Umar Farooq1, Yousef Al-Shraideh1, Ravi Katari, BS1, Alan C. Farney1, Jeffrey Rogers1, Giuseppe Orlando1, Michael D. Gautreaux1, Gloria Hairston1, Margaret Mangus1, Elizabeth Brim1, Robert J. Stratta1*, Amudha Palanisamy2, Amber Reeves-Daniel2, William Doares3, Scott Kaczmorski3 and Samy S. Iskandar4
Received Date: July 01, 2014; Accepted Date: September 08, 2014; Published Date: September 10, 2014
Citation: Farooq U, Al-Shraideh Y, Katari R, Farney AC, Rogers J, et al. (2014) Single Center Experience with Deceased Donor Kidney Transplantation in Patients Aged 70 and Older: A Matched-Pair Cohort Study. J Transplant Technol Res 4: 135. doi: 10.4172/2161-0991.1000135
Copyright: © 2014 Farooq U, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Visit for more related articles at Journal of Transplantation Technologies & Research
Aim:The purpose of this study was to compare mate deceased donor (DD) kidney transplant (KT) outcomes in patients ≥70 versus <70 years of age in a matched-pair analysis.
Methods: Single center retrospective review of adult KT cases.
Death with functioning graft; Deceased donor kidney transplantation; Elderly; End-stage renal disease; Expanded criteria donors; Outcomes; Paired kidneys; Recipient age
An ever-increasing proportion of elderly patients are receiving renal replacement therapies for end stage renal disease (ESRD) in the second decade of the new millennium . Age is an important determinant in kidney transplantation (KT) [1-6]. Increasing recipient age remains a major risk factor for mortality following KT, with the risk of death increasing proportionately with advanced age and specific co-morbidities at the time of KT [5-13]. Although the propriety of using deceased donor (DD) organs for KT in the elderly has been questioned [14-17], recent literature suggests that donor and recipient age-matched KT in both elderly and younger recipients is medically and ethically warranted compared to dialysis for the treatment of ESRD [18-22]. Although conventional wisdom once held that neither older donors nor older recipients ought to participate in KT, this paradigm has changed given the success of age-matching and the general superiority of KT as a modality of renal replacement therapy regardless of recipient age [1-25].
Nevertheless, population-based studies suggest that there is still a reluctance to place older patients on the kidney waiting list [2,14-18,26]. A recent study demonstrated that 46% of KT candidates =60 years of age placed on the waiting list will actually die before receiving a DD KT . Older age is also used as a surrogate for disease burden, functional status, co-morbidities and hospitalization [28,29]. The reluctance to accept older candidates for the kidney waiting list is mostly due to co-morbidities (e.g., cardiovascular disease, infection, and malignancy), shorter life expectancy, and the increased risk of death with a functioning graft (DWFG) [2-13,30]. With tailored immunosuppressive regimens, advances in surgical techniques, and better peri-operative management, the reluctance to incorporate elderly patients into the recipient pool has in part been mitigated. Outcomes of DD KT in patients =70 years of age are understudied [31-35]. The purpose of this study was to analyze outcomes in patients =70 compared to those <70 years of age in a matched-paired donor kidney analysis that largely controls for donor and preservation factors so that recipient factors that influence outcomes could be isolated to stratify risk and determine the optimal utilization of DD kidneys.
Design and setting
We conducted a retrospective chart review of all DD KTs performed at our center from 10/1/01 to 3/1/12 (minimum 22 months follow-up). During this 10.5 year study period, we identified 33 pairs of DD kidneys transplanted at our center in which one kidney was transplanted into a patient = age 70 and the mate kidney from the same donor was transplanted into a patient <70 years of age.
In addition to recipient factors, outcomes were evaluated according to DD category. Expanded criteria donors (ECD) were defined by United Network for Organ Sharing (UNOS) criteria . For purposes of this study, any DD not meeting ECD criteria was defined as a standard criteria donor (SCD). Delayed graft function (DGF) was defined as the need for dialysis for any reason in the first week post-transplant. Renal allograft loss was defined as DWFG, transplant nephrectomy, return to dialysis, retransplantation, or return to the pretransplant SCr level.
Recipient evaluation and selection
At our center, no specific upper age limit was an absolute contraindication to KT, although the oldest recipient in this series was 84 years at the time of KT. All patients underwent a comprehensive pre-transplant medical, psychosocial, and financial evaluation, with emphasis placed on the cardiovascular system to determine operative risks and physiologic age . Specific exclusion criteria in the elderly included the presence of dementia, nursing home residence, poor overall functional status or frailty, lack of social support, advanced disease or organ failure in an extra-renal organ system, recent malignancy, or severe cardiac or vascular disease. Patients were initially selected for transplantation according to UNOS guidelines [37,38]. Whenever possible, however, marginal donor kidneys were used by matching estimated renal functional mass to recipient nephron need . In this setting, recipient selection was usually not by standard kidney allocation but was based on age matching and identifying low immunological risk patients such as primary transplant, recipient age > 40 years, human leukocyte antigen (HLA) matching, low panel reactive antibody (PRA) level (usually 0%), body mass index (BMI) <30 kg/m2, and informed consent [37,38].
DD kidney transplant patients received depleting antibody induction with either rabbit antithymocyte globulin (rATG) at a dose of 1.5 mg/kg (maximum dose, 150 mg based on actual body weight) for 3-7 doses depending on initial graft function or alemtuzumab 30 mg intravenous as a single intra-operative dose [37,38]. Maintenance immunosuppression consisted of tacrolimus (TAC), mycophenolate mofetil (MMF), and rapid tapering doses of steroids or early steroid withdrawal based on immunological risk stratification . Specific data regarding drug dosing, target levels, and anti-infective prophylaxis have been previously published [37-39].
Data were compiled from both prospective and retrospective data bases, with confirmation by medical record review in accordance with Institutional Review Board guidelines and approval. Categorical data were summarized as proportions and percentages and continuous data were summarized as means and standard deviations. Univariate analysis was performed by the Student's t test for continuous variables, the chi-square test for categorical variables, and Fisher's exact test when data were sparse. Actual, actuarial, and death-censored survival rates were determined. A two-tailed p-value of <0.05 was considered to be significant.
From 5/03 to 3/12, we identified 33 DD kidney pairs that met the inclusion criteria. Mean donor age and BMI were 51.7 ± 16.9 years and 27.4 ± 6.8 kg/m2, respectively, including 19 (58%) expanded criteria donors. Mean recipient ages were 73.6 ± 2.7 and 55.3 ± 11.4 years in the 2 groups (p<0.01).
The majority (N=25, 76%) of DDs were donation after brain death (16 ECD, 9 SCD) whereas the remaining 8 (24%) were donation after cardiac death (DCD) DDs (5 SCD, 3 ECD). Most of the DDs were from our local donor service area (64%, n=21) whereas the remaining 12 kidney pairs (36%) were imported from other organ procurement organizations. Many were refused by multiple centers and were targeted for discard. Mean KDRI and KDPI were 1.27 ± 0.48 and 68 ± 39.6%, respectively. Twenty donors were male and 30 were Caucasian. Most of the DDs (64%) had a history of hypertension and 39% had a history of diabetes mellitus. Mean estimated glomerular filtration rate (eGFR) was 94.7 ± 37.0 ml/min and mean terminal SCr level was 1.1 ± 0.9 mg/dl. Major causes of death included stroke (60%) and trauma (21%). Fourteen (42%) of the donors were = age 60. Mean CIT was 24.7 ± 7.9 hours. Following procurement, 54 (82%) of the kidneys were managed with machine preservation for variable periods of time (mean pump time 14.8 ± 5.8 hours). Mean terminal pump flow rate was 121 ± 31 ml/min and mean terminal resistance value was 0.20 ± 0.10 mm Hg/ml/min.
Table 1 shows recipient demographic and transplant characteristics between the 2 groups. No significant differences were noted in recipient gender, race, mean BMI, mean time on dialysis or waiting time, type of dialysis, preemptive transplants, retransplants, diabetes as the cause of renal failure, or induction and maintenance immunosuppression in the older and younger recipient groups. However, the proportion of patients with 4-6 HLA mismatches (73% older versus 94% younger, p=0.04) was higher in the younger group whereas patients with a PRA level >10% (33% older versus 6% younger, p=0.01) was greater in the older group. Mean cold ischemia was similar (24.6 ± 8.8 versus 25.1 ± 7.1 hours) in the older and younger recipient groups as was the mean (57.8 versus 58 months) duration of follow-up.
|Variable Mean ± SD||Older recipients (n=33)||Younger recipients (n=33)||P-value|
|Age (years)||73.6 ± 2.7||55.3 ±11.4||<0.001|
|Males||16 (48%)||11 (33%)||NS|
|African American||8 (24%)||13 (39%)||NS|
|Recipient BMI (kg/m2)||26.5 ± 4.7||26.6 ± 5.3||NS|
|Duration of dialysis (months)||29.2 ± 22.5||29.0 ± 26.6||NS|
|Time on waiting list (months)||15 ± 11||16 ± 16.5||NS|
|Renal replacement therapy pretransplant
| 24 (73%)
| 24 (73%)
|Preemptive transplant||5 (15%)||3 (9%)||NS|
|Retransplant||1 (3%)||1 (3%)||NS|
|Number of HLA mismatches
|Cause of end stage renal disease
| 14 (42%)
| 10 (30%)
|Panel reactive antibody levels
|Cold ischemia (hours)||24.6 ± 8.8||25.1 ± 7.1||NS|
-Rabbit antithymocyte globulin
- Tacrolimus + MycophenolateMofetil
- Tacrolimus + MycophenolateMofetil + Prednisone
- Cyclosporine + MycophenolateMofetil
- Cyclosporine + MycophenolateMofetil + Prednisone
Table 1: Demographic and transplant characteristics between older and younger recipient groups.
Table 2 shows outcomes between the 2 groups. Actual patient (79% older versus 94% younger, p=0.15) and kidney graft survival ([KGS] 64% older versus 67% younger) rates were comparable. Two-year patient (97% older versus 94% younger) and KGS (91% older versus 82% younger) rates revealed few early deaths or graft losses in the older recipient group. Two early deaths (within 1 month) occurred in the younger group whereas the 7 deaths in the older group occurred at a mean of 59 months post-transplant. The 2 early deaths in the younger group were secondary to sepsis and pulmonary embolism; both in patients with primary nonfunction. Causes of death in the older group included cardiovascular (4), cerebrovascular (1), respiratory failure (1), and malignancy (1). Actuarial patient (p=0.09), uncensored kidney graft and death-censored KGS (p=NS) rates in the older and younger groups are shown in (Figures 1-3), respectively. Death-censored KGS (81% older versus 69% younger, p=0.37) rates demonstrated that the older group had more deaths with functioning grafts (DWFG, 21% versus 3%, p=0.05) but otherwise exhibited a slightly higher KGS rate in the absence of mortality. Mean length of initial hospital stay and rates of DGF, acute rejection, major infection, re-operations and readmissions were comparable. Renal function at 1 and 12 months was similar in the 2 groups (Table 2).
|Variable Mean ± SD||Older recipients (n=33)||Younger recipients (n=33)||P-value|
|Patient survival||26 (79%)||31 (94%)||0.15|
|Kidney graft survival||21 (64%)||22 (67%)||NS|
|Follow-up (months)||60 ± 24||58 ± 22||NS|
|2-year patient survival||32 (97%)||31 (94%)||NS|
|2-year kidney graft survival||30 (91%)||27 (82%)||NS|
|Death-censored graft survival||21/26 (81%)||22/32 (69%)||0.37|
|Death with a functioning graft||7 (21%)||1 (3%)||0.05|
|Delayed graft function||11 (33%)||8 (24%)||NS|
|Length of initial hospital stay (days)||6.4 ± 2.0||5.9 ± 2.4||NS|
|Acute rejection||6 (18%)||3 (9%)||NS|
|Major infection||7 (21%)||5 (15%)||NS|
|Surgical complications||3 (9%)||0||NS|
|Re-admissions||14 (42%)||10 (30%)||NS|
|Serum creatinine (mg/dl):1 month 12 months||1.8 ± 1.0 1.5 ± 0.9||1.8 ± 0.9 1.7 ± 0.9||NS NS|
|aMDRD GFR (ml/min):1 month 12 months||43 ± 16 50 ± 17||46 ± 21 50 ± 22||NS NS|
aMDRD: Estimated glomerular filtration rate [eGFR] values using the abbreviated Modification of Diet in Renal Disease formula.
Table 2: Outcomes.
In 13 patients aged 75 years and older, actual patient survival (69% >75 versus 100% younger, p=0.096), and KGS (46% >75 versus 77% younger, p=0.22) rates were numerically lower compared to the younger matched pairs. When comparing patients aged 75 years and above to the remaining 20 older patients aged 70-74 years, patient survival (69% >75 versus 85% 70-74, p=0.39), KGS (46% >75 versus 75% 70-74, p=0.14), and death-censored KGS (67% >75 versus 88% 70-74, p=0.30) rates were again slightly but not statistically lower in the oldest group. The incidences of DWFG were 31% in patients aged 75 and older, 15% in patients aged 70-74 (p=0.33 compared to those >75), and 3% in all 33 younger patients (p=0.02 compared to those >75). The timing of DWFG was at a mean of 40.5 months in patients aged 75 and older compared to 72 months for those aged 70-74 years.
Not surprisingly, actual KGS rates in the older recipient group were highest with kidneys from SCDs (88.9%) and lower with kidneys from ECDs (56.3%) and DCD donors (50%). Actual KGS rates in the younger recipient group were likewise highest with kidneys from SCDs (88.9%), intermediate with kidneys from ECDs (68.8%), and lowest with kidneys from DCD donors (37.5%). Five of the 8 DWFGs occurred in older patients receiving kidneys from ECDs, similar to the overall distribution of ECD kidneys in the study population. Death-censored KGS rates in the older recipient group were 100% with kidneys from SCDs, 81.8% with kidneys from ECDs, and 57.1% with kidneys from DCD donors. The corresponding death-censored KGS rates in the younger recipient group were 88.9% with kidneys from SCDs, 68.8% with kidneys from ECDs, and 42.9% with kidneys from DCD donors. From a death-censored perspective, the optimal utilization of an ECD kidney was transplantation into an older recipient.
The number of younger (<50 years) candidates on the kidney waiting list in the US has declined since 1990. During the same time, the number of candidates aged 50 to 69 years has doubled and those aged 70 years or more quintupled [1,40]. This is likely due, in part, to the rapidly increasing senior (>65 years) population in the US, which currently account for nearly half of incident patients with ESRD [1,40]. In short, current demographic trends suggest an increasing proportion of elderly patients in an already rising ESRD population. To add to this dilemma, waiting times and mortality on the kidney waiting list are increasing significantly because of the increasing disparity between the growing number of KT candidates and the static organ supply [1,27,28,40]. It is imperative that transplant centers are good stewards of a scarce resource and optimize utilization of DD kidneys. Given that KT is not only the most clinically effective, but also cost-effective modality for ESRD , critical analyses of outcomes in elderly recipients are necessary because kidney lifespan is reduced in this setting because of an increasing number of DWFGs [2-18].
One might contend that an important goal of KT is to have the transplanted organ “outlive” the patient. In other words, DWFG could be considered the ultimate endpoint of transplantation with the caveat that death was neither accelerated nor related to the consequences of transplantation and the requisite chronic immunosuppression. However, another important objective is to avoid large "mismatches" of donor kidney and recipient longevity so as to not lose kidney graft life-years. There is no question that a spectrum of DD kidney quality exists and that many recovered kidneys are discarded because of concerns about both initial graft function as well as expected kidney lifespan . Unfortunately, predictive tools and scoring systems are not always reliable and therein lay the challenge of determining not only the “usability” of a given kidney but also choosing the most appropriate recipient. Because older patients have a limited life expectancy and many kidneys from older donors are discarded, it is not unreasonable to age-match donors and recipients as a surrogate for matching both functional capacity and anticipated lifespan [19-22].
It is important to emphasize that the reason why we received both kidneys from each of these donors is because other centers refused the kidney offers. Many of these kidneys may have been discarded in the absence of our utilization and therefore were not appropriate for standard allocation. Consistent with recent literature regarding KT in elderly recipients, our findings demonstrate that medium-term outcomes are largely influenced by a higher incidence of DWFG in the elderly, particularly for those aged 75 and older [2-36]. Not surprisingly, the incidence and timing post-transplant of DWFG was directly related to older recipient age with patients aged 75 and older having both a higher incidence of and shorter interval post-transplant to the occurrence of DWFG.
However, a unique aspect of our study is the matched-pair cohort analysis, which in effect controls for donor quality, minimizes donor variability and bias, and provides a robust control group in an attempt to isolate transplant and recipient-related factors. Because the mean donor age in our study was 52 years and 42% were standard criteria donors, one might question whether placing these kidneys in older patients results in unrealized graft years. However, the finding that uncensored medium-term graft survival outcomes are similar irrespective of recipient age group would suggest not a loss of graft-years but rather that the causes of graft loss differ by age when one controls for donor and preservation factors. Previous studies comparing outcomes of mate kidneys transplanted sequentially to different recipients have generally been small or single center reports and have demonstrated concordance of outcomes with respect to the incidence of DGF, renal function, and KGS provided that cold ischemia times are not excessive for the second kidney [42-46].
In one of the few reports analyzing the effect of recipient age in a paired kidney analysis, Debska-Slizien et al. examined 44 pairs of mate kidneys and used an age of 60 years to differentiate between older and younger recipients . At one year follow-up, patient (93.2% versus 95.5%), KGS (88.6% versus 86.3%) and death-censored KGS (93.0% versus 90.1%) rates were comparable between the older and younger recipient groups, respectively. Similar to our study, they reported no differences in the incidences of DGF, acute rejection, surgical complications, or readmissions between the 2 groups. With follow-up ranging from 1-6 years, they also identified DWFG as the most common cause of graft loss in the older group and cardiovascular disease as the major cause of death . No differences were noted in patient or KGS (both uncensored and censored) rates with follow-up to 5 years.
A number of recent studies have attempted to identify recipient-related risk factors that predict outcomes in the elderly [3-19]. The reluctance to refer older patients for transplantation in comparison to younger patients is generally attributed to the desire to maximize graft survival and longevity, which is decreased in the long-term in the elderly primarily due to DWFG [12,48]. However, when censoring for DWFG, several studies including our own have shown that KGS in the elderly is either equivalent or even improved compared to younger recipients [3-19,48].
The primary co-morbidities responsible for DWFG are cardiovascular disease, infection, and malignancy [3-19,48]. It follows from our study and others that appropriate recipient selection with aggressive pre-transplant screening and post-transplant monitoring are paramount to improve the safety and effectiveness of KT in the older ESRD population. Proper identification and management of risk factors for DWFG such as smoking, congestive heart failure, cardiac function and arrhythmias, obesity, diabetes, and hypertension are indicated [3-17,49,50]. Clearly, however, an accurate and reproducible assessment of “physiological” age rather than “chronological” age is needed in order to guide appropriate recipient selection. Another important and under-recognized issue is the need to re-evaluate older patients on the waiting list more frequently because advanced age is also a risk factor for the development of either disqualifying features or death in the absence of timely KT [6-13]. In spite of a greater burden of co-morbidities in the older group in our study, when controlling for donor quality, no significant differences were noted in outcomes after a mean follow-up of 58 months. Because the numbers are small and the design is retrospective, we cannot convincingly show that donor and recipient age and longevity matching are warranted in order to improve organ utilization and optimize outcomes.
In summary, our single-center study using a paired-kidney analysis supports the contention that KT is a viable therapeutic modality for elderly ESRD patients, particularly with marginal donor kidneys that may not necessarily be appropriate for younger recipients who have greater projected long-term survival. A highly organized pre-transplant screening, selection, and waitlist monitoring process coupled with a robust immunosuppressant protocol and intensive post-transplant surveillance ensures that kidneys transplanted into the elderly are used to their full potential and truly enhance quality of life and life expectancy without necessarily compromising graft life-years.