当代医学
噹代醫學
당대의학
CHINA CONTEMPORARY MEDICINE
2013年
33期
145-146
,共2页
非瓣膜病房颤%华法林%初始治疗方案
非瓣膜病房顫%華法林%初始治療方案
비판막병방전%화법림%초시치료방안
Non-valvular atrial fibrillation%Warfarin%Initial treatment plan
目的:探讨非瓣膜病房颤初始治疗最佳给药方案。方法选取165例非瓣膜病房颤患者作为研究对象,所有患者随机分为联合治疗组、3mg治疗组及5mg治疗组,每组55例,联合治疗组患者给予3mg华法林联合低分子肝素钙5000U皮下注射q12h×4d作为初始治疗;3mg治疗组患者给予华法林3mg作为初始治疗;5mg治疗组患者给予华法林5mg作为初始治疗,根据INR调整华法林剂量,直至INR稳定在2.0~3.0。比较各组患者INR增高发生率及并发症情况。结果联合治疗组INR达到稳定所需时间为(11.8±4.8)d,INR增高次数发生率为5.5%,未出现血及血栓栓塞事件;3mg治疗组INR达到稳定所需时间为(12.5±4.3)d,INR增高发生率为9.1%,未出现主要出血事件,轻微出血发生率为3.6%,血栓栓塞发生率为1.8%;5mg治疗组INR达到稳定所需时间为(17.4±5.3)d,INR增高发生率为16.4%,未出现主要出血事件,轻微出血发生率为9.1%,血栓栓塞发生率为3.6%。结论华法林3mg联用皮下注射低分子肝素钙5000Uq12h×4d作为初始抗凝治疗能使INR迅速安全有效达到稳定,无严重出血并发症,对临床治疗方案的制定具有指导意义。
目的:探討非瓣膜病房顫初始治療最佳給藥方案。方法選取165例非瓣膜病房顫患者作為研究對象,所有患者隨機分為聯閤治療組、3mg治療組及5mg治療組,每組55例,聯閤治療組患者給予3mg華法林聯閤低分子肝素鈣5000U皮下註射q12h×4d作為初始治療;3mg治療組患者給予華法林3mg作為初始治療;5mg治療組患者給予華法林5mg作為初始治療,根據INR調整華法林劑量,直至INR穩定在2.0~3.0。比較各組患者INR增高髮生率及併髮癥情況。結果聯閤治療組INR達到穩定所需時間為(11.8±4.8)d,INR增高次數髮生率為5.5%,未齣現血及血栓栓塞事件;3mg治療組INR達到穩定所需時間為(12.5±4.3)d,INR增高髮生率為9.1%,未齣現主要齣血事件,輕微齣血髮生率為3.6%,血栓栓塞髮生率為1.8%;5mg治療組INR達到穩定所需時間為(17.4±5.3)d,INR增高髮生率為16.4%,未齣現主要齣血事件,輕微齣血髮生率為9.1%,血栓栓塞髮生率為3.6%。結論華法林3mg聯用皮下註射低分子肝素鈣5000Uq12h×4d作為初始抗凝治療能使INR迅速安全有效達到穩定,無嚴重齣血併髮癥,對臨床治療方案的製定具有指導意義。
목적:탐토비판막병방전초시치료최가급약방안。방법선취165례비판막병방전환자작위연구대상,소유환자수궤분위연합치료조、3mg치료조급5mg치료조,매조55례,연합치료조환자급여3mg화법림연합저분자간소개5000U피하주사q12h×4d작위초시치료;3mg치료조환자급여화법림3mg작위초시치료;5mg치료조환자급여화법림5mg작위초시치료,근거INR조정화법림제량,직지INR은정재2.0~3.0。비교각조환자INR증고발생솔급병발증정황。결과연합치료조INR체도은정소수시간위(11.8±4.8)d,INR증고차수발생솔위5.5%,미출현혈급혈전전새사건;3mg치료조INR체도은정소수시간위(12.5±4.3)d,INR증고발생솔위9.1%,미출현주요출혈사건,경미출혈발생솔위3.6%,혈전전새발생솔위1.8%;5mg치료조INR체도은정소수시간위(17.4±5.3)d,INR증고발생솔위16.4%,미출현주요출혈사건,경미출혈발생솔위9.1%,혈전전새발생솔위3.6%。결론화법림3mg련용피하주사저분자간소개5000Uq12h×4d작위초시항응치료능사INR신속안전유효체도은정,무엄중출혈병발증,대림상치료방안적제정구유지도의의。
Objective To investigate warfarin optimal dosage regimen of initial treatment of non-valvular atrial fibrillation. Methods Take 165 patients with non-valvular atrial fibrillation patients of our hospital as research objects, all the patients were randomly divided into combined treatment group, 3 mg treatment group and 5 mg treatment group, 55 cases each group. The combined treatment groups were given 3 mg warfarin combined with subcutaneous injection of 5000 units low molecular weight heparin as initial treatment. 3 mg treatment groups were treated with warfarin 3 mg as initial therapy. 5 mg treatment groups were treated with warfarin 5 mg as initial therapy. It was until the INR was stable in 2-3 according to the INR to adjust the dosage of warfarin. Compared the incidence of INR increase and complications. Results Combined treatment group:INR required to achieve stable time was 11.8 ± 4.8 d, the occurrence rate of INR increase was 5.5%and there was no bleeding and thromboembolic events. 3 mg treatment group:INR required to achieve stable time was (12.5 ± 4.3)d, the occurrence rate of INR increase was 9.1%, there was no Major bleeding events, the occurrence rate of bleeding was 3.6%, and the occurrence rate of thrombo-embolia was 1.8%. 5 mg treatment group:INR required to achieve stable time was (17.4 ±5.3) d, the occurrence rate of INR increase was 16.4%, there was no Major bleeding events, the occurrence rate of bleeding was 9.1%and the occurrence rate of thrombo-embolia was 3.6%. Conclusion Given 3 mg warfarin combined with subcutaneous injection of 5000 units low molecular weight heparin as initial treatment enable INR to reach steady rapidly, safely and effectively. It had guiding significance to planning clinical program.