Pharmaceutical Care Research Group, Department of Pharmaceutical Sciences, University of Basel, Petersplatz 14, Postfach 2148, 4051 Basel, Switzerland, Tel: +41 61 207 14 26.
Department of Neurology and Stroke Centre, University Hospital Basel and University of Basel, Basel, Switzerland, Tel: +41 61 265 44 91.
J Stroke Cerebrovasc Dis. 2021 Feb;30(2):105530. doi: 10.1016/j.jstrokecerebrovasdis.2020.105530. Epub 2020 Dec 14.
To describe how stroke survivors with atrial fibrillation implement direct oral anticoagulant treatment and propose appropriate metrics to describe adherence.
Stroke patients with atrial fibrillation electronically recorded their self-administered direct oral anticoagulants (apixaban, dabigatran, edoxaban, rivaroxaban) during a 6-month observation phase after hospitalisation for ischemic stroke. Taking and timing adherence, correct dosing days, drug holidays, time of the day and day of the week subsets, dose-to-dose intervals and longest intervals between two consecutive doses were calculated from electronic monitoring data to describe and discuss the implementation phase of adherence.
Data from 41 patients were analysed. Median age was 77 (IQR = 69-84), 63.4% were male and the majority suffered a mild stroke (median NIHSS: 1). Mean taking and timing adherence exceeded 90%. Correct dosing occurred in 86.6% of the days. Seven patients (17.1%) had intake pauses of three or more consecutive days. Patients with twice-daily regimen (70.7%) had higher taking adherence in the morning than in the evening (94.4% versus 89.9%; p = 0.001). No therapy- or anamneses-related characteristic was associated with taking adherence.
Although adherence to direct oral anticoagulants of stroke patients with atrial fibrillation exceeded 90%, deviant intake patterns such as drug holidays and missed evening doses were common and raise concerns. Appropriate adherence metrics calculated from electronic monitoring data may guide healthcare professionals elucidating patient-tailored adherence-enhancing interventions. ClinicalTrials.gov registration number: NCT03344146.
描述房颤卒中幸存者如何实施直接口服抗凝剂治疗,并提出合适的指标来描述依从性。
房颤卒中患者在因缺血性卒中住院后 6 个月的观察期内,通过电子方式记录他们自行服用的直接口服抗凝剂(阿哌沙班、达比加群、依度沙班、利伐沙班)。从电子监测数据中计算出服药和按时服药依从性、正确服药天数、药物假期、一天中的时间和一周中的天数亚组、剂量-剂量间隔和两次连续服药之间最长间隔,以描述和讨论依从性的实施阶段。
分析了 41 名患者的数据。中位年龄为 77 岁(IQR=69-84),63.4%为男性,大多数患者为轻度卒中(中位 NIHSS:1)。平均服药和按时服药依从性超过 90%。正确的剂量在 86.6%的天数内发生。7 名患者(17.1%)有连续 3 天或以上的中断。每日两次给药方案的患者(70.7%)早晨的服药依从性高于晚上(94.4%比 89.9%;p=0.001)。没有与治疗或病史相关的特征与服药依从性相关。
尽管房颤卒中患者对直接口服抗凝剂的依从性超过 90%,但常见的不规律服药模式,如药物假期和漏服晚上剂量,仍令人担忧。从电子监测数据计算出的适当依从性指标可能有助于指导医疗保健专业人员制定针对患者的依从性增强干预措施。临床试验注册号:NCT03344146。