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1.
Adv Ther ; 33(5): 727-46, 2016 05.
Article in English | MEDLINE | ID: mdl-26935830

ABSTRACT

Endophthalmitis is an intraocular inflammatory condition which may or may not be caused by infective agents. Noninfectious (sterile) endophthalmitis may be attributable to various causes including postoperative retained soft lens matter or toxicity following introduction of other agents into the eye. Infectious endophthalmitis is further subdivided into endogenous and exogenous. In endogenous endophthalmitis there is hematogenous spread of organisms from a distant source of infection whereas in exogenous endophthalmitis direct microbial inoculation may occur usually following ocular surgery or penetrating eye injury with or without intraocular foreign bodies. Acute infective endophthalmitis is usually exogenous induced by inoculation of pathogens following ocular surgery, open-globe injury and intravitreal injections. More infrequently the infective source is internal and septicemia spreads to the eye resulting in endogenous endophthalmitis. Several risk factors have been implicated including immunosuppression, ocular surface abnormalities, poor surgical wound construction, complicated cataract surgery with vitreous loss and certain types of intraocular lens. Comprehensive guidelines and recommendations on prophylaxis and monitoring of surgical cases have been proposed to minimize the risk of acute endophthalmitis. Early diagnosis and prompt management of infective endophthalmitis employing appropriately selected intravitreal antibiotics are essential to optimize visual outcome.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antibiotic Prophylaxis/methods , Endophthalmitis , Vitrectomy/methods , Disease Management , Endophthalmitis/diagnosis , Endophthalmitis/microbiology , Endophthalmitis/therapy , Humans , Visual Acuity
2.
Adv Ther ; 32(7): 705-14, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26183390

ABSTRACT

INTRODUCTION: The present study aimed to identify preoperative factors that predispose the development of subretinal fluid (SRF) following successful macular hole (MH) surgery. METHODS: Thirty-four eyes of 33 consecutive patients that underwent pars plana vitrectomy for idiopathic full-thickness MH surgery were included in this retrospective study. Best corrected visual acuity (BCVA), and spectral domain-optical coherence tomography (OCT) images were evaluated pre- and postoperatively in all cases. Patient's demographic characteristics, stage of MH, measurements of base diameter and minimum aperture diameter of the MH, preoperative foveal vitreomacular traction and selected intra-operative parameters were correlated with the development of postoperative SRF. RESULTS: Postoperative SRF was observed in 15 cases (48%). Total absorption of SRF was observed in 73% of affected eyes and was most commonly seen between the third and the fifth postoperative month. One patient developed lamellar hole leading to full-thickness MH. Postoperative BCVA was similar between the eyes that did and the eyes that did not develop postoperative SRF (0.31 ± 0.2 vs 0.35 ± 0.2; p ≥ 0.05). Development of postoperative SRF was significantly associated with the presence of preoperative foveal vitreomacular traction (p = 0.048), stage II MH (p = 0.017) and smaller size of the closest distance between the MH edges (p = 0.046). CONCLUSIONS: Postoperative SRF is a common occurrence following successful MH surgery. Meticulous evaluation of preoperative clinical and OCT findings may disclose risk factors associated with this condition. Based on our observations, idiopathic holes of early stage appear to be at a higher risk of developing postoperative SRF. This could be a point of interest with the advancing use of enzymatic proteolysis.


Subject(s)
Postoperative Complications/physiopathology , Retinal Perforations/surgery , Subretinal Fluid/physiology , Vitrectomy/adverse effects , Vitrectomy/methods , Aged , Aged, 80 and over , Female , Fovea Centralis/physiopathology , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors , Tomography, Optical Coherence , Visual Acuity
3.
Retina ; 32(8): 1624-8, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22481481

ABSTRACT

PURPOSE: To determine the long-term functional and anatomical outcome of idiopathic uveitic cystoid macular edema (UCME). METHODS: A longitudinal retrospective study was undertaken of the medical records of patients with UCME. All individuals were examined in the uveitis Service at the Moorfields Eye Hospital. The main outcome measures were change in visual acuity and anatomical outcome of UCME at diverse time points. RESULTS: A total of 109 eyes (92 patients) with UCME were included in the analysis. Mean follow-up was 60 ± 45 months (median, 48 months). Mean logarithm of the minimum angle of resolution visual acuity 1 month after the intervention improved significantly (P < 0.001) by 0.21 ± 0.27 and maintained at similar levels throughout the follow-up period. Visual acuity at the final follow-up improved in 75 eyes (69%), was deteriorated in 21 eyes (19%), and remained unchanged in 13 eyes (12%). Younger age and better visual acuity at baseline were associated with more favorable visual outcome (P < 0.001). Optical coherence tomography documentation of improvement or total resolution of UCME was observed in 84 eyes (77%) at the final follow-up. CONCLUSION: Cystoid macular edema is a major complication in uveitis. Current management provides satisfactory long-term results for the majority of those individuals. Visual acuity 1 month after the intervention is usually indicative of the final functional outcome.


Subject(s)
Macular Edema/physiopathology , Uveitis, Anterior/physiopathology , Uveitis, Intermediate/physiopathology , Uveitis, Posterior/physiopathology , Adolescent , Adult , Aged , Aged, 80 and over , Female , Fluorescein Angiography , Follow-Up Studies , Glucocorticoids/therapeutic use , Humans , Macular Edema/diagnosis , Macular Edema/drug therapy , Male , Methylprednisolone/analogs & derivatives , Methylprednisolone/therapeutic use , Methylprednisolone Acetate , Middle Aged , Prednisolone/therapeutic use , Retrospective Studies , Tomography, Optical Coherence , Triamcinolone Acetonide/therapeutic use , Uveitis, Anterior/diagnosis , Uveitis, Anterior/drug therapy , Uveitis, Intermediate/diagnosis , Uveitis, Intermediate/drug therapy , Uveitis, Posterior/diagnosis , Uveitis, Posterior/drug therapy , Visual Acuity/physiology , Young Adult
4.
Retin Cases Brief Rep ; 6(2): 219-21, 2012.
Article in English | MEDLINE | ID: mdl-25390968

ABSTRACT

PURPOSE: The purpose of this study was to report a case of vitreoretinal traction masqueraded as retinal vasculitis. METHODS: An 81-year-old woman with exudative age-related macular degeneration was treated with intravitreal injections of ranibizumab. During routine follow-up, angiographic evidence of focal, segmental, retinal vasculitis, involving both arteries and veins, was noticed in the fellow eye. Clinical examination revealed no sign of ocular inflammation in either eye. RESULTS: Spectralis optical coherence tomography revealed partial posterior vitreous detachment with multiple areas of persisting vitreoretinal adhesion. Focal vasculitis on fluorescein angiography showed absolute correspondence with sites of vitreoretinal traction on optical coherence tomography. Patient was managed by observation and 6 months later, despite persisting fluorescein leak, she was still asymptomatic with no evidence of anterior chamber or vitreous activity. CONCLUSION: This is an exceptional case of pseudovasculitis associated with mechanical traction, representing a variant of vitreomacular traction syndrome. Clinicians should be aware of this unusual manifestation, which may mimic true vasculitis associated with uveitis.

5.
Acta Ophthalmol ; 87(1): 71-6, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19178390

ABSTRACT

PURPOSE: To evaluate intraocular pressure (IOP) control over 24 hours using travoprost and timolol fixed combination (TTFC) administered in the morning or evening in primary open-angle and exfoliative glaucoma. METHODS: Patients were randomized to TTFC administered in either the morning or evening for 8 weeks. Previously treated patients underwent an untreated washout period of 4-6 weeks, after which baseline IOP was required to be > 25 mm Hg and < 38 mmHg (in two readings taken at 10.00 +/- 1 hours). During the treatment period, IOP was measured at 10.00, 14.00, 18.00, 22.00, 02.00 and 06.00 hours. Patients were then treated with the opposite dosing regimen for 8 weeks and IOP measurements were repeated. RESULTS: In 32 subjects who completed the study, the untreated baseline IOP following washout was 27.7 +/- 3.5 mmHg. Both dosing regimens reduced IOP from baseline at each time-point and throughout the 24-hour diurnal curve (p < 0.0001). When treatments were compared directly, evening dosing (18.4 +/- 3.3 mmHg) provided a statistically significant lower 24-hour curve than morning dosing (19.2 +/- 3.5 mmHg; p = 0.001). Evening dosing also resulted in a lower 24-hour IOP fluctuation (3.8 +/- 1.6 mmHg) than morning dosing (5.1 +/- 1.6 mmHg; p = 0.0002) and lower peak IOP (p = 0.0003). CONCLUSIONS: Both morning and evening administration of TTFC provide effective 24-hour IOP reduction, but evening dosing demonstrates better 24-hour pressure control.


Subject(s)
Antihypertensive Agents/administration & dosage , Circadian Rhythm , Cloprostenol/analogs & derivatives , Exfoliation Syndrome/drug therapy , Glaucoma, Open-Angle/drug therapy , Intraocular Pressure/drug effects , Timolol/administration & dosage , Adult , Antihypertensive Agents/adverse effects , Cloprostenol/administration & dosage , Cloprostenol/adverse effects , Cross-Over Studies , Double-Blind Method , Drug Administration Schedule , Drug Combinations , Exfoliation Syndrome/physiopathology , Female , Glaucoma, Open-Angle/physiopathology , Humans , Male , Middle Aged , Prospective Studies , Timolol/adverse effects , Tonometry, Ocular , Travoprost , Visual Acuity
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