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Author Topic: Ethnic and Gender Related Differences in the Risk of End-Stage Renal Disease Aft  (Read 3687 times)

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Offline Clark

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http://onlinelibrary.wiley.com/doi/10.1111/j.1600-6143.2011.03609.x/abstract

Ethnic and Gender Related Differences in the Risk of End-Stage Renal Disease After Living Kidney Donation
W. S. Cherikh1,*, C. J. Young2, B. F. Kramer1, S. E. Taranto1, H. B. Randall3, P.-Y. Fan4
Article first published online: 14 JUN 2011
American Journal of Transplantation
Early View (Online Version of Record published before inclusion in an issue)
DOI: 10.1111/j.1600-6143.2011.03609.x

Abstract

Donation;donor risk;end-stage renal disease;kidney
There is limited data pertaining to the risk of End Stage Renal Disease (ESRD) after living kidney donation. The Organ Procurement and Transplantation Network and the Center for Medicare and Medicaid Services databases were used to identify living kidney donors (LKDs) who subsequently developed ESRD and to calculate LKD ESRD rates. We found 126 cases of ESRD among 56 458 LKDs (0.22%) who donated during October 1, 1987–March 31, 2003. The overall LKD ESRD rate was 0.134 per 1000 years at risk, with an average duration of follow-up of 9.8 years. ESRD rates for LKDs overall and for Black, White, male and female donors compared favorably to the ESRD incidence in the general population. The LKD ESRD rate was nearly five times higher for Blacks than for Whites and two times higher for males than females. However, these ethnic and gender-related differences were similar to those previously reported for ESRD in the general population. Our findings do not show an increase in the risk of ESRD for LKDs and support the current practice of living kidney donation. Further research is needed to determine if improved donor screening or follow-up will reduce the risk of postdonation ESRD.
Unrelated directed kidney donor in 2003, recipient and I both well.
620 time blood and platelet donor since 1976 and still giving!
Elected to the OPTN/UNOS Boards of Directors & Executive, Kidney Transplantation, and Ad Hoc Public Solicitation of Organ Donors Committees, 2005-2011
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Offline sherri

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Not sure what conclusions can be drawn from this study means. The first sentence states there is limited data pertaining to ESRD after living donation. Is this because data has not been collected, living donors are not followed up or other reasons. The other question I have as a living donor is, these 126 donors who developed ESRD, would they have developed ESRD regardless of donating a kidney or did having one kidney contribute to their ESRD. Why did they develop ESRD? Was it due to hypertension, diabetes, subsequent glomerular disease. Were these donors educated on the importance of maintaining a healthy lifestyle, were they followed up yearly so disease could be caught early? Lots of questions for me as a donor. And did these 126 donors get transplanted?

If anyone can help explain these studies to me I would appreciate it. Want to start learning how to understand the scientific data more clearly.

Thanks,

Sherri
Sherri
Living Kidney Donor 11/12/07

Offline Clark

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Dear Sherri,

  Imagine my surprise to see that the full article is available: http://onlinelibrary.wiley.com/doi/10.1111/j.1600-6143.2011.03609.x/full

You ask, "The first sentence states there is limited data pertaining to ESRD after living donation. Is this because data has not been collected, living donors are not followed up or other reasons?"

The authors write: "To more precisely evaluate the risk of developing ESRD after kidney donation, we used the OPTN and Center for Medicare and Medicaid Services (CMS) databases to comprehensively determine the number of LKDs who donated between October 1, 1987 and March 31, 2003 and subsequently developed ESRD. We compared the characteristics of LKDs who developed ESRD with LKDs in general. In addition, we calculated the incidence of postdonation ESRD for LKDs who donated between April 1, 1994 and March 31, 2003."
  and
"Segev et al. (10) found that LKDs had similar mortality rates compared with healthy age matched controls from the National Health and Nutrition Examination Survey (NHANES) after a median of 6.3 years postdonation. However, lack of comprehensive follow-up of donors precludes definitive assessment of the long-term risks of kidney donation. OPTN data collection currently only captures data through 2 years postdonation and no other national sources of these data exist."


You ask, "The other question I have as a living donor is, these 126 donors who developed ESRD, would they have developed ESRD regardless of donating a kidney or did having one kidney contribute to their ESRD?"

The authors write: "Notably, the median time from donation to ESRD was only 10.4 years and nearly 20% of the cases progressed to ESRD within 5 years. This rapid loss of renal function after intensive predonation evaluation raises questions about incomplete donor screening, inappropriate donor acceptance and inadequate postdonation follow-up and care. Our analysis of the relationship between LKDs with ESRD and their recipients did not suggest that postdonation ESRD was due to unrecognized familial renal disease."
 and
"Unfortunately, we cannot definitively determine if kidney donation confers increased risk for ESRD. Annual ESRD incidence for the U.S. population cannot be extrapolated to LKDs as the extensive screening for renal disease for this group would be expected to dramatically lower the risk of renal failure. Estimates of ESRD rates for ‘healthy individuals’ from survey data such NHANES are incompletely validated and such data sources cannot provide a comparison group with similar levels of testing for renal disease."



You ask, "Why did they develop ESRD?  Was it due to hypertension, diabetes, subsequent glomerular disease?"

The authors write:  "While glomerulonephritis (33%) and hypertension (25%) were the most common diagnoses, analysis was limited by incomplete data as ‘other’ was reported as the etiology of ESRD in 33% of the cases. A significantly higher proportion of Black LKDs had ESRD from glomerulonephritis (39% vs. 22%) and hypertension (32% vs. 22%) than White LKDs (p = 0.02). Comparison of LKD and recipient ESRD diagnosis was also limited to 62 (49%) of LKD/recipient pairs where both diagnoses were specified. Of LKDs with specified diagnoses, 50% had the same cause of ESRD as their recipients (18 with glomerulonephritis and a total of 13 with hypertension or diabetes)."
 and
"We also attempted to compare the etiologies of LKD ESRD with those of their recipients to ascertain whether certain recipient diagnoses were associated with higher postdonation LKD ESRD risk. Unfortunately, the analysis was severely limited by incomplete data as the etiology of both LKD and recipient ESRD was available in fewer than half of the cases. Excluding those with ‘other’ or ‘unknown’ recorded as the etiology of ESRD, the most common reported diagnoses among the LKDs with postdonation ESRD were glomerulonephritis and hypertension. When compared to White LKDs, a higher proportion of Black LKDs had ESRD from glomerulonephritis (39% vs. 22%) and hypertension (32% vs. 22%). Clearly, additional follow-up data is needed to determine if specific diagnoses entail increased risk to related donors."



You ask, "Were these donors educated on the importance of maintaining a healthy lifestyle, were they followed up yearly so disease could be caught early?"

  Not addressed, except the notation of the limited follow up.

You ask, "Did these 126 donors get transplanted?"

The authors write: "Of the 56 458 LKDs who donated during October 1, 1987–March 31, 2003, 126 LKDs (0.22%) developed ESRD. One hundred and one (80%) of these LKDs were identified through records of initiation of maintenance dialysis, 24 (19%) were matched through placement on the OPTN kidney waiting list, and one received a preemptive kidney transplant without being waitlisted. Of those identified initially through dialysis records, 37% were subsequently placed on the kidney waiting list by the end of the study period."
Unrelated directed kidney donor in 2003, recipient and I both well.
620 time blood and platelet donor since 1976 and still giving!
Elected to the OPTN/UNOS Boards of Directors & Executive, Kidney Transplantation, and Ad Hoc Public Solicitation of Organ Donors Committees, 2005-2011
Proud grandpa!

Offline sherri

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Thank you John for your help in understanding the article. We can certainly conclude from this that much more research needs to be done, closer follow up for donors is required and 2 years is just the tip of the iceberg. We need to be able to follow donors for a lifetime in order to conclude how living with one kidney ultimately effects them. Two patients are involved in organ donation and there needs to be follow up for both. Medicare saves an enormous amount of money by not having to pay for dialysis. This money can certainly be allocated for serious mandatory follow ups. Hospitals should to be evaluated on both recipient and donor outcomes. One cannot truly make an informed decision if an important part of future health risks are not accurately portrayed. Doctors always say that living with one kidney is perfectly ok as the remaining one compensates. Have there been studies comparing LKD to matched healthy individuals born with one kidney? Is there more of an adverse effect on the body when a kidney is artificially removed than with a congenital anomaly.

Thanks again for posting all this great information.

Sherri
Sherri
Living Kidney Donor 11/12/07

 

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