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Organ transplants and HIV/AIDS

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General transplant requirements
Hiv transplant research

General transplant requirements
  • The United Network for Organ Sharing (UNOS) maintains a computer network that links all organ procurement organizations and transplant centers in the United States. This network is accessible 24 hours a day, seven days a week.
  • Once a doctor refers a patient, a transplant center evaluates the potential transplant candidate. Members of the transplant center conduct medical tests and consider the patient's mental and physical health, as well as his/her personal support system. Prospective transplant candidates are then added to the national patient waiting list. The patient is not placed on a ranked list at that time. Instead, the patient is added to the pool of patients who are waiting.
  • When a deceased organ donor is identified, a transplant coordinator from an organ procurement organization accesses the UNOS database. The computer creates ranked lists of patients for each organ that is procured from that donor in ranked order, based on organ allocation policies.
  • Rank is determined by factors such as blood type, length of time on the waiting list, immune status and the geographical distance between the candidate and donor. For organs such as the heart, liver and intestines, the patient's degree of medical urgency is also considered.
  • The organ is offered to the transplant team of the first person on the list. In most cases, the top patient does not end up receiving the organ. This is because when the patient is selected, he/she must be healthy enough to undergo major surgery and willing to receive the transplant immediately. In addition, a test that measures the compatibility between the donor and recipient may be necessary. For instance, patients who have high antibody levels are often incompatible with the donor because the patient's immune system is likely to reject the organ.
  • Once an organ recipient is selected and contacted, and testing is complete, surgery is scheduled.

Hiv transplant research
  • Preliminary data from a prospective study on the outcomes of HIV-infected liver or kidney transplant recipients was presented at the XVI International AIDS Conference.
  • Subjects in the study were HIV-infected patients who had CD4 cell counts higher than 200cells/mm3, an undetectable viral load (with the exception of liver transplant candidates who could not tolerate antiretroviral therapy) and no history of certain opportunistic infections. Eleven patients received liver transplants and 18 received kidney transplants. The average patient was 45 years old. Fifty-five percent of liver and 28% of kidney transplant recipients tested positive for hepatitis C virus (HCV) coinfection.
  • The researchers reported similar rates of patient and graft survival that has been reported in patients who are not infected with HIV. Three patients in the liver transplant group died. Despite relatively high rates of rejection, organ function remained high in the transplant recipients. None of the patients experienced HIV disease progression and most patients maintained stable CD4 cell counts. Lower CD4 cell counts were reported in older patients who had episodes of rejection and received the immunosuppressant anti-thymocyte globulin (Thymoglobulin®).
  • Ninety-two percent of the liver transplant recipients lived one year after surgery, and 72% lived three years after surgery. Ninety-four percent of the kidney transplant recipients lived one year after surgery, and 94% lived three years after surgery.
  • The researchers reported that two out of the three deaths among liver transplant recipients were the result of recurrent HCV disease. The third patient also experienced recurrent HCV, although it was not the cause of death. The researchers concluded that transplant risks appear to be similar in HIV-infected and non-infected patients. However, more studies are necessary to determine the proper management of HCV-coinfection after liver transplants.
  • Another study presented at the conferences examined the pharmacokinetics of protease inhibitor use in six HIV patients who received liver transplants and received immunosuppressive therapy. The patients received the protease inhibitor nelfinavir (Viracept®). Three of the patients required a dose adjustment. The study suggests that HIV patients require close monitoring and individualized treatment regimens when they receive immunosuppressants.

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The information in this monograph is intended for informational purposes only, and is meant to help users better understand health concerns. Information is based on review of scientific research data, historical practice patterns, and clinical experience. This information should not be interpreted as specific medical advice. Users should consult with a qualified healthcare provider for specific questions regarding therapies, diagnosis and/or health conditions, prior to making therapeutic decisions.

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