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1.
Neurosignals ; 30(S1): 39-58, 2022 11 11.
Artículo en Inglés | MEDLINE | ID: mdl-36354963

RESUMEN

Retinoblastoma (RB) management has evolved over the last three decades. Goals of modern RB treatment are first to protect life and prevent metastatic disease, then preservation of the globe and useful vision. With modern treatment protocols and early disease detection success rates can reach up to 100% of disease-free-globe and eye preservation. Treatment of advanced cases remains complex, requiring aggressive chemotherapy or/and external beam radiation. Treatment protocols are extremely diverse and dependent on local resources thus success rates are variable. Here we review narratively current treatment protocols and failure rates based on a PubMed search using keywords of retinoblastoma, retinoblastoma seed, retinoblastoma treatment, enucleation.


Asunto(s)
Neoplasias de la Retina , Retinoblastoma , Humanos , Lactante , Retinoblastoma/tratamiento farmacológico , Retinoblastoma/patología , Neoplasias de la Retina/tratamiento farmacológico , Neoplasias de la Retina/patología , Enucleación del Ojo/métodos , Terapia Combinada , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico
2.
Neurosignals ; 29(S1): 1-7, 2021 05 05.
Artículo en Inglés | MEDLINE | ID: mdl-33945240

RESUMEN

BACKGROUND/AIMS: Intravitreal rituximab is an off-label treatment option for primary vitreoretinal lymphoma (PVRL). The objective of this study was to monitor the therapeutic response and safety profile of intravitreal rituximab in a cohort of PVRL patients. METHODS: In this retrospective, uncontrolled, open label, multicentre study, 20 eyes from 15 consecutive patients diagnosed with PRVL received at least one intravitreal injection of 1mg in 0.1ml rituximab. Biodata of the PVRL patients was recorded as well as visual acuity and vitreous haze score immediately before rituximab intravitreal injection and at follow-up examinations. Intravitreal rituximab safety data was also recorded. Additional rituximab injections were made during control visits on a pro re nata (PRN) regime using increased vitreous haze to indicate recurrence. RESULTS: There was significant vitreous haze reduction (p=0.0002) followed by significant improvement of visual acuity (mean best visual acuity before therapy 0.57 logMAR, after therapy 0.20 logMAR (p=0.0228) during the follow-up time up to 4 years. Only mild ocular side effects were reported. Median follow-up time was 565 days (range, 7-1253 days). CONCLUSION: Intravitreal rituximab therapy shows promising PVRL regression without any severe side effects. Although our clinical data support rituximab as intravitreal therapy in PVRL disease, further study is warranted.


Asunto(s)
Linfoma Intraocular , Neoplasias de la Retina , Humanos , Recurrencia Local de Neoplasia , Neoplasias de la Retina/diagnóstico , Neoplasias de la Retina/tratamiento farmacológico , Estudios Retrospectivos , Rituximab/uso terapéutico , Cuerpo Vítreo
3.
Anesth Analg ; 126(4): 1206-1211, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-28759486

RESUMEN

Collaboration of the surgical and anesthesia teams for patient positioning is essential to assure patient comfort and safety, preventing systemic and ophthalmic complications. The goals and rationales of positioning for intraocular surgery are discussed including placing the head above the heart, elevating the chin, using a head rest that is sufficiently firm, maximizing anesthesia care team access and minimizing fire risk, and taping the patient's head to the operating table to reduce unexpected movement with intraocular injury.


Asunto(s)
Procedimientos Quirúrgicos Oftalmológicos/métodos , Posicionamiento del Paciente/métodos , Complicaciones Posoperatorias/prevención & control , Anestesistas , Conducta Cooperativa , Humanos , Comunicación Interdisciplinaria , Mesas de Operaciones , Procedimientos Quirúrgicos Oftalmológicos/efectos adversos , Grupo de Atención al Paciente , Posicionamiento del Paciente/efectos adversos , Factores de Riesgo , Cirujanos , Resultado del Tratamiento
4.
BMC Ophthalmol ; 18(1): 101, 2018 Apr 18.
Artículo en Inglés | MEDLINE | ID: mdl-29669523

RESUMEN

BACKGROUND: The critical time from onset of complete occlusion of the central retinal artery (CRA) to functionally significant inner retinal infarction represents a window of opportunity for treatment and also has medical-legal implications, particularly when central retinal artery occlusion (CRAO) complicates therapeutic interventions. Here, we review the evidence for time to infarction from complete CRAO and discuss the implications of our findings. METHODS: A Medline search was performed using each of the terms "central retinal artery occlusion", "retinal infarction", "retinal ischemia", and "cherry red spot" from 1970 to the present including articles in French and German. All retrieved references as well as their reference lists were screened for relevance. An Internet search using these terms was also performed to look for additional references. RESULTS: We find that the experimental evidence showing that inner retinal infarction occurs after 90-240 min of total CRAO, which is the interval generally accepted in the medical literature and practice guidelines, is flawed in important ways. Moreover, the retinal ganglion cells, supplied by the CRA, are part of the central nervous system which undergoes infarction after non-perfusion of 12-15 min or less. CONCLUSIONS: Retinal infarction is most likely to occur after only 12-15 min of complete CRAO. This helps to explain why therapeutic maneuvers for CRAO are often ineffective. Nevertheless, many CRAOs are incomplete and may benefit from therapy after longer intervals. To try to avoid retinal infarcton from inadvertent ocular compression by a headrest during prone anesthesia, the eyes should be checked at intervals of less than 15'.


Asunto(s)
Flujo Sanguíneo Regional/fisiología , Oclusión de la Arteria Retiniana/fisiopatología , Células Ganglionares de la Retina/fisiología , Angiografía con Fluoresceína , Humanos , Infarto , Factores de Tiempo
5.
Eur J Ophthalmol ; 34(2): 487-496, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-37461836

RESUMEN

PURPOSE: To analyze anatomic and functional response to intravitreal brolucizumab in age-related macular degeneration recalcitrant to previous intravitreal anti-VEGF therapies. METHODS: In this monocentric, one arm, retrospective study, eyes affected by neovascular age-related macular degeneration (nAMD) resistant to other intravitreally injected anti-vascular endothelial growth factor inhibitors were switched to intravitreal brolucizumab. All patients underwent ophthalmological examinations at baseline and in regular follow-up intervals. Best registered visual acuity (BRVA), Goldmann tonometry, intraocular pressure (IOP), central retinal thickness (CRT) and pigment epithelial detachment (PED) characteristics were analyzed at initiation of anti-VEGF treatment, at treatment switch, and at the end of brolucizumab loading phase. RESULTS: The study included 20 eyes of 18 consecutively treated patients (age: 77 ± 6 years). All eyes had macular neovascularization with PED. Previous treatments included intravitreal aflibercept, bevacizumab, and ranibizumab and had not resulted in a significant improvement in BRVA (0.5 ± 0.5 logMAR vs 0.5 ± 0.6 logMAR) or mean CRT (320 ± 60 µm vs 313 ± 83 µm) up to treatment switch to brolucizumab. At the end of the brolucizumab loading phase, there was significant improvement for both BRVA (0.3 ± 0.2 logMAR, P < 0.05) and CRT (264 ± 55 µm, P < 0.05). Under previous anti-VEGF therapy, there was a significant increase/deterioration in both PED area (2.68 mm2 to 5.18 mm2, P < 0.05) and PED volume (0.39 mm3 to 1.07 mm3, P < 0.05); however, both parameters improved after switching to brolucizumab (3.81 mm2 and 0.37 mm3, P < 0.05). CONCLUSION: Our results suggest a favourable anatomical and visual response after treatment switch to brolucizumab in patients with nAMD refractory to previous anti-VEGF agents.


Asunto(s)
Anticuerpos Monoclonales Humanizados , Degeneración Macular , Desprendimiento de Retina , Degeneración Macular Húmeda , Humanos , Anciano , Anciano de 80 o más Años , Inhibidores de la Angiogénesis/uso terapéutico , Estudios Retrospectivos , Ranibizumab/uso terapéutico , Receptores de Factores de Crecimiento Endotelial Vascular/uso terapéutico , Degeneración Macular/complicaciones , Degeneración Macular/diagnóstico , Degeneración Macular/tratamiento farmacológico , Desprendimiento de Retina/diagnóstico , Desprendimiento de Retina/tratamiento farmacológico , Desprendimiento de Retina/etiología , Inyecciones Intravítreas , Degeneración Macular Húmeda/complicaciones , Degeneración Macular Húmeda/diagnóstico , Degeneración Macular Húmeda/tratamiento farmacológico , Proteínas Recombinantes de Fusión/uso terapéutico
6.
Case Rep Ophthalmol ; 14(1): 104-110, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36968808

RESUMEN

We report a rare case of recurrent isolated internal ophthalmoplegia attributed to oculomotor nerve (CN III) compression by the posterior cerebral artery (PCA). A 30-year-old female patient presented with recurrent right-sided headaches, right periorbital pain, and slight anisocoria. Slit-lamp examination revealed normal anterior and posterior segments except for vermiform movements of the right pupil with a temporal hyporeactive flat area. Tonic pupils were ruled out with pilocarpine 0.1% testing. Suspecting an internal ophthalmoplegia, magnetic resonance imaging was ordered which demonstrated the right CN III indented by the PCA, fulfilling the criteria of a neurovascular conflict. The evaluation of unilateral mydriasis from internal ophthalmoplegia should prompt neuroimaging with exclusion of aneurysmal or compressive lesions. CN III palsy can rarely be caused by vascular anatomical variants because of the proximity of the posterior intracranial circulation and CN III. Newer, more precise imaging techniques will better help characterize neurovascular conflicts presenting as cranial nerve palsies.

7.
Eur J Ophthalmol ; : 11206721221124688, 2022 Sep 04.
Artículo en Inglés | MEDLINE | ID: mdl-36062617

RESUMEN

PURPOSE: We report visual and anatomical outcomes of chronic postoperative macular edema treated with a fluocinolone acetonide intravitreal implant. METHOD: Retrospective study of chronic, post-surgical CME treated with a fluocinolone acetonide intravitreal implant. Best registered visual acuity (BRVA), central retinal thickness (CRT), and Goldmann tonometry intraocular pressure (IOP) were assessed over 24 months. The need for IOP lowering treatment, top-up therapy during follow-up, and complications were also assessed. RESULTS: We analyzed 16 consecutive eyes of 16 patients with chronic, post-surgical CME treated with fluocinolone acetonide intravitreal implant. Surgical indications included cataract surgery, vitrectomy plus membrane peeling and combined phaco-vitrectomy. Baseline mean BRVA of 0.8 ± 0.65 logMAR improved to 0.60 ± 0.4 logMAR (p = 0.02) at 12 months and to 0.7 ± 0.5 logMAR (p = 0.32) at 24 months. At month 12, BRVA improved in 11 eyes, stabilized in 4 eyes, and decreased in 1 eye. At month 24, VA remained improved in 5 eyes, remained stabilized in 5 eyes, and decreased in 1 eye. Mean CRT decreased from 524 ± 132 µm at baseline to 389 µm at month 3, 347 µm at month 6, 355 ± 106 µm (p = 0.0003) at month 12, and 313 ± 83 µm (p = 0.0001) at month 24. At 12 months, CRT improved in 13 eyes and remained unchanged in 2 eyes. At 24 months, CRT improved further in 8 eyes, and stabilized in 3 eyes. Increased IOP (≥21 mmHg) was observed only in 4 eyes, all successfully managed with topical medication. No further side effects were observed in any patient. CONCLUSION: Visual and anatomic improvements were achieved by a single fluocinolone acetonide implant with few side effects up to 24 months in CME eyes with a long and heavy prior treatment history.

8.
Curr Opin Ophthalmol ; 22(1): 58-63, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21088581

RESUMEN

PURPOSE OF REVIEW: In this era of topical anesthesia for ocular surgery, anesthetic ocular blocks are still important when profound anesthesia and akinesia are required. Although injection ocular blocks, retrobulbar and peribulbar anesthesia, have been supplanted for most ocular surgery in many centers by sub-Tenon's irrigation block because of its superior safety profile, still worldwide, injection blocks remain popular. RECENT FINDINGS: We present here the results of a survey of the literature published over the last 5 years to assess current international preferences for ocular anesthesia injection blocks. We discuss the reasons why sub-Tenon's anesthesia is not more universally popular and advocate for its greater acceptance because of safety. Specific narrow indications for performing injection ocular blocks are presented. Also, guidelines for performing retrobulbar anesthesia which reduce the risk of serious ocular complications are provided as well as our rationale for preferring retrobulbar to peribulbar anesthesia. SUMMARY: Sub-Tenon's block should be performed in the operating theatre in preference to retrobulbar or peribulbar anesthesia except for limited indications. When injection ocular block is deemed necessary, we feel that retrobulbar anesthesia with the technique described may be safer than peribulbar anesthesia.


Asunto(s)
Anestesia/métodos , Anestésicos Locales/administración & dosificación , Bloqueo Nervioso/métodos , Humanos , Inyecciones Intraoculares , Órbita , Guías de Práctica Clínica como Asunto
9.
Surv Ophthalmol ; 66(4): 585-593, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33359545

RESUMEN

Pneumatic retinopexy (PR) has been widely advocated for treatment of selected rhegmatogenous retinal detachments: those with small, anterior, superior, retinal breaks and little or no proliferative vitreoretinopathy. It has been suggested that PR is underused and is advantageous because it is an outpatient clinic or office procedure, short in duration, nonincisional, and cost saving - with reduced perioperative morbidity, faster postoperative recovery, better and faster visual recovery, a low rate of complications and a high rate of overall success compared with scleral buckling or pars plana vitrectomy. We reevaluated these advantages to substantiate the effectiveness and efficiency of PR and critically define its role in the treatment of rhegmatogenous retinal detachment. We found that PR has a much higher rate of subsequent reoperation and proliferative vitreoretinopathy than scleral buckling or pars plana vitrectomy for simple, good prognosis rhegmatogenous retinal detachments. PR often involves multiple procedures that largely negates its potential cost savings and subjects the patient to prolonged stress and disability. Scleral buckling rather than PR is ideally suited for simple, good prognosis rhegmatogenous retinal detachments for surgeons who feel comfortable with the technique; alternatively, pars plana vitrectomy is indicated.


Asunto(s)
Desprendimiento de Retina , Curvatura de la Esclerótica , Humanos , Desprendimiento de Retina/etiología , Desprendimiento de Retina/cirugía , Estudios Retrospectivos , Curvatura de la Esclerótica/efectos adversos , Curvatura de la Esclerótica/métodos , Resultado del Tratamiento , Agudeza Visual , Vitrectomía/métodos
10.
Surv Ophthalmol ; 66(3): 441-460, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-32918934

RESUMEN

Radiation maculopathy and radiation-induced macular edema are common, sight-threatening complications after radiotherapy, especially that used for uveal melanoma. While many treatment and preventive strategies have been proposed, management of these conditions is still challenging. Initially, treatments were based on the use of retinal laser, but the outcomes were poor. Subsequently, management has shifted toward injection of intravitreal antivascular endothelial growth factor or corticosteroids. We reviewed current clinical evidence, which mostly relies on small sample-sized and retrospective studies, for the management of radiation maculopathy and, in particular, radiation-induced macular edema. At present, the first-line approach is usually intravitreal antivascular endothelial growth factor. Intravitreal dexamethasone implantation may be an option for those with suboptimal response or contraindications to antivascular endothelial growth factor agents. Possible preventive treatments that require future study are intravitreal bevacizumab and ranibizumab, peripheral laser photocoagulation, and subtenon triamcinolone acetonide.


Asunto(s)
Edema Macular , Inhibidores de la Angiogénesis/uso terapéutico , Bevacizumab/uso terapéutico , Glucocorticoides/uso terapéutico , Humanos , Inyecciones Intravítreas , Edema Macular/diagnóstico , Edema Macular/etiología , Edema Macular/terapia , Estudios Retrospectivos , Triamcinolona Acetonida/uso terapéutico , Factor A de Crecimiento Endotelial Vascular , Agudeza Visual
11.
Curr Opin Ophthalmol ; 21(1): 50-4, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19829113

RESUMEN

PURPOSE OF REVIEW: Posterior-assisted levitation (PAL) is a surgical maneuver for dealing with rupture of the posterior capsule or zonular dehiscence with threatened or actual subluxation of the nucleus or entire lens into the vitreous during phacoemulsification. PAL is often unknown or overlooked, especially by young or inexperienced surgeons. RECENT FINDINGS: The advantages of PAL are, first, that it often enables completion of phacoemulsification and intraocular lens placement without conversion to an open eye with nuclear expression and second, it prevents luxation of nucleus, nuclear fragments, or the lens into the vitreous avoiding the necessity for trans pars plana vitrectomy (TPPV)-lensectomy. PAL has recently been criticized by vitreoretinal surgeons as dangerous and to be avoided. However, there is no large series or controlled study showing that the PAL maneuver is associated with an excessive complication rate as compared to cases of nuclear or lens subluxation in the vitreous managed by TPPV-lensectomy with or without previous PAL. SUMMARY: PAL is a simple technique that can be extremely helpful. In cases in which the PAL maneuver is unsuccessful and in cases with complete luxation of nucleus or lens into the vitreous, the patient should be referred for TPPV-lensectomy.


Asunto(s)
Cápsula del Cristalino/lesiones , Subluxación del Cristalino/cirugía , Facoemulsificación/métodos , Humanos , Implantación de Lentes Intraoculares , Subluxación del Cristalino/etiología , Rotura
13.
Surv Ophthalmol ; 54(3): 412-6, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19422968

RESUMEN

The medical-legal problem of occult traumatic optic neuropathy diagnosed in patients who actually have feigned visual loss (malingering) is reviewed along with guidelines for suspecting and differentiating feigned visual loss from true traumatic optic neuropathy. We explain why we feel the term occult optic neuropathy is inappropriate and misleading, and the medical-legal consequences of this misdiagnosis are discussed.


Asunto(s)
Ceguera/diagnóstico , Errores Diagnósticos/legislación & jurisprudencia , Simulación de Enfermedad/diagnóstico , Traumatismos del Nervio Óptico/diagnóstico , Guías de Práctica Clínica como Asunto , Humanos , Mala Praxis/legislación & jurisprudencia
15.
Surv Ophthalmol ; 64(4): 443-451, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30707925

RESUMEN

The retinal ganglion cells infarcted in central retinal artery occlusion (CRAO) are the somata of the optic nerve axons, part of the central nervous system. Consequently, CRAO with inner retinal infarction is a small vessel stroke, usually with the devastating consequence of severe visual loss in the affected eye. At present, there is no generally accepted, evidence-based therapy of nonarteritic CRAO in contrast to ischemic cerebral stroke that has well-accepted treatment protocols. Widely divergent and controversial therapeutic options for CRAO reflect the desperation of treating physicians and disparate conflicting studies. We examine reasons why treatment of nonarteritic CRAO remains problematic and then suggest a provisional new approach to treatment based on updated understanding of CRAO pathophysiology and analysis of current therapeutic options and their rationales.


Asunto(s)
Oclusión de la Arteria Retiniana/terapia , Células Ganglionares de la Retina/fisiología , Anticoagulantes/uso terapéutico , Antihipertensivos/uso terapéutico , Fibrinolíticos/uso terapéutico , Humanos , Presión Intraocular/fisiología , Masaje/métodos , Oclusión de la Arteria Retiniana/fisiopatología
16.
Surv Ophthalmol ; 63(5): 694-699, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29649485

RESUMEN

Occult globe rupture is a traumatic dehiscence of the sclera at or posterior to the rectus muscle insertions without a visible eye wall defect on slit lamp examination. Occult scleral ruptures are important because they can be difficult to diagnose, but normally require preoperative protection against external pressure to reduce risk of herniation of ocular contents through the rupture and then urgent surgical repair to restore eye wall structural integrity and achieve optimum prognosis. A deeper-than-normal anterior chamber with posteriorly retracted plateau iris seen immediately after acute ocular trauma is virtually pathognomonic of posterior globe dehiscence. Three additional less specific signs are helpful: extensive chemosis that is often hemorrhagic, relative hypotony, and vitreous hemorrhage. Although the diagnosis is normally clinical, made by history of direct severe ocular trauma and careful anterior-segment slit lamp examination, computed tomography and ultrasonography can be helpful when thorough slit lamp examination is not possible. Strong suspicion of occult rupture should engender surgical exploration. Vitreous hemorrhage, vitreous or retinal incarceration, and retinal tears or detachment may necessitate subsequent pars plana vitrectomy or other vitreoretinal surgery. When pars plana vitrectomy is indicated, special precautions are suggested if watertight closure of the globe rupture has not been possible.


Asunto(s)
Lesiones Oculares/diagnóstico , Segmento Posterior del Ojo/lesiones , Esclerótica/lesiones , Técnicas de Diagnóstico Oftalmológico , Lesiones Oculares/fisiopatología , Lesiones Oculares/cirugía , Humanos , Hipotensión Ocular/diagnóstico , Rotura/diagnóstico , Rotura/cirugía , Esclerótica/cirugía , Tomografía Computarizada por Rayos X , Ultrasonografía/métodos , Vitrectomía/métodos , Hemorragia Vítrea/diagnóstico
18.
Surv Ophthalmol ; 66(6): 1076-1078, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33905797
20.
Surv Ophthalmol ; 61(2): 156-63, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26216341

RESUMEN

Accurate characterization of a retinal detachment as traumatic is often difficult, but is important because it may instigate a careful search for occult coexistent traumatic pathology, affect the prognosis and the treatment of both eyes, influence insurance coverage benefits and medical-legal determinations, and is essential for epidemiologic studies. We review the epidemiology and pathophysiology of traumatic retinal detachment, common obstacles to correct diagnosis, diagnostic guidelines, and outline categories of traumatic causal relationships. Because there is no generally accepted definition of traumatic retinal detachment, we offer a practical one. Categorization as traumatic should be based on the particular history and physical examination rather than epidemiologic criteria.


Asunto(s)
Lesiones Oculares/diagnóstico , Retina/lesiones , Desprendimiento de Retina/diagnóstico , Perforaciones de la Retina/diagnóstico , Lesiones Oculares/etiología , Lesiones Oculares/fisiopatología , Humanos , Desprendimiento de Retina/etiología , Desprendimiento de Retina/fisiopatología , Perforaciones de la Retina/etiología , Perforaciones de la Retina/fisiopatología
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