Evidence map›Paper›PMID 35748562›Full record

ArticleTransfusion2022

Screening platelet function in blood donors.

Pascal Pedini, Jean-Baptiste Baudey, Katia Pouymayou, Celine Falaise, Manal Ibrahim-Kosta, Melanie Vélier, Clémence Demerle, Hajer Graiet, Catherine Dragutini, Anne-Marie Dombey and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Transfusion, 2022. 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
0.8field-weighted citation impact, top 26% 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, 6 citations in OpenAlex.

  1. 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

13 authors at 4 institutions in 1 country.

Pascal PediniImmunogenetic Laboratory, EFS PACC, Marseille, France.ORCID 0000-0001-9299-3705
Jean-Baptiste BaudeyImmunogenetic Laboratory, EFS PACC, Marseille, France.
Katia PouymayouDepartment of Hematology, CHU Timone, Marseille, France.
Celine FalaiseDepartment of Hematology, CHU Timone, Marseille, France.
Manal Ibrahim-KostaDepartment of Hematology, CHU Timone, Marseille, France.
Melanie VélierImmunogenetic Laboratory, EFS PACC, Marseille, France.
Clémence DemerleImmunogenetic Laboratory, EFS PACC, Marseille, France.
Hajer GraietImmunogenetic Laboratory, EFS PACC, Marseille, France.
Catherine DragutiniDepartment of Phlebotomy, EFS PACC, Marseille, France.
Anne-Marie DombeyDepartment of Phlebotomy, EFS PACC, Marseille, France.
Jacques ChiaroniImmunogenetic Laboratory, EFS PACC, Marseille, France.
Marie Christine AlessiDepartment of Hematology, CHU Timone, Marseille, France.
Christophe PicardImmunogenetic Laboratory, EFS PACC, Marseille, France.
Centre National de la Recherche Scientifique · FRHôpital de la Timone · FRInserm · FRUnité de recherche sur les maladies cardiovasculaires et métaboliques · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransfusion of defective platelets could contribute to the inefficiency of platelet transfusion in preventing or stopping bleeding. STUDY DESIGN AND

methodsThis single-center prospective study aimed to determine the prevalence of functional platelet abnormalities in a population of blood donors with a clinical history of bleeding diathesis or with history of hematoma (>4 cm) during blood donation. Donors with positive bleeding screening questionnaire were referred to the reference center for rare platelet diseases at La Timone University Hospital (Marseille) to confirm the bleeding tendency using a more extensive bleeding questionnaire (MCMDMscore) and to assess hemostasis, including a comprehensive platelet analysis.

resultsOne hundred and ninety-five donors identified based on a history of hematoma and 2434 blood donors were included in the study. Eighty-eight donors (3.6%) had a bleeding score indicating a potential bleeding disorder. Five donors with a history of hematoma (2.5%) and 15 (17%) donors with a confirmed bleeding score underwent hemostatic analysis, including two men and 18 women with average age of 33.9 years. Minor hemostatic abnormalities were observed in three donors. Two donors exhibited accelerated fibrinolysis with reduced euglobulin lysis time and increased D-dimer levels in serum. Two donors had a platelet granule defect, without identification of genetic abnormality.

conclusionThe bleeding questionnaire proved to be a valuable tool to screen blood donors for potential platelet defects. Platelet dysfunction was rare in the blood donor population assessed. Additional studies are necessary to understand the clinical impact that the transfusion of platelets with qualitative defects has on recipients.

Indexed as

Blood Coagulation DisordersBlood Platelet DisordersHemorrhagic DisordersHemostaticsAdultBlood DonorsBlood PlateletsFemaleHematomaHemorrhageHemostasisHumansMaleProspective StudiesHemostaticsblood donorhemostatic disorderplateletprevalence

Identifiers

PMID35748562
PMCPMC9543520
OpenAlexW4283447011

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.