Evidence map›Paper›PMID 28119956›Full record

ArticleHeliyon2017

Analysis of clinical factors affecting the rates of fatal pulmonary embolism and bleeding in cancer patients with venous thromboembolism.

Javier Trujillo-Santos, Francisco Martín Martos, Carme Font, Dominique Farge-Bancel, Vladimir Rosa, Alicia Lorenzo, Manuel Barrón, Manuel Alejandro Lorente, José María Pedrajas, Manuel Monreal

Abstract read
In one paragraph

Article in Heliyon, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Patient's Awareness of Cancer-Associated Thrombosis: A Canadian Nationwide Survey.TH open : companion journal to thrombosis and haemostasis · 2025
    Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Venous Thromboembolism and Cancer.Current cardiology reports · 2018
    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

10 authors.

Javier Trujillo-SantosDepartment of Internal Medicine, Hospital General Universitario Santa Lucía, Calle Mezquita, s/n. 30202 Cartagena, Murcia, Spain.
Francisco Martín MartosDepartment of Internal Medicine, Hospital General Universitario Santa Lucía, Calle Mezquita, s/n. 30202 Cartagena, Murcia, Spain.
Carme FontDepartment of Medical Oncology, IDIBAPS/Translational Genomics and Targeted Therapeutics in Solid Tumors, Hospital Clínic, Carrer de Villarroel, 170, 08036 Barcelona, Spain.
Dominique Farge-BancelDepartment of Internal Medicine and Pathology, Hôpital Saint-Louis, Avenue Claude Vellefaux, 1, 75010 Paris, France.
Vladimir RosaDepartment of Internal Medicine, Hospital Universitario Virgen de Arrixaca, Ctra. Madrid-Cartagena, s/n. 30120, Murcia, Spain.
Alicia LorenzoDepartment of Internal Medicine, Hospital Universitario de La Paz, Paseo de la Castellana, 261, 28046, Madrid, Spain.
Manuel BarrónDepartment of pneumonology, Complejo Hospitalario San Pedro, Calle Piqueras, 98, 26006 Logroño, La Rioja, Spain.
Manuel Alejandro LorenteDepartment of Internal Medicine, Hospital de la Agencia Valenciana de Salud Vega Baja, Ctra. Orihuela-Almoradi, s/n. 03314 Orihuela, Alicante, Spain.
José María PedrajasDepartment of Internal Medicine, Hospital Clínico San Carlos, Calle Profesor Martín Lagos, s/n. 28040 Madrid, Spain.
Manuel MonrealDepartment of Internal Medicine, Hospital Universitario Germans Trias i Pujol de Badalona, Carretera de Canyet, s/n. 08916 Badalona, Barcelona, Universidad Católica de Murcia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn cancer patients with symptomatic venous thromboembolism (VTE) (deep-vein thrombosis (DVT) and/or pulmonary embolism (PE)), clinical factors that influence the benefit-risk balance of anticoagulation need to be identified so treatment intensity and duration can be optimally adjusted for the individual patient.

methodsUsing clinical data for cancer patients with VTE obtained from the RIETE registry, we compared how rates of fatal PE and fatal bleeding during and after anticoagulation vary depending on patients' clinical characteristics.

resultsData were analysed from the 10,962 cancer patients with VTE (5,740 with PE with or without DVT; 5,222 with DVT alone) in RIETE registry as of March 2016. Fatal PE occurred in 2.18% of patients, while fatal bleedings occurred in 1.55%. During the 12 months from initial VTE, fatal PE was the most common cause of death, after disseminating cancer, and bleeding the fourth most common. In patients initially presenting with PE, fatal PE during anticoagulation was 4-fold more frequent than fatal bleeding (204 vs 51 deaths) and occurred mostly during the first month of treatment (196/223, 88%). In patients initially presenting with DVT, fatal PE was 3-fold lower than fatal bleeding during (25 vs 85 deaths) and after anticoagulation treatment (8 vs 37 deaths). During the 12-month follow-up, other characteristics of cancer patients with VTE were identified as more common in fatal cases of PE and/or bleeding than in surviving cases.

interpretationBaseline clinical characteristics may determine anticoagulation outcomes in cancer patients with VTE and should be further investigated as possible factors for guiding changes in current practices of anticoagulation, such as adjusting anticoagulation intensity and duration in selected patients.

Indexed as

Health SciencesMedicine

Identifiers

PMID28119956
PMCPMC5239824

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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.