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Heidelberg spectralis sd oct

Manufactured by Heidelberg Engineering
Sourced in Germany

The Heidelberg Spectralis SD-OCT is a spectral-domain optical coherence tomography (SD-OCT) device. It is designed to produce high-resolution, cross-sectional images of the retina and other ocular structures.

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12 protocols using heidelberg spectralis sd oct

1

Papilledema Evaluation in Pediatric IIH

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This retrospective, longitudinal study evaluated children 18 years old or younger who presented to the Children's Hospital of Philadelphia between January 2016 and December 2020. The study adhered to the tenets of the Declaration of Helsinki and was approved with waiver of informed consent by the Institutional Review Board at the Children's Hospital of Philadelphia.
Subjects were included if they (1) were aged 18 years or younger, (2) underwent treatment for diagnosed or suspected papilledema in the setting of idiopathic intracranial hypertension (IIH) (i.e., primary pseudotumor cerebri syndrome), secondary pseudotumor cerebri syndrome, or papilledema secondary to a tumor, and (3) completed traditional cpRNFL and enhanced depth imaging raster scan protocol of the ONH using Heidelberg Spectralis SD-OCT (Heidelberg Engineering Inc., Heidelberg, Germany) on at least two separate visits in the first 4 months of treatment, including a pretreatment visit and one showing resolving papilledema, defined as a 10% or greater decrease in mean cpRNFL relative to pretreatment in an eye. The exclusion criteria were (1) worsening papilledema (i.e., >10% increase in mean cpRNFL relative to the pretreatment visit) before the first resolving visit and (2) poor quality OCT images precluding appropriate segmentation of the internal limiting membrane (ILM) and/or BM.
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2

Choroidal Thickness Mapping with SD-OCT

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All OCT measurements were performed using SD-OCT (Heidelberg Spectralis SD-OCT; Heidelberg Engineering; Spectralis software version 5.3.2) after pupillary dilation. Scans with quality score of less than 20 were excluded from the analysis. We also excluded scans with inadequate quality as determined by poor quality fundus images, interruption of the RNFL segmentation, or those in which the posterior border of the choroid could not be delineated (Fig. 1).

An optical coherence tomography (OCT) image shows the manual segmentation of Bruch's membrane (upper red line) and sclerochoroidal border (lower red line) in a raster line of macula. Choroidal map and volume measured in nine sectors of the Early Treatment Diabetic Retinopathy Study (ETDRS) layout profile across the central 3.45 mm zone in the macula after manual segmentation of choroidal thickness.

Fig. 1
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3

Quantifying Ellipsoid Zone Area with SD-OCT

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Macular scans were performed with Heidelberg Spectralis SD-OCT (Heidelberg Engineering, Heidelberg, Germany). Horizontal high-resolution transfoveal line scans were obtained using automated real-time tracking with an average of nine images. Each volume scan was composed of 25 horizontal b-scans in high-resolution mode with 256 µm distance between b-scans and 512 a-scans per b-scan. The EZA was measured using vendor software (Heidelberg Eye Explorer Version 1.10.2.0). The observers marked the locations of the two most distant temporal and nasal points that the EZ layer could be distinguished from the adjacent layers using the “arrow tool” at each scan (Supplementary Fig. S2b). The dots were connected to generate a circle using the “draw region” tool of the software, and the circle's area was automatically calculated by software (Supplementary Fig. S2a). The EZA was measured by three observers (YT, AH, JK) and the mean of the three measurements was used for analysis.
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4

Comprehensive Eye Evaluation of iNPH Patients

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Each iNPH patient underwent a comprehensive eye examination including best-corrected visual acuity (BCVA) assessment reported in logarithm of the minimum angle of resolution (LogMar), slit lamp examination of the anterior segment, indirect ophthalmoscopy, Goldmann applanation tonometer, assessment of axial length with Lenstar (Haag-Streit, Koniz, Swiss), and OCT Macula.
All OCT examinations were carried out using the same Heidelberg Spectralis SD-OCT (Heidelberg Engineering, Heidelberg, Germany) apparatus. The information regarding medical therapies and comorbidities was collected during the baseline ophthalmic evaluation.
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5

Choroidal Thickness Measurement Protocol

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The choroidal images were obtained by a Heidelberg Spectralis SD-OCT (Heidelberg Engineering, Heidelberg, Germany; SD-OCT) with an EDI model. The standard protocol for obtaining EDI-OCT images was reported previously.[6 7 (link)8 (link)] Briefly, the choroid was imaged by positioning an OCT device close enough to the eye to obtain an inverted image. The resultant images were viewed and measured using Heidelberg Eye Explorer software (version 1.7.0.0; Heidelberg Engineering, Heidelberg, Germany). The choroidal thickness was measured manually as the distance between the basal edge of the retinal pigment epithelium and the chorioscleral border. It was measured at nine points: Beneath the fovea, and the superior, inferior, temporal, and nasal sectors of 1 and 3 mm diameters [Fig. 1]. These measurements were performed by a single doctor who was blinded to the diagnosis and identity of the patients.
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6

Multimodal Imaging for Optic Nerve Assessment

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The implanted animals were evaluated before and immediately after the surgical procedure with the Heidelberg Spectralis™ SD-OCT (Heidelberg Engineering, Germany).
The imaging protocol was comprised of volume scans performed with SD-OCT, fluorescein angiogram (FA), fundus autofluorescence (FAF), color fundus photographs and Infrared (IR) images.
Color fundus photographs were taken of both eyes. IR images, FAF and FA were taken within 3 min of acquiring time (Heidelberg Spectralis, HRA-OCT) in both eyes. SD-OCT images (Heidelberg Spectralis-HRA) were also taken for both eyes using the following protocol: (1) High definition scans through the optic nerve; (2) volume scans (30 × 30) centered on the optic nerve; (3) volume scans (30 × 30) of the temporal retina with the optic nerve on the edge of the scan; (4) nerve fiber layer scans centered on the optic nerve.
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7

Intravitreal Ozurdex Injection Protocol

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OCT scans were carried out using the standard protocol on the Heidelberg Spectralis SD-OCT (Heidelberg Engineering, Heidelberg, Germany) [21 (link)]. All scans were performed by two experienced medical photographers.
All patients had the Ozurdex (Dexamethasone implant) intravitreal injection on week 1 (baseline). According to the protocol from OCTOME study some of the patients were eligible for a second injection at the re-treatment window between week 16 and week 24.
Changes in the patient’s VA, RG and YB thresholds were compared against the corresponding changes in CST.
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8

Comprehensive Ophthalmologic Evaluation of Ocular Lesions

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All patients who underwent a complete ophthalmologic evaluation including best-corrected visual acuity (BCVA), slit-lamp examination, fundus examination, colour fundus photography (Carl Zeiss Meditec, Inc., Jena, Germany), wide field OPTOS images, Heidelberg Spectralis SD-OCT (Heidelberg Engineering, Heidelberg, Germany) at the initial visit were included. Patients presenting with a scarred lesion without evidence of an active lesion underwent a single-color photo image directed to the scar. In cases that presented with both a scarred lesion and an active lesion, the colour photos focused on the scar lesion as well as on the active lesion were obtained. Clinical data such as lesion status (active, scarred), presentation (primary, recurrent, asymptomatic, or treated old scar, distant or satellite lesion), presence of anterior uveitis, ocular hypertension, involvement of optic nerve, presence of vitreous haze, were also collected from medical charts of subjects, retrospectively.
Clinical features such as anterior uveitis, ocular hypertension, periphlebitis, arteritic vasculitis, retinal haemorrhages, papillitis, vitreous haze score, exudative retinal detachment, hard exudates are collected from medical records of the patients and confirmed with fundus images where applicable. Vitreous haze scores are assessed from the optic nerve head centred colour fundus photographs.
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9

Prospective Study of PEVAC-like Lesions

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We prospectively recruited consecutive patients between January 2019 and October 2019, who were identified with a PEVAC(‐resembling) lesion on OCT. Identification of PEVAC lesions was based on the structural appearance on OCT, that is a round or oval lesion with hyperreflective surrounding had to be present. Lesions with similar structure and size on OCT, but in patients with a history of a retinal vascular disease, were identified as PEVAC‐resembling lesions. We divided the patients into two groups: subjects without vascular retinopathy (PEVAC group) and subjects with a vascular retinopathy, such as diabetic retinopathy or retinal vein occlusions (PEVAC‐resembling group). This was decided based on medical history, slit‐lamp examination, OCT, OCT‐A, fluorescein angiography (FA) and/or indocyanine green angiography (ICGA).
The exclusion criterium for the PEVAC group was the presence of any other retinal or choroidal vascular abnormalities, previous treatment, presence of diabetes mellitus and presence of uncontrolled hypertension. In addition, subjects that were imaged during earlier visits with the Heidelberg Spectralis SD‐OCT (Heidelberg Engineering, Heidelberg, Germany) and colour fundus photography (CFP) were retrospectively included in the study.
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10

Evaluating Pediatric Visual Acuity and pRNFL

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The results of visual eld acuity for children are less reliable due to poor patient cooperation. Changes in the peripapillary retinal nerve bre layer (pRNFL) thickness were detected using the Heidelberg Spectralis SD-OCT (Heidelberg Engineering, Heidelberg, Germany) machine according to the standard protocols to monitor glaucomatous onset and progression. All the OCT examinations were performed by the same, experienced ophthalmologist.
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