POLICY STATEMENTS/PROFESSIONAL RESOURCES:
KETOGENIC DIET FOR THE TREATMENT OF REFRACTORY EPILEPSY IN CHILDREN: A
SYSTEMATIC REVIEW OF EFFICACY
Frank Lefevre*, and Naomi Aronson
From the * Division of General Internal Medicine, Northwestern University
Medical School, and Blue Cross and Blue Shield Association Technology Evaluation
Center, Chicago, Illinois.
Objectives. To systematically review and synthesize the available
evidence on the efficacy of the ketogenic diet in reducing seizure
frequency for children with refractory epilepsy.
Data Sources. Medline searches were performed using the keywords
epilepsy/therapy, dietary therapy, and epilepsy, and the text word ketogenic
diet. The Cochrane Library of clinical trials was searched using the term
ketogenic diet. Bibliographies of recent review articles and relevant primary
research reports, as well as Current Contents were reviewed for
additional relevant citations.
Study Selection. Studies were selected for inclusion in the review
that reported the reduction of seizure frequency following treatment with the
ketogenic diet in children with refractory epilepsy. The outcome measures used
were the percentage of patients with: 1) complete elimination of seizures, 2)
>90% reduction in seizures, and 3) >50% reduction in seizures.
Results. The evidence consists entirely of uncontrolled studies. Of
11 studies identified for this review, 9 are retrospective series of
patients from a single institution. Two studies are prospective, 1 of which
is a multicenter trial. The results of these studies are consistent in showing
that some children benefit from the ketogenic diet, demonstrated by a
significant reduction in seizure frequency. Estimates of the rates of
improvement by combined analysis (confidence profile method) are complete
cessation of all seizures in 16% of children (95% confidence interval [CI]:
11.0-21.7); a greater than 90% reduction in seizures in 32% (95% CI: 25.3-39.8);
and a greater than 50% reduction in seizures in 56% (95% CI: 41.2-69.7). It is
unlikely that this degree of benefit can result from a placebo response and/or
spontaneous remission.
Conclusions. Although controlled trials are lacking, the evidence
is sufficient to determine that the ketogenic diet is efficacious in reducing
seizure frequency in children with refractory epilepsy. Key
words: ketogenic diet, refractory epilepsy, children.
Intractable or refractory epilepsy is defined by inadequate control of
seizures despite optimal treatment with conventional medications. Of the
2.5 million patients with epilepsy in the United States, 25% to 30% can be
considered to have intractable epilepsy.1,2 Poorly controlled epilepsy has been
associated with higher rates of mortality, unemployment, and cognitive
impairments.3
A number of new antiepileptic drugs (AEDs) have been approved for use in
refractory epilepsy (eg, felbamate, lamotrigine, gabapentin, and vigabatrin)and
numerous trials of these agents as add-on therapy for refractory seizures in
adult patients have demonstrated a modest benefit. A recent meta-analysis
included an analysis of 10 placebo-controlled trials of gabapentin and
11 placebo-controlled trials of lamotrigine.4 Response rates, defined as
the percentage of patients with a greater than 50% reduction in seizures, were
20% for gabapentin versus 9.3% for placebo, and 21% for lamotrigine versus 8.9%
for placebo. Although primarily labeled for adults, these agents are being used
frequently by clinicians for children with refractory seizures.5
A second option for patients with refractory epilepsy is surgery. A
resurgence of interest in surgical treatments for refractory seizures has
occurred over the last decade. Definite indications for surgery include the
presence of a epileptiform focus that is amenable to surgical resection.
Approximately 10% of patients with refractory epilepsy meet these criteria.2 In
such patients, the success rate of surgery in eliminating or substantially
improving seizures is up to 80%,3,6 and this improvement seems to be stable for
at least 4 years.7 Controversy exists in the literature concerning
indications for other types of antiepileptiform surgery (temporal lobectomy,
callosotomy, and hemispherectomy).7 The morbidity of neurosurgery for
intractable seizures is not well-reported, with small retrospective series
reporting on results from 1 type of surgery.38-10 Serious complications
have been reported, such as postoperative motor deficits, recurrent central
nervous system bleeding, hydrocephalus, and wound infections. Unfortunately, the
rates at which these complications occur remain ill defined.
Over the last decade, the ketogenic diet has gained popularity as another
treatment option for this group of patients. Dietary measures have been
described for the treatment of epilepsy since ancient times. Anecdotal reports
documenting the success of fasting or starvation in the treatment of seizures
exist as far back as the 5th century B.C.11 Interest in this form of therapy was
rekindled in the early 20th century after reports by physicians of dramatic
improvements in seizure frequency after a period of fasting.
In the 1920s, pediatricians at Johns Hopkins University postulated that the
antiepileptic effect of starvation resulted from ketosis, ie, the presence of
ketone bodies in the circulation. These physicians demonstrated that it was
possible to maintain a state of ketosis without prolonged starvation, by
severely limiting the intake of carbohydrates and proteins, and thereby forcing
the body to use ketone bodies as the predominant fuel source. The classic
ketogenic diet, developed at Johns Hopkins, contains fats in a 4:1 ratio to
carbohydrates. The amount of protein is regulated also so that ~90% of calories
are derived from fat. This diet was used as a treatment for epilepsy fairly
commonly in the 1920s and 1930s. In the late 1930s and 1940s, as effective
antiepileptic drugs, such as phenytoin and phenobarbital, were introduced into
clinical practice, the ketogenic diet was largely replaced by drug therapy.12
The mechanism of effect of ketosis on seizures is not understood. Various
theories11 have postulated that: 1) there is a direct stabilizing effect of
ketone bodies on the central nervous system; 2) resulting acidosis accompanying
ketosis modifies the seizure threshold; 3) changes in fluid and electrolyte
balance result in reduced seizures; and 4) change in lipid concentration induced
by the diet has an antiseizure effect.
Despite the lack of a well-defined mechanism of action, numerous reports have
appeared in the literature that have suggested benefit of this diet in reducing
the frequency of seizures. The objective of this present study is to
systematically review and synthesize the literature evidence reporting on the
efficacy of the ketogenic diet in reducing seizure frequency in children with
refractory epilepsy.
1. Huttenlocher PR, Hapke RJ A follow-up study of intractable seizures in
childhood. Ann Neurol 1990; 28:699-705
2. So EL Update on epilepsy. Med Clin North Am 1993; 77:203-214
3. Sperling MR, O'Connor MJ, Saykin AJ, Temporal lobectomy for refractory
epilepsy. JAMA 1996; 276:470-475
4. Marson AG, Kadir ZA, Hutton JL, The new antiepileptic drugs: a systematic
review of their efficacy and tolerability. Epilepsia 1997; 38:859-880
5. Barron TF, Hunt SL A review of the newer antiepileptic drugs and the
ketogenic diet. Clin Pediatr 1997; 36:513-521
6. Scully RE, Mark EJ, McNeely WF, Case records of the Massachusetts General
Hospital (Case 14-1997). N Engl J Med 1997; 336:1373-1379
7. So EL, Radhakrishnan K, Silbert PL, Assessing changes over time in
temporal lobectomy: outcome by scoring seizure frequency. Epilepsy Res
1997; 27:119-125
8. Davies KG, Maxwell RE, Franch LA, Hemispherectomy for intractable
seizures: long-term results in 17 patients followed for up to
38 years. J Neurosurg 1993; 78:733-740
9. Spencer DD, Schumacher J Surgical management of patients with intractable
supplementary motor area seizures. Adv Neurol 1996; 70:445-450
10. Villemure JG, Rasmussen T Functional hemispherectomy in children.
Neuropediatrics 1993; 24:53-55
11. Prasad AN, Stafstrom CF, Holmes GL
Alternative epilepsy therapies: the ketogenic diet, immunoglobulins, and
steroids. Epilepsia 1996;
37:S85-S91
|