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1.
Eye (Lond) ; 25(12): 1598-606, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21921953

ABSTRACT

AIM: To verify the safety and efficacy of Ologen (OLO) implant as adjuvant compared with low-dosage mitomycin-C (MMC) in trabeculectomy. METHODS: This was a prospective randomized clinical trial with a 24-month follow-up. Forty glaucoma patients (40 eyes) were assigned to trabeculectomy with MMC or OLO. Primary outcome includes target IOP at ≤21, ≤17, and ≤15 mm Hg; complete (target IOP without medications), and qualified success (target IOP regardless of medications). Secondary outcomes include bleb evaluation, according to Moorfields Bleb Grading System (MBGS); spectral domain optical coherence tomography (SD-OCT) examination; number of glaucoma medications; and frequency of postoperative adjunctive procedures and complications. RESULTS: The mean preoperative IOP was 26.5 (±5.2) in MMC and 27.3 (±6.0) in OLO eyes, without statistical significance. One-day postoperatively, the IOP dropped to 5.2 (±3.5) and 9.2 (±5.5) mm Hg, respectively (P=0.009). The IOP reduction was significant at end point in all groups (P=0.01), with a mean IOP of 16.0 (±2.9) and 16.5 (±2.1) mm Hg in MMC and OLO, respectively. The rates and Kaplan-Meier curves did not differ for both complete and qualified success at any target IOP. The bleb height in OLO group was higher than MMC one (P<0.05). SD-OCT analysis of successful/unsuccessful bleb in patients with or without complete success at IOP ≤17 mm Hg indicated a sensitivity of 83% and 73% and a specificity of 75% and 67%, respectively, for MMC and OLO groups. No adverse reaction to OLO was noted. CONCLUSIONS: Our results suggest that OLO implant could be a new, safe, and effective alternative to MMC, with similar long-term success rate.


Subject(s)
Collagen/therapeutic use , Cross-Linking Reagents/therapeutic use , Glaucoma/drug therapy , Glaucoma/surgery , Glycosaminoglycans/therapeutic use , Mitomycin/therapeutic use , Trabeculectomy/methods , Absorbable Implants , Aged , Female , Humans , Intraocular Pressure/drug effects , Intraoperative Care , Male , Middle Aged , Prospective Studies , Prostheses and Implants , Tomography, Optical Coherence/methods
2.
Eye (Lond) ; 24(4): 600-7, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19648904

ABSTRACT

PURPOSE: To investigate the long-term effectiveness and safety of botulinum neurotoxin A (BoNT-A) treatment in patients with blepharospasm (BEB), hemifacial spasm (HFS), and entropion (EN) and to use for the first time two modified indexes, 'botulin toxin escalation index-U' (BEI-U) and 'botulin toxin escalation index percentage' (BEI-%), in the dose-escalation evaluation. METHODS: All patients in this multicentre study were followed for at least 10 years and main outcomes were clinical efficacy, duration of relief, BEI-U and BEI-%, and frequency of adverse events. RESULTS: BEB, HFS, and EN patients received a mean BoNT-A dose with a significant inter-group difference (P<0.0005, respectively). The mean (+/-SD) effect duration was statistically different (P=0.009) among three patient groups. Regarding the BoNT-A escalation indexes, the mean (+/-SD) values of BEI-U and BEI-% were statistically different (P=0.035 and 0.047, respectively) among the three groups. In BEB patients, the BEI-% was significantly increased in younger compared with older patients (P=0.008). The most frequent adverse events were upper lid ptosis, diplopia, ecchymosis, and localized bruising. CONCLUSIONS: This long-term multicentre study supports a high efficacy and good safety profile of BoNT-A for treatment of BEB, HFS, and EN. The BEI indexes indicate a significantly greater BoNT-A-dose escalation for BEB patients compared with HFS or EN patients and a significantly greater BEI-% in younger vsolder BEB patients. These results confirm a greater efficacy in the elderly and provide a framework for long-term studies with a more flexible and reliable evaluation of drug-dose escalation.


Subject(s)
Blepharospasm/drug therapy , Botulinum Toxins, Type A/therapeutic use , Entropion/drug therapy , Hemifacial Spasm/drug therapy , Muscle Spasticity/drug therapy , Neuromuscular Agents/therapeutic use , Aged , Aged, 80 and over , Botulinum Toxins, Type A/administration & dosage , Dose-Response Relationship, Drug , Drug Combinations , Female , Follow-Up Studies , Humans , Longitudinal Studies , Male , Middle Aged , Neuromuscular Agents/administration & dosage
3.
Eye (Lond) ; 21(4): 541-6, 2007 Apr.
Article in English | MEDLINE | ID: mdl-16456585

ABSTRACT

PURPOSE: To evaluate the adequacy of common disinfection regimens for disposable tonometer tips and assess if disinfection of reusable prisms or the use of disposable tips is preferable. METHODS: We used disposable tonometer tips, using the same material and tip diameter of standard Goldmann tonometer prism. Strains of Pseudomonas aeruginosa, Staphylococcus aureus, Bacillus subtilisand Candida albicanswere tested according to the European standard guidelines for disinfectants test. Antimicrobial effectiveness of the following disinfection practices has been assessed: dry wipe, Minuten wipes (Alpro), soaking in 3% hydrogen peroxide, 0.5% benzalkonium chloride, and 0.5% Pantasept for 1, 5, and 15 min. All tests have been performed three times and all conditions tested in duplicate. RESULTS: Dry wiping and 1 min soak in 3% hydrogen peroxide were ineffective on all microrganisms. Minuten wipes, 1 min soak in 0.5% benzalkonium chloride or 3% hydrogen peroxide were ineffective on B. subtilis. 0.5% Pantasept soak was effective in 1 min for all microrganisms tested, whereas 3% hydrogen peroxide and 0.5% benzalkonium chloride soaks were effective when performed for at least 5 min. B. subtiliswas the most resistant organism to disinfectant regimes at 1 min time. CONCLUSIONS: Results of our study demonstrate a relative disinfection efficacy for the different evaluated regimens, provided that correct exposure times are adopted for the chosen disinfectants, a condition difficult to ensure in a busy clinic setting. We conclude that disposable prism tonometry provides a safe alternative to Goldmann tonometry.


Subject(s)
Communicable Diseases/transmission , Disinfection/methods , Disposable Equipment , Tonometry, Ocular/instrumentation , Anti-Infective Agents, Local/pharmacology , Bacillaceae Infections/transmission , Bacillus subtilis/drug effects , Benzalkonium Compounds/pharmacology , Candidiasis/transmission , Disinfectants/pharmacology , Humans , Hydrogen Peroxide/pharmacology , Organic Chemicals/pharmacology , Pseudomonas Infections/transmission , Risk Assessment/methods , Staphylococcal Infections/transmission , Tonometry, Ocular/adverse effects
4.
Int Ophthalmol ; 18(6): 363-71, 1994.
Article in English | MEDLINE | ID: mdl-7642339

ABSTRACT

Prevalence of cataract was studied in a population based survey performed in adults aged 40 years or more living in Casteldaccia, a small Sicilian town. Lens opacities of moderate or severe grade (type II or worse, according to the Lens Opacity Classification System II) were found at the following rates: nuclear opalescence in 18.5%, cortical cataract in 12.9%, posterior subcapsular cataract in 10.8%. All these types of cataract were much more frequent in the elderly population and were about 1.5 times more common in women than in men. Late cataract was found in about 1/3 of subjects aged 60 to 69 years, in 2/3 of subjects aged 70 or more, but rarely under 60 years of age. However, early cataract was rather common among younger subjects. Cataracts causing a reduction of visual acuity under 0.7 in the worst eye were found in 4%, 8.7% and 21.5% respectively in the three age groups ranging from 40 to 49, 50 to 59 and 60 to 69 years and in 54.4% of subjects 70 years old or over.


Subject(s)
Cataract/epidemiology , Adult , Age Factors , Aged , Aged, 80 and over , Cataract/classification , Cataract/pathology , Female , Humans , Lens, Crystalline/pathology , Male , Middle Aged , Prevalence , Sicily/epidemiology , Visual Acuity
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