Prediction of Microbial Infection and Mortality in Medical Patients with Fever: Plasma Procalcitonin, Neutrophilic Elastase-α1-Antitrypsin, and Lactoferrin Compared with Clinical Variables
Fever suggests the likelihood of severe microbial infection. Abnormal temperature, tachycardia, tachypnea, and abnormal white blood cell counts define the systemic inflammatory response syndrome (SIRS). In 300 hospitalized medical patients with fever, we determined clinical variables and procalciton...
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Veröffentlicht in: | Clinical infectious diseases 1999-08, Vol.29 (2), p.398-407 |
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description | Fever suggests the likelihood of severe microbial infection. Abnormal temperature, tachycardia, tachypnea, and abnormal white blood cell counts define the systemic inflammatory response syndrome (SIRS). In 300 hospitalized medical patients with fever, we determined clinical variables and procalcitonin, elastase-a1-antitrypsin, and lactoferrin levels in plasma. Of the patients, 71% had clinical infection (by clinical judgment) and 44% had microbial infection (by microbiological testing). SIRS occurred in 95%, and the 28-day mortality rate was 9%. The sensitivity for predicting microbial infection, bacteremia, and mortality was less but the specificity was greater for supranormal procalcitonin, elastase-a1-antitrypsin, and lactoferrin levels than for SIRS. The area under the receiver operating characteristic curve (AUC) for microbial infection was higher for procalcitonin and elastase-a1-antitrypsin levels than for clinical variables and lactoferrin level. The AUC for bacteremia was also higher for inflammatory factors (>0.70; P < .001) than for clinical variables. The AUC for mortality (P < .05) was 0.79 for the respiratory rate, 0.69 for elastase-α1-antitrypsin level, 0.65 for heart rate, 0.61 for procalcitonin level, and 0.60 for white blood cell count. In febrile medical patients, plasma procalcitonin and elastase-α1-antitrypsin levels may predict microbial infection and bacteremia better than (and mortality as well as) do clinical symptoms. |
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The area under the receiver operating characteristic curve (AUC) for microbial infection was higher for procalcitonin and elastase-a1-antitrypsin levels than for clinical variables and lactoferrin level. The AUC for bacteremia was also higher for inflammatory factors (>0.70; P < .001) than for clinical variables. The AUC for mortality (P < .05) was 0.79 for the respiratory rate, 0.69 for elastase-α1-antitrypsin level, 0.65 for heart rate, 0.61 for procalcitonin level, and 0.60 for white blood cell count. 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J.</creatorcontrib><creatorcontrib>Groeneveld, A. B. Johan</creatorcontrib><creatorcontrib>Thijs, Lambertus G.</creatorcontrib><title>Prediction of Microbial Infection and Mortality in Medical Patients with Fever: Plasma Procalcitonin, Neutrophilic Elastase-α1-Antitrypsin, and Lactoferrin Compared with Clinical Variables</title><title>Clinical infectious diseases</title><addtitle>Clinical Infectious Diseases</addtitle><description>Fever suggests the likelihood of severe microbial infection. Abnormal temperature, tachycardia, tachypnea, and abnormal white blood cell counts define the systemic inflammatory response syndrome (SIRS). In 300 hospitalized medical patients with fever, we determined clinical variables and procalcitonin, elastase-a1-antitrypsin, and lactoferrin levels in plasma. Of the patients, 71% had clinical infection (by clinical judgment) and 44% had microbial infection (by microbiological testing). SIRS occurred in 95%, and the 28-day mortality rate was 9%. The sensitivity for predicting microbial infection, bacteremia, and mortality was less but the specificity was greater for supranormal procalcitonin, elastase-a1-antitrypsin, and lactoferrin levels than for SIRS. The area under the receiver operating characteristic curve (AUC) for microbial infection was higher for procalcitonin and elastase-a1-antitrypsin levels than for clinical variables and lactoferrin level. The AUC for bacteremia was also higher for inflammatory factors (>0.70; P < .001) than for clinical variables. The AUC for mortality (P < .05) was 0.79 for the respiratory rate, 0.69 for elastase-α1-antitrypsin level, 0.65 for heart rate, 0.61 for procalcitonin level, and 0.60 for white blood cell count. In febrile medical patients, plasma procalcitonin and elastase-α1-antitrypsin levels may predict microbial infection and bacteremia better than (and mortality as well as) do clinical symptoms.</description><subject>Bacteremia</subject><subject>Bacterial diseases</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Blood plasma</subject><subject>Clinical Articles</subject><subject>Fever</subject><subject>General aspects</subject><subject>Heart rate</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Mortality</subject><subject>Neutrophils</subject><subject>Sepsis</subject><subject>Systemic inflammatory response syndrome</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNo9js1O3TAQhaOqlUpp-wRdeNFlQ_0Xx-kOXUFBuoG7gAqxiSaJLYbm2pHt_tzH6gPwCjxTfQliNaM535xziuIjo0eMavW14pRz_qo4YJWoS1U17HXeaaVLqYV-W7yL8Z5SxjStDoqHTTAjDgm9I96SFofge4SJnDtrljO4kbQ-JJgw7Qg60u4_MrKBhMalSP5guiOn5rcJ38hmgrgFsgk-IwMm79B9IRfmVwp-vsMJB3KSkQTRlI__WHnsEqawm-Me20etYUjemhBy0spvZ8gFl4TVhO4p-AcEhH4y8X3xxsIUzYfneVhcn55crc7K9eX389XxukRWqVRCzRgIZZtGM9E3SlClZD30sgdVj0oKSi0Ha4dacj3qXgk7Gs6tNaO0xlpxWHxefGeIuYAN4AaM3RxwC2HXsYbz7JmxTwt2H5MPL7KUiupmL5eLjDGZvy8yhJ-dqkVddWc3t13dVjdXrWy6W_EfcouR2Q</recordid><startdate>19990801</startdate><enddate>19990801</enddate><creator>Bossink, Ailko W. J.</creator><creator>Groeneveld, A. B. Johan</creator><creator>Thijs, Lambertus G.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><scope>BSCLL</scope><scope>IQODW</scope></search><sort><creationdate>19990801</creationdate><title>Prediction of Microbial Infection and Mortality in Medical Patients with Fever: Plasma Procalcitonin, Neutrophilic Elastase-α1-Antitrypsin, and Lactoferrin Compared with Clinical Variables</title><author>Bossink, Ailko W. J. ; Groeneveld, A. B. Johan ; Thijs, Lambertus G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i156t-a711a36f99813b96306647cb4ba67d64300f2affc7428d8b63fde22ffed4feff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Bacteremia</topic><topic>Bacterial diseases</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Blood plasma</topic><topic>Clinical Articles</topic><topic>Fever</topic><topic>General aspects</topic><topic>Heart rate</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Mortality</topic><topic>Neutrophils</topic><topic>Sepsis</topic><topic>Systemic inflammatory response syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bossink, Ailko W. J.</creatorcontrib><creatorcontrib>Groeneveld, A. B. Johan</creatorcontrib><creatorcontrib>Thijs, Lambertus G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bossink, Ailko W. J.</au><au>Groeneveld, A. B. Johan</au><au>Thijs, Lambertus G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prediction of Microbial Infection and Mortality in Medical Patients with Fever: Plasma Procalcitonin, Neutrophilic Elastase-α1-Antitrypsin, and Lactoferrin Compared with Clinical Variables</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clinical Infectious Diseases</addtitle><date>1999-08-01</date><risdate>1999</risdate><volume>29</volume><issue>2</issue><spage>398</spage><epage>407</epage><pages>398-407</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Fever suggests the likelihood of severe microbial infection. Abnormal temperature, tachycardia, tachypnea, and abnormal white blood cell counts define the systemic inflammatory response syndrome (SIRS). In 300 hospitalized medical patients with fever, we determined clinical variables and procalcitonin, elastase-a1-antitrypsin, and lactoferrin levels in plasma. Of the patients, 71% had clinical infection (by clinical judgment) and 44% had microbial infection (by microbiological testing). SIRS occurred in 95%, and the 28-day mortality rate was 9%. The sensitivity for predicting microbial infection, bacteremia, and mortality was less but the specificity was greater for supranormal procalcitonin, elastase-a1-antitrypsin, and lactoferrin levels than for SIRS. The area under the receiver operating characteristic curve (AUC) for microbial infection was higher for procalcitonin and elastase-a1-antitrypsin levels than for clinical variables and lactoferrin level. The AUC for bacteremia was also higher for inflammatory factors (>0.70; P < .001) than for clinical variables. The AUC for mortality (P < .05) was 0.79 for the respiratory rate, 0.69 for elastase-α1-antitrypsin level, 0.65 for heart rate, 0.61 for procalcitonin level, and 0.60 for white blood cell count. In febrile medical patients, plasma procalcitonin and elastase-α1-antitrypsin levels may predict microbial infection and bacteremia better than (and mortality as well as) do clinical symptoms.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><doi>10.1086/520222</doi><tpages>10</tpages></addata></record> |
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subjects | Bacteremia Bacterial diseases Biological and medical sciences Blood Blood plasma Clinical Articles Fever General aspects Heart rate Infections Infectious diseases Medical sciences Mortality Neutrophils Sepsis Systemic inflammatory response syndrome |
title | Prediction of Microbial Infection and Mortality in Medical Patients with Fever: Plasma Procalcitonin, Neutrophilic Elastase-α1-Antitrypsin, and Lactoferrin Compared with Clinical Variables |
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