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1.
Doc Ophthalmol ; 136(2): 97-111, 2018 04.
Article in English | MEDLINE | ID: mdl-29536324

ABSTRACT

PURPOSE: Pericentral visual field changes and disruption of the ellipsoid layer on spectral domain optical coherence tomography (SD-OCT) are the main features of antimalarial retinal toxicity. C-Scan OCT or "en face" enables a topographic frontal view of the changes observed within the different retinal layers in particular the ellipsoid layer. The aim of this prospective study was to compare multifocal ERG (mfERG) responses with the results of C-Scan OCT ("en face" OCT) in patients with abnormal visual field and to analyze relationships between the structural and functional abnormalities. METHODS: In 354 consecutive patients screened for antimalarial toxicity between January 1, 2014 and December 31, 2016, central visual field, mfERG recording, C-Scan OCT and short-wavelength fundus autofluorescent imaging were performed. RESULTS: Among the 17/354 patients with abnormal central visual field results, all presented with abnormalities on the mfERG at least in one eye. In 16/33 eyes, there was a good concordance between focal loss of the mfERG response and the disruption of the ellipsoid layer on C-Scan OCT. In one eye with characteristic changes in the ellipsoid layer on the C-Scan OCT, the mfERG was normal, whereas in three eyes the mfERG was abnormal in eyes with a normal C-Scan OCT. CONCLUSIONS: The contribution of the C-Scan OCT changes remains difficult to establish as there is no strict concordance with the local ERG responses. Although C-Scan OCT technology provides a new approach in analyzing focal abnormalities in the photoreceptor-retinal pigment epithelium interface, the sensitivity of this method compared with mfERG and other tests (central visual field, B-Scan OCT) needs to be evaluated. This study is still ongoing on a larger cohort.


Subject(s)
Antimalarials/toxicity , Electroretinography/methods , Hydroxychloroquine/toxicity , Retina/drug effects , Retinal Diseases/diagnosis , Tomography, Optical Coherence/methods , Adult , Aged , Female , Fundus Oculi , Humans , Male , Middle Aged , Prospective Studies , Retina/pathology , Retinal Diseases/chemically induced , Retinal Pigment Epithelium/drug effects , Visual Fields/drug effects
2.
Graefes Arch Clin Exp Ophthalmol ; 254(11): 2175-2181, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27207466

ABSTRACT

BACKGROUND: This present retrospective case control study was designed to evaluate circadian disturbance in patients with chronic idiopathic central serous chorioretinopathy (ICSC). METHODS: Between January 1st, 2012, and November 30th, 2014, 29 consecutive patients with chronic ICSC examined in a referral setting were compared with a gender-matched and age-matched control group of 29 patients. A history of pharmacologic medication (including corticosteroid treatment), sleep disturbance, irregular working hours, cardiovascular risk factors, and depressive anxiety disorders was noted. RESULTS: The median age of the patients was 52, and in the control subjects it was 50. The male-female ratio for both groups was 4.8:1. Patients with chronic ISCS were more likely to be exposed to irregular working hours (p < 0.01, OR 9.3 [2.29-37.6]) and to present with overweight than the control subjects (p = 0.016). No significant differences were found for sleeping disturbances, pharmacological medication, cardiovascular risk factors, or depressive anxiety disorders. CONCLUSIONS: In this preliminary study, the exposition of irregular working hours as a risk factor for chronic ICSC was identified, which had not been previously reported. If further studies confirm these findings, then employment with regular working hours could be recommended for chronic ICSC patients.


Subject(s)
Central Serous Chorioretinopathy/physiopathology , Chronobiology Disorders/complications , Visual Acuity , Adult , Aged , Central Serous Chorioretinopathy/epidemiology , Central Serous Chorioretinopathy/etiology , Chronobiology Disorders/physiopathology , Female , Follow-Up Studies , France/epidemiology , Humans , Incidence , Male , Middle Aged , Retrospective Studies , Risk Factors , Young Adult
3.
Acta Cytol ; 60(1): 65-73, 2016.
Article in English | MEDLINE | ID: mdl-26986556

ABSTRACT

OBJECTIVE: To describe findings in vitreous fluid samples in routine cytology practice. STUDY DESIGN: The pathology archives from 1988 to 2008 at our institution were searched for vitreous samples. The slides were reviewed and clinical and follow-up information was obtained. RESULTS: One hundred and eighty-two vitreous fluid samples from 166 patients were analyzed. Most of the samples had been collected for vitreous hemorrhage (75 cases). The second reason for vitreous sample cytological evaluation was an intraocular inflammatory process (55 cases). A specific cause of inflammation was found by combining clinical, microbiological and cytopathological findings in 19 cases, i.e. infection in 7, sarcoidosis in 3, retinal necrosis in 3, lens-induced endophthalmitis in 2, uveitis associated with systemic disease in 2, retrobulbar neuritis in 1 and sympathetic ophthalmia in 1. Among the 19 samples from 16 patients collected to rule out malignancy, 8 had a confirmed intraocular malignancy. Malignant cells were observed in 5 cases (3 lymphomas, 1 melanoma and 1 carcinoma). Undiagnosed malignancies included 2 lymphomas and 1 choroidal melanoma. Other samples were collected during surgery for retinal detachment and cataracts. CONCLUSIONS: In routine practice, cytology of the vitreous fluid is performed in many and varied situations that are most often nonneoplastic. In nonneoplastic cases, cytology is a useful adjunct to vitrectomy, in spite of its limitations.


Subject(s)
Cytodiagnosis/methods , Diagnostic Tests, Routine/methods , Vitreous Body/pathology , Aged , Aged, 80 and over , Endophthalmitis/diagnosis , Eye Diseases/diagnosis , Eye Neoplasms/diagnosis , Female , Humans , Lymphoma/diagnosis , Male , Melanoma/diagnosis , Middle Aged , Reproducibility of Results , Sarcoidosis/diagnosis , Sensitivity and Specificity , Uveitis/diagnosis , Vitrectomy
4.
J Neurosurg ; 121(1): 165-9, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24702324

ABSTRACT

UNLABELLED: OBJECT.: The authors' objective was to evaluate the predictive value of preoperative axonal loss for peripheral visual field recovery after surgery for optic chiasm compression. METHODS: Consecutive patients with optic chiasm compression in the period from October 2010 through August 2012 were retrospectively studied. Time-domain optical coherence tomography (OCT) had been performed before surgery. Kinetic automated perimetry had been performed before and after surgical decompression. The area of the peripheral isopter (square degrees [deg(2)]) was assessed. Postoperative improvement was defined as an increase of 25 deg(2) or more. RESULTS: Sixty-eight eyes in 34 patients were included in the analysis. In 44 eyes the visual field improved after surgery, and in 24 eyes it was unchanged or worse. Nasal retinal nerve fiber layer (RNFL) thickness was a good prognostic factor for peripheral visual field recovery (OR 1.56 per 15 µm, p = 0.041). CONCLUSIONS: Peripheral visual field recovery after surgery for optic chiasm compression is predicted by nasal RNFL thickness, which is in accordance with the retinotopy of retinal ganglion cells, as nasal axons decussate at the optic chiasm.


Subject(s)
Decompression, Surgical , Optic Chiasm/surgery , Optic Nerve Diseases/surgery , Retinal Neurons/physiology , Visual Fields/physiology , Adult , Aged , Female , Humans , Male , Middle Aged , Prognosis , Retrospective Studies , Treatment Outcome , Visual Acuity/physiology
5.
Graefes Arch Clin Exp Ophthalmol ; 252(2): 339-45, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24178807

ABSTRACT

BACKGROUND: In non-arteritic anterior ischemic optic neuropathy (NA-AION), no treatments have demonstrated to be effective in recovering visual loss in randomized clinical trials. Oral steroids have been evaluated, and small series of intravitreal triamcinolone acetonide (IVTA) injection in NA-AION have been reported. The purpose of our study was to report the visual outcome and morphological changes in response to a single IVTA injection as a treatment for patients with NA-AION. PATIENTS AND METHODS: The charts of 36 patients with visual symptoms and optic disc swelling caused by NA-AION were evaluated. Twenty-one patients had received 4 mg IVTA and were compared with 15 non-treated patients. Visual acuity (VA), retinal nerve fiber layer thickness and static visual field were evaluated after 6 months. RESULTS: VA improvement at 6 months is statistically better in the treated group than in the non-treated group (p = 0.0035). In the treated group, there was a significant inverse correlation between the delay of the injection and the visual acuity achieved at 6 months (p < 0.0083**, r = -0.56). A significant improvement of the visual field was noted in the injected group when compared with the non-treated group at 6 months (p < 0.0028). DISCUSSION: In this retrospective study, patients receiving IVTA in the acute phase of NA-AION have better improvement of VA and visual field during the follow-up period of 6 months. However, only a large randomized controlled trial may enable to evaluate the benefits of IVTA Injections on visual outcome in NA-AION.


Subject(s)
Glucocorticoids/therapeutic use , Optic Neuropathy, Ischemic/drug therapy , Triamcinolone Acetonide/therapeutic use , Aged , Aged, 80 and over , Arteritis/drug therapy , Arteritis/physiopathology , Female , Humans , Intraocular Pressure/physiology , Intravitreal Injections , Male , Middle Aged , Nerve Fibers/pathology , Optic Neuropathy, Ischemic/physiopathology , Retinal Ganglion Cells/pathology , Retrospective Studies , Treatment Outcome , Visual Acuity/physiology , Visual Fields/physiology
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