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

[Transfusion in sickle cell anemia].

D Bachir1, M Bonnet-Gajdos, F Galacteros

  • 1Policlinique Médecine interne, Hôpital Henri-Mondor, Créteil.

Presse Medicale (Paris, France : 1983)
|October 27, 1990
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

Deciphering Pain Experience in Adult Patients With Sickle Cell Disease: A Network Analysis of Pain-Related Factors in a Single French Sickle Cell Centre.

European journal of pain (London, England)·2025
Same author

La Revue de medecine interne·2023
Same author

La Revue de medecine interne·2023
Same author

Evaluation of a prophylactic transfusion program on obstetric outcomes in pregnant women with sickle cell disease: A single centre retrospective cohort study.

European journal of obstetrics, gynecology, and reproductive biology·2023
Same author

Delayed hemolytic transfusion reaction in the French hemovigilance system.

Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine·2019
Same author

[Prevention of genetic diseases : the return of the family practitioner ?]

Revue d'epidemiologie et de sante publique·2018
Same journal

Predictive analytics and risk stratification models in internal medicine: from risk scores to real-time machine learning.

Presse medicale (Paris, France : 1983)·2026
Same journal

Artificial Intelligence in skin disease therapeutics: from drug discovery to personalized treatment pathways.

Presse medicale (Paris, France : 1983)·2026
Same journal

AI in clinical diagnostics in dermatology: applications, validation, and real-world use cases.

Presse medicale (Paris, France : 1983)·2026
Same journal

Artificial Intelligence in medical research and publishing: progress, risks, and future perspectives.

Presse medicale (Paris, France : 1983)·2026
Same journal

Ethical, legal, and regulatory challenges in AI-based healthcare tools.

Presse medicale (Paris, France : 1983)·2026
Same journal

Decision-making for clinicians.

Presse medicale (Paris, France : 1983)·2026
See all related articles

Blood transfusions are crucial for managing sickle cell anaemia complications. This includes simple transfusions for acute anemia and exchange transfusions for severe events and general anesthesia, with specific protocols for long-term care.

Area of Science:

  • Hematology
  • Transfusion Medicine

Background:

  • Sickle cell anaemia presents unique challenges requiring tailored transfusion strategies.
  • Vascular occlusion is a significant risk associated with sickle cell disease.

Purpose of the Study:

  • To outline appropriate transfusion policies for managing sickle cell anaemia.
  • To detail the indications and methods for simple and exchange transfusions.

Main Methods:

  • Review of transfusion protocols for acute anaemia, severe occlusive/septic events, and general anaesthesia.
  • Discussion of long-term transfusion programmes, including red cell concentrate preparation and infection prevention.

Main Results:

  • Simple blood transfusion is recommended for acute anaemia and rare long-term programs.

Related Experiment Videos

  • Exchange transfusion is vital for severe occlusive/septic events and general anaesthesia to reduce sickle cell concentration.
  • Long-term transfusion programs require specific preparations and infection screening.

    • Conclusions:

    • A clear transfusion policy is essential for effective sickle cell anaemia management.
    • Appropriate use of simple and exchange transfusions, alongside long-term program considerations, improves patient outcomes.