Evidence map›Paper›PMID 25981525›Full record

ArticleVox sanguinis2015

A prospective, active haemovigilance study with combined cohort analysis of 19,175 transfusions of platelet components prepared with amotosalen-UVA photochemical treatment.

F Knutson, J Osselaer, L Pierelli, M Lozano, J Cid, R Tardivel, O Garraud, T Hervig, D Domanovic, M Cukjati and 13 more

Abstract read
In one paragraph

Article in Vox sanguinis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

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

  1. Pooled it
  2. Pathogen-reduced platelets for the prevention of bleeding.The Cochrane database of systematic reviews · 2017
    Pooled it
  3. Safety and Efficacy of Amotosalen-Ultraviolet A Pathogen-Reduced Platelets Transfused to Neonates.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026
    Article
  4. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2026
    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

23 authors.

F KnutsonDepartment of Immunology, Genetics, and Pathology, Uppsala University, Uppsala, Sweden.
J OsselaerCliniques Universitaires de Mont Godinne, Universite Catholique de Louvain, Yvoir, Belgium.
L PierelliDepartment of Experimental Medicine, Sapienza University of Roma, Rome, Italy.
M LozanoDepartment of Hemotherapy and Hemostasis, CDB, IDIBAPS, Hospital Clinic, Barcelona, Spain.ORCID http://orcid.org/0000-0003-2593-833X
J CidDepartment of Hemotherapy and Hemostasis, CDB, IDIBAPS, Hospital Clinic, Barcelona, Spain.
R TardivelEFS Bretagne, Rennes, France.
O GarraudEFS Auvergne Loire, St. Etienne, France.
T HervigDepartment of Immunology and Transfusion Medicine, University of Bergen, Bergen, Norway.
D DomanovicBlood Transfusion Centre of Slovenia, Ljubljana, Slovenia.
M CukjatiBlood Transfusion Centre of Slovenia, Ljubljana, Slovenia.
S GudmundsonBlood Bank, National University Hospital, Reykjavik, Iceland.
I B HjalmarsdottirBlood Bank, National University Hospital, Reykjavik, Iceland.
A CastrilloTransfusion Centre of Galicia, Santiago de Compostela, Spain.
R GonzalezTransfusion Centre of Galicia, Santiago de Compostela, Spain.
D BrihanteServico de Imuno-Hemoterapia, Instituto Portugues de Oncologia de Lisboa, Lisbon, Portugal.
M SantosServico de Imuno-Hemoterapia, Instituto Portugues de Oncologia de Lisboa, Lisbon, Portugal.
P SchlenkeDepartment of Blood Group Serology and Transfusion Medicine, Medical University of Graz, Graz, Austria.
A ElliottCerus Corporation, Concord, CA, USA.
J-S LinCerus Corporation, Concord, CA, USA.
D TappeCerus Corporation, Concord, CA, USA.
A StassinopoulosCerus Corporation, Concord, CA, USA.
J GreenCerus Corporation, Concord, CA, USA.
L CorashCerus Corporation, Concord, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesA photochemical treatment process (PCT) utilizing amotosalen and UVA light (INTERCEPT(™) Blood System) has been developed for inactivation of viruses, bacteria, parasites and leucocytes that can contaminate blood components intended for transfusion. The objective of this study was to further characterize the safety profile of INTERCEPT-treated platelet components (PCT-PLT) administered across a broad patient population. MATERIALS AND

methodsThis open-label, observational haemovigilance programme of PCT-PLT transfusions was conducted in 21 centres in 11 countries. All transfusions were monitored for adverse events within 24 h post-transfusion and for serious adverse events (SAEs) up to 7 days post-transfusion. All adverse events were assessed for severity (Grade 0-4), and causal relationship to PCT-PLT transfusion.

resultsOver the course of 7 years in the study centres, 4067 patients received 19,175 PCT-PLT transfusions. Adverse events were infrequent, and most were of Grade 1 severity. On a per-transfusion basis, 123 (0.6%) were classified an acute transfusion reaction (ATR) defined as an adverse event related to the transfusion. Among these ATRs, the most common were chills (77, 0.4%) and urticaria (41, 0.2%). Fourteen SAEs were reported, of which 2 were attributed to platelet transfusion (<0.1%). No case of transfusion-related acute lung injury, transfusion-associated graft-versus-host disease, transfusion-transmitted infection or death was attributed to the transfusion of PCT-PLT.

conclusionThis longitudinal haemovigilance safety programme to monitor PCT-PLT transfusions demonstrated a low rate of ATRs, and a safety profile consistent with that previously reported for conventional platelet components.

Indexed as

AdolescentAdultAgedAged, 80 and overBlood PlateletsBlood SafetyChildChild, PreschoolFemaleFurocoumarinsHumansInfantMaleMiddle AgedPhotosensitizing AgentsPlatelet TransfusionamotosalenFurocoumarinsPhotosensitizing AgentsamotosalenhaemovigilanceINTERCEPTpathogen inactivationplateletssafety

Identifiers

PMID25981525
PMCPMC4690512

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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.