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Article: Paul Kayser International Travel Scholar |
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Henry Ferreyra Pan Am J Ophthalmol 2008, 7:94 (1 July 2008) |
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Article: Report of Gillingham Fellowship Experience at the Center for Facial Appearances: Salt Lake City, Utah USA, April 2007 - March 2008 |
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Chun Cheng (Luis) Lin Yang Pan Am J Ophthalmol 2008, 7:92 (1 July 2008) |
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Article: An Introduction to a Revision of the Corneal Dystrophy Nomenclature - The IC3D Classification |
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Jayne S Weiss Pan Am J Ophthalmol 2008, 7:91 (1 July 2008) |
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Article: Introducción a la revisión a la nomenclatura de las Distrofias de Córnea - Clasificación IC3D |
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Jayne S Weiss Pan Am J Ophthalmol 2008, 7:90 (1 July 2008) |
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Article: Prova Nacional de Oftalmologia, Brasil e América Latina |
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Paulo A A Mello Pan Am J Ophthalmol 2008, 7:89 (1 July 2008) |
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Article: National Examinations for Certification in Ophthalmology in Brazil and Latin America |
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Paulo A A Mello Pan Am J Ophthalmol 2008, 7:88 (1 July 2008) |
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Article: Exámenes Nacionales para Certificación en Oftalmología en Brasil y Latinoamérica |
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Paulo A A Mello Pan Am J Ophthalmol 2008, 7:87 (1 July 2008) |
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Article: Bevacizumab (Avastin®) Intravítreo en Retinopatía Diabética |
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J Fernando Arévalo, Rafael A García-Amaris Pan Am J Ophthalmol 2008, 7:82 (1 July 2008)
Diabetic retinopathy (DR) remains the major threat to sight in the working age population. Diabetic macular edema (DME) is a manifestation of DR that produces loss of central vision. Macular edema within 1 disk diameter of the fovea is present in 9% of the diabetic population. Proliferative diabetic retinopathy (PDR) is a major cause of visual loss in diabetic patients. In PDR, the growth of new vessels from the retina or optic nerve, is thought to occur as a result of vascular endothelial growth factor (VEGF) release into the vitreous cavity as a response to ischemia. Furthermore, VEGF increases vessel permeability leading to deposition of proteins in the interstitium that facilitate the process of angiogenesis and macular edema. This review demonstrates multiple benefits of intravitreal bevacizumab on DR including DME and PDR. The results indicate that intravitreal bevacizumab injections may have a beneficial effect on macular thickness and visual acuity (VA), independent of the type of macular edema that is present. Therefore, in the future this new treatment modality could replace or complement focal/grid laser photocoagulation in DME. In addition, in PDR, this new option could be an adjuvant agent to pan-retinal photocoagulation so that more selective therapy may be applied.
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Article: Experiencia Latinoamericana con el Bevacizumab Intravítreo: Resultados del Pan-American Collaborative Retina Study (PACORES) Group |
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Lihteh Wu, Teodoro Evans Pan Am J Ophthalmol 2008, 7:75 (1 July 2008)
Vascular endothelial growth factor (VEGF) plays an important role in many diseases of the posterior segment of the eye that are characterized by macular edema and intraocular neovascularization. Recently, anti-VEGF agents such as pegaptanib sodium and ranibizumab have been shown to be of benefit in the treatment of choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD). However, in many parts of the world both pegaptanib sodium and ranibizumab are not readily available. Bevacizumab is a humanized recombinant monoclonal antibody against all VEGF isoforms. It has been proposed as an alternate treatment since it is more readily available. Since October 2005, investigators from Pan-American Collaborative Retina Study Group (PACORES) have tretaed patients with different vitreo-retinal pathologies with intravitreal bevacizumab. In our retrospective studies of relatively short follow-up, we have observed both functional and anatomic improvements in an important group of patients with diseases such as CNV secondary to different etiologies such as myopia and AMD, diabetic macular edema, as an adjuvant in proliferative diabetic retinopathy, macular edema secondary to venous vascular occlusions and pseudo-phakic cystoid macular edema. We believe that our results are promising. However, further studies are needed to determine the dose, injection interval, the number of injections and the long term safely, among other issues.
El factor de crecimiento vascular endotelial (VEGF por sus en inglés, Vascular Endothelial Growth Factor) juega un papel importante en muchas enfermedades del segmento posterior que se caracterizan por edema macular y neovascularización intraocular. Recientemente, se ha demostrado la eficacia de fármacos anti-VEGF como el ranibizumab y el pegaptabib sodio en la neovascularización coroidea (NVC) secundaria a la degeneración macular relacionada a la edad (DMRE). Sin embargo en muchas partes del mundo, tanto el pegaptanib sodio como el ranibizumab no se encuentran fácilmente disponibles. El bevacizumab es un anticuerpo monoclonal recombinado humanizado que se adhiere e inhibe todas las isoformas del VEGF. Este se ha propuesto como un tratamiento alternativo ya que es fácil de obtener. Desde octubre del 2005, los investigadores del grupo PACORES (Pan-American Collaborative Retina Study Group) hemos utilizado el bevacizumab intra-vítreo en diferentes patologías vitreoretinianas. En nuestros estudios retrospectivos de seguimiento relativamente corto, hemos observado mejoría anatómica y funcional en un grupo importante de pacientes con patologías como la NVC secundaria a diferentes etiologías incluyendo la DMRE y miopía, edema macular diabético, como adyuvante en la retinopatía diabética proliferativa (RDP), edemas maculares secundarios a oclusiones retinales venosas y edema macular cistoideo pseudofáquico. Creemos que los resultados son prometedores pero se requieren de más estudios para determinar la dosis, el intervalo entre tratamientos, el número de tratamientos y la seguridad a largo plazo entre otras consideraciones.
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Article: La kératite herpétique stromale pour le clinicien: Herpetic Stromal Keratitis for the Clinician |
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Karim Hammamji, Renaud Duval, Michèle Mabon, Hélène Boisjoly Pan Am J Ophthalmol 2008, 7:72 (1 July 2008)
HSV stromal keratitis is a frequent cause of ocular and visual morbidity. There are three recognized clinical forms: interstitial, disciform (endotheliitis), and necrotizing stromal keratitis, which all differ clinically as well as pathophysiologically. Although treatment for epithelial HSV keratitis has been standardized, it still remains controversial for the stromal form. The goal and challenge in the treatment lies in the balance of the inflammation generated by the host's immune system, and the infection from the virus. Several studies, including the cornerstone HEDS studies, consolidated the benefit of combined corticosteroid and antiviral therapy in the treatment of all forms of HSV stromal keratitis. Most studies used topical trifluridine as antiviral of choice, however several studies have demonstrated that oral acyclovir (or valacyclovir) along with topical corticosteroids is an equivalent and effective therapy, and avoids the often underestimated epithelial toxicity of long-term topical trifluridine. Prophylaxis from recurrences with oral acyclovir (or valacyclovir) is essential in the management of these patients due to the frequent relapses and its consequence on visual prognosis.
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Review: Alloplastic materials and Anophthalmic Socket Reconstruction - a literature review |
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Silvana A Schellini, Erika Hoyama Pan Am J Ophthalmol 2008, 7:69 (1 July 2008)
Reconstruction of the anophthalmic socket has historically been and continues to be a unique surgical challenge. This article reviews recent advancements in the use of alloplastic materials, as well as exciting alternatives offered by several porous materials and resorbable implants.
Resumo
Apesar do tratamento da cavidade anoftálmica ser feito há muitos séculos, persiste até os dias atuais como um desafio. Este artigo apresenta uma revisão sobre o uso de materiais aloplásticos para a reparação da cavidade anoftálmica, abordando interessantes materiais porosos e reabsorvíveis para este fim.
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Mensaje del Presidente de PAOF: Message from PAOF President: Mensajem do Presidente da PAOF: Mensaje del Presidente de PAOF: Message from PAOF President: Mensajem do Presidente da PAOF |
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Rubens Belfort Pan Am J Ophthalmol 2008, 7:68 (1 July 2008) |
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Mensaje del Presidente: Message from the President: Mensaje del Presidente: Message from the President |
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Richard L Abbott Pan Am J Ophthalmol 2008, 7:67 (1 July 2008) |
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Mensaje del Editor: Message from the Editor: Mensagem do Editor: Mensaje del Editor: Message from the Editor: Mensagem do Editor |
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Mark Mannis, Cristian Luco Pan Am J Ophthalmol 2008, 7:66 (1 July 2008) |
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