Evidence map›Paper›PMID 27823844›Full record

SynthesisThe Journal of arthroplasty2017

Safety and Efficacy of New Anticoagulants for the Prevention of Venous Thromboembolism After Hip and Knee Arthroplasty: A Meta-Analysis.

Brett T Venker, Beejal R Ganti, Hannah Lin, Elizabeth D Lee, Ryan M Nunley, Brian F Gage

Abstract readMeta-AnalysisReview
In one paragraph

Synthesis in The Journal of arthroplasty, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  17. Direct oral anticoagulants for the treatment and prevention of venous thromboembolism in patients with cancer: current evidence.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
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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

6 authors.

Brett T VenkerDepartment of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri; Department of Pharmacy, Veterans Affairs San Diego Healthcare System, San Diego, California.
Beejal R GantiDepartment of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri; Department of Pharmacy Services, Henry Ford Hospital, Detroit, Michigan.
Hannah LinDepartment of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri; University of Massachusetts Medical School, Worcester, Massachusetts.
Elizabeth D LeeDepartment of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri; Carolina Rehabilitation and Surgical Associates, Raleigh, North Carolina.
Ryan M NunleyDepartment of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri; Department of Orthopedic Surgery, Washington University in St. Louis, St. Louis, Missouri.
Brian F GageDepartment of Internal Medicine, Washington University in St. Louis, St. Louis, Missouri.

Funding

Washington University Institute of Clinical and Translational Sciences (UL1)UL1RR024992 · NCRR · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2007 to 2011
$45.4M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
GENETICS-InFORMATICS TRIAL (GIFT) OF WARFARIN TO PREVENT DVTR01HL097036 · NHLBI · WASHINGTON UNIVERSITY · PI GAGE, BRIAN F · 2009 to 2015
$5.0M
Washington University Institute of Clinical and Translational SciencesTL1TR000449 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$2.5M
Washington University Institute of Clinical and Translational Sciences (TL1)TL1RR024995 · NCRR · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2007 to 2011
$2.3M
NCATS NIH HHS TL1 TR000449NCATS NIH HHS UL1 TR000448NCRR NIH HHS TL1 RR024995NCRR NIH HHS UL1 RR024992NHLBI NIH HHS R01 HL097036
6 · The paper itself

Abstract

backgroundVenous thromboembolism (VTE) is a common and potentially fatal complication of arthroplasty.

methodsWe reviewed randomized trials to determine which anticoagulant has the best safety and efficacy in hip and knee arthroplasty patients. We searched PubMed, MEDLINE, and EMBASE through January 2016.

resultsCompared to enoxaparin (most commonly dosed 40 mg once daily), the relative risk (RR) of VTE was lowest for edoxaban 30 mg once daily (0.49; 95% confidence interval [CI], 0.32-0.75), fondaparinux 2.5 mg once daily (0.53; 95% CI, 0.45-0.63), and rivaroxaban 10 mg once daily (0.55; 95% CI, 0.46-0.66), and highest for dabigatran 150 mg once daily (1.19; 95% CI; 0.98-1.44). The RR of major/clinically relevant bleeding was lowest for apixaban 2.5 mg twice daily (0.84; 95% CI; 0.70-0.99) and highest for rivaroxaban (1.27; 95% CI, 1.01-1.59) and fondaparinux (1.64; 95% CI, 0.24-11.35). Fondaparinux was the only agent that was more effective than enoxaparin 30 mg twice daily (VTE RR = 0.58; 95% CI, 0.43-0.76).

conclusionWith the possible exception of apixaban, newer anticoagulants that lower the risk of postoperative VTE increase bleeding.

Indexed as

AnticoagulantsArthroplasty, Replacement, KneeDabigatranEnoxaparinFondaparinuxHemorrhageHumansMorpholinesPolysaccharidesPyrazolesPyridonesRivaroxabanThiophenesVenous ThromboembolismAnticoagulantsapixabanDabigatranEnoxaparinFondaparinuxMorpholinesPolysaccharidesPyrazolesPyridonesRivaroxabanThiophenesanticoagulantarthroplastybleeddeep vein thrombosismeta-analysisthromboembolism

Identifiers

PMID27823844
PMCPMC5258767

What OpenQuestion holds

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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.