Prediction of Progression in Polycystic Kidney Disease Using the Kidney Failure Risk Equation and Ultrasound Parameters
Author(s) -
Ayub Akbari,
Navdeep Tangri,
Pierre Antoine Brown,
Mohan Biyani,
Emily Rhodes,
Teerath Kumar,
Wael Shabana,
Manish M. Sood
Publication year - 2020
Publication title -
canadian journal of kidney health and disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.742
H-Index - 20
ISSN - 2054-3581
DOI - 10.1177/2054358120911274
Subject(s) - medicine , kidney disease , dialysis , population , nephrology , kidney transplantation , polycystic kidney disease , autosomal dominant polycystic kidney disease , cohort , disease , kidney , environmental health
Background: The kidney failure risk equation (KFRE) is a validated risk algorithm for predicting the risk of kidney failure in chronic kidney disease (CKD) patients regardless of etiology. Patients with autosomal dominant polycystic kidney disease (AD-PCKD) experience long disease trajectories and as such identifying individuals at risk of kidney failure would aid in interventionObjective: To examine the utility of the KFRE in predicting adverse kidney outcomes compared with existing risk factors in a cohort of patients with AD-PCKD.Methods: Retrospective cohort study of AD-PCKD patients referred to a tertiary care center with a baseline kidney ultrasound and a KFRE calculation. Cox proportional hazards were used to examine the association of the KFRE and composite of an eGFR decline of >30% or the need for dialysis/transplantation. Discrimination and calibration of a parsimonious fully adjusted model and a model containing only total kidney volume (TKV) with and without the addition of the KFRE was determined.Results: Of 340 patients with AD-PCKD eligible, 221 (65%) met inclusion criteria. Older age, cardiac disease, cancer, higher systolic blood pressure, albuminuria, lower eGFR and a higher initial TKV were more common in patients with a higher KFRE. A total of 120 events occurred over a median patient follow-up time of 3.2 years. KFRE was independently associated with the composite kidney outcome. Addition of the KFRE significantly improved discrimination and calibration in a TKV only model and a fully adjusted model.Conclusions: In a diverse, referral population with AD-PCKD, the KFRE was associated with adverse kidney outcomes and improved risk prediction.
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