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 Experiment Videos

Acquired platelet function defects.

R L Bick1

  • 1Department of Medicine, University of California, Los Angeles.

Hematology/Oncology Clinics of North America
|December 1, 1992
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Contaminants in heparins continue to be unfolded.

International angiology : a journal of the International Union of Angiology·2008
Same author

The rheological changes after cesarean section: The influence of low molecular weight or unfractionated heparin on the rheological properties of blood.

Clinical hemorheology and microcirculation·2007
Same author

Antiphospholipid thrombosis syndromes.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis·2001
Same author

Stasis ulcers refractory to therapy--accelerated healing by treatment with clopidogrel +/- dalteparin: a preliminary report.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis·2001
Same author

Proficient and cost-effective approaches for the prevention and treatment of venous thrombosis and thromboembolism.

Drugs·2000
Same author

An update on heparins at the beginning of the new millennium.

Seminars in thrombosis and hemostasis·2000
Same journal

Palliative Therapy for Liver and Biliary Neoplasms.

Hematology/oncology clinics of North America·2026
Same journal

Ablative Therapies for Liver Tumors.

Hematology/oncology clinics of North America·2026
Same journal

Pathology of Liver and Biliary Neoplasms.

Hematology/oncology clinics of North America·2026
Same journal

Minimally Invasive Surgery for Liver and Biliary Tract Neoplasms.

Hematology/oncology clinics of North America·2026
Same journal

Surgical Considerations for Primary Liver Neoplasms.

Hematology/oncology clinics of North America·2026
Same journal

Systemic Therapy for Biliary and Liver Neoplasms: Chemotherapy and Immunotherapy.

Hematology/oncology clinics of North America·2026
See all related articles

Platelet dysfunction, both inherited and acquired, can cause bleeding. Acquired platelet defects, often drug-induced, are common and require prompt diagnosis and management, including platelet transfusions and stopping offending medications.

Area of Science:

  • Hematology
  • Clinical Pathology

Background:

  • Platelet dysfunctions are significant causes of hemorrhage, particularly acquired forms linked to trauma or surgery.
  • Hereditary platelet function defects are rare, but hereditary storage-pool disease warrants suspicion in pediatric cases with specific findings.
  • Acquired platelet function defects, frequently drug-induced, are common and should be suspected in patients with bruising or mucosal bleeding.

Purpose of the Study:

  • To summarize the clinical significance and diagnostic approaches to platelet dysfunctions.
  • To outline therapeutic strategies for managing bleeding due to platelet defects.

Main Methods:

  • Review of clinical presentations and diagnostic utility of bleeding time tests.
  • Discussion of laboratory tests like platelet aggregation and lumi-aggregation.

Related Experiment Videos

  • Emphasis on clinical history and physical examination in diagnosing platelet disorders.
  • Main Results:

    • Template bleeding time is a useful screening tool but not definitive; normal results do not exclude dysfunction.
    • Prolonged bleeding time is an unreliable predictor of bleeding risk.
    • Platelet aggregation or lumi-aggregation tests are crucial in specific clinical scenarios.

    Conclusions:

    • Promptly suspect acquired platelet function defects in patients with bleeding symptoms, especially if on medication.
    • Platelet concentrates are the primary treatment for significant bleeding from platelet defects.
    • Managing acquired defects involves addressing underlying conditions and discontinuing causative drugs.