Evidence map›Paper›PMID 30738978›Full record

Observational studyJACC. Heart failure2019

Target Doses of Heart Failure Medical Therapy and Blood Pressure: Insights From the CHAMP-HF Registry.

Poghni A Peri-Okonny, Xiaojuan Mi, Yevgeniy Khariton, Krishna K Patel, Laine Thomas, Gregg C Fonarow, Puza P Sharma, Carol I Duffy, Nancy M Albert, Javed Butler and 6 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in JACC. Heart failure, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
9.7field-weighted citation impact, top 1% of its field
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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 99 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 9 institutions in 1 country.

Poghni A Peri-OkonnyUniversity of Missouri, Kansas City, Missouri. Electronic address: periokonnyp@umkc.edu.
Xiaojuan MiDuke Clinical Research Institute, Durham, North Carolina.
Yevgeniy KharitonUniversity of Missouri, Kansas City, Missouri.
Krishna K PatelUniversity of Missouri, Kansas City, Missouri.
Laine ThomasDuke Clinical Research Institute, Durham, North Carolina.
Gregg C FonarowUniversity of California Los Angeles, Los Angeles, California.
Puza P SharmaNovartis Pharmaceuticals Corporation, East Hanover, New Jersey.
Carol I DuffyNovartis Pharmaceuticals Corporation, East Hanover, New Jersey.
Nancy M AlbertCleveland Clinic, Cleveland, Ohio.
Javed ButlerUniversity of Mississippi, University, Mississippi.
Adrian F HernandezDuke Clinical Research Institute, Durham, North Carolina.
Kevin McCagueNovartis Pharmaceuticals Corporation, East Hanover, New Jersey.
Fredonia B WilliamsMended Hearts, Hunstville, Alabama.
Adam D DeVoreDuke Clinical Research Institute, Durham, North Carolina.
J Herbert PattersonUniversity of North Carolina, Chapel Hill, North Carolina.
John A SpertusUniversity of Missouri, Kansas City, Missouri; Saint Luke's Mid America Heart Institute, Kansas City, Missouri.
Clinical Research Institute · USNovartis (United States) · USUniversity of Missouri–Kansas City · USCleveland Clinic · USHeartsong · USSaint Luke's Health System · USUniversity of California, Los Angeles · USUniversity of Mississippi · USUniversity of North Carolina at Chapel Hill · US

Funding

Tracking and Evaluation CoreU54GM115428 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI HALL, JOHN E · 2016 to 2025
$38.2M
CARDIOVASCULAR OUTCOMES RESEARCH TRAINING PROGRAMT32HL110837 · NHLBI · UNIVERSITY OF MISSOURI KANSAS CITY · PI JOHN A SPERTUS · 2012 to 2026
$5.0M
NHLBI NIH HHS T32 HL110837NIGMS NIH HHS U54 GM115428
6 · The paper itself

Abstract

objectivesThis study sought to determine the rate of use of target doses of foundational guideline-directed medical therapy (GDMT) in a contemporary cohort of patients with heart failure with reduced ejection fraction (HFrEF) across systolic blood pressure (SBP) categories.

backgroundPatients with HFrEF are infrequently titrated to recommended doses of GDMT. The relationship between SBP and achieving GDMT target doses is not well studied.

methodsPatients enrolled in the CHAMP-HF (Change the Management of Patients With Heart Failure) registry without documented intolerance to angiotensin-converting enzyme inhibitors (ACEIs), angiotensin receptor blockers (ARBs), angiotensin receptor-neprilysin inhibitors (ARNIs), and beta blockers (BBs) were assessed at enrollment. We estimated the proportion receiving target doses (% of target dose [95% confidence interval (CI)]) based on the most recent American College of Cardiology/American Heart Association/Heart Failure Society of America heart failure guidelines at baseline in all patients, and by SBP category (≥110 vs. <110 mm Hg).

resultsOf the 3,095 patients eligible for analysis, 2,421 (78.2%) had SBP ≥110 mm Hg. The proportion of patients receiving target doses were 18.7% (95% CI: 17.3% to 20.0%; BB), 10.8% (95% CI: 9.7% to 11.9%; ACEI/ARB), and 2.0% (95% CI: 1.5% to 2.5%; ARNI). Among those with SBP <110 mm Hg (n = 674), 17.5% (95% CI: 14.6% to 20.4%; BB), 6.2% (95% CI: 4.4% to 8.1%; ACEI/ARB), and 1.8% (95% CI: 0.8% to 2.8%; ARNI) were receiving target doses. Among those with SBP ≥110 mm Hg (n = 2,421), 19.0% (95% CI: 17.4% to 20.6%; BB), 12.1% (95% CI: 10.8% to 13.4%; ACEI/ARB), and 2.0% (95% CI: 1.5% to 2.6%; ARNI) were receiving target doses.

conclusionsIn a large, contemporary registry of outpatients with chronic HFrEF eligible for treatment with BBs and ACEI/ARB/ARNI, <20% of patients were receiving target doses, even among those with SBP ≥110 mm Hg.

Indexed as

RegistriesAdrenergic beta-AntagonistsAdultAgedAged, 80 and overAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsBlood PressureCross-Sectional StudiesDose-Response Relationship, DrugFemaleFollow-Up StudiesHeart FailureHospitalizationHumansMaleAdrenergic beta-AntagonistsAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor Antagonistsheart failuresystolic blood pressuretarget dose

Identifiers

PMID30738978
PMCPMC6440823
OpenAlexW2913792930

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.