ABSTRACT
PURPOSE: to evaluate demarcation laser photocoagulation (DLP) for macula-sparing rhegmatogenous retinal detachments (RRD) with and without symptoms of posterior vitreous separation or progressive visual field defect. METHODS: retrospective, interventional, single surgeon case series of consecutive patients with RRD treated with demarcation laser photocoagulation between March 1999 and February 2008 at an academic center. The null hypothesis was that there exists no difference in the rate of progression for retinal detachment irrespective of the presence ('symptomatic') or absence ('asymptomatic') of symptoms of posterior vitreous separation or visual field defect at presentation. RESULTS: a total of 27 eyes of 26 patients were included in the study. In all, 22 of the 27 eyes (81.4%) did not require additional treatment and remained attached during mean follow-up of 38.4 months. None of the 14 asymptomatic patients required surgery (0%) whereas 5 out of the 13 patients (38.5%) who were symptomatic at presentation required further intervention (p=0.016): one patient required additional laser only and four patients required scleral buckling or vitrectomy. Pre- and post- DLP logMAR visual acuity was 0.15 and 0.14, respectively. CONCLUSION: demarcation laser photocoagulation is an effective alternative to scleral buckling or vitrectomy for treating asymptomatic RRDs. It has a high failure rate among eyes with symptomatic RRD.
Subject(s)
Laser Coagulation/methods , Retinal Detachment/surgery , Adolescent , Adult , Aged , Child , Disease Progression , Female , Follow-Up Studies , Humans , Male , Middle Aged , Retinal Detachment/physiopathology , Retrospective Studies , Visual Acuity , Young AdultABSTRACT
PURPOSE: To report a case of fungal keratitis with consecutive endophthalmitis caused by Microsphaeropsis olivacea. METHODS: Case report. RESULTS: A 51-year-old man developed fungal keratitis and consecutive endophthalmitis after sustaining a penetrating injury to the right eye. Cultures of the aqueous humor yielded M. olivacea. Infection resolved after intraocular fungal debridement, intravitreous amphotericin B, and aggressive topical natamycin and oral fluconazole. Persistent, low-grade smoldering corneal and intraocular inflammation required topical corticosteroid therapy. CONCLUSION: M. olivacea is an exceedingly rare ocular pathogen. The intraocular portion of the infection responded quickly to intravitreal antifungal treatment; however, the course was prolonged by smoldering corneal inflammation. Prompt recognition of intraocular spread and aggressive treatment may be beneficial in fungal infections caused by unusual organisms with uncertain virulence.
Subject(s)
Endophthalmitis/microbiology , Eye Infections, Fungal/microbiology , Eye Injuries, Penetrating/microbiology , Keratitis/microbiology , Mitosporic Fungi/isolation & purification , Mycoses/microbiology , Prednisolone/analogs & derivatives , Antifungal Agents/therapeutic use , Aqueous Humor/microbiology , Corneal Injuries , Debridement , Endophthalmitis/diagnosis , Endophthalmitis/drug therapy , Eye Infections, Fungal/diagnosis , Eye Infections, Fungal/drug therapy , Eye Injuries, Penetrating/diagnosis , Eye Injuries, Penetrating/drug therapy , Humans , Keratitis/diagnosis , Keratitis/drug therapy , Lens, Crystalline/injuries , Male , Middle Aged , Mycoses/diagnosis , Mycoses/drug therapy , Prednisolone/therapeutic useSubject(s)
Purpura, Thrombotic Thrombocytopenic/complications , Retinal Artery Occlusion/etiology , Retinal Vein Occlusion/etiology , Adult , Blindness/etiology , Female , Humans , Purpura, Thrombotic Thrombocytopenic/pathology , Retinal Artery Occlusion/pathology , Retinal Vein Occlusion/pathology , Retinal Vessels/pathology , Visual AcuityABSTRACT
PURPOSE: To report a case of persistent polymicrobial postoperative endophthalmitis caused by Alcaligenes xylosoxidans and Propionibacterium acnes in a pseudophakic eye. A. xylosoxidans is a gram-negative bacteria resistant to most antibiotics. METHODS: Case report. RESULTS: A 72-year-old man presented with clinical signs of endophthalmitis on the first postoperative day after a phacoemulsification procedure with posterior chamber intraocular lens, left eye. Initial treatment included topical, subconjunctival, and oral antibiotics. After initial clearing, there was recrudescence of infection on postoperative day 37 that prompted referral of the patient to the Cullen Eye Institute. Treatment at that time included anterior chamber and vitreous taps with intravitreal antibiotic injections. Complete pars plana vitrectomy and intraocular lens explantation were eventually required because of persistent infection with a resistant organism. Cultures from the first procedure grew A. xylosoxidans and P. acnes. Cultures from the vitrectomy grew only A. xylosoxidans. At the final follow-up visit 6 months after the initial procedure. The eye was without inflammation with best-corrected visual acuity of 20/40. CONCLUSION: Both A. xylosoxidans and P. acnes can cause chronic progressive endophthalmitis after cataract extraction often resistant to corrective antibiotic therapy. Successful intervention may require complete vitrectomy with intraocular lens and capsule removal.
Subject(s)
Alcaligenes/isolation & purification , Endophthalmitis/microbiology , Eye Infections, Bacterial/microbiology , Gram-Negative Bacterial Infections/microbiology , Gram-Positive Bacterial Infections/microbiology , Postoperative Complications/microbiology , Propionibacterium acnes/isolation & purification , Pseudophakia/microbiology , Aged , Anti-Bacterial Agents , Aqueous Humor/microbiology , Device Removal , Drug Therapy, Combination/therapeutic use , Endophthalmitis/therapy , Eye Infections, Bacterial/therapy , Gram-Negative Bacterial Infections/therapy , Gram-Positive Bacterial Infections/therapy , Humans , Lens Implantation, Intraocular , Male , Phacoemulsification , Postoperative Complications/therapy , Vitrectomy , Vitreous Body/microbiologyABSTRACT
PURPOSE: To report an unusual case of familial exudative vitreoretinopathy in an infant. METHODS: Case report. A 6-day-old girl had unilateral microphthalmia in the right eye, with a retrolental plaque initially diagnosed as persistent hyperplastic primary vitreous. Three months later, peripheral retinal vascular changes and a fibrovascular ridge were noted in the left eye, suggesting familial exudative vitreoretinopathy as the cause in both eyes. RESULTS: The microphthalmic right eye was unsalvageable. The left eye developed an exudative retinal detachment despite photocoagulation of the peripheral avascular retina. Additional cryotherapy resulted in resolution of the detachment and regression of the vascular changes. CONCLUSIONS: With highly asymmetric involvement, neonatal familial exudative vitreoretinopathy can mimic persistent hyperplastic primary vitreous. Fellow eye involvement can progress rapidly.
