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1.
Biomaterials ; 22(24): 3305-10, 2001 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-11700802

RESUMEN

This study was performed to test viscoelastic artificial tears (VAT) based on both subjective and clinical parameters in patients with keratoconjunctivitis sicca (KCS). Twenty-eight patients were evaluated in a randomized double-blind study. Sodium hyaluronate was used in two different concentrations (0.4%, 0.25%) and in combination with chondroitin sulfate. Each preparation was used for one week preceded by another weekly cycle using a sodium chloride solution. Before and after each cycle, clinical examinations were performed: tear film break-up time, Schirmer's test, lipid-layer thickness and fluorescein staining. Patients kept a record of the drop-frequency, subjective response and side effects. After the study, they were asked to give a rating of the various preparations. The severity of KCS was expressed based on a sicca score and correlated with response to viscoelastic treatment. Both the subjective and the clinical parameters revealed no statistically significant differences between the various viscoelastic agents or between the viscoelastics and the sodium chloride solutions. Severe side effects did not occur. There was a positive correlation of response to viscoelastic treatment with severe KCS (+ 0.36) but not with mild KCS (-0.07). The VAT seems to be indicated in severe cases of dry-eye syndrome. Sodium chloride solutions may be a useful short-term alternative to other tear formulations.


Asunto(s)
Síndromes de Ojo Seco/tratamiento farmacológico , Soluciones Oftálmicas/uso terapéutico , Adulto , Anciano , Estudios Cruzados , Método Doble Ciego , Elasticidad , Femenino , Humanos , Queratoconjuntivitis Seca/tratamiento farmacológico , Masculino , Ensayo de Materiales , Persona de Mediana Edad , Soluciones Oftálmicas/química , Cloruro de Sodio/uso terapéutico , Viscosidad
2.
J Cataract Refract Surg ; 27(2): 233-8, 2001 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11226788

RESUMEN

PURPOSE: To evaluate inflammation after cataract surgery in patients with nonproliferative diabetic retinopathy (NPDR) and compare results with 2 intraocular lenses (IOLs): a foldable hydrophobic acrylic and a heparin-surface-modified (HSM) poly(methyl methacrylate) (PMMA). SETTING: Department of Ophthalmology, University of Vienna, Vienna, Austria. METHODS: Patients with NPDR were randomized for implantation of an HSM PMMA IOL (811C, Pharmacia) through a 6.0 mm sclerocorneal incision (30 patients) or a foldable hydrophobic acrylic IOL (AcrySof, Alcon) through a 4.0 mm sclerocorneal incision (32 patients). Both IOLs had 6.0 mm optics. All patients were treated according to a standardized protocol. The degree of flare in the anterior chamber was measured with the Kowa 1000 laser flare-cell meter 1 day preoperatively and 1 day, 1 week, and 1 and 3 months postoperatively. RESULTS: In both IOL groups, flare was highest on the first postoperative day and decreased to preoperative levels by 3 months after surgery. There was no statistically significant difference in relative flare values between the 2 groups. CONCLUSION: There was no difference in postoperative inflammation in eyes with a foldable hydrophobic acrylic IOL implanted through a small incision and those with a rigid HSM PMMA IOL. Postoperative inflammation results indicate that the lenses are equally suitable for the use in patients with diabetic retinopathy.


Asunto(s)
Materiales Biocompatibles Revestidos , Retinopatía Diabética/complicaciones , Endoftalmitis/etiología , Heparina , Lentes Intraoculares , Facoemulsificación/efectos adversos , Resinas Acrílicas , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Implantación de Lentes Intraoculares , Masculino , Persona de Mediana Edad , Polimetil Metacrilato
3.
Cornea ; 19(4): 487-91, 2000 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-10928764

RESUMEN

PURPOSE: Patients with diabetic retinopathy (DRP) seldom report symptoms of ocular surface irritation, but evaluations of dryness are pathologic. This study was designed to evaluate the correlation between the severity of DRP and dry eyes. METHODS: We included 144 eyes of 72 patients. Severity of retinopathy was graded according to the Early Treatment Diabetic Retinopathy Study. The examinations for dry eyes included Schirmer's test, break-up time, lipid layer thickness, fluorescein and rose bengal staining of the cornea, impression cytology, and a questionnaire. A sicca severity score was calculated using a point system of the results of these tests. Patients were divided into three groups: postpanretinal laser coagulation (PPL), postcentral laser coagulation (PCL), and those with no laser treatment (0-L). For statistics, we used the correlation coefficient to determine relationships and the unpaired Student t test for statistical difference. RESULTS: The correlation (c) of keratoconjunctivitis sicca (KCS) and DRP after laser treatment was c = 0.24 and after central laser treatment was c = 0.22; the correlation without laser treatment was 0.54. The best correlation is 1 or -1, the worst was 0. The score of those patients with mild to moderate retinopathy was compared to that of patients with severe to proliferative disease. There was a significant statistical difference in the sicca severity score between both groups, (p < 0.006. Student t test). CONCLUSION: KCS represents another manifestation of diabetes mellitus and its severity--measured by a many-membered score--correlates with the severity of the DRP.


Asunto(s)
Retinopatía Diabética/diagnóstico , Queratoconjuntivitis Seca/diagnóstico , Conjuntiva/patología , Medios de Contraste/administración & dosificación , Córnea/patología , Córnea/cirugía , Retinopatía Diabética/cirugía , Fluoresceína/administración & dosificación , Colorantes Fluorescentes/administración & dosificación , Humanos , Queratoconjuntivitis Seca/cirugía , Coagulación con Láser , Soluciones Oftálmicas , Retina/cirugía , Rosa Bengala/administración & dosificación , Índice de Severidad de la Enfermedad , Propiedades de Superficie , Lágrimas/química
4.
J Ocul Pharmacol Ther ; 15(5): 439-45, 1999 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-10530705

RESUMEN

The aim of this study was to determine the penetration of intravenously administered meropenem into the human aqueous humor and vitreous. Thirty patients about to undergo cataract surgery and fourteen patients about to undergo vitrectomy received a 2 g dose of meropenem before surgery. Specimens of aqueous humor or vitreous and blood were obtained intraoperatively and analyzed by high performance liquid chromatography (HPLC). The study was designed as a non-randomized prospective trial. Thirty min to 12 hr after administration, mean aqueous humor levels of 13.4 and 1.1 mg/l and vitreous levels between 8.94 and 1.08 mg/l were found, respectively. The peak concentrations are distinctly above the in vitro measured minimum inhibitory concentration of meropenem for 90% (MIC90) of almost all relevant gram-positive and gram-negative organisms, including Pseudomonas aeruginosa and Enterobacteriaceae. With regard to its broad spectrum, high antibacterial activity, and good penetration into ocular fluids, meropenem seems to be an alternative to currently used systemic drugs. Its usefulness in perioperative prophylaxis, as initial therapy after perforating or penetrating injuries, or in the therapy of bacterial endophthalmitis has yet to be proved.


Asunto(s)
Humor Acuoso/metabolismo , Tienamicinas/farmacocinética , Cuerpo Vítreo/metabolismo , Cromatografía Líquida de Alta Presión , Humanos , Infusiones Intravenosas , Meropenem , Tienamicinas/metabolismo , Factores de Tiempo
6.
Acta Ophthalmol Scand ; 77(4): 471-3, 1999 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-10463426

RESUMEN

PURPOSE: To report on AIDS patients having combination antiretroviral therapy whose cytomegalovirus (CMV) retinitis remained inactive after discontinuation of anti-CMV maintenance therapy. METHODS: We describe the course of CMV-retinitis in 3 patients with AIDS after initiation of combination antiretroviral therapy. RESULTS: After cessation of anti-CMV therapy no relapse of CMV-retinitis has been observed for up to 18 months. Two of the patients developed new CMV-retinitis in the first months after initiation of combination therapy, nevertheless after further improvement of immunological parameters retinitis remained stable without anti-CMV therapy. CONCLUSION: The sustained immunological effects of combination therapy are possibly sufficient enough to provide protection against CMV-retinitis.


Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/prevención & control , Fármacos Anti-VIH/uso terapéutico , Retinitis por Citomegalovirus/prevención & control , Ganciclovir/uso terapéutico , Indinavir/uso terapéutico , Saquinavir/uso terapéutico , Infecciones Oportunistas Relacionadas con el SIDA/complicaciones , Infecciones Oportunistas Relacionadas con el SIDA/inmunología , Adulto , Recuento de Linfocito CD4 , Retinitis por Citomegalovirus/complicaciones , Retinitis por Citomegalovirus/inmunología , Quimioterapia Combinada , Estudios de Seguimiento , VIH/genética , Humanos , Masculino , Persona de Mediana Edad , ARN Viral/análisis
7.
Klin Monbl Augenheilkd ; 215(4): 228-32, 1999 Oct.
Artículo en Alemán | MEDLINE | ID: mdl-10572884

RESUMEN

BACKGROUND: Conjunctivitis sicca is a chronic disease of the ocular surface. The substitution of tear deficiency with artificial tears is not satisfying in many patients. In a series of patients successfully treated with acupuncture we observed very different effects on each patient. In this study we evaluate the correlation between the effect of acupuncture and the etiology of the dry eyes treated. PATIENTS AND METHODS: 102 patients (87 women, 15 men) with dry-eye syndrome have been needed 10 sessions, once per week, for 30 minutes. We recorded causal factors according to the traditional chinese medicine (TCM): external and internal factors. External factors were: toxic, allergic, drug-induced, ocular surface inflammation and infection, contact lens and generally external irritations. Internal factors were disorders of hormones, immune system, psychic, and vitamin-A deficiency. Ophthalmologic observation included the slit-lamp examination, Schirmers test II, break-up time of tear film (BUT) and a drop-frequency protocol--before and 1 week after acupuncture treatment. RESULTS: There was a statistically significant difference (p < 0.001) in Schirmers test, BUT and drop frequency between before and after acupuncture. There was no significant difference between internal and external factors, but the effect on external induced sicca was better. The best effect of acupuncture was found in external factors after inflammation and in patients with imbalance of the autonomic nervous system, the least effects in Sjögren Syndrome. The effect was better in younger then in patients over 50 years. CONCLUSION: The study demonstrate, according DeLa Fuye that the best effect of acupuncture is seen on functionally disorders.


Asunto(s)
Terapia por Acupuntura , Queratoconjuntivitis Seca/terapia , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Queratoconjuntivitis Seca/etiología , Masculino , Medicina Tradicional China , Persona de Mediana Edad , Resultado del Tratamiento
8.
Int Ophthalmol ; 20(1-3): 125-9, 1996.
Artículo en Inglés | MEDLINE | ID: mdl-9112176

RESUMEN

PURPOSE: To compare the efficacy and complication rate of two standard cataract extraction techniques with different incision lengths when combined with trabeculectomy. METHODS: 54 eyes after combined ECCE, posterior chamber lens implantation and trabeculectomy (ECCE-group) are compared with 49 eyes following phacoemulsification, trabeculectomy and implantation of a folded flexible posterior chamber lens (small-incision group). Minimum follow-up was 24 months. RESULTS: Glaucoma control was achieved in all eyes of both groups. There was a tendency towards a higher number of patients without therapy in the small-incision group (82% versus 65%, p = 0.07). Final mean IOP (14.2 +/- 3.0 mmHg versus 15.5 +/- 2.7 mmHg, p = 0.02) and mean therapy index (0.2 +/- 0.5 versus 0.4 +/- 0.6, p = 0.03) were significantly lower in the small-incision group. Postoperative complications such as severe fibrin effusion (41% versus 18%, p = 0.018), early postoperative IOP rises > 25 mmHg (18% versus 2%, p = 0.009), filtering bleb scarring (63% versus 8%, p < 0.0001) and the total number of complications (87% versus 63%, p = 0.006) were significantly higher in the ECCE-group. CONCLUSION: With the decrease of the incision size necessary for the cataract extraction a reduction of postoperative complications and better functional results are achieved in combined cataract/glaucoma surgery.


Asunto(s)
Glaucoma/cirugía , Lentes Intraoculares , Facoemulsificación , Suturas , Trabeculectomía , Anciano , Anciano de 80 o más Años , Catarata/complicaciones , Femenino , Estudios de Seguimiento , Glaucoma/fisiopatología , Humanos , Presión Intraocular , Lentes Intraoculares/efectos adversos , Masculino , Persona de Mediana Edad , Facoemulsificación/efectos adversos , Complicaciones Posoperatorias , Estudios Retrospectivos , Trabeculectomía/efectos adversos , Resultado del Tratamiento , Campos Visuales
9.
Ophthalmologica ; 212(4): 239-43, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9672212

RESUMEN

Cytomegalovirus (CMV) is the most common pathogen of opportunistic viral infections in patients with the acquired immunodeficiency syndrome. In this study, we assessed the therapeutic outcome of our treatment regimen of CMV retinitis by analysing retrospectively 33 consecutive patients. The clinical utility of CMV cultures from blood, urine and throat specimens obtained at the time of diagnosis was additionally evaluated. Treatment started with ganciclovir (GCV) therapy. In case of relapsing retinitis, re-induction therapy was initiated, and if unsuccessful, the patient was switched to foscarnet. Patients developing resistant retinitis despite foscarnet therapy were offered a GCV-foscarnet combination therapy. Under primary GCV therapy, the median first stable interval of the whole group was 202 days (mean 238 days). Twenty-five out of 33 CMV retinitis patients (76%) responded to initial GCV therapy. Eleven of these patients showed relapsing retinitis that could be stabilised in 3 patients solely with combination therapy. Eight patients did not respond to primary GCV therapy. Three of them improved with foscarnet, but 3 patients did not respond to either treatment. In 18 (56%) out of 32 patients, CMV cultures yielded positive results. Considering our series, we may conclude that in the majority of patients primary or secondary viral resistance can be overcome by dose increase, switching to the alternative drug or a combination therapy.


Asunto(s)
Antivirales/uso terapéutico , Retinitis por Citomegalovirus/tratamiento farmacológico , Foscarnet/uso terapéutico , Ganciclovir/uso terapéutico , Infecciones Oportunistas Relacionadas con el SIDA/diagnóstico , Infecciones Oportunistas Relacionadas con el SIDA/tratamiento farmacológico , Infecciones Oportunistas Relacionadas con el SIDA/inmunología , Líquidos Corporales/virología , Recuento de Linfocito CD4 , Citomegalovirus/aislamiento & purificación , Retinitis por Citomegalovirus/diagnóstico , Retinitis por Citomegalovirus/inmunología , Progresión de la Enfermedad , Quimioterapia Combinada , Estudios de Seguimiento , Humanos , Estudios Retrospectivos , Resultado del Tratamiento
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