Ketogenic diet treatment for super-refractory status epilepticus in the intensive care unit: feasibility, safety and effectiveness.
Study Goal
The researchers aimed to investigate the feasibility, safety, and effectiveness of the ketogenic diet (KD) for treating super-refractory status epilepticus (SRSE) in ICU patients.
Results Summary
The KD resolved SRSE in 75% of patients within a median of 3 days, with successful weaning off anesthetic agents and ventilators. Side effects included gastrointestinal intolerances and metabolic abnormalities, but most were correctable, and no deaths were attributed to the KD.
Population
ICU patients with super-refractory status epilepticus (12 participants, median age 34 years).
Effective Dosage
Not specified
Duration
Median duration of KD treatment until SRSE resolution was 3 days (range 1-18), with continued therapy for weaning off anesthetic agents (median 16 days).
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
ketogenic diet (KD) | decrease | super-refractory status epilepticus (SRSE) | patients with SRSE | 75% (9/12) | resolved | #1 |
ketogenic diet (KD) | decrease | anesthetic agents | KD responders | median of 16 days (range 4-32) after KD initiation | successfully weaned off | #2 |
ketogenic diet (KD) | decrease | ventilator | KD responders | - | successfully weaned off | #3 |
ketogenic diet (KD) | increase | neurofunctions | patients with SRSE | - | continued to improve | #4 |
ketogenic diet (KD) | increase | side effects | patients with SRSE | - | varied | #5 |
ketogenic diet (KD) | no change | mortality | patients with SRSE | - | no patient died due to | #6 |
BACKGROUND AND AIMS: To investigate the feasibility, safety and effectiveness of the ketogenic diet (KD) for super-refractory status epilepticus (SRSE) in the intensive care unit (ICU). METHODS: We conducted a prospective investigation on patients with SRSE treated with the KD. The primary outcome measures were ketosis development as a biomarker of feasibility and resolution of SRSE as effectiveness. KD-related side effects were also investigated. RESULTS: Twelve patients (9 females and 3 males) with SRSE, with a median age of 34 years [range 16-69, interquartile range (IQR) 18-52], were treated with a KD. The median duration of SRSE prior to KD treatment was 21 days (range 4-46). SRSE resolved in 75% (9/12) of patients at a median of 3 days (range 1-18) after KD initiation. Among the nine KD responders, all were successfully weaned off anesthetic agents at a median of 16 days (range 4-32) after KD initiation, and all were also successfully weaned off ventilator. Side effects varied, and included gastrointestinal intolerances, malnutrition and metabolic abnormalities, electrolyte disturbance, and acute weight loss, although most of them could be corrected. No patient died due to KD, and neurofunctions continued to improve under KD therapy. CONCLUSION: The KD may be feasible and effective for the treatment of SRSE in the ICU. Moreover, it is relatively safe. However, there are numerous adverse events that can be corrected under close monitoring.