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Dalfampridine in patients with downbeat nystagmus--an observational study.
Author: BardinsStanislav, ClaassenJens, FeilKatharina, JahnKlaus, KallaRoger, SchneiderErich, SchnieppRoman, SpiegelRainer, StruppMichael, TeufelJulian
Original Abstract of the Article :
We investigated the effects of dalfampridine, the sustained-release form of 4-aminopyridine, on slow phase velocity (SPV) and visual acuity (VA) in patients with downbeat nystagmus (DBN) and the side effects of the drug. In this proof-of-principle observational study, ten patients received dalfampri...See full text at original site
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引用元:
https://doi.org/10.1007/s00415-013-6911-5
データ提供:米国国立医学図書館(NLM)
Dalfampridine: A New Hope for Downbeat Nystagmus?
Downbeat nystagmus (DBN) is a rare neurological condition causing involuntary eye movements. This observational study investigated the effects of dalfampridine, a drug used to treat multiple sclerosis, on reducing slow phase velocity (SPV) and improving visual acuity (VA) in patients with DBN. The study aimed to evaluate the potential of dalfampridine as a therapeutic option for DBN.
Dalfampridine Shows Promise in Reducing Downbeat Nystagmus
The study found that dalfampridine significantly reduced SPV and improved VA in patients with DBN. The results suggest that dalfampridine may be an effective treatment for DBN, providing relief from the debilitating symptoms associated with this condition. However, the study was small and further research is needed to confirm these findings.
A Potential New Treatment for Downbeat Nystagmus
This study highlights the potential of dalfampridine as a new treatment option for DBN. The drug's effectiveness in reducing SPV and improving VA suggests that it could be a valuable tool in managing this neurological condition. However, as with any new treatment, more research is needed to fully understand its benefits and risks.
Dr. Camel's Conclusion
This observational study provides promising evidence for the potential of dalfampridine in treating DBN. The drug's ability to reduce SPV and improve VA suggests that it could offer a valuable therapeutic option for patients with this rare condition. It underscores the need for further research to confirm its efficacy and explore its long-term effects.
Date :
- Date Completed 2014-02-28
- Date Revised 2021-10-21
Further Info :
Related Literature
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