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1.
Eye (Lond) ; 27(3): 443-6, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23238443

RESUMEN

AIM: Bacterial keratitis results in corneal scarring and subsequent visual impairment. The long-term evolution of corneal scars has not been well described. In this case series, we identified patients who had improvement in corneal scarring and visual acuity from a clinical trial for bacterial keratitis. METHODS: We searched the records of the Steroids for Corneal Ulcers Trial (SCUT) for patients who had improvement in vision between the 3-month and 12-month visits and reviewed their clinical photographs. RESULTS: Of the 500 patients enrolled in SCUT, five patients with large central corneal scars due to bacterial keratitis are presented. All experienced improvement in rigid contact lens-corrected visual acuity from months 3 to 12. All patients also had marked improvement in corneal opacity during the same time period. None of the patients opted to have penetrating keratoplasty. CONCLUSIONS: Corneal scars may continue to improve even many months after a bacterial corneal ulcer has healed. The corneal remodeling can be accompanied by considerable improvement in visual acuity, such that corneal transplantation may not be necessary.


Asunto(s)
Cicatriz/fisiopatología , Úlcera de la Córnea/fisiopatología , Infecciones Bacterianas del Ojo/fisiopatología , Infecciones Neumocócicas/fisiopatología , Infecciones por Pseudomonas/fisiopatología , Trastornos de la Visión/fisiopatología , Adulto , Anciano , Compuestos Aza/uso terapéutico , Úlcera de la Córnea/tratamiento farmacológico , Úlcera de la Córnea/microbiología , Infecciones Bacterianas del Ojo/tratamiento farmacológico , Infecciones Bacterianas del Ojo/microbiología , Femenino , Fluoroquinolonas , Humanos , Masculino , Persona de Mediana Edad , Moxifloxacino , Soluciones Oftálmicas , Infecciones Neumocócicas/tratamiento farmacológico , Infecciones Neumocócicas/microbiología , Prednisolona/análogos & derivados , Prednisolona/uso terapéutico , Infecciones por Pseudomonas/tratamiento farmacológico , Infecciones por Pseudomonas/microbiología , Quinolinas/uso terapéutico , Agudeza Visual/fisiología
2.
Eye (Lond) ; 26(9): 1226-31, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22744392

RESUMEN

PURPOSE: To analyse predictors of clinical outcome in fungal keratitis. METHODS: Data was collected during a prospective, randomized, controlled, double-masked clinical trial of treatment for fungal keratitis. Clinical features at presentation and demographics were collected at the enrollment visit for all patients. Pre-specified clinical outcomes included 3-month visual acuity and infiltrate/scar size, time to re-epithelialization, and corneal perforation. A separate multivariable model with each outcome as the dependent variable included all predictor variables. RESULTS: Predictors for worse 3-month visual acuity include older age (P=0.024), worse presentation visual acuity (P<0.001), larger infiltrate size at presentation (P<0.001), and pigmented ulcer (P=0.030). Larger infiltrate size at presentation was a significant predictor of worse 3-month infiltrate/scar size (P<0.001). Larger epithelial defect size was a significant predictor of perforation (P=0.0013). Predictors of longer time to re-epithelialization include infiltrate size at presentation (P<0.001) and older age (P=0.025). CONCLUSION: Ulcer severity at presentation is highly predictive of worse outcomes. Presentation of clinical characteristics such as baseline acuity and infiltrate scar can provide important information to clinicians about prognosis, and may help guide management and treatment decisions. Prevention of corneal ulcer remains important, as it is difficult to change the course of the ulcer once it has begun.


Asunto(s)
Úlcera de la Córnea/diagnóstico , Infecciones Fúngicas del Ojo/diagnóstico , Administración Tópica , Antifúngicos/uso terapéutico , Perforación Corneal/diagnóstico , Úlcera de la Córnea/tratamiento farmacológico , Úlcera de la Córnea/microbiología , Desbridamiento , Método Doble Ciego , Infecciones Fúngicas del Ojo/tratamiento farmacológico , Infecciones Fúngicas del Ojo/microbiología , Femenino , Humanos , Masculino , Natamicina/uso terapéutico , Soluciones Oftálmicas , Evaluación de Procesos y Resultados en Atención de Salud , Pronóstico , Estudios Prospectivos , Pirimidinas/uso terapéutico , Repitelización , Factores de Riesgo , Factores de Tiempo , Triazoles/uso terapéutico , Agudeza Visual/fisiología , Voriconazol
3.
Eye (Lond) ; 25(9): 1155-60, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21637300

RESUMEN

AIMS: The purpose of this study was to estimate the duration of treatment necessary for sequential acanthamoeba laboratory tests from corneal scrapings to become negative, and to assess predictors that affect this duration period. METHODS: We included all patients with at least one positive acanthamoeba culture or Giemsa stain at the F.I. Proctor Foundation Microbiology Laboratory from 1996 to 2009. A parametric survival analysis was performed among patients with repeat cultures to assess significant predictors for extended clearance time. Simulations were performed to estimate clearance time in the entire patient population, assuming imperfect sensitivity. RESULTS: Thirty-seven patients with laboratory evidence of acanthamoeba had testing at 69 time points. The median clearance time among eyes with repeat cultures was 42.5 days (interquartile range (IQR) 22.0-82.0 days; unadjusted parametric model). Initial visual acuity was the only predictor significantly associated with clearance time in univariate analyses (P<0.0001). Using initial visual acuity as a predictor for clearance time among the entire patient population, the estimated clearance time decreased to 38.7 days (95% confidence interval (CI) 27.9-53.5 days). When the imperfect sensitivity of the culture technique was also taken into account, the estimated clearance time was 44.1 days (95% CI 31.9-61.0 days). CONCLUSION: The duration of infection with acanthamoeba keratitis undergoing treatment has not been well characterized. In this report we estimate a median clearance time of approximately 6 weeks, with an IQR of 22-82 days.


Asunto(s)
Queratitis por Acanthamoeba/microbiología , Acanthamoeba/aislamiento & purificación , Queratitis por Acanthamoeba/tratamiento farmacológico , Queratitis por Acanthamoeba/fisiopatología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Antiparasitarios/uso terapéutico , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Factores de Tiempo , Agudeza Visual/fisiología , Adulto Joven
5.
Br J Ophthalmol ; 93(1): 116-9, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18952649

RESUMEN

BACKGROUND/AIMS: To study the susceptibility of Fusarium and Aspergillus isolated from keratitis to amoxicillin, cefazolin, chloramphenicol, moxifloxacin, tobramycin and benzalkonium chloride (BAK). METHODS: 10 isolates of Fusarium and 10 isolates of Aspergillus from cases of fungal keratitis at Aravind Eye Hospital in South India were tested using microbroth dilution for susceptibility to amoxicillin, cefazolin, chloramphenicol, moxifloxacin, tobramycin and BAK. The minimum inhibitory concentration (MIC) median and 90th percentile were determined. RESULTS: BAK had the lowest MIC for both Fusarium and Aspergillus. Chloramphenicol had activity against both Fusarium and Aspergillus, while moxifloxacin and tobramycin had activity against Fusarium but not Aspergillus. CONCLUSIONS: The susceptibility of Fusarium to tobramycin, moxifloxacin, chloramphenicol and BAK and of Aspergillus to chloramphenicol and BAK may explain anecdotal reports of fungal ulcers that improved with antibiotic treatment alone. While some of the MICs of antibiotics and BAK are lower than the typically prescribed concentrations, they are not in the range of antifungal agents such as voriconazole, natamycin and amphotericin B. Antibiotics may, however, have a modest effect on Fusarium and Aspergillus when used as initial treatment prior to identification of the pathological organism.


Asunto(s)
Antibacterianos/uso terapéutico , Antifúngicos/uso terapéutico , Aspergillus/efectos de los fármacos , Fusarium/efectos de los fármacos , Aspergilosis/microbiología , Úlcera de la Córnea/microbiología , Farmacorresistencia Fúngica/efectos de los fármacos , Infecciones Fúngicas del Ojo/microbiología , Femenino , Humanos , India , Masculino , Pruebas de Sensibilidad Microbiana , Micosis/microbiología , Estudios Prospectivos
6.
Br J Ophthalmol ; 93(2): 198-202, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-18829631

RESUMEN

AIMS: The aim of the study was to conduct a preliminary clinical trial to assess whether adjunctive topical corticosteroids improve outcomes in bacterial keratitis and, if no difference was found, to determine the feasibility and sample size necessary for conducting a larger trial to answer this question. METHODS: In this single centre, double-masked clinical trial, 42 patients with culture-confirmed bacterial keratitis at Aravind Eye Hospital in India were randomised to receive either topical prednisolone phosphate or placebo. All patients received topical moxifloxacin. The primary outcome was best spectacle-corrected visual acuity (BSCVA) at 3 months, adjusting for enrolment BSCVA and arm. Other pre-specified outcomes included re-epithelialisation time, infiltrate/scar size and adverse events. RESULTS: Compared with placebo, patients in the steroid group re-epithelialised more slowly (hazard ratio 0.47, 95% CI 0.23 to 0.94). There was no significant difference in BSCVA or infiltrate/scar size at 3 weeks or 3 months. To have 80% power to detect a two-line difference in acuity, 360 cases would be required. CONCLUSIONS: Although corticosteroid treatment resulted in a statistically significant delay in re-epithelialisation, this did not translate to a significant difference in visual acuity, infiltrate/scar size or adverse events. To assess the effect of steroids on acuity, a larger trial is warranted and feasible.


Asunto(s)
Úlcera de la Córnea/tratamiento farmacológico , Infecciones Bacterianas del Ojo/tratamiento farmacológico , Glucocorticoides/uso terapéutico , Prednisolona/análogos & derivados , Adulto , Anciano , Úlcera de la Córnea/microbiología , Úlcera de la Córnea/fisiopatología , Método Doble Ciego , Epitelio Corneal/fisiología , Infecciones Bacterianas del Ojo/fisiopatología , Estudios de Factibilidad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Soluciones Oftálmicas , Prednisolona/uso terapéutico , Resultado del Tratamiento , Agudeza Visual/efectos de los fármacos , Cicatrización de Heridas/efectos de los fármacos
7.
Eur J Ophthalmol ; 18(3): 351-5, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18465715

RESUMEN

PURPOSE: Prior cataract surgery is a recognized risk factor for the development of Mooren''s ulcer, but the demographic and clinical features of a large cohort of such patients have not been described. METHODS: The authors performed a retrospective review of demographic and clinical data from 14 eyes in 13 patients who developed Mooren's ulcer following extracapsular cataract extraction at Aravind Eye Hospital in Madurai, South India. RESULTS: Eight (62%) of the 13 patients were men and 5 (39%) were women. The median age in our population was 65 years, with a range of 45 to 85 years. The median number of months from surgery to the onset of Mooren's ulcer was 19, with a range of 4 to 156 months. Of the 14 eyes with prior cataract surgery, the location of the ulcer was at or contiguous with the wound in 10 eyes (71%), which was 2.5 times more likely than other circumlimbal locations, and only one patient (8%) had bilateral disease. CONCLUSIONS: Mooren''s ulcer may occur following extracapsular cataract extraction and when it does it is most likely to be unilateral and contiguous with the wound. These findings support the notion that exposure of normally concealed corneal antigens may contribute to the pathogenesis of Mooren''s ulcer in some patients.


Asunto(s)
Extracción de Catarata/efectos adversos , Úlcera de la Córnea/etiología , Adulto , Anciano , Anciano de 80 o más Años , Afaquia Poscatarata/etiología , Conjuntiva/cirugía , Úlcera de la Córnea/diagnóstico , Úlcera de la Córnea/terapia , Femenino , Glucocorticoides/uso terapéutico , Humanos , Implantación de Lentes Intraoculares , Masculino , Persona de Mediana Edad , Seudofaquia/etiología , Estudios Retrospectivos , Factores de Riesgo , Factores de Tiempo
10.
Indian Heart J ; 45(1): 53-5, 1993.
Artículo en Inglés | MEDLINE | ID: mdl-8365742

RESUMEN

The present study was carried out in 33 cases of cyanotic congenital heart disease (CCHD) to determine the prevalence of iron deficiency anemia (IDA) and its correlation to hyperviscosity symptoms in terms of hematocrit levels. Furthermore, the study was aimed at assessing the response to low dose iron therapy (60 mg of elemental iron once daily) in relieving symptoms of hyperviscosity. All these cases were evaluated for presence of symptoms of hyperviscosity and later subjected to various hematological & biochemical parameters of iron deficiency anemia including hemoglobin (Hb), pack cell volume (PCV), mean corpuscular volume (MCV), mean corpuscular hemoglobin concentration (MCHC), serum iron, total iron binding capacity respectively. Results showed presence of IDA in 6/33 cases (18.2%) and hyperviscosity symptoms in 10/33 cases (30.3%). Amongst the group with symptoms of hyperviscosity, in the subset having IDA these symptoms were observed at PCV levels of 0.52 L/L to 0.58 L/L in contrast to the subset not deficient in iron where the symptoms occurred at a PCV 0.68 L/L. Relief of symptoms of hyperviscosity was evident with a minimal rise of mean hemoglobin by 2.1 gm/dl. It was concluded that IDA was not an uncommon finding in CCHD cases and that it leads to symptoms of hyperviscosity at a level of PCV much lower than those known to produce these symptoms. Finally low dose iron therapy was found effective in relieving the symptoms of hyperviscosity.


Asunto(s)
Anemia Hipocrómica/sangre , Viscosidad Sanguínea/fisiología , Cardiopatías Congénitas/sangre , Adolescente , Adulto , Anemia Hipocrómica/complicaciones , Cianosis , Femenino , Cardiopatías Congénitas/complicaciones , Humanos , Masculino
11.
Acta Ophthalmol (Copenh) ; 70(4): 515-7, 1992 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-1414297

RESUMEN

Serum alpha-1 acid glycoprotein levels were measured in 27 patients with idiopathic peripheral retinal vasculitis (Eales' disease) and 31 healthy subjects by single radial immunodiffusion technique. The levels were found to be significantly increased in both moderate and severe types of the disease. The serum levels of this protein paralleled the severity of the disease. The increased alpha-1 acid glycoprotein in serum showed a significant fall to near normal levels during the quiescent stage. Our observations support the hypothesis that idiopathic peripheral retinal vasculitis is an immune mediated disease. It is proposed that serum alpha-1 acid glycoprotein may be considered as a reliable parameter of the activity and the degree of severity of the disease, as well as an useful tool for monitoring the efficacy of treatment.


Asunto(s)
Orosomucoide/análisis , Hemorragia Retiniana/sangre , Vasos Retinianos , Vasculitis/sangre , Hemorragia Vítrea/sangre , Adolescente , Adulto , Biomarcadores , Niño , Humanos , Inmunodifusión , Masculino , Persona de Mediana Edad , Enfermedades de la Retina/sangre
12.
Trop Gastroenterol ; 10(3): 167-72, 1989.
Artículo en Inglés | MEDLINE | ID: mdl-2815325

RESUMEN

Of the 20 cases with biliary colics who had normal OCG and ultrasound, 11 (55%) showed microlithiasis in the form of cholesterol monohydrate crystals and/or calcium bilirubinate granules on polarized light microscopy of the duodenal bile. Microlithiasis was noted in gallbladder bile of all (100%) the cases with proven gallstones but in none of the duodenal bile samples from healthy subjects. This study suggests that polarized microscopy may be a useful method to detect microlithiasis in patients with repeated biliary colics who have normal OCG and ultrasound examination.


Asunto(s)
Bilis/análisis , Colelitiasis/diagnóstico , Cólico/diagnóstico , Colelitiasis/análisis , Humanos , Microscopía de Polarización
13.
Adv Myocardiol ; 2: 407-14, 1980.
Artículo en Inglés | MEDLINE | ID: mdl-7423054

RESUMEN

The isozyme profile of lactic dehydrogenase (LDH) is being studied in this laboratory, mainly for the diagnosis in the suspected cases of myocardial infarction (MI). The isozymes are separated by polyacrylamide gel electrophoresis and the quantitative assay of the isoenzymes is done by enzyme staining followed by scanning with the help of an automatic scanner. In normal cases, the ratio of the two isozymes H4 and H3M is approximately 0.5. In almost all cases of myocardial infarction the ratio becomes 1 or more and sometimes increases up to 2. In the suspected and potential cases of infarction the ratio tends to become more than 0.5 (usually 0.7) but remains lower than 1. Thus, the measurement of the ratio may be a very helpful diagnostic index in the suspected and potential cases and may also be used for prognostic purposes as well.


Asunto(s)
Isoenzimas/análisis , L-Lactato Deshidrogenasa/análisis , Infarto del Miocardio/enzimología , Electroforesis en Gel de Poliacrilamida , Femenino , Humanos , Masculino , Infarto del Miocardio/diagnóstico
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