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Dexamethasone concentration in the subretinal fluid after a subconjunctival injection, a peribulbar injection, or an oral dose.

机译:结膜下注射,球周注射或口服给药后,视网膜下液中地塞米松的浓度。

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PURPOSE: To determine dexamethasone concentrations in the subretinal fluid of patients after a peribulbar injection, a subconjunctival injection, or an oral dose of dexamethasone and to compare the results with those of previous similar studies of dexamethasone concentrations in the vitreous. DESIGN: Prospective, nonrandomized, comparative trial. PARTICIPANTS: One hundred forty-eight patients with a rhegmatogenous retinal detachment. METHODS: Fifty patients received a peribulbar injection of 5 mg dexamethasone disodium phosphate, 49 received a subconjunctival injection of 2.5 mg dexamethasone disodium phosphate, and 49 received an oral dose of 7. 5 mg dexamethasone at various time intervals before surgery. At the time of surgery, a subretinal fluid sample was taken from each patient. MAIN OUTCOME MEASURES: The dexamethasone concentration in the subretinal fluid measured by radioimmunoassay. RESULTS: The estimated maximum dexamethasone concentrations in the subretinal fluid after the peribulbar injection, the subconjunctival injection, and the oral dose were, respectively, 82.2 ng/ml (standard error, 17. 6), 359 ng/ml (standard error, 80.2), and 12.3 ng/ml (standard error, 1.61). Corrected for dose, the maximum dexamethasone concentrations after subconjunctival injection and peribulbar injection were, respectively, 120 (95% confidence interval, 54/180) and 13 (95% confidence interval, 6.8/20) times greater than after oral administration. CONCLUSIONS: A subconjunctival injection of dexamethasone disodium phosphate is more effective in delivering dexamethasone into the subretinal fluid of patients with a rhegmatogenous retinal detachment compared with peribulbar injection or oral administration. The subretinal dexamethasone concentrations were higher than concentrations measured in the vitreous in previous studies with a similar setup after all three delivery methods.
机译:目的:确定球周注射,结膜下注射或口服地塞米松后患者视网膜下液中地塞米松的浓度,并将该结果与先前玻璃体中地塞米松浓度的类似研究进行比较。设计:前瞻性,非随机,比较试验。参与者:148名患有流变性视网膜脱离的患者。方法:50例患者在球囊周围注射5 mg地塞米松磷酸二钠,49例在结膜下注射2.5 mg地塞米松磷酸二钠,49例在手术前的不同时间口服7毫克。5 mg地塞米松。在手术时,从每位患者中提取视网膜下液样品。主要观察指标:放射免疫法测定视网膜下液中地塞米松的浓度。结果:估计在球周注射,结膜下注射和口服剂量后,视网膜下液中地塞米松的最大浓度分别为82.2 ng / ml(标准误为17. 6),359 ng / ml(标准误为80.2)。 )和12.3 ng / ml(标准误,1.61)。校正剂量后,结膜下注射和球周注射后的最大地塞米松浓度分别比口服后高120倍(95%置信区间54/180)和13倍(95%置信区间6.8 / 20)。结论:与球周注射或口服给药相比,结膜下注射地塞米松磷酸二钠更有效地将地塞米松递送至具有流变性视网膜脱离的患者的视网膜下液中。在所有三种递送方法之后,视网膜下地塞米松的浓度均高于先前研究中玻璃体中的浓度,之前的研究采用类似的设置。

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