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Is diabetes a risk factor for central venous access port-related bloodstream infection in oncological patients?
It was a dogma that patients with diabetes mellitus (DM) are at increased risk of infection or death associated with an infection. However, in cancer patients, this has not been well investigated. The aim was to investigate whether diabetic patients with cancer are at high risk of central venous acc...
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Published in: | European journal of clinical microbiology & infectious diseases 2013, Vol.32 (1), p.133-138 |
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container_title | European journal of clinical microbiology & infectious diseases |
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creator | Touré, A. Vanhems, P. Lombard-Bohas, C. Souquet, J.-C. Lauverjat, M. Chambrier, C. |
description | It was a dogma that patients with diabetes mellitus (DM) are at increased risk of infection or death associated with an infection. However, in cancer patients, this has not been well investigated. The aim was to investigate whether diabetic patients with cancer are at high risk of central venous access port (CVAP)-related bloodstream infection (BSI), and to analyse mortality after CVAP-BSI. A total of 17 patients with type 1 DM (T1DM), 66 with type 2 DM (T2DM) and 307 non-diabetic patients were included. Each patient was followed up until the first late CVAP-BSI or for a maximum for 1 year in the absence of a CVAP-BSI. Fifty-three CVAP-BSIs occurred in 66,528 catheter-days. The cumulative incidence of CVAP-BSI was not higher in T1DM (5.9 %;
p
= 0.17) and T2DM (19.7 %;
p
= 0.70) compared with the non-diabetic patients (12.7 %). However, in patients with CVAP-BSI, the 1-month crude mortality rate was higher in DM patients (42.9 % vs. 15.4 %;
p
= 0.04), whereas the mortality in patients without CVAP-BSI was similar in both groups of patients (19.8 % vs. 17.1 %;
p
= 0.58). Of the 12 deaths that occurred within 1 month of CVAP-BSI, 16.66 % was attributable to CVAP-BSI. The predictive factor of 1-month mortality was DM (
p
= 0.04). Parenteral nutrition (PN) was independently associated with CVAP-BSI in diabetic patients (
p
= 0.001). In this study, diabetes did not increase the risk of CVAP-BSI, but mortality was higher in diabetic patients who had a CVAP-BSI. This suggests, in addition to medical treatment, CVAP should be withdrawn after infection onset. |
doi_str_mv | 10.1007/s10096-012-1728-1 |
format | article |
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p
= 0.17) and T2DM (19.7 %;
p
= 0.70) compared with the non-diabetic patients (12.7 %). However, in patients with CVAP-BSI, the 1-month crude mortality rate was higher in DM patients (42.9 % vs. 15.4 %;
p
= 0.04), whereas the mortality in patients without CVAP-BSI was similar in both groups of patients (19.8 % vs. 17.1 %;
p
= 0.58). Of the 12 deaths that occurred within 1 month of CVAP-BSI, 16.66 % was attributable to CVAP-BSI. The predictive factor of 1-month mortality was DM (
p
= 0.04). Parenteral nutrition (PN) was independently associated with CVAP-BSI in diabetic patients (
p
= 0.001). In this study, diabetes did not increase the risk of CVAP-BSI, but mortality was higher in diabetic patients who had a CVAP-BSI. This suggests, in addition to medical treatment, CVAP should be withdrawn after infection onset.</description><identifier>ISSN: 0934-9723</identifier><identifier>EISSN: 1435-4373</identifier><identifier>DOI: 10.1007/s10096-012-1728-1</identifier><identifier>PMID: 22930406</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Aged ; Bacterial diseases ; Bacterial sepsis ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Body mass index ; Catheter-Related Infections ; Catheter-Related Infections - epidemiology ; Catheter-Related Infections - mortality ; Catheterization, Central Venous ; Catheterization, Central Venous - adverse effects ; Catheters ; Chemotherapy ; Diabetes ; Diabetes Complications ; Diabetes. Impaired glucose tolerance ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Epidemiology ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Follow-Up Studies ; Health risks ; Hospitals ; Human bacterial diseases ; Humans ; Incidence ; Infections ; Infectious diseases ; Intensive care ; Internal Medicine ; Life Sciences ; Male ; Medical instruments ; Medical Microbiology ; Medical sciences ; Medical treatment ; Middle Aged ; Mortality ; Neoplasms ; Neoplasms - complications ; Pancreatic cancer ; Parenteral nutrition ; Patients ; Risk Assessment ; Risk Factors ; Sepsis ; Sepsis - epidemiology ; Sepsis - mortality ; Survival Analysis ; Venous access</subject><ispartof>European journal of clinical microbiology & infectious diseases, 2013, Vol.32 (1), p.133-138</ispartof><rights>Springer-Verlag 2012</rights><rights>2014 INIST-CNRS</rights><rights>Springer-Verlag Berlin Heidelberg 2013</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-9524835cc4ba88abc702d12488e7bb24aaface972a1b52a0a0be63f3291eb3803</citedby><cites>FETCH-LOGICAL-c436t-9524835cc4ba88abc702d12488e7bb24aaface972a1b52a0a0be63f3291eb3803</cites><orcidid>0000-0003-3188-1456</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27588255$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22930406$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00965791$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Touré, A.</creatorcontrib><creatorcontrib>Vanhems, P.</creatorcontrib><creatorcontrib>Lombard-Bohas, C.</creatorcontrib><creatorcontrib>Souquet, J.-C.</creatorcontrib><creatorcontrib>Lauverjat, M.</creatorcontrib><creatorcontrib>Chambrier, C.</creatorcontrib><title>Is diabetes a risk factor for central venous access port-related bloodstream infection in oncological patients?</title><title>European journal of clinical microbiology & infectious diseases</title><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><description>It was a dogma that patients with diabetes mellitus (DM) are at increased risk of infection or death associated with an infection. However, in cancer patients, this has not been well investigated. The aim was to investigate whether diabetic patients with cancer are at high risk of central venous access port (CVAP)-related bloodstream infection (BSI), and to analyse mortality after CVAP-BSI. A total of 17 patients with type 1 DM (T1DM), 66 with type 2 DM (T2DM) and 307 non-diabetic patients were included. Each patient was followed up until the first late CVAP-BSI or for a maximum for 1 year in the absence of a CVAP-BSI. Fifty-three CVAP-BSIs occurred in 66,528 catheter-days. The cumulative incidence of CVAP-BSI was not higher in T1DM (5.9 %;
p
= 0.17) and T2DM (19.7 %;
p
= 0.70) compared with the non-diabetic patients (12.7 %). However, in patients with CVAP-BSI, the 1-month crude mortality rate was higher in DM patients (42.9 % vs. 15.4 %;
p
= 0.04), whereas the mortality in patients without CVAP-BSI was similar in both groups of patients (19.8 % vs. 17.1 %;
p
= 0.58). Of the 12 deaths that occurred within 1 month of CVAP-BSI, 16.66 % was attributable to CVAP-BSI. The predictive factor of 1-month mortality was DM (
p
= 0.04). Parenteral nutrition (PN) was independently associated with CVAP-BSI in diabetic patients (
p
= 0.001). In this study, diabetes did not increase the risk of CVAP-BSI, but mortality was higher in diabetic patients who had a CVAP-BSI. This suggests, in addition to medical treatment, CVAP should be withdrawn after infection onset.</description><subject>Aged</subject><subject>Bacterial diseases</subject><subject>Bacterial sepsis</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Body mass index</subject><subject>Catheter-Related Infections</subject><subject>Catheter-Related Infections - epidemiology</subject><subject>Catheter-Related Infections - mortality</subject><subject>Catheterization, Central Venous</subject><subject>Catheterization, Central Venous - adverse effects</subject><subject>Catheters</subject><subject>Chemotherapy</subject><subject>Diabetes</subject><subject>Diabetes Complications</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Epidemiology</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Health risks</subject><subject>Hospitals</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Incidence</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Intensive care</subject><subject>Internal Medicine</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical instruments</subject><subject>Medical Microbiology</subject><subject>Medical sciences</subject><subject>Medical treatment</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Neoplasms</subject><subject>Neoplasms - complications</subject><subject>Pancreatic cancer</subject><subject>Parenteral nutrition</subject><subject>Patients</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Sepsis</subject><subject>Sepsis - epidemiology</subject><subject>Sepsis - mortality</subject><subject>Survival Analysis</subject><subject>Venous access</subject><issn>0934-9723</issn><issn>1435-4373</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kU2LFDEQhoMo7uzoD_AiDSLooTUfnU73SZbFdRcGvOg5VNLVa9aezphkFvz3VtPjKoKHfFB5qvJWvYy9EPyd4Ny8z7T3bc2FrIWRXS0esY1olK4bZdRjtuG9aureSHXGznO-45TTGfOUnUnZK97wdsPiTa6GAA4L5gqqFPL3agRfYqpGWh7nkmCq7nGORwK8x5yrQ0ylTjhBwaFyU4xDLglhX4V5RF9CnOlWxdnHKd4GT_kHKIFK5Q_P2JMRpozPT-eWfb36-OXyut59_nRzebGrfaPaUvdaNp3S3jcOug6cN1wOgmIdGudkA0AikVoD4bQEDtxhq0Yle4FOdVxt2du17jeY7CGFPaSfNkKw1xc7u8SWyWnTi3tB7JuVPaT444i52H3IHqcJZqSurZBGaS0a3RL66h_0Lh7TTJ0sFFdatjT6LRMr5VPMOeH4oEBwuzhnV-csOWcX5-wi4uWp8tHtcXjI-G0VAa9PAGQa6Zhg9iH_4YzuOqk1cXLlMj3Nt5j-kvjf338Bz7KwDg</recordid><startdate>2013</startdate><enddate>2013</enddate><creator>Touré, A.</creator><creator>Vanhems, P.</creator><creator>Lombard-Bohas, C.</creator><creator>Souquet, J.-C.</creator><creator>Lauverjat, M.</creator><creator>Chambrier, C.</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><general>Springer Verlag</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>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-3188-1456</orcidid></search><sort><creationdate>2013</creationdate><title>Is diabetes a risk factor for central venous access port-related bloodstream infection in oncological patients?</title><author>Touré, A. ; Vanhems, P. ; Lombard-Bohas, C. ; Souquet, J.-C. ; Lauverjat, M. ; Chambrier, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-9524835cc4ba88abc702d12488e7bb24aaface972a1b52a0a0be63f3291eb3803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Bacterial diseases</topic><topic>Bacterial sepsis</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Body mass index</topic><topic>Catheter-Related Infections</topic><topic>Catheter-Related Infections - epidemiology</topic><topic>Catheter-Related Infections - mortality</topic><topic>Catheterization, Central Venous</topic><topic>Catheterization, Central Venous - adverse effects</topic><topic>Catheters</topic><topic>Chemotherapy</topic><topic>Diabetes</topic><topic>Diabetes Complications</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Epidemiology</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Health risks</topic><topic>Hospitals</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Incidence</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Intensive care</topic><topic>Internal Medicine</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical instruments</topic><topic>Medical Microbiology</topic><topic>Medical sciences</topic><topic>Medical treatment</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Neoplasms</topic><topic>Neoplasms - complications</topic><topic>Pancreatic cancer</topic><topic>Parenteral nutrition</topic><topic>Patients</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Sepsis</topic><topic>Sepsis - epidemiology</topic><topic>Sepsis - mortality</topic><topic>Survival Analysis</topic><topic>Venous access</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Touré, A.</creatorcontrib><creatorcontrib>Vanhems, P.</creatorcontrib><creatorcontrib>Lombard-Bohas, C.</creatorcontrib><creatorcontrib>Souquet, J.-C.</creatorcontrib><creatorcontrib>Lauverjat, M.</creatorcontrib><creatorcontrib>Chambrier, C.</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>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>European journal of clinical microbiology & infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Touré, A.</au><au>Vanhems, P.</au><au>Lombard-Bohas, C.</au><au>Souquet, J.-C.</au><au>Lauverjat, M.</au><au>Chambrier, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Is diabetes a risk factor for central venous access port-related bloodstream infection in oncological patients?</atitle><jtitle>European journal of clinical microbiology & infectious diseases</jtitle><stitle>Eur J Clin Microbiol Infect Dis</stitle><addtitle>Eur J Clin Microbiol Infect Dis</addtitle><date>2013</date><risdate>2013</risdate><volume>32</volume><issue>1</issue><spage>133</spage><epage>138</epage><pages>133-138</pages><issn>0934-9723</issn><eissn>1435-4373</eissn><abstract>It was a dogma that patients with diabetes mellitus (DM) are at increased risk of infection or death associated with an infection. However, in cancer patients, this has not been well investigated. The aim was to investigate whether diabetic patients with cancer are at high risk of central venous access port (CVAP)-related bloodstream infection (BSI), and to analyse mortality after CVAP-BSI. A total of 17 patients with type 1 DM (T1DM), 66 with type 2 DM (T2DM) and 307 non-diabetic patients were included. Each patient was followed up until the first late CVAP-BSI or for a maximum for 1 year in the absence of a CVAP-BSI. Fifty-three CVAP-BSIs occurred in 66,528 catheter-days. The cumulative incidence of CVAP-BSI was not higher in T1DM (5.9 %;
p
= 0.17) and T2DM (19.7 %;
p
= 0.70) compared with the non-diabetic patients (12.7 %). However, in patients with CVAP-BSI, the 1-month crude mortality rate was higher in DM patients (42.9 % vs. 15.4 %;
p
= 0.04), whereas the mortality in patients without CVAP-BSI was similar in both groups of patients (19.8 % vs. 17.1 %;
p
= 0.58). Of the 12 deaths that occurred within 1 month of CVAP-BSI, 16.66 % was attributable to CVAP-BSI. The predictive factor of 1-month mortality was DM (
p
= 0.04). Parenteral nutrition (PN) was independently associated with CVAP-BSI in diabetic patients (
p
= 0.001). In this study, diabetes did not increase the risk of CVAP-BSI, but mortality was higher in diabetic patients who had a CVAP-BSI. This suggests, in addition to medical treatment, CVAP should be withdrawn after infection onset.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>22930406</pmid><doi>10.1007/s10096-012-1728-1</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-3188-1456</orcidid></addata></record> |
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source | Springer Nature |
subjects | Aged Bacterial diseases Bacterial sepsis Biological and medical sciences Biomedical and Life Sciences Biomedicine Body mass index Catheter-Related Infections Catheter-Related Infections - epidemiology Catheter-Related Infections - mortality Catheterization, Central Venous Catheterization, Central Venous - adverse effects Catheters Chemotherapy Diabetes Diabetes Complications Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Epidemiology Etiopathogenesis. Screening. Investigations. Target tissue resistance Female Follow-Up Studies Health risks Hospitals Human bacterial diseases Humans Incidence Infections Infectious diseases Intensive care Internal Medicine Life Sciences Male Medical instruments Medical Microbiology Medical sciences Medical treatment Middle Aged Mortality Neoplasms Neoplasms - complications Pancreatic cancer Parenteral nutrition Patients Risk Assessment Risk Factors Sepsis Sepsis - epidemiology Sepsis - mortality Survival Analysis Venous access |
title | Is diabetes a risk factor for central venous access port-related bloodstream infection in oncological patients? |
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