Evidence map›Paper›PMID 29263773›Full record

ArticleAmerican health & drug benefits2017

Major Cardiovascular Events in Patients with Gout and Associated Cardiovascular Disease or Heart Failure and Chronic Kidney Disease Initiating a Xanthine Oxidase Inhibitor.

JoAnne Foody, Robin S Turpin, Beni A Tidwell, Debra Lawrence, Kathy L Schulman

Open access · greenAbstract read
In one paragraph

Article in American health & drug benefits, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
5.6field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  5. Observational
  6. Article
  7. Article
  8. Managing Gout in Women: Current Perspectives.Journal of inflammation research · 2022
    Review
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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

5 authors at 4 institutions in 4 countries.

JoAnne FoodyAssociate Professor, Harvard Medical School, Boston, MA, and Executive Director-Cardiovascular, Janssen Pharmaceuticals, New Brunswick, NJ.
Robin S TurpinDirector and Head, Health Economics and Outcomes Research, Medical Affairs, Takeda Pharmaceuticals USA, Deerfield, IL.
Beni A TidwellResearch Associate, Outcomes Research Solutions, Shrewsbury, MA.
Debra LawrenceDirector, Health Economics and Outcomes Research; Medical Affairs, Takeda Pharmaceuticals USA.
Kathy L SchulmanResearch Scientist and Principal, Outcomes Research Solutions, Shrewsbury, MA.
Health Outcomes Solutions (United States) · USHealth Economics and Outcomes Research (United Kingdom) · GBJanssen (Belgium) · BETakeda (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral observational studies and meta-analyses have suggested that treating hyperuricemia in patients with gout and moderate or severe chronic kidney disease (CKD) may improve renal and cardiovascular (CV) outcomes.

objectiveTo evaluate the impact of initiating allopurinol or febuxostat treatment on major CV events in patients with gout, preexisting CV disease (CVD) or heart failure (HF), and stage 3 or 4 CKD in a real-world setting.

methodsPatients with gout (aged >18 years) who initiated allopurinol or febuxostat treatment between 2009 and 2013 after a diagnosis of stage 3 or 4 CKD and CVD-including coronary artery disease (CAD), cerebrovascular disease, and peripheral vascular disease (PVD)-or HF were selected from the MarketScan databases. The major CV events included CAD-specific, cerebrovascular disease-specific, and PVD-specific events. Cox proportional hazards modeling identified the predictors of major CV events in aggregate, and of CAD, cerebrovascular disease, and PVD events, individually.

resultsDuring follow-up, 2426 patients (370 receiving febuxostat and 2056 receiving allopurinol; 63% male; mean age, 73 years) had 162 major CV events (3.8% in those receiving febuxostat vs 7.2% in those receiving allopurinol;

conclusionPatients with moderate-to-severe CKD and CVD or HF who initiated febuxostat treatment had a significantly lower rate of major CV events than patients who initiated allopurinol.

Indexed as

allopurinolcardiovascular diseasechronic kidney diseasefebuxostatgouthyperuricemiamajor CV eventsurate-lowering therapiesxanthine oxidase inhibitors

Identifiers

PMID29263773
PMCPMC5726059
OpenAlexW3024496456

What OpenQuestion holds

Textmetadata
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.