Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Disorders of Hemostasis01:24

Disorders of Hemostasis

Hemostasis, the process that stops bleeding after a blood vessel injury, is crucial for maintaining the integrity of the circulatory system. However, disorders of hemostasis can disrupt this delicate balance, leading to either excessive clotting or bleeding. These disorders can be broadly classified into thromboembolic disorders and bleeding disorders.
Thromboembolic Disorders
Two factors primarily cause thromboembolic conditions.
Venous Thrombosis I: Introduction01:30

Venous Thrombosis I: Introduction

Venous thrombosis, the most common disorder of the veins, involves the formation of a thrombus or blood clot associated with vein inflammation. It can be classified as either superficial vein thrombosis or deep vein thrombosis.Superficial Vein Thrombosis: This involves the formation of a thrombus in a superficial vein, usually the greater or lesser saphenous vein. Though less severe than deep vein thrombosis (DVT), SVT can lead to complications if untreated.Deep Vein Thrombosis (DVT): This...
Bone Marrow Sampling and Transplants01:22

Bone Marrow Sampling and Transplants

Bone marrow transplant is a potential cure for several diseases, including cancer and specific genetic disorders. Notably, this procedure is applicable for patients suffering from aplastic anemia, certain types of leukemia, severe combined immunodeficiency disease (SCID), Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, thalassemia, sickle-cell disease, and certain cancers.
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy the...
Anticoagulant Drugs: Low-Molecular-Weight Heparins01:30

Anticoagulant Drugs: Low-Molecular-Weight Heparins

Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
Regulation of Hematopoietic Stem Cells01:01

Regulation of Hematopoietic Stem Cells

All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
Hematopoiesis01:21

Hematopoiesis

The process of blood cell formation is called hematopoiesis. Hematopoiesis starts early during development, on the seventh day of embryogenesis. This phase of hematopoiesis is called the primitive wave, wherein the extraembryonic yolk sac allows the production of erythroid cells and endothelial cells from a common precursor called hemangioblast. The erythroid cells provide oxygen to support the growth of the rapidly dividing embryo. Hemangioblasts later develop into hematopoietic stem cells or...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Thrombopoietin receptor agonists in hereditary thrombocytopenias.

Journal of thrombosis and haemostasis : JTHยท2018
Same author

Fifth ร…land Island conference on von Willebrand disease.

Haemophilia : the official journal of the World Federation of Hemophiliaยท2018
Same author

Desmopressin and type II B von Willebrand disease.

Haemophilia : the official journal of the World Federation of Hemophiliaยท2016
Same author

Acquired haemophilia: experience of two Italian centres with 17 new cases.

Haemophilia : the official journal of the World Federation of Hemophiliaยท2016
Same author

Practice-relevant revision of IPSET-thrombosis based on 1019 patients with WHO-defined essential thrombocythemia.

Blood cancer journalยท2015
Same author

Diagnosing type 1 von Willebrand disease: good for patient's health or for doctor's prestige? reply.

Journal of thrombosis and haemostasis : JTHยท2014
Same journal

Apoptotic versus procoagulant platelets: similar "necrotic" phenotype and procoagulant activity in vitro, but distinct adhesive protein composition.

Thrombosis researchยท2026
Same journal

Heatstroke-induced coagulopathy: A scoping review of therapeutic strategies and outcome reporting.

Thrombosis researchยท2026
Same journal

Mapping thrombus habitat: Non-contrast MRI radiomics and pixel-tile histomics approach to track venous thrombosis evolution in mice.

Thrombosis researchยท2026
Same journal

A study protocol for a randomised controlled trial evaluating the safety and efficiency of the YEARS algorithm versus computed tomography pulmonary angiography only for suspected acute pulmonary embolism in patients with cancer: the Hydra Study.

Thrombosis researchยท2026
Same journal

Associating the phenotypic expression of platelets with disease type through image-based single-cell profiling.

Thrombosis researchยท2026
Same journal

The mechanisms of contractile dysfunction following chronic limited platelet activation in (pro)thrombotic conditions.

Thrombosis researchยท2026
See all related articles

Related Experiment Video

Updated: May 26, 2026

Venous Thrombosis Assay in a Mouse Model of Cancer
04:40

Venous Thrombosis Assay in a Mouse Model of Cancer

Published on: January 5, 2024

Hematologic malignancies and thrombosis.

F Elice1, F Rodeghiero

  • 1Department of Cell Therapy and Hematology, San Bortolo Hospital, Vicenza, Italy.

Thrombosis Research
|December 27, 2011
PubMed
Summary
This summary is machine-generated.

Patients with blood cancers face a high risk of blood clots (venous thromboembolism or VTE). Proactive VTE prevention strategies are crucial for these patients, despite treatment challenges.

More Related Videos

Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome
06:39

Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome

Published on: October 3, 2018

Related Experiment Videos

Last Updated: May 26, 2026

Venous Thrombosis Assay in a Mouse Model of Cancer
04:40

Venous Thrombosis Assay in a Mouse Model of Cancer

Published on: January 5, 2024

Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome
06:39

Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome

Published on: October 3, 2018

Area of Science:

  • Hematology
  • Oncology
  • Vascular Medicine

Background:

  • Patients with hematologic malignancies exhibit elevated venous thromboembolism (VTE) risk, especially during diagnosis and treatment.
  • Risk factors include disease-specific hypercoagulability, chemotherapy, asparaginase, immunomodulatory drugs (IMiDs), central venous catheters (CVCs), immobility, and infections.
  • Thrombotic complications significantly increase morbidity and mortality in onco-hematologic patients.

Purpose of the Study:

  • To highlight the need for thromboprophylaxis in hematologic malignancies.
  • To address challenges in managing anticoagulant/antiaggregant therapy due to thrombocytopenia and bleeding risks.
  • To advocate for institutional policies on VTE prevention and treatment in this patient population.

Main Methods:

  • Review of existing literature on VTE in hematologic malignancies.
  • Analysis of risk factors and complications associated with VTE in these patients.
  • Evaluation of current guideline limitations and clinical practice needs.

Main Results:

  • Current guidelines offer limited recommendations, primarily for multiple myeloma patients on specific therapies.
  • Thrombocytopenia and bleeding complications complicate anticoagulant and antiplatelet therapy.
  • A significant unmet need exists for comprehensive VTE management strategies.

Conclusions:

  • Hematologic malignancy patients require tailored VTE prevention and treatment protocols.
  • Clinical departments should develop and implement specific policies for managing thromboembolic complications.
  • Further research is needed to optimize thromboprophylaxis in this high-risk group.