Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome

Pedro Nuno Brito,1 Sérgio Estrela Silva,1 José Silva Cotta,1 Fernando Falcão-Reis1,21Ophthalmology Department, Hospital S João, Porto, Portugal; 2Faculty of Medicine of Porto, University of Porto, Porto, PortugalPurpose: To report a case of...

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Autores principales: Brito PN, Silva SE, Cotta JS, Falcão-Reis F
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Publicado: Dove Medical Press 2012
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spelling oai:doaj.org-article:762f84e6c03342078144baa801b205452021-12-02T04:07:13ZSevere ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome1177-54671177-5483https://doaj.org/article/762f84e6c03342078144baa801b205452012-10-01T00:00:00Zhttp://www.dovepress.com/severe-ocular-hypertension-secondary-to-systemic-corticosteroid-treatm-a11282https://doaj.org/toc/1177-5467https://doaj.org/toc/1177-5483Pedro Nuno Brito,1 Sérgio Estrela Silva,1 José Silva Cotta,1 Fernando Falcão-Reis1,21Ophthalmology Department, Hospital S João, Porto, Portugal; 2Faculty of Medicine of Porto, University of Porto, Porto, PortugalPurpose: To report a case of severe, acute ocular hypertension in a 6-year-old child, 7 days after initiating treatment with oral prednisolone, due to nephrotic syndrome.Methods: A 6-year-old female Caucasian child was diagnosed with nephrotic syndrome and treated with oral prednisolone (60 mg/day). Seven days later the child initiated complaints of headache, vomiting, ocular pain, and photophobia. Ophthalmologic examination revealed a severely increased intraocular pressure (IOP) of 52 mmHg in the right eye and 56 mmHg in the left eye. Anterior segment morphology was evaluated with ultrasound biomicroscopy. Optic disc status was evaluated by disc photography, kinetic perimetry, and optical coherence tomography.Results: Treatment was initiated with latanoprost, brimonidine, and the fixed association of timolol and dorzolamide. At each follow-up examination, progressively better control of IOP was obtained. Simultaneous with corticosteroid dosage decrease we were able to reduce antiglaucomatous medication while maintaining IOP under control. Ultrasound biomicroscopy revealed an open angle with normal anterior segment echographic findings. Perimetric evaluation revealed normal visual fields in both eyes. Four months after presentation, steroid treatment had been completed and IOP was 10 mmHg in both eyes without any antiglaucomatous medication. Optical coherence tomography revealed normal retinal nerve fiber layer thickness in all peripapillary sectors.Conclusions: Systemic steroid treatment can cause a severe, acute increase in IOP in children. Children undergoing steroid treatment should have routine ophthalmologic examinations during treatment duration. Prompt antiglaucomatous treatment prevents retinal nerve fiber layer damage and visual acuity loss.Keywords: glaucoma, children, corticosteroid, nephroticBrito PNSilva SECotta JSFalcão-Reis FDove Medical PressarticleOphthalmologyRE1-994ENClinical Ophthalmology, Vol 2012, Iss default, Pp 1675-1679 (2012)
institution DOAJ
collection DOAJ
language EN
topic Ophthalmology
RE1-994
spellingShingle Ophthalmology
RE1-994
Brito PN
Silva SE
Cotta JS
Falcão-Reis F
Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome
description Pedro Nuno Brito,1 Sérgio Estrela Silva,1 José Silva Cotta,1 Fernando Falcão-Reis1,21Ophthalmology Department, Hospital S João, Porto, Portugal; 2Faculty of Medicine of Porto, University of Porto, Porto, PortugalPurpose: To report a case of severe, acute ocular hypertension in a 6-year-old child, 7 days after initiating treatment with oral prednisolone, due to nephrotic syndrome.Methods: A 6-year-old female Caucasian child was diagnosed with nephrotic syndrome and treated with oral prednisolone (60 mg/day). Seven days later the child initiated complaints of headache, vomiting, ocular pain, and photophobia. Ophthalmologic examination revealed a severely increased intraocular pressure (IOP) of 52 mmHg in the right eye and 56 mmHg in the left eye. Anterior segment morphology was evaluated with ultrasound biomicroscopy. Optic disc status was evaluated by disc photography, kinetic perimetry, and optical coherence tomography.Results: Treatment was initiated with latanoprost, brimonidine, and the fixed association of timolol and dorzolamide. At each follow-up examination, progressively better control of IOP was obtained. Simultaneous with corticosteroid dosage decrease we were able to reduce antiglaucomatous medication while maintaining IOP under control. Ultrasound biomicroscopy revealed an open angle with normal anterior segment echographic findings. Perimetric evaluation revealed normal visual fields in both eyes. Four months after presentation, steroid treatment had been completed and IOP was 10 mmHg in both eyes without any antiglaucomatous medication. Optical coherence tomography revealed normal retinal nerve fiber layer thickness in all peripapillary sectors.Conclusions: Systemic steroid treatment can cause a severe, acute increase in IOP in children. Children undergoing steroid treatment should have routine ophthalmologic examinations during treatment duration. Prompt antiglaucomatous treatment prevents retinal nerve fiber layer damage and visual acuity loss.Keywords: glaucoma, children, corticosteroid, nephrotic
format article
author Brito PN
Silva SE
Cotta JS
Falcão-Reis F
author_facet Brito PN
Silva SE
Cotta JS
Falcão-Reis F
author_sort Brito PN
title Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome
title_short Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome
title_full Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome
title_fullStr Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome
title_full_unstemmed Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome
title_sort severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome
publisher Dove Medical Press
publishDate 2012
url https://doaj.org/article/762f84e6c03342078144baa801b20545
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AT cottajs severeocularhypertensionsecondarytosystemiccorticosteroidtreatmentinachildwithnephroticsyndrome
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