The effect of chronic administration of oral contraceptive steroids (OCS) on the pharmacokinetics of the oral anticoagulant phenprocoumon was investigated in seven healthy females. 2. Plasma concentrations of phenprocoumon and the urinary recovery of unchanged as well as conjugated drug were measured following a single oral dose of 0.22 mg kg-1. A group of seven non-smoking, drug-free women matched for age and body weight served as controls. 3. Administration of OCS was associated with a significant increase in the clearance of phenprocoumon from 1.6 +/- 0.7 to 2.0 +/- 0.7 ml min-1 kg-1 (P less than 0.05). The urinary recovery of phenprocoumon glucuronide was significantly higher in OCS users (21.0 +/- 16 vs 14.0 +/- 10 (% of dose); P less than 0.05). No difference in plasma protein binding of phenprocoumon was observed, being 99.2 +/- 0.07 in both groups. 4. The accelerated glucuronidation of phenprocoumon in OCS users suggests the need for careful monitoring of the anticoagulatory response in these subjects, especially when the OCS are withdrawn.
摘要
在7名健康女性中研究了长期口服避孕药类固醇(OCS)对口服抗凝剂苯丙香豆素药代动力学的影响。2. 在单次口服0.22 mg kg-1剂量后,测量苯丙香豆素的血浆浓度以及未变化和结合药物的尿回收率。一组7名年龄和体重匹配的不吸烟、未用药女性作为对照。3. 服用OCS与苯丙香豆素清除率从1.6±0.7显著增加到2.0±0.7 ml min-1 kg-1相关(P<0.05)。OCS使用者中苯丙香豆素葡萄糖醛酸苷的尿回收率显著更高(21.0±16对14.0±10(剂量百分比);P<0.05)。未观察到苯丙香豆素血浆蛋白结合的差异,两组均为99.2±0.07。4. OCS使用者中苯丙香豆素葡萄糖醛酸化加速表明需要仔细监测这些受试者的抗凝反应,尤其是在停用OCS时。