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1.
Eye (Lond) ; 21(9): 1155-61, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16732214

RESUMEN

AIMS: To evaluate the safety and efficacy of propofol sedation combined with sub-Tenon's anaesthesia for strabismus surgery in adults. METHODS: Thirty-two consecutive patients aged 31-85 years underwent strabismus surgery under general (n=16) or local (n=16) anaesthesia. In the local anaesthesia (study) group, sedation was induced with a loading dose of midazolam, fentanyl, and propofol, followed by continuous infusion of propofol, 3-6 mg/k/h to deep sedation. A nasal tube was inserted to prevent airway obstruction. Sub-Tenon's anaesthesia included infusion of a 3-4 ml mixture (50 : 50) of lidocaine 2%/mercaine 0.5%. General anaesthesia consisted of premedication with midazolam, followed by fentanyl, esmeron-bromate, propofol, and tracheal intubation. Duration of surgery and anaesthesia, intraoperative oculocardiac reflex and arrhythmias, time to discharge, postoperative pain, nausea and vomiting, and patient and surgeon satisfaction were evaluated. RESULTS: The local anaesthesia group had a significantly shorter operative and anaesthesia time, fewer episodes of oculocardiac reflex or arrythmia/bradycardia requiring treatment, fewer early or late episodes of nausea and vomiting, and less pain. The patients and surgeon in this group reported higher satisfaction. CONCLUSION: Propofol sedation with local sub-Tenon's injection of lidocaine/mercaine is recommended for the induction and maintenance of anaesthesia during unilateral or bilateral strabismus surgery in adults. The method is quick and effective, without systemic or ocular side effects.


Asunto(s)
Anestesia General/métodos , Anestesia Local/métodos , Sedación Profunda/métodos , Estrabismo/cirugía , Adulto , Anciano , Anciano de 80 o más Años , Anestésicos Combinados/administración & dosificación , Anestésicos Locales/administración & dosificación , Actitud del Personal de Salud , Bupivacaína/administración & dosificación , Femenino , Humanos , Complicaciones Intraoperatorias , Periodo Intraoperatorio , Tiempo de Internación , Lidocaína/administración & dosificación , Masculino , Persona de Mediana Edad , Dimensión del Dolor , Dolor Postoperatorio , Satisfacción del Paciente , Complicaciones Posoperatorias , Náusea y Vómito Posoperatorios/etiología , Propofol
2.
Ophthalmology ; 107(10): 1884-8, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11013193

RESUMEN

OBJECTIVE: To compare the efficacy of topical diclofenac sodium 0.1% versus dexamethasone 0.1% on the conjunctival healing process and on intraocular pressure (IOP) after strabismus surgery. DESIGN: A randomized clinical trial. PARTICIPANTS: Forty consecutive pediatric patients who underwent strabismus surgery. INTERVENTION: The patients were assigned before surgery to receive topical diclofenac 0.1% (study group, 20 patients) or dexamethasone 0.1% (control group, 20 patients) from immediately after surgery to up to 4 weeks after surgery (both combined with chloramphenicol 0.2%, polymyxin B sulfate 2500 U). MAIN OUTCOME MEASURES: Between-group comparison of five parameters: patient discomfort, conjunctival chemosis, inflammation, gap, and intraocular pressure (IOP) at 1, 2, and 4 weeks after surgery. RESULTS: At postoperative week 2, the diclofenac-treated group showed significantly less patient discomfort and less conjunctival inflammation, edema, and gap than the dexamethasone group (P: = 0.003, P: = 0.04, P: = 0.02, P: = 0. 001, respectively). At week 4, the study patients continued to show less discomfort and conjunctival gap (P: = 0.02). The dexamethasone group showed a significant change in IOP between the preoperative and the fourth postoperative week (P: = 0.001 in the right eye, P: = 0.0005 in the left eye) and an increased prevalence of higher IOP during the fourth postoperative week (P: = 0.01 in the right eye, P: = 0.02 in the left eye). Thirty-eight percent of the dexamethasone group showed an increase in IOP to more than 21 mmHg during the four postoperative weeks. No increase in IOP was noted in the diclofenac group. CONCLUSIONS: Topical diclofenac is superior to dexamethasone for each of the five postoperative parameters examined. Its maximal effect occurred at 2 weeks after surgery, without an increase in IOP or in local subconjunctival hemorrhage.


Asunto(s)
Antiinflamatorios no Esteroideos/uso terapéutico , Antiinflamatorios/uso terapéutico , Conjuntivitis/prevención & control , Dexametasona/uso terapéutico , Diclofenaco/uso terapéutico , Dolor Postoperatorio/prevención & control , Estrabismo/cirugía , Cicatrización de Heridas/efectos de los fármacos , Adolescente , Antiinflamatorios/administración & dosificación , Antiinflamatorios no Esteroideos/administración & dosificación , Niño , Preescolar , Cloranfenicol/administración & dosificación , Conjuntiva/efectos de los fármacos , Dexametasona/administración & dosificación , Diclofenaco/administración & dosificación , Método Doble Ciego , Quimioterapia Combinada/administración & dosificación , Femenino , Humanos , Presión Intraocular/efectos de los fármacos , Masculino , Soluciones Oftálmicas/administración & dosificación , Soluciones Oftálmicas/uso terapéutico , Polimixina B/administración & dosificación , Seguridad
3.
Ophthalmic Surg Lasers ; 27(12): 1039-40, 1996 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-8976525

RESUMEN

A 2-month-old female infant with intractable congenital glaucoma and diffuse corneal opacification underwent trabeculectomy with 5-fluorouracil (5-FU) injection in both eyes followed by penetrating keratoplasty (PKP) combined with partial cyclocryotherapy in the right eye. The latter procedure was undertaken despite the B-scan ultrasonographic finding of extensive optic disc cupping in order to provide the infant with some degree of improved visual function. The anatomic and functional results are discussed.


Asunto(s)
Glaucoma/congénito , Glaucoma/diagnóstico por imagen , Disco Óptico/diagnóstico por imagen , Antimetabolitos/administración & dosificación , Opacidad de la Córnea/complicaciones , Opacidad de la Córnea/cirugía , Crioterapia , Femenino , Fluorouracilo/administración & dosificación , Estudios de Seguimiento , Glaucoma/cirugía , Humanos , Lactante , Presión Intraocular , Queratoplastia Penetrante , Trabeculectomía , Ultrasonografía , Agudeza Visual
4.
J Pediatr Ophthalmol Strabismus ; 33(3): 171-4, 1996.
Artículo en Inglés | MEDLINE | ID: mdl-8771520

RESUMEN

PURPOSE: Surfactant therapy in premature infants has reduced the severity of respiratory distress syndrome (RDS), thus leading to a reduction in mortality. However, the anticipated effect of surfactant therapy on the incidence and severity of retinopathy of prematurity (ROP) is ambiguous. The acute rise in PaO2 and the increased survival of low-birth-weight infants may augment the risk of ROP, whereas their improved health and respiratory status may lower it. METHODS: We reviewed the findings of sequential ophthalmologic examinations performed in our neonatal intensive care unit. Premature infants of gestational age under 32 weeks and weighing less than 1500 g at birth who received surfactant treatment were compared with a group of historical controls consisting of premature infants of the same mean birth weight and gestational age who did not get this supplement. RESULTS: ROP was present in 13 (65%) of the 20 surfactant-treated babies, and threshold disease was noted in six (30%). In the historical control group, 20 (77%) of 25 infants had ROP, of whom 10 (40%) were treated for threshold disease. These differences were not statistically significant. CONCLUSION: Surfactant therapy was not associated with an increased incidence of ROP in our series.


Asunto(s)
Alcoholes Grasos/uso terapéutico , Fosforilcolina , Polietilenglicoles/uso terapéutico , Surfactantes Pulmonares/uso terapéutico , Retinopatía de la Prematuridad/epidemiología , Edad de Inicio , Combinación de Medicamentos , Femenino , Humanos , Incidencia , Recién Nacido de Bajo Peso , Recién Nacido , Masculino , Síndrome de Dificultad Respiratoria del Recién Nacido/prevención & control , Retinopatía de la Prematuridad/etiología , Retinopatía de la Prematuridad/fisiopatología , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Tasa de Supervivencia
5.
Br J Ophthalmol ; 65(3): 184-8, 1981 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-6784747

RESUMEN

A 23-year-old man suffering from Crohn's disease developed a bilateral maculopathy simulating 'cherry-red spot' with vision impairment and normal electroretinogram during total parenteral hyperalimentation, when copper and zinc serum levels were considerably decreased. The maculopathy rapidly subsided after cessation of the parenteral hyperalimentation and the addition of cooper and zinc. The cause of this maculopathy may be ocular involvement as part of the systemic disease owing to storage of the supplementary free amines and intravenous lipids, and the deficiency of zinc and copper.


Asunto(s)
Enfermedad de Crohn/complicaciones , Enfermedades de la Retina/etiología , Adulto , Cobre/sangre , Enfermedad de Crohn/sangre , Enfermedad de Crohn/terapia , Humanos , Mácula Lútea/patología , Masculino , Nutrición Parenteral Total , Enfermedades de la Retina/sangre , Enfermedades de la Retina/patología , Escotoma/etiología , Zinc/sangre
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