Application of therapeutic drug monitoring to the treatment of bacterial central nervous system infection: a scoping review
Bacterial central nervous system (CNS) infection is challenging to treat and carries high risk of recurrence, morbidity, and mortality. Low CNS penetration of antibiotics may contribute to poor clinical outcomes from bacterial CNS infections. The current application of therapeutic drug monitoring (T...
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Veröffentlicht in: | Journal of antimicrobial chemotherapy 2022-11, Vol.77 (12), p.3408-3413 |
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container_title | Journal of antimicrobial chemotherapy |
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creator | Arkell, Paul Wilson, Richard Watkins, Killian Antcliffe, David B Gilchrist, Mark Wilson, Mark Rawson, Timothy M Holmes, Alison |
description | Bacterial central nervous system (CNS) infection is challenging to treat and carries high risk of recurrence, morbidity, and mortality. Low CNS penetration of antibiotics may contribute to poor clinical outcomes from bacterial CNS infections. The current application of therapeutic drug monitoring (TDM) to management of bacterial CNS infection was reviewed.
Studies were included if they described adults treated for a suspected/confirmed bacterial CNS infection and had antibiotic drug concentration(s) determined that affected individual treatment.
One-hundred-and-thirty-six citations were retrieved. Seventeen manuscripts were included describing management of 68 patients. TDM for vancomycin (58/68) and the beta-lactams (29/68) was most common. Timing of clinical sampling varied widely between studies and across different antibiotics. Methods for setting individual PK-PD targets, determining parameters and making treatment changes varied widely and were sometimes unclear.
Despite increasing observational data showing low CNS penetration of various antibiotics, there are few clinical studies describing practical implementation of TDM in management of CNS infection. Lack of consensus around clinically relevant CSF PK-PD targets and protocols for dose-adjustment may contribute. Standardised investigation of TDM as a tool to improve treatment is required, especially as innovative drug concentration-sensing and PK-PD modelling technologies are emerging. Data generated at different centres offering TDM should be open access and aggregated to enrich understanding and optimize application. |
doi_str_mv | 10.1093/jac/dkac332 |
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Studies were included if they described adults treated for a suspected/confirmed bacterial CNS infection and had antibiotic drug concentration(s) determined that affected individual treatment.
One-hundred-and-thirty-six citations were retrieved. Seventeen manuscripts were included describing management of 68 patients. TDM for vancomycin (58/68) and the beta-lactams (29/68) was most common. Timing of clinical sampling varied widely between studies and across different antibiotics. Methods for setting individual PK-PD targets, determining parameters and making treatment changes varied widely and were sometimes unclear.
Despite increasing observational data showing low CNS penetration of various antibiotics, there are few clinical studies describing practical implementation of TDM in management of CNS infection. Lack of consensus around clinically relevant CSF PK-PD targets and protocols for dose-adjustment may contribute. Standardised investigation of TDM as a tool to improve treatment is required, especially as innovative drug concentration-sensing and PK-PD modelling technologies are emerging. Data generated at different centres offering TDM should be open access and aggregated to enrich understanding and optimize application.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkac332</identifier><identifier>PMID: 36227686</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Adult ; Anti-Bacterial Agents - therapeutic use ; beta-Lactams - therapeutic use ; Central Nervous System Infections - drug therapy ; Drug Monitoring ; Humans ; Original Research ; Vancomycin - therapeutic use</subject><ispartof>Journal of antimicrobial chemotherapy, 2022-11, Vol.77 (12), p.3408-3413</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy.</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-4eaba50e8394a5737c3b5b8148351c9cbfa063ccd3a644262f56c31738c4e43d3</citedby><cites>FETCH-LOGICAL-c381t-4eaba50e8394a5737c3b5b8148351c9cbfa063ccd3a644262f56c31738c4e43d3</cites><orcidid>0000-0002-3275-6932</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36227686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arkell, Paul</creatorcontrib><creatorcontrib>Wilson, Richard</creatorcontrib><creatorcontrib>Watkins, Killian</creatorcontrib><creatorcontrib>Antcliffe, David B</creatorcontrib><creatorcontrib>Gilchrist, Mark</creatorcontrib><creatorcontrib>Wilson, Mark</creatorcontrib><creatorcontrib>Rawson, Timothy M</creatorcontrib><creatorcontrib>Holmes, Alison</creatorcontrib><title>Application of therapeutic drug monitoring to the treatment of bacterial central nervous system infection: a scoping review</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Bacterial central nervous system (CNS) infection is challenging to treat and carries high risk of recurrence, morbidity, and mortality. Low CNS penetration of antibiotics may contribute to poor clinical outcomes from bacterial CNS infections. The current application of therapeutic drug monitoring (TDM) to management of bacterial CNS infection was reviewed.
Studies were included if they described adults treated for a suspected/confirmed bacterial CNS infection and had antibiotic drug concentration(s) determined that affected individual treatment.
One-hundred-and-thirty-six citations were retrieved. Seventeen manuscripts were included describing management of 68 patients. TDM for vancomycin (58/68) and the beta-lactams (29/68) was most common. Timing of clinical sampling varied widely between studies and across different antibiotics. Methods for setting individual PK-PD targets, determining parameters and making treatment changes varied widely and were sometimes unclear.
Despite increasing observational data showing low CNS penetration of various antibiotics, there are few clinical studies describing practical implementation of TDM in management of CNS infection. Lack of consensus around clinically relevant CSF PK-PD targets and protocols for dose-adjustment may contribute. Standardised investigation of TDM as a tool to improve treatment is required, especially as innovative drug concentration-sensing and PK-PD modelling technologies are emerging. Data generated at different centres offering TDM should be open access and aggregated to enrich understanding and optimize application.</description><subject>Adult</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>beta-Lactams - therapeutic use</subject><subject>Central Nervous System Infections - drug therapy</subject><subject>Drug Monitoring</subject><subject>Humans</subject><subject>Original Research</subject><subject>Vancomycin - therapeutic use</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUFv1DAQRi0EokvhxB35iIRC7YztJByQqqoFpEq9lLPlTCZblyQOtrOo4s-TqEsFp5Fmnt6M_TH2VoqPUjRwdu_wrPvhEKB8xnZSGVGUopHP2U6A0EWlNJywVyndCyGMNvVLdgKmLCtTmx37fT7Pg0eXfZh46Hm-o-hmWrJH3sVlz8cw-Ryin_Y8h23McySXR5ryxrcOM0XvBo5rJ651ongIS-LpIWUauZ96ws3-iTueMMybKdLB06_X7EXvhkRvjvWUfb-6vL34WlzffPl2cX5dINQyF4pc67SgGhrldAUVQqvbWqoatMQG294JA4gdOKNUacpeGwRZQY2KFHRwyj4_euelHak7Hmrn6EcXH2xw3v4_mfyd3YeDbSqxCVfB-6Mghp8LpWxHn5CGwU20PtWWVal0LdcfXdEPjyjGkFKk_mmNFHaLy65x2WNcK_3u38ue2L_5wB8MgpXV</recordid><startdate>20221128</startdate><enddate>20221128</enddate><creator>Arkell, Paul</creator><creator>Wilson, Richard</creator><creator>Watkins, Killian</creator><creator>Antcliffe, David B</creator><creator>Gilchrist, Mark</creator><creator>Wilson, Mark</creator><creator>Rawson, Timothy M</creator><creator>Holmes, Alison</creator><general>Oxford University Press</general><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3275-6932</orcidid></search><sort><creationdate>20221128</creationdate><title>Application of therapeutic drug monitoring to the treatment of bacterial central nervous system infection: a scoping review</title><author>Arkell, Paul ; Wilson, Richard ; Watkins, Killian ; Antcliffe, David B ; Gilchrist, Mark ; Wilson, Mark ; Rawson, Timothy M ; Holmes, Alison</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-4eaba50e8394a5737c3b5b8148351c9cbfa063ccd3a644262f56c31738c4e43d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>beta-Lactams - therapeutic use</topic><topic>Central Nervous System Infections - drug therapy</topic><topic>Drug Monitoring</topic><topic>Humans</topic><topic>Original Research</topic><topic>Vancomycin - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arkell, Paul</creatorcontrib><creatorcontrib>Wilson, Richard</creatorcontrib><creatorcontrib>Watkins, Killian</creatorcontrib><creatorcontrib>Antcliffe, David B</creatorcontrib><creatorcontrib>Gilchrist, Mark</creatorcontrib><creatorcontrib>Wilson, Mark</creatorcontrib><creatorcontrib>Rawson, Timothy M</creatorcontrib><creatorcontrib>Holmes, Alison</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arkell, Paul</au><au>Wilson, Richard</au><au>Watkins, Killian</au><au>Antcliffe, David B</au><au>Gilchrist, Mark</au><au>Wilson, Mark</au><au>Rawson, Timothy M</au><au>Holmes, Alison</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of therapeutic drug monitoring to the treatment of bacterial central nervous system infection: a scoping review</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2022-11-28</date><risdate>2022</risdate><volume>77</volume><issue>12</issue><spage>3408</spage><epage>3413</epage><pages>3408-3413</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Bacterial central nervous system (CNS) infection is challenging to treat and carries high risk of recurrence, morbidity, and mortality. Low CNS penetration of antibiotics may contribute to poor clinical outcomes from bacterial CNS infections. The current application of therapeutic drug monitoring (TDM) to management of bacterial CNS infection was reviewed.
Studies were included if they described adults treated for a suspected/confirmed bacterial CNS infection and had antibiotic drug concentration(s) determined that affected individual treatment.
One-hundred-and-thirty-six citations were retrieved. Seventeen manuscripts were included describing management of 68 patients. TDM for vancomycin (58/68) and the beta-lactams (29/68) was most common. Timing of clinical sampling varied widely between studies and across different antibiotics. Methods for setting individual PK-PD targets, determining parameters and making treatment changes varied widely and were sometimes unclear.
Despite increasing observational data showing low CNS penetration of various antibiotics, there are few clinical studies describing practical implementation of TDM in management of CNS infection. Lack of consensus around clinically relevant CSF PK-PD targets and protocols for dose-adjustment may contribute. Standardised investigation of TDM as a tool to improve treatment is required, especially as innovative drug concentration-sensing and PK-PD modelling technologies are emerging. Data generated at different centres offering TDM should be open access and aggregated to enrich understanding and optimize application.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>36227686</pmid><doi>10.1093/jac/dkac332</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-3275-6932</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Adult Anti-Bacterial Agents - therapeutic use beta-Lactams - therapeutic use Central Nervous System Infections - drug therapy Drug Monitoring Humans Original Research Vancomycin - therapeutic use |
title | Application of therapeutic drug monitoring to the treatment of bacterial central nervous system infection: a scoping review |
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