Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Neurologia (Engl Ed) ; 37(3): 216-228, 2022 Apr.
Article in English | MEDLINE | ID: mdl-35241415

ABSTRACT

INTRODUCTION: Spinal muscular atrophy (SMA) is a neurodegenerative disease caused by a biallelic mutation of the SMN1 gene, located on the long arm of chromosome 5, and predominantly affects the motor neurons of the anterior horn of the spinal cord, causing progressive muscle weakness and atrophy. The development of disease-modifying treatments is significantly changing the natural history of SMA, but uncertainty remains about which patients can benefit from these treatments and how that benefit should be measured. METHODOLOGY: A group of experts specialised in neurology, neuropediatrics, and rehabilitation and representatives of the Spanish association of patients with SMA followed the Delphi method to reach a consensus on 5 issues related to the use of these new treatments: general aspects, treatment objectives, outcome assessment tools, requirements of the treating centres, and regulation of their use. Consensus was considered to be achieved when a response received at least 80% of votes. RESULTS: Treatment protocols are useful for regulating the use of high-impact medications and should guide treatment, but should be updated regularly to take into account the most recent evidence available, and their implementation should be assessed on an individual basis. Age, baseline functional status, and, in the case of children, the type of SMA and the number of copies of SMN2 are characteristics that should be considered when establishing therapeutic objectives, assessment tools, and the use of such treatments. The cost-effectiveness of these treatments in paediatric patients is mainly influenced by early treatment onset; therefore, the implementation of neonatal screening is recommended. CONCLUSIONS: The RET-AME consensus recommendations provide a frame of reference for the appropriate use of disease-modifying treatments in patients with SMA.


Subject(s)
Muscular Atrophy, Spinal , Neurodegenerative Diseases , Child , Consensus , Delphi Technique , Humans , Infant, Newborn , Muscular Atrophy, Spinal/genetics , Muscular Atrophy, Spinal/therapy , Spain
2.
Euro Surveill ; 17(8)2012 Feb 23.
Article in English | MEDLINE | ID: mdl-22401506

ABSTRACT

Research is ongoing on eighteen cases of Legionellosis, including four deaths, identified among tourists and employees in a hotel in Calp, Spain. Cases occurred during a period of two months, indicating the possibility of a point-source transmission at the hotel. An environmental investigation identified several positive samples in the hotel, which as a precautionary measure, was closed until requested improvements were made. Surveillance measures currently remain active.


Subject(s)
Disease Outbreaks , Drinking Water/microbiology , Legionnaires' Disease/epidemiology , Travel , Adult , Aged , Aged, 80 and over , Female , Humans , Legionella pneumophila/isolation & purification , Legionnaires' Disease/diagnosis , Legionnaires' Disease/microbiology , Legionnaires' Disease/transmission , Male , Middle Aged , Population Surveillance , Spain/epidemiology
SELECTION OF CITATIONS
SEARCH DETAIL
...