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1.
J Neurol ; 269(3): 1651-1662, 2022 Mar.
Artículo en Inglés | MEDLINE | ID: covidwho-1733983

RESUMEN

OBJECTIVE: To investigate the safety and efficacy of N-acetyl-L-leucine (NALL) on symptoms, functioning, and quality of life in pediatric (≥ 6 years) and adult Niemann-Pick disease type C (NPC) patients. METHODS: In this multi-national, open-label, rater-blinded Phase II study, patients were assessed during a baseline period, a 6-week treatment period (orally administered NALL 4 g/day in patients ≥ 13 years, weight-tiered doses for patients 6-12 years), and a 6-week post-treatment washout period. The primary Clinical Impression of Change in Severity (CI-CS) endpoint (based on a 7-point Likert scale) was assessed by blinded, centralized raters who compared randomized video pairs of each patient performing a pre-defined primary anchor test (8-Meter Walk Test or 9-Hole Peg Test) during each study periods. Secondary outcomes included cerebellar functional rating scales, clinical global impression, and quality of life assessments. RESULTS: 33 subjects aged 7-64 years with a confirmed diagnosis of NPC were enrolled. 32 patients were included in the primary modified intention-to-treat analysis. NALL met the CI-CS primary endpoint (mean difference 0.86, SD = 2.52, 90% CI 0.25, 1.75, p = 0.029), as well as secondary endpoints. No treatment-related serious adverse events occurred. CONCLUSIONS: NALL demonstrated a statistically significant and clinical meaningfully improvement in symptoms, functioning, and quality of life in 6 weeks, the clinical effect of which was lost after the 6-week washout period. NALL was safe and well-tolerated, informing a favorable benefit-risk profile for the treatment of NPC. CLINICALTRIALS. GOV IDENTIFIER: NCT03759639.


Asunto(s)
Enfermedad de Niemann-Pick Tipo C , Adolescente , Adulto , Niño , Método Doble Ciego , Humanos , Leucina/análogos & derivados , Leucina/uso terapéutico , Persona de Mediana Edad , Enfermedad de Niemann-Pick Tipo C/diagnóstico , Enfermedad de Niemann-Pick Tipo C/tratamiento farmacológico , Calidad de Vida , Resultado del Tratamiento , Adulto Joven
2.
Eur J Neurol ; 29(4): 1243-1253, 2022 04.
Artículo en Inglés | MEDLINE | ID: covidwho-1583572

RESUMEN

BACKGROUND AND PURPOSE: The scientific literature on COVID-19 is increasingly growing. METHODS: In this paper, we review the literature on movement disorders in the context of the COVID-19 pandemic. RESULTS: First, there are a variety of transient movement disorders that may manifest in the acute phase of COVID-19, most often myoclonus, with more than 50 patients described in the literature. New onset parkinsonism, chorea, and tic-like behaviours have also been reported. Movement disorders as a side effect after COVID-19 vaccination are rare, occurring with a frequency of 0.00002-0.0002 depending on the product used, mostly manifesting with tremor. Current evidence for potential long-term manifestations, for example, long COVID parkinsonism, is separately discussed. Second, the pandemic has also had an impact on patients with pre-existing movement disorder syndromes, with negative effects on clinical status and overall well-being, and reduced access to medication and health care. In many parts, the pandemic has led to reorganization of the medical system, including the development of new digital solutions. The movement disorder-related evidence for this is reviewed and discussed. CONCLUSIONS: The pandemic and the associated preventive measures have had a negative impact on the clinical status, access to health care, and overall well-being of patients with pre-existing movement disorders.


Asunto(s)
COVID-19 , Trastornos del Movimiento , COVID-19/complicaciones , Vacunas contra la COVID-19 , Humanos , Trastornos del Movimiento/epidemiología , Trastornos del Movimiento/etiología , Pandemias , SARS-CoV-2 , Síndrome Post Agudo de COVID-19
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