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PROPOSALS TO PROTECT
LIVING ORGAN DONORS

September 16, 2003

FWD: SHOULD A PATIENT BE TOLD THAT HEPATITIS C CAN RETURN AND INFECT THE NEW LIVER!

Several organizations have made recommendations aimed at protecting living organ donors.

The United Network for Organ Sharing, which runs the nation's transplant network under a government contract, agreed at its June meeting:

  • Hospitals that want to perform living donor transplants should meet minimum criteria, such as having surgeons with significant experience. Other hospitals may still perform the transplants, but lack of UNOS approval could be a red flag to patients and/or insurance companies.
  • The questionnaire used to track the well-being of living donors will be updated. But many donors are never interviewed, and the network's action will not change that.
  • Potential living donors "should have a psychosocial evaluation." The network rejected a proposal to make this mandatory.
  • The network will develop educational materials for potential living donors explaining the risks and the donation process.

    The New York State Transplant Council Committee on Quality Improvement issued a series of recommendations, now under review by the state Health Department, after a 35-year-old donor died in 2002:
  • Hospitals performing living donor transplants would be required to have donor advocate teams with power to veto any donor candidates. Hospital transplant programs would have to have minimum staffing ratios and experienced surgeons.
  • Only patients age 55 and under, who have suffered at least one complication from their disease, would be eligible to get livers from living donors.
  • The state would create a donor registry with reporting of donor short- and long-term outcomes mandatory.
  • Hospital could only take organs from people who have a "vital emotional relationship" to the recipient, thus nixing "good Samaritan" donations from strangers.

    The federal Advisory Committee on Transplantation made several recommendations to the secretary of the Department of Health and Human Services, and they have been forwarded to UNOS or other agencies for consideration:
  • The government should create a standardized informed consent document to make sure all potential donors understand the risks.
  • All hospitals must have independent donor advocates.
  • HHS should establish a database of health outcomes of all live donors.
  • An independent resource center should be considered to assist living donors and their families.
  • The organ allocation system should be changed to give all living donors preference should they someday need an organ transplant. Current policy only gives preference to kidney donors who later need a kidney.
  • Hospitals that take organs from living donors should have to meet certain standards.


  • (AP)
    Continue to the article source
    The Dark Side Of Organ Donation

 

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