Background: Children with pharmacoresistant epilepsy usually receive ketogenic diet (KD) as an inpatient, which makes it an expensive treatment. Objective: To compare the effectiveness, safety, and costs of outpatient versus inpatient initiated KD.
Design: Retrospective observational non-inferiority study. Patients/setting: Patients (1–18 years of age) who started KD either inpatient or outpatient.
Main outcome measures: Effectiveness was defined as ≥50% seizure reduction. Safety was measured by the numbers of emergency visits and complications. Economic impact was analyzed by calculating total costs of treatment.
Statistical analyses: Non-inferiority of outpatient initiation was tested using 95% confidence intervals of the differences in effectiveness and safety endpoints between groups with non-inferiority margins of 10%. Nonparametric bootstrap techniques were used to derive a 95% confidence interval for the mean difference in total costs between the groups.
Results: Hundred and five patients started KD in the period 2001 to 2017: 43 inpatient and 62 outpatient. At three months, the KD was effective in 61% of outpatients versus 63% of inpatients. The KD was considered safe in 36% of the outpatients, as compared to 29% in the inpatients. Outpatient initiation was shown to be non-inferior to inpatient initiation in terms of safety. Total health care costs of outpatient initiation were € 2901, as compared to € 8195 of inpatient initiation per patient (mean difference € 5294, 95% CI; -€ 7653 to -€ 2935).
Conclusions: Our study suggests that outpatient KD initiation is no worse than inpatient initiation in terms of effectiveness and safety, while carrying lower health care costs.

, , , ,
doi.org/10.1016/j.ejpn.2019.06.001, hdl.handle.net/1765/117916
European Journal of Paediatric Neurology

van der Louw, E., Olieman, J., Poley, M., Wesstein, T., Vehmeijer, F. O. L., Catsman-Berrevoets, C., & Neuteboom, R. (2019). Outpatient initiation of the ketogenic diet in children with pharmacoresistant epilepsy. European Journal of Paediatric Neurology, 23(5), 740–748. doi:10.1016/j.ejpn.2019.06.001