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1.
Retina ; 41(6): 1242-1250, 2021 Jun 01.
Article in English | MEDLINE | ID: mdl-33079789

ABSTRACT

PURPOSE: To evaluate the clinical course of patients with neovascular age-related macular degeneration (nAMD) after developing endophthalmitis during their treatment with intravitreal injections. METHODS: Multicenter, retrospective series. RESULTS: From April 2013 to October 2018, 196,598 intravitreal anti-vascular endothelial growth factor (VEGF) injections were performed, with 75 cases of endophthalmitis (incidence 0.0381%). There was no association between intravitreal anti-VEGF drug (P = 0.29), anesthetic method (P = 0.26), povidone concentration (P = 0.22), or any intraprocedure variable and endophthalmitis incidence. Seventy-two patients (96%) were treated with intravitreal tap and inject , while 3 underwent immediate pars plana vitrectomy. After endophthalmitis resolution, 17 patients (22.7%) were not re-treated for nAMD (in 10 cases due to inactive disease; follow-up, 115 Ā± 8.4 weeks). Patients required less frequent anti-VEGF injections after infection (7.4 Ā± 0.61 weeks vs. 11.5 Ā± 1.8 weeks; P = 0.004). Preinfection logarithm of the minimum angle of resolution visual acuity was 0.585 Ā± 0.053 (Ć¢ĀˆĀ¼20/77). It worsened with endophthalmitis (1.67 Ā± 0.08, Ć¢ĀˆĀ¼20/935; P < 0.001) and again on postendophthalmitis treatment day 1 (1.94 Ā± 0.064; count fingers; P < 0.001), but improved after reinitiating nAMD therapy (1.02 Ā± 0.11; Ć¢ĀˆĀ¼20/209; P < 0.001). Better visual acuity on postendophthalmitis week 1 (P = 0.002) and reinitiation of nAMD treatment (P = 0.008) were associated with better final visual acuity, and streptococcal culture with worse visual acuity (P = 0.028). The postendophthalmitis treatment interval was associated with the anti-VEGF drug used (aflibercept = ranibizumab > bevacizumab; P < 0.001). CONCLUSION: Patients with nAMD required fewer injections after endophthalmitis, suggesting a biological change in disease activity. Neovascular age-related macular degeneration became quiescent in 13.3% of eyes. Most achieved better outcomes with anti-VEGF reinitiation.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Endophthalmitis/etiology , Risk Assessment/methods , Wet Macular Degeneration/drug therapy , Aged , Aged, 80 and over , Angiogenesis Inhibitors/adverse effects , Endophthalmitis/epidemiology , Female , Humans , Incidence , Intravitreal Injections/adverse effects , Male , Middle Aged , Retrospective Studies , Risk Factors , Tomography, Optical Coherence/methods , United States/epidemiology , Vascular Endothelial Growth Factor A/antagonists & inhibitors , Visual Acuity , Wet Macular Degeneration/diagnosis
2.
Article in English | MEDLINE | ID: mdl-38276812

ABSTRACT

Mercury (Hg) is a toxic metal that is easily released into the atmosphere as a gas or a particulate. Since Hg has serious health impacts based on human exposure, it is a major concern where it accumulates. Southern Florida is a region of high Hg deposition in the United States. It has entered the southern Florida environment for over 56 MY. For the past 3000 to 8000 years, Hg has accumulated in the Everglades peatlands, where approximately 42.3 metric tons of Hg was deposited. The pre-industrial source of mercury that was deposited into the Everglades was from the atmosphere, consisting of combined Saharan dust and marine evasion. Drainage and the development of the Everglades for agriculture, and other mixed land uses have caused a 65.7% reduction in the quantity of peat, therefore releasing approximately 28 metric tons of Hg into the southern Florida environment over a period of approximately 133 years. Both natural and man-made fires have facilitated the Hg release. The current range in mercury release into the southern Florida environment lies between 994.9 and 1249 kg/yr. The largest source of Hg currently entering the Florida environment is from combined atmospheric sources, including Saharan dust, aerosols, sea spray, and ocean flux/evasion at 257.1-514.2 kg/yr. The remobilization of Hg from the Everglades peatlands and fires is approximately 215 kg/yr. Other large contributors include waste to energy incinerators (204.1 kg/yr), medical waste and crematory incinerators (159.7+ kg/yr), and cement plant stack discharge (150.6 kg/yr). Minor emissions include fuel emissions from motorized vehicles, gas emissions from landfills, asphalt plants, and possible others. No data are available on controlled fires in the Everglades in sugar farming, which is lumped with the overall peatland loss of Hg to the environment. Hg has impacted wildlife in southern Florida with recorded excess concentrations in fish, birds, and apex predators. This bioaccumulation of Hg in animals led to the adoption of regulations (total maximum loads) to reduce the impacts on wildlife and warnings were given to consumers to avoid the consumption of fish that are considered to be contaminated. The deposition of atmospheric Hg in southern Florida has not been studied sufficiently to ascertain where it has had the greatest impacts. Hg has been found to accumulate on willow tree leaves in a natural environment in one recent study. No significant studies of the potential impacts on human health have been conducted in southern Florida, which should be started based on the high rates of Hg fallout in rainfall and known recycling for organic sediments containing high concentrations of Hg.


Subject(s)
Mercury , Animals , Humans , Mercury/analysis , Public Health , Florida , Environmental Monitoring , Fishes , Dust
3.
Retina ; 33(2): 387-91, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23064425

ABSTRACT

PURPOSE: To describe the effect of scleral buckle (SB) removal on preoperative symptoms and signs prompting removal and to assess the risk of recurrent retinal detachment (RD) after SB removal. METHODS: A retrospective study of 36 patients who underwent SB removal between August 1988 and December 2007 was performed. Indications for SB removal, presence or absence of pain or diplopia, and recurrence of RD were recorded. Composite RD rates were estimated from previously published studies and stratified into those occurring during the previtrectomy era versus later (1980 to present). RESULTS: Mean follow-up time was 75.5 months after SB removal. Thirty-two of 33 patients (97%) who had preoperative pain had symptom relief. Twelve of 12 patients who had clinical infection had resolution. Of the four patients with diplopia, two experienced complete resolution and two reported substantial improvement but required prisms to obtain single vision. Four of 34 patients (12%) whose retinas were attached at the time of SB removal developed recurrent RD but were successfully repaired without significant visual loss from the RD. CONCLUSION: Scleral buckle removal is effective in eliminating SB-related pain and infection. Symptomatic diplopia can sometimes improve after SB removal. The rates of RD after SB removal observed in this study (12%) and in others performed in the era of vitrectomy were notably lower than those of previous reports.


Subject(s)
Device Removal , Diplopia/therapy , Eye Infections/therapy , Eye Pain/therapy , Retinal Detachment/surgery , Scleral Buckling/adverse effects , Vitrectomy , Diplopia/etiology , Eye Infections/etiology , Eye Pain/etiology , Female , Follow-Up Studies , Humans , Male , Middle Aged , Recurrence , Retinal Detachment/etiology , Retrospective Studies , Time Factors
4.
Ophthalmology ; 117(1): 49-54, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19815281

ABSTRACT

PURPOSE: To determine if the 1-month postoperative error of predicted refraction of the first eye can be used to alter intraocular lens (IOL) power selection and improve refractive results for the second eye in patients undergoing bilateral, sequential phacoemulsification with IOL implantation (phaco/IOL). DESIGN: Retrospective, consecutive, case series. PARTICIPANTS: Three hundred consecutive patients who underwent uncomplicated bilateral, sequential phaco/IOL between January 1, 2006, and December 31, 2007, by a single surgeon using a single IOL platform. METHODS: The observed second eye 1-month postoperative spherical equivalent refractive error was compared with calculations of the hypothetic 1-month postoperative spherical equivalent refractive error if the first eye error had been fully or partially incorporated into the choice of IOL power for the second eye. The optimal amount of partial adjustment was determined. MAIN OUTCOME MEASURES: The error of predicted refraction: the difference between the actual or hypothetic spherical equivalent refractive errors and those predicted by preoperative calculations. RESULTS: A total of 206 patients met inclusion criteria. The average of the absolute value of the unadjusted second eye error (|E(UNADJ)|) was +0.44 diopters (D) compared with +0.42 D for the fully adjusted second eye error (|E(FULL)|). The optimal amount of adjustment of the second eye IOL power was determined to be 50%; the average of the absolute value of this partially adjusted second eye error (|E(PARTIAL,50%)|) was +0.36 D; this was statistically different from |E(UNADJ)| (P<0.0001) and |E(FULL)| (P = 0.001). The statistically significant benefit was observed for patients with either myopic or hyperopic errors in the first eye. The percentages of patients achieving postoperative refractions within 0.5 D and 1.0 D of the predicted refraction were 66.5% and 90.3%, respectively, for the unadjusted second eye, 67.0% and 90.8%, respectively, for the hypothetic fully adjusted second eye, and 74.3% and 93.7%, respectively, for the hypothetic partially adjusted (50%) second eye. CONCLUSIONS: Accounting for 50% of the observed error of predicted refraction of the first eye reduced the error of predicted refraction in the second eye. This novel methodology has the potential to improve the refractive outcomes in the second eye of patients with cataract. FINANCIAL DISCLOSURE(S): The author(s) have no proprietary or commercial interest in any materials discussed in this article.


Subject(s)
Lens Implantation, Intraocular , Lenses, Intraocular , Phacoemulsification , Refraction, Ocular/physiology , Refractive Errors/prevention & control , Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Optics and Photonics , Preoperative Care , Refractive Errors/diagnosis , Retrospective Studies , Young Adult
6.
Article in English | MEDLINE | ID: mdl-33198342

ABSTRACT

Isopropylbenzene (cumene) is commonly encountered in groundwater at petroleum release sites due to its natural occurrence in crude oil and historical use as a fuel additive. The cumene concentrations detected at these sites often exceed regulatory guidelines or standards for states with stringent groundwater regulations. Recent laboratory analytical data collected at historical petroleum underground storage tank (UST) release sites have revealed that cumene persists at concentrations exceeding the default cleanup criterion, while other common petroleum constituents are below detection limits or low enough to allow natural attenuation as a remediation strategy. This effectively makes cumene the driver for active remediation at some sites. An insignificant amount of research has been conducted for the in-situ remediation of cumene. Sulfate Enhanced Biodegradation (SEB) is evaluated in a field case study. The results from the field case study show an approximate 92% decrease in plume area following three rounds of SEB injections. An additional objective of this research was to determine the cumene concentration in fuels currently being used to determine future impacts. A review of safety data sheets from several fuel suppliers revealed that cumene concentrations in gasoline are reported typically as wide ranges due to the proprietary formulations. Several fuels from different suppliers were analyzed to determine a baseline of cumene concentration in modern fuels. The results of the analysis indicated that cumene accounts for approximately 0.01% (diesel) to 0.13% (premium gasoline) of the overall fuel composition. Cumene generally is considered to be of low human health toxicity, with the principal concern being eye, skin, and respiratory irritation following inhalation of vapors in an occupational setting, but it has been regulated in Florida at very low concentrations based on organoleptic considerations.


Subject(s)
Benzene Derivatives , Biodegradation, Environmental , Environmental Monitoring , Groundwater , Public Health , Sulfates , Benzene Derivatives/analysis , Benzene Derivatives/metabolism , Florida , Groundwater/chemistry , Humans , Sulfates/chemistry , Water Pollutants, Chemical/analysis , Water Pollutants, Chemical/chemistry
7.
Ophthalmic Surg Lasers Imaging ; 40(6): 554-60, 2009.
Article in English | MEDLINE | ID: mdl-19928720

ABSTRACT

BACKGROUND AND OBJECTIVE: To quantify the interpretation of fluorescein angiograms of evolving predominantly classic choroidal neovascularization in age-related macular degeneration. PATIENTS AND METHODS: Thirty-six fluorescein angiograms of predominantly classic choroidal neovascularization were used to define 22 fluorescein angiogram pairs. Imaging software was used to measure surface area and greatest linear dimension (GLD). Six retina physicians estimated the change in surface area and GLD for each pair before and after demarcation of the lesions' borders and GLD. RESULTS: For enlarging lesions, the smallest changes consistently detected by physicians were a 5% to 15% increase in surface area and a 5% to 15% increase in GLD; for shrinking lesions, they were a 5% to 15% decrease in surface area and a 5% to 15% decrease in GLD. Linear regression demonstrated moderate correlation between physician and software estimates of surface area and GLD change (r(2) = 0.50 and 0.67, respectively; P < .001), which was higher with lesion demarcation (r(2) = 0.91 and 0.93, respectively; P < .001). CONCLUSION: Computer-assisted demarcation of lesion surface area and GLD reduced variability in physicians' estimates of choroidal neovascularization size change and improved correlation with software measurements.


Subject(s)
Choroidal Neovascularization/diagnosis , Clinical Competence , Fluorescein Angiography/methods , Macular Degeneration/diagnosis , Choroidal Neovascularization/etiology , Fundus Oculi , Humans , Image Processing, Computer-Assisted/methods , Macular Degeneration/complications , Prospective Studies , Reproducibility of Results
8.
Ophthalmic Surg Lasers Imaging ; 40(2): 201-2, 2009.
Article in English | MEDLINE | ID: mdl-19320315

ABSTRACT

Scleral buckle removal is an uncommon procedure performed for various reasons. Microbiological information on explanted scleral buckles remains limited. The authors identified 37 cases of scleral buckle removal during an 18-year period. Bacterial cultures isolated an organism in 4 of 9 patients (44%) with clinical infection. Organisms identified included methicillin-resistant Staphylococcus aureus, Pseudomonas aeruginosa, Mycobacterium abscessus, and coagulase-negative Staphylococcus species. Bacterial cultures isolated an organism in 3 of 11 patients (27%) without clinical infection. Organisms identified included Nocardia species, Alcaligenes xylosoxidans, and Mycobacterium chelonae. Scleral buckles appearing clinically infected may be associated with more virulent organisms and a greater chance of identifying an organism. Bacterial cultures may be of value for scleral buckles upon removal.


Subject(s)
Bacteria/isolation & purification , Eye Infections, Bacterial/microbiology , Prostheses and Implants , Scleral Buckling/adverse effects , Device Removal , Humans , Middle Aged , Retrospective Studies
9.
Article in English | MEDLINE | ID: mdl-31117171

ABSTRACT

Southern Florida is underlain by rocks and sediments that naturally contain radioactive isotopes. The primary origin of the radioactive isotopes is Miocene-aged phosphate deposits that can be enriched in uranium-238 and its daughter isotopes. Nodular phosphate containing radionuclides from the Miocene has been reworked into younger formations and is ubiquitous in southern Florida. When the nodular phosphate is exposed to groundwater with geochemical conditions favorable for its dissolution, uranium, radium, and radon may be released into the groundwater system. Uranium concentrations have been measured above the 30 Āµg/L drinking water standard at only one location in Lee County. Radium226/228 exceedances of the drinking water standard have been documented in numerous wells in Sarasota County. Indoor radon activities have exceeded the 4 piC/L guideline in five southern Florida counties. The exceedance of radioactivity standards in drinking water does not occur in municipal drinking water supplies, but rather only in some domestic self-supply wells. Health risks for exposure to radiation from domestic self-supply wells could be mitigated by testing of well water and, if necessary, switching to the use of a different aquifer or treatment process. While the risk of exposure to radon in indoor air in southern Florida is generally low, some areas are enriched in soil radon that migrates into structures, which could be addressed by improved ventilation.


Subject(s)
Background Radiation , Geology , Groundwater/chemistry , Soil Pollutants, Radioactive/analysis , Uranium/analysis , Water Pollutants, Radioactive/analysis , Florida , Radiation Monitoring , Radium/analysis , Radon/analysis
10.
Ophthalmol Retina ; 3(1): 3-7, 2019 01.
Article in English | MEDLINE | ID: mdl-30929813

ABSTRACT

PURPOSE: To determine the incidence of endophthalmitis after anti-vascular endothelial growth factor (VEGF) therapy at our institution and to identify potential risk factors for endophthalmitis occurring after injection. DESIGN: Retrospective, single-center cohort study. PARTICIPANTS: All patients who received an intravitreal injection of an anti-VEGF medication between January 1, 2014, and March 31,Ā 2017. METHODS: Current Procedural Terminology and International Classification of Diseases billing codes were used to identify instances of anti-VEGF administration and cases of endophthalmitis. Medical records and injection technique were reviewed carefully in each case. Multivariable logistic regression analysis was performed in a stepwise fashion to determine independent predictors of endophthalmitis based on injection protocol. MAIN OUTCOME MEASURES: Incidence of endophthalmitis after injection and odds of endophthalmitis by injection technique with 95% confidence intervals (CIs). RESULTS: A total of 154 198 anti-VEGF injections were performed during the period of interest, resulting in 58 cases of endophthalmitis (0.038% [1:2659]). After adjustment for confounders, both 2% lidocaine jelly (odds ratio [OR], 11.28; 95% CI, 3.39-37.46; P < 0.001) and 0.5% Tetravisc (Ocusoft, Richmond, TX; OR, 3.95; 95% CI, 1.15-13.50; PĀ = 0.03) use were independent risk factors for endophthalmitis after injection. Lid speculum use, povidone iodine strength (5% vs. 10%), injection location (superior or inferior), conjunctival displacement, use of provider gloves, use of a strict no-talking policy, use of subconjunctival lidocaine, and topical antibiotic use were not statistically significant predictors of endophthalmitis after injection. There was no difference in endophthalmitis rate among the anti-VEGF agents (bevacizumab, ranibizumab 0.3 mg, ranibizumab 0.5 mg, and aflibercept). CONCLUSIONS: The incidence of endophthalmitis after anti-VEGF injections is low. Use of lidocaine jelly or Tetravisc may increase the risk of endophthalmitis after injection.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Endophthalmitis/epidemiology , Eye Infections, Bacterial/epidemiology , Intravitreal Injections/adverse effects , Povidone-Iodine/administration & dosage , Adult , Bevacizumab/administration & dosage , Endophthalmitis/diagnosis , Endophthalmitis/microbiology , Eye Infections, Bacterial/diagnosis , Eye Infections, Bacterial/microbiology , Female , Humans , Incidence , Male , Middle Aged , Ranibizumab/administration & dosage , Retinal Diseases/drug therapy , Retrospective Studies , Risk Factors , Vascular Endothelial Growth Factor A/antagonists & inhibitors
11.
Am J Ophthalmol ; 146(3): 434-439, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18614132

ABSTRACT

PURPOSE: To identify preoperative, perioperative, and postoperative risk factors for scleral buckle (SB) removal. DESIGN: Retrospective, consecutive, matched, case-control study. METHODS: Cases included all patients undergoing SB removal between August 1988 and December 2007 at a single academic center. Cases were matched against four randomly selected control patients who underwent SB implantation during the same year as the case. Odds ratios (OR) were calculated for each factor investigated. RESULTS: Forty cases of SB removal and 148 matched control cases were identified. Three cases of SB removal were omitted from analysis because of incomplete records. Factors associated with SB removal for any reason, using univariate analysis, included concurrent globe-penetrating injury at time of SB placement (OR, 24; 95% confidence interval [CI], 2.9 to 200), concurrent pars plana vitrectomy (PPV) (OR, 17.3; 95% CI, 4.9 to 61), diabetes mellitus (DM) (OR, 7.3; 95% CI, 1.8 to 30), prior chronic topical ocular therapy (OR, 4.3; 95% CI, 1.7 to 11), and subsequent ocular procedures (OR, 3.4; 95% CI, 1.5 to 7.5). Factors independently associated with SB removal using multivariate analysis included concurrent globe-penetrating injury (OR, 27.3; 95% CI, 1.7 to 426), concurrent PPV (OR, 11.3; 95% CI, 2.9 to 45), DM (OR, 8.9; 95% CI, 1.3 to 58), and subsequent ocular procedures (OR, 3.9; 95% CI, 1.4 to 11). Factors that did not alter SB removal risk included patient age; gender; and type, size, or location of buckling elements used. CONCLUSIONS: Awareness of these risk factors may be valuable for the surgical planning of retinal detachment repair in patients at higher risk for subsequent SB removal and for risk stratification subsequent to SB implantation.


Subject(s)
Device Removal , Retinal Detachment/surgery , Scleral Buckling/instrumentation , Adolescent , Adult , Aged , Aged, 80 and over , Case-Control Studies , Child , Child, Preschool , Diabetes Complications , Female , Humans , Infant , Intraoperative Complications , Male , Middle Aged , Postoperative Complications , Retrospective Studies , Rheumatic Diseases/complications , Risk Factors
12.
Article in English | MEDLINE | ID: mdl-30336588

ABSTRACT

Florida geologic units and soils contain a wide range in concentrations of naturally-occurring arsenic. The average range of bulk rock concentrations is 1 to 13.1 mg/kg with concentrations in accessary minerals being over 1000 mg/kg. Florida soils contain natural arsenic concentrations which can exceed 10 mg/kg in some circumstances, with organic-rich soils often having the highest concentrations. Anthropogenic sources of arsenic have added about 610,000 metric tons of arsenic into the Florida environment since 1970, thereby increasing background concentrations in soils. The anthropogenic sources of arsenic in soils include: pesticides (used in Florida beginning in the 1890's), fertilizers, chromated copper arsenate (CCA)-treated wood, soil amendments, cattle-dipping vats, chicken litter, sludges from water treatment plants, and others. The default Soil Cleanup Target Level (SCTL) in Florida for arsenic in residential soils is 2.1 mg/kg which is below some naturally-occurring background concentrations in soils and anthropogenic concentrations in agricultural soils. A review of risk considerations shows that adverse health impacts associated with exposure to arsenic is dependent on many factors and that the Florida cleanup levels are very conservative. Exposure to arsenic in soils at concentrations that exceed the Florida default cleanup level set specifically for residential environments does not necessarily pose a meaningful a priori public health risk, given important considerations such as the form of arsenic present, the route(s) of exposure, and the actual circumstances of exposure (e.g., frequency, duration, and magnitude).


Subject(s)
Arsenic , Environmental Exposure , Groundwater/chemistry , Soil Pollutants , Soil/chemistry , Animals , Arsenates , Fertilizers , Florida , Pesticides , Risk , Sewage , Water , Water Pollutants, Chemical , Water Purification , Wood
13.
Ophthalmology ; 114(2): 221-6, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17156845

ABSTRACT

PURPOSE: To describe our technique and early results of Descemet's stripping and automated endothelial keratoplasty (DSAEK), identify perioperative complications, and discuss their management. DESIGN: Prospective, noncomparative, surgical case series. PARTICIPANTS: Twenty-six eyes of 26 patients who had corneal edema from Fuchs' endothelial dystrophy, pseudophakic bullous keratopathy, or aphakic bullous keratopathy. INTERVENTION: The donor corneal lenticule was prepared using a microkeratome and an artificial anterior chamber maintainer. Stripping of the diseased host endothelium was performed under viscoelastic using a 2.75-mm clear corneal temporal incision. The incision was enlarged to approximately 4.2 mm to allow placement of a folded 8.5-mm-diameter donor corneal lenticule. The donor graft was positioned using a temporary air bubble that was partially evacuated after 7 minutes. The corneal wound was closed with a single 10-0 nylon suture. MAIN OUTCOME MEASURES: Preoperative and postoperative best spectacle-corrected visual acuity (BSCVA), manifest refraction, keratometry, topographic astigmatism, corneal pachymetry, and perioperative complications. RESULTS: Three months postoperatively, all donor grafts remained clear. The average 3-month postoperative BSCVA was 20/45 (range, 20/20-20/150). The average change in refractive astigmatism was 0.12+/-1.15 diopters (D) (range, -1.50 to 3.25). In patients who underwent simple DSAEK (i.e., no intraocular lens implantation), the average postoperative shift in spherical equivalent refractive error was 1.15+/-1.35 D (range, -0.25 to +4.25). Nine of 26 initial grafts dislocated postoperatively and had to be repositioned. Three of the repositioned grafts dislocated again and were replaced with new donor corneal lenticules, all of which remained clear. CONCLUSIONS: Descemet's stripping and automated endothelial keratoplasty uses a mechanical microkeratome to harvest the donor corneal lenticule and mechanical stripping of the diseased host endothelium and Descemet's membrane. Despite a smooth graft-host interface, only 2 patients in the series achieved > or =20/25 vision. The average visual results were comparable to vision after deep lamellar endothelial keratoplasty. Although patients experienced excellent postoperative acuity with minimally induced surgical astigmatism, nearly one third of the donor lenticules needed to be either repositioned or replaced. Nevertheless, DSAEK offers significant advantages over standard penetrating keratoplasty for patients with Fuchs' dystrophy in pseudophakic bullous keratopathy.


Subject(s)
Corneal Transplantation/methods , Descemet Membrane/surgery , Endothelium, Corneal/transplantation , Fuchs' Endothelial Dystrophy/surgery , Aged , Aged, 80 and over , Astigmatism/physiopathology , Blister/physiopathology , Blister/surgery , Corneal Topography , Descemet Membrane/physiology , Endothelium, Corneal/physiology , Female , Fuchs' Endothelial Dystrophy/physiopathology , Graft Survival , Humans , Intraoperative Complications , Male , Microsurgery , Middle Aged , Postoperative Complications , Prognosis , Prospective Studies , Refraction, Ocular/physiology , Visual Acuity/physiology
14.
Ophthalmology ; 114(7): 1272-7, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17433835

ABSTRACT

PURPOSE: To evaluate visual acuity (VA), graft clarity, and refractive outcome of Descemet's stripping and automated endothelial keratoplasty (DSAEK) combined with phacoemulsification and intraocular lens (IOL) implantation in patients with coexisting Fuchs' endothelial dystrophy and immature senile cataracts. DESIGN: Pilot, prospective, noncomparative, surgical case series. PARTICIPANTS: Twenty-one eyes of 21 consecutive patients with coexisting visually significant immature senile cataracts and Fuchs' corneal dystrophy with guttata of Descemet's membrane and either microcystic epithelial edema or stromal edema presenting to a single academic eye institute. METHODS: All patients underwent phacoemulsification and posterior chamber IOL implantation through temporal clear corneal incision, followed by DSAEK. The intent was to render all eyes as close to emmetropia as possible. MAIN OUTCOME MEASURES: Six-month postoperative best spectacle-corrected VA (BSCVA), refractive spherical equivalent (SE), refractive astigmatism, and keratometry. RESULTS: Average BSCVAs were 20/68 preoperatively and 20/34 postoperatively (P<0.0001). The postoperative SE refractive error was +0.45 diopters (D), on average +1.13 D more hyperopic than predicted by preoperative lens power calculations. Overall, 13 patients (62%) were within 1.00 D and 21 (100%) were within 2.00 D of emmetropia postoperatively. Preoperative and postoperative average refractive astigmatisms were 1.46 D and 1.56 D, respectively (P = 0.69). Complications included graft dislocations requiring repositioning (3), 2 of which experienced recurrent dislocation requiring reoperation with a new graft; acute graft rejection (3); and pupillary block glaucoma (2). CONCLUSIONS: This pilot case series of 6-month results of DSAEK combined with phacoemulsification and IOL implantation suggests that it provides rapid visual rehabilitation with predictable refractive outcomes.


Subject(s)
Cataract Extraction , Cataract/complications , Corneal Transplantation , Descemet Membrane/surgery , Fuchs' Endothelial Dystrophy/complications , Fuchs' Endothelial Dystrophy/surgery , Lens Implantation, Intraocular , Phacoemulsification , Aged , Aged, 80 and over , Automation , Female , Fuchs' Endothelial Dystrophy/physiopathology , Humans , Male , Middle Aged , Pilot Projects , Postoperative Period , Prospective Studies , Refraction, Ocular , Treatment Outcome , Visual Acuity
15.
J Cataract Refract Surg ; 33(2): 189-90, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17276256

ABSTRACT

We describe a technique to facilitate unfolding and prevent inversion of the donor corneal lenticule during Descemet's stripping and automated endothelial keratoplasty (DSAEK). The donor corneal lenticule is unfolded in the anterior chamber using a bent 30-gauge needle on a 3 cc air syringe. The needle tip is used to pinion the edge of the lenticule while an air bubble is simultaneously injected between the folded edges of the donor graft. A gentian-violet dye mark placed on the peripheral stromal surface of the donor lenticule is used to confirm proper graft orientation. The simple technique of simultaneously fixating the donor lenticule while injecting air ensures that the graft unfolds correctly and minimizes potential mechanical trauma to the endothelium.


Subject(s)
Corneal Transplantation/methods , Descemet Membrane/surgery , Endothelium, Corneal/transplantation , Humans , Tissue Donors
16.
J Cataract Refract Surg ; 33(12): 2091-7, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18053910

ABSTRACT

PURPOSE: To assess the accuracy of surrogate decision making for elective cataract surgery. SETTING: Comprehensive Ophthalmology Department of Tertiary Care Hospital. METHODS: Decisions regarding elective cataract surgery of currently competent, elderly patients were compared with the predictions of patient-identified surrogate decision makers in scenarios of current state of mental health and progressive dementia. Patients were identified (age >50 years, Mini-Mental Status Score >20, absence of significant noncataract pathology) consecutively at a scheduled clinic visit to a single provider. Preferences for cataract surgery in the current state of health and hypothetical progressive dementia were assessed on a Likert scale. The same interviewer contacted patient-identified surrogate decision makers within 48 hours. Independently, a survey of community ophthalmologists was performed. The concordance of surrogate predictions with patient preferences (32 pairs) was assessed using percentage agreement, the kappa coefficient with dichotomous Likert scale data, and chi-square analyses (concordance beyond chance). RESULTS: In their current state of health, most patients said they would prefer to have surgery if they were deemed to have a visually significant cataract, which was accurately predicted by surrogates (72% agreement, kappa = 0.65, chi square = 16.5). In a hypothetical dementia scenario, contrary to perceptions of patients and their surrogates, proxies were unable to accurately represent a patient's wishes for elective cataract surgery (34% agreement, kappa = 0.23, chi square = 14.4). Physicians tended to withhold intervention in the dementia scenario. CONCLUSIONS: The findings suggest that current methods of decision making in elective surgery for patients unable to make autonomous decisions may be seriously flawed. This extends previous findings of inaccuracy with the substituted judgment approach to end-of-life issues to reflect elective surgical scenarios.


Subject(s)
Cataract Extraction/standards , Decision Making , Elective Surgical Procedures/standards , Third-Party Consent , Aged , Female , Humans , Male , Middle Aged , Reproducibility of Results , Surveys and Questionnaires
17.
J Cataract Refract Surg ; 33(5): 770-2, 2007 May.
Article in English | MEDLINE | ID: mdl-17466845

ABSTRACT

Dislocation of the graft is a well-recognized complication of Descemet's stripping automated endothelial keratoplasty (DSAEK). We describe a technique to promote adhesion of the graft during DSAEK using an anterior chamber air-fluid infusion and exchange for direct control of the pressure and medium used to tamponade the graft against the host stroma.


Subject(s)
Corneal Transplantation/methods , Descemet Membrane/surgery , Endothelium, Corneal/transplantation , Graft Survival/physiology , Acetates , Air , Descemet Membrane/physiology , Drug Combinations , Humans , Minerals , Sodium Chloride , Tissue Adhesions
18.
Cornea ; 26(6): 692-6, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17592318

ABSTRACT

PURPOSE: To report our results of using Descemet stripping and automated endothelial keratoplasty (DSAEK) in eyes with failed penetrating keratoplasty (PK). METHODS: An institutional review board-approved, prospective, surgical case series of 7 eyes of 7 consecutive patients undergoing DSAEK for graft failure after 1 or more PKs at 1 academic eye center. RESULTS: The mean follow-up period was 13.3 months (range, 9-18 months). One eye suffered recurrent donor graft dislocation and elected to undergo repeat PK instead of repeat DSAEK. Of the remaining 6 patients, the average preoperative visual acuity (VA) was 20/851 compared with a best-corrected visual acuity (BCVA) of 20/65 postoperatively (P = 0.008). After DSAEK, 6 (100%) eyes showed improved BCVA, and 4 of 6 eyes (67%) achieved a BCVA of 20/40 or better. All 6 grafts remained clear at the last follow-up visit. Two eyes showed graft dislocation on the first postoperative day and underwent repositioning of the lenticule with good results. Two other eyes were diagnosed with primary iatrogenic graft failure within 1 week of DSAEK and underwent repeat DSAEK with new donor tissue with good results. One eye experienced acute graft rejection that was successfully treated with topical steroids. CONCLUSIONS: This pilot series of DSAEK in eyes with graft failure from previous PK shows favorable VA and graft clarity outcomes. The complications observed were similar to those observed for DSAEK for Fuchs dystrophy and pseudophakic bullous keratopathy and include graft dislocation, iatrogenic graft failure, and homograft rejection.


Subject(s)
Corneal Transplantation/methods , Descemet Membrane/surgery , Endothelium, Corneal/transplantation , Keratoplasty, Penetrating , Adult , Aged , Aged, 80 and over , Female , Follow-Up Studies , Graft Rejection/surgery , Humans , Male , Middle Aged , Pilot Projects , Prospective Studies , Reoperation , Treatment Failure , Treatment Outcome , Visual Acuity
19.
Cornea ; 26(6): 670-4, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17592314

ABSTRACT

PURPOSE: To evaluate visual acuity, refractive outcomes, and endothelial cell density 6 months after Descemet stripping and automated endothelial keratoplasty (DSAEK). METHODS: We performed an institutional review board-approved prospective study of a surgical case series of 34 patients at 2 institutions undergoing DSAEK for Fuchs endothelial dystrophy, pseudophakic bullous keratopathy, or aphakic bullous keratopathy with or without simultaneous phacoemulsification and intraocular lens implantation. Clinical outcomes, including best spectacle-corrected visual acuity (BSCVA), spherical equivalent refraction, and refractive astigmatism and topographic or keratometric astigmatism, were assessed at the 6-month postoperative examination and compared with preoperative values with paired Student t tests. The change in endothelial cell density from the eye bank examination to 6 months after transplantation was similarly evaluated. RESULTS: BSCVA averaged 20/99 preoperatively and 20/42 postoperatively (P < 0.0001). After DSAEK, 30 (88.2%) of 34 patients showed improved BSCVA, and 21 (61.8%) of the 34 patients achieved a BSCVA of 20/40 or better. For patients not undergoing simultaneous phacoemulsification and intraocular lens implantation, a hyperopic shift in refraction of 1.19 +/- 1.32 D was noted. Refractive astigmatism, topographic astigmatism, and keratometry showed no statistically significant change. Endothelial cell density of donor corneas averaged 2826 +/- 370 cells/mm, whereas the mean postoperative density was 1396 +/- 440 cells/mm. This finding corresponded to an average loss of 1426 cells/mm (50% loss; P = 0.0001). The first half of cases experienced an average cell loss of 1674 cells/mm (59% loss) compared with 1181 (41% loss) in the second half of cases (P = 0.005). Three (9%) of 34 grafts experienced iatrogenic graft failure and required reoperation with new donor tissue. Also, 9 (27%) of 34 grafts experienced dislocation in the early postoperative period and required repositioning. CONCLUSIONS: In this prospective study of DSAEK for bullous keratopathy and Fuchs endothelial corneal dystrophy, improvement of visual acuity was achieved with only a mild tendency toward hyperopic shift and without significant induced astigmatism. Endothelial cell loss was significant, however, and may be related to surgical experience.


Subject(s)
Corneal Transplantation/methods , Descemet Membrane/surgery , Endothelium, Corneal/pathology , Endothelium, Corneal/transplantation , Refractive Errors/physiopathology , Visual Acuity/physiology , Aged , Aged, 80 and over , Cell Count , Corneal Diseases/surgery , Corneal Topography , Female , Graft Rejection , Humans , Lens Implantation, Intraocular , Male , Middle Aged , Phacoemulsification , Postoperative Complications , Prospective Studies , Reoperation
20.
Br J Ophthalmol ; 96(5): 723-9, 2012 May.
Article in English | MEDLINE | ID: mdl-22328813

ABSTRACT

PURPOSE: To evaluate the utility of ring ratios in detecting hydroxychloroquine (HCQ) related retinal toxicity using the 103-hexagon multifocal electroretinogram (mfERG). DESIGN: Retrospective cross-sectional study. METHODS: 23 patients taking HCQ were consecutively evaluated for retinal toxicity and divided into those without (HCQ-non-toxic group) and with documented visual field loss (HCQ-toxic group). A control patient group without retinal disease and not on HCQ was used for comparison. 103-hexagon P(1) mfERG amplitude response densities were analysed by averaging the 103 responses into six (age-corrected) concentric rings (R(1)-R(6)), calculating standard ring ratios (R(1):R(2)-R(1):R(6)) and R(5) ring ratios (R(5):R(1)-R(5):R(6)). Receiver operating characteristic curves were used to compare these tests for detecting toxicity. RESULTS: Relative to HCQ-non-toxic and control groups, the HCQ-toxic group showed generalised reduction of the 103-hexagon mfERG absolute responses most prominent in the foveal/pericentral regions. R(5) ring ratios were superior to standard ring ratios in discriminating the HCQ-toxic from the HCQ-non-toxic and control groups and were approximately equivalent to pericentral absolute ring responses in detecting HCQ retinal toxicity by receiver operating characteristic criteria, with R(5):R(4) and R(5):R(3) ratios performing best. However, R(5) ring ratios revealed improved sensitivity over absolute ring responses (89% vs 73%) at a 95% specificity threshold. CONCLUSIONS: Ring ratio analysis using the R(5) ring response as the 'internal reference ring' appeared equivalent to pericentral absolute ring responses in detecting HCQ retinal toxicity, and possibly superior at clinically desirable specificity thresholds. R(5) ring ratios did not require age correction, a potential clinical advantage over absolute ring responses.


Subject(s)
Antirheumatic Agents/adverse effects , Electroretinography/drug effects , Hydroxychloroquine/adverse effects , Retina/pathology , Retinal Diseases/diagnosis , Adolescent , Adult , Aged , Area Under Curve , Child , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , ROC Curve , Retina/drug effects , Retinal Diseases/chemically induced , Retrospective Studies , Visual Fields
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