DALI: Defining Antibiotic Levels in Intensive Care Unit Patients: Are Current β-Lactam Antibiotic Doses Sufficient for Critically Ill Patients?
Background. Morbidity and mortality for critically ill patients with infections remains a global healthcare problem. We aimed to determine whether β-lactam antibiotic dosing in critically ill patients achieves concentrations associated with maximal activity and whether antibiotic concentrations affe...
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Veröffentlicht in: | Clinical infectious diseases 2014-04, Vol.58 (8), p.1072-1083 |
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creator | Roberts, Jason A. Paul, Sanjoy K. Akova, Murat Bassetti, Matteo De Waele, Jan J. Dimopoulos, George Kaukonen, Kirsi-Maija Koulenti, Despoina Martin, Claude Montravers, Philippe Rello, Jordi Rhodes, Andrew Starr, Therese Wallis, Steven C. Lipman, Jeffrey |
description | Background. Morbidity and mortality for critically ill patients with infections remains a global healthcare problem. We aimed to determine whether β-lactam antibiotic dosing in critically ill patients achieves concentrations associated with maximal activity and whether antibiotic concentrations affect patient outcome. Methods. This was a prospective, multinational pharmacokinetic point-prevalence study including 8 β-lactam antibiotics. Two blood samples were taken from each patient during a single dosing interval. The primary pharmacokinetic/pharmacodynamic targets were free antibiotic concentrations above the minimum inhibitory concentration (MIC) of the pathogen at both 50% (50% f T> MIC ) and 100% (100% f T> MIC ) of the dosing interval. We used skewed logistic regression to describe the effect of antibiotic exposure on patient outcome. Results. We included 384 patients (361 evaluable patients) across 68 hospitals. The median age was 61 (interquartile range [IQR], 48–73) years, the median Acute Physiology and Chronic Health Evaluation II score was 18 (IQR, 14–24), and 65% of patients were male. Of the 248 patients treated for infection, 16% did not achieve 50% f T> MIC and these patients were 32% less likely to have a positive clinical outcome (odds ratio [OR], 0.68; P=.009). Positive clinical outcome was associated with increasing 50% f T>MIC and 100% f T> MIC ratios (OR, 1.02 and 1.56, respectively; P |
doi_str_mv | 10.1093/cid/ciu027 |
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Morbidity and mortality for critically ill patients with infections remains a global healthcare problem. We aimed to determine whether β-lactam antibiotic dosing in critically ill patients achieves concentrations associated with maximal activity and whether antibiotic concentrations affect patient outcome. Methods. This was a prospective, multinational pharmacokinetic point-prevalence study including 8 β-lactam antibiotics. Two blood samples were taken from each patient during a single dosing interval. The primary pharmacokinetic/pharmacodynamic targets were free antibiotic concentrations above the minimum inhibitory concentration (MIC) of the pathogen at both 50% (50% f T> MIC ) and 100% (100% f T> MIC ) of the dosing interval. We used skewed logistic regression to describe the effect of antibiotic exposure on patient outcome. Results. We included 384 patients (361 evaluable patients) across 68 hospitals. The median age was 61 (interquartile range [IQR], 48–73) years, the median Acute Physiology and Chronic Health Evaluation II score was 18 (IQR, 14–24), and 65% of patients were male. Of the 248 patients treated for infection, 16% did not achieve 50% f T> MIC and these patients were 32% less likely to have a positive clinical outcome (odds ratio [OR], 0.68; P=.009). Positive clinical outcome was associated with increasing 50% f T>MIC and 100% f T> MIC ratios (OR, 1.02 and 1.56, respectively; P<.03), with significant interaction with sickness severity status. Conclusions. Infected critically ill patients may have adverse outcomes as a result of inadeqaute antibiotic exposure; a paradigm change to more personalized antibiotic dosing may be necessary to improve outcomes for these most seriously ill patients.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciu027</identifier><identifier>PMID: 24429437</identifier><language>eng</language><publisher>United States: OXFORD UNIVERSITY PRESS</publisher><subject>Aged ; Anti-Bacterial Agents - administration & dosage ; Anti-Bacterial Agents - pharmacokinetics ; Antibiotics ; ARTICLES AND COMMENTARIES ; Bacterial Infections - drug therapy ; beta-Lactams - administration & dosage ; beta-Lactams - pharmacokinetics ; Blood Chemical Analysis ; Critical care ; Critical Illness ; Female ; Health care industry ; Health outcomes ; Hospitals ; Humans ; Infections ; Intensive Care Units ; International Cooperation ; Male ; Microbial Sensitivity Tests ; Middle Aged ; Models, Statistical ; Pathogens ; Pharmacokinetics ; Prospective Studies ; Treatment Outcome ; University hospitals</subject><ispartof>Clinical infectious diseases, 2014-04, Vol.58 (8), p.1072-1083</ispartof><rights>Copyright © 2014 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24031748$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24031748$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24429437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roberts, Jason A.</creatorcontrib><creatorcontrib>Paul, Sanjoy K.</creatorcontrib><creatorcontrib>Akova, Murat</creatorcontrib><creatorcontrib>Bassetti, Matteo</creatorcontrib><creatorcontrib>De Waele, Jan J.</creatorcontrib><creatorcontrib>Dimopoulos, George</creatorcontrib><creatorcontrib>Kaukonen, Kirsi-Maija</creatorcontrib><creatorcontrib>Koulenti, Despoina</creatorcontrib><creatorcontrib>Martin, Claude</creatorcontrib><creatorcontrib>Montravers, Philippe</creatorcontrib><creatorcontrib>Rello, Jordi</creatorcontrib><creatorcontrib>Rhodes, Andrew</creatorcontrib><creatorcontrib>Starr, Therese</creatorcontrib><creatorcontrib>Wallis, Steven C.</creatorcontrib><creatorcontrib>Lipman, Jeffrey</creatorcontrib><creatorcontrib>DALI Studya</creatorcontrib><creatorcontrib>DALI Study</creatorcontrib><title>DALI: Defining Antibiotic Levels in Intensive Care Unit Patients: Are Current β-Lactam Antibiotic Doses Sufficient for Critically Ill Patients?</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Background. Morbidity and mortality for critically ill patients with infections remains a global healthcare problem. We aimed to determine whether β-lactam antibiotic dosing in critically ill patients achieves concentrations associated with maximal activity and whether antibiotic concentrations affect patient outcome. Methods. This was a prospective, multinational pharmacokinetic point-prevalence study including 8 β-lactam antibiotics. Two blood samples were taken from each patient during a single dosing interval. The primary pharmacokinetic/pharmacodynamic targets were free antibiotic concentrations above the minimum inhibitory concentration (MIC) of the pathogen at both 50% (50% f T> MIC ) and 100% (100% f T> MIC ) of the dosing interval. We used skewed logistic regression to describe the effect of antibiotic exposure on patient outcome. Results. We included 384 patients (361 evaluable patients) across 68 hospitals. The median age was 61 (interquartile range [IQR], 48–73) years, the median Acute Physiology and Chronic Health Evaluation II score was 18 (IQR, 14–24), and 65% of patients were male. Of the 248 patients treated for infection, 16% did not achieve 50% f T> MIC and these patients were 32% less likely to have a positive clinical outcome (odds ratio [OR], 0.68; P=.009). Positive clinical outcome was associated with increasing 50% f T>MIC and 100% f T> MIC ratios (OR, 1.02 and 1.56, respectively; P<.03), with significant interaction with sickness severity status. Conclusions. Infected critically ill patients may have adverse outcomes as a result of inadeqaute antibiotic exposure; a paradigm change to more personalized antibiotic dosing may be necessary to improve outcomes for these most seriously ill patients.</description><subject>Aged</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Anti-Bacterial Agents - pharmacokinetics</subject><subject>Antibiotics</subject><subject>ARTICLES AND COMMENTARIES</subject><subject>Bacterial Infections - drug therapy</subject><subject>beta-Lactams - administration & dosage</subject><subject>beta-Lactams - pharmacokinetics</subject><subject>Blood Chemical Analysis</subject><subject>Critical care</subject><subject>Critical Illness</subject><subject>Female</subject><subject>Health care industry</subject><subject>Health outcomes</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Infections</subject><subject>Intensive Care Units</subject><subject>International Cooperation</subject><subject>Male</subject><subject>Microbial Sensitivity Tests</subject><subject>Middle Aged</subject><subject>Models, Statistical</subject><subject>Pathogens</subject><subject>Pharmacokinetics</subject><subject>Prospective Studies</subject><subject>Treatment Outcome</subject><subject>University hospitals</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkEtOwzAQhi0EoqWwYQ_ykk3AE8dx0g2qUh6VIoEEXVdOYiNXqVNsp1JvwVk4CGfCqIC6GM3j_-bXaBA6B3INJKc3tW5C9CTmB2gIjPIoZTkchpqwLEoymg3QiXNLQgAywo7RIE6SOE8oH6KP6aScjfFUKm20ecMT43WlO69rXMqNbB3WBs-Ml8bpjcSFsBLPjfb4WXgtjXdjPAmjorc2dPjrMypF7cVq32jaOenwS6-Urn92sOosLqwOmmjbLZ617b_d7Sk6UqJ18uw3j9D8_u61eIzKp4dZMSmjJeSpjxioOKa0YrRRVcolFSQGJWtCISW8UZxmUjCqWM4SATnEkMQ1haaBTAWJ0xG62vmubffeS-cXK-1q2bbCyK53C-AEkgwogYBe_qJ9tZLNYm31Stjt4u-LAbjYAUvnO7unh2t4-P83-VB-HQ</recordid><startdate>20140415</startdate><enddate>20140415</enddate><creator>Roberts, Jason A.</creator><creator>Paul, Sanjoy K.</creator><creator>Akova, Murat</creator><creator>Bassetti, Matteo</creator><creator>De Waele, Jan J.</creator><creator>Dimopoulos, George</creator><creator>Kaukonen, Kirsi-Maija</creator><creator>Koulenti, Despoina</creator><creator>Martin, Claude</creator><creator>Montravers, Philippe</creator><creator>Rello, Jordi</creator><creator>Rhodes, Andrew</creator><creator>Starr, Therese</creator><creator>Wallis, Steven C.</creator><creator>Lipman, Jeffrey</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>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20140415</creationdate><title>DALI: Defining Antibiotic Levels in Intensive Care Unit Patients: Are Current β-Lactam Antibiotic Doses Sufficient for Critically Ill Patients?</title><author>Roberts, Jason A. ; Paul, Sanjoy K. ; Akova, Murat ; Bassetti, Matteo ; De Waele, Jan J. ; Dimopoulos, George ; Kaukonen, Kirsi-Maija ; Koulenti, Despoina ; Martin, Claude ; Montravers, Philippe ; Rello, Jordi ; Rhodes, Andrew ; Starr, Therese ; Wallis, Steven C. ; Lipman, Jeffrey</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j196t-51f2233b53dfb67e3a021fec031607df738ea53f5954a1912142c31dd18f38e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Anti-Bacterial Agents - pharmacokinetics</topic><topic>Antibiotics</topic><topic>ARTICLES AND COMMENTARIES</topic><topic>Bacterial Infections - drug therapy</topic><topic>beta-Lactams - administration & dosage</topic><topic>beta-Lactams - pharmacokinetics</topic><topic>Blood Chemical Analysis</topic><topic>Critical care</topic><topic>Critical Illness</topic><topic>Female</topic><topic>Health care industry</topic><topic>Health outcomes</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Infections</topic><topic>Intensive Care Units</topic><topic>International Cooperation</topic><topic>Male</topic><topic>Microbial Sensitivity Tests</topic><topic>Middle Aged</topic><topic>Models, Statistical</topic><topic>Pathogens</topic><topic>Pharmacokinetics</topic><topic>Prospective Studies</topic><topic>Treatment Outcome</topic><topic>University hospitals</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roberts, Jason A.</creatorcontrib><creatorcontrib>Paul, Sanjoy K.</creatorcontrib><creatorcontrib>Akova, Murat</creatorcontrib><creatorcontrib>Bassetti, Matteo</creatorcontrib><creatorcontrib>De Waele, Jan J.</creatorcontrib><creatorcontrib>Dimopoulos, George</creatorcontrib><creatorcontrib>Kaukonen, Kirsi-Maija</creatorcontrib><creatorcontrib>Koulenti, Despoina</creatorcontrib><creatorcontrib>Martin, Claude</creatorcontrib><creatorcontrib>Montravers, Philippe</creatorcontrib><creatorcontrib>Rello, Jordi</creatorcontrib><creatorcontrib>Rhodes, Andrew</creatorcontrib><creatorcontrib>Starr, Therese</creatorcontrib><creatorcontrib>Wallis, Steven C.</creatorcontrib><creatorcontrib>Lipman, Jeffrey</creatorcontrib><creatorcontrib>DALI Studya</creatorcontrib><creatorcontrib>DALI Study</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roberts, Jason A.</au><au>Paul, Sanjoy K.</au><au>Akova, Murat</au><au>Bassetti, Matteo</au><au>De Waele, Jan J.</au><au>Dimopoulos, George</au><au>Kaukonen, Kirsi-Maija</au><au>Koulenti, Despoina</au><au>Martin, Claude</au><au>Montravers, Philippe</au><au>Rello, Jordi</au><au>Rhodes, Andrew</au><au>Starr, Therese</au><au>Wallis, Steven C.</au><au>Lipman, Jeffrey</au><aucorp>DALI Studya</aucorp><aucorp>DALI Study</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DALI: Defining Antibiotic Levels in Intensive Care Unit Patients: Are Current β-Lactam Antibiotic Doses Sufficient for Critically Ill Patients?</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2014-04-15</date><risdate>2014</risdate><volume>58</volume><issue>8</issue><spage>1072</spage><epage>1083</epage><pages>1072-1083</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Background. Morbidity and mortality for critically ill patients with infections remains a global healthcare problem. We aimed to determine whether β-lactam antibiotic dosing in critically ill patients achieves concentrations associated with maximal activity and whether antibiotic concentrations affect patient outcome. Methods. This was a prospective, multinational pharmacokinetic point-prevalence study including 8 β-lactam antibiotics. Two blood samples were taken from each patient during a single dosing interval. The primary pharmacokinetic/pharmacodynamic targets were free antibiotic concentrations above the minimum inhibitory concentration (MIC) of the pathogen at both 50% (50% f T> MIC ) and 100% (100% f T> MIC ) of the dosing interval. We used skewed logistic regression to describe the effect of antibiotic exposure on patient outcome. Results. We included 384 patients (361 evaluable patients) across 68 hospitals. The median age was 61 (interquartile range [IQR], 48–73) years, the median Acute Physiology and Chronic Health Evaluation II score was 18 (IQR, 14–24), and 65% of patients were male. Of the 248 patients treated for infection, 16% did not achieve 50% f T> MIC and these patients were 32% less likely to have a positive clinical outcome (odds ratio [OR], 0.68; P=.009). Positive clinical outcome was associated with increasing 50% f T>MIC and 100% f T> MIC ratios (OR, 1.02 and 1.56, respectively; P<.03), with significant interaction with sickness severity status. Conclusions. Infected critically ill patients may have adverse outcomes as a result of inadeqaute antibiotic exposure; a paradigm change to more personalized antibiotic dosing may be necessary to improve outcomes for these most seriously ill patients.</abstract><cop>United States</cop><pub>OXFORD UNIVERSITY PRESS</pub><pmid>24429437</pmid><doi>10.1093/cid/ciu027</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - pharmacokinetics Antibiotics ARTICLES AND COMMENTARIES Bacterial Infections - drug therapy beta-Lactams - administration & dosage beta-Lactams - pharmacokinetics Blood Chemical Analysis Critical care Critical Illness Female Health care industry Health outcomes Hospitals Humans Infections Intensive Care Units International Cooperation Male Microbial Sensitivity Tests Middle Aged Models, Statistical Pathogens Pharmacokinetics Prospective Studies Treatment Outcome University hospitals |
title | DALI: Defining Antibiotic Levels in Intensive Care Unit Patients: Are Current β-Lactam Antibiotic Doses Sufficient for Critically Ill Patients? |
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