首页> 外文期刊>Obstetrics and Gynecology: Journal of the American College of Obstetricians and Gynecologists >A comparison of the bioavailability of oral and intramuscular dexamethasone in women in late pregnancy.
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A comparison of the bioavailability of oral and intramuscular dexamethasone in women in late pregnancy.

机译:妊娠晚期妇女口服和肌肉内地塞米松的生物利用度比较。

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OBJECTIVE: To compare the bioavailability of oral and intramuscular (i.m.) dexamethasone in third-trimester pregnant women. METHODS: Oral and i.m. dexamethasone levels were compared in a randomized, parallel, crossover bioavailability study involving 11 gravid women in the third trimester of pregnancy. Subjects were randomized to receive either 6 mg of i.m. or 8 mg of oral dexamethasone. The following week, the alternative regimen was administered. Serial blood samples were obtained after drug administration. Dexamethasone concentrations were measured by radioimmunoassay. Total area under the curve was compared for the oral and i.m. groups using a paired t test. RESULTS: Eight of the 11 women completed the study through 12 hours; all 11 women completed the study through 6 hours. Among the 11 women, peak levels of dexamethasone occurred 30 minutes after i.m. injection (mean +/- standard deviation, 101.7 +/- 19.2 ng/mL) and 120 minutes after oral administration (65.9 +/- 20.5 ng/mL). Area under the curvedid not differ significantly between those receiving i.m. dexamethasone (258.3 +/- 50.0 ng/minute/mL) and those receiving oral dexamethasone (251.8 +/- 59.7 ng/minute/mL) when measured 6 hours after administration of the drug. Terminal half-lives were similar in the i.m. and oral groups. Similar findings were noted among the eight women who were studied through 12 hours. This study had a power of 87% to detect a 20% difference in area under the curve between the two groups. CONCLUSION: The bioavailability of 8 mg of oral dexamethasone is similar to that of a 6-mg IM dose, as determined by the area under the curve.
机译:目的:比较妊娠晚期孕妇口服和肌肉注射地塞米松的生物利用度。方法:口服和上午在一项随机,平行,交叉的生物利用度研究中,对地塞米松的水平进行了比较,该研究涉及11个妊娠晚期的妊娠妇女。使受试者随机接受6mgi.m。或口服地塞米松8毫克。接下来的一周,进行了替代治疗。给药后获得连续血样。地塞米松浓度通过放射免疫测定法测量。比较曲线下的总面积用于口服和口服。组使用配对t检验。结果:11名妇女中有8名在12个小时内完成了研究。所有11名妇女在6个小时内完成了研究。在这11名妇女中,地塞米松的峰值水平出现在i.m.后30分钟。注射后(平均+/-标准偏差,101.7 +/- 19.2 ng / mL)和口服后120分钟(65.9 +/- 20.5 ng / mL)。接受i.m的人的下颌弯曲面积没有明显差异。地塞米松(258.3 +/- 50.0 ng / min / mL)和接受口服地塞米松(251.8 +/- 59.7 ng / min / mL)的人在给药6小时后进行测量。最终半衰期在上午相似和口头小组。在研究了12小时的八名女性中,也发现了类似的发现。这项研究具有87%的功效,可检测出两组之间曲线下面积的20%差异。结论:根据曲线下的面积确定,口服地塞米松8 mg的生物利用度与IM剂量6 mg的生物利用度相似。

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