Diagnosing Ventilator-Associated Pneumonia: The Role of Bronchoscopy

To discuss the two diagnostic procedures used most frequently to obtain uncontaminated lower airway secretions during bronchoscopy. This article reviews the contributing risk factors of ventilator-associated pneumonia (VAP) and the recent studies that have assessed the usefulness of the protected sp...

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Veröffentlicht in:Mayo Clinic proceedings 1994-10, Vol.69 (10), p.962-968
Hauptverfasser: ALLEN, ROBERT M., DUNN, WILLIAM F., LEMPER, ANDREW H.
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DUNN, WILLIAM F.
LEMPER, ANDREW H.
description To discuss the two diagnostic procedures used most frequently to obtain uncontaminated lower airway secretions during bronchoscopy. This article reviews the contributing risk factors of ventilator-associated pneumonia (VAP) and the recent studies that have assessed the usefulness of the protected specimen brush (PSB) and bronchoalveolar lavage (BAL) in the nonimmunocompromised host. A prompt, accurate diagnosis of VAP, including specific identification of the bacterial pathogen, remains a common challenge in the intensive-care unit. Standard clinical criteria are of suboptimal specificity for making decisions, including selecting antibiotic therapy. Bronchoscopic techniques of lung secretion sampling can be used in the intensive-care unit in an effort to overcome the effects of oropharyngeal contamination. The PSB and BAL, used appropriately, can help intensive-care clinicians formulate specific antimicrobial therapy. Evaluation of intracellular bacteria obtained by BAL has been reported to be useful in guiding empiric antibiotic therapy while the final results of cultures obtained with the PSB are pending. Prior antibiotic therapy, however, may confound the interpretation and clinical utility of results. Currently, for a patient taking antibiotic therapy, no reliable technique nor quantitative culture threshold exists to help in diagnosing suspected VAP or in guiding antibiotic therapy. If the clinical situation allows, antibiotic therapy should be discontinued for 48 hours; then, the PSB, BAL, protected BAL, or endobronchial aspiration should be used. These contemporary modalities, however, necessitate further clinical trials before widespread use is warranted.
doi_str_mv 10.1016/S0025-6196(12)61821-7
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Prior antibiotic therapy, however, may confound the interpretation and clinical utility of results. Currently, for a patient taking antibiotic therapy, no reliable technique nor quantitative culture threshold exists to help in diagnosing suspected VAP or in guiding antibiotic therapy. If the clinical situation allows, antibiotic therapy should be discontinued for 48 hours; then, the PSB, BAL, protected BAL, or endobronchial aspiration should be used. These contemporary modalities, however, necessitate further clinical trials before widespread use is warranted.</description><identifier>ISSN: 0025-6196</identifier><identifier>EISSN: 1942-5546</identifier><identifier>DOI: 10.1016/S0025-6196(12)61821-7</identifier><identifier>PMID: 7934193</identifier><identifier>CODEN: MACPAJ</identifier><language>eng</language><publisher>Rochester, MN: Elsevier Inc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. 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This article reviews the contributing risk factors of ventilator-associated pneumonia (VAP) and the recent studies that have assessed the usefulness of the protected specimen brush (PSB) and bronchoalveolar lavage (BAL) in the nonimmunocompromised host. A prompt, accurate diagnosis of VAP, including specific identification of the bacterial pathogen, remains a common challenge in the intensive-care unit. Standard clinical criteria are of suboptimal specificity for making decisions, including selecting antibiotic therapy. Bronchoscopic techniques of lung secretion sampling can be used in the intensive-care unit in an effort to overcome the effects of oropharyngeal contamination. The PSB and BAL, used appropriately, can help intensive-care clinicians formulate specific antimicrobial therapy. Evaluation of intracellular bacteria obtained by BAL has been reported to be useful in guiding empiric antibiotic therapy while the final results of cultures obtained with the PSB are pending. Prior antibiotic therapy, however, may confound the interpretation and clinical utility of results. Currently, for a patient taking antibiotic therapy, no reliable technique nor quantitative culture threshold exists to help in diagnosing suspected VAP or in guiding antibiotic therapy. If the clinical situation allows, antibiotic therapy should be discontinued for 48 hours; then, the PSB, BAL, protected BAL, or endobronchial aspiration should be used. These contemporary modalities, however, necessitate further clinical trials before widespread use is warranted.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bronchi - microbiology</subject><subject>Bronchoalveolar Lavage Fluid - microbiology</subject><subject>Bronchoscopy - methods</subject><subject>Cross Infection - diagnosis</subject><subject>Cross Infection - drug therapy</subject><subject>Cross Infection - etiology</subject><subject>Emergency and intensive respiratory care</subject><subject>Humans</subject><subject>Intensive care medicine</subject><subject>Medical sciences</subject><subject>Pneumonia - diagnosis</subject><subject>Pneumonia - drug therapy</subject><subject>Pneumonia - etiology</subject><subject>Respiration, Artificial - adverse effects</subject><subject>Risk Factors</subject><subject>Specimen Handling - instrumentation</subject><issn>0025-6196</issn><issn>1942-5546</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhi0EggD9CUh7qFA5LHi8_lj3UqWBAhISVRtxtRzvbGK0sYO9qcS_Z0OiXHuakeaZmVcPIRdAr4GCvPlLKROlBC2_AbuSUDMo1QEZgeasFILLQzLaIyfkNOdXSqnSmh-TY6UrDroakdtbb-chZh_mxQuG3ne2j6kc5xydtz02xe-A62UM3n4vpgss_sQOi9gWP1MMbhGzi6v3c3LU2i7jl109I9Nfd9PJQ_n0fP84GT-VjnPoS6ktMjuzstFUVagbXqFTMHQoh7wNQN20vK6Bcgas1mLGBICiggrV1rw6I5fbs6sU39aYe7P02WHX2YBxnY2SSlZSqwEUW9ClmHPC1qySX9r0boCajTzzKc9szBhg5lOe2exd7B6sZ0ts9ls7W8P8625us7Ndm2xwPu8xzoRkNQzYjy2Gg4t_HpPJzmNw2PiErjdN9P8J8gFdsoma</recordid><startdate>19941001</startdate><enddate>19941001</enddate><creator>ALLEN, ROBERT M.</creator><creator>DUNN, WILLIAM F.</creator><creator>LEMPER, ANDREW H.</creator><general>Elsevier Inc</general><general>Mayo Medical Ventures</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>19941001</creationdate><title>Diagnosing Ventilator-Associated Pneumonia: The Role of Bronchoscopy</title><author>ALLEN, ROBERT M. ; DUNN, WILLIAM F. ; LEMPER, ANDREW H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-69ae2aba6d9073e9d43ec713e9e6546d118df488104212895b2511705057f843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bronchi - microbiology</topic><topic>Bronchoalveolar Lavage Fluid - microbiology</topic><topic>Bronchoscopy - methods</topic><topic>Cross Infection - diagnosis</topic><topic>Cross Infection - drug therapy</topic><topic>Cross Infection - etiology</topic><topic>Emergency and intensive respiratory care</topic><topic>Humans</topic><topic>Intensive care medicine</topic><topic>Medical sciences</topic><topic>Pneumonia - diagnosis</topic><topic>Pneumonia - drug therapy</topic><topic>Pneumonia - etiology</topic><topic>Respiration, Artificial - adverse effects</topic><topic>Risk Factors</topic><topic>Specimen Handling - instrumentation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ALLEN, ROBERT M.</creatorcontrib><creatorcontrib>DUNN, WILLIAM F.</creatorcontrib><creatorcontrib>LEMPER, ANDREW H.</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>Mayo Clinic proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ALLEN, ROBERT M.</au><au>DUNN, WILLIAM F.</au><au>LEMPER, ANDREW H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnosing Ventilator-Associated Pneumonia: The Role of Bronchoscopy</atitle><jtitle>Mayo Clinic proceedings</jtitle><addtitle>Mayo Clin Proc</addtitle><date>1994-10-01</date><risdate>1994</risdate><volume>69</volume><issue>10</issue><spage>962</spage><epage>968</epage><pages>962-968</pages><issn>0025-6196</issn><eissn>1942-5546</eissn><coden>MACPAJ</coden><abstract>To discuss the two diagnostic procedures used most frequently to obtain uncontaminated lower airway secretions during bronchoscopy. This article reviews the contributing risk factors of ventilator-associated pneumonia (VAP) and the recent studies that have assessed the usefulness of the protected specimen brush (PSB) and bronchoalveolar lavage (BAL) in the nonimmunocompromised host. A prompt, accurate diagnosis of VAP, including specific identification of the bacterial pathogen, remains a common challenge in the intensive-care unit. Standard clinical criteria are of suboptimal specificity for making decisions, including selecting antibiotic therapy. Bronchoscopic techniques of lung secretion sampling can be used in the intensive-care unit in an effort to overcome the effects of oropharyngeal contamination. The PSB and BAL, used appropriately, can help intensive-care clinicians formulate specific antimicrobial therapy. Evaluation of intracellular bacteria obtained by BAL has been reported to be useful in guiding empiric antibiotic therapy while the final results of cultures obtained with the PSB are pending. Prior antibiotic therapy, however, may confound the interpretation and clinical utility of results. Currently, for a patient taking antibiotic therapy, no reliable technique nor quantitative culture threshold exists to help in diagnosing suspected VAP or in guiding antibiotic therapy. If the clinical situation allows, antibiotic therapy should be discontinued for 48 hours; then, the PSB, BAL, protected BAL, or endobronchial aspiration should be used. These contemporary modalities, however, necessitate further clinical trials before widespread use is warranted.</abstract><cop>Rochester, MN</cop><pub>Elsevier Inc</pub><pmid>7934193</pmid><doi>10.1016/S0025-6196(12)61821-7</doi><tpages>7</tpages></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Anti-Bacterial Agents - therapeutic use
Biological and medical sciences
Bronchi - microbiology
Bronchoalveolar Lavage Fluid - microbiology
Bronchoscopy - methods
Cross Infection - diagnosis
Cross Infection - drug therapy
Cross Infection - etiology
Emergency and intensive respiratory care
Humans
Intensive care medicine
Medical sciences
Pneumonia - diagnosis
Pneumonia - drug therapy
Pneumonia - etiology
Respiration, Artificial - adverse effects
Risk Factors
Specimen Handling - instrumentation
title Diagnosing Ventilator-Associated Pneumonia: The Role of Bronchoscopy
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