Evidence map›Paper›PMID 39530109›Full record

ArticleClinical kidney journal2024

Dynamic prediction of kidney allograft and patient survival using post-transplant estimated glomerular filtration rate trajectory.

Khandoker Shuvo Bakar, Armando Teixeira-Pinto, Ryan Gately, Farzaneh Boroumand, Wai H Lim, Germaine Wong

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Article in Clinical kidney journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Khandoker Shuvo BakarSydney School of Public Health, University of Sydney, Sydney, Australia.
Armando Teixeira-PintoSydney School of Public Health, University of Sydney, Sydney, Australia.
Ryan GatelyDepartment of Kidney and Transplant Services, Princess Alexandra Hospital, Brisbane, Australia.
Farzaneh BoroumandSydney School of Public Health, University of Sydney, Sydney, Australia.
Wai H LimDepartment of Renal Medicine, Sir Charles Gairdner Hospital, Perth, Australia.
Germaine WongSydney School of Public Health, University of Sydney, Sydney, Australia.ORCID https://orcid.org/0000-0001-8422-7269

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Allograft loss is the most feared outcome of kidney transplant recipients. We aimed to develop a dynamic Bayesian model using estimated glomerular filtration rate (eGFR) trajectories to predict long-term allograft and patient survivals. Methods: We used data from the Australian and New Zealand Dialysis and Transplant registry and included all adult kidney transplant recipients (1980-2017) in Australia (derivation cohort) and New Zealand (NZ, validation cohort). Using a joint model, the temporal changes of eGFR trajectories were used to predict patient and allograft survivals. Results: The cohort composed of 14 915 kidney transplant recipients [12 777 (86%) from Australia and 2138 (14%) from NZ] who were followed for a median of 8.9 years. In the derivation cohort, eGFR trajectory was inversely associated with allograft loss [every 10 ml/min/1.73 m Conclusion: This straightforward model, using a single metric of eGFR trajectory, shows good model performance, and effectively distinguish transplant recipients who are at risk of death and allograft loss from those who are not. This simple bedside tool may facilitate early identification of individuals at risk of allograft loss and death.

Indexed as

allograft lossdeathdynamic modelingeGFR trajectorykidney transplant

Identifiers

PMID39530109
PMCPMC11551522

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.