Pharmacokinetics in children with chronic kidney disease
In children, the main causes of chronic kidney disease (CKD) are congenital diseases and glomerular disorders. CKD is associated with multiple physiological changes and may therefore influence various pharmacokinetic (PK) parameters. A well-known consequence of CKD on pharmacokinetics is a reduction...
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Veröffentlicht in: | Pediatric nephrology (Berlin, West) West), 2020-07, Vol.35 (7), p.1153-1172 |
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description | In children, the main causes of chronic kidney disease (CKD) are congenital diseases and glomerular disorders. CKD is associated with multiple physiological changes and may therefore influence various pharmacokinetic (PK) parameters. A well-known consequence of CKD on pharmacokinetics is a reduction in renal clearance due to a decrease in the glomerular filtration rate. The impact of renal impairment on pharmacokinetics is, however, not limited to a decreased elimination of drugs excreted by the kidney. In fact, renal dysfunction may lead to modifications in absorption, distribution, transport, and metabolism as well. Currently, insufficient evidence is available to guide dosing decisions on many commonly used drugs. Moreover, the impact of maturation on drug disposition and action should be taken into account when selecting and dosing drugs in the pediatric population. Clinicians should take PK changes into consideration when selecting and dosing drugs in pediatric CKD patients in order to avoid toxicity and increase efficiency of drugs in this population. The aim of this review is to summarize known PK changes in relation to CKD and to extrapolate available knowledge to the pediatric CKD population to provide guidance for clinical practice. |
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CKD is associated with multiple physiological changes and may therefore influence various pharmacokinetic (PK) parameters. A well-known consequence of CKD on pharmacokinetics is a reduction in renal clearance due to a decrease in the glomerular filtration rate. The impact of renal impairment on pharmacokinetics is, however, not limited to a decreased elimination of drugs excreted by the kidney. In fact, renal dysfunction may lead to modifications in absorption, distribution, transport, and metabolism as well. Currently, insufficient evidence is available to guide dosing decisions on many commonly used drugs. Moreover, the impact of maturation on drug disposition and action should be taken into account when selecting and dosing drugs in the pediatric population. Clinicians should take PK changes into consideration when selecting and dosing drugs in pediatric CKD patients in order to avoid toxicity and increase efficiency of drugs in this population. The aim of this review is to summarize known PK changes in relation to CKD and to extrapolate available knowledge to the pediatric CKD population to provide guidance for clinical practice.</description><identifier>ISSN: 0931-041X</identifier><identifier>EISSN: 1432-198X</identifier><identifier>DOI: 10.1007/s00467-019-04304-9</identifier><identifier>PMID: 31375913</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Age Factors ; Animals ; Child ; Children ; Chronic kidney failure ; Complications and side effects ; Dose-Response Relationship, Drug ; Drug dosages ; Drug therapy ; Glomerular filtration rate ; Glomerular Filtration Rate - drug effects ; Humans ; Kidney diseases ; Liver - metabolism ; Medicine ; Medicine & Public Health ; Nephrology ; Pediatric research ; Pediatrics ; Pharmacokinetics ; Rats ; Renal function ; Renal Insufficiency, Chronic - physiopathology ; Review ; Toxicity ; Urology ; What’s New in Chronic Kidney Disease</subject><ispartof>Pediatric nephrology (Berlin, West), 2020-07, Vol.35 (7), p.1153-1172</ispartof><rights>The Author(s) 2019</rights><rights>COPYRIGHT 2020 Springer</rights><rights>The Author(s) 2019. 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CKD is associated with multiple physiological changes and may therefore influence various pharmacokinetic (PK) parameters. A well-known consequence of CKD on pharmacokinetics is a reduction in renal clearance due to a decrease in the glomerular filtration rate. The impact of renal impairment on pharmacokinetics is, however, not limited to a decreased elimination of drugs excreted by the kidney. In fact, renal dysfunction may lead to modifications in absorption, distribution, transport, and metabolism as well. Currently, insufficient evidence is available to guide dosing decisions on many commonly used drugs. Moreover, the impact of maturation on drug disposition and action should be taken into account when selecting and dosing drugs in the pediatric population. Clinicians should take PK changes into consideration when selecting and dosing drugs in pediatric CKD patients in order to avoid toxicity and increase efficiency of drugs in this population. The aim of this review is to summarize known PK changes in relation to CKD and to extrapolate available knowledge to the pediatric CKD population to provide guidance for clinical practice.</description><subject>Age Factors</subject><subject>Animals</subject><subject>Child</subject><subject>Children</subject><subject>Chronic kidney failure</subject><subject>Complications and side effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>Glomerular filtration rate</subject><subject>Glomerular Filtration Rate - drug effects</subject><subject>Humans</subject><subject>Kidney diseases</subject><subject>Liver - metabolism</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nephrology</subject><subject>Pediatric research</subject><subject>Pediatrics</subject><subject>Pharmacokinetics</subject><subject>Rats</subject><subject>Renal function</subject><subject>Renal Insufficiency, Chronic - physiopathology</subject><subject>Review</subject><subject>Toxicity</subject><subject>Urology</subject><subject>What’s New in Chronic Kidney Disease</subject><issn>0931-041X</issn><issn>1432-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kltrFTEUhYMo9lj9Az7IgODb1NwvL0Ip3qBgHyr0LWQye86knUlqMqfSf2_qqW0PHCSBsLO_tRI2C6G3BB8RjNXHgjGXqsXEtJgzzFvzDK0IZ7QlRl88RytsGKktcnGAXpVyiTHWQsuX6IARpoQhbIX02ejy7Hy6ChGW4EsTYuPHMPUZYvM7LGOtcorBN1ehj3Db9KGAK_AavRjcVODN_XmIfn75fH7yrT398fX7yfFp6yXBSwtEdqpuTHgvwDguhl7pjuKeMj1QT71RwwCMSeG5YIoLKUXXAfbaaGOAHaJPW9_rTTdD7yEu2U32OofZ5VubXLC7nRhGu043VlGuseDV4P29QU6_NlAWe5k2OdY_W0qlMkZJpR6ptZvAhjikaubnULw9ltXJaC5Npdo91Boi1JdThCHU6x3-aA9fVw9z8HsFH54IRnDTMpY0bZaQYtkF6Rb0OZWSYXiYCMH2Lh12mw5b02H_psPeid49neWD5F8cKsC2QKmtuIb8OKv_2P4BkKzDAQ</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Schijvens, Anne M.</creator><creator>de Wildt, Saskia N.</creator><creator>Schreuder, Michiel F.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2418-8928</orcidid></search><sort><creationdate>20200701</creationdate><title>Pharmacokinetics in children with chronic kidney disease</title><author>Schijvens, Anne M. ; 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subjects | Age Factors Animals Child Children Chronic kidney failure Complications and side effects Dose-Response Relationship, Drug Drug dosages Drug therapy Glomerular filtration rate Glomerular Filtration Rate - drug effects Humans Kidney diseases Liver - metabolism Medicine Medicine & Public Health Nephrology Pediatric research Pediatrics Pharmacokinetics Rats Renal function Renal Insufficiency, Chronic - physiopathology Review Toxicity Urology What’s New in Chronic Kidney Disease |
title | Pharmacokinetics in children with chronic kidney disease |
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