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

Hemolytic anemia: a systematic approach to management

M C Brain

    Postgraduate Medicine
    |October 1, 1978
    PubMed
    Summary

    This review covers hemolytic anemia, focusing on its recognition, diagnosis, and treatment. It classifies causes based on erythrocyte defects, inheritance, and origin.

    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

    Acute effects of varying doses of propranolol upon oxygen haemoglobin affinity in man.

    British journal of clinical pharmacology·2012
    Same author

    First successful unrelated bone marrow transplant in Canada: A look at the longest surviving recipient.

    Canadian family physician Medecin de famille canadien·2011
    Same author

    Letter from Ontario: Research at long odds.

    British medical journal·2010
    Same author

    Hammersmith postgraduate association.

    Canadian Medical Association journal·2010
    Same author

    Reinduction of remission of chronic myeloid leukemia by donor leukocyte transfusion following relapse after bone marrow transplantation: recovery complicated by initial pancytopenia and late dermatomyositis.

    Bone marrow transplantation·1993
    Same author

    B-cell lymphoma of recipient origin 9 years after allogeneic bone marrow transplantation for T-cell acute lymphoblastic leukaemia.

    British journal of haematology·1993

    Area of Science:

    • Hematology
    • Internal Medicine
    • Pathophysiology

    Background:

    • Hemolytic anemia is a condition characterized by premature destruction of red blood cells.
    • Understanding the diverse causes of hemolysis is crucial for effective management.
    • Erythrocyte disorders can stem from intrinsic defects or extrinsic factors.

    Purpose of the Study:

    • To provide a comprehensive review of hemolytic anemia.
    • To outline the classification of hemolytic anemia causes.
    • To guide the recognition, investigation, diagnosis, and treatment of hemolytic anemia.

    Main Methods:

    • Classification of hemolytic anemia based on erythrocyte membrane, hemoglobin, or metabolism disorders.
    • Categorization by congenital/familial versus acquired causes.
    • Differentiation between intrinsic and extrinsic factors leading to hemolysis.

    Main Results:

    • Hemolytic anemias can be systematically classified into distinct etiological groups.
    • This classification aids in understanding the underlying mechanisms of red blood cell destruction.
    • Recognizing these categories is key for targeted diagnostic and therapeutic approaches.

    Conclusions:

    • A structured classification system is essential for the comprehensive management of hemolytic anemia.
    • Understanding the specific cause of hemolysis (membrane, hemoglobin, metabolism, etc.) directs clinical strategy.
    • Effective treatment relies on accurate diagnosis informed by etiological classification.

    Related Experiment Videos