Evidence map›Paper›PMID 31041550›Full record

ReviewCurrent atherosclerosis reports2019

Current Role of Lipoprotein Apheresis.

Gilbert Thompson, Klaus G Parhofer

Open access · hybridAbstract readReview
In one paragraph

Review in Current atherosclerosis reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
11.0field-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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Article
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  10. Bibliometric analysis of residual cardiovascular risk: trends and frontiers.Journal of health, population, and nutrition · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Apheresis: What Should a Clinician Know?Current atherosclerosis reports · 2023
    Review
  16. Review
  17. Review
  18. Editorial: Highlights in Lipids in Cardiovascular Disease: 2021.Frontiers in cardiovascular medicine · 2022
    Article
  19. Review
  20. 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

2 authors at 2 institutions in 2 countries.

Gilbert ThompsonDepartment of Metabolic Medicine, Imperial College London, Hammersmith Hospital, Ducane Road, London, W12 0NN, UK. g.thompson@imperial.ac.uk.
Klaus G ParhoferMedical Dept. IV - Grosshadern, Ludwig-Maximilians-University Munich, Munich, Germany.
Imperial College London · GBLudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewLipoprotein apheresis is a very efficient but time-consuming and expensive method of lowering levels of low-density lipoprotein cholesterol, lipoprotein(a)) and other apoB containing lipoproteins, including triglyceride-rich lipoproteins. First introduced almost 45 years ago, it has long been a therapy of "last resort" for dyslipidaemias that cannot otherwise be managed. In recent years new, very potent lipid-lowering drugs have been developed and the purpose of this review is to define the role of lipoprotein apheresis in the current setting. RECENT

findingsLipoprotein apheresis still plays an important role in managing patients with homozygous FH and some patients with other forms of hypercholesterolaemia and cardiovascular disease. In particular, patients not achieving treatment goals despite modern lipid-lowering drugs, either because these are not tolerated or the response is insufficient. Recently, lipoprotein(a) has emerged as an important cardiovascular risk factor and lipoprotein apheresis has been used to decrease lipoprotein(a) concentrations in patients with marked elevations and cardiovascular disease. However, there is considerable heterogeneity concerning the recommendations by scientific bodies as to which patient groups should be treated with lipoprotein apheresis. Lipoprotein apheresis remains an important tool for the management of patients with severe drug-resistant dyslipidaemias, especially those with homozygous FH.

Indexed as

Blood Component RemovalCholesterol, LDLHomozygoteHumansHypercholesterolemiaHyperlipoproteinemia Type IIHypolipidemic AgentsLipoprotein(a)LipoproteinsPCSK9 InhibitorsProprotein Convertase 9TriglyceridesCholesterol, LDLHypolipidemic AgentsLipoprotein(a)Lipoproteinslipoprotein triglyceridePCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9TriglyceridesApheresis guidelinesHeterozygous familial hypercholesterolaemiaHomozygous familial hypercholesterolaemiaLipoprotein(a)

Identifiers

PMID31041550
PMCPMC6491397
OpenAlexW2942575020

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.