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

Using a mock trial to make a difficult clinical decision.

R Smith1

  • 1British Medical Journal, London.

BMJ (Clinical Research Ed.)
|November 21, 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

Paget's disease of bone.

BMJ (Clinical research ed.)·1992
Same author

Nonuniform expression of a mouse mammary tumor virus-driven int-2/Fgf-3 transgene in pregnancy-responsive breast tumors.

Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research·1992
Same author

Proviral insertions near cyclin D1 in mouse lymphomas: a parallel for BCL1 translocations in human B-cell neoplasms.

Oncogene·1992
Same author

Beta-endrophin immunoreactivity during human pregnancy.

The Journal of clinical endocrinology and metabolism·1992
Same author

Whistle blowing: a curse on ineffective organisations.

BMJ (Clinical research ed.)·1992
Same author

Eating disorders. Thin excuses.

Nursing times·1992
Same journal

The UK's visa brake will limit Sudan's healthcare recovery.

BMJ (Clinical research ed.)·2026
Same journal

Miscarriage: poor access to care leaves thousands of UK women desperately searching for answers.

BMJ (Clinical research ed.)·2026
Same journal

Amos maternity review: Doctors must work differently as units "no longer fit for purpose," but report is dogged by controversy.

BMJ (Clinical research ed.)·2026
Same journal

WHO's misguided push for complementary and alternative medicine.

BMJ (Clinical research ed.)·2026
Same journal

Why the GMC should not retain a right of appeal against MPTS decisions.

BMJ (Clinical research ed.)·2026
Same journal

Resident doctors' strikes end with latest pay offer accepted.

BMJ (Clinical research ed.)·2026
See all related articles

A mock trial determined that bone marrow transplantation (BMT) should not be offered to all children with symptomatic sickle cell disease due to its risks and the inability to predict patient outcomes.

Area of Science:

  • Medical Ethics
  • Hematology
  • Clinical Decision-Making

Background:

  • Clinical decisions are often made with limited scientific evidence.
  • Expert consensus is one approach to address this uncertainty.
  • Legal processes can also be utilized to analyze complex medical questions.

Purpose of the Study:

  • To explore the use of a mock trial to decide on a controversial clinical intervention.
  • To evaluate the ethical considerations of offering bone marrow transplantation (BMT) for symptomatic sickle cell disease in children.

Main Methods:

  • A mock trial was conducted involving legal professionals and expert witnesses.
  • A jury was presented with evidence regarding the benefits and risks of BMT for sickle cell disease.
  • The trial focused on whether BMT should be universally offered to symptomatic children.
Keywords:
Professional Patient Relationship

Related Experiment Videos

Main Results:

  • Bone marrow transplantation offers a potential 90% cure rate for sickle cell disease.
  • However, BMT carries a 10% risk of death or severe disability.
  • Doctors cannot accurately predict which children will experience severe sickle cell disease complications.

Conclusions:

  • The jury reached a majority decision against offering BMT to all symptomatic children with sickle cell disease at this time.
  • The decision highlights the challenges in balancing potential cures with significant treatment risks when scientific information is incomplete.