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Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation

BACKGROUND: A Minimal Clinically Meaningful Difference (MCMD) has not been defined for Estimated glomerular filtration rate (eGFR). Our goal was to define the MCMD for eGFR anchored to kidney graft failure. METHODS: A systematic review of studies with 12‐month eGFR and subsequent renal graft failure...

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Autores principales: Mayne, Tracy J., Nordyke, Robert J., Schold, Jesse D., Weir, Matthew R., Mohan, Sumit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365649/
https://www.ncbi.nlm.nih.gov/pubmed/33896052
http://dx.doi.org/10.1111/ctr.14326
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author Mayne, Tracy J.
Nordyke, Robert J.
Schold, Jesse D.
Weir, Matthew R.
Mohan, Sumit
author_facet Mayne, Tracy J.
Nordyke, Robert J.
Schold, Jesse D.
Weir, Matthew R.
Mohan, Sumit
author_sort Mayne, Tracy J.
collection PubMed
description BACKGROUND: A Minimal Clinically Meaningful Difference (MCMD) has not been defined for Estimated glomerular filtration rate (eGFR). Our goal was to define the MCMD for eGFR anchored to kidney graft failure. METHODS: A systematic review of studies with 12‐month eGFR and subsequent renal graft failure was conducted. For observational studies, we calculated hazard ratio (HR) differences between adjacent eGFR intervals weighted by population distribution. Interventional trials yielded therapeutically induced changes in eGFR and failure risk. OPTN data analysis divided 12‐month eGFR into bands for Cox regressions comparing adjacent eGFR bands with a death‐censored graft survival outcome. RESULTS: Observational studies indicated that lower eGFR was associated with increased death‐censored graft failure risk; each 5 ml/min/1.73 m(2) 12‐month eGFR band associated with a weighted incremental HR = 1.12 to 1.23. Clinical trial data found a 5 ml/min/1.73 m(2) difference was associated with incremental HR = 1.16 to 1.35. OPTN analyses showed weighted mean HRs across 10, 7, and 5 ml/min/1.73 m(2) bands of 1.47, 1.30, and 1.19. CONCLUSIONS: A 5 ml/min/1.73 m(2) difference in 12‐month eGFR was consistently associated with ~20% increase in death‐censored graft failure risk. The magnitude of effect has been interpreted as clinically meaningful in other disease states and should be considered the MCMD in renal transplantation clinical trials.
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spelling pubmed-83656492021-08-23 Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation Mayne, Tracy J. Nordyke, Robert J. Schold, Jesse D. Weir, Matthew R. Mohan, Sumit Clin Transplant Original Articles BACKGROUND: A Minimal Clinically Meaningful Difference (MCMD) has not been defined for Estimated glomerular filtration rate (eGFR). Our goal was to define the MCMD for eGFR anchored to kidney graft failure. METHODS: A systematic review of studies with 12‐month eGFR and subsequent renal graft failure was conducted. For observational studies, we calculated hazard ratio (HR) differences between adjacent eGFR intervals weighted by population distribution. Interventional trials yielded therapeutically induced changes in eGFR and failure risk. OPTN data analysis divided 12‐month eGFR into bands for Cox regressions comparing adjacent eGFR bands with a death‐censored graft survival outcome. RESULTS: Observational studies indicated that lower eGFR was associated with increased death‐censored graft failure risk; each 5 ml/min/1.73 m(2) 12‐month eGFR band associated with a weighted incremental HR = 1.12 to 1.23. Clinical trial data found a 5 ml/min/1.73 m(2) difference was associated with incremental HR = 1.16 to 1.35. OPTN analyses showed weighted mean HRs across 10, 7, and 5 ml/min/1.73 m(2) bands of 1.47, 1.30, and 1.19. CONCLUSIONS: A 5 ml/min/1.73 m(2) difference in 12‐month eGFR was consistently associated with ~20% increase in death‐censored graft failure risk. The magnitude of effect has been interpreted as clinically meaningful in other disease states and should be considered the MCMD in renal transplantation clinical trials. John Wiley and Sons Inc. 2021-05-05 2021-07 /pmc/articles/PMC8365649/ /pubmed/33896052 http://dx.doi.org/10.1111/ctr.14326 Text en © 2021 The Authors. Clinical Transplantation published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Mayne, Tracy J.
Nordyke, Robert J.
Schold, Jesse D.
Weir, Matthew R.
Mohan, Sumit
Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation
title Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation
title_full Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation
title_fullStr Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation
title_full_unstemmed Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation
title_short Defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation
title_sort defining a minimal clinically meaningful difference in 12‐month estimated glomerular filtration rate for clinical trials in deceased donor kidney transplantation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365649/
https://www.ncbi.nlm.nih.gov/pubmed/33896052
http://dx.doi.org/10.1111/ctr.14326
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