Daniel Oliveira Dantas

Dr. Daniel Oliveira Dantas

Universidade Federal de Sergipe, Aracaju, Sergipe, Brazil
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Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 November 2002
Verified
Conference Paper
Closed access
RHRoberto Hirata
Roberto Hirata
JBJ. Barrera
J. Barrera
Ronaldo HashimotoRonaldo Hashimoto
Ronaldo Hashimoto
DDDaniel Oliveira Dantas
Daniel Oliveira Dantas

1 December 2002 in Real-Time Imaging
Verified
Journal Article
Closed access
RHRoberto Hirata
Roberto Hirata
JBJunior Barrera
Junior Barrera
Ronaldo HashimotoRonaldo Hashimoto
Ronaldo Hashimoto
DDDaniel Oliveira Dantas
Daniel Oliveira Dantas
GEGustavo H. Esteves
Gustavo H. Esteves

1 January 2021
Verified
Conference Paper
Open access
AOArtur Oliveira
Artur Oliveira
ACAndré Britto de Carvalho
André Britto de Carvalho
DDDaniel Oliveira Dantas
Daniel Oliveira Dantas

1 January 2021
Verified
Conference Paper
Open access
JOJosé Maurício de Oliveira
José Maurício de Oliveira
DDDaniel Oliveira Dantas
Daniel Oliveira Dantas

1 February 2016 in Clinics
Verified
Journal Article
Open access
DJDaniela Lima de Jesus
Daniela Lima de Jesus
FVFlávio Fernandes Villela
Flávio Fernandes Villela
LOLuis Fernando Orlandin
Luis Fernando Orlandin
FEFernando Naves Eiji
Fernando Naves Eiji
DDDaniel Oliveira Dantas
Daniel Oliveira Dantas
MAMilton Ruiz Alves
Milton Ruiz Alves
The purpose of this study was to evaluate the accuracy of Spot Vision Screening™ as an autorefractor by comparing refraction measurements to subjective clinical refractometry results in children and adult patients. One-hundred and thirty-four eyes of 134 patients were submitted to refractometry by Spot and clinical refractometry under cycloplegia. Patients, students, physicians, staff and children of staff from the Hospital das Clínicas (School of Medicine, University of São Paulo) aged 7-50 years without signs of ocular disease were examined. Only right-eye refraction data were analyzed. The findings were converted in magnitude vectors for analysis. The difference between Spot Vision Screening™ and subjective clinical refractometry expressed in spherical equivalents was +0.66±0.56 diopters (D), +0.16±0.27 D for the vector projected on the 90 axis and +0.02±0.15 D for the oblique vector. Despite the statistical significance of the difference between the two methods, we consider the difference non-relevant in a clinical setting, supporting the use of Spot Vision Screening™ as an ancillary method for estimating refraction.

1 June 2017 in Journal of Glaucoma
Verified
Journal Article
Closed access
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RGRenato A.S. Germano
Renato A.S. Germano
CMCarlos Gustavo de Moraes
Carlos Gustavo de Moraes
RSRemo Susanna
Remo Susanna
DDDaniel Oliveira Dantas
Daniel Oliveira Dantas
ENEdson D.S. Neto
Edson D.S. Neto
Purpose: To describe the Glaucoma Staging Application (GSA), a new application for automated classification of visual field (VF) severity that can be used in any Humphrey perimeters. We also tested and validated its performance in staging glaucomatous VFs defects and assessed its reproducibility. Materials and Methods: The GSA is based upon the modified University of São Paulo Glaucoma Visual Field Staging System, and consists of 3 sections: severity based on the visual field index; defect location based on eccentricity; and extent of topographic damage by hemifields. We analyzed 612 VFs of 32 patients. VFs were analyzed by a glaucoma expert and then compared with the output of the GSA. To evaluate the repeatability, the same search criteria were repeated 1 week later using the same GSA. The classification given by the software was considered correct if it completely agreed in all variables (severity, location, and extent of topographic damage) with the classification performed manually by the glaucoma expert. Results: One hundred seventy-eight eyes were classified as early VF damage, 148 moderate, and 156 severe. One hundred thirty-one VFs were classified as normal. When repeated, 1 week later, the GSA showed excellent repeatability. The automated classification agreed with the expert’s grading in 100% of cases. Conclusions: The GSA allows an automated, fast, reproducible, and objective classification system for multiple 24-2 VFs of Humphrey perimetry. This study is a proof-of-concept that could translate into a useful tool to analyze and stage VFs more objectively and thus help detecting progression of different types of VFs defects.