|Year : 2018 | Volume
| Issue : 4 | Page : 108-114
Use of donors at age extremes for simultaneous pancreas-kidney transplant
Clifford Akateh, Elmahdi Elkhammas, Ronald Pelletier, Amer Rajab, Mitchell Henry, Ashraf El-Hinnawi
Comprehensive Transplant Center, Ohio State University College of Medicine, Columbus, Ohio, USA
|Date of Web Publication||3-Aug-2018|
Dr. Ashraf El-Hinnawi
OSU Wexner Medical Center, Faculty Tower, 395 W 12th Ave, First Floor, Columbus, OH - 43210-1267
Source of Support: None, Conflict of Interest: None
Introduction: There is a shortage of optimal pancreatic donors for simultaneous pancreas and kidney transplant (SPKT), as such there is interest in utilizing donors at extremes of age to expand the donor pool. We sought to evaluate outcomes in SPKT from pediatric donors (PDs) to older donors (ODs). Patients and Methods: We identified patients who underwent simultaneous pancreas and kidney transplant at a single, high-volume institution from 1988–2013. We evaluated for differences in transplant organ function (estimated glomerular filtration rate [GFR], serum glucose, and urine amylase), early (technical) graft loss, and patient and graft survival. Results: A total of 729 SPKT were performed during the study, with 32 PDs, 652 standard donors (SDs), and 45 ODs. Renal function was slightly worse in OD. Otherwise, graft function was similar between all three groups at up to 5 years. There was no difference in censored survival analyses for both kidney and pancreas allografts. There was comparable short-term and long-term patient survival among all groups. Conclusions: Overall, the use of pancreas from pediatric and ODs for SPKT has comparable outcome to SDs. Kidneys from donors above 50 may have lower GFR, but otherwise, have comparable long-term patient and graft survival.
Keywords: End-stage renal disease, graft survival, kidney transplantation, older donor, pancreas transplantation, pediatric donor, survival analysis, type 1 diabetes mellitus
|How to cite this article:|
Akateh C, Elkhammas E, Pelletier R, Rajab A, Henry M, El-Hinnawi A. Use of donors at age extremes for simultaneous pancreas-kidney transplant. Ibnosina J Med Biomed Sci 2018;10:108-14
|How to cite this URL:|
Akateh C, Elkhammas E, Pelletier R, Rajab A, Henry M, El-Hinnawi A. Use of donors at age extremes for simultaneous pancreas-kidney transplant. Ibnosina J Med Biomed Sci [serial online] 2018 [cited 2022 Jan 22];10:108-14. Available from: http://www.ijmbs.org/text.asp?2018/10/4/108/238530
| Introduction|| |
Type 1 diabetes mellitus (T1DM) is a major cause of morbidity and mortality in the United States and accounts for about 245 billion annual health-care costs.,,, There are 1.25 million Americans are living with T1DM, 85% of who are adults, with 40, 000 new diagnoses each year, and an estimated 5 million people with T1DM in the U. S. by 2050.,,,, Simultaneous pancreas-kidney transplant (SPKT) is a well-established treatment for patients with T1DM complicated by end-stage renal disease.,,,,, Despite an increase in the number of deceased donor pancreata recovered over the last decade, the overall number of pancreas transplants has continued to decline., This is, in part, due to historically poor outcomes from pancreas transplant. The recent implementation of a new pancreas allocation system, along with the proposal for a consistent definition of pancreas graft failure, as well as improving outcomes (graft and patient survival), is expected to improve the overall rates of SPKT being performed., Unfortunately, the number of diabetic patients on the pancreas transplant waiting list continues to rise and exceeds the number of available donor organs., This mandates different options to expand the donor pool while maintaining excellent outcome.
Conventionally, pediatric donors (PDs) have been underutilized for SPKT. This was mostly driven by the lack of standard criteria for an acceptable pancreas graft., PDs are considered by most centers to be marginal grafts due to perceived lower islet mass, higher technical demand, and potential complications.,, Older donors (ODs) are equally also underutilized due to a perceived shorter graft survival and less optimal function., However, there is growing evidence from single-center studies that these organs may provide comparable outcomes to standard age donors.,,,,,, Nevertheless, there remains a paucity of the literature to encourage the use of these donors, and as such, many centers remain reluctant to use these organs in the absence of stronger evidence to support their use. Our study aims to evaluate the outcome of SPKT in donors at extremes of age using our over 20-year institutional database.
| Methods|| |
We performed a retrospective review of a prospectively collected database registry for all SPKTs performed between 1988 and 2013. During that period, we performed 32 SPKT using PDs, 652 using standard (control) donors, and 45 using ODs. Those cases were reviewed and compared based on 1-, 3-, 5-, and 10-year patient and graft survival, transplanted organs function (estimated glomerular filtration rate [eGFR], serum glucose, and urine amylase), and incidence of early graft loss. The study was approved by the Institutional Review Board.
The surgical management of T1DM evolved over the period of data collection but consisted of either simultaneous pancreas-kidney (SPK), pancreas-after-kidney, pancreas-transplant-alone, or more recently pancreatic islet cell transplantation. The operative technique for SPK transplantation has equally changed over the years and remains a subject of great debate. Our preferred approach, including changes in our immunosuppression protocols, has been previously published elsewhere.,,,, All organ procurements were done by standard techniques and preserved in the University of Wisconsin solution.
Data collection and statistics
A prospectively maintained database of all transplant patients (total 729) was utilized for demographic data and patient outcome, survival, and graft failure. In this study, pediatric kidney and pancreas deceased donors (PDs) were defined as being between the age of 0–13 years (n = 32; 4.4%), and more than 20 kg body weight. We considered standard (control) donors (SDs) to be between the age of 13–50 years (N = 652; 89.4%) and ODs to be older than 50 years (n = 45;6.2%). Chi-square tests and Fisher's exact tests were used to analyze categorical variables, and Student t-test and ANOVA were used to compare continuous variables. Univariate analyses were performed to characterize transplanted organ-specific outcomes over time including creatinine, average glucose levels, hemoglobin A1c (HgA1c), average urinary amylase, and average GFR. The Kaplan–Meier product limit methods were used to estimate overall patient and graft death-censored survival, and log-rank tests were used to compare the overall long-term patient and graft survival between age groups. IBM Corp. Data analysis was performed in SPSS (IBM SPSS Statistics for Windows, Version 24.0, IBM Corp., Armonk, NY, USA).
| Results|| |
Organs from younger donors tended to be transplanted into younger recipients (P = 0.018). There was a significantly higher proportion of male recipients in the SD group, compared to the pediatric and OD groups, which had a higher proportion of female recipients. A high proportion of the PDs suffered from a cerebrovascular accident. There were no statistically significant differences in other baseline characteristics including race and pretransplant diagnosis between the three groups [Table 1] and [Table 2]. A small percentage of patients underwent transplantation due to end-stage renal disease not directly related to their diabetes, and an even smaller percentage underwent SPKT due to Type 2 diabetes. Technical graft loss, described as graft loss within 30 days of transplant, was equivalent between PD and control groups. The same was true for ODs.
|Table 1: Comparison of baseline characteristics of pediatric donor group to control donor group (n, percentage, or mean, standard deviation)|
Click here to view
|Table 2: Comparison of baseline characteristics of older donor group to control donor group (n, %, or mean, standard deviation)|
Click here to view
There was no significant difference in average HgA1c between groups at up to 5-year post-transplantation [Table 2] and [Figure 1]. Similarly, the average urine amylase was similar across all three groups at up to 5-year postkidney transplant [Table 3] and [Figure 1]. Due to the paucity of data available, c-peptides were not analyzed. With regard to kidney function, there was no difference in the average GFR between the PD group and SD group. However, there was a significantly lower GFR in the OD group, and this persisted for 5-year post-transplantation [Table 3] and [Figure 1].
|Figure 1: Trends of hemoglobin A1c (a), urine amylase trends (b) and glomerular filtration rate (c) post-transplant (up to five years).|
Click here to view
|Table 3: Hemoglobin A1c values. Urine amylase and Glomerular filtration rate measurements averaged over time.|
Click here to view
In multivariate analyses, there was a trend toward early pancreas graft survival advantage in the PD group, although no significant difference was seen in the long. Furthermore, there was a trend toward between early and long-term kidney survival advantage in the PD group compared to SD group and OD group, although this did not reach statistical significance [Figure 2] and [Figure 3]. Overall, there was no short-term or long-term patient survival difference between all three groups [Figure 4].
| Discussion|| |
Despite the overall improving outcomes in SPK transplant, fewer SPK transplants are performed nationally. This trend is probably multifactorial. Better medical management for diabetic patients has resulted in delayed diabetic complications and is reflected by fewer patient or delay in referrals and listing for SPK transplant. In addition, less optimal donor quality may be limiting perceived donor options. In 2014, there were 954 pancreas transplants were performed, while there were 1233 patients waiting for a pancreas transplant. Hence, although great progress has been made in minimally invasive techniques for pancreatic endocrine replacement therapy, SPK transplant remains the treatment of choice for diabetic patients with the end-stage renal disease. SPK achieves normoglycemia, improves the quality of life, prolongs patient survival, and prevents of the progression of most of the diabetic complications. Unfortunately, these results cannot be realized for all patients as most transplant centers shy away from using pancreata from donors at extreme of age due to fear of technical complications and concerns about transplant organ function. Our study demonstrates that these organs can be used safely and effectively. Although kidneys from ODs may have a lower GFR, initially, there is no difference in long-term patient and graft survival related to this finding. Per Organ Procurement and Transplantation Network data, between 2010 and 2014, an average of 434/year donors between the ages of 6–10 years underwent organ recovery. However, only 5% of pancreata from those donors were transplanted. Furthermore, an average of 8175/year donors between the ages of 50–65 years underwent organ recovery, and only 1% of pancreata from those donors were transplanted.
One of the most feared complications of pancreatic transplantation is arterial thrombosis, as this often results in graft loss. Humar et al. showed reported the highest graft failure rates in SPK, with a majority of graft failures resulting from graft thrombosis., The technical challenges associated with transplantation of smaller grafts have resulted in an added fear of using PDs for transplantation. Although previous large center trials ,, have demonstrated similar findings of equal outcomes from PDs, use of PDs is not yet widely accepted. We found no difference in technical complications or early graft loss between the pediatric and donor groups. At this center, the cutoff for PDs was 20 kg, which might eliminate some of the technical concerns alluded to above. Although some studies have the use of smaller weight patients, these were limited to a few centers, and more data are needed to encourage its use.
The use of ODs for SPK transplant in our results was not associated with inferior patient and graft survival. When compared to patients on the waitlist and those not transplanted, the OD age group had a better patient survival. Our study showed a 5-year patient survival of more than 70%, which is higher than a previous report by White et al. who reported a 46% 4-year patient survival. Previous studies have raised concerns about the pancreas allograft from ODs. These grafts are thought to have a lower islet cell mass and function,, raising concerns of early graft failure. In addition, grafts from ODs have been associated with increased graft thrombosis and graft failure., Our results show similar long-term outcomes in this patient group with respect to graft and patient survival. Although baseline GFR was lower in this group, this did not translate to the worse long-term outcome.
Our study is limited by its retrospective nature, and although the different cohorts are evenly matched except for age, the absence of randomization could introduce bias in the data. Transplant centers make an effort to size match the donors to the recipients, which can introduce bias in the observed outcomes. This, likely, explains the higher proportion of female recipients in the PD group. Pediatric donations tend to be transplanted in other younger patients or women, who have similar body surface area, and thus vessel size. In addition, all pancreas transplants in the study were done by bladder drainage, which in some studies have been shown to have a favorable outcome in SPK., Finally, the database did not capture immediate reoperation rates, rejection episodes, length of hospital stay, or rehospitalizations, all of which could potentially impact postoperative morbidity and quality of life.
| Conclusions|| |
Using PDs for SPKT have comparable outcomes to using SDs, and associated with similar long-term survival without increased risk of technical complications. Compared to other age groups, ODs are associated with significantly lower eGFR but otherwise comparable pancreas function, patient, and graft survival. The decreasing number of ideal pancreas donors mandates exploring other options to care for patients waiting for needed life-saving organs. Donors at extremes of age should be considered for donation as they provide excellent and comparable short- and long-term recipient outcomes. Their use can increase donor pool and decrease waiting time on the transplant list.
All authors contributed to the conception, planning, conduct of the study, drafting, and revising of the manuscript, and approval of its last version.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
Compliance with ethical principles
This work has been approved by the Institutional Review Board of The Ohio State University (IRB #: 2015H0402).
| References|| |
Writing Group for the DCCT/EDIC Research Group, Orchard TJ, Nathan DM, Zinman B, Cleary P, Brillon D, et al.
Association between 7 years of intensive treatment of type 1 diabetes and long-term mortality. JAMA 2015;313:45-53.
Diabetes Control and Complications Trial Research Group, Nathan DM, Genuth S, Lachin J, Cleary P, Crofford O, et al.
The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med 1993;329:977-86.
Dall TM, Mann SE, Zhang Y, Quick WW, Seifert RF, Martin J, et al.
Distinguishing the economic costs associated with type 1 and type 2 diabetes. Popul Health Manag 2009;12:103-10.
Menke A, Orchard TJ, Imperatore G, Bullard KM, Mayer-Davis E, Cowie CC, et al.
The prevalence of type 1 diabetes in the United States. Epidemiology 2013;24:773-4.
Dabelea D, Mayer-Davis EJ, Saydah S, Imperatore G, Linder B, Divers J, et al.
Prevalence of type 1 and type 2 diabetes among children and adolescents from 2001 to 2009. JAMA 2014;311:1778-86.
Morel P, Goetz FC, Moudry-Munns K, Freier E, Sutherland DE. Long-term glucose control in patients with pancreatic transplants. Ann Intern Med 1991;115:694-9.
Gruessner AC, Sutherland DE, Gruessner RW. Pancreas transplantation in the United States: A review. Curr Opin Organ Transplant 2010;15:93-101.
Wiseman AC. The role of kidney-pancreas transplantation in diabetic kidney disease. Curr Diab Rep 2010;10:385-91.
White SA, Nicholson ML, London NJ. Vascularized pancreas allotransplantation – Clinical indications and outcome. Diabet Med 1999;16:533-43.
Becker BN, Odorico JS, Becker YT, Groshek M, Werwinski C, Pirsch JD, et al.
Simultaneous pancreas-kidney and pancreas transplantation. J Am Soc Nephrol 2001;12:2517-27.
Israni AK, Skeans MA, Gustafson SK, Schnitzler MA, Wainright JL, Carrico RJ, et al.
OPTN/SRTR 2012 annual data report: Pancreas. Am J Transplant 2014;14 Suppl 1:45-68.
Kandaswamy R, Skeans MA, Gustafson SK, Carrico RJ, Tyler KH, Israni AK, et al.
OPTN/SRTR 2013 annual data report: Pancreas. Am J Transplant 2015;15 Suppl 2:1-20.
Kandaswamy R, Skeans MA, Gustafson SK, Carrico RJ, Prentice MA, Israni AK, et al.
Pancreas. Am J Transplant 2016;16 Suppl 2:47-68.
Krieger NR, Odorico JS, Heisey DM, D'Alessandro AM, Knechtle SJ, Pirsch JD, et al.
Underutilization of pancreas donors. Transplantation 2003;75:1271-6.
Ihm SH, Matsumoto I, Sawada T, Nakano M, Zhang HJ, Ansite JD, et al.
Effect of donor age on function of isolated human islets. Diabetes 2006;55:1361-8.
Humar A, Ramcharan T, Kandaswamy R, Gruessner RW, Gruessner AC, Sutherland DE, et al.
Technical failures after pancreas transplants: Why grafts fail and the risk factors – A multivariate analysis. Transplantation 2004;78:1188-92.
Schulz T, Schenker P, Flecken M, Kapischke M. Donors with a maximum body weight of 50 kg for simultaneous pancreas-kidney transplantation. Transplant Proc 2005;37:1268-70.
Ihm SH, Moon HJ, Kang JG, Park CY, Oh KW, Jeong IK, et al.
Effect of aging on insulin secretory function and expression of beta cell function-related genes of islets. Diabetes Res Clin Pract 2007;77 Suppl 1:S150-4.
Van der Werf WJ, Odorico J, D'Alessandro AM, Knechtle S, Becker Y, Collins B, et al.
Utilization of pediatric donors for pancreas transplantation. Transplant Proc 1999;31:610-1.
Singh RP, Rogers J, Farney AC, Moore PS, Hartmann EL, Reeves-Daniel A, et al.
Outcomes of extended donors in pancreatic transplantation with portal-enteric drainage. Transplant Proc 2008;40:502-5.
Biglarnia AR, Bennet W, Nilsson T, Larsson E, Magnusson A, Yamamoto S, et al.
Utilization of small pediatric donors including infants for pancreas and kidney transplantation: Exemplification of the surgical technique and the surveillance. Ann Surg 2014;260:e5-7.
Rhein T, Metzner R, Uhlmann D, Serr F, Caca K, Weinert D, et al.
Pediatric donor organs for pancreas transplantation: An underutilized resource? Transplant Proc 2003;35:2145-6.
Stratta RJ, Sundberg AK, Farney AC, Rohr MS, Hartmann EL, Adams PL, et al.
Successful simultaneous kidney-pancreas transplantation from extreme donors. Transplant Proc 2005;37:3535-7.
Elkhammas EA, Henry ML, Yilmaz S, Pelletier RP, Bumgardner GL, Ferguson RM. Simultaneous pancreas-kidney transplantation at the Ohio State University Medical Center. Clin Transpl 1997;11:167-72.
Elkhammas EA, Henry ML, Akin B, Ferguson RM, Bumgardner GL, Davies EA, et al
. Simultaneous pancreas-kidney transplantation at a single center. Clin Transpl 2003;17:221-7.
Elkhammas EA, Henry ML, Ferguson RM, Bumgardner GL, Pelletier RP, Rajab A, et al.
Simultaneous pancreas-kidney transplantation: Overview of the ohio state experience. Yonsei Med J 2004;45:1095-100.
Henry ML, Elkhammas EA, Bumgardner GL, Pelletier RP, Ferguson RM. Outcome of 300 consecutive pancreas-kidney transplants. Transplant Proc 1998;30:291.
Rajab A, Pelletier RP, Ferguson RM, Elkhammas EA, Bumgardner GL, Henry ML, et al.
Steroid-free maintenance immunosuppression with rapamune and low-dose neoral in pancreas transplant recipients. Transplantation 2007;84:1131-7.
White SA, Shaw JA, Sutherland DE. Pancreas transplantation. Lancet 2009;373:1808-17.
Socci C, Orsenigo E, Santagostino I, Caumo A, Caldara R, Parolini D, et al.
Pancreata from pediatric donors restore insulin independence in adult insulin-dependent diabetes mellitus recipients. Transplant Proc 2010;42:2068-70.
Fernandez LA, Di Carlo A, Odorico JS, Leverson GE, Shames BD, Becker YT, et al.
Simultaneous pancreas-kidney transplantation from donation after cardiac death: Successful long-term outcomes. Ann Surg 2005;242:716-23.
Finger EB, Radosevich DM, Dunn TB, Chinnakotla S, Sutherland DE, Matas AJ, et al.
A composite risk model for predicting technical failure in pancreas transplantation. Am J Transplant 2013;13:1840-9.
Gruessner RW, Sutherland DE, Gruessner AC. Mortality assessment for pancreas transplants. Am J Transplant 2004;4:2018-26.
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3]