Evaluation of Guideline-Directed Medical Therapy for Outpatients Living with Heart Failure with Reduced Ejection Fraction.

The Canadian journal of hospital pharmacy Pub Date : 2024-03-13 eCollection Date: 2024-01-01 DOI:10.4212/cjhp.3373
Taylor McVannel, Lori Albers, Lynette Kosar, Brittani Reid, Colin Yeung, Muhammad Siddiqui, Oleksandr Baran
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Abstract

Background: Pharmacotherapy is the cornerstone of treatment for heart failure with reduced ejection fraction (HFrEF). The Canadian Cardiovascular Society and Canadian Heart Failure Society have defined guideline-directed medical therapy (GDMT) as 4 foundational medications. Despite strong recommendations for use of GDMT in HFrEF, current practice alignment with guidelines is unknown.

Objectives: The primary objectives were to determine the proportion of patients for whom optimized GDMT for HFrEF was prescribed, to describe the doses of foundational medications achieved, and to describe any documented rationale limiting the optimization of GDMT. The secondary objectives were to describe documented pharmacist activities outside of scheduled multidisciplinary appointments at the heart function clinic (HFC) and to describe heart failure-related hospital encounters in 2021.

Methods: A retrospective cohort study using medical records of patients with HFrEF who were receiving treatment at the Regina HFC as of December 31, 2021, was conducted.

Results: Of the 129 patients included in the study, 61 (47.3%) were prescribed optimized GDMT. Specifically, within the individual foundational medication classes, 82.2% (106/129), 80.6% (104/129), 79.1% (102/129), and 74.4% (96/129) of patients received optimized therapy with a renin-angiotensin system inhibitor, mineralocorticoid receptor antagonist, β-blocker, and sodium-glucose cotransporter 2 inhibitor, respectively. Documented rationale was not available in 35.8% (38/106) of instances of suboptimal utilization of GDMT and in 41.7% (60/144) of instances of suboptimal dosing of GDMT. The most common documented rationale for suboptimal utilization was intolerance to the medication (33.0% [35/106]), and the most common rationale for suboptimal dosing was intolerance to dose increases (57.6% [83/144]). Pharmacists documented a total of 553 patient care activities for 58.9% (76/129) of the patients, outside scheduled multidisciplinary appointments in the HFC. Sixteen patients (12.4%) had heart failure-related hospital encounters a total of 31 times in 2021.

Conclusions: Although many patients were receiving the benefits of multidisciplinary care at the Regina HFC, there remained a treatment gap in the use of GDMT for HFrEF. These findings will be used to inform strategies to improve clinic processes, including efficient identification of patients requiring optimization of GDMT, who would benefit the most from multidisciplinary care.

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评估针对射血分数降低型心力衰竭门诊患者的指导性医疗疗法。
背景:药物疗法是治疗射血分数降低型心力衰竭(HFrEF)的基石。加拿大心血管协会和加拿大心力衰竭协会将指南指导下的药物治疗(GDMT)定义为 4 种基础药物。尽管指南强烈建议在 HFrEF 中使用 GDMT,但目前的实践与指南的一致性尚不清楚:首要目标是确定为 HFrEF 开具优化 GDMT 的患者比例,描述所达到的基础药物剂量,并描述限制 GDMT 优化的任何有据可查的理由。次要目标是描述药剂师在心脏功能门诊(HFC)预定的多学科预约之外的活动记录,并描述 2021 年与心衰相关的医院就诊情况:方法: 使用截至 2021 年 12 月 31 日在里贾纳心功能门诊接受治疗的心衰患者的医疗记录进行了一项回顾性队列研究:在纳入研究的 129 名患者中,61 人(47.3%)使用了优化的 GDMT 处方。具体来说,在各个基础药物类别中,分别有82.2%(106/129)、80.6%(104/129)、79.1%(102/129)和74.4%(96/129)的患者接受了肾素-血管紧张素系统抑制剂、矿物质皮质激素受体拮抗剂、β-受体阻滞剂和钠-葡萄糖共转运体2抑制剂的优化治疗。35.8%(38/106)的 GDMT 使用量不达标病例和 41.7%(60/144)的 GDMT 剂量不达标病例没有文件说明。记录的最常见的非最佳用药理由是对药物不耐受(33.0% [35/106]),最常见的非最佳剂量理由是对剂量增加不耐受(57.6% [83/144])。药剂师共为 58.9% 的患者(76/129)记录了 553 次患者护理活动,这些活动都是在 HFC 预定的多学科预约之外进行的。16 名患者(12.4%)在 2021 年共 31 次与心衰相关的住院治疗:尽管许多患者在里贾纳 HFC 得到了多学科治疗的益处,但在使用 GDMT 治疗 HFrEF 方面仍存在差距。这些发现将用于制定改善诊所流程的策略,包括有效识别需要优化 GDMT 的患者,这些患者将从多学科治疗中获益最多。
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