Evidence map›Paper›PMID 30071043›Full record

ArticlePloS one2018

Evolution of platelet functions in cirrhotic patients undergoing liver transplantation: A prospective exploration over a month.

Daniel Eyraud, Ludovic Suner, Axelle Dupont, Christilla Bachelot-Loza, David M Smadja, Dominique Helley, Sébastien Bertil, Ovidiu Gostian, Jean Szymezak, Yann Loncar and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 33% 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, 11 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Observational
  6. Review
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

16 authors at 3 institutions in 1 country.

Daniel EyraudAP-HP, Pitié-Salpêtrière University Hospital, Department of Anesthesiology and Reanimation, Paris, France.ORCID 0000-0001-9503-7129
Ludovic SunerAP-HP, European University Hospital Georges Pompidou, Hematology Department, Paris, France.ORCID 0000-0002-5107-4961
Axelle DupontUniversité Pierre et Marie Curie, Paris, France.
Christilla Bachelot-LozaInserm UMR-S1140, Faculté de Pharmacie, Paris, France.ORCID 0000-0002-6264-902X
David M SmadjaAP-HP, European University Hospital Georges Pompidou, Hematology Department, Paris, France.
Dominique HelleyAP-HP, European University Hospital Georges Pompidou, Hematology Department, Paris, France.
Sébastien BertilAP-HP, European University Hospital Georges Pompidou, Hematology Department, Paris, France.
Ovidiu GostianAP-HP, Pitié-Salpêtrière University Hospital, Department of Anesthesiology and Reanimation, Paris, France.
Jean SzymezakAP-HP, European University Hospital Georges Pompidou, Hematology Department, Paris, France.
Yann LoncarAP-HP, Pitié-Salpêtrière University Hospital, Department of Anesthesiology and Reanimation, Paris, France.
Louis PuybassetAP-HP, Pitié-Salpêtrière University Hospital, Department of Anesthesiology and Reanimation, Paris, France.
Pascal LebrayAP-HP, Pitié-Salpêtrière University Hospital, Hepatology Department, Paris, France.
Corinne VezinetAP-HP, Pitié-Salpêtrière University Hospital, Department of Anesthesiology and Reanimation, Paris, France.
Jean-Christophe VaillantAP-HP, Pitié-Salpêtrière University Hospital, Department of Digestive, HPB Surgery, and Liver Transplantation, Paris, France.
Benjamin GrangerUniversité Pierre et Marie Curie, Paris, France.
Pascale GaussemAP-HP, European University Hospital Georges Pompidou, Hematology Department, Paris, France.
Sorbonne Université · FRDélégation Paris 5 · FRAssistance Publique – Hôpitaux de Paris · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This prospective observational study was designed to analyze platelet functions across time in 50 patients scheduled for liver transplantation (LT) secondary to decompensated cirrhosis or hepatocellular carcinoma. Platelet functions were assessed before LT (pre-LT), one week (D7) and 1 month (D28) after LT. Platelet count significantly increased from pre-LT time to day 28 as well as circulating CD34+hematopoietic stem cells. To avoid any influence of platelet count on assays, platelet function was evaluated on platelet-rich-plasma adjusted to pre-LT platelet count. Although platelet secretion potential did not differ between time-points, as evaluated by the expression of CD62P upon strong activation, platelet aggregation in response to various agonists significantly increased along time, however with no concomitant increase of circulating markers of platelet activation: platelet microvesicles, platelet-leukocyte complexes, soluble CD40L and soluble CD62P. In the multivariate analysis, hepatic function was associated with platelet count and function. A lower platelet aggregation recovery was correlated with Child C score. History of thrombosis or bleeding was associated with respective higher or lower values of platelet aggregation. This longitudinal analysis of platelet functions in LT patients showed an improvement of platelet functions along time together with platelet count increase, with no evidence of platelet hyperactivation at any time-point.

Indexed as

Liver TransplantationBlood PlateletsCarcinoma, HepatocellularCD40 LigandFemaleHemorrhageHumansLiverLiver CirrhosisLiver NeoplasmsMaleMiddle AgedPlatelet ActivationPlatelet AggregationPlatelet CountPlatelet Function TestsCD40 LigandP-Selectin

Identifiers

PMID30071043
PMCPMC6072007
OpenAlexW2886083098

What OpenQuestion holds

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Registered trials

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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.