Evidence mapPaperPMID 27709253Full record

Trial reportEuropean journal of clinical pharmacology2016

Statin use decreases coagulation in users of vitamin K antagonists.

Nienke van Rein, J S Biedermann, S M Bonafacio, M J H A Kruip, F J M van der Meer, W M Lijfering

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in European journal of clinical pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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 1 country.

Nienke van ReinDepartment of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands. n.van_rein@lumc.nl.
J S BiedermannDepartment of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
S M BonafacioDepartment of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands.
M J H A KruipDepartment of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
F J M van der MeerDepartment of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands.
W M LijferingDepartment of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands.
Leiden University Medical Center · NLErasmus MC · NLStar Medisch Diagnostisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purpose of the study is to determine the immediate and long-term effect of statins on coagulation in patients treated with vitamin K antagonists (VKAs).

methodsWe selected patients on VKAs of two Dutch anticoagulation clinics who initiated treatment with a statin between 2009 and 2013. Patients who initiated or stopped concomitant drugs that interact with VKAs or were hospitalised during follow-up were excluded. The VKA dosage (mg/day) after statin initiation was compared with the last VKA dosage before the statin was started. Immediate and long-term differences in VKA dosage (at 6 and 12 weeks) were calculated with a paired student t test.

resultsFour hundred thirty-five phenprocoumon users (mean age 70 years, 60 % men) and 303 acenocoumarol users (mean age 69 years, 58 % men) were included. After start of statin use, the immediate phenprocoumon dosage was 0.02 mg/day (95 % CI, 0.00 to 0.03) lower. At 6 and 12 weeks, these phenprocoumon dosages were 0.03 (95 % CI, 0.01 to 0.05) and 0.07 mg/day (95 % CI, 0.04 to 0.09) lower as compared with the dosage before first statin use. In acenocoumarol users, VKA dosage was 0.04 mg/day (95%CI, 0.01 to 0.07) (immediate effect), 0.10 (95 % CI, 0.03 to 0.16) (at 6 weeks), and 0.11 mg/day (95 % CI, 0.04 to 0.18) (after 12 weeks) lower.

conclusionsInitiation of statin treatment was associated with an immediate and long-term minor although statistically significant decrease in VKA dosage in both phenprocoumon and acenocoumarol users, which suggests that statins may have anticoagulant properties.

Indexed as

AcenocoumarolAgedAged, 80 and overAnticoagulantsBlood CoagulationFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsInternational Normalized RatioMaleMiddle AgedPhenprocoumonVitamin KAcenocoumarolAnticoagulantsHydroxymethylglutaryl-CoA Reductase InhibitorsPhenprocoumonVitamin KCoumarinsDrug interactionsHydroxymethylglutaryl-CoA reductase inhibitorsPharmacokineticsPharmacology

Identifiers

PMID27709253
PMCPMC5110601
OpenAlexW2528428023

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.