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首页> 外文期刊>Ophthalmology >Prospective randomized trial of trimethoprim/sulfamethoxazole versus pyrimethamine and sulfadiazine in the treatment of ocular toxoplasmosis.
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Prospective randomized trial of trimethoprim/sulfamethoxazole versus pyrimethamine and sulfadiazine in the treatment of ocular toxoplasmosis.

机译:甲氧苄氨嘧啶/磺胺甲恶唑与乙胺嘧啶和磺胺嘧啶在眼弓形虫病治疗中的前瞻性随机试验。

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OBJECTIVE: To compare the efficacy of the classic treatment of ocular toxoplasmosis (pyrimethamine, sulfadiazine, and prednisolone) with a regimen consisting of trimethoprim/sulfamethoxazole (co-trimoxazole) plus prednisolone. DESIGN: Prospective randomized single-blind clinical trial. PARTICIPANTS: Fifty-nine patients with active ocular toxoplasmosis were randomly assigned to 2 treatment groups: 29 were treated with pyrimethamine/sulfadiazine, and 30 patients received trimethoprim/sulfamethoxazole. INTERVENTION: Treatment consisted of 6 weeks' treatment with antibiotics plus steroids. Antitoxoplasmosis antibodies (immunoglobulin M [IgM] and IgG) were measured using an enzyme-linked immunosorbent assay. MAIN OUTCOME MEASURES: Changes in retinochoroidal lesion size after 6 weeks' treatment, visual acuity (VA) before and after intervention, adverse drug reactions during follow-up, and rate of recurrence. RESULTS: Active toxoplasmosis retinochoroiditis resolved in all patients over 6 weeks' treatment, with no significant difference in mean reduction of retinochoroidal lesion size between the 2 treatment groups (61% reduction in the classic treatment group and 59% in the trimethoprim/sulfamethoxazole group, P = 0.75). Similarly, no significant difference was found in VA after treatment between the 2 groups (mean VAs after treatment were 0.12 logarithm of the minimum angle of resolution [logMAR] [20/25] in the classic treatment group and 0.09 logMAR [20/25] in the trimethoprim/sulfamethoxazole group, P = 0.56). Adverse effects were similar in both groups, with one patient in each suffering from any significant drug side effects. The overall recurrence rate after 24 months' follow-up was 10.16%, with no significant difference between the treatment groups (P = 0.64). CONCLUSIONS: Drug efficacies in terms of reduction in retinal lesion size and improvement in VA were similar in a regimen of trimethoprim/sulfamethoxazole and the classic treatment of ocular toxoplasmosis with pyrimethamine and sulfadiazine. Therapy with trimethoprim/sulfamethoxazole seems to be an acceptable alternative for the treatment of ocular toxoplasmosis.
机译:目的:比较传统的治疗眼弓形虫病(乙胺嘧啶,磺胺嘧啶和泼尼松龙)与甲氧苄氨嘧啶/磺胺甲恶唑(三甲唑)联合泼尼松龙的治疗方案的疗效。设计:前瞻性随机单盲临床试验。参与者:59例活动性眼弓形虫病患者被随机分为2个治疗组:29例接受乙胺嘧啶/磺胺嘧啶治疗,30例接受甲氧苄啶/磺胺甲恶唑治疗。干预:治疗包括用抗生素加类固醇治疗6周。使用酶联免疫吸附测定法测定抗弓形虫抗体(免疫球蛋白M [IgM]和IgG)。主要观察指标:治疗6周后视网膜脉络膜病变大小,干预前后的视力(VA),随访过程中药物不良反应和复发率的变化。结果:活动弓形虫视网膜脉络膜炎在治疗6周以上的所有患者中均得到解决,两个治疗组之间视网膜脉络膜病变大小的平均减少量无显着差异(传统治疗组减少61%,甲氧苄啶/磺胺甲恶唑组减少59%, P = 0.75)。同样,两组之间治疗后的VA也无显着差异(治疗后VA的平均值为经典治疗组的最小分辨角[logMAR] [20/25]的0.12对数和0.09 logMAR [20/25]的最小对数)。在甲氧苄氨嘧啶/磺胺甲恶唑基团中,P = 0.56)。两组的不良反应相似,每例一名患者均患有任何明显的药物副作用。随访24个月后的总复发率为10.16%,各治疗组之间无显着差异(P = 0.64)。结论:在甲氧苄氨嘧啶/磺胺甲基异恶唑的治疗方案以及用乙胺嘧啶和磺胺嘧啶经典治疗眼弓形体病的方案中,减少视网膜病变大小和改善视力的药物疗效相似。甲氧苄啶/磺胺甲基异恶唑的治疗似乎是治疗眼弓形体病的一种可接受的替代方法。

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