Evidence map›Paper›PMID 27156005›Full record

Trial reportJournal of veterinary internal medicine2016

The Effects of Cyclosporine and Aspirin on Platelet Function in Normal Dogs.

J Thomason, T Archer, R Wills, S Press, A Mackin

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of veterinary internal medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Article
  3. Urinary 11-dehydrothromboxane BJournal of veterinary internal medicine · 2022
    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

5 authors at 1 institution in 1 country.

J ThomasonDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, MS, 39762-6100.
T ArcherDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, MS, 39762-6100.
R WillsDepartment of Pathobiology and Population Medicine, College of Veterinary Medicine, Mississippi State University, MS, 39762-6100.
S PressDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, MS, 39762-6100.
A MackinDepartment of Clinical Sciences, College of Veterinary Medicine, Mississippi State University, MS, 39762-6100.
Mississippi State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCyclosporine increases thromboxane synthesis in dogs, potentially increasing the thrombogenic properties of platelets. HYPOTHESIS/

objectivesOur hypothesis was that the concurrent administration of low-dose aspirin and cyclosporine would inhibit cyclosporine-associated thromboxane synthesis without altering the antiplatelet effects of aspirin. The objective was to determine the effects of cyclosporine and aspirin on primary hemostasis. ANIMALS: Seven healthy dogs.

methodsA randomized, crossover study utilized turbidimetric aggregometry and a platelet function analyzer to evaluate platelet function during the administration of low-dose aspirin (1 mg/kg PO q24h), high-dose aspirin (10 mg/kg PO q12h), cyclosporine (10 mg/kg PO q12h), and combined low-dose aspirin and cyclosporine. The urine 11-dehydro-thromboxane-B2 (11-dTXB2 )-to-creatinine ratio also was determined.

resultsOn days 3 and 7 of administration, there was no difference in the aggregometry amplitude or the platelet function analyzer closure time between the low-dose aspirin group and the combined low-dose aspirin and cyclosporine group. On day 7, there was a significant difference in amplitude and closure time between the cyclosporine group and the combined low-dose aspirin and cyclosporine group. High-dose aspirin consistently inhibited platelet function. On both days, there was a significant difference in the urinary 11-dTXB2 -to-creatinine ratio between the cyclosporine group and the combined low-dose aspirin and cyclosporine group. There was no difference in the urinary 11-dTXB2 -to-creatinine ratio among the low-dose aspirin, high-dose aspirin, and combined low-dose aspirin and cyclosporine groups. CONCLUSIONS AND CLINICAL IMPORTANCE: Low-dose aspirin inhibits cyclosporine-induced thromboxane synthesis, and concurrent use of these medications does not alter the antiplatelet effects of aspirin.

Indexed as

AnimalsAspirinBlood PlateletsCross-Over StudiesCyclosporineDogsImmunosuppressive AgentsNephelometry and TurbidimetryPlatelet AggregationPlatelet Aggregation InhibitorsAspirinCyclosporineImmunosuppressive AgentsPlatelet Aggregation InhibitorsCanineImmune-mediated hemolytic anemiaImmunosuppressionThromboxane

Identifiers

PMID27156005
PMCPMC5084737
OpenAlexW2366484497

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.