Etiology and PRESENTATION of Acute Bacterial
Meningitis in Children AT
Abdul Khaliq A. Sallam
Department
of Pediatrics, Al-Thawrah Teaching Hospital, Sana'a,
Background: This study was carried out
to determine the etiology and management outcome of acute bacterial meningitis among
children presenting at Al-Thawrah hospital, Sana’a,
Key words: Acute bacterial
meningitis, Etiology, Febrile convulsion, CSF culture
INTRODUCTION
Acute
Bacterial Meningitis (ABM) is one of the most severe infectious diseases in the
childhood. The global burden of the disease is high. Apart from epidemic, at
least 1.2 million cases of meningitis are estimated to occur every year with
135000 deaths.1 It is caused by a variety of microorganisms but,
beyond the neonate period, the most important ones are streptococcus pneumonia
and Haemophilus influenza.2-4 Acute
bacterial meningitis is seen more in children than adults.1 Haemophilus influenza ,N.meningitides,
S.pneumonae are the most common cause of bacterial
meningitis in children.2
ABM is an important disease of early childhood with high fatality and
risk of neurological handicaps.3 The prevalence of these organisms
varies from place to place, by age and season.4 The specific
pathogen causing bacterial meningitis varies around the World.2,5,6 There
is predominance of gram negative organisms as the etiological agents of
bacterial meningitis.7
Various factors that determine the outcome of the disease are age, early
diagnosis, early treatment, duration of treatment and type of microorganism.8
The exact etiological diagnosis is often not possible because of poor
culture facilities.9,10 But similar studies showed that, the common
causative organisms responsible for bacterial meningitis beyond neonatal period
were H.influenzae type B, S. pneumonia and N.meningitides were found in different regions of Saudia Arabia and abroad.11,12 Ceftrixone was used as drug of choice in many centers in
treating bacterial meningitis, especially with H.influenzae
type B infection.13,14,15 As well as it has excellent penetration
into the CSF with a ratio of achievable CSF concentration to minimum inhibitory
concentration levels in the range of 100:1.16 The management of ABM
include, a suitable combination of antibiotics, dexamethasone
for first few days (reduces meningeal inflammation
and improves the clinical outcome,19,20) and importantly, intensive
care thereby especially for shock and raised intracranial pressure.8,17,18
CSF latex agglutination test (LAT) is of great promise. Various authors
have suggested it to be simple with superior sensitivity and specificity and
unaffected by previous antibiotics thereby.21-23 This is
particularly important for N.meningitides which is
known to be not detected by in smear, CSF and blood culture, and even in
antigen detection tests.24 About 76% of ABM in children admitted to
hospital had received antibiotics, had similar observation by Murphy.25
A high percentage of ampicilline- resistant (23%) and
choromphinicol-resistant (11%) and similar findings
have been observed by other workers 26,27 and the incidence of these
antibiotics resistant was higher than those reported by other workers.10,28
CT scan is an important diagnostic tool to detect the intracranial
complications, which was also suggested by Lancy et
al.29 The mortality rate among these children with ABM have been
reported in industrialized countries such as the USA 2.6%.30 High
rates have been reported in some developing countries and countries in the
Middle East such as Turkey 38%,31 Saudia
Arabia 14.7%,32 Sudan 28.6%33 and India 21.8%.34
This current study was carried out to determine etiology and management
outcome of acute bacterial meningitis in Yemeni children, with a goal of help
in reduction of morbidity and mortality associated with this disease.
MATERIAL AND METHODS
This
study was carried out from
The information obtained at the time of admission included patient age,
weight, sex, presenting complaints, birth history, family history,
developmental history, any history of trauma/wound, drugs, immunization and ear
problems, exam findings and duration of illness. Investigations done were CSF
exam, stain, culture, complete blood counts. Blood film for malaria, random
blood sugar, chest x-ray, renal and liver function tests, serum electrolyte and
trans-frontal ultrasound/CT scan of the head were carried out whenever required.
Drugs used before admission, final diagnosis and the outcome were also
recorded.
Bacteriological studies were carried out in the Department of
Microbiology of the same hospital. Those children in whom CSF culture was
negative (no organism was grew) but they were having signs of meningeal irritation/raised anterior fontanel were
considered suspected cases of bacterial meningitis.
Data were analyzed manually to calculator using rates & percentages.
RESULTS
Over a 20
months period, only 63 children (44 males, 19 females) with a presumptive
diagnosis of acute bacterial meningitis were seen. The most affected group were those between 4 months to 3 years. The mean age at the
presentation was 4.1±0.71 years.
The positive findings of CSF analysis (turbid, decrease glucose
<40mg.dl, increase protein >80mg.dl and leucocytes neutrophils
>5cells.cu.mm) were found in 23 (36.50%) cases. The findings of CSF analysis
with respect to cell count, protein and glucose levels were suggestive of
partially treated meningitis.
CSF culture detected 21 cases (33.33%) while the remaining 19 cases
showed normal CSF pictures although they did have clinical signs of acute
meningitis.
Fatality was 14.28%. The predominant organism in CSF culture was Klebsiella (33.33%), Haemophilius
influenza (23.80%), streptococcal pneumonia (14.28%), 2 cases each of E-coli
and Pseudomonas while with one cases each of tuberculus
meningitis and staphylococcus aurus.
From those 21 with positive CSF culture (proved acute bacterial
meningitis) major clinical presentation at pediatric emergency room were 7
patients with high fever, 7 cases were toxic look, 3 cases with altered
consciousness, 2 cases looks ill and lethargic and 2 cases with neck rigidity.
Among 63 patients with ABM, only
6 CT scan were performed.
Table 1: Cases
showing positive CSF findings
|
Males |
Females |
Total |
Turbid CSF |
2 |
1 |
3 |
CSF glucose <40mg.dl |
2 |
2 |
4 |
CSF protein >80 mg.dl. |
7 |
4 |
11 |
CSF polymorph
>05cells.cumm. |
2 |
3 |
5 |
Total |
13 |
10 |
23 |
No
neonate was seen in above group.
Table 2: Type of microorganism isolated:
Age group |
Male |
Female |
Type of organism |
Total |
0-3 months |
1 |
2 |
2 with E-coli, 1strept.pneumonae. |
3 |
4mon-3 Yrs |
10 |
3 |
5H.influenzae, 4Klebesiellae spp, 2strep.pneumonia,
1Psudomonas, 1staph.aureus. |
13 |
>3.1 Yrs |
3 |
2 |
3Klebesialla pnu, 1TBM, 1Pseudomonas. |
5 |
Total |
14 |
7 |
21 |
21 |
The outcome from the confirmed cases (organism isolated from CSF n=21)
12 (57.14%) cases improved, 3 (14.28%) left against medical advise, 3 (14.28%)
expired (2 with H.infleunzae and one with
Pseudomonas), 2 cases got complications and one case absconded.
White blood cell count (WBC) showed; in those positive isolated
micro-organism, there were 15 cases with raised WBC >11000cell.cu.mm (71.4%)
and decrease WBC <5000 with only 6 cases (28.5%). Other WBC relation to
those complicated cases n=2; one patient with increased & one patient with
decrease WBC. The same WBC relation to those expired cases n=3 it showed one
case with increase WBC >11000 and 2 cases with decreased WBC <5000 cells
mm3.
The mean hospital stay was 2 weeks.
DISCUSSION
From this
study, it is evident that, the common causative organism responsible for
bacterial meningitis beyond the neonatal period were H. Influenza type B and Klebsiellae spp.
The main complaint of our patients when attended at our hospital was
fever and convulsions (47.6%) compared to children studied in Saudi Arabia
(KSA)6 in amongst whom 97% had high fever and 58.8% convulsions.
Then the second major presented signs were nuchal
rigidity (36.5%) compare to the same KSA study6 were (47.1%) and to
that done at
Fourty Eight (76.19%) patients had received
antibiotics before admission to this hospital, and this might have caused low
bacteriological yield of CSF culture, A similar
observation was reported by Murphy.25
The positive CSF culture obtained organism in our study in total were
n=21 (33.33%) out of them, Klebsillae spp was the predominant one n=7 (33.33%) (That affect 4
cases in those 4 months-3years & 3 cases to those >3.1 years) then H.Infleunzae type b was n=5 (23.80%) which seen mainly
beyond neonatal period, then streptococcal pneumonia n=3 (14.28%) mainly seen
in those 4months-3years, then of 2 cases each E. coli (seen in neonatal
period), Pseudomonas (9.52%) then one case each with tuberculus
meningitis and staph.aurous.
The other 14 cases of fever and convulsion were examined and
investigated without any clinical signs/or lab finding suggestive of ABM, but
did have the related clinical pictures and lab finding toward that illness.
They were as 7 as febrile convulsions (9.09%), 4 cases with cerebral malaria
(5.19%), 2 cases with acute gastroenteritis (2.59%), and one case with pertussis (1.29%).
Before admission to our hospital, 48 patients (76.19%) had received
antibiotics, a similar observation was reported by Murphy.25
Complications were seen in 15 cases of our study, recurrent convulsions
in 4, 1 got 7th cranial nerve palsy, 2 cerebral atrophy, 2
persisting coma, 1 hydrocephalus, 1 hemiparesis, 1 subdural effusion, 2 encephalitis and 1 decreased lower
limbs tone.
Our complications among those with isolated organism in CSF were only 2
cases, along with other 13 cases from the remaining groups, all gives 23.80%
and the fatality rates (3 patients among those positive isolated organism from
CSF & 5 cases from other group, all gives n=8 (12.69%).
The Ampicilline & Chloramphenicol
resistance in our study was 12.69% compare to those study in a rural
In the KSA study positive isolated organism in CSF culture among those
with suspected ABM patients only 43%, the predominant organism obtained were H.
Influenza 44.1% then strep.pneumoniae 29.4% and their
complication were 46%, fatality 14.7% their ampicilline
& chloromphinicol were 12%.6
Other similar study was done at
As regards WBC count it showed that in those with positive isolated
micro-organism, there were 15 cases with raised WBC >11000 cell.cu.mm (71.4%) and decrease WBC <5000 with only 06
cases (28.5%). Other WBC relation to those complicated cases n=2; one patient
with increased & one patient with decrease WBC. The same WBC relation to those
expired cases n=3 it showed one case with increase WBC >11000 and 2 cases
with decrease WBC <5000 cells.cu.mm.
In this above WBC relation, which mean that there were an early
indicator sign to the major illnesses (ABM) as well as it may give an alarm to
the prognosis (there were correlation between the increase/decrease WBC and the
major illness with their outcome).
We did not isolate any N.Meningitidis in those
CSF positive isolated organism, although, it is one of common organism causing
ABM in children, it could be due to lack of this organism in the smear or in
CSF. The development of new and very sensitive tests may throw light on this
group.
In our study there were 12.69% of ampicilline
& chloromphnicol resistant, that resistant was
mainly due to the production of B-lactamase against ampicilline and transferase
against chloromphinicol, a similar finding have been
observed by other workers.26,27
In our study , we found that the majority of isolated organisms were
highly sensitive to gentamycine, cefotaxime
and ceftrixone.
No patient came back for post-treatment follow-up. Blood cultured was
not done in our hospital.
CONCLUSION
Proper
knowledge of etiology and presentation of ABM along with timely vaccination can
help reduce mortality and morbidity associated with this deadly disease.
REFERENCES
1.
Babiker MA, Taha SA. Meningitis in children of
2.
Schiech WF. Bacterial
Meningitis in the
3.
Bell WE, Silber DL. Meningococcal meningitis. Past and present
concepts. Military medicine 1971;136:601-4.
4.
Dagbjartsson A, Ludvigsson P. Bacterial meningitis: diagnosis and initial
antibiotic therapy. Peditr Clin
N Am 1987;34:219-30.
5.
Cadoz M. An
epidemiological study of purulent meningitis cases admitted to hospital in
6.
7.
Gorman CA. Bacterial meningitis, Infections
caused by certain Gram-negative enteric organisms. Proceedings of the staff
Meetings of the Mayo Clinic 1962;37:703-5.
8.
Bridger RC. Diagnosis and treatment of bacterial
meningitis. Postgrad Doctor 1986;9:282-7.
9.
Kabra SK, Praveen Kumar, Verma IC, Mukherjee D, Chowdhary BH, Sengupta S, et al.
Bacterial meningitis in India: An IJP survey. Indian J Pediatr
1991;58:505-11.
10.
11.
Azubuike JC. Childhood
bacterial meningitis in Tabuk, Saudia
Arabia. Ann Saudi Med 1990;10:145-8.
12.
Zaki M,
13.
Osoba AO. Susceptibility
of common bacterial isolates to ceftrixone. Saudi Med
J1990;11:187-90.
14.
Hell K. [Ceftrixone:
worldwide experience with its clinical use. Antibiotiki
I khimioterapiia 1992;37:34-7](In Russian).
15.
Craig JC. Cefrtixone
for paediatric bacterial meningitis: report of 62
children and a review of the literature.
16.
Steel RW, Bradsher RW.
Comparison of ceftrixone with standard therapy for
bacterial meningitis. J Pediatric 1983;103:138-41.
17.
Kim M. Pneumococcal
conjugate vaccine-relevance for developing countries. Indian Pediatr 2001;38:453-60.
18.
Thirumoorthi MC. Bacterial
meningitis in children. Indian J Pediatr
1995;62:265-79.
19.
Odio CM, Faingezicht I, Paris M. The beneficial effects of early dexamethasone administration in infants and children with
bacterial meningitis. N Eng J Med 1991;324:1525-31.
20.
Finch RG, Mandragos C.
corticosteroids in bacterial meningitis. Br Med J 1991;302:607-8.
21.
Singh H, Sarkar R, Sachdev HPS, Saini L.
Immunological tests in acute bacterial meningitis. Indian Peditr
1988;25:323-8.
22.
Mirdha BR, Gupta U, Bhujwala RA. Latex agglutination test: An adjunct to the
lab diagnosis of pyogenic bacterial meningitis.
Indian J Peditr 1991;58:521-4.
23.
Choo KE, Ariffin WA, Ahmad T, Lim WL, Gururaj
AK. Pyogenic meningitis in hospitalized children in
24.
25.
Murphy PA. Bacterial infections of the nervous
system with special reference to tuberculosis. Saudi Med J 1988;9:569-79.
26.
Wafaa M. Acute bacterial
meningitis in neonates and infants in
27.
Nabi G. Bacterial
meningitis in children. Saudi Med J 1992;13:348-51.
28.
Abdullah A, Uduman SA,
Saleh MF, AL Rajeh S, Sibai MS, Agib A. Childhood
bacterial meningitis. Ann Saudi Med 1988;8:274-8.
29.
Lancy MS, Woody RC,
Sullivan JA. Computed tomography in childhood intracranial infections. Am Fam Physician 1987;335:179-81.
30.
Pomeroy SL. Seizures and other neurological sequelae of bacterial meningitis in children.
31.
Gurses N. Bacterial
meningitis. Proceeding of the 8th European Congress of Clinical
Microbiology and infectious diseases,
32.
Srair HA. Bacterial
meningitis in Saudi Children. Indian J
of Peditr 1992;59:719-21.
33.
Ahmed AA. Post-endemic acute bacterial
meningitis in Sudanese children. East African Med J 1996;73:527-32.
34.
Deivananyagam N. Bacterial
meningitis: diagnosis by latex agglutination test and clinical feature. Indian Pedtr 1993;30:495-500.
35.
Rao BN. Eitology and occurrence of acute bacterial meningitis in
children in
______________________________________________________________________________
Address For Correspondence:
Abdul Khaliq
A. Sallam,
Department of Paediatrics, Faculty of Medicine,
Sana’a University, PO Box 4228, Sana’a, Yemen. Fax: +9671605229, Tel: +967-77946670, +9671245248.
Email : draks@yemen.net.ye