Evidence map›Paper›PMID 30940751›Full record

Observational studyBMJ open2019

Clinical characteristics and lipid lowering treatment of patients initiated on proprotein convertase subtilisin-kexin type 9 inhibitors: a nationwide cohort study.

Jakob Solgaard Jensen, Peter Ejvin Weeke, Lia Evi Bang, Dan Eik Høfsten, Maria Sejersten Ripa, Anne-Marie Schjerning, Juliane Elizabeth Theilade, Lars Valeur Køber, Gunnar Hilmar Gislason, Jannik Pallisgaard

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in BMJ open, 2019. 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
0.9field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. Article
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

10 authors at 4 institutions in 3 countries.

Jakob Solgaard JensenDepartment of Cardiology, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0003-3255-4406
Peter Ejvin WeekeDepartment of Cardiology, Copenhagen University Hospital, Bispebjerg, Copenhagen, Denmark.
Lia Evi BangDepartment of Cardiology, Rigshospitalet, Copenhagen, Denmark.
Dan Eik HøfstenDepartment of Cardiology, Rigshospitalet, Copenhagen, Denmark.
Maria Sejersten RipaDepartment of Cardiology, Copenhagen University Hospital Herlev and Gentofte, Hellerup, Denmark.
Anne-Marie SchjerningDepartment of Cardiology, Copenhagen University Hospital Herlev and Gentofte, Hellerup, Denmark.
Juliane Elizabeth TheiladeDepartment of Cardiology, Copenhagen University Hospital Herlev and Gentofte, Hellerup, Denmark.
Lars Valeur KøberDepartment of Cardiology, Rigshospitalet, Copenhagen, Denmark.
Gunnar Hilmar GislasonDepartment of Cardiology, Copenhagen University Hospital Herlev and Gentofte, Hellerup, Denmark.
Jannik PallisgaardDepartment of Cardiology, Copenhagen University Hospital Herlev and Gentofte, Hellerup, Denmark.
Gentofte Hospital · DKRigshospitalet · DKBispebjerg Hospital · DKNovo Nordisk (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesGiven the novelty of proprotein convertase subtilisin-kexin type 9 inhibitors (PCSK9i), little is known regarding overall implementation or clinical characteristics among patients who initiate treatment. We aimed to assess the total number of patients initiated on PCSK9i along with a description of the clinical characteristics and lipid lowering treatment (LLT) of such patients.

settingA register-based descriptive cohort study of patients receiving a PCSK9i in the time period from 01 January 2016 to 31 March 2017 using a cross linkage between three nationwide Danish registers. Information regarding PCSK9i prescriptions, patient demographics, concurrent pharmacotherapy, comorbidities and previous coronary procedures was identified.

resultsOverall, 137 patients initiated treatment with PCSK9i in the study period from 11 in the first quarter of 2016 to 40 in the first quarter of 2017. The majority had a history of ischaemic heart disease (IHD) (67.9%) with ischaemic stroke and diabetes mellitus being present in 7.3% and 16.8% of patients, respectively. All patients initiated on PCSK9i had been previously prescribed statin treatment with atorvastatin and simvastatin being most frequently prescribed in 53% and 36% of patients, respectively. The majority of patients had received both statins and ezetimibe (94.9%) and approximately half of these patients had also received bile acid sequestrant (45.3%). Clinical characteristics mainly differed in patients receiving triple LLT compared with patients not receiving triple LLT in the regards of heart failure.

conclusionPatients treated with PCSK9i were rare, characterised by having IHD and had received various and intensive conventional LLT prior to PCSK9i initiation in agreement with current international guidelines.

Indexed as

PCSK9 InhibitorsPractice Patterns, Physicians'AgedAnticholesteremic AgentsCholesterol, LDLDenmarkDiabetes MellitusEzetimibeFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHypercholesterolemiaMaleMiddle AgedMyocardial IschemiaStrokeAnticholesteremic AgentsCholesterol, LDLEzetimibeHydroxymethylglutaryl-CoA Reductase InhibitorsPCSK9 Inhibitorscardiovascular diseasedescriptive cohortlipid lowering treatmentproprotein convertase subtilisin–kexin type 9 inhibitor

Identifiers

PMID30940751
PMCPMC6500097
OpenAlexW2913284942

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC
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.