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Cystatin C: A Primer for Pharmacists
Pharmacists are at the forefront of dosing and monitoring medications eliminated by or toxic to the kidney. To evaluate the effectiveness and safety of these medications, accurate measurement of kidney function is paramount. The mainstay of kidney assessment for drug dosing and monitoring is serum c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151673/ https://www.ncbi.nlm.nih.gov/pubmed/32182861 http://dx.doi.org/10.3390/pharmacy8010035 |
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author | Teaford, Hilary R. Barreto, Jason N. Vollmer, Kathryn J. Rule, Andrew D. Barreto, Erin F. |
author_facet | Teaford, Hilary R. Barreto, Jason N. Vollmer, Kathryn J. Rule, Andrew D. Barreto, Erin F. |
author_sort | Teaford, Hilary R. |
collection | PubMed |
description | Pharmacists are at the forefront of dosing and monitoring medications eliminated by or toxic to the kidney. To evaluate the effectiveness and safety of these medications, accurate measurement of kidney function is paramount. The mainstay of kidney assessment for drug dosing and monitoring is serum creatinine (SCr)-based estimation equations. Yet, SCr has known limitations including its insensitivity to underlying changes in kidney function and the numerous non-kidney factors that are incompletely accounted for in equations to estimate glomerular filtration rate (eGFR). Serum cystatin C (cysC) is a biomarker that can serve as an adjunct or alternative to SCr to evaluate kidney function for drug dosing. Pharmacists must be educated about the strengths and limitations of cysC prior to applying it to medication management. Not all patient populations have been studied and some evaluations demonstrated large variations in the relationship between cysC and GFR. Use of eGFR equations incorporating cysC should be reserved for drug management in scenarios with demonstrated outcomes, including to improve pharmacodynamic target attainment for antibiotics or reduce drug toxicity. This article provides an overview of cysC, discusses evidence around its use in medication dosing and in special populations, and describes practical considerations for application and implementation. |
format | Online Article Text |
id | pubmed-7151673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71516732020-04-20 Cystatin C: A Primer for Pharmacists Teaford, Hilary R. Barreto, Jason N. Vollmer, Kathryn J. Rule, Andrew D. Barreto, Erin F. Pharmacy (Basel) Review Pharmacists are at the forefront of dosing and monitoring medications eliminated by or toxic to the kidney. To evaluate the effectiveness and safety of these medications, accurate measurement of kidney function is paramount. The mainstay of kidney assessment for drug dosing and monitoring is serum creatinine (SCr)-based estimation equations. Yet, SCr has known limitations including its insensitivity to underlying changes in kidney function and the numerous non-kidney factors that are incompletely accounted for in equations to estimate glomerular filtration rate (eGFR). Serum cystatin C (cysC) is a biomarker that can serve as an adjunct or alternative to SCr to evaluate kidney function for drug dosing. Pharmacists must be educated about the strengths and limitations of cysC prior to applying it to medication management. Not all patient populations have been studied and some evaluations demonstrated large variations in the relationship between cysC and GFR. Use of eGFR equations incorporating cysC should be reserved for drug management in scenarios with demonstrated outcomes, including to improve pharmacodynamic target attainment for antibiotics or reduce drug toxicity. This article provides an overview of cysC, discusses evidence around its use in medication dosing and in special populations, and describes practical considerations for application and implementation. MDPI 2020-03-09 /pmc/articles/PMC7151673/ /pubmed/32182861 http://dx.doi.org/10.3390/pharmacy8010035 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Teaford, Hilary R. Barreto, Jason N. Vollmer, Kathryn J. Rule, Andrew D. Barreto, Erin F. Cystatin C: A Primer for Pharmacists |
title | Cystatin C: A Primer for Pharmacists |
title_full | Cystatin C: A Primer for Pharmacists |
title_fullStr | Cystatin C: A Primer for Pharmacists |
title_full_unstemmed | Cystatin C: A Primer for Pharmacists |
title_short | Cystatin C: A Primer for Pharmacists |
title_sort | cystatin c: a primer for pharmacists |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7151673/ https://www.ncbi.nlm.nih.gov/pubmed/32182861 http://dx.doi.org/10.3390/pharmacy8010035 |
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