Donor renal functionDate written: August 2009nep_1223 137..145
Final submission: June 2009Author: Solomon Cohney, John Kanellis, Martin Howell
GUIDELINES
No recommendations possible based on Level I or II evidence
SUGGESTIONS FOR CLINICAL CARE
(Suggestions are based primarily on Level III and IVevidence)
• An accurate assessment of the glomerular filtration rate(GFR) should be undertaken in all potential donors. Thebenefit of obtaining a directly measured GFR (thought tobe more accurate) over an estimated GFR, has not beenproven in live donors (refer to CARI guidelines titled‘Use of estimated glomerular filtration rate to assess levelof kidney function’ and ‘Direct measurement of glomeru-lar filtration rate’).• When the GFR is estimated it is recommended that thisbe on the basis of serum creatinine using, for example, theCockcroft-Gault (CG) formula or the Modified Dietin Renal Disease (MDRD). Measurement of creatinineclearance calculated from a 24 h urine collection is alsoacceptable, if collected accurately. The estimated glomeru-lar filtration rate (eGFR) should be confirmed on at leasttwo separate occasions.• If there is doubt regarding the GFR from estimatedmethods, further techniques can be used to assess orclarify this. Acceptable methods include a direct evalua-tion of the GFR by methods such as Cr-EDTA (nuclearGFR), iohexol or inulin clearance.• It is preferable not to accept kidneys from donors withGFR < 80 mL/min per 1.73 m2.
IMPLEMENTATION AND AUDIT
1. Ensure all donors are followed and results submitted tothe Donor Registry.2. Monitor outcomes in the Donor Registry.
BACKGROUND
The aim of this guideline is to provide an indication as tothe acceptable lower limit of renal function for livingdonors prior to donation. This is primarily with a view toproviding sufficient residual (donor) renal function post-donation. A separate consideration is that the donated
kidney needs to provide sufficient function for the trans-plant recipient.
While long-term outcomes of renal donors reported inthe literature have generally been good, these reports arefrom an era when more stringent criteria for organ donorswere used, and selection criteria generally ensured healthydonors with normal renal function. Studies of donors withreduced renal function are limited.1
The increasing success and safety of transplantation(including for marginal recipients), the associated wideninggap between transplant and dialysis outcomes, and thelengthening waiting lists for cadaveric kidneys have led to agreater demand for donors. In turn, this has led to a greaterwillingness to consider and accept donors with isolatedmedical abnormalities (IMA) (e.g. hypertension, obesityand lower GFR) and older age.2
Concerns with respect to living donors with lower GFRare the following:(i) Outcome for the recipient: Transplant GFR is an impor-tant determinant of graft and patient outcome post kidneytransplantation.3–5 Lower GFR is likely to be associated withpoorer outcome but is still almost always superior tooutcome on dialysis.(ii) Risk of renal insufficiency in the donor: The risk ofend-stage kidney disease (ESKD) in donors is in the order of0.04–0.5%. In comparison, the prevalence of patientsundergoing treatment for ESKD in Australia at the end of2006 was 0.08%.6
(iii) Consequences of reduced GFR for the donor in lightof the current knowledge of the association betweenreduced GFR and cardiovascular risk*: The clinical signifi-cance of a reduced GFR may not be the same for an indi-vidual with a single healthy kidney compared with anindividual with disease and/or diseased kidneys and thesame level of renal function.7
*There may be additional considerations in relation toreduced renal mass such as mineral/bone metabolism andanaemia.
The following factors also warrant consideration:(i) GFR normally decreases with age.(ii) After donation, there is an initial decline in GFR of25–35%, followed by a small increase, and then mainte-nance of GFR at 60–75% of pre-nephrectomy GFR.
NEPHROLOGY 2010; 15, S137–S145 doi:10.1111/j.1440-1797.2009.01223.x
© 2010 The AuthorsJournal compilation © 2010 Asian Pacific Society of Nephrology
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(iii) The amount of reserve required post-nephrectomyneeds to consider the number of years of life remaining –therefore, lower GFR may be acceptable in an older donor.8
(iv) Dialysis dependency after donor nephrectomy is almostalways due to de novo renal disease.9
Renal function is most widely assessed by GFR, eithermeasured or estimated. An accurate measure of GFR can beundertaken using low molecular weight markers of kidneyfunction such as inulin, iohexol, technetium (labelledDTPA) or labelled EDTA, however, the methods are time-consuming, expensive and generally not available.10 In addi-tion to the direct measurement of GFR, there are severalmethods for estimating GFR. The measurement of 24 hcreatinine clearance tends to underestimate hyperfiltrationand overestimate low GFR levels and is subject to errors inurine collection unless great care is taken. The regular mea-surement of serum creatinine levels is easy to perform and iscurrently the most common method. However, because crea-tinine is invariably reabsorbed by the renal tubules, serumcreatinine and creatinine clearance measurements tend tounderestimate the GFR in the context of hyperfiltration andoverestimate the GFR in the context of hypofiltration.11
Estimation of GFR by serum creatinine-based equationssuch as the CG or MDRD equations are commonly used forchronic kidney disease (CKD) screening, however, theapplication in healthy populations and for the screening ofpotential living kidney donors is less clear. For example, theAustralasian Creatinine Consensus Working Group cur-rently recommend that eGFR values greater than 90 mL/min per 1.73 m2, estimated using the MDRD equation, onlybe reported as >90 mL/min per 1.73 m2.12
SEARCH STRATEGY
Databases searched: MeSH terms and text words for kidneytransplantation were combined with MeSH terms and textwords for living donor, and combined with MeSH terms andtext words for renal function. The search was carried out inMedline (1950–January Week 2, 2009). The CochraneRenal Group, Trials Register was also searched for trials notindexed in Medline.Date of searches: 20 January 2009.
WHAT IS THE EVIDENCE?
Defining normal renal function
Grewal and Blake report GFR reference data (measured by51Cr-EDTA clearance) in a population of 428 potentialliving donors (50.9% women) aged 19–72 years.13 The ref-erence data indicated a mean GFR until the age of 40 yearsof 103.4 mL/min per 1.73 m2 after which the GFR declinedat a mean rate of 9.1 mL/min per 1.73 m2 per decade. Therewere no significant gender differences either in the mean orthe rate of decline of GFR. These reference data have beenused as the basis for defining minimal age dependent GFRsin living donors by the British Transplantation Society(refer to later section in this document). An earlier evalu-
ation of GFR reference values based on 51Cr-EDTA clear-ance values obtained from eight studies of healthyindividuals, reported GFR to decline at all ages14 with agreater rate at ages after 50 years. The average rate of GFRdecline with age prior to 50 was 4 mL/min per 1.73 m2 perdecade and 10 mL/min per 1.73 m2 per decade thereafter.No significant differences between sexes were noted.
A significant (P = 0.0002) annual decline of 1.05 mL/min per 1.73 m2 in GFR (iohexol) with age was alsoreported by Fehrman-Ekholm and Skeppholm in 52 healthyindividuals aged 70–110 years.15 In this group, the CG equa-tion was found to underestimate the average GFR byapproximately 30% (46.2 1 11.3 mL/min per 1.73 m2 com-pared with 67.7 mL/min per 1.73 m2) and there was nocorrelation between serum creatinine and age.
Rule et al. examined the performance of creatinine-based equations in a population of healthy living kidneydonors older than 18 years.16 A total of 365 patients (56.2%women) aged from 18 to 71 years (mean 41.1 years) hadtheir GFR measured using non-radiolabelled iothalamateand GFR estimated using the CG and MDRD equations.The measured GFR declined by 4.6 mL/min per 1.73 m2 perdecade in men and 7.1 mL/min per 1.73 m2 per decade inwomen, however, the difference between sexes was not sig-nificant. Regression analysis was significant for age but notsex with an all patient decline of GFR of 4.9 mL/min per1.73 m2 per decade for all age groups. This is in contrast toearlier studies where age-related GFR decline increasedafter the age of 4013 or 50 years.14
Assessment of MDRD and CG equations was undertakenby Rule et al. after exclusion of 67 non-white and non-African–American individuals (for MDRD) and 24 indi-viduals for whom no body weight data were available (forCG).16 In the healthy population, both equations appearedto underestimate GFR by 29 mL/min per 1.73 m2 and14 mL/min per 1.73 m2 for the MDRD and CG equations,respectively. A large cause of the difference can be attrib-uted to laboratory calibration bias, however, even whencorrected, correlation between estimated and measuredGFR remained weak.16
Modelled estimates by Douville et al.17 of decline in GFRby age, based on creatinine clearance measurements in 7551outpatients (aged 18–90 years) with normal serum creati-nine, suggest a decline in GFR from approximately 120 mL/min per 1.73 m2 in early adulthood down to approximately60 mL/min per 1.73 m2 when people are in their 80s. Therewas a continuous downward trend over 50 years of age andno significant differences between males and females.
In contrast to the above, the study by Berg of 112 poten-tial kidney donors (55% female) aged 21–67 years indicateda significant decline in GFR with age in males but not infemales, over the age range of 20–50 years.18 The mean GFR(measured by inulin clearance) at 20–30 years was 119(112) mL/min per 1.73 m2 and 102 (115) mL/min per1.73 m2 in males and females, respectively, and were signifi-cantly different. The mean GFR at 40–50 years was 100(111) mL/min per 1.73 m2 and 105 (111) mL/min per1.73 m2 in males and females, respectively, and the differ-ences were not significant. The data suggested to the author
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that women seem to be protected in the pre-menopausalperiod. The apparent decline in males 20–50 years of agewas consistent with the data reported by Rule et al.16
Donor outcomes
A critical analysis of studies on long-term medical outcomes(including renal function) in living kidney donors byOmmen and colleagues19 identified the following issues thatlimit the ability to assess medical risks:• virtually all studies are retrospective and commonly havelarge losses to follow up,• studies commonly have small sample sizes,• a lack of suitably matched controls, and• a lack of consideration of potential risk factors for devel-opment of hypertension and renal dysfunction in donorgroups.
As a consequence, assessment of the significance of find-ings of long-term renal function including the incidence ofESKD among donors is limited. Overall, in relation to renaloutcomes, Ommen et al. consider that the available studiesindicate no large decreases in GFR or increases in ESKDamong donors. However, some studies suggest the potentialfor an increased risk of renal dysfunction in certain donorsand given the limitations of the evidence, this suggests acautionary approach should be taken in relation to ‘mar-ginal living donors’.19
The systematic review by Garg et al.20 considered thefollowing two questions for kidney donors:• What proportion of kidney donors develop proteinuria ora GFR < 60 mL/min?• Do kidney donors compared with controls have an accel-erated loss of GFR after the initial decrement followingnephrectomy?
The systematic review considered any study where 10 ormore healthy adults donated a kidney and where proteinuriaor GFR was assessed at least 1 year later. Studies that did notseparate healthy donors from those with overt proteinuria orGFR < 80 mL/min per 1.73 m2 were excluded. Forty-eightstudies from 27 countries that followed a total of 5048donors were identified. Eleven studies collected data onsuitable non-donor controls, which allowed assessment ofthe risk of proteinuria and reduced kidney function follow-ing nephrectomy. Overall, studies with internal controlswere limited and loss to follow up was high.
The average decrement in GFR (22 studies) in donorswith normal renal function after donation was 26 mL/minper 1.73 m2 (range 8–50). After 10 years (8 studies), 40%(range 23–52%) of donors had a GFR between 60 and80 mL/min per 1.73 m2, 12% (range 0–28%) had a GFRbetween 30 and 59 mL/min per 1.73 m2 and 0.2% (range0–2.2%) had a GFR less than 30 mL/min per 1.73 m2. In the6 controlled studies where average follow up was at least5 years, the post-donation weighted mean difference inGFR among the donors compared with controls was-10 mL/min per 1.73 m2 (95% CI: 6–15). Garg and col-leagues note no evidence of an accelerated loss of GFR overthat anticipated with normal ageing with the lower absolute
GFR being attributable to the decrement occurring as aresult of nephrectomy. However, they also note that theprognostic significance of the reduced GFR in healthydonors is unknown given the mechanism of reduction isdifferent to that which occurs in CKD.
The evidence with respect to the outcome of livingkidney donors who have reduced GFR at the time of dona-tion is limited. A systematic review and meta analysis ofhealth outcomes for living donors with isolated medicalabnormalities including age, obesity, hypertension or anti-hypertensive medication, haematuria, proteinuria, neph-rolithiasis and reduced GFR (defined as 280 mL/min) hasbeen recently completed by Young et al.1 Only one studywas identified that compared donors with a reduced GFR(n = 16) with those having normal GFR (n = 75).21 This wasalso the only study identified that considered proteinuriaas an IMA. Although this was a prospective study, theproportion lost to follow up was not reported. One yearafter donation, the GFR was lower in the IMA group(51.7 1 11 mL/min) compared with the control (68.0 115 mL/min). At follow up 8 years after nephrectomy, thedonor with the lowest GFR at 1 year (44 mL/min) had aGFR of 63 mL/min.
Young and colleagues also note that there are very fewstudies documenting important health outcomes amongliving kidney donors with IMAs. Across all IMA groups,longer term assessments (31 year) of blood pressure, pro-teinuria and renal function have been reported in only 3, 2and 10 studies, respectively. Only 17 of the 37 studiesincluded prospective data. A limited number provided lossto follow up and the studies were small. Overall, the abilityof the primary studies to identify significant differences inlong-term medical risks, including long-term renal functionis limited.1
In the study by Rook et al. examining the predictivecapacity of pre-donation GFR, 31 of 125 donors had a post-donation GFR < 60 mL/min per 1.73 m2.7 In this group, themean pre-donation GFR measured by iothalamate was99 mL/min 1 12 mL/min (88 1 10 mL/min per 1.73 m2),while the pre-donation CG GFR was 83 1 21 mL/min andthe pre-donation GFR by simplified MDRD was 69 1 8 mL/min. Follow up beyond 1 year (mean duration 161 months)was available for 63 donors. No significant deterioration inrenal function occurred from <1 year to >1 year afternephrectomy as indicated by mean eGFR. Some studieshave suggested that greater losses of GFR are seen inpatients with low GFR,20 while other studies have foundthat larger reductions in GFR occur in patients with higherpre-donation GFR.22
Ramcharan and Matas23 conducted a follow up of 773living donor transplants 20–37 years after nephrectomy.Information was able to be obtained from 464 (60%) of thedonors, of these, 380 were living at the time of the study andresponses were obtained for 256. Serum creatinine levelsand proteinuria assessments were available for 74 and 92donors, respectively. The authors conclude that the long-term retrospective analysis indicates minimal deteriorationin average serum creatinine levels and little proteinuria, buta few donors developed kidney dysfunction and ESKD. As
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laboratory data were only available for 16% of the originaldonors, it is not possible to determine whether the inci-dence of kidney dysfunction was increased compared withnon-donors.
The retrospective study by Gossman et al.22 achieved a93% follow up of 152 living donors aged 45 1 11 years at thetime of donation and an average of 11 years (range1–28 years) from the time of nephrectomy. The averageeGFR (MDRD) showed a significant (P < 0.001) decreasefrom 92 1 20 mL/min per 1.73 m2 to 71 1 15 mL/min per1.73 m2 at the time of evaluation. There was no significantcorrelation between the magnitude of loss of eGFR andduration since nephrectomy. No significant risk factors forthe percentage loss of eGFR were identified (e.g. age, sex,smoking status, body mass index and blood pressure) otherthan the magnitude of the eGFR before donation.
A retrospective study of 1112 consecutive living kidneydonors found an incidence of ESKD of 0.5%, occurring14–27 years post donation (beginning 36 years after thestart of the living donor program).24 The age at the time ofESKD was 73–89 years, except for one younger donor whohad developed renal cell carcinoma. The other renal diag-noses were nephrosclerosis in four patients, and obstructiveuropathy in the other.
In an attempt to examine the cardiovascular risk ofdonor nephrectomy and the associated reduced GFR,Seyahi and colleagues used multidetector spiral computedtomography to examine coronary artery calcification(CAC) in 101 living kidney donors and 99 age- and sex-matched healthy controls without diabetes and a history ofcoronary artery disease.25 GFR was calculated using theabbreviated MDRD formula. The frequency of risk factorsfor coronary artery disease was compared in kidney donorsand controls, and the relation between kidney donors’ clini-cal characteristics and the presence or absence of CAC wasexamined. The authors wished to examine the effect of thereduced GFR in the absence of other cardiovascular riskfactors and used the following exclusion criteria: age olderthan 65 years, history of coronary artery disease (myocardialinfarction, coronary artery angioplasty or bypass graftingsurgery), stroke, diabetes mellitus, documented hyperten-sion before nephrectomy or malignancy. Hypertension thatdeveloped after nephrectomy was not an exclusion crite-rion. Of 282 patients who donated between 1986 and 2000,69 donors could not be contacted. Sixty-nine donors wereolder than 65 years, 6 had diabetes mellitus, 1 had a historyof coronary artery disease, 4 had malignancy and 5 haddocumented hypertension before nephrectomy, leaving 101patients for comparison with the control group. Patients hadto be at least 12 months post-nephrectomy and the mediantime post-donation was 5 years. The mean GFR of kidneydonors was 75 mL/min, which was approximately 25 mL/min per 1.73 m2 (0.42 mL/min per 1.73 m2) less than that ofcontrols.
The frequency of CAC and mean calcification scoreswere similar for kidney donors (13.9%; 4.5 1 22.6) and con-trols (17.2%; 13.2 1 89.2). CAC was not associated withdecreased GFR, and the correlation between CAC and GFRwas not statistically significant. Kidney donors with calcifi-
cation were more likely to be older (P = 0.003) and male(P = 0.001). Age- and sex-adjusted analysis showed an asso-ciation between greater parathyroid hormone (PTH) levels(odds ratio 1.023; 95% CI: 1.001–1.045; P = 0.037) andCAC in kidney donors.25
Recognizing that a fixed lower limit of GFR does notadequately define donor acceptability (probably too low foryoung donors and too high for older donors), Thiel andcolleagues developed calculations taking into account thelife expectancy of the donor – the Minimum CreatinineClearance.8 Discussions with nephrologists and gerontolo-gists in Switzerland led them to define a creatinine clear-ance (CrCl) of 40 mL/min at age 80 years as adequate tomaintain fluid and electrolyte homeostasis in the donor aswell as maintaining adequate levels of erythropoietin andactive Vitamin D. A second calculation was made targetinga CrCl of at least 30 mL/min per 1.73 m2 at age 80 years asthe absolute minimum acceptable for an elderly person (butpossibly requiring some intervention to maintain normal,age-related quality of life). Using such a formula, a 30-year-old donor may require a CrCl of 123 mL/min per 1.73 m2
while the level for a 70-year-old may be of the order of68 mL/min per 1.73 m2.
SUMMARY OF THE EVIDENCE
Most of the evidence relating to renal function in livingdonors comes from retrospective cohort studies commonlyof small size and with poor follow up (see Table 1). There isa lack of prospective long-term data regarding live donorrenal function following donation, particularly in relation toconsequences of donation in certain donor subgroups suchas those with reduced GFR. There are few studies thatinclude appropriately matched control groups to allowassessment of the significance of long-term changes in renaloutcomes, in particular, the small incidence of ESKD fol-lowing live kidney donation.
The available data in healthy populations (i.e. withnormal renal function) indicate GFR declines with age. Therate of decline appears to be greater after the age of 40 or50 years and may be constant or close to constant at youngerages (i.e. less than 40 years). The rate of decline in GFRafter 40 or 50 years is in the order of 1 mL/min per 1.73 m2
per year and the average GFR for young adults is in the orderof 100–110 mL/min per 1.73 m2.
Overall, the evidence indicates that renal function, asmeasured by GFR, declines between 65% and 75% follow-ing donation with a long-term GFR around 10 mL/min per1.73 m2 less than would be expected without nephrectomy.There is no evidence of an accelerated decline comparedwith age-matched controls. The absolute decrement in GFRappears to remain constant with ageing. The prognosticimplication of the reduced GFR in living kidney donors isunknown.
It is commonly acknowledged that there is a need formore precise information regarding long-term risks faced bydonors. This would ideally be obtained from prospectivelycollected live donor registry data.
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WHAT DO THE OTHER GUIDELINES SAY?
British Transplant Society (2005)26
The potential kidney donor must have sufficient kidneyfunction prior to donation to have an effective GFR at theage of 80 years independent of the age at which he/shedonated. Acceptable GFR by donor age have been derivedbased on the reference data reported by Grewal and Blake13
and therefore assumes a constant GFR up until age 40. Theacceptable GFR prior to donation have been established soas to achieve a predicted GFR at 80 greater than 37.5 mL/min per 1.73 m2 which is equal to the population mean at 80minus 2 standard deviations. The acceptable GFR by donorage are as listed in the table below:
Donor age (years)Acceptable corrected GFR prior to
donation (mL/min per 1.73 m2)
Up to 40 8650 7760 6870 5980 50
GFR should be measured using an isotopic marker in allpotential donors as alternate methods based on serum crea-tinine are not sufficiently accurate in this context and mea-sured creatinine clearance, using timed urine collections, issusceptible to considerable inaccuracy. When renal functionis normal but there is a significant difference in functionbetween the two kidneys, the kidney with lower functionshould be used for transplantation.
European Renal Association-European Dialysis andTransplant Association (2000)27
It is recommended that donor renal function be assessed by24 h urine for creatinine clearance or a direct evaluation ofthe GFR by Cr-EDTA or iohexol or inulin clearance. As anoptional assessment radionuclide determination of GFR as aseparate evaluation of the function of the two kidneys.Donors with a reduced GFR in comparison to the normalrange for age should be excluded.
The Amsterdam Forum on The Care of the Live KidneyDonor (2005)28
Adopted the following consensus guideline regardingacceptable renal function:• A GFR < 80 mL/min or 2 standard deviations belownormal (based on age, gender and body surface area cor-rected to 1.73 m2) generally precludes donation.• Kidneys from live donors with GFR 2 80 mL/min areassociated with a relative risk of graft loss of 2.28 comparedwith those with greater pre-nephrectomy GFR.5
• However, successful transplantation was noted fromsome, usually elderly living donors, with GFR as low as65–70 mL/min, indicating a need for individualization andcareful follow up of donors with GFR of <80 mL/min per1.73 m2.
The Canadian Council for Donation and Transplantation(2006)29
It is recommended that in the absence of higher qualityevidence, it is reasonable to refer to existing guidelinesregarding the assessment and eligibility of potential livingkidney donors (e.g. Amsterdam Forum). However, it is rec-ommended that these guidelines not be used as absolutecriteria where risk is poorly quantified or uncertain.
American Society of Transplantation Position Statementon the Medical Evaluation of Living Kidney Donors(2007)30
Renal focused evaluation to determine the presence ofunderlying kidney disease in the potential donor shouldinclude measurement of GFR (method not specified).
CKD Stage 3 or less (defined as 30–59 mL/min per1.73 m2) will typically exclude a living donor candidatefrom donating based upon scientific data of medical risk.
The Organ Procurement and Transplantation Network(2008)31
Medical evaluation of potential donors should include:• measurement of GFR by 24 h urine collection or equiva-lent testing. Possible exclusion criteria that may make anindividual unsuitable for living donation includes:• creatinine clearance < 80 mL/min per 1.73 m2, or pro-jected GFR with removal of one kidney at 80 years old of<40 mL/min per 1.73 m2.
SUGGESTIONS FOR FUTURE RESEARCH
Perform a prospective assessment of donors with respect tothe relationship between pre-donation GFR and:(i) mortality(ii) cardiovascular system complications(iii) long-term renal function(iv) pre-donation GFR(v) haemoglobin(vi) vitamin D/calcium, PTH(vii) renal function (isotopic GFR) and graft outcome ofrecipients.
CONFLICT OF INTEREST
Solomon Cohney has a Level IIb conflict of interest whileJohn Kanellis and Martin Howell have no relevant finan-cial affiliations that would cause a conflict of interestaccording to the conflict of interest statement set down byCARI.
REFERENCES
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7. Rook M, Hofker HS, van Son WJ et al. Predictive capacity ofpre-donation GFR and renal reserve capacity for donor renal func-tion after living kidney donation. Am. J. Transplant. 2006; 6:1653–59.
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12. Mathew TH, Johnson DW, Jones RD. Chronic kidney disease andautomatic reporting of estimated glomerular filtration rate:Revised recommendations. Med. J. Aust. 2007; 187: 459–63.
13. Grewal GS, Blake GM. Reference data for 51Cr-EDTA measure-ments of the glomerular filtration rate derived from live kidneydonors. Nucl. Med. Comm. 2005; 26: 61–5.
14. Granerus G, Aurell M. Reference values for 51Cr-EDTA clearanceas a measure of glomerular filtration rate. Scand. J. Clin. Lab.Invest. 1981; 41: 611–16.
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16. Rule AD, Gussak HM, Pond GR et al. Measured and estimatedGFR in healthy potential kidney donors. Am. J. Kidney Dis. 2004;43: 112–19.
17. Douville P, Martel AR, Talbot J et al. Impact of age on glomerularfiltration estimates. Nephrol. Dial. Transplant. 2009; 24: 97–103.
18. Berg UB. Differences in decline in GFR with age between males andfemales. Reference data on clearances of inulin and PAH in poten-tial kidney donors. Nephrol. Dial. Transplant. 2006; 21: 2577–82.
19. Ommen ES, Winston JA, Murphy B. Medical risks in living kidneydonors: Absence of proof is not proof of absence. Clin. J. Am. Soc.Nephrol. 2006; 1: 885–95.
20. Garg AX, Muirhead N, Knoll G et al. Proteinuria and reducedkidney function in living kidney donors: A systematic review,meta-analysis, and meta-regression. Kidney Int. 2006; 70: 1801–10.
21. Tsinalis D, Binet I, Steiger J et al. Can ‘borderline’ living kidneydonors (BLKD) be used safely for transplantation? Kidney BloodPress. Res. 1999; 22: 388–89.
22. Gossmann J, Wilhelm A, Kachel HG et al. Long-term conse-quences of live kidney donation follow-up in 93% of living kidneydonors in a single transplant center. Am. J. Transplant. 2005; 5:2417–24.
23. Ramcharan T, Matas AJ. Long-term (20–37 years) follow-up ofliving kidney donors. Am. J. Transplant. 2002; 2: 959–64.
24. Fehrman-Ekholm I, Norden G, Lennerling A et al. Incidence ofend-stage renal disease among live kidney donors. Transplantation2006; 82: 1646–48.
25. Seyahi N, Kahveci A, Bolayirli M et al. Coronary artery calcifica-tion and chronically decreased GFR in living kidney donors. Am.J. Kidney Dis. 2007; 49: 143–52.
26. British Transplant Society and the Renal Association. UnitedKingdom Guidelines for Living Donor Kidney Transplantation, 2ndedn. British Transplant Society and the Renal Association, 2005.
27. European Renal Association and European Dialysis and TransplantAssociation. European Best Practice Guidelines for Renal Trans-plantation (Part 1). II.3 Living kidney donors. Nephrol. Dial.Transplant. 2000; 15 (Suppl 7): 47.
28. Delmonico F. Council of the Transplantation Society. A Report ofthe Amsterdam Forum on the Care of the Live Kidney Donor:Data and Medical Guidelines. Transplantation 2005; 79 (6 Suppl):S53–S66.
29. The Canadian Council for Donation and Transplantation.Enhancing Living Donation: A Canadian Forum. February 9–12 2006Vancouver [Cited July 2009.] Available from URL: http://www.ccdt.ca/.
30. AST Position Statement on the Medical Evaluation of LivingKidney Donors. American Society Transplantation 2007. [Cited July2009.] Available from URL: http://www.a-s-t.org/files/pdf/public_policy/key_position/EvalLivingKidney.pdf
31. The Organ Procurement and Transplantation Network. Guidancefor the Development of Program-Specific Living Kidney Donor MedicalEvaluation Protocols 2008. [Cited July 2009.] Available from URL:http://optn.transplant.hrsa.gov/
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005)
1342
8R
etro
spec
tive
anal
ysis
.G
FRm
easu
red
by51
Cr-
EDTA
.
Pote
ntia
lUK
live
kidn
eydo
nors
afte
rsc
reen
ing
and
excl
usio
nfo
rno
n-re
nal
cont
rain
dica
tion
sfo
rdo
nati
on.2
18fe
mal
es,2
10m
ales
;age
rang
e19
–72
year
s.
NA
Pool
edG
FRfo
rm
ales
and
fem
ales
was
cons
tant
at10
3.4
mL/
min
per
1.73
m2
unti
lthe
age
of40
and
then
decl
ined
ata
rate
of9.
1m
L/m
inpe
r1.
73m
2
per
deca
deth
erea
fter
.
Gra
neru
sG
and
Aur
ellM
(198
1)14
503
Com
bine
dan
alys
isof
8re
tros
pect
ive
stud
ies.
GFR
mea
sure
dby
inul
inor
51C
r-ED
TA.
Hea
lthy
men
and
wom
enof
diffe
rent
ages
.145
fem
ales
,358
men
;ag
es17
–75.
NA
No
syst
emat
icdi
ffere
nce
betw
een
mea
sure
dm
ean
51C
r-ED
TAcl
eara
nce
valu
esan
dm
ean
valu
esca
lcul
ated
from
inul
incl
eara
nce.
Dec
reas
ew
ith
incr
easi
ngag
eof
appr
oxim
atel
y4
mL/
min
per
deca
deat
age
less
than
50ye
ars
and
10m
L/m
inpe
rde
cade
atag
egr
eate
rth
an50
year
s.T
hem
ean
(12
stan
dard
devi
atio
ns)
was
1051
26m
L/m
inat
30ye
ars;
981
23m
L/m
inat
50ye
ars;
and
781
24m
L/m
inat
70ye
ars.
Fehr
man
-Ekh
olm
and
Skep
phol
m(2
004)
15
52C
ross
-sec
tion
al.G
FRm
easu
red
byio
hexo
lcl
eara
nce
and
esti
mat
edfr
omse
rum
crea
tini
neby
ara
nge
ofeq
uati
ons.
20fe
mal
es,3
2m
ales
;age
s71
–110
NA
GFR
byio
hexo
lcle
aran
cesh
owed
alin
ear
corr
elat
ion
wit
hag
ew
ith
am
ean
annu
alde
clin
eof
1.05
mL/
min
(i.e
.app
roxi
mat
ely
11m
L/m
inpe
rde
cade
).G
FRra
nged
from
113
to38
mL/
min
per
1.73
m2
wit
ha
mea
nof
67.7
mL/
min
per
1.73
m2 .
The
CG
form
ula
unde
rest
imat
edG
FR.
Rul
eet
al.
(200
4)16
365
Ret
rosp
ecti
vean
alys
is.
GFR
mea
sure
dus
ing
non-
radi
olab
elle
dio
thal
amat
ecl
eara
nce
and
esti
mat
edfr
omse
rum
crea
tini
neus
ing
CG
and
MD
RD
equa
tion
s.
Pote
ntia
lliv
ing
dono
rs.2
05fe
mal
es,1
06m
ales
;age
s18
–71
year
s;pr
edom
inan
tly
whi
teA
mer
ican
s
NA
Line
arre
gres
sion
anal
ysis
sign
ifica
ntfo
rag
ebu
tno
tge
nder
wit
han
over
alld
eclin
eof
4.9
mL/
min
per
1.73
m2
per
deca
de.M
ean
GFR
decl
ined
from
111
mL/
min
per
1.73
m2
atag
e20
to84
mL/
min
per
1.73
m2
atag
e75
.The
rate
ofde
clin
ebe
fore
and
afte
r50
year
sw
asno
tsi
gnifi
cant
lydi
ffere
nt.
Bot
hth
eC
Gan
dM
DR
Deq
uati
ons
prov
ided
wea
kco
rrel
atio
nw
ith
mea
sure
dG
FR.
Dou
ville
etal
.(2
009)
17G
roup
A–
773
Cro
ss-s
ecti
onal
anal
ysis
.G
FRes
tim
ated
from
seru
mcr
eati
nine
(Gro
upA
and
B)
and
crea
tini
necl
eara
nce
(Gro
upA
only
).eG
FRby
MD
RD
,M
AY
Oan
dC
HU
Q.
Gro
upA
outp
atie
nts
wit
hco
mpl
eted
24h
crea
tini
necl
eara
nce
(45%
fem
ale;
ages
18–9
0ye
ars)
.No
excl
usio
nfo
rch
roni
cki
dney
dise
ase.
NA
Rel
ativ
ely
stab
leG
FRup
unti
lage
30fo
llow
edby
asl
owde
clin
e.M
odel
ling
sugg
ests
are
gula
rde
crea
sein
GFR
from
appr
oxim
atel
y12
0m
L/m
inpe
r1.
73m
2in
earl
yad
ulth
ood
toap
prox
imat
ely
60m
L/m
inpe
r1.
73m
2in
the
80s
wit
ha
cont
inuo
str
end
over
50ye
ars
ofag
e.A
naly
sis
did
not
incl
ude
ago
ldst
anda
rdfo
rG
FR.
Gro
upB
–75
51G
roup
Bno
n-ho
spit
aliz
edcl
inic
pati
ents
wit
hno
rmal
seru
mcr
eati
nine
(56%
fem
ale;
ages
18–1
02)
Living Kidney Donor S143
OUT OF D
ATE
Tab
le1
Con
tinue
d
Stud
yID
NSt
udy
desi
gnPa
rtic
ipan
tsFo
llow
upC
omm
ents
and
resu
lts
Ber
g(2
006)
1812
2C
ross
-sec
tion
alan
alys
is.
GFR
mea
sure
dby
inul
incl
eara
nce.
Pote
ntia
lliv
eki
dney
dono
rs.6
2fe
mal
e,60
mal
e;ag
es21
–67
year
s.N
AG
FRno
tsi
gnifi
cant
lydi
ffere
ntbe
twee
nm
enan
dw
omen
(105
and
106
mL/
min
per
1.73
m2
resp
ecti
vely
).Si
gnifi
cant
mea
nde
clin
ew
ith
age
of5.
1m
L/m
inpe
r1.
73m
2pe
rde
cade
.The
rate
ofde
clin
ein
mal
esw
as8.
1m
L/m
inpe
r1.
73m
2w
hich
was
sign
ifica
ntly
diffe
rent
tofe
mal
es(1
.4m
L/m
inpe
r1.
73m
2 ).
Don
orou
tcom
esO
mm
enet
al.
(200
6)19
I25
stud
ies
Syst
emat
icre
view
Livi
ngdo
nors
.N
ASt
udie
sar
epr
edom
inan
tly
smal
l,re
tros
pect
ive
wit
ha
low
part
icip
atio
nra
tean
dte
ndto
lack
suit
able
cont
rols
.Cha
ract
eris
tica
llyun
derp
ower
edto
dete
ctcl
inic
ally
mea
ning
fuld
iffer
ence
sbe
twee
ndo
nors
and
com
pari
son
grou
ps.G
iven
the
diffi
cult
yin
mea
suri
ngre
nalf
unct
ion,
stud
ies
may
unde
rest
imat
eth
eim
pact
ofdo
nati
on.
Gar
get
al.
(200
6)20
5048
dono
rsSy
stem
atic
revi
ew,m
eta
anal
ysis
and
met
are
gres
sion
.
10or
mor
ehe
alth
kidn
eydo
nors
and
eith
erpr
otei
nuri
aor
GFR
asse
ssed
at1
year
orla
ter.
Tota
lof4
8st
udie
sof
whi
ch36
(352
9do
nors
)re
port
eda
post
-don
atio
nse
rum
crea
tini
neor
GFR
.
Ove
rall
high
loss
tofo
llow
upof
abou
ton
e-th
ird
onav
erag
e.In
22st
udie
sth
eav
erag
ede
crem
ent
inG
FRaf
ter
dona
tion
was
26m
L/m
inpe
r1.
73m
2
(ran
geof
8–50
).In
nine
stud
ies
afte
ra
mea
nof
10ye
ars
post
-don
atio
n40
%ha
da
GFR
betw
een
60an
d80
mL/
min
per
1.73
m2 ,1
2%be
twee
n30
and
59m
L/m
inpe
r1.
73m
2 ,and
0.2%
less
than
30m
L/m
inpe
r1.
73m
2 .In
six
stud
ies
wit
hco
ntro
lsth
epo
st-d
onat
ion
GFR
was
10m
L/m
inpe
r1.
73m
2
low
erin
dono
rsco
mpa
red
wit
hco
ntro
ls.T
hedi
ffere
nce
did
not
vary
sign
ifica
ntly
wit
hti
me
from
dona
tion
.No
evid
ence
ofan
acce
lera
ted
loss
inG
FRov
erth
atan
tici
pate
dw
ith
norm
alag
eing
.
Youn
get
al.
(200
8)1
37 stud
ies
Syst
emat
icre
view
Livi
ngki
dney
dono
rsw
ith
isol
ated
med
ical
abno
rmal
itie
s.G
reat
erth
an1
year
dura
tion
wit
hth
ree
orm
ore
livin
gki
dney
dono
rs.
Min
imum
1ye
arO
nly
one
stud
yw
asid
enti
fied
that
incl
uded
redu
ced
GFR
(defi
ned
as<7
0m
L/m
inby
inul
incl
eara
nce)
.Ove
rall
the
abili
tyof
the
stud
ies
toid
enti
fysi
gnifi
cant
diffe
renc
esin
long
-ter
mm
edic
alri
sks
islim
ited
.
Tsin
alis
etal
.(1
999)
2118
0Pr
ospe
ctiv
eco
hort
.GFR
byin
ulin
clea
ranc
em
easu
red
befo
rean
d1
year
afte
rdo
nati
on
‘Nor
mal
’and
‘Bor
derl
ine’
livin
gki
dney
dono
rsof
who
m16
had
GFR
<70
mL/
min
.
1ye
arN
orm
algr
oup
GFR
decl
ined
from
101.
8m
L/m
into
68.0
mL/
min
1ye
araf
ter
dona
tion
.No
sign
ifica
ntdi
ffere
nce
inab
norm
algr
oup
wit
hlo
wG
FRpr
ior
todo
nati
on.I
nsuf
ficie
ntlo
ngte
rmfo
llow
upto
give
are
com
men
dati
onw
ith
resp
ect
toab
norm
ally
low
GFR
.
The CARI GuidelinesS144
OUT OF D
ATE
Roo
ket
al.
(200
6)7
125
Pros
pect
ive
anal
ysis
.GFR
and
dopa
min
est
imul
ated
GFR
mea
sure
dus
ing
125
I-io
thal
amat
ecl
eara
nce
Con
secu
tive
dono
rs(4
5m
ales
;age
491
11ye
ars)
571
16da
ysT
heav
erag
eba
selin
eG
FRw
as10
41
15m
L/m
inpe
r1.
73m
2 .GFR
fell
to641
7%of
the
pre-
dona
tion
valu
e.eG
FRby
MD
RD
fell
to711
7%of
pre-
dona
tion
eGFR
.Ren
alfu
ncti
onim
pair
men
t(G
FR<
60m
L/m
inpe
r1.
73m
2 )oc
curr
edin
25%
ofdo
nors
afte
rdo
nati
on.
Inde
pend
ent
risk
fact
ors
for
low
GFR
post
-don
atio
nw
ere,
low
GFR
pre-
dona
tion
,age
and
body
mas
sin
dex.
Gos
sman
net
al.
(200
5)22
152
Ret
rosp
ecti
vean
alys
is.
Pre-
dona
tion
data
take
nfr
omre
cord
s.Po
st-d
onat
ion
from
24h
urin
ean
dbl
ood
sam
ples
.A
bbre
viat
edM
DR
Dus
edto
esti
mat
eG
FR.
Live
dono
rsco
hort
from
asi
ngle
cent
refr
omth
epe
riod
1973
–200
1(9
6fe
mal
es;a
geat
dona
tion
451
11)
111
1ye
ars
Ach
ieve
d93
%fo
llow
upof
the
145
dono
rsw
how
ere
aliv
eat
follo
wup
.Cre
atin
ine
clea
ranc
ede
clin
edfr
om11
91
30m
L/m
inpe
r1.
73m
2to
991
30m
L/m
inpe
r1.
73m
2af
ter
dona
tion
(P<
0.00
1)an
deG
FRfr
om921
20m
L/m
inpe
r1.
73m
2to
711
15m
L/m
inpe
r1.
73m
2(P
<0.
001)
.N
osi
gnifi
cant
corr
elat
ion
betw
een
the
loss
ofG
FRw
ith
tim
eaf
ter
dona
tion
.The
only
sign
ifica
ntri
skfa
ctor
for
the
perc
enta
gelo
ssof
GFR
was
ahi
gher
GFR
atth
eti
me
ofdo
nati
on.
Ram
char
anan
dM
atas
(200
2)23
464
Ret
rosp
ecti
vean
alys
isLa
bora
tory
resu
lts
avai
labl
efo
r12
5liv
ing
dono
rsw
hodo
nate
dov
erth
epe
riod
1963
–197
9
20–3
7ye
ars
Obt
aine
din
form
atio
non
60%
and
labo
rato
ryre
sult
sfr
om16
%of
the
dono
rs.O
fthe
84do
nors
know
nto
have
died
thre
ew
ere
know
nto
have
had
kidn
eyfa
ilure
.Oft
he38
0al
ive,
thre
eha
dab
norm
alki
dney
func
tion
and
two
unde
rgon
etr
ansp
lant
atio
n.R
emai
nder
had
norm
alki
dney
func
tion
.Mos
tdo
nors
had
norm
alki
dney
func
tion
20–3
7ye
ars
afte
rdo
nati
on.T
here
tros
pect
ive
natu
rean
dth
ela
rge
loss
tofo
llow
uplim
itth
eab
ility
toas
sess
the
sign
ifica
nce
ofth
esm
all
num
ber
who
deve
lope
dre
nald
ysfu
ncti
onan
dre
nal
failu
re.
Fehr
man
-Ekh
olm
etal
.(2
006)
241,
112
Ret
rosp
ecti
vean
alys
isof
med
ical
reco
rds
Con
secu
tive
livin
gdo
nors
who
dona
ted
over
the
peri
od19
65–2
005
1–40
year
s(m
edia
n14
year
s)
Six
(0.5
%)
had
deve
lope
dES
KD
.Maj
orit
yw
ere
mal
es,m
ost
com
mon
diag
nosi
sw
asne
phro
scle
rosi
san
dth
eag
eat
tim
eof
urae
mia
was
73–8
9ye
ars.
Tim
esi
nce
dona
tion
was
14–2
7ye
ars,
med
ian
20ye
ars.
Seya
hiet
al.
(200
7)25
101
(don
ors)
Cro
ss-s
ecti
onal
anal
ysis
GFR
esti
mat
edus
ing
MD
RD
Live
dono
rs3
1ye
araf
ter
neph
rect
omy.
Excl
usio
ncr
iter
ia,a
geol
der
than
65ye
ars,
hist
ory
ofco
rona
ryar
tery
dise
ase,
stro
ke,
diab
etes
,hyp
erte
nsio
nbe
fore
dona
tion
and
mal
igna
ncy.
The
mea
neG
FRof
dono
rsw
assi
gnifi
cant
lylo
wer
than
the
cont
rolg
roup
(P<
0.00
1)be
ing
751
16.0
mL/
min
per
1.73
m2
com
pare
dw
ith
99.81
20.7
mL/
min
per
1.73
m2 .T
hein
cide
nce
ofES
KD
was
inth
esa
me
orde
ras
expe
cted
for
the
Swed
ish
popu
lati
onta
king
age
into
acco
unt.
99 (con
trol
s)
CG
,Coc
kcro
ft-G
ault
;GFR
,glo
mer
ular
filtr
atio
nra
te;E
SKD
,end
-sta
geki
dney
dise
ase;
MD
RD
,Mod
ified
Die
tin
Ren
alD
isea
se.
Living Kidney Donor S145
OUT OF D
ATE