2023
DOI: 10.1016/j.nrl.2021.09.015
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Diagnóstico y tratamiento de la neuralgia del trigémino: documento de consenso del Grupo de Estudio de Cefaleas de la Sociedad Española de Neurología

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Cited by 16 publications
(16 citation statements)
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“…ej., tumor, accidente cerebrovascular, placa de esclerosis múltiple, malformación vascular, otras lesiones que comprimen el nervio trigémino o interrumpen sus vías en el tronco encefálico). (Rubin, 2022) Asimismo, Latorre et al, (2021) en su documento de consenso del Grupo de Estudio de Cefaleas de la Sociedad Espanola de Neurología acerca del diagnóstico y tratamiento de la neuralgia del trigémino, recomiendan la realización de una Resonancia Magnética (RM) craneal a todo paciente con diagnóstico clínico de NT para descartar causas secundarias. Se utilizan técnicas de reconstrucción en 3D que reemplazan a las clásicas secuencias en 2D, permitiendo una óptima evaluación anatómica del nervio.…”
Section: Diagnósticounclassified
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“…ej., tumor, accidente cerebrovascular, placa de esclerosis múltiple, malformación vascular, otras lesiones que comprimen el nervio trigémino o interrumpen sus vías en el tronco encefálico). (Rubin, 2022) Asimismo, Latorre et al, (2021) en su documento de consenso del Grupo de Estudio de Cefaleas de la Sociedad Espanola de Neurología acerca del diagnóstico y tratamiento de la neuralgia del trigémino, recomiendan la realización de una Resonancia Magnética (RM) craneal a todo paciente con diagnóstico clínico de NT para descartar causas secundarias. Se utilizan técnicas de reconstrucción en 3D que reemplazan a las clásicas secuencias en 2D, permitiendo una óptima evaluación anatómica del nervio.…”
Section: Diagnósticounclassified
“…(Marín Medina & Gámez Cárdenas, 2019, pág. 196) Latorre et al, (2021) refiere acerca de la lamotrigina o baclofeno son fármacos de se-gunda línea. En consecuencia, se recomienda el uso de lamotrigina en monoterapia en caso de contraindicación o intolerancia a los fármacos de primera línea.…”
Section: Tratamientounclassified
“…Many drugs have been assessed as potential monotherapy alternatives or as adjunctive treatments, including baclofen, lamotrigine, gabapentin, pimozide, lidocaine, phenytoin, and onabotulinumtoxinA injections. Nevertheless, none of these therapies have reached a sufficient level of evidence due to a low number of patients and inconsistent results 6 ; thus, they are not recommended as treatments of choice in clinical guidelines, and their prescription is only resorted to after first‐line treatment failure, either as a switch or an add‐on treatment at the discretion of the treating physician 5,7 …”
Section: Introductionmentioning
confidence: 99%
“…Nevertheless, none of these therapies have reached a sufficient level of evidence due to a low number of patients and inconsistent results 6 ; thus, they are not recommended as treatments of choice in clinical guidelines, and their prescription is only resorted to after first-line treatment failure, either as a switch or an add-on treatment at the discretion of the treating physician. 5,7 Recently, there has been a growing interest in new drugs that act by blocking voltage-gated sodium channels, 8,9 similar to carbamazepine or oxcarbazepine, but with novel mechanisms of action that may decrease the very common side effects of these drugs. 10 For instance, lacosamide blocks voltage-gated sodium channels in a slow inactivating manner 11 and has recently shown efficacy in the treatment of neuropathic pain.…”
mentioning
confidence: 99%
“…11 Although much work has focused on the processing of peripheral pain signals in neuropathic pain conditions, less is known about the mechanisms by which trigeminal neuropathies lead to a dysregulation of signaling in the trigeminal pathway, leading to a paucity of therapeutic avenues to combat trigeminal neuralgia. 15 Anticonvulsants, such as carbamazepine and oxcarbazepine, that target voltage-gated sodium channels are first-line treatment options, 3,14 indicating that sodium channels may be potential targets for trigeminal pain. In this current issue of PAIN, Loya-Lopez et al 16 present new evidence that selectively targeting Na v 1.7 channel expression offered protection from trigeminal pain in preclinical models.…”
mentioning
confidence: 99%