Evidence map›Paper›PMID 39503006›Full record

ArticleAmerican heart journal plus : cardiology research and practice2024

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

James C Coons, Jennifer Kliner, Michael A Mathier, Suresh Mulukutla, Floyd Thoma, Ahmet Sezer, Mary Keebler

Abstract read
In one paragraph

Article in American heart journal plus : cardiology research and practice, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

James C CoonsDepartment of Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, United States of America.
Jennifer KlinerHeart and Vascular Institute, UPMC Presbyterian-Shadyside Hospital, Pittsburgh, PA, United States of America.
Michael A MathierHeart and Vascular Institute, UPMC Presbyterian-Shadyside Hospital, Pittsburgh, PA, United States of America.
Suresh MulukutlaHeart and Vascular Institute, UPMC Presbyterian-Shadyside Hospital, Pittsburgh, PA, United States of America.
Floyd ThomaHeart and Vascular Institute, UPMC Presbyterian-Shadyside Hospital, Pittsburgh, PA, United States of America.
Ahmet SezerHeart and Vascular Institute, UPMC Presbyterian-Shadyside Hospital, Pittsburgh, PA, United States of America.
Mary KeeblerHeart and Vascular Institute, UPMC Presbyterian-Shadyside Hospital, Pittsburgh, PA, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 all-cause 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 < 0.0001), angiotensin-receptor neprilysin inhibitor (62 % vs. 45 %; p < 0.0001), beta blocker (92 % vs. 88 %; p < 0.0001), mineralocorticoid receptor antagonist (69 % vs. 45 %; p < 0.0001), and sodium glucose cotransporter-2 inhibitor (68 % vs. 35 %; p < 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 < 0.001). All-cause mortality was significantly lower at 6 months (p = 0.006) and 12 months (p < 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.

Indexed as

Guideline-directed medical therapyHeart failureMedication optimizationReadmissions

Identifiers

PMID39503006
PMCPMC11535887

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.