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In meningitis, one antibiotic is better than than two
EDITOR There is no sound microbiological basis for using a cephalosporin and a
penicillin together, with the exception of patients who may be infected
with Listeria monocytogenes. Listeriosis is extremely
uncommon in England and Wales, with only 64 reported cases in the first
seven months of 1997, including a total of 14 neonatal
cases.4 A third generation cephalosporin is adequate cover
for Neisseria meningitidis, Streptococcus
pneumoniae, Haemophilus pneumoniae, or
Escherichia coli, and benzylpenicillin provides no extra
benefit. Two We recommend that empirical treatment for patients aged between 3 months and 18 years who are suspected of having bacterial meningitis
(not thought to be due to listeria or tuberculosis) should be
monotherapy with high doses of a third generation cephalosporin, such
as cefotaxime or ceftriaxone. Patients in the United Kingdom with a
rash typical of meningococcal sepsis may be treated with a high dose of
benzylpenicillin alone.
Use of dexamethasone remains contentious
EDITOR Interestingly, the first child Mactier et al described did not
receive intravenous dexamethasone, whereas the child in the second case
did, but when the drug was started, or its role in treating acute
obstructive hydrocephalus, was not mentioned. Despite the drug's early
promise, its use remains contentious. A recent meta-analysis showed
that if it is started with or before parenteral antibiotics,
dexamethasone can benefit children with pneumococcal meningitis.3 However, there were limitations on the
analysis undertaken.
The use of dexamethasone in meningitis clearly requires further
research, but questioning whether it should be used should not delay
the administration of intravenous antibiotics.
Hydrocephalus was probably non-obstructive
EDITOR The failure to diagnose meningitis on examination of ventricular
cerebrospinal fluid is well recognised. Samples of lumbar and
ventricular cerebrospinal fluid may show considerable disparity even
when the meningeal inflammatory process is severe, and the diagnosis of
acute bacterial meningitis should not be discounted when ventricular
cerebrospinal fluid is normal or mildly inflammatory. The authors
are correct in advising that lumbar puncture should not be performed in
patients who have impairment of consciousness before brain imaging.
Finally, the comment that "diagnosing critically high intracranial
pressure is difficult" is wrong. Intracranial pressure is easily,
reliably, and safely monitored in the appropriate setting Neuroimaging has limitations
EDITOR Lumbar puncture should be avoided in children with clinically diagnosed
meningitis if consciousness is impaired or there are clinical signs of
raised intracranial pressure, as it may precipitate herniation of the
brain or coning. Coning may occur after lumbar puncture in children
with meningitis even when neuroimaging has been normal.2
Brain imaging is of no value in the immediate diagnosis of meningitis
and is an insensitive method for the detection of raised intracranial
pressure.3 The role of brain imaging is to identify complications of meningitis or to exclude focal brain pathology simulating meningitis. Positive indications for computed tomography or
magnetic resonance imaging are progressive focal neurological signs,
prolonged decreased level of consciousness, prolonged or focal
seizures, increasing head circumference, evidence of continuing infection, or recurrence of symptoms. Brain imaging should not be done
until antibiotic treatment has been started, raised intracranial pressure has been controlled, and intubation and ventilation started, if necessary.
A recent lesson of the week highlighted the possibility of
meningitis in childhood presenting as obstructive hydrocephalus, with
cerebrospinal fluid from ventriculostomy proving sterile but subsequent
lumbar fluid yielding Streptococcus
pneumoniae.1 In the two paediatric cases
described, treatment consisted of both a third generation cephalosporin
and benzylpenicillin. In children between 3 months and 18 years of age,
however, it is recommended practice for empirical treatment to consist
of a third generation cephalosporin alone.
2 3
The article
may be misleading in giving the impression that use of two antibiotics
in this type of case is routine.
lactam antibiotics should not be given together unless
this is unavoidable: there is potential for antagonistic interaction
between agents, as both act by inhibiting cell wall synthesis. It is
not likely that the penicillin was used to cover the possibility of
listeriosis, as the drug of choice in such cases is ampicillin (with or
without an aminoglycoside).5
Mark H Wilcox
Department of Microbiology, General Infirmary and University
of Leeds, Leeds LS2 9JT
Mactier et al illustrate an important complication of bacterial
meningitis
namely, acute obstructive hydrocephalus.1 The
authors say that they could not find any record of the incidence of
this complication in children. A series of 79 cases over 11 years in
Australia has been published; it shows an incidence of 2.8%.2
New South Wales Newborn and Paediatric Transport Service,
Westmead, Sydney 2145, Australia
Mactier et al make important points about the management of
patients who are seriously ill with acute bacterial meniningitis, particularly about draining cerebrospinal fluid via
ventriculostomy.1 Raised intracranial pressure leading to
cerebral herniation is well recognised in patients with bacterial
meningitis.2 It is probably multifactorial in origin, with
inflammatory cytotoxic oedema, interstitial oedema due to increased
permeability of the blood-brain barrier, venous thrombosis, infarction,
and hydrocephalus contributing.3 Mactier et al, however,
refer to "obstructive" hydrocephalus. In fact the hydrocephalus in
both cases is likely to be non-obstructive or communicating in origin,
as there does not seem to be any evidence for obstruction of the
internal cerebrospinal fluid pathway. In particular, figure 3 (computed
tomography scan of case 2) shows a dilated fourth ventricle, indicating
obstruction ouside the ventricular system. Communicating hydrocephalus
in bacterial meningitis reflects failure of cerebrospinal fluid
circulation in the basal cisterns and failure of resorption through
arachnoid granulations.
which is a
neurosciences intensive care unit. Although there is no hard proof that
such monitoring, the use of ventricular drainage, or other methods of
controlling intracranial pressure will improve outcome, it seems
logical that the experience and knowledge of those involved in
neurological intensive care, particularly with regard to the management
of raised intracranial pressure, altered cerebral perfusion, and
autoregulation, should be available for patients with bacterial
meningitis. Unfortunately the lack of available beds in such units in
the United Kingdom may prevent these patients benefiting from modern,
targeted treatment.
Victor Patterson
Royal Victoria Hospital, Belfast BT12 6BA
Mactier et al's lesson of the week concludes with a
recommendation that all patients with suspected meningitis and decreased level of consciousness should urgently have brain imaging to
exclude obstructive hydrocephalus before lumbar puncture.1 It is most important to understand the limitations of neuroimaging in
children with acute meningitis, and to avoid the commonly held misconception that lumbar puncture is safe if neuroimaging is normal.
Royal Liverpool Children's Hospital, Alder Hey, Liverpool L12
2AP abernet{at}cybase.co.uk
© BMJ 1999
Israeli students are refusing to perform intimate examinations on anaesthetised women without their informed consent.