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1.
Brain Sci ; 11(6)2021 Jun 11.
Artigo em Inglês | MEDLINE | ID: mdl-34208347

RESUMO

Non-motor symptoms (NMS) in Parkinson's disease (PD), including neuropsychiatric or dysautonomic complaints, fatigue, or pain, are frequent and have a high impact on the patient's quality of life. They are often poorly recognized and inadequately treated. In the recent years, the growing awareness of NMS has favored the development of techniques that complement the clinician's diagnosis. This review provides an overview of the most important ultrasonographic findings related to the presence of various NMS. Literature research was conducted in PubMed, Scopus, and Web of Science from inception until January 2021, retrieving 23 prospective observational studies evaluating transcranial and cervical ultrasound in depression, dementia, dysautonomic symptoms, psychosis, and restless leg syndrome. Overall, the eligible articles showed good or fair quality according to the QUADAS-2 assessment. Brainstem raphe hypoechogenicity was related to the presence of depression in PD and also in depressed patients without PD, as well as to overactive bladder. Substantia nigra hyperechogenicity was frequent in patients with visual hallucinations, and larger intracranial ventricles correlated with dementia. Evaluation of the vagus nerve showed contradictory findings. The results of this systematic review demonstrated that transcranial ultrasound can be a useful complementary tool in the evaluation of NMS in PD.

2.
Atheroscler Plus ; 45: 32-38, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-36643997

RESUMO

Background and aims: The benefits of the PCSK9 inhibitors, alirocumab and evolocumab, in lowering LDL-cholesterol and preventing major adverse cardiac events (MACE) have been demonstrated in pivotal clinical trials. However, few studies of routine clinical practice have been conducted to analyse and compare the efficacy and safety of the two drugs. Methods: Retrospective observational study of patients treated with a PCSK9 inhibitor in five hospitals in Andalusia (southern Spain). Baseline demographic and clinical data, LDL-cholesterol levels and the occurrence of MACEs during the follow-up period were recorded. Results: A total of 141 patients were included in the study: 90 were treated with alirocumab and 51 with evolocumab. The patients' mean age (IQR) was 58 (11) years and 58 (41%) were women. The most frequent concomitant medications were statins, 94 (66.7%), followed by antiplatelet therapy (66%) and ezetimibe (65.2%). The median (IQR) follow-up period was 18 (18) months, with 18 (24) for alirocumab and 11 (18) for evolocumab. At the six-month follow-up visit, LDL-cholesterol values had decreased to pre-treatment levels and remained significantly decreased (p < 0.05) over time, for both drugs, and a greater reduction was achieved in patients with established cardiovascular disease and concomitant treatment with statins. With respect to adverse effects, there were nine MACEs (6.4%), of which seven were with alirocumab (7.8%) and two with evolocumab (3.9%) (p NS). Other adverse effects (9.2%) included local erythema (3.5%), muscle cramps (2.1%), respiratory symptoms (2.1%) and asthaenia (1.4%). Conclusions: The efficacy and safety of alirocumab and evolocumab in routine clinical practice are consistent with the findings of the pivotal clinical trials.

4.
Epilepsy Res ; 138: 81-87, 2017 12.
Artigo em Inglês | MEDLINE | ID: mdl-29096133

RESUMO

OBJECTIVE: Evaluate if eslicarbazepine acetate (ESL) in combination with other non-inducer antiepileptic drugs (AEDs) in the treatment of epilepsy may represent a positive impact in the cardiovascular risk profile. METHODS: multicentre, retrospective, observational, non-interventional, real-life study comparing patients treated with cytochrome P450 (CYP) inducer vs. ESL plus non-inducer AEDs. Primary endpoint: Carotid intima-media thickness (CIMT) measured following the Manheim Consensus criteria. RESULTS: Patients included: 163. The main demographic, clinical and vascular risk parameters were comparable between the two groups except for duration of the disease, prevalence of dyslipidemia and use of lipid-lowering drugs (significantly higher in the inducers group) and number of previous antiepileptic drugs (significantly higher in the non-inducers group). Bivariate analysis of the main endpoint showed almost significant differences (p=0.05) in CIMT measures favourable to non-inducers (average 0.617mm+SD=0.148) vs. inducers (average 0.663mm+SD=0.147). Other variables reaching statistical significance were: age >50 years (p<0.001), high blood pressure (p<0.01) and dyslipidemia (p<0.05). A multivariate analysis including these variables and biochemical vascular risk factors showed a predictor model including two variables: inducers group (p=0.031; Coefficient ß=0.234) and age >50 years (p=0.001; Coefficient ß=0.387). Regarding gender, the mean CIMT in males was significantly higher in the inducers (0.693mm; SD=0.139) than in the non- inducers groups (0.628mm; SD=0.151; p<0.05). In females the differences were not significant. SIGNIFICANCE: The use of CYP inducer AEDs is associated with a significant increase in CIMT as compared with ESL and other non-inducer AEDs. The study shows a decrease in the vascular risk measured by ultrasound criteria in male patients treated with ESL compared with patients treated with inducer AEDs.


Assuntos
Espessura Intima-Media Carotídea , Dibenzazepinas/uso terapêutico , Epilepsias Parciais/tratamento farmacológico , Epilepsias Parciais/patologia , Bloqueadores do Canal de Sódio Disparado por Voltagem/uso terapêutico , Adolescente , Adulto , Idoso , Epilepsias Parciais/complicações , Feminino , Humanos , Hipertensão/etiologia , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Estatísticas não Paramétricas , Ultrassonografia , Adulto Jovem
5.
Rev Neurol ; 56(6): 309-14, 2013 Mar 16.
Artigo em Espanhol | MEDLINE | ID: mdl-23483464

RESUMO

INTRODUCTION. Eslicarbazepine acetate (ESL) is a new antiepileptic drug (AED) licensed in Spain in February 2011 as an adjunctive therapy in adults with partial seizures with or without secondary generalization. Clinical trials with ESL have demonstrated acceptable efficacy and safety. AIM. To evaluate the results of ESL in our epilepsy unit during its first year of clinical experience with this AED. PATIENTS AND METHODS. We included all patients who started treatment with ESL at our epilepsy unit from March 2011 to May 2012. We collected the following variables: gender, aetiology of epilepsy, epileptogenic area, reason for switch to ESL, clinical response after initiation of ESL, adverse effects of ESL, refractoriness criteria and treatment discontinuation. A bivariate factor-to-factor correlation study was carried out to establish associations between the independent variables and the clinical response. RESULTS. We recruited 105 patients (51.4% male). 20,7% of patients remained seizure-free and 58.4% showed > 50% improvement after introduction of ESL. At 6 months, 18.1% had experienced some type of side effect, with cognitive disorders being the most common, and 11.5% had discontinued treatment. Combination with lacosamide proved to be significantly less effective in the control of seizures. Combination of ESL with the rest of sodium channel inhibitors was similar in efficacy to others combinations. CONCLUSIONS. ESL is a well-tolerated and effective AED when is used as adjunctive treatment with most of other AED in clinical practice.


Assuntos
Anticonvulsivantes/uso terapêutico , Dibenzazepinas/uso terapêutico , Epilepsia/tratamento farmacológico , Bloqueadores dos Canais de Sódio/uso terapêutico , Acetamidas/administração & dosagem , Acetamidas/uso terapêutico , Adolescente , Adulto , Idoso , Anticonvulsivantes/administração & dosagem , Anticonvulsivantes/efeitos adversos , Transtornos Cognitivos/induzido quimicamente , Depressão/induzido quimicamente , Dibenzazepinas/administração & dosagem , Dibenzazepinas/efeitos adversos , Quimioterapia Combinada , Epilepsias Parciais/tratamento farmacológico , Epilepsia Generalizada/tratamento farmacológico , Feminino , Seguimentos , Humanos , Lacosamida , Masculino , Pessoa de Meia-Idade , Bloqueadores dos Canais de Sódio/administração & dosagem , Bloqueadores dos Canais de Sódio/efeitos adversos , Aumento de Peso/efeitos dos fármacos , Adulto Jovem
6.
Rev. neurol. (Ed. impr.) ; 56(6): 309-314, 16 mar., 2013. tab, graf
Artigo em Espanhol | IBECS | ID: ibc-110757

RESUMO

Introducción. El acetato de eslicarbazepina (ESL) es un nuevo fármaco antiepiléptico aprobado en España en febrero de 2011 como tratamiento adyuvante en adultos con crisis parciales, con o sin generalización secundaria. Los ensayos clínicos con ESL han demostrado una aceptable eficacia y seguridad. Objetivo. Evaluar los resultados de la ESL tras el primer año de experiencia en la práctica clínica. Pacientes y métodos. Incluimos a todos los pacientes que, habiendo iniciado tratamiento con ESL entre marzo de 2011 y mayo de 2012 en nuestra unidad, habían completado los seis meses de tratamiento continuado. Se recogieron siete variables independientes clínicas y demográficas. Se realizó un análisis de correlación bivariante factor a factor para establecer las posibles asociaciones entre las variables independientes recogidas y la respuesta clínica. Resultados. Incluimos un total de 105 pacientes (el 51,4%, hombres). El 58,4% mostró una mejoría superior al 50% en el número de crisis tras la introducción de la ESL (el 20,7% quedó libre de crisis). Al cabo de seis meses, un 18,1% experimentó algún tipo de efecto adverso, siendo los más frecuentes las quejas cognitivas, y un 11,5% abandonó el tratamiento. La combinación con lacosamida mostró menos eficacia estadística en el control de las crisis que el resto de las combinaciones. La combinación de ESL con el resto de los inhibidores de los canales del sodio no mostró diferencias significativas de eficacia. Conclusiones. La ESL constituye un fármaco antiepiléptico con buena tolerancia, y con una tasa de efectos adversos y de retención aceptables cuando se usa en combinación con la mayoría de los antiepilépticos disponibles (AU)


Introduction. Eslicarbazepine acetate (ESL) is a new antiepileptic drug (AED) licensed in Spain in February 2011 as an adjunctive therapy in adults with partial seizures with or without secondary generalization. Clinical trials with ESL have demonstrated acceptable efficacy and safety. Aim. To evaluate the results of ESL in our epilepsy unit during its first year of clinical experience with this AED. Patients and methods. We included all patients who started treatment with ESL at our epilepsy unit from March 2011 to May 2012. We collected the following variables: gender, aetiology of epilepsy, epileptogenic area, reason for switch to ESL, clinical response after initiation of ESL, adverse effects of ESL, refractoriness criteria and treatment discontinuation. A bivariate factor-to-factor correlation study was carried out to establish associations between the independent variables and the clinical response. Results. We recruited 105 patients (51.4% male). 20,7% of patients remained seizure-free and 58.4% showed > 50% improvement after introduction of ESL. At 6 months, 18.1% had experienced some type of side effect, with cognitive disorders being the most common, and 11.5% had discontinued treatment. Combination with lacosamide proved to be significantly less effective in the control of seizures. Combination of ESL with the rest of sodium channel inhibitors was similar in efficacy to others combinations. Conclusions. ESL is a well-tolerated and effective AED when is used as adjunctive treatment with most of other AED in clinical practice (AU)


Assuntos
Humanos , Epilepsia/tratamento farmacológico , Anticonvulsivantes/uso terapêutico , Adjuvantes Farmacêuticos/uso terapêutico , Epilepsias Parciais/tratamento farmacológico , Epilepsia , Carbamazepina/uso terapêutico
7.
Clin Neurol Neurosurg ; 115(8): 1338-42, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23369403

RESUMO

INTRODUCTION: The predominant manifestations of temporal lobe epilepsy (TLE) are partial seizures with impairment of consciousness (type I.B of ILAE classification), although consciousness impairment is not necessary in all seizures of patients with TLE. Nevertheless, there have been very few reports of TLE patients with exclusive seizures with no impairment of consciousness (i.e. isolated auras). The objective of this study was to determine any differential characteristics of this subgroup of TLE patients. MATERIAL AND METHODS: Retrospective case-control study in 163 consecutive TLE patients from our hospital database. The patients were divided between those with and without ictal impairment of consciousness, based on directed semi-structured questionnaire to the patient and relatives and on video-EEG records. Ten independent variables (8 clinical and 2 paraclinical) were compared between the groups. RESULTS: 14 patients (8.5%) formed the "TLE without ictal impairment of consciousness" group. This group was less refractory to medical treatment [Odds Ratio: 0.14 (0.03-0.64); p<0.01] and had frequent ictal motor behaviour [Odds ratio: 5.33 (1.65-17.14); p=0.008] and less frequent presence of automatisms [p<0.001]. Non-significant tendencies were observed for a higher frequency of lesional substrate and fewer generalization episodes. DISCUSSION: TLE without ictal impairment of consciousness appears to be more frequent than previously thought. This subgroup of TLE patients shows differential characteristics that may possibly result from a differential propagation of the original epileptic activity towards frontal areas rather than towards neocortical and diencephalic structures, which may be related to the more frequent presence of structural lesions.


Assuntos
Transtornos da Consciência/etiologia , Transtornos da Consciência/psicologia , Epilepsia do Lobo Temporal/fisiopatologia , Epilepsia do Lobo Temporal/psicologia , Adolescente , Adulto , Idoso , Anticonvulsivantes/uso terapêutico , Automatismo/etiologia , Comportamento , Estudos de Casos e Controles , Estudos de Coortes , Resistência a Medicamentos , Eletroencefalografia , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Razão de Chances , Estudos Retrospectivos , Convulsões/psicologia , Inconsciência/etiologia , Inconsciência/psicologia , Adulto Jovem
9.
Prog. obstet. ginecol. (Ed. impr.) ; 55(10): 514-517, dic. 2012.
Artigo em Espanhol | IBECS | ID: ibc-107505

RESUMO

La histerosalpingografía (HSG) es un procedimiento utilizado en el estudio de la infertilidad. La embolia del medio de contraste es una complicación infrecuente y está favorecida por ciertos factores. La persistencia del foramen oval permeable (FOP) complica el pronóstico, ya que puede producir embolias paradójicas. Presentamos el caso de una mujer de 32 años, derivada de un hospital comarcal por accidente cerebrovascular isquémico tras realizarse una HSG informada como dificultosa, precisando una dosis mayor de contraste (ácido diazitroico) que la habitual. Se realizó una tomografía computarizada craneal que mostró infarto cerebral hemisférico derecho. La ecocardiografía posterior al acontecimiento reveló la existencia de un FOP. Tras 8 días de evolución, la paciente presentó mejoría progresiva del déficit, con capacidad para deambular autónomamente, por lo que se procedió al alta hospitalaria con tratamiento antiagregante domiciliario. La clínica acontecida en esta paciente y los hallazgos encontrados en las pruebas diagnósticas son altamente sugestivos de ictus isquémico de la arteria cerebral media secundario a embolismo paradójico del medio de contraste a través del FOP, por lo que resulta interesante realizar una revisión del tema (AU)


Hysterosalpingography is a procedure used in the study of infertility. Embolism of contrast dye is a rare complication and is facilitated by certain factors. Persistence of permeable foramen ovale (PFO) complicates the prognosis and may produce paradoxical embolisms. We present the case of a 32-year-old woman who was referred from a district hospital due to an ischemic stroke following a hysterosalpingography reported as difficult, requiring a higher dose of contrast medium (diatrizoic acid) than usual. A cranial computed tomography scan was performed, which showed a right hemispheric stroke. Post-event echocardiography revealed a PFO. Eight days after the event, the patient showed progressive improvement and was able to walk without assistance. Consequently, she was discharged from hospital with antiplatelet therapy. The symptomology in this patient, as well as the findings of the diagnostic tests, are highly suggestive of ischemic stroke of the middle cerebral artery secondary to paradoxical embolism of the contrast medium through the PFO. A review of the topic is provided (AU)


Assuntos
Humanos , Feminino , Adulto , Acidente Vascular Cerebral/complicações , Acidente Vascular Cerebral/diagnóstico , Histerossalpingografia/instrumentação , Histerossalpingografia/métodos , Embolia Paradoxal/complicações , Embolia Paradoxal/diagnóstico , Embolia Paradoxal/terapia , Forame Oval Patente/complicações , Forame Oval Patente/cirurgia , Forame Oval Patente , Acidente Vascular Cerebral/fisiopatologia , Acidente Vascular Cerebral , Histerossalpingografia/efeitos adversos , Histerossalpingografia , Embolia Paradoxal/fisiopatologia , Embolia Paradoxal , /métodos
10.
Epilepsy Res ; 101(1-2): 113-21, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22472321

RESUMO

INTRODUCTION: Temporal Lobe Epilepsy (TLE) is frequently resistant to drug treatment, but a high percentage of these patients can be free of seizures after epilepsy surgery. Delay in the surgical decision has been related to quality of life impairment, social and work limitations, and increased mortality risk. A predictive model for refractoriness based on clinical and diagnostic factors may allow its earlier detection and a shorter delay before surgery. MATERIAL AND METHODS: A case-control study was conducted in TLE patients over 16 years old. The dependent variable was resistance to medical treatment according to ILAE 2010 criteria. Independent variables were clinical, semiological, therapeutic, neurophysiological, radiological, and neuropsychological variables. A multivariate study was conducted to identify the variables associated with refractoriness, calculating the positive and negative predictive values and positive likelihood ratios of these variables individually and in combination. These data were used to construct a refractoriness predictive model. RESULTS: ILAE refractoriness criteria were met by 83 patients (50.9%). In the multivariate analysis, refractoriness was significantly associated with one semiological variable, one neuroradiological variable, one neurophysiological variable, and two therapeutic variables but not with neuropsychological test outcomes. These significant variables were used to construct a predictive model. CONCLUSION: Assessment of semiological, neurophysiological, and neuroradiological data can serve to stratify the risk of refractory epilepsy in TLE patients.


Assuntos
Epilepsia do Lobo Temporal/diagnóstico , Epilepsia do Lobo Temporal/tratamento farmacológico , Adolescente , Adulto , Idoso , Anticonvulsivantes/uso terapêutico , Estudos de Casos e Controles , Criança , Pré-Escolar , Interpretação Estatística de Dados , Progressão da Doença , Resistência a Medicamentos , Eletroencefalografia , Epilepsia/complicações , Epilepsia/psicologia , Epilepsia do Lobo Temporal/psicologia , Feminino , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Testes Neuropsicológicos , Valor Preditivo dos Testes , Medição de Risco , Adulto Jovem
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