Medication optimization clinic decreases hospitalizations and mortality for patients with heart failure with reduced ejection fraction

被引:0
作者
Coons, James C. [1 ,2 ]
Kliner, Jennifer [2 ]
Mathier, Michael A. [2 ]
Mulukutla, Suresh [2 ]
Thoma, Floyd [2 ]
Sezer, Ahmet [2 ]
Keebler, Mary [2 ]
机构
[1] Univ Pittsburgh, Sch Pharm, Dept Pharm & Therapeut, Pittsburgh, PA USA
[2] UPMC Presbyterian Shadyside Hosp, Heart & Vasc Inst, Pittsburgh, PA USA
来源
AMERICAN HEART JOURNAL PLUS: CARDIOLOGY RESEARCH AND PRACTICE | 2024年 / 47卷
关键词
Heart failure; Medication optimization; Readmissions; Guideline-directed medical therapy;
D O I
10.1016/j.ahjo.2024.100470
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Study objective: To evaluate the impact of a medication optimization clinic (MOC) on GDMT and outcomes for patients with HFrEF versus usual care. Design: Retrospective evaluation of a multi-site MOC was conducted. Setting: Large health system with academic and community hospitals. Participants: Patients with HFrEF referred to MOC by their cardiologist versus usual care. Interventions: GDMT use managed by an advanced practice provider or clinical pharmacist through weekly telemedicine visits. Main outcome measures: The primary outcome was HF hospitalization. Cardiovascular hospitalization and allcause mortality were also assessed. Kaplan-Meier Curve, Cumulative Incidence Function, and competing risk analysis with regression models were conducted. Results: 1419 patients in MOC group were compared to 5116 control patients. GDMT use was significantly higher in MOC: quadruple therapy (49 % vs. 19 %; p G 0.0001), angiotensin-receptor neprilysin inhibitor (62 % vs. 45 %; p G 0.0001), beta blocker (92 % vs. 88 %; p G 0.0001), mineralocorticoid receptor antagonist (69 % vs. 45 %; p G 0.0001), and sodium glucose cotransporter-2 inhibitor (68 % vs. 35 %; p G 0.0001). Competing risk analyses showed that HF and CV hospitalizations were significantly lower at all times points (3, 6, and 12 months) for MOC vs. control (p G 0.001). All-cause mortality was significantly lower at 6 months (p = 0.006) and 12 months (p G 0.001), but did not differ at 3 months (p = 0.35), for MOC vs. control. Conclusions: MOC was associated with improved GDMT and lower risks of hospitalizations due to HF and any cardiovascular cause, and all-cause mortality in patients with HFrEF.
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页数:7
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