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      Living kidney donor evaluation for all candidates with normal estimated GFR for age

      1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 2 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36
      Transplant International
      Wiley

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          A new equation to estimate glomerular filtration rate.

          Equations to estimate glomerular filtration rate (GFR) are routinely used to assess kidney function. Current equations have limited precision and systematically underestimate measured GFR at higher values. To develop a new estimating equation for GFR: the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. Cross-sectional analysis with separate pooled data sets for equation development and validation and a representative sample of the U.S. population for prevalence estimates. Research studies and clinical populations ("studies") with measured GFR and NHANES (National Health and Nutrition Examination Survey), 1999 to 2006. 8254 participants in 10 studies (equation development data set) and 3896 participants in 16 studies (validation data set). Prevalence estimates were based on 16,032 participants in NHANES. GFR, measured as the clearance of exogenous filtration markers (iothalamate in the development data set; iothalamate and other markers in the validation data set), and linear regression to estimate the logarithm of measured GFR from standardized creatinine levels, sex, race, and age. In the validation data set, the CKD-EPI equation performed better than the Modification of Diet in Renal Disease Study equation, especially at higher GFR (P < 0.001 for all subsequent comparisons), with less bias (median difference between measured and estimated GFR, 2.5 vs. 5.5 mL/min per 1.73 m(2)), improved precision (interquartile range [IQR] of the differences, 16.6 vs. 18.3 mL/min per 1.73 m(2)), and greater accuracy (percentage of estimated GFR within 30% of measured GFR, 84.1% vs. 80.6%). In NHANES, the median estimated GFR was 94.5 mL/min per 1.73 m(2) (IQR, 79.7 to 108.1) vs. 85.0 (IQR, 72.9 to 98.5) mL/min per 1.73 m(2), and the prevalence of chronic kidney disease was 11.5% (95% CI, 10.6% to 12.4%) versus 13.1% (CI, 12.1% to 14.0%). The sample contained a limited number of elderly people and racial and ethnic minorities with measured GFR. The CKD-EPI creatinine equation is more accurate than the Modification of Diet in Renal Disease Study equation and could replace it for routine clinical use. National Institute of Diabetes and Digestive and Kidney Diseases.
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            Is Open Access

            KDIGO Clinical Practice Guideline on the Evaluation and Care of Living Kidney Donors

            Abstract The 2017 Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice Guideline on the Evaluation and Care of Living Kidney Donors is intended to assist medical professionals who evaluate living kidney donor candidates and provide care before, during and after donation. The guideline development process followed the Grades of Recommendation Assessment, Development, and Evaluation (GRADE) approach and guideline recommendations are based on systematic reviews of relevant studies that included critical appraisal of the quality of the evidence and the strength of recommendations. However, many recommendations, for which there was no evidence or no systematic search for evidence was undertaken by the Evidence Review Team, were issued as ungraded expert opinion recommendations. The guideline work group concluded that a comprehensive approach to risk assessment should replace decisions based on assessments of single risk factors in isolation. Original data analyses were undertaken to produce a “proof-in-concept” risk-prediction model for kidney failure to support a framework for quantitative risk assessment in the donor candidate evaluation and defensible shared decision making. This framework is grounded in the simultaneous consideration of each candidate's profile of demographic and health characteristics. The processes and framework for the donor candidate evaluation are presented, along with recommendations for optimal care before, during, and after donation. Limitations of the evidence are discussed, especially regarding the lack of definitive prospective studies and clinical outcome trials. Suggestions for future research, including the need for continued refinement of long-term risk prediction and novel approaches to estimating donation-attributable risks, are also provided. In citing this document, the following format should be used: Kidney Disease: Improving Global Outcomes (KDIGO) Living Kidney Donor Work Group. KDIGO Clinical Practice Guideline on the Evaluation and Care of Living Kidney Donors. Transplantation. 2017;101(Suppl 8S):S1–S109.
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              Long-term consequences of kidney donation.

              The long-term renal consequences of kidney donation by a living donor are attracting increased appropriate interest. The overall evidence suggests that living kidney donors have survival similar to that of nondonors and that their risk of end-stage renal disease (ESRD) is not increased. Previous studies have included relatively small numbers of donors and a brief follow-up period. We ascertained the vital status and lifetime risk of ESRD in 3698 kidney donors who donated kidneys during the period from 1963 through 2007; from 2003 through 2007, we also measured the glomerular filtration rate (GFR) and urinary albumin excretion and assessed the prevalence of hypertension, general health status, and quality of life in 255 donors. The survival of kidney donors was similar to that of controls who were matched for age, sex, and race or ethnic group. ESRD developed in 11 donors, a rate of 180 cases per million persons per year, as compared with a rate of 268 per million per year in the general population. At a mean (+/-SD) of 12.2+/-9.2 years after donation, 85.5% of the subgroup of 255 donors had a GFR of 60 ml per minute per 1.73 m(2) of body-surface area or higher, 32.1% had hypertension, and 12.7% had albuminuria. Older age and higher body-mass index, but not a longer time since donation, were associated with both a GFR that was lower than 60 ml per minute per 1.73 m(2) and hypertension. A longer time since donation, however, was independently associated with albuminuria. Most donors had quality-of-life scores that were better than population norms, and the prevalence of coexisting conditions was similar to that among controls from the National Health and Nutrition Examination Survey (NHANES) who were matched for age, sex, race or ethnic group, and body-mass index. Survival and the risk of ESRD in carefully screened kidney donors appear to be similar to those in the general population. Most donors who were studied had a preserved GFR, normal albumin excretion, and an excellent quality of life. 2009 Massachusetts Medical Society
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                Author and article information

                Contributors
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                Journal
                Transplant International
                Transpl Int
                Wiley
                0934-0874
                1432-2277
                June 2021
                May 20 2021
                June 2021
                : 34
                : 6
                : 1123-1133
                Affiliations
                [1 ]Department of Nephrology Hôpital Bichat Assistance Publique‐Hôpitaux de Paris Centre de recherche sur l’inflammation INSERM UMR1149 CNRS EL8252 Laboratoire d’Excellence Inflamex Université de Paris Paris France
                [2 ]Nephrology and Renal Transplantation Department CHU Nantes Nantes France
                [3 ]Nephrology Department Hopital Européen Georges Pompidou Paris France
                [4 ]Nephrology and Renal Transplantation Department Pasteur Hospital Nice France
                [5 ]Urology Department Pitié‐Salpêtrière Paris France
                [6 ]Nephrology, Dialysis, Transplantation Department CHU Cote de Nacre Caen University Caen France
                [7 ]Service de Néphrologie et Immunologie Clinique CHU Tours Université de Tours Tours France
                [8 ]Nephrology, Dialysis and Transplantation Department University Hospital Amiens France
                [9 ]Nephrology, Transplantation and Dialysis CHU Bordeaux CNRS UMR 5164 Bordeaux University Bordeaux France
                [10 ]Nephrology, Dialysis and Renal Transplantation Department Foch Hospital Suresnes France
                [11 ]Nephrology, Dialysis and Transplantation Department CHU Besançon Besançon France
                [12 ]Nephrology Department CHU Rouen France
                [13 ]Nephrology, Dialysis and Transplantation Department CHU Nancy France
                [14 ]Nephrology, Dialysis and Transplantation Department CHU Clermont Ferrand France
                [15 ]Department of Nephrology and Renal Transplantation Hopital Saint Louis Paris France
                [16 ]Nephrology and Transplantation Department UPEC University Créteil France
                [17 ]Nephrology Department University Hospital Lille France
                [18 ]Nephrology and Transplantation Hopital Pitié Salpétrière Paris France
                [19 ]Department of Nephrology, Dialysis and Organ Transplantation CHU Rangueil INSERM U1043 IFR‐BMT University Paul Sabatier Toulouse France
                [20 ]Department of Nephrology and Renal Transplantation CHU Brest Brest France
                [21 ]Nephrology, Transplantation and Dialysis Department CHU Lapeyronie, and IRMB INSERM U1183 Montpellier France
                [22 ]Nephrology and Renal Transplantation Department Hopital Necker Paris France
                [23 ]Nephrology and Renal Transplantation APHM Marseille France
                [24 ]Nephrology and Transplantation Department University Hospital Strasbourg France
                [25 ]Nephrology Department University Hospital Dijon France
                [26 ]Renal Transplantation Department Hospices Civils de Lyon Claude Bernard University Lyon France
                [27 ]Nephrology and Renal Transplantation Department University Hospital Reims France
                [28 ]Nephrology and Renal Transplantation Hopital Tenon Paris France
                [29 ]Nephrology, Hemodialysis, Apheresis and Transplantation Department University Hospital Grenoble France
                [30 ]Nephrology Department University Hospital and Poitiers University INSERM U1082 Poitiers France
                [31 ]Nephrology, Dialysis and Renal Transplantation Department CHU Limoges France
                [32 ]Nephrology, Dialysis and Transplantation Department University Hospital Rennes France
                [33 ]Department of Nephrology‐Dialysis‐Transplantation University of Liège (ULg CHU) Liège Belgium
                [34 ]Department of Nephrology‐Dialysis‐Apheresis Hopital Universitaire Caremeau Nimes France
                [35 ]Department of Physiology European Georges Pompidou Hospital APHP INSERM U1151 Paris University Paris France
                [36 ]Nephrology, Dialysis and Renal Transplantation Department Hôpital Nord CHU de Saint‐Etienne Jean Monnet University COMUE Université de Lyon Lyon France
                Article
                10.1111/tri.13870
                816c4380-fbd5-4041-ab25-e5fc42e92d3f
                © 2021

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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