Carris Nicholas W, Spinelli Alisa, Pierini Danielle, Taylor James R, Anderson Katherine Vogel, Sando Karen, Powell Jason, Rosenberg Eric I, Zumberg Marc S, Smith Steven M, Gums John G, Dietrich Eric
Department of Community Health and Family Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
Department of Pharmacotherapy and Translational Research, College of Pharmacy, University of Florida, Gainesville, FL, USA.
Cardiovasc Ther. 2015 Jun;33(3):98-103. doi: 10.1111/1755-5922.12115.
The 2012 American College of Chest Physician Evidence-Based Management of Anticoagulant Therapy guidelines suggest an international normalized ratio (INR) testing interval of up to 12 weeks, rather than every 4 weeks, for patients with consistently stable INRs while taking vitamin K antagonists. We aimed to examine the feasibility of extended-interval follow-up in a real-world setting.
Patients receiving stable warfarin therapy for ≥ 12 weeks at baseline began extended-interval follow-up with visits occurring at 6 weeks, 14 weeks, and every 12 weeks thereafter to a maximum of 68 weeks or until they were no longer suitable for extended-interval follow-up. A single INR excursion >0.3 from goal was permitted if a reversible precipitating factor was identified and the INR was expected to return to goal without dose adjustment. The primary outcome was the proportion of patients completing all study follow-up visits.
Of 48 patients enrolled, 47 had evaluable data. The most common indication for anticoagulation was atrial fibrillation/flutter (53.2%). At baseline, mean prior warfarin treatment duration was 6.7 ± 6 years and median number of weeks on a stable regimen was 24 weeks (IQR, 19-37.5). Eleven patients (23%) completed all study follow-up visits, whereas 17 (36%) did not maintain a stable INR past the 14-week follow-up.
A large proportion of patients with previously stable (≥ 3 months) INRs were not able to maintain stable INRs during extended-interval follow-up. More research is needed to identify patient characteristics predictive of success with extended-interval follow-up prior to broad implementation.
2012年美国胸科医师学会抗凝治疗循证管理指南建议,对于服用维生素K拮抗剂且国际标准化比值(INR)持续稳定的患者,INR检测间隔可长达12周,而非每4周检测一次。我们旨在探讨在现实环境中延长检测间隔随访的可行性。
基线时接受稳定华法林治疗≥12周的患者开始延长检测间隔随访,随访时间为6周、14周,此后每12周随访一次,最长随访68周或直至不再适合延长检测间隔随访。如果确定存在可逆性促发因素且预计INR无需调整剂量即可恢复至目标值,则允许INR单次偏离目标值>0.3。主要结局是完成所有研究随访的患者比例。
48例入组患者中,47例有可评估数据。抗凝最常见的适应证是心房颤动/扑动(53.2%)。基线时,既往华法林平均治疗时间为6.7±6年,稳定治疗方案的中位周数为24周(四分位间距,19 - 37.5)。11例患者(23%)完成了所有研究随访,而17例患者(36%)在14周随访后未维持INR稳定。
很大一部分既往INR稳定(≥3个月)的患者在延长检测间隔随访期间无法维持INR稳定。在广泛实施之前,需要更多研究来确定预测延长检测间隔随访成功的患者特征。