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Clinical and microbiological factors associated with early patient mortality from methicillin-resistant Staphylococcus aureus bacteremia
Methicillin-resistant Staphylococcus aureus bacteremia (MRSAB) is a major bloodstream infection with a high mortality rate. Identification of factors associated with early mortality in MRSAB patients would be useful for predicting prognosis and developing new therapeutic options. A prospective cohor...
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Published in: | The Korean journal of internal medicine 2019-01, Vol.34 (1), p.184-194 |
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creator | Kim, Tark Chong, Yong Pil Park, Ki-Ho Bang, Kyung Mi Park, Su-Jin Kim, Sung-Han Jeong, Jin-Yong Lee, Sang-Oh Choi, Sang-Ho Woo, Jun Hee Kim, Yang Soo |
description | Methicillin-resistant Staphylococcus aureus bacteremia (MRSAB) is a major bloodstream infection with a high mortality rate. Identification of factors associated with early mortality in MRSAB patients would be useful for predicting prognosis and developing new therapeutic options.
A prospective cohort of MRSAB patients was examined between August 2008 and June 2011. Early and late mortality was defined as death within 2 and 28 days of blood culture, respectively. The clinical and microbiological characteristics in the early and late mortality and survival groups were compared. Risk factors associated with severe sepsis or septic shock were also investigated.
A total of 385 adult MRSAB patients whose S. aureus isolates were available were enrolled; of these patients, 25 patients (6.5%) and 50 (13%) died early and late, respectively. Compared with both the late-mortality group and the survival group, severe sepsis or septic shock was a statistically significant independent risk factor associated with early mortality. Rapidly or ultimately fatal McCabe and Jackson classification (adjusted odds ratio [aOR], 1.94; 95% confidence interval [CI], 1.25 to 3.02) and pneumonia (aOR, 2.04; 95% CI, 1.03 to 4.02) were independently associated with severe sepsis or septic shock. A vancomycin minimum inhibitory concentration (MIC) ≥ 1.5 μg/mL was associated with a reduced incidence of severe sepsis or septic shock (aOR, 0.53; 95% CI, 0.34 to 0.84).
Severity of illness seems to be the most important risk factor associated with early mortality in MRSAB. Although vancomycin MIC was not independently associated with early mortality, reduced vancomycin susceptibility appears to be linked to reduced disease severity. |
doi_str_mv | 10.3904/kjim.2016.351 |
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A prospective cohort of MRSAB patients was examined between August 2008 and June 2011. Early and late mortality was defined as death within 2 and 28 days of blood culture, respectively. The clinical and microbiological characteristics in the early and late mortality and survival groups were compared. Risk factors associated with severe sepsis or septic shock were also investigated.
A total of 385 adult MRSAB patients whose S. aureus isolates were available were enrolled; of these patients, 25 patients (6.5%) and 50 (13%) died early and late, respectively. Compared with both the late-mortality group and the survival group, severe sepsis or septic shock was a statistically significant independent risk factor associated with early mortality. Rapidly or ultimately fatal McCabe and Jackson classification (adjusted odds ratio [aOR], 1.94; 95% confidence interval [CI], 1.25 to 3.02) and pneumonia (aOR, 2.04; 95% CI, 1.03 to 4.02) were independently associated with severe sepsis or septic shock. A vancomycin minimum inhibitory concentration (MIC) ≥ 1.5 μg/mL was associated with a reduced incidence of severe sepsis or septic shock (aOR, 0.53; 95% CI, 0.34 to 0.84).
Severity of illness seems to be the most important risk factor associated with early mortality in MRSAB. Although vancomycin MIC was not independently associated with early mortality, reduced vancomycin susceptibility appears to be linked to reduced disease severity.</description><identifier>ISSN: 1226-3303</identifier><identifier>EISSN: 2005-6648</identifier><identifier>DOI: 10.3904/kjim.2016.351</identifier><identifier>PMID: 28859468</identifier><language>eng</language><publisher>Korea (South): The Korean Association of Internal Medicine</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Algorithms ; bacteremia ; Bacteremia - drug therapy ; Bacteremia - microbiology ; Bacteremia - mortality ; Cohort Studies ; Female ; Genes, Bacterial ; Humans ; Male ; methicillin-resistant staphylococcus aureus ; Methicillin-Resistant Staphylococcus aureus - drug effects ; Methicillin-Resistant Staphylococcus aureus - genetics ; Methicillin-Resistant Staphylococcus aureus - pathogenicity ; Middle Aged ; mortality ; Multivariate Analysis ; Original ; Prospective Studies ; Republic of Korea - epidemiology ; Risk Factors ; Shock, Septic - drug therapy ; Shock, Septic - microbiology ; Shock, Septic - mortality ; Staphylococcal Infections - drug therapy ; Staphylococcal Infections - microbiology ; Staphylococcal Infections - mortality ; Time Factors ; Vancomycin - therapeutic use ; Vancomycin Resistance - genetics ; Virulence - genetics ; Young Adult</subject><ispartof>The Korean journal of internal medicine, 2019-01, Vol.34 (1), p.184-194</ispartof><rights>Copyright © 2019 The Korean Association of Internal Medicine 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-fef6ba964ee929d14ff2aaf01d09f3c3c60197aed928f45a1edad3af35bb95983</citedby><cites>FETCH-LOGICAL-c453t-fef6ba964ee929d14ff2aaf01d09f3c3c60197aed928f45a1edad3af35bb95983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325428/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325428/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28859468$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Tark</creatorcontrib><creatorcontrib>Chong, Yong Pil</creatorcontrib><creatorcontrib>Park, Ki-Ho</creatorcontrib><creatorcontrib>Bang, Kyung Mi</creatorcontrib><creatorcontrib>Park, Su-Jin</creatorcontrib><creatorcontrib>Kim, Sung-Han</creatorcontrib><creatorcontrib>Jeong, Jin-Yong</creatorcontrib><creatorcontrib>Lee, Sang-Oh</creatorcontrib><creatorcontrib>Choi, Sang-Ho</creatorcontrib><creatorcontrib>Woo, Jun Hee</creatorcontrib><creatorcontrib>Kim, Yang Soo</creatorcontrib><title>Clinical and microbiological factors associated with early patient mortality from methicillin-resistant Staphylococcus aureus bacteremia</title><title>The Korean journal of internal medicine</title><addtitle>Korean J Intern Med</addtitle><description>Methicillin-resistant Staphylococcus aureus bacteremia (MRSAB) is a major bloodstream infection with a high mortality rate. Identification of factors associated with early mortality in MRSAB patients would be useful for predicting prognosis and developing new therapeutic options.
A prospective cohort of MRSAB patients was examined between August 2008 and June 2011. Early and late mortality was defined as death within 2 and 28 days of blood culture, respectively. The clinical and microbiological characteristics in the early and late mortality and survival groups were compared. Risk factors associated with severe sepsis or septic shock were also investigated.
A total of 385 adult MRSAB patients whose S. aureus isolates were available were enrolled; of these patients, 25 patients (6.5%) and 50 (13%) died early and late, respectively. Compared with both the late-mortality group and the survival group, severe sepsis or septic shock was a statistically significant independent risk factor associated with early mortality. Rapidly or ultimately fatal McCabe and Jackson classification (adjusted odds ratio [aOR], 1.94; 95% confidence interval [CI], 1.25 to 3.02) and pneumonia (aOR, 2.04; 95% CI, 1.03 to 4.02) were independently associated with severe sepsis or septic shock. A vancomycin minimum inhibitory concentration (MIC) ≥ 1.5 μg/mL was associated with a reduced incidence of severe sepsis or septic shock (aOR, 0.53; 95% CI, 0.34 to 0.84).
Severity of illness seems to be the most important risk factor associated with early mortality in MRSAB. Although vancomycin MIC was not independently associated with early mortality, reduced vancomycin susceptibility appears to be linked to reduced disease severity.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Algorithms</subject><subject>bacteremia</subject><subject>Bacteremia - drug therapy</subject><subject>Bacteremia - microbiology</subject><subject>Bacteremia - mortality</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Genes, Bacterial</subject><subject>Humans</subject><subject>Male</subject><subject>methicillin-resistant staphylococcus aureus</subject><subject>Methicillin-Resistant Staphylococcus aureus - drug effects</subject><subject>Methicillin-Resistant Staphylococcus aureus - genetics</subject><subject>Methicillin-Resistant Staphylococcus aureus - pathogenicity</subject><subject>Middle Aged</subject><subject>mortality</subject><subject>Multivariate Analysis</subject><subject>Original</subject><subject>Prospective Studies</subject><subject>Republic of Korea - epidemiology</subject><subject>Risk Factors</subject><subject>Shock, Septic - drug therapy</subject><subject>Shock, Septic - microbiology</subject><subject>Shock, Septic - mortality</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcal Infections - mortality</subject><subject>Time Factors</subject><subject>Vancomycin - therapeutic use</subject><subject>Vancomycin Resistance - genetics</subject><subject>Virulence - genetics</subject><subject>Young Adult</subject><issn>1226-3303</issn><issn>2005-6648</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkk1vEzEQhlcIREPhyBXtkcsGf62zviChCEqlShyAszVrjxMH7zrYTlH-AT-7TlMqehpp_OiZkedtmreULLki4sOvnZ-WjFC55D191iwYIX0npRieNwvKmOw4J_yieZXzjhC5IgN_2VywYeiVkMOi-bsOfvYGQguzbSdvUhx9DHFz33NgSky5hZyj8VDQtn982bYIKRzbPRSPc2mnmAoEX46tS3FqJyxbb3yo4i5h9rlAhb4X2G-PIZpozKEaDwlrGesATDh5eN28cBAyvnmol83PL59_rL92N9-urtefbjojel46h06OoKRAVExZKpxjAI5QS5TjhhtJqFoBWsUGJ3qgaMFycLwfR9WrgV8212evjbDT--QnSEcdwev7RkwbDal4E1BzM64c0N6ujBTKjCMwVNQ5iwSZ6011fTy79odxQmvqZyQIT6RPX2a_1Zt4qyVnvWCnZd4_CFL8fcBc9OSzwRBgxnjImiouqaRE0Ip2Z7ReKOeE7nEMJfqUBH1Kgj4lQdckVP7d_7s90v9Oz-8AtOC2_g</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Kim, Tark</creator><creator>Chong, Yong Pil</creator><creator>Park, Ki-Ho</creator><creator>Bang, Kyung Mi</creator><creator>Park, Su-Jin</creator><creator>Kim, Sung-Han</creator><creator>Jeong, Jin-Yong</creator><creator>Lee, Sang-Oh</creator><creator>Choi, Sang-Ho</creator><creator>Woo, Jun Hee</creator><creator>Kim, Yang Soo</creator><general>The Korean Association of Internal Medicine</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><scope>DOA</scope></search><sort><creationdate>20190101</creationdate><title>Clinical and microbiological factors associated with early patient mortality from methicillin-resistant Staphylococcus aureus bacteremia</title><author>Kim, Tark ; Chong, Yong Pil ; Park, Ki-Ho ; Bang, Kyung Mi ; Park, Su-Jin ; Kim, Sung-Han ; Jeong, Jin-Yong ; Lee, Sang-Oh ; Choi, Sang-Ho ; Woo, Jun Hee ; Kim, Yang Soo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-fef6ba964ee929d14ff2aaf01d09f3c3c60197aed928f45a1edad3af35bb95983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Algorithms</topic><topic>bacteremia</topic><topic>Bacteremia - drug therapy</topic><topic>Bacteremia - microbiology</topic><topic>Bacteremia - mortality</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Genes, Bacterial</topic><topic>Humans</topic><topic>Male</topic><topic>methicillin-resistant staphylococcus aureus</topic><topic>Methicillin-Resistant Staphylococcus aureus - drug effects</topic><topic>Methicillin-Resistant Staphylococcus aureus - genetics</topic><topic>Methicillin-Resistant Staphylococcus aureus - pathogenicity</topic><topic>Middle Aged</topic><topic>mortality</topic><topic>Multivariate Analysis</topic><topic>Original</topic><topic>Prospective Studies</topic><topic>Republic of Korea - epidemiology</topic><topic>Risk Factors</topic><topic>Shock, Septic - drug therapy</topic><topic>Shock, Septic - microbiology</topic><topic>Shock, Septic - mortality</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcal Infections - microbiology</topic><topic>Staphylococcal Infections - mortality</topic><topic>Time Factors</topic><topic>Vancomycin - therapeutic use</topic><topic>Vancomycin Resistance - genetics</topic><topic>Virulence - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Tark</creatorcontrib><creatorcontrib>Chong, Yong Pil</creatorcontrib><creatorcontrib>Park, Ki-Ho</creatorcontrib><creatorcontrib>Bang, Kyung Mi</creatorcontrib><creatorcontrib>Park, Su-Jin</creatorcontrib><creatorcontrib>Kim, Sung-Han</creatorcontrib><creatorcontrib>Jeong, Jin-Yong</creatorcontrib><creatorcontrib>Lee, Sang-Oh</creatorcontrib><creatorcontrib>Choi, Sang-Ho</creatorcontrib><creatorcontrib>Woo, Jun Hee</creatorcontrib><creatorcontrib>Kim, Yang Soo</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><collection>DOAJ Directory of Open Access Journals</collection><jtitle>The Korean journal of internal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Tark</au><au>Chong, Yong Pil</au><au>Park, Ki-Ho</au><au>Bang, Kyung Mi</au><au>Park, Su-Jin</au><au>Kim, Sung-Han</au><au>Jeong, Jin-Yong</au><au>Lee, Sang-Oh</au><au>Choi, Sang-Ho</au><au>Woo, Jun Hee</au><au>Kim, Yang Soo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and microbiological factors associated with early patient mortality from methicillin-resistant Staphylococcus aureus bacteremia</atitle><jtitle>The Korean journal of internal medicine</jtitle><addtitle>Korean J Intern Med</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>34</volume><issue>1</issue><spage>184</spage><epage>194</epage><pages>184-194</pages><issn>1226-3303</issn><eissn>2005-6648</eissn><abstract>Methicillin-resistant Staphylococcus aureus bacteremia (MRSAB) is a major bloodstream infection with a high mortality rate. Identification of factors associated with early mortality in MRSAB patients would be useful for predicting prognosis and developing new therapeutic options.
A prospective cohort of MRSAB patients was examined between August 2008 and June 2011. Early and late mortality was defined as death within 2 and 28 days of blood culture, respectively. The clinical and microbiological characteristics in the early and late mortality and survival groups were compared. Risk factors associated with severe sepsis or septic shock were also investigated.
A total of 385 adult MRSAB patients whose S. aureus isolates were available were enrolled; of these patients, 25 patients (6.5%) and 50 (13%) died early and late, respectively. Compared with both the late-mortality group and the survival group, severe sepsis or septic shock was a statistically significant independent risk factor associated with early mortality. Rapidly or ultimately fatal McCabe and Jackson classification (adjusted odds ratio [aOR], 1.94; 95% confidence interval [CI], 1.25 to 3.02) and pneumonia (aOR, 2.04; 95% CI, 1.03 to 4.02) were independently associated with severe sepsis or septic shock. A vancomycin minimum inhibitory concentration (MIC) ≥ 1.5 μg/mL was associated with a reduced incidence of severe sepsis or septic shock (aOR, 0.53; 95% CI, 0.34 to 0.84).
Severity of illness seems to be the most important risk factor associated with early mortality in MRSAB. Although vancomycin MIC was not independently associated with early mortality, reduced vancomycin susceptibility appears to be linked to reduced disease severity.</abstract><cop>Korea (South)</cop><pub>The Korean Association of Internal Medicine</pub><pmid>28859468</pmid><doi>10.3904/kjim.2016.351</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Algorithms bacteremia Bacteremia - drug therapy Bacteremia - microbiology Bacteremia - mortality Cohort Studies Female Genes, Bacterial Humans Male methicillin-resistant staphylococcus aureus Methicillin-Resistant Staphylococcus aureus - drug effects Methicillin-Resistant Staphylococcus aureus - genetics Methicillin-Resistant Staphylococcus aureus - pathogenicity Middle Aged mortality Multivariate Analysis Original Prospective Studies Republic of Korea - epidemiology Risk Factors Shock, Septic - drug therapy Shock, Septic - microbiology Shock, Septic - mortality Staphylococcal Infections - drug therapy Staphylococcal Infections - microbiology Staphylococcal Infections - mortality Time Factors Vancomycin - therapeutic use Vancomycin Resistance - genetics Virulence - genetics Young Adult |
title | Clinical and microbiological factors associated with early patient mortality from methicillin-resistant Staphylococcus aureus bacteremia |
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