Procalcitonin vs C-Reactive Protein as Predictive Markers of Response to Antibiotic Therapy in Acute Exacerbations of COPD
Rational prescription of antibiotics in acute exacerbations of COPD (AECOPD) requires predictive markers. We aimed to analyze whether markers of systemic inflammation can predict response to antibiotics in AECOPD. We used data from 243 exacerbations out of 205 patients from a placebo-controlled tria...
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description | Rational prescription of antibiotics in acute exacerbations of COPD (AECOPD) requires predictive markers. We aimed to analyze whether markers of systemic inflammation can predict response to antibiotics in AECOPD.
We used data from 243 exacerbations out of 205 patients from a placebo-controlled trial on doxycycline in addition to systemic corticosteroids for AECOPD. Clinical and microbiologic response, serum C-reactive protein (CRP) level (cutoffs 5 and 50 mg/L), and serum procalcitonin level (PCT) (cutoffs 0.1 and 0.25 μg) were assessed.
Potential bacterial pathogens were identified in the majority of exacerbations (58%). We found a modest positive correlation between PCT and CRP (r = 0.46, P < .001). The majority of patients (75%) had low PCT levels, with mostly elevated CRP levels. Although CRP levels were higher in the presence of bacteria (median, 33.0 mg/L [interquartile range, 9.75-88.25] vs 17 mg/L [interquartile range, 5.0-61.0] [P = .004]), PCT levels were similar. PCT and CRP performed similarly as markers of clinical success, and we found a clinical success rate of 90% in patients with CRP ≤ 5 mg/L. A significant effect of doxycycline was observed in patients with a PCT level < .1 μg/L (treatment effect, 18.4%; P = .003). A gradually increasing treatment effect of antibiotics (6%, 10%, and 18%), although not significant, was found for patients with CRP values of ≤ 5, 6-50, and > 50 mg/L, respectively.
Contrary to the current literature, this study suggests that patients with low PCT values do benefit from antibiotics. CRP might be a more valuable marker in these patients. |
doi_str_mv | 10.1378/chest.09-2927 |
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We used data from 243 exacerbations out of 205 patients from a placebo-controlled trial on doxycycline in addition to systemic corticosteroids for AECOPD. Clinical and microbiologic response, serum C-reactive protein (CRP) level (cutoffs 5 and 50 mg/L), and serum procalcitonin level (PCT) (cutoffs 0.1 and 0.25 μg) were assessed.
Potential bacterial pathogens were identified in the majority of exacerbations (58%). We found a modest positive correlation between PCT and CRP (r = 0.46, P < .001). The majority of patients (75%) had low PCT levels, with mostly elevated CRP levels. Although CRP levels were higher in the presence of bacteria (median, 33.0 mg/L [interquartile range, 9.75-88.25] vs 17 mg/L [interquartile range, 5.0-61.0] [P = .004]), PCT levels were similar. PCT and CRP performed similarly as markers of clinical success, and we found a clinical success rate of 90% in patients with CRP ≤ 5 mg/L. A significant effect of doxycycline was observed in patients with a PCT level < .1 μg/L (treatment effect, 18.4%; P = .003). A gradually increasing treatment effect of antibiotics (6%, 10%, and 18%), although not significant, was found for patients with CRP values of ≤ 5, 6-50, and > 50 mg/L, respectively.
Contrary to the current literature, this study suggests that patients with low PCT values do benefit from antibiotics. CRP might be a more valuable marker in these patients.</description><identifier>ISSN: 0012-3692</identifier><identifier>EISSN: 1931-3543</identifier><identifier>DOI: 10.1378/chest.09-2927</identifier><identifier>PMID: 20576731</identifier><identifier>CODEN: CHETBF</identifier><language>eng</language><publisher>Northbrook, IL: American College of Chest Physicians</publisher><subject>Aged ; Anti-Bacterial Agents - therapeutic use ; Biological and medical sciences ; Biomarkers - blood ; C-Reactive Protein - metabolism ; Calcitonin - blood ; Calcitonin Gene-Related Peptide ; Cardiology. Vascular system ; Chronic obstructive pulmonary disease, asthma ; Doxycycline - therapeutic use ; Female ; Follow-Up Studies ; Glycoproteins ; Humans ; Male ; Medical sciences ; Nephelometry and Turbidimetry ; Pneumology ; Protein Precursors - blood ; Pulmonary Disease, Chronic Obstructive - blood ; Pulmonary Disease, Chronic Obstructive - drug therapy ; Pulmonary Disease, Chronic Obstructive - physiopathology ; Recurrence ; Retrospective Studies ; Treatment Outcome</subject><ispartof>Chest, 2010-11, Vol.138 (5), p.1108-1115</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c322t-8c83843616631a48fd69086c6c8e7c55647239caa6c3f5ad9e09bc24cb4d4c553</citedby><cites>FETCH-LOGICAL-c322t-8c83843616631a48fd69086c6c8e7c55647239caa6c3f5ad9e09bc24cb4d4c553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23382716$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20576731$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DANIELS, Johannes M. A</creatorcontrib><creatorcontrib>SCHOORL, Marianne</creatorcontrib><creatorcontrib>SNIJDERS, Dominic</creatorcontrib><creatorcontrib>KNOL, Dirk L</creatorcontrib><creatorcontrib>LUTTER, René</creatorcontrib><creatorcontrib>JANSEN, Henk M</creatorcontrib><creatorcontrib>BOERSMA, Wim G</creatorcontrib><title>Procalcitonin vs C-Reactive Protein as Predictive Markers of Response to Antibiotic Therapy in Acute Exacerbations of COPD</title><title>Chest</title><addtitle>Chest</addtitle><description>Rational prescription of antibiotics in acute exacerbations of COPD (AECOPD) requires predictive markers. We aimed to analyze whether markers of systemic inflammation can predict response to antibiotics in AECOPD.
We used data from 243 exacerbations out of 205 patients from a placebo-controlled trial on doxycycline in addition to systemic corticosteroids for AECOPD. Clinical and microbiologic response, serum C-reactive protein (CRP) level (cutoffs 5 and 50 mg/L), and serum procalcitonin level (PCT) (cutoffs 0.1 and 0.25 μg) were assessed.
Potential bacterial pathogens were identified in the majority of exacerbations (58%). We found a modest positive correlation between PCT and CRP (r = 0.46, P < .001). The majority of patients (75%) had low PCT levels, with mostly elevated CRP levels. Although CRP levels were higher in the presence of bacteria (median, 33.0 mg/L [interquartile range, 9.75-88.25] vs 17 mg/L [interquartile range, 5.0-61.0] [P = .004]), PCT levels were similar. PCT and CRP performed similarly as markers of clinical success, and we found a clinical success rate of 90% in patients with CRP ≤ 5 mg/L. A significant effect of doxycycline was observed in patients with a PCT level < .1 μg/L (treatment effect, 18.4%; P = .003). A gradually increasing treatment effect of antibiotics (6%, 10%, and 18%), although not significant, was found for patients with CRP values of ≤ 5, 6-50, and > 50 mg/L, respectively.
Contrary to the current literature, this study suggests that patients with low PCT values do benefit from antibiotics. CRP might be a more valuable marker in these patients.</description><subject>Aged</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>C-Reactive Protein - metabolism</subject><subject>Calcitonin - blood</subject><subject>Calcitonin Gene-Related Peptide</subject><subject>Cardiology. Vascular system</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Doxycycline - therapeutic use</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glycoproteins</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nephelometry and Turbidimetry</subject><subject>Pneumology</subject><subject>Protein Precursors - blood</subject><subject>Pulmonary Disease, Chronic Obstructive - blood</subject><subject>Pulmonary Disease, Chronic Obstructive - drug therapy</subject><subject>Pulmonary Disease, Chronic Obstructive - physiopathology</subject><subject>Recurrence</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><issn>0012-3692</issn><issn>1931-3543</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1vEzEQhi0EomnhyBX5gjhtsT27_jhGaSlIRa2qcl55Z2dVQ7IOtlNRfj0OCXCamXeemcPD2BspziUY-wEfKJdz4RrllHnGFtKBbKBr4TlbCCFVA9qpE3aa8zdRZ-n0S3aiRGe0Ablgv25TRL_GUOIcZv6Y-aq5I48lPBKvu0I19bm2NIZD-sWn75QyjxO_o7yNcyZeIl_OJQwhloD8_oGS3z7xerrEXSF--dMjpcGXUOn94erm9uIVezH5dabXx3rGvn68vF99aq5vrj6vltcNglKlsWjBtqCl1iB9a6dRO2E1arRksOt0axQ49F4jTJ0fHQk3oGpxaMe27uGMvT_83ab4Y1dt9ZuQkdZrP1Pc5d5opa2B1lSyOZCYYs6Jpn6bwsanp16Kfm-7_2O7F67f26782-Pn3bCh8R_9V28F3h0Bn6vlKfkZQ_7PAVhlpIbf3V6JDA</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>DANIELS, Johannes M. A</creator><creator>SCHOORL, Marianne</creator><creator>SNIJDERS, Dominic</creator><creator>KNOL, Dirk L</creator><creator>LUTTER, René</creator><creator>JANSEN, Henk M</creator><creator>BOERSMA, Wim G</creator><general>American College of Chest Physicians</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20101101</creationdate><title>Procalcitonin vs C-Reactive Protein as Predictive Markers of Response to Antibiotic Therapy in Acute Exacerbations of COPD</title><author>DANIELS, Johannes M. A ; SCHOORL, Marianne ; SNIJDERS, Dominic ; KNOL, Dirk L ; LUTTER, René ; JANSEN, Henk M ; BOERSMA, Wim G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c322t-8c83843616631a48fd69086c6c8e7c55647239caa6c3f5ad9e09bc24cb4d4c553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Aged</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>C-Reactive Protein - metabolism</topic><topic>Calcitonin - blood</topic><topic>Calcitonin Gene-Related Peptide</topic><topic>Cardiology. Vascular system</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>Doxycycline - therapeutic use</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Glycoproteins</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nephelometry and Turbidimetry</topic><topic>Pneumology</topic><topic>Protein Precursors - blood</topic><topic>Pulmonary Disease, Chronic Obstructive - blood</topic><topic>Pulmonary Disease, Chronic Obstructive - drug therapy</topic><topic>Pulmonary Disease, Chronic Obstructive - physiopathology</topic><topic>Recurrence</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DANIELS, Johannes M. A</creatorcontrib><creatorcontrib>SCHOORL, Marianne</creatorcontrib><creatorcontrib>SNIJDERS, Dominic</creatorcontrib><creatorcontrib>KNOL, Dirk L</creatorcontrib><creatorcontrib>LUTTER, René</creatorcontrib><creatorcontrib>JANSEN, Henk M</creatorcontrib><creatorcontrib>BOERSMA, Wim G</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Chest</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DANIELS, Johannes M. A</au><au>SCHOORL, Marianne</au><au>SNIJDERS, Dominic</au><au>KNOL, Dirk L</au><au>LUTTER, René</au><au>JANSEN, Henk M</au><au>BOERSMA, Wim G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Procalcitonin vs C-Reactive Protein as Predictive Markers of Response to Antibiotic Therapy in Acute Exacerbations of COPD</atitle><jtitle>Chest</jtitle><addtitle>Chest</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>138</volume><issue>5</issue><spage>1108</spage><epage>1115</epage><pages>1108-1115</pages><issn>0012-3692</issn><eissn>1931-3543</eissn><coden>CHETBF</coden><abstract>Rational prescription of antibiotics in acute exacerbations of COPD (AECOPD) requires predictive markers. We aimed to analyze whether markers of systemic inflammation can predict response to antibiotics in AECOPD.
We used data from 243 exacerbations out of 205 patients from a placebo-controlled trial on doxycycline in addition to systemic corticosteroids for AECOPD. Clinical and microbiologic response, serum C-reactive protein (CRP) level (cutoffs 5 and 50 mg/L), and serum procalcitonin level (PCT) (cutoffs 0.1 and 0.25 μg) were assessed.
Potential bacterial pathogens were identified in the majority of exacerbations (58%). We found a modest positive correlation between PCT and CRP (r = 0.46, P < .001). The majority of patients (75%) had low PCT levels, with mostly elevated CRP levels. Although CRP levels were higher in the presence of bacteria (median, 33.0 mg/L [interquartile range, 9.75-88.25] vs 17 mg/L [interquartile range, 5.0-61.0] [P = .004]), PCT levels were similar. PCT and CRP performed similarly as markers of clinical success, and we found a clinical success rate of 90% in patients with CRP ≤ 5 mg/L. A significant effect of doxycycline was observed in patients with a PCT level < .1 μg/L (treatment effect, 18.4%; P = .003). A gradually increasing treatment effect of antibiotics (6%, 10%, and 18%), although not significant, was found for patients with CRP values of ≤ 5, 6-50, and > 50 mg/L, respectively.
Contrary to the current literature, this study suggests that patients with low PCT values do benefit from antibiotics. CRP might be a more valuable marker in these patients.</abstract><cop>Northbrook, IL</cop><pub>American College of Chest Physicians</pub><pmid>20576731</pmid><doi>10.1378/chest.09-2927</doi><tpages>8</tpages></addata></record> |
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subjects | Aged Anti-Bacterial Agents - therapeutic use Biological and medical sciences Biomarkers - blood C-Reactive Protein - metabolism Calcitonin - blood Calcitonin Gene-Related Peptide Cardiology. Vascular system Chronic obstructive pulmonary disease, asthma Doxycycline - therapeutic use Female Follow-Up Studies Glycoproteins Humans Male Medical sciences Nephelometry and Turbidimetry Pneumology Protein Precursors - blood Pulmonary Disease, Chronic Obstructive - blood Pulmonary Disease, Chronic Obstructive - drug therapy Pulmonary Disease, Chronic Obstructive - physiopathology Recurrence Retrospective Studies Treatment Outcome |
title | Procalcitonin vs C-Reactive Protein as Predictive Markers of Response to Antibiotic Therapy in Acute Exacerbations of COPD |
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