Crussell-Porter L L, Rindone J P, Ford M A, Jaskar D W
Pharmacy Service, Veterans Affairs Medical Center, Mountain Home, Tenn.
Arch Intern Med. 1993 Jan 11;153(1):102-4.
Fluconazole has been reported to interact with many medications. This study examined the effect of low-dose fluconazole therapy on the hypoprothrombinemic response of warfarin sodium in patients.
Patients receiving low-intensity anticoagulation therapy with warfarin were recruited. All patients were taking stable doses of warfarin and had two baseline prothrombin times (PTs) within 10% of each other. Each patient received 100 mg of fluconazole daily for 7 days. Prothrombin times were measured on days 2, 5, and 8 during fluconazole administration.
All patients had a progressive increase in PTs. Mean (+/- SD) of PTs increased from 15.8 +/- 1 seconds before the administration of fluconazole to 18.9 +/- 1.9 seconds on day 5 and 21.9 +/- 2.2 seconds on day 8. Fluconazole therapy was stopped early in the three patients due to high PTs. The largest change in PT was 9.7 seconds. No bleeding was noted during the study.
Fluconazole predictably potentiates the hypoprothrombinemic response of warfarin. Prothrombin times must be monitored when fluconazole is administered to patients taking warfarin.
据报道,氟康唑可与多种药物相互作用。本研究检测了低剂量氟康唑治疗对患者华法林钠低凝血酶原血症反应的影响。
招募接受华法林低强度抗凝治疗的患者。所有患者均服用稳定剂量的华法林,且两次基线凝血酶原时间(PT)相差不超过10%。每位患者每天服用100mg氟康唑,共7天。在服用氟康唑期间的第2、5和8天测量凝血酶原时间。
所有患者的PT均逐渐升高。PT的平均值(±标准差)从服用氟康唑前的15.8±1秒增加到第5天的18.9±1.9秒和第8天的21.9±2.2秒。3例患者因PT过高而提前停止氟康唑治疗。PT的最大变化为9.7秒。研究期间未观察到出血情况。
氟康唑可预测地增强华法林的低凝血酶原血症反应。在给服用华法林的患者使用氟康唑时,必须监测凝血酶原时间。