, and cerebrospinal fluid were obtained. The specimens were tested at the Central Pathology Laboratory at MNH. Short-term clinical outcome was also determined for recruited participants. One hundred and twenty-six neonates met the inclusion criteria and were recruited, males were 67 (53.2%) and the mean age of participants was 10.4 ± 7.9 days. Features of meningitis were noted among 19% (24/126) and very low birth weight neonates were observed to have a statistically higher prevalence of meningitis (p=0.038). Bacterial isolates from cerebrospinal fluid (CSF) culture were Klebsiella spp and E. coli, while predominant isolates from blood culture were Klebsiella spp (35%) and E. coli (20.6%). There was high resistance to ampicillin (91.2%), cloxacillin (94.1%), gentamycin (50%), and ceftriaxone (50%). A high mortality of 24.9% was noted. Neonatal meningitis is common among neonates with sepsis, and bacterial isolates were resistant to routinely used antibiotics. High mortality attributed to meningitis was noted at Muhimbili National Hospital.

 

 

Introduction    Down

Meningitis is a form of sepsis that contributes to high morbidity and mortality among neonates globally and the burden of this condition is high in low-income countries including Tanzania [1,2]. Most affected neonates include those with low birth weight, prematurity, and maternal colonization with group B streptococcus (GBS), the most common offending organisms include GBS, E. coli, Klebsiella spp listeria monocytogenes [3-5].

Neonatal sepsis is attributed to many factors including maternal colonization, and because of low immature immune systems, these babies are at increased risk for meningitis [6,7]. Characterizing the clinical profile of meningitis among neonates is valuable in managing affected babies, the existing lacunae in the information of this condition was the reason for conducting this study at Muhimbili National Hospital.

 

 

Methods Up    Down

Study design, setting, and participants: this cross-sectional study was conducted in the neonatal ward at Muhimbili National Hospital from May to December 2015. All neonates admitted in the neonatal ward meeting the World Health Organization (WHO) definition of neonatal sepsis [8] were eligible, 126 met the criteria for neonatal sepsis and were recruited consecutively.

Sample size: Kish and Leslie formula using a prevalence of 17.9% neonatal meningitis reported by Laving et al. from a study conducted in Kenya was used for sample size calculation, a margin error of 5% and a 95% confidence interval were utilized [5].

Variables: the main variables for this study were clinical meningitis, aetiological pathogens, and antimicrobial susceptibility patterns of isolates. Meningitis was defined by either cell count abnormality in the CSF (white cell count > 32/mm3 for term and > 29/mm3 for preterm) or positive biochemical results of CSF specimen (proteins > 1.7g/dl for preterm babies or > 1.5g/dl for term babies, CSF glucose < 50% of random blood glucose test (RBG test) or isolation of bacterial pathogens from culture of CSF specimens.

Measurements: structured questionnaires were used to collect data including demographic, clinical presentation, and outcome. Weight was measured using SECA beam balance to the nearest 100 g. From each participant, 2 ml of venous blood was aseptically drawn from the anterior cubital fossa of each neonate and inoculated into pediatric blood culture bottles. A lumbar puncture was performed aseptically to obtain cerebral spinal fluid (CSF) and concurrent random blood glucose was also checked using the ACCU-CHEK Active machine.

Cerebral spinal fluid (CSF) glucose and protein were determined by the use of an ARCHITECT c4000 clinical chemistry analyzer. Cell count was carried out by a counting chamber that is an improved Neubauer Chamber. CSF specimens were inoculated onto solid agar plates; MacConkey, blood, and chocolate agars for up to 48 hours before being regarded as no growth. Blood culture bottles were incubated at 37°C for 24 hours after which aliquots were sub-cultured on solid agar plates; MacConkey, blood, and chocolate agars for up to 96 hours before being regarded as having no growth. Colonies on solid agar plates were identified based on characteristic morphology, gram stain appearance, and standard commercially prepared biochemical tests.

Antimicrobial sensitivity testing was performed for routinely used antimicrobials for treating neonatal sepsis at MNH, drug concentrations used were; ampicillin 10µg, cloxacillin 30µg, gentamicin 10µg, ceftriaxone 30µg, amikacin 30µg and vancomycin 30µg, results were recorded as resistance and sensitive [7]. Bacterial meningitis was defined by either cell count abnormality in the CSF (white cell count > 32/mm3 for term and > 29/mm3 for preterm) or positive biochemical results of CSF specimen (proteins > 1.7g/dl for preterm babies or > 1.5g/dl for term babies, CSF glucose < 50% of RBG) or isolation of bacterial pathogens from culture of CSF specimens.

Statistical methods: Package for Social Sciences (SPSS) was used for data entry, cleaning, and analysis using the Chi-square test and Fishers' exact test, a p-value of < 0.05 was considered statistically significant.

Ethical considerations: Muhimbili University of Health and Allied Sciences (MUHAS) ethical review board and MNH administration provided approval and permission respectively for this study. Informed consent was obtained from the parents/guardians before recruitment.

 

 

Results Up    Down

Maternal and neonatal demographic and baseline characteristics of the study population: one hundred and ninety-five neonates were screened, 69 were excluded; 32 refused consent, 17 had neural tube defects, 20 had a septic shock with disseminated intravascular coagulopathy and lumbar puncture could not be performed. Out of 126 neonates who were included in the study, 67 (53.2%) were male and the mean age was 10.4 ± 7.9 days ranging from 2 to 24 days. Sixty-five (51.5%) neonates had low birth weight, and suspected sepsis were admission reasons for 35 (27.8%) and 75 (60%) neonates respectively. The majority of neonates (64.3%) were delivered by Spontaneous Vaginal Delivery (SVD) and foul-smelling amniotic fluid was noted in 17/126 (13.5%) deliveries. Five out of 126 (4%) mothers tested positive for HIV during pregnancy.

Clinical features of study participants: tachypnea (72.2%), lethargy/coma (66.7%), difficulty in feeding (65.1%), fever (63.5%), severe chest in-drawing (58.7%) convulsion (54.8%), and skin mottling/sclerema (51.6%). Other clinical features included hypothermia (36.1%) and bulging fontanel (4.8%).

The proportion of children with features of meningitis among the septic infants (Table 1): twenty-four participants (19%) had features of meningitis, of which 3 (12.5%) had bacterial isolation from CSF, 11 (45.8%) had aseptic CSF, raised protein, and low glucose levels in CSF while 10 (41.7%) leukocytosis on CSF microscopy. Neonates with very low birth weight were noted to have a higher prevalence of meningitis (37.5%) as compared to those with low birth weight (14.6%) and normal birth weight (14.8%), p = 0.038 (Table 2). The mean CSF protein and mean cell count were significantly higher in children with meningitis as compared to those without (p < 0.001), while the mean CSF glucose level was lower in those with features of meningitis (p < 0.001).

Isolated organisms from blood and CSF culture (Table 2): bacteria were isolated from 34 blood culture and three CSF specimens, blood isolates included Klebsiella spp (35.3%), E. coli (20.6%), S. aureus (17.6%) coagulase-negative Staphylococcus (11.8%), Pseudomonas spp (8.8%), and S. pneumoniae (5.9%) while CSF isolates included E. coli (2 specimens) and Klebsiella spp. Two neonates had similar organisms isolated from blood, and CSF growing E. coli and Klebsiella spp. One neonate had isolation of E. coli from CSF and S. aureus from blood.

Sixteen neonates out of 34 (47%) with positive blood culture had features of coagulase-negative staphylococci (CNS) involvement while 58.3% (14/24) of those with features of meningitis had positive growth on blood culture. Only 3 (8.8%) and 2 (5.9%) out of all blood isolates were sensitive to ampicillin and cloxacillin respectively, and 18/34 (53%) isolates were sensitive to gentamicin. The three isolates from CSF were resistant to ampicillin, cloxacillin, ceftriaxone, gentamycin, and vancomycin, they were only sensitive to amikacin.

Outcome of study participants: the overall mortality rate was 29.4%, it was higher among neonates with features of meningitis as compared to those without (37.5% vs 27.5%) although there was no statistically significant difference (Table 1). Seizures were noted in 12.5% (3/24) and 13.7% (14/102) of neonates with and without features of meningitis respectively. Hospital stay was longer for neonates with features of meningitis, with 80% staying for more than 2 weeks as compared to 43% of those without (p- value 0.009).

 

 

Discussion Up    Down

There is a significant burden of meningitis among neonates in our setting, with common aetiology comprising of E. coli and Klebsiella spp, prolonged hospital stay and higher mortality was noted among neonates with meningitis in this study, similar to other reports in the region [4,5]. Commonly reported risk factors for neonatal meningitis including premature rupture of membranes and stained liquor did not show any influence on meningitis in this study, highlighting the possibility of these infections even in the absence of known risk factors [5]. Low birth weight and premature who have low immunity were noted to be more vulnerable to meningitis in this study, which is agreement with existing literature [9,10].

Positive CSF culture was noted in only three out of 24 neonates with features of meningitis, majority of which (70%) were delivered in other facilities, and had antibiotics before referral to MNH. Delayed lumbar puncture and use of antibiotics may have contributed to poor yield, making it important to improve capacity for evaluating neonates in primary care level in neonates with presumed sepsis, and to limit the use of treatment based on clinical judgment [11].

Concordant bacterial isolates from CSF and blood were noted for E. coli and Klebsiella spp in this study, these are commonly reported causative organisms for neonatal meningitis [3-5]. This growth emphasized considering meningitis for neonates with sepsis. Other organisms isolated from blood culture were similar to findings from other studies conducted in Tanzania [6].

High resistance to routinely used antibiotics and those recommended by WHO for treatment of neonatal sepsis was noted, this is similar to other reports in the region [6]. High mortality and prolonged hospital noted in this study, particularly among neonates with features of neonatal meningitis, and high resistance of isolates call for robust community-based studies to examine applicability of the current antibiotic recommendations for neonatal sepsis.

Limitations: this was a single-center hospital-based study therefore findings may not be generalizable to the community setting.

Funding: this study was funded by Fogarty Global Infectious Disease (GID) training grant (NIH/Fogarty GID grant number: 2 D43 TW007886-05).

 

 

Conclusion Up    Down

Features of meningitis were common among neonates with presumed sepsis, bacterial isolates from CSF included E. coli and Klebsiella spp while Klebsiella spp, E. coli, and S. aureus were isolated from blood. High resistance to ampicillin, cloxacillin, and gentamycin were noted. Participants with features of meningitis had prolonged hospital stays and high mortality.

What is known about this topic

  • Neonatal infections are common and contribute to mortality.

What this study adds

  • Central nervous system involvement is common with neonatal sepsis;
  • There is high mortality with central nervous system involvement;
  • There is high resistance to organisms isolated from cerebral spinal fluid.

 

 

Competing interests Up    Down

The authors declare no competing interests.

 

 

Authors' contributions Up    Down

Taher Pishori designed the study, collected data, and wrote the initial report; Francis Fredrick Furia and Karim Manji participated in the design and supervised data collection and analysis. Francis Fredrick Furia wrote the manuscript. All the authors read and approved the final version of this manuscript.

 

 

Tables Up    Down

Table 1: baseline characteristics and factors associated with neonatal meningitis

Table 2: sensitivity pattern of bacterial isolates from blood

 

 

References Up    Down

  1. Liang LD, Kotadia N, English L, Kissoon N, Ansermino JM, Kabakyenga J et al. Predictors of Mortality in Neonates and Infants Hospitalized With Sepsis or Serious Infections in Developing Countries: A Systematic Review. Front Pediatr. 2018 Oct 4;6:277. PubMed | Google Scholar

  2. Zunt JR, Kassebaum NJ, Blake N, Glennie L, Wright C, Nichols E et al. Global, regional, and national burden of meningitis, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 2018 Dec;17(12):1061-1082. PubMed | Google Scholar

  3. Furyk JS, Swann O, Molyneux E. Systematic review: neonatal meningitis in the developing world. Trop Med Int Health. 2011;16(6):672-9. PubMed | Google Scholar

  4. Reta MA, Zeleke TA. Neonatal bacterial meningitis in Tikur Anbessa Specialized Hospital, Ethiopia: a 10-year retrospective review. Springerplus. 2016 Nov 14;5(1):1971. PubMed | Google Scholar

  5. Laving AM, Musoke RN, Wasunna AO, Revathi G. Neonatal bacterial meningitis at the newborn unit of Kenyatta National Hospital. East Afr Med J. 2003;80(9):456-462. PubMed | Google Scholar

  6. Mkony MF, Mizinduko MM, Massawe A, Matee M. Management of neonatal sepsis at Muhimbili National Hospital in Dar es Salaam: diagnostic accuracy of C - reactive protein and newborn scale of sepsis and antimicrobial resistance pattern of etiological bacteria. BMC Pediatr. 2014;14:293. PubMed | Google Scholar

  7. Joachim A, Matee MI, Massawe FA, Lyamuya EF. Maternal and neonatal colonisation with Group B Streptococcus at Muhimbili National Hospital, Dar es Salaam, Tanzania: Prevalence, risk factors and antimicrobial resistance. BMC Public Health. 2009;9:437. PubMed | Google Scholar

  8. World Health Organization Young Infants Study Group. Clinical prediction of serious bacterial infections in young infants in developing countries. Pediatr Infect Dis J. 1999 Oct;18(10 Suppl):S23-31. PubMed | Google Scholar

  9. Airede KI, Adeyemi O, Ibrahim T. Neonatal Bacterial Meningitis and dexamethasone adjunctive usage in Nigeria. Niger J Clin Pract. 2008;11(3):235-245. PubMed | Google Scholar

  10. Lin MC, Chiu NC, Chi H, Ho CS, Huang FY. Evolving trends of neonatal and childhood bacterial meningitis in northern Taiwan. J Microbiol Immunol Infect. 2015 Jun;48(3):296-301. PubMed | Google Scholar

  11. Smith PB, Garges HP, Cotton CM, Walsh TJ, Clark RH, Benjamin DK Jr. Meningitis in Preterm Neonates: Importance of Cerebrospinal Fluid Parameters. Am J Perinatol. 2008;25(7):421-426. PubMed | Google Scholar