Evidence map›Paper›PMID 35664276›Full record

ArticleClinical kidney journal2022

Trimming the fat: is there a health economic case for the use of new lipid-lowering drugs in chronic kidney disease? A scoping review.

Alexandra Gallagher, Blaise Agresta, Brendan Smyth, Meg Jardine, Charles Ferro, Rachael L Morton

Open access · goldAbstract readScoping Review
In one paragraph

Article in Clinical kidney journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 72% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 2 countries.

Alexandra GallagherNational Health and Medical Research Council Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.ORCID https://orcid.org/0000-0002-4101-6776
Blaise AgrestaNational Health and Medical Research Council Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
Brendan SmythNational Health and Medical Research Council Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
Meg JardineNational Health and Medical Research Council Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
Charles FerroInstitute of Cardiovascular Science, University of Birmingham, Birmingham, UK.ORCID https://orcid.org/0000-0003-0577-7081
Rachael L MortonNational Health and Medical Research Council Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.ORCID https://orcid.org/0000-0001-7834-0572
The University of Sydney · AUUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Individuals with chronic kidney disease (CKD) are at a very high risk for atherosclerotic cardiovascular disease (ASCVD). New lipid-lowering agents offer hope of improved outcomes where traditional agents have been less efficacious, yet the cost of these agents needs consideration in this population before their widespread application. Objective: We sought to evaluate the cost-effectiveness of novel lipid-lowering therapies for a CKD population. Methods: We searched four electronic databases, one government registry and the reference lists of included literature to identify cost-effectiveness analyses of novel lipid-lowering agents in CKD. Costs were converted to a single currency to allow cross-country comparisons. Completeness of reporting was analysed using the Consolidated Health Economic Evaluation Reporting Standards checklist. Results were synthesized in narrative form with graphical representation of cost-effectiveness ratios. Results: Of the 1041 identified studies, 4 met the inclusion criteria. None were specific to a CKD-only population. All examined the impact of proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9is) in the secondary prevention of ASCVD. Incremental cost-effectiveness ratios of new agents compared with standard care were between €7288 and €112 530 per quality-adjusted life year gained. Cost-effectiveness was sensitive to the degree of cardiovascular risk of the underlying populations. Conclusion: This review found PCSK9is were moderately cost-effective in populations with high cardiovascular risk. People with CKD were included as an undifferentiated subpopulation in the primary studies, but application of these findings to CKD-specific populations should be interpreted with caution. There is insufficient evidence for a health economic case to support novel lipid-lowering therapies for advanced CKD.

Indexed as

CKDcost-effectivenessnovel lipid-lowering therapiesPCSK9 inhibitorscoping review

Identifiers

PMID35664276
PMCPMC9155226
OpenAlexW4205843721

What OpenQuestion holds

Textmetadata
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.