3-month post-procedural evaluation of a combined intense pulsed light and photo-biomodulation system in the treatment of meibomian gland dysfunction.

PURPOSE: Meibomian gland dysfunction (MGD) is the leading cause of dry eye syndrome. It is a frequent and underdiagnosed condition with a significant socioeconomic impact. We propose here the evaluation of a platform combining intense pulsed light and photo-biomodulation in the treatment of Meibomian gland dysfunction. METHODS: We conducted a retrospective study at Brest University Hospital analyzing a cohort of 74 eyes (37 patients) at 1 month and 3 months after a protocol of 3 Eye-Light® (Espansione Group, Italy) sessions 14 days apart between January 2019 and April 2020. The primary outcome was the change in OSDI quality of life score. Secondary outcomes were the SPEED questionnaire score; tear break-up time (BUT), Oxford score, non-invasive break-up time (NIBUT), lipid layer thickness, lacrimal meniscus height and Meibomian gland atrophy rate. Tolerance of the treatment was also evaluated. RESULTS: We found a significant improvement in OSDI scores at 1 month (-17.32; 95% CI (-25.84; -8.79), P<0.0001) and 3 months (-16.95; 95% CI (-25.26; -8.64), P<0.0001). The SPEED score, BUT, Oxford score, Meibomian gland atrophy and NIBUT were also statistically significantly improved. Tolerance to treatment was very good despite two cases of herpetic keratitis, which resolved on treatment. CONCLUSION: Treatment with the Eye-Light® in three sessions every two weeks significantly reduced symptoms and ocular surface damage in patients with MGD. This data suggests that the use of Eye-Light® may represent a good option for patients with MGD.

Impact of virtual reality headset use on eye blinking and lipid layer thickness.

PURPOSE: Blinking plays an important role in protecting the eyes, and the use of computers has been associated with a reduction in the blink rate. The goal of this study was to evaluate the effect of a virtual reality headset on blinking and lipid layer thickness and to compare these data to those associated with a conventional desktop monitor. METHODS: Two experiments were performed to compare the effect of 20minutes of use of a virtual reality headset (FOVE) and 20minutes of use of a desktop monitor on the frequency and length of blinks (experiment 1, 15 participants) and on the thickness of the lipid layer as measured by Lipiview (experiment 2, 12 participants). RESULTS: In the first experiment, the blink rate [F(1.83)=4.3, P=0.04, ß=0.36] and duration [F(1.83)=13, P=0.001, ß=0.35] increased with time under both conditions, but no statistical difference was found between the two conditions (headset vs. desktop monitor) either for blink rate [rmANOVA F(1.11)=0.01, P=0.92; headset: 15.1 blinks, 95% CI: 12.6 to 17.6 blinks; desktop: 14.6 blinks, 95% CI: 13.6 to 15.7 blinks] or for blink duration [rmANOVA F(1.11)=4.534, P=0.06; headset: 205.75ms, 95% CI: 200.9 to 210.6ms; desktop: 202.82ms, 95% CI: 198.2 to 207.5ms]. However, strong individual variations were observed. Evaluation of simulator sickness and visual fatigue by questionnaire showed no significant differences between the two conditions (SSQ simulator sickness questionnaire: V=46, P=0.62; VFQ visual fatigue questionnaire: V=15.5, P=0.13). In the second experiment, the lipid layer thickness increased significantly after use of the VR headset [F(1.18)=11.03, P=0.004, headset: 76.2nm, desktop: 58.8nm]. CONCLUSION: In terms of recommendations, the effect of virtual reality headsets on blink duration and frequency during a moderate exposure (20minutes) is comparable to that of a conventional desktop monitor. However, the strong individual variations observed, the lack of reliable tests to evaluate this individual sensitivity, and the significant increase in lipid layer thickness in experiment 2 suggest the value of a more detailed investigation, in particular with consideration of a longer exposure time and other tear film parameters.

Association of sensitive skin with sensitive corneas and sensitive eyelids.

BACKGROUND: Sensitive scalp or irritable bowel syndrome has been previously shown to be associated with sensitive skin. We wondered whether sensitive eyelids and sensitive eyes could also be associated with sensitive skin. METHODS: A cross-sectional epidemiological study was carried out on a representative sample of French people, according to the quota method, using a questionnaire. RESULTS: A total of 2048 subjects were included in the present study. Notably, 52.2% declared sensitive eyes, which was more frequent in women than in men. The subjects who reported sensitive eyes were more numerous according to the severity of skin sensitivity, the severity of sleep disorders and the presence of bright eyes. More than half of the subjects with sensitive eyes thought that they were sensitive to sun exposure, dust, computer or touch pads or dry air. The presence of sensitive eyelids was reported by 18.65% (more frequent in women) and was associated with sensitive skin and sensitive eyes, sun exposure and exposure to dust. CONCLUSION: This study is the first to investigate sensitive eyelids or sensitive eyes. Sensitive eyelids can be considered a localization of sensitive skin. The concept of sensitive eyes is not commonly used by ophthalmologists and remains to be more precisely defined.

Cascaded multi-scale convolutional encoder-decoders for breast mass segmentation in high-resolution mammograms.

This paper addresses breast mass segmentation from high-resolution mammograms. To cope with strong class imbalance, huge diversity of size, shape, texture and contour as well as limited receptive field, mass segmentation is achieved through a multi-scale cascade of deep convolutional encoder-decoders without any pre-detection scheme. Multi-scale information is integrated using auto-context to make long-range spatial context arising from lower scale impact training at higher resolution. The pipeline is trained end-to-end to benefit from simultaneous segmentation refinement performed at each level. It incorporates transfer learning and fine tuning from DDSM-CBIS to INbreast datasets to further improve mass delineations. The comprehensive evaluation provided for high-resolution INbreast images highlights promising model generalizability against standard encoder-decoder strategies.

Healing of resistant corneal neurotrophic ulcers using a matrix regenerating agent.

PURPOSE: To assess the success rate of a matrix regenerating agent (RGTA) in the treatment of chronic corneal ulcers resistant to conventional treatments. METHODS: Uncontrolled prospective observational study in patients with corneal neurotrophic ulcer (Stage 2 or 3 of the Mackie classification), unresponsive to standard medical or surgical treatments and managed with RGTA as an adjunctive treatment. Corneal ulcers were evaluated using slit-lamp examination and optical coherence tomography after 2 weeks, 1 month, 2 months and 3 months. Success was defined as complete corneal healing. RESULTS: RGTA was administered to 20 patients (20 eyes) with chronic corneal ulcers of various causes, including keratoplasty (7 eyes, 35.0%), herpetic keratitis (5 eyes, 25.0%) and intracorneal ring (3 eyes, 15.0%). Total corneal healing was observed in 13/20 patients (65.0%) within 1 to 3 months. RGTA was discontinued due to partial healing/ulcer stagnation in 6 patients (30.0%), and aggravation of the ulcer in 1 patient (5.0%). Relapses were reported in 4 patients (20.0%) several months after cessation of RGTA treatment. No adverse reactions were noted. CONCLUSIONS: In the event of failure of conventional treatments, RGTA may be an alternative medical treatment for patients with chronic corneal ulcers, avoiding the need to resort to surgical treatment.

[Assessment of a 3D digital orthoptic test platform]. / Évaluation d'une plateforme d'orthoptie numérique 3D.

PURPOSE: To compare standard orthoptic tests with a novel digital 3D orthoptic platform, 3DeltaEasy(©) from Orthoptica(®). MATERIALS AND METHODS: This study tests the 3D digital orthoptics platform, 3DeltaEasy(©) from Orthoptica(®) and compares it to the corresponding standard orthoptic tests. This platform consists of a computer equipped with dedicated software, a video projector and 3D liquid crystal glasses. Three tests were compared: Wirt test, measurement of horizontal and vertical phorias, and the horizontal fusional amplitude in convergence and divergence. A total of 102 subjects, 53 males (52 %) and 49 females (48 %), aged between 9 years and 72 years (mean age 33±16.4 years) were examined at the ophthalmologic department of the Brest Hospital (France) and included in this observational cross-sectional study. Subjects recruited in this study were patients requiring orthoptic screening or therapy. Patients without their optimal visual corrections were excluded. All patients underwent both ophthalmological and orthoptic examination including Wirt fly stereotest with polarizing spectacles, cover tests to evaluate and measure the horizontal and vertical deviation of the lines of sight, horizontal vergence ranges using prism bar and their equivalent tests implemented in the digital 3D orthoptic tests 3DeltaEasy(©) from Orthoptica(®). RESULTS: All data were processed using MedCalc Statistical Software version 14.12.0 (MedCalc Software bvba, Ostend, Belgium). The main result of this study is that 3DeltaEasy(©) and the classical Wirt test are correlated (Spearman's coefficient of rank correlation: ρ=0.74; P<0.0001), cover tests are equivalent for intermediate and far vision (paired t-test; P=0.46 and P=0.51), and horizontal and vertical vergence range are comparable for distance vision (paired t-test; P=0.34 and P=0.94). CONCLUSION: New digital 3D tools could easily substitute for some orthoptic tests with better ergonomics. Eventually, by increasing the number of tests performed, it could substitute for nearly all tests.

[Endoscopy-guided 20-G vitrectomy in severe endophthalmitis: Report of 18 cases and literature review]. / Vitrectomie endoscopique 20Ga dans les endophtalmies sévères : série de 18 cas et revue de la littérature.

OBJECTIVE: To report the anatomical and functional outcomes after endoscopy-guided vitrectomy in a series of cases of severe endophthalmitis. Also to identify and compare the outcomes of two different modes of clinical presentation. PATIENTS AND METHODS: Retrospective case study, single center; all patients who underwent endoscopic 20Ga vitrectomy (Endo optiks E4 system) for severe endophthalmitis were included. For each case, data were recorded for: etiology, surgical indication, preoperative and postoperative visual acuity, comorbidity factors and postoperative complications, and whether any additional surgery was performed. Two groups were distinguished according to their initial mode of presentation; results were then compared in terms of complications and visual prognosis to those found in the literature. RESULTS: Eighteen patients were included, with mean age 62±19years. Severe endophthalmitis was initially obvious for 8 cases (group 1). For 10 cases, disease progression had been considered unfavorable despite adequate medical treatment (group 2). There was no statistically significant difference between the two groups (P=0.55). Endophthalmitis occurred: after intravitreal injections (4 cases), after intraocular foreign body (n=2), after cataract surgery (n=5), following a trabeculectomy (n=2), after epiretinal membrane peeling (n=3), 1 case caused by a corneal infection and 1 case of endogenous leptospirosis. Mean follow-up was 13.7months. The surgical technique was a complete 20Ga vitrectomy under endoscopic visual control. The mean operative time was 70±27minutes. The causative organism was identified in 72% of cases in vitreous humor samples, among which 77% were gram-positive organisms. The infection was controlled in 89% of cases, and these patients have recovered useful visual acuity. CONCLUSION: The value of endoscopic visualization in ophthalmology has been proven for 30 S. aureus years, but its miniaturization enhances the current enthusiasm for the use of this instrumentation. When visualization is compromised, endoscopic guided vitrectomy is very useful and may assist the surgeon in the management of these difficult cases. Our anatomical and functional outcomes are encouraging, but we must keep in mind the poor long-term prognosis of severe endophthalmitis.

[Quality of vision studied by comparative measurement of light scattering]. / Qualité de vision étudiée par mesure comparative de la diffusion de la lumière.

PURPOSE: To assess quality of vision by measuring ocular light scattering with two platforms and comparing them to traditional tests, in healthy subjects and cataract patients. PATIENTS AND METHODS: One hundred and sixty-eight eyes divided in two groups were examined by the same clinician in a prospective study (group 1, healthy controls, with a mean age of 31.22 [± 6.76]; and group 2, patients presenting with cataract, with a mean age of 60.36 [± 10.27]). Patients with ocular surface disease were excluded from this study. Each group responded to the VF-14 questionnaire, underwent an examination with lens opacities assessed by LOCS III and a measurement of ocular light scattering with two platforms: the OQAS (Visiometrics(©)) and the C-Quant (Oculus(©)). We analyzed correlations between indices of light scattering with the two platforms (respectively OSI and log(s)) and traditional quality of vision tests (VF-14 questionnaire and LOCS III). RESULTS: Strong correlations were found between the OSI and LOCS III. Moderate correlations were found between the OSI and the VF-14 questionnaire, as well as between log(s), VF-14 questionnaire and LOCS III. CONCLUSION: Indices of light scattering seems to be valid tools to assess quality of vision, thus lending themselves to routine testing of visual function.

[Multifocal IOLs in the high myope, 6-year follow-up]. / Implants multifocaux chez le grand myope, résultats à 6ans.

INTRODUCTION: Currently, the use of multifocal IOL's remains controversial for patients with high myopia, especially because of the risk of retinal complications and poor quality of vision. Our goal was to evaluate this retinal risk and clarify the benefits obtained in this population in terms of visual acuity. PATIENTS AND METHODS: Twenty-nine highly myopic patients (52 eyes with over 6 diopters of myopia) aged 40-69 years with early cataract by LOCSIII were selected for multifocal lens implantation, based on a healthy endothelium and retina as well as better visual acuity corrected to at least 0.5 - J2. Thirteen of them (21 eyes) had been previously implanted with a phakic IOL. The AT Lisa IOL (Zeiss©) was chosen because of the low powers available and ease of exchange. Data collection was conducted prospectively, at each visit. The main study parameters were the development of retinal complications, occurrence of PCO, patient satisfaction rate and rate of spectacle independence. RESULTS: At the end of the 6-year follow-up, we found 2 rhegmatogenous retinal detachments (3.8%) occurring at approximately 20 months and favorably treated without IOL explantation. We also found one case of macular atrophy secondary to cystoid edema. Twenty-seven uncomplicated YAG posterior capsulotomies were performed for posterior capsule opacification. Ninety-eight percent of patients reached best corrected visual acuity of at least 0.5 and 38% of at least 0.8 without correction. Finally, 85% of patients achieved spectacle independence, and all would be willing to undergo the same procedure. DISCUSSION AND CONCLUSION: Multifocal IOL implantation in the high myope provided favorable results at 6 years, in carefully selected cases, providing optimal binocular visual comfort, including near vision. However, the fragility of the highly myopic retina mandates long-term follow-up. It would be beneficial to compare results of multifocal vs. monofocal IOL implantation in terms of visual performance and safety.

[Meibomian gland dysfunction: a comparative study of modern treatments]. / Évaluation des moyens modernes de prise en charge du dysfonctionnement meibomien.

PURPOSE: To evaluate a thermal pulsation treatment compared to a warming eyelid device for the management of meibomian gland dysfunction. METHODS: Thirty patients were randomized into two groups: the first had a treatment with MeiboPatch(®) on a daily basis for three months while the second had a single treatment with LipiFlow(®). The evaluation focused on a classical approach but also on a modern approach of the ocular surface (interferometry lipid layer LipiView(®)), analysis of the tear film by Oquas(®) (osmolarity by TearLab(®)) before treatment, then a month and three months later. RESULTS: Both treatments proved to be effective with almost three times more functional meibomian glands at 3 months in the LipiFlow group and almost twice more in the MeiboPatch group (P<0.05) but the LipiFlow allows a more rapid improvement at the first month of treatment. Functional scores and classic exploration of the ocular surface except the Schirmer test also undergo a significant improvement in both groups after three months of treatment. CONCLUSION: The combination of heat applied to the inner eyelid surface, together with simultaneous expression of the glands, during a single 12-minute treatment shows to be highly effective in treating cases of meibomian gland disease. Whilst results were excellent, and continued lid hygiene remains advised, the benefit of being able to simultaneous address potential compliance issues relating to ongoing treatment is significant. The convenience of a single 12-minute treatment versus an ongoing daily heating regime was shown to be highly desirable and a welcome relief in our patients' busy lifestyles.

Automatic correction of rotating ultrasound bio microscopy acquisitions for the segmentation of the eye anterior segment.

We have developed a rotating 3D probe prototype in order to acquire the anterior segment of the eye in three dimensions. The acquisition accuracy has to be sufficient to allow for the use of automatic segmentation of the provided data, and thus generate a 3D structure of the eye, for which it could be easier to obtain measurements than in 2D images. We have created an image post processing scheme in order to compensate for vibrations and eye movements during acquisition that are associated with increased noise. These tools have been applied to 92 volume datasets acquired on 21 patients in pre-operative conditions. Acquisition noise was reduced by 97% in specific conditions with respect to data acquired without correction.

[Neuro-ophthalmological assessments in the Ophthalmology Department at University Medical Center, Brest: retrospective study of 269 patients (January 2004-October 2009)]. / Bilans neuro-ophtalmologiques dans le service d'ophtalmologie du CHU de Brest : étude rétrospective sur 269 patients (janvier 2004-octobre 2009).

AIMS: To evaluate the neuro-ophthalmological assessments carried out in the ophthalmology department of the university medical center, Brest, identifying the population seen, the examinations performed, the pathologies treated and patient outcomes, so as to suggest solutions to improve quality of care. METHODOLOGY: Retrospective study over a period of more than five years, between January 1st, 2004 and October 31st, 2009. Data were collected from each patient's chart with the help of a standardized spreadsheet including epidemiological, clinical, paraclinical and treatment data. RESULTS: Analysis of the 269 charts reveals that optic neuropathies are the most frequently encountered etiologies. In addition to the standardized assessment currently used on the service, we suggest adding a specific neuro-ophthalmological clinical intake form so as to standardize and perfect the diagnostic approach. CONCLUSION: Optimization of quality of care in neuro-ophthalmology involves a multidisciplinary approach, requiring close collaboration between ophthalmologists, neurologists and radiologists. A careful, regular analysis of our practice patterns with respect to scientific advances should improve consistency and quality of care for our patients.

[Long-term results of posterior chamber phakic intraocular lens implantation for correction of high ametropia]. / Résultats à long terme de l'implantation phaque de chambre postérieure pour la correction des amétropies fortes.

PURPOSE: To assess efficacy, stability and safety of posterior chamber phakic intraocular lens implantation with STAAR Visian ICL for correction of high ametropia, with a mean follow-up of 5 years (3.5-10 years). PATIENTS AND METHODS: Ninety eyes of 53 highly ametropic patients (45 myopia, ten hyperopia and 35 with mixed astigmatism) were included in a retrospective single-surgeon study, using primarily the V4 ICL model (87 eyes). We studied pre- and postoperative refractive efficacy, endothelial cell density, crystalline lens opacification and intraocular clearances within the various compartments of the eye. RESULTS: Mean uncorrected visual acuity was 0.77 at the 12th postoperative month; 17 of 90 eyes required adjunctive photoablation for residual astigmatism. Forty-eight percent of eyes gained at least one line of best corrected visual acuity. After implantation, the decrease in endothelial cell density remained stable at 0.69%/year, and 91% of eyes showed no opacification of the crystalline lens. Mean endothelium-ICL and ICL-crystalline lens distances were 2.41 mm and 0.52 mm respectively. Overall patient satisfaction achieved was 96% at 36 months postoperatively. DISCUSSION AND CONCLUSION: These results demonstrate efficacy, stability and safety of the ICL V4 phakic IOL for the correction of high ametropia. Long-term follow-up did not show a significant increase in cataract formation in implanted eyes.

[Endogenous bacterial endophthalmitis related to dental abscess: case report]. / Endophtalmie endogène bactérienne sur abcès dentaire: à propos d'un cas.

INTRODUCTION: Endogenous bacterial endophthalmitis (EBE) is an intraocular bacterial infection transmitted via a hemotogenous route, usually occuring in immunocompromised patients with bacteremia spreading from extraocular foci of infection. We report a case of EBE secondary to a dental infection occurring in an immunocompetent patient. CASE REPORT: A 61-year-old-man with no past medical history other than a dental bridge on the 13th tooth was referred for rapid onset hypertensive fibrinous panuveitis of the right eye. He presented with profound visual loss in this eye, an absent pupillary reflex and an obscured fundus. The left eye was normal. Neither fever nor constitutional symptoms were noted at presentation. Work-up revealed a mild inflammatory syndrome with increased C-reactive protein, a high antistreptolysin O titer, and an abscess of the dental bridge. The clinical picture worsened rapidly, suggesting the possibility of EBE secondary to an organism of dental origin. Aqueous humor polymerase chain reaction (PCR) was positive for streptococci, which could not be identified more specifically. Removal of the dental bridge in combination with systemic and intravitreal multiple antiobiotic therapy achieved a rapid cure of the EBE. Vitrectomy combined with phacoemulsification was performed later in order to clear media opacities. At 6 months follow-up, best-corrected visual acuity was 8/10 with no recurrent inflammation. CONCLUSION: This case shows that EBE can occur in the absence of predisposing factors but with an extraocular infectious focus as simple as a dental abscess. In the absence of associated septicemia, with the involved tooth superior and ipsilateral to the affected eye, a spread of the infection by retrograde venous flow should be suspected. The prognosis for visual function may be good if early diagnosis and immediate treatment can be provided.

[Management of neovascular glaucoma related to the persistence after retinal detachment surgery of a circumferential peripheral retinal detachment]. / Traitement du glaucome néovasculaire lié à la persistance après chirurgie du décollement de rétine d'un décollement de rétine périphérique annulaire.

OBSERVATION: A 41-year-old male with a medical history of high myopia and several retinal detachment (RD) surgeries was referred for vitreous hemorrhage coexisting with neovascular glaucoma occurring 2 months after uncomplicated silicone oil removal on his left and single eye. The right eye had been lost to RD. The retina behind the equator was reattached on ultrasonography. We performed a washout pars plana vitrectomy on the left eye, revealing a chronic circumferential RD of the anterior retina stopped in its posterior spread by dense photocoagulation scars. We combined a retinectomy of the detached retina with an intracamerular injection of bevacizumab, resulting in complete disappearance of rubeosis and normalization of the intraocular pressure. CONCLUSIONS: The retinal ischemia related to the persistence of a chronic and circumferential RD anterior to dense photocoagulation scars after ab-interno RD surgery, whereas the rest of the retina appears reattached, is probably the causative factor of neovascular glaucoma. In the present case, the removal of RD by circumferential retinectomy combined with an intraocular injection of anti-VEGF allowed the complete and definitive regression of neovascular glaucoma.

[Treatment of circumscribed choroidal haemangiomas by photodynamic therapy: a review]. / Traitement des hémangiomes choroïdiens circonscrits par photothérapie dynamique : revue de la littérature.

Circumscribed choroidal hemangioma (CCH) is an uncommon benign vascular tumor of the choroid that is usually diagnosed when it causes a decrease in vision due to exudative retinal detachment. The classical treatments of CCH were photocoagulation and radiotherapy, which induced additional chorioretinal damage, explaining the poor visual prognosis even in adequately treated patients. It is difficult to compare these two therapeutic options, laser photocoagulation having been abandoned for many years due to the retractile retinal scars that it induced. Conventional radiotherapy and proton therapy with a total dose of 20 Gy gave and give good results but can be performed only by teams used to these types of treatment. Recently, photodynamic therapy (PDT), which allows a selective occlusion of vascular lesions without damaging overlying retinal structures, has emerged as a sound alternative for the treatment of CCH. Most of the clinicians used the standard treatment of age related macular degeneration by photodynamic therapy (TAP) study protocol with or without variations. The main variations brought to the TAP study protocol were the duration of the verteporfin infusion, and/or the increase of the laser power settings, and/or the increase of the duration of exposure, and/or the number of PDT spots (single spot or multiple spots, overlapping or not). Mid-term PDT results are very encouraging. PDT has been reported to bring about resolution of subretinal fluid and to reduce tumor thickness in almost all cases. Visual acuity was improved or stabilized in at least 80% of the cases. Several studies reported on minor local side effects following PDT, consisting of atrophy and proliferation of the retinal pigment epithelium, atrophy of the choroid, transient choroidal effusion, and mild subretinal fibrosis. Published data demonstrated that PDT is a safe and effective alternative to radiotherapy or photocoagulation as first-line therapy for CCH.

Wavelet optimization for content-based image retrieval in medical databases.

We propose in this article a content-based image retrieval (CBIR) method for diagnosis aid in medical fields. In the proposed system, images are indexed in a generic fashion, without extracting domain-specific features: a signature is built for each image from its wavelet transform. These image signatures characterize the distribution of wavelet coefficients in each subband of the decomposition. A distance measure is then defined to compare two image signatures and thus retrieve the most similar images in a database when a query image is submitted by a physician. To retrieve relevant images from a medical database, the signatures and the distance measure must be related to the medical interpretation of images. As a consequence, we introduce several degrees of freedom in the system so that it can be tuned to any pathology and image modality. In particular, we propose to adapt the wavelet basis, within the lifting scheme framework, and to use a custom decomposition scheme. Weights are also introduced between subbands. All these parameters are tuned by an optimization procedure, using the medical grading of each image in the database to define a performance measure. The system is assessed on two medical image databases: one for diabetic retinopathy follow up and one for screening mammography, as well as a general purpose database. Results are promising: a mean precision of 56.50%, 70.91% and 96.10% is achieved for these three databases, when five images are returned by the system.

[Peribulbar anesthesia: efficacy of a single injection with a limited local anesthetic volume]. / Anesthésie péribulbaire: efficacité d'une seule injection et d'un volume d'anesthésiques locaux limité.

INTRODUCTION: Cataract surgery can be performed with peribulbar anesthesia. The classical technique consists of two injections of local anesthetics. The purpose of our study was to assess peribulbar anesthesia with a single injection and a limited volume of local anesthetics. MATERIAL AND METHOD: After local ethics committee agreement and oral consent, patients scheduled for cataract surgery using peribulbar anesthesia were prospectively included. The lower temporal puncture was performed with a peribulbar needle with propofol sedation. The mixture of local anesthetics was administered with tactile control of orbital pressure. The puncture was followed by a 10-min compression of the ocular globe. Akinesia, analgesia, complications, and surgical conditions were noted. RESULTS: A total of 101 successive patients were included. We administered 1.2 mg/kg of propofol. The volume of local anesthetics administered was 5.0 +/- 0.9 ml. Ninety patients had akinesia at 10 min and 6.7% moderate chemosis. No puncture complication occurred. At the end of surgery, the pain noted by the patients was 0.4 +/- 2.1 out of 100 (range, 0-10). Surgical conditions were good for all patients. CONCLUSION: Peribulbar anesthesia performed with a single injection and a limited volume of local anesthetics allows cataract surgery in good conditions for the surgeon with very good analgesia for the patient.