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1.
Rev Neurol ; 72(6): 203-212, 2021 03 16.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33710610

RESUMO

INTRODUCTION: The coronavirus disease 2019 (COVID-19) pandemic is a major worldwide health disorder. There is an increasing number of neurological complications recognized with COVID-19 including patients with GBS and its variants. DEVELOPMENT: A review of the clinical cases of GBS associated to COVID-19 infection published in the last months has been developed. We included 48 patients (31 men, mean age 56.4 years). The most common COVID-19 symptoms were cough (60.4%) and fever (56.3%). Mean time from COVID-19 symptoms to neurologic manifestations was 12.1 days, but in nine patients (18.8%) developed GBS within seven days. Eleven patients (22.9%) presented cranial nerve involvement in the absence of muscle weakness; 36 presented the classic sensory motor variant (75%) and one had a pure motor variant (2.1%). The electrodiagnostic pattern was considered demyelinating in 82.4% of the generalized variants. The presence of hyposmia/dysgeusia was associated with a latency shorter than seven days to GBS onset of symptoms (30% vs 15.6%), and cranial nerve involvement in the absence of weakness (30.8% vs 17.1%). Most patients (87.5%) were treated with intravenous immunoglobulin. Neurological outcome was favorable in 64.6%; 29.2% had respiratory failure and 4.2% died shortly after being admitted. CONCLUSIONS: GBS in patients with SARS-CoV-2 infection resembles clinically and electrophysiology the classical forms. Further studies are necessary to understand whether GBS frequency is actually increased due to SARS-CoV-2 infection and explore pathogenic mechanisms.


TITLE: Síndrome de Guillain-Barré asociado a infección por COVID-19: revisión de casos publicados.Introducción. La pandemia por la enfermedad por coronavirus 2019 (COVID-19) es un importante problema para la salud mundial. Hay un incremento en las complicaciones neurológicas reconocidas por la COVID-19, incluyendo el síndrome de Guillain-Barré (SGB) y sus variantes. Desarrollo. Se realizó una revisión de los casos publicados en los últimos meses de SGB asociado a infección por COVID-19. Incluimos a 48 pacientes (31 hombres; edad media: 56,4 años). Los síntomas de COVID-19 más comunes fueron tos (60,4%) y fiebre (56,3%). El tiempo promedio entre los síntomas de COVID-19 y el SGB fue de 12,1 días, pero nueve pacientes (18,8%) desarrollaron SGB en menos de siete días. Once pacientes (22,9%) presentaron afectación de los nervios craneales en ausencia de debilidad muscular, 36 presentaron la variante clásica sensitivomotora (75%) y uno tuvo una variante motora pura (2,1%). El patrón electrofisiológico se consideró desmielinizante en el 82,4% de las variantes generalizadas. La presencia de hiposmia/disgeusia estuvo asociada con una latencia menor a los siete días hasta el inicio de los síntomas del SGB (30 frente a 15,6%) y a la afectación de los nervios craneales en ausencia de debilidad (30,8 frente a 17,1%). La mayoría de los pacientes (87,5%) fueron tratados con inmunoglobulina endovenosa. La evolución neurológica fue favorable en el 64,6%, el 29,2% tuvo insuficiencia respiratoria y hubo un 4,2% de muertes. Conclusiones. El SGB en pacientes con infección por SARS-CoV-2 es similar clínica y electrofisiológicamente a las formas clásicas. Se requieren más estudios para comprender si la frecuencia del SGB realmente aumentó debido a la pandemia por COVID-19 y explorar los mecanismos patógenos involucrados.


Assuntos
COVID-19/complicações , Síndrome de Guillain-Barré/etiologia , Pandemias , SARS-CoV-2 , Adolescente , Adulto , Idoso , Anosmia/etiologia , Autoanticorpos/sangue , Autoanticorpos/imunologia , Autoantígenos/imunologia , Doenças dos Nervos Cranianos/etiologia , Disgeusia/etiologia , Feminino , Gangliosídeos/imunologia , Síndrome de Guillain-Barré/líquido cefalorraquidiano , Síndrome de Guillain-Barré/imunologia , Síndrome de Guillain-Barré/terapia , Humanos , Imunoglobulinas Intravenosas/uso terapêutico , Masculino , Pessoa de Meia-Idade , Plasmaferese , Insuficiência Respiratória/etiologia , Estudos Retrospectivos , Avaliação de Sintomas , Resultado do Tratamento , Adulto Jovem
2.
J Fr Ophtalmol ; 40(9): 723-730, 2017 11.
Artigo em Francês | MEDLINE | ID: mdl-29055730

RESUMO

PURPOSE AND CONTEXT: Intravitreal administration of anti-VEGF agents, available in France since 2007, allows stabilization and improvement in visual acuity in wet age-related macular degeneration (AMD). In the past few years, the management of this disease has evolved in terms of both diagnostic methods and treatment schedules, which have been adapted to the pathophysiology of AMD. The goal of this survey, performed in a representative sample of French ophthalmologists, was to describe the evolution of medical practices one year after a similar survey (Massé et al., J Fr Ophtalmol 2016; 39: 40-7). METHOD: The survey was performed from December, 2014 to March, 2015 in 191 ophthalmologists (53 general ophthalmologists and 98 retina specialists) with an on-line questionnaire. This questionnaire was designed by a committee of ophthalmologists to describe practices concerning screening, diagnosis, treatment and follow-up of wet AMD. RESULTS: An initial intravitreal injection of an anti-VEGF agent was usually performed within 10 days after the diagnosis of wet AMD by 98% of ophthalmologists and within 5 days by 63%. The treatment protocols favored by retina specialists were pro re nata (PRN) for 58%, Observe and Plan for 25% and Treat and Extend for 17%. Bilateral intravitreal injections were performed on the same day by 46% of retina specialists, mostly for the convenience of the patient and because of the low infectious risk. The initial protocol was maintained by one third of retina specialists throughout the course of treatment, while two thirds of them reported that they reassessed the protocol on average after 5 months. CONCLUSION: This survey on the practices of the ophthalmologists in wet AMD highlights an improvement in the time course of patient management and an evolution of treatment schedules toward individualized protocols.


Assuntos
Procedimentos Clínicos , Padrões de Prática Médica , Degeneração Macular Exsudativa/terapia , Adulto , Inibidores da Angiogênese/administração & dosagem , Bevacizumab/administração & dosagem , Protocolos Clínicos , Procedimentos Clínicos/história , Procedimentos Clínicos/estatística & dados numéricos , Procedimentos Clínicos/tendências , Feminino , França/epidemiologia , História do Século XXI , Humanos , Injeções Intravítreas , Masculino , Pessoa de Meia-Idade , Oftalmologistas/estatística & dados numéricos , Padrões de Prática Médica/história , Padrões de Prática Médica/estatística & dados numéricos , Padrões de Prática Médica/tendências , Fator A de Crescimento do Endotélio Vascular/antagonistas & inibidores , Degeneração Macular Exsudativa/epidemiologia
3.
Nucleic Acids Res ; 29(24): E122, 2001 12 15.
Artigo em Inglês | MEDLINE | ID: mdl-11812859

RESUMO

Nucleic acid fragmentation (footprinting) by *OH radicals is used often as a tool to probe nucleic acid structure and nucleic acid-protein interactions. This method has proven valuable because it provides structural information with single base pair resolution. Recent developments in the field introduced the 'synchrotron X-ray footprinting' method, which uses a high-flux X-ray source to produce single base pair fragmentation of nucleic acid in tens of milliseconds. We developed a complementary method that utilizes X-rays generated from a conventional rotating anode machine in which nucleic acid footprints can be generated by X-ray exposures as short as 100-300 ms. Our theoretical and experimental studies indicate that efficient cleavage of nucleic acids by X-rays depends upon sample preparation, energy of the X-ray source and the beam intensity. In addition, using this experimental set up, we demonstrated the feasibility of conducting X-ray footprinting to produce protein-DNA protection portraits at sub-second timescales.


Assuntos
Pegada de DNA/métodos , DNA Bacteriano/química , Proteínas de Bactérias/química , Proteínas de Ligação a DNA/química , Escherichia coli/química , Escherichia coli/genética , Fatores Hospedeiros de Integração , Conformação de Ácido Nucleico , Conformação Proteica , Fatores de Tempo , Raios X
4.
J Fr Ophtalmol ; 39(1): 40-7, 2016 Jan.
Artigo em Francês | MEDLINE | ID: mdl-26747017

RESUMO

BACKGROUND AND OBJECTIVES: Wet AMD is characterized by the formation of choroidal neovascularization, mediated by vascular endothelial growth factor (VEGF) and responsible for a decrease in visual acuity and metamorphopsia of sudden onset. Intravitreal anti-VEGF can stabilize or even improve visual acuity. Although there is a consensus among ophthalmologists about the induction phase injection of anti-VEGF, there appear to be differences in practice regarding therapeutic treatment modalities. The goal of this work was to explore this hypothesis and to better understand real life practices. METHOD: The Ipsos institute conducted a qualitative survey of 16 retinal specialists and 9 general ophthalmologists in September and October 2013, using a questionnaire developed by a scientific committee of experts. Fifteen telephone interviews and 4 face-to-face meetings with a retina specialist and an ophthalmologist were conducted. This qualitative study allowed the development of a quantitative survey of 200 retina specialists and general ophthalmologists, conducted between November 2013 and January 2014, to describe practices in diagnosis, treatment and follow-up of wet AMD. RESULTS: A distribution of roles between the ophthalmologist making the initial diagnosis and the retinal specialists responsible for treatment and follow-up was noted. Treatment was initiated within 10 days of diagnosis as recommended by the HAS in only one third of patients. After the induction phase of treatment, i.e. three monthly injections of anti-VEGF, treatment and monitoring practices were heterogeneous with 74% of physicians using a PRN treatment protocol, 22% a bimonthly protocol (with monthly monitoring in 19.4% of cases) and 4% a "treat and extend" protocol. There was little change in the protocol chosen in the case of recurrence. CONCLUSION: Three quarters of ophthalmologists report using a PRN protocol, and over 90% report seeing their patients monthly, either for injection or for a check-up. This apparent uniformity is in reality more complex: for the large majority, they prefer to closely follow the patient so as to treat the slightest recurrence, but with great variability in practices with regard to individualization of treatment.


Assuntos
Oftalmologia/estatística & dados numéricos , Padrões de Prática Médica/estatística & dados numéricos , Degeneração Macular Exsudativa/terapia , Adulto , Idoso , Protocolos Clínicos , Gerenciamento Clínico , Esquema de Medicação , Feminino , França/epidemiologia , Humanos , Injeções Intravítreas , Masculino , Pessoa de Meia-Idade , Receptores de Fatores de Crescimento do Endotélio Vascular/antagonistas & inibidores , Recidiva , Inquéritos e Questionários , Fator A de Crescimento do Endotélio Vascular/antagonistas & inibidores , Degeneração Macular Exsudativa/diagnóstico , Degeneração Macular Exsudativa/epidemiologia
6.
J Fr Ophtalmol ; 30(6): 578-84, 2007 Jun.
Artigo em Francês | MEDLINE | ID: mdl-17646746

RESUMO

PURPOSE: To assess the quality of vision in pseudophakic patients with aspheric intraocular lens (IOL) without spherical aberration compared to patients with spherical IOL. METHODS: Twenty-four patients (48 eyes) undergoing cataract surgery were randomly divided into two groups: 12 patients received an aspheric IOL in both eyes and 12 received spherical IOLs. The integrity of ocular functions was assessed with clinical examination and multifocal electroretinogram. Postoperative evaluations were conducted 3 months after surgery. Refraction, best-corrected visual acuity, contrast sensitivities, and wavefront ocular aberrations were analyzed. Patient-centered visual functions were evaluated according to the Activities of Daily Vision Scale. RESULTS: The ADVS score was better in the aspheric IOL group (p=0.01), particularly concerning the best-corrected near vision (p=0.006). Refraction and BCVA were similar. Contrast sensitivities in photopic conditions was better in the aspherical IOL group (p<0.001). Higher-order aberration was not different, except from spherical aberration (p=0.022). CONCLUSION: Patients with the aspherical IOLs felt they had better quality of vision, particularly near vision, compared with the spherical IOL group. These patient-centered benefits were associated with better photopic contrast sensitivity and reduced spherical aberration.


Assuntos
Sensibilidades de Contraste , Lentes Intraoculares , Pseudofacia/fisiopatologia , Acuidade Visual , Idoso , Idoso de 80 Anos ou mais , Extração de Catarata , Eletrorretinografia , Desenho de Equipamento , Feminino , Humanos , Implante de Lente Intraocular , Masculino , Óptica e Fotônica , Índice de Gravidade de Doença , Resultado do Tratamento , Testes Visuais
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