Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/29997
Title: | Treatment of severe keratoconus hydrops with intracameral platelet-rich plasma injection | Authors: | Alio, J.L. Toprak, İbrahim Rodriguez, A.E. |
Keywords: | corneal surgery corneal transplantation Down syndrome keratoconus platelet-rich plasma sulfur hexafluoride adult Article case report clinical article clinical examination controlled study cornea edema cornea transplantation corrected distance visual acuity disease severity eye pain female follow up human intraocular pressure keratometry optical coherence tomography photophobia postoperative period priority journal slit lamp microscopy thrombocyte rich plasma treatment failure visual impairment anterior eye chamber complication diagnostic imaging drug effect intraocular drug administration treatment outcome visual acuity Adult Anterior Chamber Corneal Edema Down Syndrome Female Humans Injections, Intraocular Intraocular Pressure Keratoconus Platelet-Rich Plasma Tomography, Optical Coherence Treatment Outcome Visual Acuity |
Publisher: | Lippincott Williams and Wilkins | Abstract: | Purpose: To present successful management of severe corneal hydrops by corneal optical coherence tomography (OCT) guidance and intracameral application of eye platelet-rich plasma (E-PRP) in a case with Down syndrome. Methods: A 36-year-old woman with Down syndrome presented with acute vision loss, pain, photophobia, and corneal edema in the left eye. Clinical examination revealed keratoconus in the right eye and extreme keratoconus with severe corneal hydrops in the left eye. Anterior segment OCT (MS-39, Costruzione Strumenti Oftalmici, Firenze, Italy) showed intrastromal cystic fluid collection and ruptured and detached Descemet membrane. The OCT-guided management of hydrops is first described in this case report. Results: Medical treatment and intracameral sulfur hexafluoride injection failed. A sterile 0.3 mL of E-PRP was injected into the anterior chamber. Clinical and anatomical improvement began from the first postoperative day, and corneal edema totally resolved at 1 week. Postoperatively, no significant side effect was noted except an early transient moderate (28 mm Hg) intraocular pressure peak. Anterior segment-OCT demonstrated dramatic normalization in corneal morphology with total disappearance of fluid in the cystic intracorneal space, closure of the DM rupture, and DM reattachment. The patient was stable during the 6-month follow-up.Conclusions:In this case, intraocular E-PRP was a promising, apparently safe, and effective treatment option in management of corneal hydrops, in which conventional approaches failed. This is the first case in the literature to describe OCT appearance of corneal hydrops and intracameral use of E-PRP for the resolution of DM rupture in acute corneal hydrops. © 2019 Wolters Kluwer Health, Inc. All rights reserved. | URI: | https://hdl.handle.net/11499/29997 https://doi.org/10.1097/ICO.0000000000002070 |
ISSN: | 0277-3740 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
Show full item record
CORE Recommender
SCOPUSTM
Citations
16
checked on Nov 16, 2024
WEB OF SCIENCETM
Citations
9
checked on Nov 21, 2024
Page view(s)
30
checked on Aug 24, 2024
Google ScholarTM
Check
Altmetric
Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.