Evidence map›Paper›PMID 30863448›Full record

ArticleInternational journal of rheumatology2019

Febuxostat and Cardiovascular Events: A Systematic Review and Meta-Analysis.

John A Cuenca, Javier Balda, Ana Palacio, Larry Young, Michael H Pillinger, Leonardo Tamariz

Open access · hybridAbstract read
In one paragraph

Article in International journal of rheumatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Comparative Cardiovascular Risks of Febuxostat and Allopurinol in Patients with Diabetes Mellitus and Chronic Kidney Disease.Medical science monitor : international medical journal of experimental and clinical research · 2024
    Observational
  9. Observational
  10. Toxicity Profiling and Antihyperuricemic Activity of Goubion: A Polyherbal Formulation.Evidence-based complementary and alternative medicine : eCAM · 2023
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Clinical Effects of Xanthine Oxidase Inhibitors in Hyperuricemic Patients.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2021
    Review
  16. Musculoskeletal Pain in Older Adults: A Clinical Review.The Medical clinics of North America · 2020
    Review
  17. Article
  18. Article
  19. Uric Acid and Arterial Stiffness.Therapeutics and clinical risk management · 2020
    Review
  20. 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

6 authors at 3 institutions in 2 countries.

John A CuencaUniversidad Catolica de Santiago de Guayaquil, Ecuador.ORCID 0000-0003-3228-2244
Javier BaldaUniversidad Catolica de Santiago de Guayaquil, Ecuador.
Ana PalacioDivision of Population Health and Computational Medicine, Miller School of Medicine, University of Miami, Miami, FL, USA.
Larry YoungVeterans Affairs Medical Center, Miami, FL, USA.
Michael H PillingerDivision of Rheumatology, New York University School of Medicine, USA.
Leonardo TamarizDivision of Population Health and Computational Medicine, Miller School of Medicine, University of Miami, Miami, FL, USA.ORCID 0000-0003-1583-3534
University of Miami · USUniversidad Católica de Santiago de Guayaquil · ECVeterans Health Administration · US

Funding

Project-005UL1TR001445 · NCATS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BREDELLA, MIRIAM ANTOINETTE, HOCHMAN, JUDITH S · 2015 to 2025
$103.5M
NCATS NIH HHS UL1 TR001445
6 · The paper itself

Abstract

backgroundFebuxostat is approved in the United States for the management of hyperuricemia in patients with gout. In November 2017 the FDA released a warning alert on a possible link between febuxostat and cardiovascular disease (CVD) reported in a single clinical trial.

objectiveTo conduct a systematic review and meta-analysis and assess the risk of major adverse cardiovascular events (MACE) in patients receiving febuxostat compared to a control group.

methodsWe searched the MEDLINE and EMBASE database for studies published up until March 2018. We included randomized clinical trials (RCTs) that compared febuxostat to control groups including placebo and allopurinol. We calculated the pooled relative risk (RR) of MACE and cardiovascular disease (CVD) mortality with the corresponding 95% confidence intervals (CI).

resultsOur search yielded 374 potentially relevant studies. Among the 25 RCTs included in the systematic review, 10 qualified for the meta-analysis. Among the 14,402 subjects included, the median age was 54 years (IQR 52-67) and 90% were male (IQR 82-96); 8602 received febuxostat, 5118 allopurinol, and 643 placebo. The pooled RR of MACE for febuxostat was 0.9; 95% CI 0.6-1.5 (p= 0.96) compared to the control. The RR of CV-related death for febuxostat was 1.29; 95% CI 1.01-1.66 (p=0.03).

conclusionsCompared with other SU-lowering treatments, febuxostat does not increase or decrease the risk of cardiovascular disease but may increase the risk of CVD death. More RCTs measuring cardiovascular safety as a primary outcome are needed to adequately evaluate the risk of CVD with febuxostat.

Identifiers

PMID30863448
PMCPMC6378016
OpenAlexW2912716476

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.