Identification of Patients with Pentosan Polysulfate Sodium-Associated Maculopathy through Screening of the Electronic Medical Record at an Academic Center.


Journal

Journal of ophthalmology
ISSN: 2090-004X
Titre abrégé: J Ophthalmol
Pays: United States
ID NLM: 101524199

Informations de publication

Date de publication:
2020
Historique:
received: 12 09 2020
revised: 07 11 2020
accepted: 28 11 2020
entrez: 25 1 2021
pubmed: 26 1 2021
medline: 26 1 2021
Statut: epublish

Résumé

This chart review of a quaternary academic medical center electronic medical record (EMR) aimed to identify patients at risk of development of maculopathy with exposure to pentosan polysulfate sodium (PPS). A review of electronic medical records of a quaternary medical center of patients with either documented exposure to PPS or diagnosis of interstitial cystitis (IC) from 2007 to 2019 was performed for retinal imaging and visual acuity; the study was conducted in August of 2019. 216 charts were included for analysis, of which 96 had documented eye exams and 24 had retinal imaging done. We identified three patients with maculopathy in the context of long-term exposure to PPS via chart review, and one additional patient was identified by referral. The median PPS exposure duration was 11 years (range 7 to 19 years). Median logMAR BCVA OD 0.6 range was 0.0-1.9 (approximate Snellen equivalent 20/80 range (20/20-20/1600)) and OS 0.7 range was 0.1-1.9 (approximate Snellen equivalent 20/100 range (20/25-20/1600)). Ultrawidefield color fundus imaging and fundus autofluorescence revealed findings of pigmentary changes and patchy macular atrophy. Optical coherence tomography (OCT) demonstrated outer retinal thinning and increased choroidal transmission coincident with areas of atrophy seen on fundus imaging. Less than half of patients at risk for development of maculopathy due to exposure to PPS had received eye examinations, suggesting that those at risk are not receiving adequate screening. We found two patients with PPS maculopathy who had relatively preserved central vision, one patient with bitemporal vision loss, and one patient who developed vision loss in both eyes.

Identifiants

pubmed: 33489347
doi: 10.1155/2020/8866961
pmc: PMC7803106
doi:

Types de publication

Journal Article

Langues

eng

Pagination

8866961

Subventions

Organisme : NEI NIH HHS
ID : K08 EY027463
Pays : United States

Informations de copyright

Copyright © 2020 Kendall Higgins et al.

Déclaration de conflit d'intérêts

No conflicts of interest exist for any author.

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Auteurs

Kendall Higgins (K)

Department of Ophthalmology & Vision Science, School of Medicine, University of California Davis, Sacramento, CA, USA.
Department of Urologic Surgery, School of Medicine, University of California Davis, Sacramento, CA, USA.

R Joel Welch (RJ)

Department of Ophthalmology & Vision Science, School of Medicine, University of California Davis, Sacramento, CA, USA.

Colin Bacorn (C)

Department of Ophthalmology & Vision Science, School of Medicine, University of California Davis, Sacramento, CA, USA.

Glenn Yiu (G)

Department of Ophthalmology & Vision Science, School of Medicine, University of California Davis, Sacramento, CA, USA.

Jennifer Rothschild (J)

The University of Miami, Leonard M. Miller School of Medicine, Miami, FL, USA.

Susanna S Park (SS)

Department of Ophthalmology & Vision Science, School of Medicine, University of California Davis, Sacramento, CA, USA.

Ala Moshiri (A)

Department of Ophthalmology & Vision Science, School of Medicine, University of California Davis, Sacramento, CA, USA.

Classifications MeSH