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  4. Strategies to improve monitoring disease progression, assessing cardiovascular risk, and defining prognostic biomarkers in chronic kidney disease
 
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Strategies to improve monitoring disease progression, assessing cardiovascular risk, and defining prognostic biomarkers in chronic kidney disease

Journal
Kidney International Supplements
ISSN
2157-1716
Date Issued
2017
Author(s)
Pena, Michelle J.
Stenvinkel, Peter
Kretzler, Matthias
Adu, Dwomoa
Agarwal, Sanjay Kumar
Coresh, Josef
Feldman, Harold I.
Fogo, Agnes B.
Gansevoort, Ron T.
Harris, David C.
Vivekanand, Jha
Zhi-Hong, Liu
Luyckx, Valerie A.
Massy, Ziad A.
Ravindra, Mehta
Nelson, Robert G.
O'Donoghue, Donal J.
Obrador, Gregorio  
Facultad de Ciencias de la Salud - CampCM  
Roberts, Charlotte J.
Sola, Laura
Sumaili, Ernest K.
Tatiyanupanwong, Sajja
Thomas, Bernadette
Wiecek, Andrzej
Parikh, Chirag R.
Heerspink, Hiddo J.L.
Type
Resource Types::text::journal::journal article
DOI
10.1016/j.kisu.2017.07.005
URL
https://scripta.up.edu.mx/handle/123456789/2267
Abstract
Chronic kidney disease (CKD) is a major global public health problem with significant gaps in research, care, and policy. In order to mitigate the risks and adverse effects of CKD, the International Society of Nephrology has created a cohesive set of activities to improve the global outcomes of people living with CKD. Improving monitoring of renal disease progression can be done by screening and monitoring albuminuria and estimated glomerular filtration rate in primary care. Consensus on how many times and how often albuminuria and estimated glomerular filtration rate are measured should be defined. Meaningful changes in both renal biomarkers should be determined in order to ascertain what is clinically relevant. Increasing social awareness of CKD and partnering with the technological community may be ways to engage patients. Furthermore, improving the prediction of cardiovascular events in patients with CKD can be achieved by including the renal risk markers albuminuria and estimated glomerular filtration rate in cardiovascular risk algorithms and by encouraging uptake of assessing cardiovascular risk by general practitioners and nephrologists. Finally, examining ways to further validate and implement novel biomarkers for CKD will help mitigate the global problem of CKD. The more frequent use of renal biopsy will facilitate further knowledge into the underlying etiologies of CKD and help put new biomarkers into biological context. Real-world assessments of these biomarkers in existing cohorts is important, as well as obtaining regulatory approval to use these biomarkers in clinical practice. Collaborations among academia, physician and patient groups, industry, payer organizations, and regulatory authorities will help improve the global outcomes of people living with CKD.
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