Loading…
Selective digestive tract decontamination and selective oropharyngeal decontamination and antibiotic resistance in patients in intensive-care units: an open-label, clustered group-randomised, crossover study
Summary Background Previously, we assessed selective digestive tract decontamination (SDD) and selective oropharyngeal decontamination (SOD) on survival and prevention of bacteraemia in patients in intensive-care units. In this analysis, we aimed to assess effectiveness of these interventions for pr...
Saved in:
Published in: | The Lancet infectious diseases 2011-05, Vol.11 (5), p.372-380 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c476t-d0921210d61acee955e8015f87e153d8d8c12a03a2cfc980cebb96dfe4fd569f3 |
---|---|
cites | cdi_FETCH-LOGICAL-c476t-d0921210d61acee955e8015f87e153d8d8c12a03a2cfc980cebb96dfe4fd569f3 |
container_end_page | 380 |
container_issue | 5 |
container_start_page | 372 |
container_title | The Lancet infectious diseases |
container_volume | 11 |
creator | de Smet, Anne Marie GA, Dr Kluytmans, Jan AJW, Prof Blok, Hetty EM, MSc Mascini, Ellen M, MD Benus, Robin FJ, MD Bernards, Alexandra T, MD Kuijper, Ed J, MD Leverstein-van Hall, Maurine A, MD Jansz, Arjan R, MD de Jongh, Bartelt M, MD van Asselt, Gerard J, MD Frenay, Ine HME, MD Thijsen, Steven FT, MD Conijn, Simon NM Kaan, Jan A, MD Arends, Jan P, MD Sturm, Patrick DJ, MD Bootsma, Martin CJ, PhD Bonten, Marc JM, Prof |
description | Summary Background Previously, we assessed selective digestive tract decontamination (SDD) and selective oropharyngeal decontamination (SOD) on survival and prevention of bacteraemia in patients in intensive-care units. In this analysis, we aimed to assess effectiveness of these interventions for prevention of respiratory tract colonisation and bacteraemia with highly resistant microorganisms acquired in intensive-care units. Methods We did an open-label, clustered group-randomised, crossover study in 13 intensive-care units in the Netherlands between May, 2004, and July, 2006. Participants admitted to intensive-care units with an expected duration of mechanical ventilation of more than 48 h or an expected stay of more than 72 h received SOD (topical tobramycin, colistin, and amphotericin B in the oropharynx), SDD (SOD antibiotics in the oropharynx and stomach plus 4 days' intravenous cefotaxime), or standard care. The computer-randomised order of study regimens was applied by an independent clinical pharmacist who was masked to intensive-care-unit identity. We calculated crude odds ratios (95% CI) for rates of bacteraemia or respiratory tract colonisation with highly resistant microorganisms in patients who stayed in intensive-care units for more than 3 days (ie, acquired infection). This trial is registered at http://isrctn.org , number ISRCTN35176830. Findings Data were available for 5927 (>99%) of 5939 patients, of whom 5463 (92%) were in intensive-care units for more than 3 days. 239 (13%) of 1837 patients in standard care acquired bacteraemia after 3 days, compared with 158 (9%) of 1758 in SOD (odds ratio 0·66, 95% CI 0·53–0·82), and 124 (7%) of 1868 in SDD (0·48, 0·38–0·60). Eight patients acquired bacteraemia with highly resistant microorganisms during SDD, compared with 18 patients (with 19 episodes) during standard care (0·41, 0·18–0·94; rate reduction [RR] 59%, absolute risk reduction [ARR] 0·6%) and 20 during SOD (0·37, 0·16–0·85; RR 63%, ARR 0·7%). Of the patients staying in intensive-care units for more than 3 days, we obtained endotracheal aspirate cultures for 881 (49%) patients receiving standard care, 886 (50%) receiving SOD, and 828 (44%) receiving SDD. 128 (15%) patients acquired respiratory tract colonisation with highly resistant microorganisms during standard care, compared with 74 (8%) during SDD (0·58, 0·43–0·78; RR 38%, ARR 5·5%) and 88 (10%) during SOD (0·65, 0·49–0·87; RR 32%, ARR 4·6%). Acquired respiratory tract colonisation w |
doi_str_mv | 10.1016/S1473-3099(11)70035-4 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_864782058</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1473309911700354</els_id><sourcerecordid>2334639381</sourcerecordid><originalsourceid>FETCH-LOGICAL-c476t-d0921210d61acee955e8015f87e153d8d8c12a03a2cfc980cebb96dfe4fd569f3</originalsourceid><addsrcrecordid>eNqFkduKFDEQhhtR3IM-ghIEWQVbU93pkxeKLJ5gwYvV65BJqsesPUmbSg_MU_pKpnvGERbBqxTpr76u1J9lj4C_BA71q2sQTZmXvOueATxvOC-rXNzJTtO1yIWomrtLvUdOsjOiG86hAS7uZycFiIJ3vD3Nfl3jgDraLTJj10hLFYPSkRnU3kW1sU5F6x1TzjA60j748bsKO7dGNfyTVS7alfXRahaQLEXlNDLr2JgYdJHm2rqIjpIw1yogm5yN9Dq1Mj-iywe1wuEF08NEEQMatg5-GvOQ9H5jCU36FjyR32JgFCeze5Dd69VA-PBwnmffPrz_evkpv_ry8fPlu6tci6aOueFdAQVwU4PSiF1VYcuh6tsGoSpNa1oNheKlKnSvu5ZrXK262vQoelPVXV-eZxd77xj8zyntTaZ5NA6Dcugnkm0tmrbgVZvIJ7fIGz8Fl4abIWih4TNU7aHlOQF7OQa7SeuVwOWct1zylnOYEkAueUuR-h4f5NNqg-bY9SfgBDw9AIq0Gvq0Om3pLycKUYtyFr3dc5iWtrUYJOkUkkZjQ0pcGm__O8qbWwY9WGfTT3_gDun4aJBUSL6XzA6AxSDK3_2k4ro</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>864181708</pqid></control><display><type>article</type><title>Selective digestive tract decontamination and selective oropharyngeal decontamination and antibiotic resistance in patients in intensive-care units: an open-label, clustered group-randomised, crossover study</title><source>ScienceDirect Freedom Collection</source><creator>de Smet, Anne Marie GA, Dr ; Kluytmans, Jan AJW, Prof ; Blok, Hetty EM, MSc ; Mascini, Ellen M, MD ; Benus, Robin FJ, MD ; Bernards, Alexandra T, MD ; Kuijper, Ed J, MD ; Leverstein-van Hall, Maurine A, MD ; Jansz, Arjan R, MD ; de Jongh, Bartelt M, MD ; van Asselt, Gerard J, MD ; Frenay, Ine HME, MD ; Thijsen, Steven FT, MD ; Conijn, Simon NM ; Kaan, Jan A, MD ; Arends, Jan P, MD ; Sturm, Patrick DJ, MD ; Bootsma, Martin CJ, PhD ; Bonten, Marc JM, Prof</creator><creatorcontrib>de Smet, Anne Marie GA, Dr ; Kluytmans, Jan AJW, Prof ; Blok, Hetty EM, MSc ; Mascini, Ellen M, MD ; Benus, Robin FJ, MD ; Bernards, Alexandra T, MD ; Kuijper, Ed J, MD ; Leverstein-van Hall, Maurine A, MD ; Jansz, Arjan R, MD ; de Jongh, Bartelt M, MD ; van Asselt, Gerard J, MD ; Frenay, Ine HME, MD ; Thijsen, Steven FT, MD ; Conijn, Simon NM ; Kaan, Jan A, MD ; Arends, Jan P, MD ; Sturm, Patrick DJ, MD ; Bootsma, Martin CJ, PhD ; Bonten, Marc JM, Prof</creatorcontrib><description>Summary Background Previously, we assessed selective digestive tract decontamination (SDD) and selective oropharyngeal decontamination (SOD) on survival and prevention of bacteraemia in patients in intensive-care units. In this analysis, we aimed to assess effectiveness of these interventions for prevention of respiratory tract colonisation and bacteraemia with highly resistant microorganisms acquired in intensive-care units. Methods We did an open-label, clustered group-randomised, crossover study in 13 intensive-care units in the Netherlands between May, 2004, and July, 2006. Participants admitted to intensive-care units with an expected duration of mechanical ventilation of more than 48 h or an expected stay of more than 72 h received SOD (topical tobramycin, colistin, and amphotericin B in the oropharynx), SDD (SOD antibiotics in the oropharynx and stomach plus 4 days' intravenous cefotaxime), or standard care. The computer-randomised order of study regimens was applied by an independent clinical pharmacist who was masked to intensive-care-unit identity. We calculated crude odds ratios (95% CI) for rates of bacteraemia or respiratory tract colonisation with highly resistant microorganisms in patients who stayed in intensive-care units for more than 3 days (ie, acquired infection). This trial is registered at http://isrctn.org , number ISRCTN35176830. Findings Data were available for 5927 (>99%) of 5939 patients, of whom 5463 (92%) were in intensive-care units for more than 3 days. 239 (13%) of 1837 patients in standard care acquired bacteraemia after 3 days, compared with 158 (9%) of 1758 in SOD (odds ratio 0·66, 95% CI 0·53–0·82), and 124 (7%) of 1868 in SDD (0·48, 0·38–0·60). Eight patients acquired bacteraemia with highly resistant microorganisms during SDD, compared with 18 patients (with 19 episodes) during standard care (0·41, 0·18–0·94; rate reduction [RR] 59%, absolute risk reduction [ARR] 0·6%) and 20 during SOD (0·37, 0·16–0·85; RR 63%, ARR 0·7%). Of the patients staying in intensive-care units for more than 3 days, we obtained endotracheal aspirate cultures for 881 (49%) patients receiving standard care, 886 (50%) receiving SOD, and 828 (44%) receiving SDD. 128 (15%) patients acquired respiratory tract colonisation with highly resistant microorganisms during standard care, compared with 74 (8%) during SDD (0·58, 0·43–0·78; RR 38%, ARR 5·5%) and 88 (10%) during SOD (0·65, 0·49–0·87; RR 32%, ARR 4·6%). Acquired respiratory tract colonisation with Gram-negative bacteria or cefotaxime-resistant and colistin-resistant pathogens was lowest during SDD. Interpretation Widespread use of SDD and SOD in intensive-care units with low levels of antibiotic resistance is justified. Funding None.</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(11)70035-4</identifier><identifier>PMID: 21420908</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Anti-Bacterial Agents - pharmacology ; Antibacterial agents ; Antibiotic resistance ; Antibiotics ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Antifungal Agents - pharmacology ; Bacteria ; Bacteria - drug effects ; Biological and medical sciences ; Colonization ; Cross-Over Studies ; Decontamination ; Decontamination - methods ; Drug Resistance, Bacterial ; Drug Resistance, Fungal ; Epidemiology. Vaccinations ; Gastrointestinal Tract - microbiology ; General aspects ; Humans ; Infectious Disease ; Infectious diseases ; Intensive Care Units ; Medical sciences ; Microorganisms ; Oropharynx - microbiology ; Pharmacology. Drug treatments ; Prevention ; Respiratory tract</subject><ispartof>The Lancet infectious diseases, 2011-05, Vol.11 (5), p.372-380</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited May 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-d0921210d61acee955e8015f87e153d8d8c12a03a2cfc980cebb96dfe4fd569f3</citedby><cites>FETCH-LOGICAL-c476t-d0921210d61acee955e8015f87e153d8d8c12a03a2cfc980cebb96dfe4fd569f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24246434$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21420908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Smet, Anne Marie GA, Dr</creatorcontrib><creatorcontrib>Kluytmans, Jan AJW, Prof</creatorcontrib><creatorcontrib>Blok, Hetty EM, MSc</creatorcontrib><creatorcontrib>Mascini, Ellen M, MD</creatorcontrib><creatorcontrib>Benus, Robin FJ, MD</creatorcontrib><creatorcontrib>Bernards, Alexandra T, MD</creatorcontrib><creatorcontrib>Kuijper, Ed J, MD</creatorcontrib><creatorcontrib>Leverstein-van Hall, Maurine A, MD</creatorcontrib><creatorcontrib>Jansz, Arjan R, MD</creatorcontrib><creatorcontrib>de Jongh, Bartelt M, MD</creatorcontrib><creatorcontrib>van Asselt, Gerard J, MD</creatorcontrib><creatorcontrib>Frenay, Ine HME, MD</creatorcontrib><creatorcontrib>Thijsen, Steven FT, MD</creatorcontrib><creatorcontrib>Conijn, Simon NM</creatorcontrib><creatorcontrib>Kaan, Jan A, MD</creatorcontrib><creatorcontrib>Arends, Jan P, MD</creatorcontrib><creatorcontrib>Sturm, Patrick DJ, MD</creatorcontrib><creatorcontrib>Bootsma, Martin CJ, PhD</creatorcontrib><creatorcontrib>Bonten, Marc JM, Prof</creatorcontrib><title>Selective digestive tract decontamination and selective oropharyngeal decontamination and antibiotic resistance in patients in intensive-care units: an open-label, clustered group-randomised, crossover study</title><title>The Lancet infectious diseases</title><addtitle>Lancet Infect Dis</addtitle><description>Summary Background Previously, we assessed selective digestive tract decontamination (SDD) and selective oropharyngeal decontamination (SOD) on survival and prevention of bacteraemia in patients in intensive-care units. In this analysis, we aimed to assess effectiveness of these interventions for prevention of respiratory tract colonisation and bacteraemia with highly resistant microorganisms acquired in intensive-care units. Methods We did an open-label, clustered group-randomised, crossover study in 13 intensive-care units in the Netherlands between May, 2004, and July, 2006. Participants admitted to intensive-care units with an expected duration of mechanical ventilation of more than 48 h or an expected stay of more than 72 h received SOD (topical tobramycin, colistin, and amphotericin B in the oropharynx), SDD (SOD antibiotics in the oropharynx and stomach plus 4 days' intravenous cefotaxime), or standard care. The computer-randomised order of study regimens was applied by an independent clinical pharmacist who was masked to intensive-care-unit identity. We calculated crude odds ratios (95% CI) for rates of bacteraemia or respiratory tract colonisation with highly resistant microorganisms in patients who stayed in intensive-care units for more than 3 days (ie, acquired infection). This trial is registered at http://isrctn.org , number ISRCTN35176830. Findings Data were available for 5927 (>99%) of 5939 patients, of whom 5463 (92%) were in intensive-care units for more than 3 days. 239 (13%) of 1837 patients in standard care acquired bacteraemia after 3 days, compared with 158 (9%) of 1758 in SOD (odds ratio 0·66, 95% CI 0·53–0·82), and 124 (7%) of 1868 in SDD (0·48, 0·38–0·60). Eight patients acquired bacteraemia with highly resistant microorganisms during SDD, compared with 18 patients (with 19 episodes) during standard care (0·41, 0·18–0·94; rate reduction [RR] 59%, absolute risk reduction [ARR] 0·6%) and 20 during SOD (0·37, 0·16–0·85; RR 63%, ARR 0·7%). Of the patients staying in intensive-care units for more than 3 days, we obtained endotracheal aspirate cultures for 881 (49%) patients receiving standard care, 886 (50%) receiving SOD, and 828 (44%) receiving SDD. 128 (15%) patients acquired respiratory tract colonisation with highly resistant microorganisms during standard care, compared with 74 (8%) during SDD (0·58, 0·43–0·78; RR 38%, ARR 5·5%) and 88 (10%) during SOD (0·65, 0·49–0·87; RR 32%, ARR 4·6%). Acquired respiratory tract colonisation with Gram-negative bacteria or cefotaxime-resistant and colistin-resistant pathogens was lowest during SDD. Interpretation Widespread use of SDD and SOD in intensive-care units with low levels of antibiotic resistance is justified. Funding None.</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibacterial agents</subject><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antifungal Agents - pharmacology</subject><subject>Bacteria</subject><subject>Bacteria - drug effects</subject><subject>Biological and medical sciences</subject><subject>Colonization</subject><subject>Cross-Over Studies</subject><subject>Decontamination</subject><subject>Decontamination - methods</subject><subject>Drug Resistance, Bacterial</subject><subject>Drug Resistance, Fungal</subject><subject>Epidemiology. Vaccinations</subject><subject>Gastrointestinal Tract - microbiology</subject><subject>General aspects</subject><subject>Humans</subject><subject>Infectious Disease</subject><subject>Infectious diseases</subject><subject>Intensive Care Units</subject><subject>Medical sciences</subject><subject>Microorganisms</subject><subject>Oropharynx - microbiology</subject><subject>Pharmacology. Drug treatments</subject><subject>Prevention</subject><subject>Respiratory tract</subject><issn>1473-3099</issn><issn>1474-4457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkduKFDEQhhtR3IM-ghIEWQVbU93pkxeKLJ5gwYvV65BJqsesPUmbSg_MU_pKpnvGERbBqxTpr76u1J9lj4C_BA71q2sQTZmXvOueATxvOC-rXNzJTtO1yIWomrtLvUdOsjOiG86hAS7uZycFiIJ3vD3Nfl3jgDraLTJj10hLFYPSkRnU3kW1sU5F6x1TzjA60j748bsKO7dGNfyTVS7alfXRahaQLEXlNDLr2JgYdJHm2rqIjpIw1yogm5yN9Dq1Mj-iywe1wuEF08NEEQMatg5-GvOQ9H5jCU36FjyR32JgFCeze5Dd69VA-PBwnmffPrz_evkpv_ry8fPlu6tci6aOueFdAQVwU4PSiF1VYcuh6tsGoSpNa1oNheKlKnSvu5ZrXK262vQoelPVXV-eZxd77xj8zyntTaZ5NA6Dcugnkm0tmrbgVZvIJ7fIGz8Fl4abIWih4TNU7aHlOQF7OQa7SeuVwOWct1zylnOYEkAueUuR-h4f5NNqg-bY9SfgBDw9AIq0Gvq0Om3pLycKUYtyFr3dc5iWtrUYJOkUkkZjQ0pcGm__O8qbWwY9WGfTT3_gDun4aJBUSL6XzA6AxSDK3_2k4ro</recordid><startdate>20110501</startdate><enddate>20110501</enddate><creator>de Smet, Anne Marie GA, Dr</creator><creator>Kluytmans, Jan AJW, Prof</creator><creator>Blok, Hetty EM, MSc</creator><creator>Mascini, Ellen M, MD</creator><creator>Benus, Robin FJ, MD</creator><creator>Bernards, Alexandra T, MD</creator><creator>Kuijper, Ed J, MD</creator><creator>Leverstein-van Hall, Maurine A, MD</creator><creator>Jansz, Arjan R, MD</creator><creator>de Jongh, Bartelt M, MD</creator><creator>van Asselt, Gerard J, MD</creator><creator>Frenay, Ine HME, MD</creator><creator>Thijsen, Steven FT, MD</creator><creator>Conijn, Simon NM</creator><creator>Kaan, Jan A, MD</creator><creator>Arends, Jan P, MD</creator><creator>Sturm, Patrick DJ, MD</creator><creator>Bootsma, Martin CJ, PhD</creator><creator>Bonten, Marc JM, Prof</creator><general>Elsevier Ltd</general><general>Lancet Publishing Group</general><general>Elsevier Limited</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>0TZ</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20110501</creationdate><title>Selective digestive tract decontamination and selective oropharyngeal decontamination and antibiotic resistance in patients in intensive-care units: an open-label, clustered group-randomised, crossover study</title><author>de Smet, Anne Marie GA, Dr ; Kluytmans, Jan AJW, Prof ; Blok, Hetty EM, MSc ; Mascini, Ellen M, MD ; Benus, Robin FJ, MD ; Bernards, Alexandra T, MD ; Kuijper, Ed J, MD ; Leverstein-van Hall, Maurine A, MD ; Jansz, Arjan R, MD ; de Jongh, Bartelt M, MD ; van Asselt, Gerard J, MD ; Frenay, Ine HME, MD ; Thijsen, Steven FT, MD ; Conijn, Simon NM ; Kaan, Jan A, MD ; Arends, Jan P, MD ; Sturm, Patrick DJ, MD ; Bootsma, Martin CJ, PhD ; Bonten, Marc JM, Prof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-d0921210d61acee955e8015f87e153d8d8c12a03a2cfc980cebb96dfe4fd569f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antibacterial agents</topic><topic>Antibiotic resistance</topic><topic>Antibiotics</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Antifungal Agents - pharmacology</topic><topic>Bacteria</topic><topic>Bacteria - drug effects</topic><topic>Biological and medical sciences</topic><topic>Colonization</topic><topic>Cross-Over Studies</topic><topic>Decontamination</topic><topic>Decontamination - methods</topic><topic>Drug Resistance, Bacterial</topic><topic>Drug Resistance, Fungal</topic><topic>Epidemiology. Vaccinations</topic><topic>Gastrointestinal Tract - microbiology</topic><topic>General aspects</topic><topic>Humans</topic><topic>Infectious Disease</topic><topic>Infectious diseases</topic><topic>Intensive Care Units</topic><topic>Medical sciences</topic><topic>Microorganisms</topic><topic>Oropharynx - microbiology</topic><topic>Pharmacology. Drug treatments</topic><topic>Prevention</topic><topic>Respiratory tract</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Smet, Anne Marie GA, Dr</creatorcontrib><creatorcontrib>Kluytmans, Jan AJW, Prof</creatorcontrib><creatorcontrib>Blok, Hetty EM, MSc</creatorcontrib><creatorcontrib>Mascini, Ellen M, MD</creatorcontrib><creatorcontrib>Benus, Robin FJ, MD</creatorcontrib><creatorcontrib>Bernards, Alexandra T, MD</creatorcontrib><creatorcontrib>Kuijper, Ed J, MD</creatorcontrib><creatorcontrib>Leverstein-van Hall, Maurine A, MD</creatorcontrib><creatorcontrib>Jansz, Arjan R, MD</creatorcontrib><creatorcontrib>de Jongh, Bartelt M, MD</creatorcontrib><creatorcontrib>van Asselt, Gerard J, MD</creatorcontrib><creatorcontrib>Frenay, Ine HME, MD</creatorcontrib><creatorcontrib>Thijsen, Steven FT, MD</creatorcontrib><creatorcontrib>Conijn, Simon NM</creatorcontrib><creatorcontrib>Kaan, Jan A, MD</creatorcontrib><creatorcontrib>Arends, Jan P, MD</creatorcontrib><creatorcontrib>Sturm, Patrick DJ, MD</creatorcontrib><creatorcontrib>Bootsma, Martin CJ, PhD</creatorcontrib><creatorcontrib>Bonten, Marc JM, Prof</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>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Lancet Titles</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 One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Collection</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</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><jtitle>The Lancet infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Smet, Anne Marie GA, Dr</au><au>Kluytmans, Jan AJW, Prof</au><au>Blok, Hetty EM, MSc</au><au>Mascini, Ellen M, MD</au><au>Benus, Robin FJ, MD</au><au>Bernards, Alexandra T, MD</au><au>Kuijper, Ed J, MD</au><au>Leverstein-van Hall, Maurine A, MD</au><au>Jansz, Arjan R, MD</au><au>de Jongh, Bartelt M, MD</au><au>van Asselt, Gerard J, MD</au><au>Frenay, Ine HME, MD</au><au>Thijsen, Steven FT, MD</au><au>Conijn, Simon NM</au><au>Kaan, Jan A, MD</au><au>Arends, Jan P, MD</au><au>Sturm, Patrick DJ, MD</au><au>Bootsma, Martin CJ, PhD</au><au>Bonten, Marc JM, Prof</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective digestive tract decontamination and selective oropharyngeal decontamination and antibiotic resistance in patients in intensive-care units: an open-label, clustered group-randomised, crossover study</atitle><jtitle>The Lancet infectious diseases</jtitle><addtitle>Lancet Infect Dis</addtitle><date>2011-05-01</date><risdate>2011</risdate><volume>11</volume><issue>5</issue><spage>372</spage><epage>380</epage><pages>372-380</pages><issn>1473-3099</issn><eissn>1474-4457</eissn><coden>LANCAO</coden><abstract>Summary Background Previously, we assessed selective digestive tract decontamination (SDD) and selective oropharyngeal decontamination (SOD) on survival and prevention of bacteraemia in patients in intensive-care units. In this analysis, we aimed to assess effectiveness of these interventions for prevention of respiratory tract colonisation and bacteraemia with highly resistant microorganisms acquired in intensive-care units. Methods We did an open-label, clustered group-randomised, crossover study in 13 intensive-care units in the Netherlands between May, 2004, and July, 2006. Participants admitted to intensive-care units with an expected duration of mechanical ventilation of more than 48 h or an expected stay of more than 72 h received SOD (topical tobramycin, colistin, and amphotericin B in the oropharynx), SDD (SOD antibiotics in the oropharynx and stomach plus 4 days' intravenous cefotaxime), or standard care. The computer-randomised order of study regimens was applied by an independent clinical pharmacist who was masked to intensive-care-unit identity. We calculated crude odds ratios (95% CI) for rates of bacteraemia or respiratory tract colonisation with highly resistant microorganisms in patients who stayed in intensive-care units for more than 3 days (ie, acquired infection). This trial is registered at http://isrctn.org , number ISRCTN35176830. Findings Data were available for 5927 (>99%) of 5939 patients, of whom 5463 (92%) were in intensive-care units for more than 3 days. 239 (13%) of 1837 patients in standard care acquired bacteraemia after 3 days, compared with 158 (9%) of 1758 in SOD (odds ratio 0·66, 95% CI 0·53–0·82), and 124 (7%) of 1868 in SDD (0·48, 0·38–0·60). Eight patients acquired bacteraemia with highly resistant microorganisms during SDD, compared with 18 patients (with 19 episodes) during standard care (0·41, 0·18–0·94; rate reduction [RR] 59%, absolute risk reduction [ARR] 0·6%) and 20 during SOD (0·37, 0·16–0·85; RR 63%, ARR 0·7%). Of the patients staying in intensive-care units for more than 3 days, we obtained endotracheal aspirate cultures for 881 (49%) patients receiving standard care, 886 (50%) receiving SOD, and 828 (44%) receiving SDD. 128 (15%) patients acquired respiratory tract colonisation with highly resistant microorganisms during standard care, compared with 74 (8%) during SDD (0·58, 0·43–0·78; RR 38%, ARR 5·5%) and 88 (10%) during SOD (0·65, 0·49–0·87; RR 32%, ARR 4·6%). Acquired respiratory tract colonisation with Gram-negative bacteria or cefotaxime-resistant and colistin-resistant pathogens was lowest during SDD. Interpretation Widespread use of SDD and SOD in intensive-care units with low levels of antibiotic resistance is justified. Funding None.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>21420908</pmid><doi>10.1016/S1473-3099(11)70035-4</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1473-3099 |
ispartof | The Lancet infectious diseases, 2011-05, Vol.11 (5), p.372-380 |
issn | 1473-3099 1474-4457 |
language | eng |
recordid | cdi_proquest_miscellaneous_864782058 |
source | ScienceDirect Freedom Collection |
subjects | Anti-Bacterial Agents - pharmacology Antibacterial agents Antibiotic resistance Antibiotics Antibiotics. Antiinfectious agents. Antiparasitic agents Antifungal Agents - pharmacology Bacteria Bacteria - drug effects Biological and medical sciences Colonization Cross-Over Studies Decontamination Decontamination - methods Drug Resistance, Bacterial Drug Resistance, Fungal Epidemiology. Vaccinations Gastrointestinal Tract - microbiology General aspects Humans Infectious Disease Infectious diseases Intensive Care Units Medical sciences Microorganisms Oropharynx - microbiology Pharmacology. Drug treatments Prevention Respiratory tract |
title | Selective digestive tract decontamination and selective oropharyngeal decontamination and antibiotic resistance in patients in intensive-care units: an open-label, clustered group-randomised, crossover study |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-03-07T19%3A04%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Selective%20digestive%20tract%20decontamination%20and%20selective%20oropharyngeal%20decontamination%20and%20antibiotic%20resistance%20in%20patients%20in%20intensive-care%20units:%20an%20open-label,%20clustered%20group-randomised,%20crossover%20study&rft.jtitle=The%20Lancet%20infectious%20diseases&rft.au=de%20Smet,%20Anne%20Marie%20GA,%20Dr&rft.date=2011-05-01&rft.volume=11&rft.issue=5&rft.spage=372&rft.epage=380&rft.pages=372-380&rft.issn=1473-3099&rft.eissn=1474-4457&rft.coden=LANCAO&rft_id=info:doi/10.1016/S1473-3099(11)70035-4&rft_dat=%3Cproquest_cross%3E2334639381%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c476t-d0921210d61acee955e8015f87e153d8d8c12a03a2cfc980cebb96dfe4fd569f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=864181708&rft_id=info:pmid/21420908&rfr_iscdi=true |