Evidence map›Paper›PMID 40551211›Full record

ArticleThrombosis journal2025

Α 6-month, multicenter, observational study investigating the treatment of venous thromboembolism in Greece (VICTORIA study).

Paraskevi Savvari, Ioannis Skiadas, Evgenia Mavrokefalou, Stavros Kakkos, Ioulia Antoniou, Georgios A Pitoulias, Effrosyni Dima, Emmanouil Ferdoutsis, Georgios Ntaios, Athanasios Giannoukas and 15 more

Abstract read
In one paragraph

Article in Thrombosis journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

25 authors.

Paraskevi SavvariMedical Affairs, Pfizer Hellas S.A, 243 Messoghion Ave, Athens, N. Psychiko, 154 51, Greece.
Ioannis SkiadasMedical Affairs, Pfizer Hellas S.A, 243 Messoghion Ave, Athens, N. Psychiko, 154 51, Greece.
Evgenia Mavrokefalou4th Department of Internal Medicine, Evangelismos Hospital, Athens, Greece.
Stavros KakkosDepartment of Vascular Surgery, University of Patras Medical School, Patras, Greece.
Ioulia AntoniouMedical Affairs, Pfizer Hellas S.A, 243 Messoghion Ave, Athens, N. Psychiko, 154 51, Greece. ioulia.antoniou@pfizer.com.
Georgios A PitouliasDivision of Vascular Surgery, 2nd Surgery Clinic, School of Health Sciences, Faculty of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Effrosyni Dima1st Department of Critical Care and Pulmonary Services, Evangelismos Hospital, Athens, Greece.
Emmanouil FerdoutsisPulmonary Medicine Department, General Hospital of Heraklion "VENIZELEIO", Heraklion, Greece.
Georgios NtaiosDepartment of Internal Medicine, School of Health Sciences, University of Thessaly, Larissa, Greece.
Athanasios GiannoukasVascular Surgery Department, Faculty of Medicine, School of Health Sciences, University Hospital of Larissa, University of Thessaly, Larissa, Greece.
Ourania KotsiouRespiratory Medicine Department, School of Medicine, University of Thessaly, University Hospital of Larissa, Larissa, Greece.
Flora ZagouriOncology Department of Clinical Therapeutics, Alexandra Hospital, National Kapodistrian University of Athens School of Medicine, Athens, Greece.
Georgios Tsoukalas4th Respiratory Medicine Department, General Hospital for Chest Diseases of Athens "SOTIRIA", Athens, Greece.
Konstantinos KostikasRespiratory Medicine Department, University of Ioannina, Ioannina, Greece.
Dimitrios StaramosVascular Surgery Department, "Konstantopouleion" General Hospital of Nea Ionia, Athens, Greece.
Haralampos Milionis1st Department of Internal Medicine, School of Medicine, University Hospital of Ioannina, Ioannina, Greece.
Konstantinos FilisVascular Surgery Unit, 1st Department of Propaedeutic Surgery, National and Kapodistrian University of Athens, Hippocration Hospital, Athens, Greece.
Christos Savopoulos1st Propaedeutic Internal Medicine Department, AHEPA University General Hospital of Thessaloniki, Thessaloniki, Greece.
Ioannis KakisisVascular Surgery Department, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Vasileios TzilalisVascular Surgery Department, 401 General Military Hospital of Athens, Athens, Greece.
Nikolaos KoulourisRespiratory Medicine Department, Rehabilitation Unit, 1st Sotiria Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Theophanis PapasVascular Surgery Department, "Red Cross" General Hospital of Athens, Athens, Greece.
Ioanna Skrapari1st Department of Internal Medicine, Evangelismos General Hospital, Athens, Greece.
Damianos MenegasMedical Affairs, Pfizer Hellas S.A, 243 Messoghion Ave, Athens, N. Psychiko, 154 51, Greece.
VICTORIA Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReal-world data are needed to inform clinical practice with regards to anticoagulation treatment for persons with venous thromboembolism (VTE).

objectivesTo identify the type and duration of antithrombotic treatment in persons with VTE. Anticoagulation dosage and persistence/adherence were among the secondary objectives.

methodsA multicenter, observational, prospective study conducted in Greek adults with VTE with two on-site visits -baseline and at three months- and a telephone follow-up at 6 months.

resultsA total of 600 eligible persons were enrolled. The index event was 'PE only' in 50%, 'DVT only' in 40%, and 'DVT+PE' in 10%. Risk factors were categorized as temporary major (21%), temporary minor (37%), and persistent (43%), with active cancer present in 18% of patients. All VTE patients received anticoagulants: 73% received oral anticoagulants (72% DOACs, 1% VKAs) and 70% received parenteral anticoagulants. Treatment was oral only in 30%, parenteral only in 27%, and both in 43%. The most common DOAC was apixaban (47%). Extended anticoagulation (>6 months) was administered to 41% with only 9% (18/198) of those on DOACs receiving a reduced dose. Persistent risk factors predicted extended anticoagulation, while diabetes, COVID-19, and temporary minor risk factors did not. Adherence/persistence rates were similar between DOAC and non-DOAC-treated patients.

conclusionVTE was mainly treated with a combination of parenteral and oral anticoagulants. DOACs, primarily apixaban, were the most common oral treatments. Forty percent of patients received extended anticoagulation, mostly at standard dosages. Adherence and persistence rates were high for both DOAC and non-DOAC treatments.

Indexed as

AnticoagulantDeep vein thrombosisDuration of anticoagulationPulmonary embolism

Identifiers

PMID40551211
PMCPMC12183886

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.