Evidence map›Paper›PMID 36943661›Full record

ArticleJournal of thrombosis and thrombolysis2023

Direct oral anticoagulants in patients with venous thromboembolism and hematological malignancies.

Renana Robinson, Galia Spectre, Michael Lishner, Ofek Sharabi, Eyal Robinson, Orly Hamburger Avnery, Anat Gafter-Gvili, Pia Raanani, Avi Leader

Abstract read
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In one paragraph

Article in Journal of thrombosis and thrombolysis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.7field-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, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. 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

9 authors at 3 institutions in 1 country.

Renana RobinsonInstitute of Hematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Israel. renana.robinson@gmail.com.ORCID http://orcid.org/0000-0003-0239-9265
Galia SpectreInstitute of Hematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Israel.
Michael LishnerSackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Ofek SharabiSackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Eyal RobinsonIntensive Care Unit, Rabin Medical Centre, Petah Tikva, Israel.
Orly Hamburger AvneryInstitute of Hematology, Meir Medical Center, Kfar Saba, Israel.
Anat Gafter-GviliInstitute of Hematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Israel.
Pia RaananiInstitute of Hematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Israel.
Avi LeaderInstitute of Hematology, Davidoff Cancer Centre, Rabin Medical Centre, Petah Tikva, Israel.
Tel Aviv University · ILMeir Medical Center · ILRabin Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Data are needed on direct oral anticoagulants (DOACs) for the treatment of venous thromboembolism (VTE) in hematological malignancies (HM). Retrospective studies to date lacked a control group and did not focus on patients with VTE. Out aim was to assess the incidence of VTE recurrence and bleeding in HM patients treated with low molecular weight heparin (LMWH) or DOACs for acute VTE. This is a retrospective cohort study including patients with active HM and newly-diagnosed VTE, indexed on the first day of anticoagulation and followed for 12 months. The outcome was a composite of recurrent VTE, major bleeding or clinically relevant non-major bleeding. Cumulative incidence [95% confidence interval (CI)] was calculated for each anticoagulation group (LMWH, DOAC) and hazard ratios (HR) were calculated using cox-proportional hazards model, with death as a competing risk. 143 HM patients treated with LMWH (96) or DOACs (47) for acute VTE were included. The most common HM types were lymphoma in 83 (58%) and plasma cell dyscrasia in 32 (22.3%). The 12-month cumulative incidence of the composite outcome was 24.2% (95% CI 15.9-33.5%; n = 22) in the LMWH group and 18.5% (8.5-31.5%; n = 8) in the DOAC group (HR 1.51 [0.695-3.297]). Two recurrent VTE occurred (both in the DOAC group while off-treatment). Nine (9.4%) LMWH-treated patients had major bleeding compared to 1 (2.1%) DOAC-treated patient (HR 4.85 [0.64-36.56]). This study generates the hypothesis that DOACs may be a safe and effective alternative to LMWH for VTE in patients with HM types represented in the study.

Indexed as

Hematologic NeoplasmsNeoplasmsVenous ThromboembolismAdministration, OralAnticoagulantsHemorrhageHeparin, Low-Molecular-WeightHumansRetrospective StudiesAnticoagulantsHeparin, Low-Molecular-WeightDirect oral anticoagulantsHematological malignanciesVenous thromboembolism

Identifiers

PMID36943661
OpenAlexW4328049727

What OpenQuestion holds

Textmetadata
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.