Evidence map›Paper›PMID 28328015›Full record

ReviewClinical cardiology2017

PCSK9 inhibitor access barriers-issues and recommendations: Improving the access process for patients, clinicians and payers.

Seth J Baum, Peter P Toth, James A Underberg, Paul Jellinger, Joyce Ross, Katherine Wilemon

Abstract readReview
In one paragraph

Review in Clinical cardiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 citing papers in PubMed.

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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

6 authors.

Seth J BaumDepartment of Integrated Medical Sciences, Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, Florida.ORCID http://orcid.org/0000-0001-9045-6607
Peter P TothCGH Medical Center, Sterling, Illinois, and Ciccarone Center for the Prevention of Heart Disease, Johns Hopkins University School of Medicine, Baltimore, Maryland.
James A UnderbergCenter for the Prevention of Cardiovascular Disease at New York University Langone Medical Center, New York, New York.
Paul JellingerCenter for Diabetes and Endocrine Care, Ft. Lauderdale, Florida, and University of Miami Miller School of Medicine, Miami, Florida.
Joyce RossUniversity of Pennsylvania Health System, Philadelphia, Pennsylvania.
Katherine WilemonThe Familial Hypercholesterolemia Foundation, Pasadena, California.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The proprotein convertase subtilisin/kexin type 9 inhibitors or monoclonal antibodies likely represent the greatest advance in lipid management in 30 years. In 2015 the US Food and Drug Administration approved both alirocumab and evolocumab for high-risk patients with familial hypercholesterolemia (FH) and clinical atherosclerotic cardiovascular disease requiring additional lowering of low-density lipoprotein cholesterol. Though many lipid specialists, cardiovascular disease prevention experts, endocrinologists, and others prescribed the drugs on label, they found their directives denied 80% to 90% of the time. The high frequency of denials prompted the American Society for Preventive Cardiology (ASPC), to gather multiple stakeholder organizations including the American College of Cardiology, National Lipid Association, American Association of Clinical Endocrinologists (AACE), and FH Foundation for 2 town hall meetings to identify access issues and implement viable solutions. This article reviews findings recognized and solutions suggested by experts during these discussions. The article is a product of the ASPC, along with each author writing as an individual and endorsed by the AACE.

Indexed as

Drug CostsHypercholesterolemiaPCSK9 InhibitorsPractice Guidelines as TopicAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCost-Benefit AnalysisHumansIndole AlkaloidsProprotein Convertase 9alirocumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedevodamineIndole AlkaloidsPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9Coronary Artery DiseaseFamilial HypercholesterolemiaHepatocyteLow-Density Lipoprotein CholesterolPharmacy Benefits ManagerProprotein Convertase Subtilisin/Kexin Type 9

Identifiers

PMID28328015
PMCPMC5412679

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.