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Originally posted by AGWskeptic
I did not watch the videos, but I will in fairness.
Originally posted by AGWskeptic
I researched this topic 2 years ago when it came up and found that while there are isolated cases it is not widespread and reports of abduction harvests were unsubstantiated.
It's one of those issues the media likes to overhype and fabricate.
Originally posted by AGWskeptic
As I said before, the amount of testing you have to go through is extensive, the odds of some Joe off the street being a match are mighty slim, and by the time you get the test results and match it with a donor, it's a dead organ.
Originally posted by AGWskeptic
I'll watch the videos to see if there is anything new, but being approached online by a willing seller is a far cry from back alley abductions of children.
Originally posted by hotbread
I think it is a standard procedure for funeral homes to remove organs before burial, where do the organs go?
If someone has indicated that he or she wishes to donate organs after death, a transplant team can immediately move in and initiate the organ harvesting process after consent forms are signed by someone with the power of attorney for the patient. In other instances, someone's wishes may be unclear, and hospital staff may discuss options with a family. In all cases, a transplant coordinator discusses the possibility of organ donation before a harvest is begun, and the wishes of surviving family members are always respected; organ harvesting will never take place without consent.
Once a medical team has received approval, the organ donor is wheeled into an operating room and cut open so that his or her organs and tissues can be removed. Typically, the donor has been blood typed and screened first, and a transplant coordination agency, such as the United Network for Organ Sharing in the United States, has assigned organs to people in need. Medical staff work quickly to keep organs usable, but they are also respectful, and they ensure that the patient is sewn up when the procedure is finished so that the family can visit the body as part of their grieving process, if desired.
After organ harvesting, the organs and tissues are rushed to their new destinations, and transplanted into patients in need. Some tissues have a shelf life, and they may be stored in medical facilities until they are needed. In the event that any donated organ or tissue is not usable, it is respectfully disposed of.
Link.
Originally posted by AGWskeptic
It would mean there are more being done on the black market than in the open.
Originally posted by AGWskeptic
Do you have any idea how many transplants that would be.
...
That's an awful lot of rich sick people.
MedScape
Question
I'm trying to find a source for data describing the worldwide statistics of organ transplantation. Can you please help me?
Response from Francis Leo Delmonico, MD
The worldwide statistics on organ transplantation would likely have to be an ad hoc compilation of multiple databases: the United Network for Organ Sharing (UNOS) Scientific Registry on Organ Transplantation, Eurotransplant and others. By organ specificity there are international registries for kidney, pancreas, liver, heart and lung transplantation. Selected transplantation registries and databases are described below.
UNOS Scientific Registry on Organ Transplantation - www.unos.org...
The volume, accuracy, and reliability of the data available on transplantation are unprecedented in medicine. The UNOS Scientific Registry on Organ Transplantation (www.unos.org) is the most extensive single source of information available for a single form of medical treatment. Because of a federal mandate, solid organ transplantation is the only discipline in medicine in which complete demographic, risk, and outcome data [in the traditional sense] are available. UNOS administers the National Organ Procurement and Transplantation Network (OPTN) and the U.S. Scientific Registry on Organ Transplantation under contracts with the U.S. Department of Health and Human Services. The OPTN portion of the database contains pretransplant information pertaining to transplant candidates on the OPTN waiting list, donor-recipient matching, cadaveric and living donors, and histocompatibility. The Scientific Registry Transplant database is the most complete medical database in the world, tracking outcomes of all solid organ transplants since October 1987.
Eurotransplant - www.eurotransplant.nl...
The Eurotransplant Foundation is a non-profit organization whose main aim is to encourage organ transplantation. Eurotransplant coordinates international exchange of donor organs across a region with 116 million inhabitants. Transplant centers and tissue-typing laboratories as well as donor hospitals in Belgium, the Netherlands, Luxembourg, Germany and Austria share in this effort. For Transplantation Statistics go to www.eurotransplant.nl...
Australia and New Zealand Dialysis and Transplant Registry (ANZDATA) - www.anzdata.org.au...
The ANZDATA collects a wide range of statistics that relate to the outcomes of treatment of those with end stage renal failure. The data are collected twice a year. The main results are published in an annual report, with interim analyses and publications occurring throughout the year. Data is collected from all dialysis and transplant units in Australia and New Zealand at 31st March and 30th September each year. This encompasses all patient events that have occurred in the previous six months as well as a "snapshot" of all dialysis and transplants patients on those dates. The Annual Reports of the ANZDATA Registry are available. The full Reports are available since the 20th Report. Excerpts of the 19th Report are available.
United States Renal Data System (USRDS) - www.med.umich.edu...
The USRDS Database is a national data system that collects, analyzes, and distributes information about end-stage renal disease in the United States. Data on approximately 95% of all adult and kidney transplant recipients in the U.S. are in the USRDS Renal Transplant Database. The USRDS is funded directly by NIDDK in conjunction with the Health Care Financing Administration. The USRDS Coordinating Center is operated under a contract with the University of Michigan.
International Pancreas Transplant Registry
The IPTR is a scientific database collected from institutions performing pancreas transplants worldwide. The goals of the IPTR are to: collect data on all pancreas transplants performed worldwide, perform scientific analysis on collected pancreas transplantation data, and communicate information on pancreas transplantation to member institutions, the health care community, and the interested general public. The International Pancreas Transplant Registry is located at the University of Minnesota in Minneapolis. The IPTR maintains a database of all reported pancreas transplants worldwide. In cooperation with over 200 centers, the pretransplant and posttransplant courses of over 10,000 patients who have received pancreas transplants are followed. Biostatistical analyses are performed regularly and the results are presented at international and national scientific meetings. The original goal of the Registry was to collect information on both pancreas and islet cell transplants. However, with the growth in pancreas transplantation data, the responsibility for the records of the islet cell transplantation component was transferred in 1987 as the International Islet Transplant Registry (IITR) to the University of Giessen, in Germany. The IPTR remained at the University of Minnesota and in 1997, the IPTR was contracted with the UNOS to collect the data on U.S. pancreas transplants for the Scientific Studies Committee of UNOS. This led to organization of a UNOS/US Pancreas Transplant Registry. Today, the IPTR continues to maintain a close working relationship with UNOS, ITR, Eurotransplant, and other registries throughout the world. The IPTR databases currently include information on the following parameters: recipient demographics, recipient history, immunological information, operative techniques, preservation regimen, transplantation of other organs to the same recipient, donor information, recipient graft function, transplant complications, and recipient/graft survival.
International Islet Transplant Registry (IITR) - www.insulin-free.org...
The IITR was originally part of the IPTR, but with the growth in pancreas transplantation data the responsibility for the records of the islet cell transplantation component was transferred in 1987 as the IITR to the University of Giessen, in Germany. The function of the IITR is to collect, analyze, and report data on all islet (allo-, auto, xeno-) transplants performed throughout the world.
International Society for Heart and Lung Transplantation (ISHLT) Heart/Lung Registry Database - www.ishlt.org...
The ISHLT has over 1800 members from more than 45 countries, representing more than 10 different disciplines involved in the management and treatment of end-stage heart and lung disease. The ISHLT Heart/Lung Registry Database reports worldwide heart transplantation experience since 1982, and is maintained in Dallas, Texas.
Intestinal Transplant Registry (ITR) - www.lhsc.on.ca...
The Intestinal Transplant Registry was established in 1994 to review the worldwide experience for the 4th International Symposium on Small Bowel Transplantation. The ITR collects data and prepares a report every 2 years. The ITR collects the following types of information from all intestinal transplants: demographics, such as gender and age of recipient; pretransplant diagnosis leading to transplant; pretransplant status; type of transplant (bowel, bowel-liver, or "cluster transplant"); posttransplant status and complications; antirejection drugs taken by patients and donor information.
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Liver Transplantation Database - www.niddk.nih.gov...
The NIDDK LTD is leading the way for building consensus on methods for assessment of patient-reported outcomes in transplantation. The NIDDK LTD was established to prospectively investigate questions related to the experience of patients evaluated for and undergoing liver transplantation. An initial 4-year planning phase was used to develop data collection instruments and quality control procedures. The project was funded by the NIH and the contract was awarded to the Epidemiology Data Coordinating Center at the University of Pittsburgh and five liver transplant centers that carried out the pilot program between 1985 and 1989. During the implementation phase beginning in 1990, 3 clinical centers (Mayo Clinic, University of Nebraska Medical Center, and University of California at San Francisco) refined the data collection instruments and enrolled and followed consecutive liver transplant candidates who consented to be included in the protocol. The definitive phase of the NIDDK LTD was a prospective study (1990-1995) of follow-up data on consecutive patients referred for liver transplantation at these 3 centers.
Pulmonary Retransplant Registry - www.lhsc.on.ca...
The Pulmonary Retransplant Registry was established in late 1991 in order to provide a summary of the worldwide experience with redo lung transplantation at the 12th annual meeting of the International Society for Heart and Lung Transplantation in 1992. All known centers performing pulmonary transplants were invited to join the Pulmonary Retransplant Registry and to provide information about their retransplant patients for the database. Programs from approximately 50 centers in North America, Europe and Australia participate in this registry. The Pulmonary Retransplant Registry has been able to identify the predictors of survival and graft function after pulmonary retransplantation. The Registry collects the following types of information on all pulmonary retransplantations: demographics, pretransplant diagnosis leading to the initial lung transplant procedure, cause of graft failure after primary lung transplantation,recipient's condition before retransplantation, type of retransplant procedure (single lung or bilateral lung), posttransplantation complications and duration of intensive care unit and hospital stays, antirejection drugs taken by patients, long-term survival and lung graft function and donor information.
North American Pediatric Renal Transplant Cooperative Study (NAPRTCS) - camelot.emmes.com...
The purpose of the NAPRTCS is to identify, characterize and follow current practices and trends in therapy for children receiving renal allografts, dialysis or treatment for chronic renal insufficiency in participating centers in North America. Since 1987, the NAPRTCS has enrolled more than 10,000 children and adolescents from more than 140 participating transplant centers. Specific aims of the NAPRTCS are to:
--Characterize patient survival, graft survival and patient morbidity among pediatric renal allograft recipients, dialysis and chronic renal insufficiency patients.
--Follow growth of children who receive renal allografts, dialysis, or care for chronic renal insufficiency.
--Conduct special studies designed to answer questions pertaining to such topics as quality of life, rehabilitation and physical and mental development among selected subgroups of patients.
--Compare the data obtained from this North American study with information on pediatric renal transplantation and dialysis generated by the European Dialysis and Transplant Association (EDTA) and other pediatric renal care registries.
Originally posted by AGWskeptic
Do you have any idea how many transplants that would be.
Originally posted by loam
A few months ago, the European division of CNN produced this report concerning and even sinister problem in the Sinai. And as you will see, these 'organ donors' aren't simply duped into selling their organs. They are taken by force.
Society makes me nervous about the future. But so do the people on ATS who SHOULD care about things like this, yet can't be bothered.
On Wikipedia, the CURRENT article on organ harvesting says:
Organ harvesting (is) a general fiction...