2017
DOI: 10.1016/j.nrleng.2016.02.003
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Consensus statement on the treatment of multiple sclerosis by the Spanish Society of Neurology in 2016

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Cited by 16 publications
(14 citation statements)
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References 39 publications
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“…Based on our findings, fingolimod was used mainly as a second-line drug in patients diagnosed with RRMS, and only two of the 55 patients in our dataset started treatment with fingolimod immediately after diagnosis. These data are in alignment with the recommendations of the RRMS clinical treatment guidelines, in which fingolimod is recommended as second-line therapy, thus restricting its use as a first-line option in patients presenting with aggressive forms of RRMS 2 14. In a previous study by Ontaneda et al ,15 only 3.5% of patients were treatment-naïve and 41.6% of patients started fingolimod as second-line treatment, compared with 74.6% in our study.…”
Section: Discussionsupporting
confidence: 89%
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“…Based on our findings, fingolimod was used mainly as a second-line drug in patients diagnosed with RRMS, and only two of the 55 patients in our dataset started treatment with fingolimod immediately after diagnosis. These data are in alignment with the recommendations of the RRMS clinical treatment guidelines, in which fingolimod is recommended as second-line therapy, thus restricting its use as a first-line option in patients presenting with aggressive forms of RRMS 2 14. In a previous study by Ontaneda et al ,15 only 3.5% of patients were treatment-naïve and 41.6% of patients started fingolimod as second-line treatment, compared with 74.6% in our study.…”
Section: Discussionsupporting
confidence: 89%
“…In the case of relapsing-remitting MS (RRMS), outbreaks occur frequently—that is, episodes of neurological dysfunction that last for days or weeks and usually remit partially or totally, especially in the initial stages of the disease. However, approximately 10% of patients experience progressive neurological deterioration without outbreaks, suffering so-called primary progressive MS 2…”
Section: Introductionmentioning
confidence: 99%
“…The country of primary clinical practice was also identified as an independent predictor of TI. The observed differences among countries can be partially explained by variations in adherence to published MS management guidelines, regional differences regarding eligibility and access to DMTs, public funding of DMTs, and physician-related factors, such as risk preferences and education in risk management and decision making.…”
Section: Discussionmentioning
confidence: 99%
“…Another limitation is that physicians' decisions to escalate therapy are influenced by factors like availability of the drug, local policies, drug costs, variations in treatment guidelines in different countries, and other unmeasured variables that can alter the assessment of TI. 26,31,32 However, all included countries shared private and government-funded MS drug coverage in the absence of private health insurance. 33,34 A previous study 35 showed a limited role of costs in explaining therapeutic decisions and TI.…”
Section: Limitationsmentioning
confidence: 99%
“…National and regional recommendations include escalating therapy from a first-line agent to a second-line agent when there is evidence of clinical and radiological disease progression. 6 , 11 15 However, switching to a second-line agent is not supported by best practice recommendations if an MS patient has been clinically stable, with no new lesions on a follow-up magnetic resonance imaging (MRI) or no progression on the disability scale. 6 , 11 15 For the current analysis, we used the aforementioned scheme according to the current clinical practice.…”
Section: Methodsmentioning
confidence: 99%