Sharow Anna, Champigny Joey, Gamble John-Michael, Houle Sherilyn K D, Carter Caitlin, Nagge Jeff
University of Waterloo School of Pharmacy, Kitchener, ON, Canada.
J Pharm Pract. 2025 Dec;38(6):540-550. doi: 10.1177/08971900251347506. Epub 2025 Jun 2.
Growing evidence suggests that non-physician providers (NPPs) can effectively and safely manage warfarin therapy. This systematic review and meta-analysis aimed to evaluate warfarin management by NPPs compared to usual medical care (UMC) in ambulatory patients. We conducted a systematic search of PubMed (MEDLINE), Ovid Embase, Ovid International Pharmaceutical Abstracts, Scopus, CINAHL (EBSCO), and the Cochrane Central Register of Controlled Trials (CENTRAL) from inception to January 2024. Studies were included if they were randomized controlled trials or quasi-experimental designs comparing warfarin management across professions. Two independent reviewers performed title and abstract screening, full-text review, data extraction, and risk of bias assessment. Results were pooled using random effects models. Of 19 122 citations identified, 6 met the inclusion criteria. NPPs included pharmacists (4), nurse practitioners (1), and multidisciplinary teams (1). Meta-analysis showed no significant difference in time spent in therapeutic range (TTR) (mean difference [MD] 1.64%; 95% confidence interval [CI]-1.86 to 5.16, I = 0%)) for NPPs vs UMC. There were no differences in thrombosis (relative risk [RR] 1.23; 95% CI 0.36 to 4.23, I = 0%), hemorrhage (RR = 1.07; 95% CI 0.44 to 2.63, I = 0%), mortality (RR = 0.94; 95% CI 0.33 to 2.67, I = 0%), or patient satisfaction (standardized mean difference [SMD] 0.56; 95% CI -0.04 to 1.15, I = 85%). NPP management resulted in similar TTR as UMC. Due to few thromboembolic and hemorrhagic events, more studies are needed to determine the effects of NPP warfarin management on clinical outcomes.
越来越多的证据表明,非医师医疗服务提供者(NPPs)能够有效且安全地管理华法林治疗。本系统评价和荟萃分析旨在评估在门诊患者中,与常规医疗护理(UMC)相比,NPPs对华法林的管理情况。我们对PubMed(MEDLINE)、Ovid Embase、Ovid国际药学文摘、Scopus、CINAHL(EBSCO)以及Cochrane对照试验中心注册库(CENTRAL)进行了从建库至2024年1月的系统检索。纳入的研究需为比较不同专业对华法林管理情况的随机对照试验或准实验设计。两名独立评审员进行标题和摘要筛选、全文评审、数据提取以及偏倚风险评估。结果采用随机效应模型进行汇总。在检索到的19122篇文献中,有6篇符合纳入标准。NPPs包括药剂师(4篇)、执业护士(1篇)以及多学科团队(1篇)。荟萃分析显示,NPPs与UMC相比,在治疗范围内花费的时间(TTR)无显著差异(平均差[MD] 1.64%;95%置信区间[CI] -1.86至5.16,I² = 0%)。在血栓形成(相对风险[RR] 1.23;95% CI 0.36至4.23,I² = 0%)、出血(RR = 1.07;95% CI 0.44至2.63,I² = 0%)、死亡率(RR = 0.94;95% CI 0.33至2.67,I² = 0%)或患者满意度(标准化平均差[SMD] 0.56;95% CI -0.04至1.15,I² = 85%)方面均无差异。NPPs管理的TTR与UMC相似。由于血栓栓塞和出血事件较少,需要更多研究来确定NPPs对华法林的管理对临床结局的影响。