Literature DB >> 25444639

Penetrating keratoplasty for corneal amyloidosis in familial amyloidosis, Finnish type.

Jaakko S Mattila1, Kari Krootila1, Tero Kivelä1, Juha M Holopainen2.   

Abstract

PURPOSE: To analyze the outcome of penetrating keratoplasty (PK) to the first eye for corneal amyloidosis in familial amyloidosis, Finnish type (FAF).
DESIGN: Single-center, retrospective, nonrandomized, interventional, noncomparative case series. PARTICIPANTS: Thirty-one eyes of 31 patients with FAF. INTERVENTION: All patients with FAF who had their first PK in Helsinki University Eye Hospital between January 1, 1990, and August 1, 2011, were identified and a retrospective analysis of the patient charts was performed. MAIN OUTCOME MEASURES: Best spectacle-corrected visual acuity (BCVA), intraoperative and postoperative complications, graft survival, reason for graft failure, and frequency of regrafting.
RESULTS: The median follow-up period was 32 months (range, 5-114). After 24 months, the median BCVA was 1.15 on a logarithm of the minimum angle of resolution scale (20/280; mean, 1.1; SD, 0.5) in comparison with the preoperative median BCVA of 1.3 (20/400; mean, 1.3; SD, 0.4). At 24 months, 3 of 18 eyes (17%) had a visual acuity of ≥0.5 (20/63) and 13 of 18 grafts (72%) were clear. Rejection occurred in 6 of 31 primary grafts (19%). Graft failure occurred in 16 of 31 eyes and resulted from surface complications in 11 eyes and additionally from rejection in 5 eyes. Seven eyes needed regrafting (twice in 1 eye). Complications were frequent in the early and late postoperative periods. Presence of preoperative corneal or graft neovascularization was an indicator of a high risk of graft failure and poor visual outcome.
CONCLUSIONS: In a minority of FAF patients, PK improves vision. Owing to the high failure risk and guarded visual prognosis after PK, it is important that both the surgeon and the patient have realistic expectations. It may be reasonable to limit PK to cases with bilateral advanced disease. It seems reasonable to optimize ocular surface health and to delay PK.
Copyright © 2015 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 25444639     DOI: 10.1016/j.ophtha.2014.09.035

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  3 in total

1.  Deep Learning Algorithms for Corneal Amyloid Deposition Quantitation in Familial Amyloidosis.

Authors:  Klaus Kessel; Jaakko Mattila; Nina Linder; Tero Kivelä; Johan Lundin
Journal:  Ocul Oncol Pathol       Date:  2019-07-15

2.  A novel missense TGFBI variant p.(Ser591Phe) in a Finnish family with variant lattice corneal dystrophy.

Authors:  Aino Maaria Jaakkola; Petri J Järventausta; Reetta-Stiina Järvinen; Pauliina Repo; Tero T Kivelä; Joni A Turunen
Journal:  Eur J Ophthalmol       Date:  2021-03-01       Impact factor: 1.922

3.  The First Argentinian Family with Familial Amyloidosis of the Finnish Type.

Authors:  Francisco Lucero Saá; Federico Andrés Cremona; Natalia Ximena Mínguez; María Laura Igarzabal; Pablo Chiaradía
Journal:  Case Rep Ophthalmol       Date:  2017-08-31
  3 in total

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