The pace at which neurotechnological developments are being translated into clinical applications calls for a preparatory neuroethical model that can plot the benefits, burdens, and risks of neurosurgery as a step toward minimizing risks and maximizing benefits.
Unclear regulations and informal data gathering on immigrants who receive or donate organs can cause mistrust and suspicion of the organ allocation system and affect donation rates.
Parents’ right to choose the culture of their children and a child’s right to an open future outweigh the right of the Deaf to perpetuate their culture by disallowing government funding of cochlear implant research to restore hearing.
Media coverage of information presented at medical meetings often fails to qualify the findings reported, and scientists and the media need to develop a better working relationship to ensure the accuracy of early-stage research reports.
Organ procurement organization representatives play a pivotal role in serving families of a deceased donor and mediating disagreements about the donation while physicians' involvement in these discussions is minimal.
Physicians who treat patients who are on the organ transplant wait list are obligated to share with the rest of the transplant team pertinent confidential information that can affect the patient's eligibility or clinical status.
Physicians who treat patients who are on the organ transplant wait list are obligated to share with the rest of the transplant team pertinent confidential information that can affect the patient's eligibility or clinical status.