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1.
Cornea ; 33(2): 161-8, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24322804

ABSTRACT

PURPOSE: The aim was to describe a geographically and clinically diverse sample of cases of Acanthamoeba keratitis (AK) and establish the risk factors for poor outcomes among patients with this disease. METHODS: We conducted a retrospective, population-based case series of 116 patients with AK identified through a national surveillance network. Data were collected via a medical record review by diagnosing ophthalmologists and by phone interviews with patients. Exact logistic regression modeling was used to determine risk factors for poor visual outcomes. RESULTS: Among patients with data available on contact lens use, it was found that 93.3% wore contact lenses. The median time from symptom onset to care seeking was 2 days, whereas the median time from symptom onset to diagnosis was 27 days. Keratoplasty was performed in 27 of 81 patients with available outcome data and was more likely in patients >40 years old [odds ratio (OR) 5.25, 95% confidence interval (CI) 1.49-21.92]. When adjusted for age, the risk factors for keratoplasty included the presence of a ring infiltrate (OR 40.00, 95% CI 3.58-447.0) or any sign of stromal invasion (OR 10.48, 95% CI 2.56-55.09). One-third of patients with available data on best-corrected visual acuity had a best-corrected visual acuity <20/200, with the presence of a ring infiltrate as the only significant predictor of this outcome when adjusted for age (aOR 3.45, 95% CI 1.01-12.31). CONCLUSIONS: AK remains challenging to diagnose. Consequently, patients with advanced disease are more likely to have poor outcomes, particularly if they are older. The increasing awareness of AK among general eye care providers may shorten referral times and potentially improve outcomes.


Subject(s)
Acanthamoeba Keratitis/diagnosis , Acanthamoeba Keratitis/epidemiology , Acanthamoeba Keratitis/drug therapy , Acanthamoeba Keratitis/parasitology , Adult , Amebicides/therapeutic use , Female , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors , United States/epidemiology , Visual Acuity , Young Adult
3.
J Refract Surg ; 28(8): 575-86, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22869235

ABSTRACT

PURPOSE: To describe the etiology, diagnosis, clinical course, and management of LASIK interface complications. METHODS: Literature review. RESULTS: Primary interface complications include infectious keratitis, diffuse lamellar keratitis, central toxic keratopathy, pressure-induced stromal keratopathy (PISK), and epithelial ingrowth. Infectious keratitis is most commonly caused by Methicillin-resistant Staphylococcus aureus (early onset) or atypical Mycobacterium (late onset) postoperatively, and immediate treatment includes flap lift and irrigation, cultures, and initiation of broad-spectrum topical antibiotics, with possible flap amputation for recalcitrant cases. Diffuse lamellar keratitis is a white blood cell infiltrate that appears within the first 5 days postoperatively and is acutely responsive to aggressive topical and oral steroid use in the early stages, but may require flap lift and irrigation to prevent flap necrosis if inflammation worsens. In contrast, PISK is caused by acute steroid response and resolves only with cessation of steroid use and intraocular pressure lowering. Without appropriate therapy PISK can result in severe optic nerve damage. Central toxic keratopathy mimics stage 4 diffuse lamellar keratitis, but occurs early in the postoperative period and is noninflammatory. Observation is the only effective treatment, and flap lift is usually not warranted. Epithelial ingrowth is easily distinguishable from other interface complications and may be self-limited or require flap lift to treat irregular astigmatism and prevent flap melt. CONCLUSIONS: Differentiating between interface entities is critical to rapid appropriate diagnosis, treatment, and ultimate visual outcome. Although initial presentations may overlap significantly, the conditions can be readily distinguished with close follow-up, and most complications can resolve without significant visual sequelae when treated appropriately.


Subject(s)
Corneal Diseases/etiology , Corneal Diseases/therapy , Corneal Stroma/pathology , Keratomileusis, Laser In Situ/adverse effects , Surgical Flaps/pathology , Corneal Diseases/diagnosis , Corneal Topography , Humans
5.
Ophthalmology ; 119(2): 256-60, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21982414

ABSTRACT

PURPOSE: To report spontaneous corneal clearing with improved visual acuity and central endothelial cell repopulation after Descemet's stripping without endothelial replacement. DESIGN: Interventional case report. METHODS: A 34-year-old woman with bilateral decreased vision secondary to corneal edema from endothelial dysfunction underwent Descemet's stripping endothelial keratoplasty (DSEK) in the right eye and Descemet's stripping only in the left eye. Histopathologic evaluation confirmed a dual diagnosis of Fuchs' endothelial dystrophy and posterior polymorphous membrane dystrophy from Descemet's membrane specimens removed from each eye. After primary graft failure with regraft in the right eye, the second posterior corneal lenticule detached and was removed and not replaced. The cornea cleared, and central endothelial cell repopulation was documented by confocal microscopy. Therefore, Descemet's stripping without endothelial replacement was performed in the left eye. The left cornea also cleared with central endothelial cell repopulation. MAIN OUTCOME MEASURES: Postoperative visual acuity and central endothelial cell repopulation. RESULTS: Endothelial migration after Descemet's stripping alone in the left eye, with probable host endothelial cell repopulation in the right eye. CONCLUSIONS: Endothelial cell migration after Descemet's stripping procedure without insertion of endothelial graft can occur, resulting from host endothelial cell repopulation with corneal clearing and improved visual acuity.


Subject(s)
Corneal Edema/surgery , Descemet Stripping Endothelial Keratoplasty/methods , Fuchs' Endothelial Dystrophy/surgery , Vision Disorders/surgery , Adult , Cell Movement/physiology , Corneal Edema/complications , Corneal Edema/pathology , Endothelium, Corneal/pathology , Female , Fuchs' Endothelial Dystrophy/complications , Fuchs' Endothelial Dystrophy/pathology , Humans , Microscopy, Confocal , Reoperation , Vision Disorders/etiology , Visual Acuity/physiology
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