Evidence map›Paper›PMID 27217043›Full record

Trial reportJournal of thrombosis and thrombolysis2016

Renal function in atrial fibrillation patients switched from warfarin to a direct oral anticoagulant.

Anum S Minhas, Qingmei Jiang, Xiaokui Gu, Brian Haymart, Eva Kline-Rogers, Steve Almany, Jay Kozlowski, Gregory D Krol, Scott Kaatz, James B Froehlich and 1 more

Abstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Journal of thrombosis and thrombolysis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Guideline
  3. Article
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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

11 authors.

Anum S MinhasDepartment of Internal Medicine, University of Michigan Medical Center, 2F208 UH , 1500 E. Medical Center Dr., SPC 5052, Ann Arbor, MI, 48109-5052, USA. aminhas@umich.edu.
Qingmei JiangFrankel Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, MI, USA.
Xiaokui GuFrankel Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, MI, USA.
Brian HaymartFrankel Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, MI, USA.
Eva Kline-RogersFrankel Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, MI, USA.
Steve AlmanyOakland University/Beaumont Hospital, Royal Oak, MI, USA.
Jay KozlowskiHuron Valley Sinai Hospital, Commerce Township, MI, USA.
Gregory D KrolHenry Ford Hospital, Detroit, MI, USA.
Scott KaatzHurley Medical Center, Flint, MI, USA.
James B FroehlichFrankel Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, MI, USA.
Geoffrey D BarnesFrankel Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All available direct oral anticoagulants (DOACs) are at least partially eliminated by the kidneys. These agents are increasingly being used as alternatives to warfarin for stroke prevention in patients with atrial fibrillation. The aim of this study was to identify changes in renal function and associated DOAC dosing implications in a multicenter cohort of atrial fibrillation patients switched from warfarin to DOAC treatment. We included all patients in the Michigan Anticoagulation Quality Improvement Initiative cohort who switched from warfarin to a DOAC with atrial fibrillation as their anticoagulant indication between 2009 and 2014, and who had at least two creatinine values. Compliance with FDA-recommended dosing based on renal function was assessed. Of the 189 patients switched from warfarin to a DOAC, 34 (18.0 %) had a baseline creatinine clearance <50 mL/min and 23 (12.2 %) experienced important fluctuations in renal function. Of these 23 patients, 6 (26.1 %) should have impacted the DOAC dosing, but only 1 patient actually received an appropriate dose adjustment. Additionally, 15 (7.9 %) of patients on DOACs had a dose change performed, but only one patient demonstrated a change in renal function to justify the dose adjustment. Most atrial fibrillation patients who switched from warfarin to a DOAC had stable renal function. However, the majority of patients who had a change in renal function did not receive the indicated dose change. As the use of DOACs expands, monitoring of renal function and appropriate dose adjustments are critical.

Indexed as

Atrial FibrillationDrug SubstitutionKidneyAdministration, OralAgedAged, 80 and overAnticoagulantsCreatinineFemaleHumansKidney Function TestsMaleMiddle AgedWarfarinAnticoagulantsCreatinineWarfarinAnticoagulantsApixabanDabigatranRenal insufficiencyRivaroxaban

Identifiers

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.