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.
Heidelberg spectralis sd oct
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.
12 protocols using heidelberg spectralis sd oct
Papilledema Evaluation in Pediatric IIH
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.
Choroidal Thickness Mapping with SD-OCT
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.
Quantifying Ellipsoid Zone Area with SD-OCT
Comprehensive Eye Evaluation of iNPH Patients
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.
Choroidal Thickness Measurement Protocol
Multimodal Imaging for Optic Nerve Assessment
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.
Intravitreal Ozurdex Injection Protocol
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.
Comprehensive Ophthalmologic Evaluation of Ocular Lesions
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.
Prospective Study of PEVAC-like Lesions
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.
Evaluating Pediatric Visual Acuity and pRNFL
About PubCompare
Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.
We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.
However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.
Ready to get started?
Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required
Revolutionizing how scientists
search and build protocols!