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1.
Eur J Ophthalmol ; 31(3): 920-931, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33736500

RESUMO

BACKGROUND: To date there are yet no available approved therapies for Geographic Atrophy (GA) secondary to age-related macular degeneration (AMD). METHODS: Single site, non-randomized safety and efficacy study presenting the preliminary results in a cohort of five late stage AMD (GA) patients successfully implanted with the Argus II Retinal Prosthesis System (Second Sight Medical Products Inc., Sylmar, CA, USA). Extensive fundus imaging including retinal photographs from which the GA area was measured. A combination of custom and traditional tests designed for very low vision subjects assessed visual function in study subjects. A Functional Low-Vision Observer Rated Assessment was carried out to evaluate the impact of the system on the subject's daily life. In addition, a study to evaluate structural characteristics of the visual cortex of the brain was performed in one subject using magnetic resonance imaging. RESULTS: Seven device-related adverse events were reported, four of which were classed as serious adverse events. Retinal detachment was reported in three patients and was successfully treated within 12 months of onset. Testing showed an improvement in visual function in three of five patients with the system turned on. Magnetic resonance imaging assessed in one patient after implantation indicates a selective increase in cortical myelin and thickness in visual brain regions 1 year post implantation. CONCLUSIONS: Epiretinal prostheses can successfully be implanted in those affected by GA secondary to late-stage AMD and can elicit visual percepts by electrical stimulation of residual neuroretinal elements and improve basic visual function in those affected.


Assuntos
Atrofia Geográfica , Degeneração Macular , Baixa Visão , Próteses Visuais , Eletrônica , Atrofia Geográfica/diagnóstico , Atrofia Geográfica/etiologia , Humanos , Degeneração Macular/complicações
2.
Retina ; 40(2): 303-311, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31972801

RESUMO

PURPOSE: To analyze and provide an overview of the incidence, management, and prevention of conjunctival erosion in Argus II clinical trial subjects and postapproval patients. METHODS: This retrospective analysis followed the results of 274 patients treated with the Argus II Retinal Prosthesis System between June 2007 and November 2017, including 30 subjects from the US and European clinical trials, and 244 patients in the postapproval phase. Results were gathered for incidence of a serious adverse event, incidence of conjunctival erosion, occurrence sites, rates of erosion, and erosion timing. RESULTS: Overall, 60% of subjects in the clinical trial subjects versus 83% of patients in the postapproval phase did not experience device- or surgery-related serious adverse events. In the postapproval phase, conjunctival erosion had an incidence rate of 6.2% over 5 years and 11 months. In 55% of conjunctival erosion cases, erosion occurred in the inferotemporal quadrant, 25% in the superotemporal quadrant, and 20% in both. Sixty percent of the erosion events occurred in the first 15 months after implantation, and 85% within the first 2.5 years. CONCLUSION: Reducing occurrence of conjunctival erosion in patients with the Argus II Retinal Prosthesis requires identification and minimization of risk factors before and during implantation. Implementing inverted sutures at the implant tabs, use of graft material at these locations as well as Mersilene rather than nylon sutures, and accurate Tenon's and conjunctiva closure are recommended for consideration in all patients.


Assuntos
Túnica Conjuntiva/cirurgia , Doenças da Túnica Conjuntiva/etiologia , Complicações Pós-Operatórias/etiologia , Implantação de Prótese/efeitos adversos , Retinose Pigmentar/cirurgia , Próteses Visuais/efeitos adversos , Doenças da Túnica Conjuntiva/epidemiologia , Doenças da Túnica Conjuntiva/prevenção & controle , Europa (Continente)/epidemiologia , Feminino , Humanos , Incidência , Masculino , Pessoa de Meia-Idade , Complicações Pós-Operatórias/epidemiologia , Complicações Pós-Operatórias/prevenção & controle , Implantação de Prótese/métodos , Estudos Retrospectivos , Estados Unidos/epidemiologia
4.
Br J Ophthalmol ; 97(5): 632-6, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23426738

RESUMO

BACKGROUND: Retinal prosthesis systems (RPS) are a novel treatment for profound vision loss in outer retinal dystrophies. Ideal prostheses would offer stable, long-term retinal stimulation and reproducible spatial resolution in a portable form appropriate for daily life. METHODS: We report a prospective, internally controlled, multicentre trial of the Argus II system. Twenty-eight subjects with light perception vision received a retinal implant. Controlled, closed-group, forced-choice letter identification, and, open-choice two-, three- and four-letter word identification tests were carried out. RESULTS: The mean±SD percentage correct letter identification for 21 subjects tested were: letters L, T, E, J, F, H, I, U, 72.3±24.6% system on and 17.7±12.9% system off; letters A, Z, Q, V, N, W, O, C, D, M, 55.0±27.4% system on and 11.8%±10.7% system off, and letters K, R, G, X, B, Y, S, P, 51.7±28.9% system on and 15.3±7.4% system off. (p<0.001 for all groups). A subgroup of six subjects was able to consistently read letters of reduced size, the smallest measuring 0.9 cm (1.7°) at 30 cm, and four subjects correctly identify unrehearsed two-, three- and four-letter words. Average implant duration was 19.9 months. CONCLUSIONS: Multiple blind subjects fitted with the Argus II system consistently identified letters and words using the device, indicating reproducible spatial resolution. This, in combination with stable, long-term function, represents significant progress in the evolution of artificial sight.


Assuntos
Coroideremia/fisiopatologia , Leitura , Retinose Pigmentar/fisiopatologia , Baixa Visão/fisiopatologia , Acuidade Visual/fisiologia , Percepção Visual/fisiologia , Próteses Visuais , Adulto , Idoso , Coroideremia/cirurgia , Eletrodos Implantados , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Implantação de Prótese , Retinose Pigmentar/cirurgia , Baixa Visão/cirurgia
5.
J Shoulder Elbow Surg ; 19(8): 1184-90, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20951609

RESUMO

HYPOTHESIS: We hypothesized that the malpositioning of the humeral component can preclude the long-term success of anatomical total shoulder arthroplasty. The goal of this study was to evaluate the mechanical consequences of superior and inferior malpositioning of the humeral head. MATERIALS AND METHODS: A numerical musculoskeletal model of the shoulder joint allowing natural humeral head translation was used to simulate a loaded abduction movement controlled by muscular activation. An inferior and superior malpositioning of 5 mm were compared to an optimal positioning. Impingements, articular contact pattern, and cement stress were evaluated. RESULTS: Inferior malpositioning of the humeral head induced impingement and limited the abduction level, while superior malpositioning increased the subluxation risk. Both inferior and superior malpositioning increased the stress level within the cement mantle. DISCUSSION: This numerical study highlights the importance of an anatomical reconstruction of the glenohumeral surfaces for the success rate of anatomical total shoulder arthroplasty.


Assuntos
Artroplastia de Substituição/métodos , Cabeça do Úmero , Articulação do Ombro/cirurgia , Fenômenos Biomecânicos , Humanos , Modelos Anatômicos , Estresse Mecânico
6.
J Shoulder Elbow Surg ; 18(3): 360-5, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19243979

RESUMO

HYPOTHESIS: Supraspinatus deficiency associated with total shoulder arthroplasty (TSA) provokes eccentric loading and may induce loosening of the glenoid component. A downward inclination of the glenoid component has been proposed to balance supraspinatus deficiency. METHODS: This hypothesis was assessed by a numeric musculoskeletal model of the glenohumeral joint during active abduction. Three cases were compared: TSA with normal muscular function, TSA with supraspinatus deficiency, and TSA with supraspinatus deficiency and downward inclination of the glenoid. RESULTS: Supraspinatus deficiency increased humeral migration and eccentric loading. A downward inclination of the glenoid partly balanced the loss of stability, but this potential advantage was counterbalanced by an important stress increase within the glenoid cement. The additional subchondral bone reaming required to incline the glenoid component indeed reduced the bone support, increasing cement deformation and stress. CONCLUSION: Glenoid inclination should not be obtained at the expense of subchondral bone support.


Assuntos
Artroplastia de Substituição/efeitos adversos , Prótese Articular , Músculo Esquelético/fisiologia , Falha de Prótese , Amplitude de Movimento Articular/fisiologia , Articulação do Ombro/cirurgia , Artroplastia de Substituição/métodos , Fenômenos Biomecânicos , Simulação por Computador , Análise de Elementos Finitos , Humanos , Instabilidade Articular/fisiopatologia , Instabilidade Articular/prevenção & controle , Modelos Anatômicos , Contração Muscular/fisiologia , Desenho de Prótese , Sensibilidade e Especificidade , Articulação do Ombro/fisiopatologia , Estresse Mecânico
7.
Comput Methods Biomech Biomed Engin ; 12(1): 95-100, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18651261

RESUMO

A combined experimental/numerical study was performed to calculate the 3D octahedral shear strain map in a mouse tibia loaded axially. This study is motivated by the fact that the bone remodelling analysis, in this in vivo mouse model should be performed at the zone of highest mechanical stimulus to maximise the measured effects. Accordingly, it is proposed that quantification of bone remodelling should be performed at the tibial crest and at the distal diaphysis. The numerical model could also be used to furnish a more subtle analysis as a precise correlation between local strain and local biological response can be obtained with the experimentally validated numerical model.


Assuntos
Remodelação Óssea/fisiologia , Modelos Biológicos , Tíbia/fisiologia , Suporte de Carga/fisiologia , Animais , Força Compressiva/fisiologia , Simulação por Computador , Módulo de Elasticidade/fisiologia , Imageamento Tridimensional/métodos , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Resistência ao Cisalhamento , Estresse Mecânico
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