Key result
Intraventricular administration of ribavirin using a subcutaneous continuous infusion pump maintained target CSF concentrations and temporarily relieved clinical symptoms in 3 patients with SSPE.
Why the study?
Does intraventricular administration of ribavirin using a subcutaneous continuous infusion pump maintain target CSF concentrations in patients with new-onset SSPE?
Case Report (n=3)
Does intraventricular administration of ribavirin using a subcutaneous continuous infusion pump maintain target CSF concentrations in patients with new-onset SSPE?
Intraventricular administration of ribavirin via a subcutaneous continuous infusion pump can safely maintain target CSF concentrations and may temporarily relieve clinical symptoms in patients with SSPE.
Answers are grounded in this paper and cite their sources.
Provides initial evidence for continuous intraventricular ribavirin in SSPE; hypothesis-generating and should not yet change practice.
BACKGROUND: Subacute sclerosing panencephalitis (SSPE) is a slow virus infectious disease resulting from persistent infection with mutant measles virus. At present, there is no effective treatment for SSPE. Interferon-α and inosine pranobex have both been used for the treatment of SSPE, and partial success has been reported for the antiviral drug, ribavirin (RBV). The standardization of dosage method is necessary to carry out treatment with RBV more safely and effectively. In this study, RBV concentrations in cerebrospinal fluid (CSF) were monitored during the intraventricular administration using a subcutaneous continuous infusion pump. METHODS: Three patients with new-onset SSPE were treated with RBV using a subcutaneous continuous infusion pump. On days 3-10 after the start of RBV infusion, CSFs were obtained by lumbar tap, and the concentration of RBV in the CSF was measured using high-performance liquid chromatography. RESULTS: RBV concentration increased in a dose-dependent manner in all 3 patients, and the target concentration could be generally maintained without any severe side effects. We observed that the clinical symptoms were temporarily relieved in each case. In the 2 cases for whom treatment is continuing, the patients remain in stage III, while the patient who discontinued the therapy progressed to stage IV. CONCLUSION: The target RBV concentration in the CSF could be maintained continuously by intraventricular administration using a subcutaneous continuous infusion pump. The accumulation of further cases is necessary to confirm the safety and efficacy of this medical treatment.
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Miyazaki et al. (2018) conducted a case report in Subacute sclerosing panencephalitis (SSPE) (n=3). Ribavirin via subcutaneous continuous infusion pump was evaluated on Ribavirin concentration in cerebrospinal fluid. Intraventricular administration of ribavirin using a subcutaneous continuous infusion pump maintained target CSF concentrations and temporarily relieved clinical symptoms in 3 patients with SSPE.
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