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1.
Eur Rev Med Pharmacol Sci ; 27(8): 3664-3669, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-37140316

RESUMO

OBJECTIVE: Intravitreal injections (IVI) of therapeutic substances are one of the most common procedures in ophthalmology and, for sure, the most feared complication of them is endophthalmitis. Nowadays, a precise prophylactic protocol does not exist to avoid these infections, and the role of new antiseptic drops is an interesting field of research in this regard. In this article we are going to discuss the tolerability and the efficacy of a new antiseptic drop based on a solution of hexamidine diisethionate 0.05% (Keratosept®; Bruschettini Srl, Genoa, Italy). PATIENTS AND METHODS: This was a single-center, case-control study, comparing the in vivo effect of hexamidine diisethionate 0.05% with povidone iodine 0.6% solution during IVI program. Ocular bacterial flora composition was analyzed with a conjunctival swab on day 0. After injection patients underwent antibacterial prophylaxis with Keratosept for 3 days or povidone iodine 0.6%. A second conjunctival swab was collected on day 4 and patients were asked to fulfill a questionnaire based on the OSDi model, to investigate the ocular tolerability of the drug administered. RESULTS: Efficacy was tested on 50 patients, 25 of whom received hexamidine diisethionate 0.05% drops and the other 25 received povidone iodine 0.6% solution drops, 100 total conjunctival swabs, 18 positive swabs before and 9 after treatment for the first group and 13 before and 5 after for the second one. Tolerability was tested on 104 patients, 55 underwent Keratosept therapy and 49 povidone iodine one. CONCLUSIONS: Keratosept demonstrated a good efficacy profile with better tolerability against povidone iodine in the analyzed sample.


Assuntos
Anti-Infecciosos Locais , Povidona-Iodo , Humanos , Povidona-Iodo/uso terapêutico , Povidona-Iodo/farmacologia , Injeções Intravítreas , Estudos de Casos e Controles , Túnica Conjuntiva
2.
Eur Rev Med Pharmacol Sci ; 27(5): 1759-1766, 2023 03.
Artigo em Inglês | MEDLINE | ID: mdl-36930491

RESUMO

OBJECTIVE: Fluocinolone acetonide is a valid alternative treatment for patients with chronic diabetic macular edema (DME) with poor response to anti-vascular endothelial growth factor (VEGF) therapy. The purpose of this study is to report the efficacy and safety of ILUVIEN® implant in pseudophakic eyes with persistent DME. PATIENTS AND METHODS: This is a single-centre pilot-study of 8 patients with persistent DME treated with the ILUVIEN implant, despite previous anti-vascular endothelial growth factor and/or steroid treatment. Best-corrected visual acuity (BCVA), optical coherence tomography (OCT) central retinal thickness, intraocular pressure (IOP) and microperimetric data were evaluated at baseline and month 1, 3 and 6 post treatment. RESULTS: All data are presented as mean and standard deviation. At baseline, 1, 3 and 6 months, we had BCVA of 0.26±0.22, 0.38±0.27, 0.48±0.27 and 0.46±0.24; IOP of 15.00±2.67, 15.50±3.16, 14.88±2.42 and 15.63±2.67 mmHg; macular thickness of 652±231, 487±278, 475±287 and 413±211 µm; macular sensitivity of 6.83±4.20, 6.13±3.72, 7.68±3.40 and 7.71±3.33 dB; bivariate contour elliptic area (BCEA) 95.4% 3.8±3.42, 6.06±10.06, 3.05±2.46 and 2.59±2.19°2. CONCLUSIONS: According to the results of our study, fluocinolone acetonide (FAc) is a valid therapy option despite some limitations. It has been evidenced that FAc is more effective in patients with mild central macular thickening, while in those with modest to severe central macular thickness (CMT), different therapy strategies should be considered.


Assuntos
Retinopatia Diabética , Edema Macular , Humanos , Fluocinolona Acetonida/uso terapêutico , Glucocorticoides/uso terapêutico , Retinopatia Diabética/tratamento farmacológico , Tomografia de Coerência Óptica , Fatores de Crescimento Endotelial/uso terapêutico , Projetos Piloto , Testes de Campo Visual , Edema Macular/tratamento farmacológico , Injeções Intravítreas , Implantes de Medicamento/uso terapêutico
7.
Pediatr Med Chir ; 7(4): 503-11, 1985.
Artigo em Italiano | MEDLINE | ID: mdl-3837213

RESUMO

This paper reports observations on 160 patients, aged between 1 and 30 days, submitted to general anaesthesia for surgery in the period within 1/1/81 and 31/12/84, at the Pediatric Surgery Department - Vicenza Regional Hospital. First we mentioned the main anatomo-physiological features in newborns, and on the grounds of the most recent bibliography and of our own experience, we propose a general anaesthesia record, as much as possible univocal, still bearing in mind the difficulty of this piece of advice, related to the various neonatal malformations, to the very poor conditions, and sometimes to dramatic emergency. This record as come out to be as much as possible corresponding to the main physiopathological features in newborns and doesn't modify the weak balance in these young patients.


Assuntos
Anestesia Geral/métodos , Recém-Nascido , Equilíbrio Ácido-Base , Anestesiologia/instrumentação , Metabolismo Energético , Hemodinâmica , Humanos , Rim/fisiologia , Monitorização Fisiológica , Medicação Pré-Anestésica , Respiração , Sistema Respiratório/anatomia & histologia
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