Jt Comm J Qual Patient Saf. 2022 Jan;48(1):25-32. doi: 10.1016/j.jcjq.2021.10.004. Epub 2021 Oct 29.
Improved utilization of guideline-directed medical therapy (GDMT) in the management of heart failure with reduced ejection fraction (HFrEF) can reduce mortality, reduce heart failure hospitalizations, and improve quality of life. Despite well-established clinical guidelines, these therapies remain significantly underprescribed. The goal of this intervention was to increase prescribing of angiotensin-converting enzyme inhibitor (ACEI)/angiotensin II receptor blocker (ARB), angiotensin receptor neprilysin inhibitor (ARNI), and beta-blockers at ≥ 50% target doses.
The study team identified key drivers to adequate dosing of GDMT: (1) frequent and reliable follow-up visits for titration opportunities, (2) identification of actionable patients for therapy initiation and titration, and (3) reduction in prescribing practice variability. The interventions were implemented at an outpatient clinical site and consisted of three main components: (1) establishing a pharmacist-led heart failure medication titration clinic, (2) creation of a standardized titration protocol, and (3) utilization of a patient dashboard to identify eligible patients.
For patients seen in the titration clinic, in 14 months, the mean dose per patient increased from 31.3% to 70.5% of target dose for ACEI/ARB/ARNI, and from 45.8% to 85.4% for beta-blockers. At this clinical site, the percentage of HFrEF patients receiving > 50% of targeted dose increased from 39.7% to 46.7% for ACEI/ARB/ARNI, and from 39.5% to 42.9% for beta-blockers. For ACEI/ARB/ARNI, use of target doses was 5.9% higher (95% confidence interval [CI] = 3.6%-8.3%, p < 0.0001) for the intervention site, 0.2% higher (95% CI = -2.2%-2.5%, p = 0.89) during the intervention period, and 10.4% higher (95% CI = 6.9%-13.9%, p < 0.0001) for the interaction (intervention site during the intervention time period). For beta-blockers, use of target doses was 1.0% higher (95% CI = -0.6%-2.6%, p = 0.20) for the intervention site, 0.8% lower (95% CI = -2.4%-0.8%, p = 0.29) for the intervention period, and 5.8% higher (95% CI = 3.5%-8.1%, p < 0.0001) for the interaction (intervention site during the intervention time period).
Through this project's interventions, the prescribing of ACEI/ARB/ARNI and beta-blocker therapy at ≥ 50% target doses for patients with HFrEF was increased. This study demonstrates the value of a multifaceted, team-based approach that integrates population-level interventions such as clinical dashboard management with a pharmacist-led heart failure medication titration clinic.
改善射血分数降低的心力衰竭(HFrEF)患者的指南指导的医学治疗(GDMT)的利用可以降低死亡率,减少心力衰竭住院次数,提高生活质量。尽管有明确的临床指南,但这些治疗方法的应用仍然明显不足。该干预的目标是将血管紧张素转换酶抑制剂(ACEI)/血管紧张素 II 受体阻滞剂(ARB)、血管紧张素受体脑啡肽酶抑制剂(ARNI)和β受体阻滞剂的处方剂量提高到≥50%的目标剂量。
研究小组确定了实现 GDMT 充分剂量的关键驱动因素:(1)频繁且可靠的随访以进行滴定机会,(2)确定开始和滴定治疗的可操作患者,以及(3)减少处方实践的变异性。干预措施在一个门诊临床地点实施,包括三个主要组成部分:(1)建立一个由药剂师主导的心衰药物滴定诊所,(2)制定一个标准化的滴定方案,以及(3)利用患者仪表板来确定合格的患者。
在接受滴定诊所治疗的患者中,在 14 个月内,ACEI/ARB/ARNI 的每位患者的平均剂量从 31.3%增加到 70.5%的目标剂量,β受体阻滞剂的平均剂量从 45.8%增加到 85.4%。在该临床地点,接受 HFrEF 治疗的患者中,接受 ACEI/ARB/ARNI 治疗的患者中接受>50%目标剂量的比例从 39.7%增加到 46.7%,接受β受体阻滞剂治疗的患者比例从 39.5%增加到 42.9%。ACEI/ARB/ARNI 的目标剂量使用率在干预地点高 5.9%(95%置信区间[CI]:3.6%-8.3%,p<0.0001),在干预期间高 0.2%(95% CI:-2.2%-2.5%,p=0.89),在干预时间期间高 10.4%(95% CI:6.9%-13.9%,p<0.0001)。β受体阻滞剂的目标剂量使用率在干预地点高 1.0%(95% CI:-0.6%-2.6%,p=0.20),在干预期间低 0.8%(95% CI:-2.4%-0.8%,p=0.29),在干预时间期间高 5.8%(95% CI:3.5%-8.1%,p<0.0001)。
通过该项目的干预措施,提高了射血分数降低的心力衰竭患者的 ACEI/ARB/ARNI 和β受体阻滞剂治疗的≥50%目标剂量处方。这项研究证明了一种多方面、以团队为基础的方法的价值,该方法将基于人群的干预措施(如临床仪表板管理)与由药剂师主导的心衰药物滴定诊所相结合。