eMedicine Specialties > Pediatrics: Surgery > Transplantation

Kidney Transplantation: Follow-up

Author: David Hatch, MD, Chief, Section of Pediatric Urology, Professor of Urology & Pediatrics, Departments of Urology and Pediatrics, Foster G McGaw Hospital and Loyola University of Chicago
Coauthor(s): Rekha Agrawal, MD, Director, Division of Pediatric Nephrology, Professor, Department of Pediatrics, Loyola University Medical Center
Contributor Information and Disclosures

Updated: Mar 24, 2009

Outcome and Prognosis

Graft survival

Kidney transplant survival increased dramatically with the use of cyclosporine A in the late 1980s. Since that time, a steady increase in kidney and patient survival has followed the advent of new immunosuppressive medications and modifications in the way immunosuppressive drugs are used. Actual kidney transplant survival as reported by US Renal Data Systems is illustrated in Media file 15.

Actual kidney transplantation survival in North A...

Actual kidney transplantation survival in North American children. Data from US Renal Data Systems, 2008.

Actual kidney transplantation survival in North A...

Actual kidney transplantation survival in North American children. Data from US Renal Data Systems, 2008.


Actual kidney transplantation survival in North American children. Data from US Renal Data Systems, 2008.

The most recent report from North American Pediatric Renal Trials and Collaborative Studies (NAPRTCS) demonstrates that kidney transplant survival rates in very young children (aged 0-1 y) is approximately 10 percentage points lower than that for older children. This difference is due to graft losses within the first year following transplantation. As in the adult population, black children experience graft loss at a higher rate than people of other races. Children who receive kidney transplants from pediatric donors appear to have more capacity to increase their glomerular filtration rate as they grow compared with children who receive adult kidneys.52

Cause of graft loss

The most common etiology of allograft loss among children and adolescents is rejection. Acute and chronic rejection caused almost half of the kidney transplant losses reported by members of the NAPRTCS. This was true for both initial and second kidney transplant failures. Other causes in order of decreasing frequency include technical complications including thrombosis, death with a functioning kidney, recurrent or de novo kidney diseases, primary nonfunction, noncompliance with immunosuppression, and others (see Media file 16).

Etiology of kidney transplant loss in children. D...

Etiology of kidney transplant loss in children. Data from US Renal Data Systems, 2008.

Etiology of kidney transplant loss in children. D...

Etiology of kidney transplant loss in children. Data from US Renal Data Systems, 2008.


Patient survival

Patient survival for pediatric recipients of kidney transplants reported by the US Renal Data System is illustrated in Media file 17.16

Pediatric patient survival following kidney trans...

Pediatric patient survival following kidney transplantation. Data from US Renal Data Systems, 2008.

Pediatric patient survival following kidney trans...

Pediatric patient survival following kidney transplantation. Data from US Renal Data Systems, 2008.


Patient survival is significantly lower for very young (<1 y) recipients. Infant recipients of cadaveric kidneys have the highest mortality rate.

Etiology of patient death

The NAPRTCS report from 2007 lists cardiopulmonary event as the most common cause of death among children with kidney transplants. Infection (bacterial more common than viral) was the second most common cause of mortality. Other causes are illustrated in Media file 18.

Cause of death among pediatric recipients of kidn...

Cause of death among pediatric recipients of kidney transplantation. Data from US Renal Data System, 2008.

Cause of death among pediatric recipients of kidn...

Cause of death among pediatric recipients of kidney transplantation. Data from US Renal Data System, 2008.


Currently, of any of the options for treatment, renal transplantation offers children with end-stage renal disease (ESRD) the best opportunity for growth and development. Allograft and patient survival both have demonstrated consistent improvement in the 5 decades during which renal transplantation has been available. This has been the result of improved understanding of the immune response to allografting and the development of increasingly specific strategies to protect a kidney transplant from the body's natural defenses while leaving a recipient protected from infection.

Future and Controversies

General

The greatest challenges facing those who treat children with end-stage renal disease (ESRD) are to provide more organs for children waiting for transplant and to prevent acute and chronic rejection without increasing the complications of immunosuppressive drugs.

Non–heart-beating cadaver donors

In the United States and Europe, most cadaver organs used in transplantation come from heart-beating cadavers. In some countries that have no legal recognition of brain death, transplant surgeons use organs from non–heart-beating cadavers, patients who experienced nonsurvivable injury (but did not meet the criteria for brain death), and those for whom life support systems did not preserve life. Within the last decade, several US and European centers have reported success in this technique. In general, graft survival rates are not as high and renal function is somewhat poorer when kidneys from non–heart-beating cadavers are used. Ongoing research in preservation and harvesting techniques may improve outcomes for transplantation with such organs.

Newer immunosuppressive agents

In the 1990s, several new immunosuppressive drugs became available. This explosion in transplant pharmacology has left transplant physicians wondering how these new medications should be used. In addition, new techniques in dosing and monitoring of older immunosuppressive regimens have improved graft survival. With the dramatic improvements in graft survival observed in the past decade, proving superiority of newer immunosuppressive agents is more difficult, especially in the short term (1-3 y). Lower rates of chronic rejection are expected as acute rejection rates decrease. Therefore, comparison of long-term graft survival likely is necessary to determine the best combination of immunosuppressive drugs.

Xenotransplantation

Since the infancy of human kidney transplantation, physicians have sought to use organs from animals. Early experimentation with sheep and primate organs were unsuccessful because of immunologic barriers. More is being learned about such impediments; however, currently xenotransplantation remains an unrealized dream. The two approaches under investigation are (1) immunologic blockade to the antigen-initiated response to interspecies transplantation and (2) genetic engineering to produce animals that lack the antigens against which human recipients mount an immunologic response.

For further information, see Mayo Clinic - Kidney Transplant Information.

 


More on Kidney Transplantation

Overview: Kidney Transplantation
Workup: Kidney Transplantation
Treatment: Kidney Transplantation
Follow-up: Kidney Transplantation
Multimedia: Kidney Transplantation
References

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Further Reading

Keywords

kidney transplantation, transplant, kidney transplant, end-stage renal disease, ESRD, renal transplant, renal transplantation, kidney donation, dialysis, hemodialysis, glomerulonephritis, histocompatibility antigens, HLAs, kidney rejection, nephrectomy, systemic lupus erythematosus, Goodpasture syndrome, Goodpasture disease, focal segmental glomerulosclerosis, membranoproliferative glomerulonephritis, hemolytic-uremic syndrome, Henoch-Schönlein purpura, continuous ambulatory peritoneal dialysis, CAPD, treatment, kidney failure, renal failure 

Contributor Information and Disclosures

Author

David Hatch, MD, Chief, Section of Pediatric Urology, Professor of Urology & Pediatrics, Departments of Urology and Pediatrics, Foster G McGaw Hospital and Loyola University of Chicago
David Hatch, MD is a member of the following medical societies: American Academy of Pediatrics, American College of Surgeons, American Society of Transplant Surgeons, and American Urological Association
Disclosure: Watson Pharma Grant/research funds Other; Mentor Corporation Grant/research funds Other

Coauthor(s)

Rekha Agrawal, MD, Director, Division of Pediatric Nephrology, Professor, Department of Pediatrics, Loyola University Medical Center
Rekha Agrawal, MD is a member of the following medical societies: American Society of Pediatric Nephrology and International Society of Nephrology
Disclosure: Nothing to disclose.

Medical Editor

Casimir F Firlit, MD, PhD, Attending Urologist, Department of Urology, Cardinal Glennon Children's Medical Center; Surgical Director, Pediatric Urology Specialists, PC, Cardinal Glennon Children's Medical Center
Casimir F Firlit, MD, PhD is a member of the following medical societies: American Academy of Pediatrics, American College of Surgeons, American Medical Association, American Society of Transplant Surgeons, American Urological Association, and Illinois State Medical Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Brian F Gilchrist, MD, Surgeon-in-Chief of Pediatric Surgery, The Floating Hospital for Children at Tufts-New England Medical Center; Associate Professor, Department of Surgery, Tufts University School of Medicine
Brian F Gilchrist, MD is a member of the following medical societies: American College of Surgeons, American Pediatric Surgical Association, and Society for Surgery of the Alimentary Tract
Disclosure: Nothing to disclose.

CME Editor

Ron Shapiro, MD, Professor of Surgery, Robert J Corry Chair in Transplantation Surgery, Director, Kidney, Pancreas, and Islet Transplantation, Thomas E Starzl Transplantation Institute, University of Pittsburgh Medical Center
Ron Shapiro, MD is a member of the following medical societies: American College of Surgeons, American Society of Transplant Surgeons, Association for Academic Surgery, Central Surgical Association, and Society of University Surgeons
Disclosure: Astellas Honoraria Speaking and teaching; Brystol Meyer Squibb StemCell Data Monitoring Committee Consulting fee Review panel membership; Wyeth Honoraria Speaking and teaching; Stem Cells, Inc Consulting fee Review panel membership; Up To Date contracted Author; Medscape contracted Video Blogger

Chief Editor

Stuart M Greenstein, MD, Professor of Surgery, Albert Einstein College of Medicine; Consulting Surgeon, Department of Surgery, Division of Transplantation, Montefiore Medical Center
Stuart M Greenstein, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Surgeons, American Society of Transplant Surgeons, American Society of Transplantation, Association for Academic Surgery, International College of Surgeons, Medical Society of New Jersey, National Kidney Foundation, New York Academy of Sciences, and Southeastern Surgical Congress
Disclosure: Nothing to disclose.

 
 
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