Carris Nicholas W, Hwang Andrew Y, Smith Steven M, Taylor James R, Sando Karen, Powell Jason, Rosenberg Eric I, Zumberg Marc S, Gums John G, Dietrich Eric A, Anderson Katherine Vogel
Department of Pharmacotherapeutics and Clinical Research, College of Pharmacy, University of South Florida, 12901 Bruce B. Downs Blvd., MDC 30, Tampa, FL, 33612-4749, USA.
Department of Family Medicine, Morsani College of Medicine, University of South Florida, 12901 Bruce B. Downs Blvd., MDC 30, Tampa, FL, 33612, USA.
J Thromb Thrombolysis. 2016 Nov;42(4):486-93. doi: 10.1007/s11239-016-1385-9.
Extended-interval monitoring of warfarin has been proposed to reduce follow-up burden and improve patient satisfaction. We aimed to make an initial assessment of anticoagulation satisfaction before and after an extended-interval warfarin monitoring intervention. We conducted a translational prospective single-arm pilot study of extended-interval warfarin monitoring in five pharmacist-managed anticoagulation clinics. Patients meeting CHEST guideline criteria for extended-interval warfarin monitoring began progressive extended-interval follow-up (6, 8, and 12 weeks thereafter). The Duke Anticoagulation Satisfaction Scale (DASS) was administered at baseline and at end-of-study or study removal (in patients no longer appropriate for extended interval follow-up). Forty-six patients had evaluable pre- and post-intervention DASS survey data. Mean age of patients was 66.5 years, 74 % were non-Hispanic whites, and 48 % were men. Patients completed a mean ± SD of 34 ± 22 weeks of follow-up. Mean ± SD total DASS score at baseline was 45.2 ± 14.2 versus 49.1 ± 14.9 at end-of-study (mean change, +3.9 [95 % CI -0.6-8.4; p = 0.09]), indicating no benefit-and trending toward decrement-to anticoagulation satisfaction. Change in anticoagulation satisfaction varied substantially following extended-interval monitoring, with no evidence of improved satisfaction. Plausible reasons for patients not preferring extended-interval monitoring include increased anxiety and disengagement from self-management activities, both potentially related to less frequent feedback and reassurance during extended interval-monitoring. Additional research is needed to identify who is likely to benefit most from extended-interval monitoring. Anticoagulation satisfaction should be considered with clinical factors and shared-decision making when implementing extended-interval warfarin monitoring.
有人提议延长对华法林的监测间隔,以减轻随访负担并提高患者满意度。我们旨在对华法林监测间隔延长干预前后的抗凝满意度进行初步评估。我们在五家由药剂师管理的抗凝诊所进行了一项关于延长华法林监测间隔的前瞻性单臂试点研究。符合CHEST指南中延长华法林监测间隔标准的患者开始进行逐步延长间隔的随访(此后分别为6周、8周和12周)。在基线时以及研究结束时或退出研究时(对于不再适合延长间隔随访的患者)使用杜克抗凝满意度量表(DASS)进行评估。46例患者有可评估的干预前后DASS调查数据。患者的平均年龄为66.5岁,74%为非西班牙裔白人,48%为男性。患者完成随访的平均时间为34±22周。基线时DASS总评分的平均值±标准差为45.2±14.2,而研究结束时为49.1±14.9(平均变化为+3.9[95%置信区间-0.6-8.4;p=0.09]),表明抗凝满意度没有改善,且有下降趋势。延长间隔监测后,抗凝满意度的变化差异很大,没有证据表明满意度有所提高。患者不倾向于延长间隔监测的合理原因包括焦虑增加以及自我管理活动参与度降低,这两者都可能与延长间隔监测期间反馈和安心程度降低有关。需要进一步研究以确定谁最可能从延长间隔监测中获益。在实施延长华法林监测间隔时,应结合临床因素和共同决策来考虑抗凝满意度。