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1.
Ophthalmology ; 108(10): 1789-95, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11581050

ABSTRACT

PURPOSE: To report the long-term outcomes of patients with iridocorneal endothelial (ICE) syndrome who required surgery for glaucoma. DESIGN: Retrospective, noncomparative case series. PARTICIPANTS: Twenty-six patients with ICE syndrome who underwent surgery for glaucoma at one institution between January 1987 and January 2000. MAIN OUTCOME MEASURES: Intraocular pressure (IOP), visual acuity, number of glaucoma medications, and further surgical interventions were measured. RESULTS: Five eyes had a trabeculectomy with an antifibrotic agent alone, seven eyes had a trabeculectomy with an antifibrotic agent and a subsequent glaucoma drainage implant (GDI), and 14 eyes had a GDI alone. In eyes that underwent a trabeculectomy with an antifibrotic agent, preoperative IOP was reduced from a mean of 38.8 +/- 10.5 mmHg on 2.3 +/- 0.8 glaucoma medications to a mean of 11.8 +/- 4.3 mmHg on 1.2 +/- 1.4 medications at last follow-up after surgery (83.8 +/- 40.3 months). In eyes that underwent GDI surgery, preoperative IOP was reduced from a mean of 35.2 +/- 13.0 mmHg on 2.0 +/- 1.3 glaucoma medications to a mean of 8.7 +/- 11.2 mmHg on 1.2 +/- 1.1 medications at last follow-up after surgery (50.5 +/- 40.7 months). Twenty-four eyes (92%) had an IOP less than 22 mmHg, and 22 eyes (85%) had visual acuity 20/400 or better at last follow-up (55.8 +/- 41.5 months). Mean number of glaucoma surgeries per patient over the follow-up period was 1.6 +/- 1.2. Trabeculectomy with antifibrotic agents had a survival of 73% at 1 year, 44% at 3 years, and 29% at 5 years. Glaucoma drainage implants had a survival of 71% at 1 year, 71% at 3 years, and 53% at 5 years. CONCLUSIONS: Glaucoma associated with ICE syndrome can be managed successfully surgically, although multiple procedures are often needed.


Subject(s)
Corneal Diseases/complications , Endothelium, Corneal/pathology , Glaucoma/surgery , Iris Diseases/complications , Adult , Antihypertensive Agents/therapeutic use , Fluorouracil/therapeutic use , Follow-Up Studies , Glaucoma/etiology , Glaucoma Drainage Implants , Humans , Intraocular Pressure , Middle Aged , Mitomycin/therapeutic use , Reoperation , Syndrome , Tissue Adhesions , Trabeculectomy , Treatment Outcome , Visual Acuity
2.
Am J Ophthalmol ; 132(2): 261-3, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11476693

ABSTRACT

PURPOSE: To report acute onset lens particle glaucoma associated with pseudoexfoliation-related dislocation of an intraocular lens implant 12 years after cataract surgery. METHODS: Case report. RESULTS: An 80-year-old woman presented with acute onset of left eye pain that was associated with white fleck-like particles circulating in the anterior chamber and an intraocular pressure of 48 mm Hg. The posterior chamber intraocular lens within the capsular bag was positioned more posteriorly to the iris plane than usual, and pseudoexfoliative material was present on the lens capsule and the zonules. Anterior chamber aspirate confirmed the presence of lens cortical fibers. CONCLUSION: Spontaneous dislocation of the posterior chamber intraocular lens in patients with pseudoexfoliation syndrome several years after cataract surgery may liberate lens cortical material, causing lens particle glaucoma.


Subject(s)
Exfoliation Syndrome/complications , Foreign-Body Migration/etiology , Glaucoma, Angle-Closure/etiology , Lens Subluxation/etiology , Lenses, Intraocular , Acute Disease , Aged , Aged, 80 and over , Cataract Extraction , Exfoliation Syndrome/diagnosis , Exfoliation Syndrome/surgery , Female , Foreign-Body Migration/diagnosis , Foreign-Body Migration/surgery , Glaucoma, Angle-Closure/diagnosis , Glaucoma, Angle-Closure/surgery , Humans , Intraocular Pressure , Lens Subluxation/diagnosis , Lens Subluxation/surgery , Pain/etiology , Visual Acuity
3.
Ophthalmology ; 106(10): 2033-7, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10519604

ABSTRACT

OBJECTIVE: To determine whether brimonidine 0.2% can control intraocular pressure (IOP) spikes as well as apraclonidine 1.0% can in those patients undergoing argon laser trabeculoplasty (ALT). DESIGN: Prospective, randomized, double-masked, clinical trial. PARTICIPANTS: A total of 56 eyes of 41 patients with open-angle glaucoma or ocular hypertension were entered in the study; 46 eyes of 41 patients were eventually used for the final analysis. INTERVENTION: Patients were randomized to receive either brimonidine 0.2% or apraclonidine 1.0% before and after 360 degrees ALT. Both patient and physician were masked as to which agent each patient received. MAIN OUTCOME MEASURES: Intraocular pressure measurements were recorded before surgery and at 1, 2, and 4 hours after surgery. The difference between the preoperative IOP (baseline) and the highest recorded postoperative IOP was recorded as the maximum IOP change. The mean of the maximum IOP change for each group was analyzed using a two-sample, one-tailed t test. RESULTS: The mean of the maximum IOP change in the brimonidine 0.2% group was -2.6+/-3.6 mmHg, and the mean for the apraclonidine 1.0% group was -2.3+/-3.7 mmHg (P = 0.8). No patient had a pressure spike greater than 10 mmHg. CONCLUSIONS: Brimonidine 0.2% appears to be as effective as apraclonidine 1.0% in preventing IOP spikes after argon laser trabeculoplasty.


Subject(s)
Adrenergic alpha-Agonists/therapeutic use , Clonidine/analogs & derivatives , Intraocular Pressure/drug effects , Laser Therapy , Quinoxalines/therapeutic use , Trabeculectomy/methods , Adrenergic alpha-Agonists/administration & dosage , Aged , Brimonidine Tartrate , Clonidine/administration & dosage , Clonidine/therapeutic use , Double-Blind Method , Female , Glaucoma, Open-Angle/therapy , Humans , Male , Middle Aged , Ocular Hypertension/therapy , Ophthalmic Solutions/administration & dosage , Ophthalmic Solutions/therapeutic use , Prospective Studies , Quinoxalines/administration & dosage
4.
J Pediatr Ophthalmol Strabismus ; 35(5): 264-9; 286-7, 1998.
Article in English | MEDLINE | ID: mdl-9782437

ABSTRACT

BACKGROUND: Prophylactic administration of an antiemetic is a common procedure for patients undergoing strabismus surgery. Droperidol and ondansetron hydrochloride are commonly used antiemetics. This study compared the rates of postoperative nausea and vomiting (PONV) in adult patients undergoing strabismus surgery with prophylactically administered Droperidol or ondansetron hydrochloride. METHODS: A double-masked, randomized, prospective study was conducted comparing droperidol with ondansetron hydrochloride when administered prophylactically to adults undergoing strabismus surgery. RESULTS: Forty-five patients entered the study with a mean age of 30 years. Twenty percent of patients had nausea immediately postoperatively and 37% had nausea before discharge with no significant differences between groups. Overall rate of emesis, time in the recovery room, and time to discharge was not significantly different between the droperidol and ondansetron hydrochloride group. CONCLUSION: No real differences in the ability to prevent PONV between the two medications were found in this study.


Subject(s)
Antiemetics/therapeutic use , Droperidol/therapeutic use , Nausea/prevention & control , Ondansetron/therapeutic use , Strabismus/surgery , Vomiting/prevention & control , Adolescent , Adult , Aged , Double-Blind Method , Follow-Up Studies , Humans , Middle Aged , Postoperative Complications/prevention & control , Prospective Studies , Treatment Outcome
5.
J Ocul Pharmacol Ther ; 14(1): 1-4, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9493778

ABSTRACT

To determine if pilocarpine 4% produces miosis when delivered via a spray, eleven eyes of ten patients undergoing a laser peripheral iridotomy for occludable angles were pretreated with one application of pilocarpine spray to closed eyelids. Standardized pupil photographs for pupil diameter measurements were taken before and thirty minutes after the spray. Contralateral eyes served as controls (9 eyes) All treated eyes achieved miosis. The mean pupil diameter in the treated group was 4.1+/-0.9 mm before the spray and 1.5+/-0.3 mm after the spray (p < 0.0001). The average change in pupil diameter in the treated group was 2.6+/-0.9 mm compared to 0.0+/-0.2 mm in the control eyes (p < 0.0001). Pilocarpine spray is an effective delivery modality for intraocular miosis.


Subject(s)
Miotics/administration & dosage , Pilocarpine/administration & dosage , Pupil/drug effects , Aerosols , Humans , Miosis/chemically induced , Nebulizers and Vaporizers , Pupil/physiology
6.
Acad Emerg Med ; 4(2): 142-3, 147-9, 1997 Feb.
Article in English | MEDLINE | ID: mdl-9043543
7.
Fam Med ; 25(8): 536-9, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8405803

ABSTRACT

BACKGROUND: The Medical Outcomes Study Short-Form General Health Survey (MOS-SF) and the Duke Health Profile (DUKE) are brief, reliable, valid, and practical health status measures with potential applications in clinical research. We compared patient acceptance, ease of completion, and adequacy of capture (of the patient's self-perception of health) of these instruments in a primary care setting. METHODS: The MOS-SF, DUKE, and assessment questionnaires were administered to 79 patients in a university-based family practice. Patient acceptance of each instrument was assessed with Likert scale questions. Patients then compared the two instruments for relative ease of completion, preference, and completeness of capture. RESULTS: Both forms assessed each item well, but the DUKE scored statistically significantly better than the MOS-SF on four of six patient acceptance questions and both ease of completion items. There were no significant differences for capture items. CONCLUSIONS: Although both instruments are well accepted, investigators may favor the DUKE over the MOS-SF for situations in which patient acceptance or ease of completion is a key issue.


Subject(s)
Health Status Indicators , Patient Acceptance of Health Care , Adult , Family Practice , Female , Humans , Male , North Carolina , Patient Satisfaction , Surveys and Questionnaires/standards
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