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25 protocols using visante

1

Ocular Biometry Measurements in Mice

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Mice were stabilized and oriented for OCT performed with a Visante instrument (Carl Zeiss Canada Ltd., Toronto, ON) using a custom-designed platform permitting adjustment through the X, Y and Z planes [36 (link)]. Diophenyl-T (Alcon) was applied topically to dilate the pupil of both eyes and the instrument was focused at the apex of the corneal surface of each eye prior to image capture. Measurements of central corneal thickness, anterior chamber width, anterior chamber depth, pupil diameter, ratio of pupil diameter to anterior chamber diameter, posterior retina thickness and anterior retina thickness were obtained for each eye using a digital caliper tool (Carl Zeiss Canada Ltd.). Anterior chamber angle of OCT images was measured using ImageJ software (National Institute of Health, Bethesda, Maryland). All measurements for both eyes were taken by two independent scorers blinded to mouse genotype.
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2

Anterior Segment OCT for Postoperative IOP Monitoring

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Anterior segment Optical Coherence Tomography (Visante, Carl Zeiss Meditec, USA) was performed on postoperative day 1, 1 week,1 month, 2 months, and at the onset of postoperative IOP spike in cases where this occurred. The angle was imaged at four quadrants including additional areas in the nasal quadrant where the angle was incised. The degrees of open TM shelf or visible TM leaflet (Figure 1) and presence of PAS, supraciliary effusions/cleft or clots, or additional angle features, were quantified by noting the number of quadrants of that feature seen on ASOCT.

A-H shows the trabecular leaflet (Arrows) with open shelf on gonioscopy ((A and B) Patient 1, (D) Patient 2, (G and H) Patient 3) and anterior segment optical coherence tomography ((C, E and F), respectively).

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3

Clinical Evaluation of Ocular Disorders

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All investigations were conducted in accordance with the principles of the Declaration of Helsinki. The study was approved by the following local ethics committees; Moorfields and Whittington Hospital UK, The Royal Victorian Eye and Ear Hospital Australia, Odense University Hospital Denmark and University Hospital of Wales UK. Informed written consent, including permission to publish photographs, was obtained from all participating individuals or parental guardians on behalf of the minors enrolled in this study. Blood samples were donated and genomic DNA was extracted from peripheral blood lymphocytes using conventional methodologies. Patients and their relatives were clinically assessed by experienced ophthalmologists. Standard evaluation consisted of detailed ophthalmic examination and the additional measurement of the axial length of the eye and imaging of the anterior segment of the eye performed with ocular coherence tomography (OCT; Visante, Carl Zeiss Meditec), b-scan ultrasonography, and optical interferometry (IOLMaster, Carl Zeiss Meditec). Proband of Family K was clinically assessed by a geneticist (DTP), a paediatric ophthalmologist (DL) and a paediatrician (MG). He had standard MRI with a 1.5 Tesla scanner.
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4

Comprehensive Eye Examination Protocol

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Cycloplegia was induced using 1 drop of tropicamide HCI 1% (Minims, Bausch & Lomb, Kingston-Upon-Thames, UK). An objective measure of the refractive error and central corneal curvature was determined with a binocular open view autorefractor/keratometer (Shin-Nippon SRW-5000, Ryusyo Industrial Co. Ltd, Osaka, Japan). Five measurements were taken, averaged and converted to MSE (sphere power + 0.5 x cylinder power). AL and anterior chamber depth (ACD) measurements were taken with the commercially available IOLMaster (Carl Zeiss Meditec, Inc., Dublin, California, USA). Five separate measurements were averaged for AL, whereas three separate measurements were averaged for central corneal curvature (mm), and a single capture shot automatically generated and averaged five measurements of ACD. Corneal pachymetry measurements were obtained with the global pachymetry scan protocol on the AS-OCT (Visante; Carl Zeiss Meditec). The Visante system automatically processes 16 line scans and represents a map of the pachymetry values. The average reading for the central 2 mm was used for analysis.
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5

Penetrating Donor Cornea Transplant Technique

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For the donor cornea, the posterior side cut was set to be penetrating. A 0.2 mm undersized recipient cornea was trephined with similar settings, except that the depth of the posterior side cut was programmed to begin 70 μm anterior to the endothelium at the thinnest point on the optical coherence tomography pachymetry map (Visante, Carl Zeiss Meditec, Inc., Dublin, CA). In the operating room, the adhesions along the cut surface of the recipient cornea were dissected with a Sinskey hook (Rhein Medical, Tampa, FL), and the residual posterior stroma was cut with corneal scissors. The pupil was constricted with miotic (pilocarpine 1 %), and viscoelastic material was put into the anterior chamber to protect the lens. The donor button was then placed on the recipient and sutured with 16 interrupted 10–0 nylon sutures.
Tobramycin-dexamethasone ointment was applied to the eye at the end of the surgery. Eyes were patched and shielded. Postoperatively, patients were commenced on tobramycin- dexamethasone eyedrops with one drop 3 hourly, and slowly tapered over several months. Sutures were removed as clinically indicated.
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6

Corneal Thickness Measurement by AS-OCT

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All patients were examined and photographed using a slit-lamp biomicroscope (Haag-Streit BM900; Haag-Streit USA, Inc., Mason, Ohio) by experienced technicians at each visit. The lesion sites were analyzed by AS-OCT (Visante, Carl Zeiss Meditec, Inc., Dublin, CA). In addition, the central corneal thickness (CCT) and the corneal thickness at the site of the lesion (CTL) were also measured by AS-OCT. The same operator adjusted the software system to position the vertex at the center of the AS-OCT image. The thickness was measured using the software on the Visante AS-OCT. The CCT was measured with the caliper position at zero and recorded as the distance from the surface epithelium to the endothelium. CTL evaluation was performed manually at the site of the lesions. Cursors were placed perpendicular to the anterior corneal surface at the point of measurement.
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7

Femtosecond-Assisted DSAEK Outcomes

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The 126 consecutive eyes with endothelial failure of 120 patients, who had corneal endothelial decompensation and underwent femtosecond-assisted DSAEK using the VisuMax femtosecond laser system in the Department of Ophthalmology, Peking University 3rd Hospital, were included in the study. General data, corneal diseases, combined ocular diseases, and previous ocular surgical history were obtained from each patient. A detailed examination was performed that included a slit-lamp examination, confocal microscopy using the Heidelberg retina tomography with the cornea module (HRT III, Heidelberg Engineering, Heidelberg, Germany), anterior segment-optical coherence tomography (AS-OCT, Visante, Carl Zeiss Meditec, Dublin, CA, USA), and conventional photography. DSAEK with femtosecond laser-assisted corneal endothelial graft preparation using the VisuMax femtosecond laser system was performed in all eyes by the same surgeon. Central endothelial cell density (ECD) was recorded postoperatively at 2 weeks (n = 126), 1 month (n = 126), 3 months (n = 110), 6 months (n = 101), and 12 months (n = 71) by the same examination technician. ECD measurements were compared with the preoperative eye bank measurements.
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8

Postoperative Examination of FCVB Implantation

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Postoperative examinations include assessment of the FCVB position, slit lamp microscopy (Nikon FS-2, Nikon Inc, NY), scanning laser ophthalmoscope (SLO) (OPTOSPLC, Daytona, England), VA through E Standard Logarithm Eyesight, IOP with Goldmann applanation tonometry (CT80A, Topcon, Japan), optical coherence tomography (OCT) (Visante, Carl Zeiss Meditec, Dublin, CA), ultrasound biomicroscopy (UBM) (SW-3200L, Suoer, China), B-scan (HC00504598, Cinescan, France), computed tomography scans (Ingenuity128, Philips, Holland), as well as monitoring the postoperative complications. The primary effectiveness outcome measure was retinal reattachment after FCVB implantation at the six-month follow-up at the latest. The secondary effectiveness outcome measures were VA and IOP, and the safety outcome was postoperative complications.
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9

Comprehensive Ophthalmic Examination Protocol

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All of the study participants were examined between January 2010 and August 2013 at the glaucoma and cataract service of Seoul National University Hospital, Seoul, Korea. All eligible participants were consecutively enrolled by retrospective medical-record review. At the initial clinic visit, all underwent a complete ophthalmic examination, including medical history review, best-corrected visual acuity measurement, slit-lamp biomicroscopy, Goldmann applanation tonometry (Haag-Streit, Koniz, Switzerland), funduscopic examination (90 diopter lens), stereoscopic optic disc photography, retinal nerve fiber layer photography, and gonioscopy, performed in the dark using a Sussman 4-mirror lens at high magnification (x16). Indentation gonioscopy with the same lens was used to establish the presence or absence of peripheral anterior synechiae. The cataract type and grade was evaluated, based on the Lens Opacity Classification System II [9 (link)]. Additionally, AS-OCT imaging (Visante, Carl Zeiss Meditec, Dublin, CA) and axial length (AL) measurement (IOL Master; Carl Zeiss Meditec) were performed at the initial or follow-up clinic visit.
This study, approved by the Seoul National University Hospital institutional review board adhered to the tenets of the Declaration of Helsinki. Informed consent was obtained from all subjects.
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10

Comprehensive Ocular Examinations for FCVB Implantation

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Ocular examinations were performed at baseline, 1, 2, 3, 6 and 12 months after FCVB implantation. The arrangements of ocular examinations consist of VA with Snellen eye charts (transformed to logMAR) and IOP with Goldmann applanation tonometry (GAT; Haag-Streit AG, Köniz, Switzerlan), traditional slit lamp biomicroscopy (Nikon FS-2, Nikon Inc., Melville, NY), direct ophthalmoscopy, and fundus photography (TRC- 50EX; Topcon, Tokyo, Japan). A-scan ultrasound (CineScan A/B; Quantel Medical, Bozeman, MT), B-scan ultrasound (CineScan A/B; Quantel Medical, Bozeman, MT), noncontact specular microscopy (SP-3000P; Topcon, Tokyo, Japan), optical coherence tomography (OCT, Visante; Carl Zeiss Meditec, Dublin, CA), ultrasound biomicroscopy (UBM, SW-3200 Kinscan; Suoer, Tianjin, China) and were performed at baseline and 3 months after implantation.
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