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1.
J Glaucoma ; 11(4): 306-14, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12169967

RESUMO

PURPOSE: To compare the safety and efficacy of topical versus retrobulbar anesthesia for primary trabeculectomy METHODS: A prospective study of 36 consecutive patients undergoing trabeculectomy who were randomized to receive topical (n = 18) or retrobulbar (n = 18) anesthesia. Operating conditions, patient comfort, and surgical outcome were evaluated. SETTINGS: Tertiary-care university hospital ambulatory surgical center. RESULTS: There were no differences in operating conditions (P = 0.14), pain during (P = 0.54) or after (P = 0.76) surgery, or supplemental anesthesia required (P = 0.34) between the two groups. Very few patients in either group were bothered by touch sensation, tissue manipulation, or the microscope light. Chemosis, subconjunctival hemorrhage and eyelid hemorrhage were seen exclusively in the retrobulbar group (P <0.03), and were all attributable to the injection. Inadvertent eye movement was present more frequently in the topical group (P = 0.01), although this did not pose a problem to the surgeon. No surgical complications were encountered in either group. CONCLUSION: Topical anesthesia is a safe and effective alternative to retrobulbar anesthesia for primary trabeculectomy.


Assuntos
Anestesia Local/métodos , Anestésicos Combinados/administração & dosagem , Anestésicos Locais/administração & dosagem , Glaucoma/cirurgia , Bloqueio Nervoso/métodos , Trabeculectomia/métodos , Idoso , Idoso de 80 Anos ou mais , Bupivacaína/administração & dosagem , Feminino , Humanos , Hialuronoglucosaminidase/administração & dosagem , Injeções , Lidocaína/administração & dosagem , Masculino , Pessoa de Meia-Idade , Órbita , Medição da Dor , Dor Pós-Operatória/diagnóstico , Estudos Prospectivos , Segurança
2.
J Cataract Refract Surg ; 28(4): 631-8, 2002 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11955903

RESUMO

PURPOSE: To compare the safety and efficacy of topical and retrobulbar anesthesia for combined phacotrabeculectomy. SETTING: Tertiary-care university hospital ambulatory surgical center. METHODS: In this prospective study, 40 consecutive patients having combined phacotrabeculectomy were randomized to receive topical (n = 20) or retrobulbar (n = 20) anesthesia. Operating conditions, patient comfort, and surgical outcome were evaluated. RESULTS: There was no significant between-group difference in operating conditions (P =.56), pain during (P =.41) or after (P =.23) surgery, or supplemental anesthesia required (P =.49). Few patients in either group were bothered by tissue manipulation or the microscope light, although more patients in the topical group were slightly bothered by touch sensation (P =.05). Chemosis, subconjunctival hemorrhage, and eyelid hematoma were seen almost exclusively in the retrobulbar group (P <.05). Inadvertent eye movement was present more frequently in the topical group (P =.04), although this did not pose a problem to the surgeon. CONCLUSION: Topical anesthesia is a safe and effective alternative to retrobulbar anesthesia for combined phacotrabeculectomy.


Assuntos
Anestesia Local/métodos , Anestésicos Locais/administração & dosagem , Facoemulsificação , Trabeculectomia , Administração Tópica , Idoso , Idoso de 80 Anos ou mais , Catarata/complicações , Catarata/terapia , Feminino , Glaucoma/complicações , Glaucoma/cirurgia , Humanos , Masculino , Pessoa de Meia-Idade , Soluções Oftálmicas , Órbita , Estudos Prospectivos , Segurança , Resultado do Tratamento
3.
J Cataract Refract Surg ; 28(4): 656-61, 2002 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11955907

RESUMO

PURPOSE: To determine the difference between the predicted and postoperative refraction in eyes after implantation of the Mentor MemoryLens intraocular lens (IOL) and compare these results with those of 2 other types of foldable IOLs implanted by the same surgeons. SETTING: Community-based group practice ophthalmology clinic. METHODS: All operated eyes (341) of all patients who had routine phacoemulsification with implantation of a MemoryLens IOL performed by 1 of 2 surgeons were evaluated retrospectively. The predicted refractive error and actual postoperative refractive error were compared in each eye in the MemoryLens group and in 2 smaller control groups with an AcrySof acrylic (Alcon) or SI-40 silicone (Allergan Medical Optics) IOL implanted by the same surgeons using identical technique and IOL calculation parameters. Patients in whom the difference between the predicted and actual postoperative refraction fell significantly outside expected parameters were rechecked with repeat axial length and keratometric readings, and these measurements were used to back-calculate the effective in vivo IOL power. RESULTS: The MemoryLens group had significantly greater variability in postoperative refractive results from those predicted by the Hoffer program than the 2 control groups. The postoperative refractive error in the MemoryLens group differed from +1.50 to -5.50 diopters (D) from that predicted by the IOL calculation formulas. When the outlier groups (ie, greater than +0.50 D or less than -1.00 D from predicted refractive error) were evaluated and compared to the rest of the MemoryLens group and the 2 control groups, no significant difference in axial length, keratometric measurements, operative surgeon, surgical technique, or patient age was found. Repeat axial length and keratometric measurements in the outlier group were not significantly different from those in the same eyes preoperatively. Back-calculation using postoperative axial length and keratometric measurements in the highly myopic outlier group showed that the mean difference between the labeled IOL power and actual in vivo IOL power in the outlier group was -3.08 D (range -1.98 to -7.54 D). The best corrected visual acuity was not affected in patients in the outlier groups despite the refractive variability. CONCLUSION: The variation in postoperative refractive results in the MemoryLens group was significantly greater than in the 2 other foldable IOL groups.


Assuntos
Materiais Biocompatíveis/efeitos adversos , Lentes Intraoculares/efeitos adversos , Complicações Pós-Operatórias , Erros de Refração/etiologia , Resinas Acrílicas , Adulto , Idoso , Idoso de 80 Anos ou mais , Humanos , Implante de Lente Intraocular , Pessoa de Meia-Idade , Facoemulsificação , Refração Ocular , Estudos Retrospectivos , Elastômeros de Silicone , Acuidade Visual
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