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Vitreous cavity penetration of ceftazidime after intravenous administration.

机译:静脉给药后头孢他啶的玻璃体腔穿透。

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PURPOSE: Penetration of ceftazidime, a third generation cephalosporin, into the vitreous cavity after intravenous administration was investigated. METHODS: Because antimicrobial penetration varies with surgical status of the eye and with inflammation, studies were conducted in phakic, aphakic, and aphakic, vitrectomized eyes in both normal and inflamed conditions. Ceftazidime 50 mg/kg was administered every 8 hours and vitreous cavity concentrations were tested at intervals from 2 to 72 hours after the initial dose. RESULTS: No penetration was found into control phakic and aphakic eyes, but drug concentrations were detected in inflamed eyes at 24 hours. Vitreous concentrations of ceftazidime in aphakic, vitrectomized eyes reached levels well above the minimal inhibitory concentration (MIC) for Pseudomonas organisms within 2 hours of intravenous administration in control eyes (8.5 micrograms/ml) and inflamed eyes (35.4 micrograms/ml). Inflammation and removal of the lens and vitreous significantly enhanced ceftazidime penetration at all time periods tested. CONCLUSION: Ceftazidime penetrates into the vitreous cavity of inflamed eyes after intravenous administration and achieves concentrations above the MIC for Pseudomonas organisms. Penetration is greatest in aphakic, vitrectomized eyes.
机译:目的:研究了第三代头孢菌素头孢他啶在静脉内给药后渗透入玻璃体腔的情况。方法:由于抗菌素的渗透随眼睛的手术状态和发炎而变化,因此在正常和发炎的情况下,均在有晶状体,无晶状体和无晶状体,无晶状体的眼中进行了研究。头孢他啶50 mg / kg每8小时施用一次,并在初始剂量后2至72小时的间隔内测试玻璃体腔的浓度。结果:未发现有晶状体和无晶状体对照眼有渗透,但在24小时发炎的眼睛中检测到药物浓度。无晶状体,无玻璃体切除术的眼睛中的头孢他啶的玻璃体内浓度在对照眼(8.5微克/毫升)和发炎眼(35.4微克/毫升)的静脉注射后2小时内达到远高于假单胞菌生物的最小抑制浓度(MIC)。在所有测试的时间段内,晶状体和玻璃体的炎症和去除显着增强了头孢他啶的渗透。结论:头孢他啶静脉内给药后会渗透到发炎的眼睛的玻璃体腔中,并达到假单胞菌生物体MIC以上的浓度。无晶状体,无玻璃体切除的眼睛的穿透力最大。

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