Microbiology of Bronchoalveolar Lavage Fluid in Children With Acute Nonresponding or Recurrent Community-Acquired Pneumonia: Identification of Nontypeable Haemophilus influenzae as a Major Pathogen
Background. Precise etiologic diagnosis in pediatric community-acquired pneumonia (CAP) remains challenging. Methods. We conducted a retrospective study of CAP etiology in 2 groups of pediatric patients who underwent flexible bronchoscopy (FOB) with bronchoalveolar lavage (BAL); children with acute...
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description | Background. Precise etiologic diagnosis in pediatric community-acquired pneumonia (CAP) remains challenging. Methods. We conducted a retrospective study of CAP etiology in 2 groups of pediatric patients who underwent flexible bronchoscopy (FOB) with bronchoalveolar lavage (BAL); children with acute nonresponsive CAP (NR-CAP; n = 127) or recurrent CAP (Rec-CAP; n = 123). Procedural measures were taken to limit contamination risk and quantitative bacterial culture of BAL fluid (significance cutoff point, ≥10⁴ colony-forming units/mL) was used. Blood culture results, serological test results, nasopharyngeal secretion findings, and pleural fluid culture results were also assessed, where available. Results. An infectious agent was detected in 76.0% of cases. In 51.2% of infections, aerobic bacteria were isolated, of which 75.0%, 28.9%, and 13.3% were Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae, respectively. Most (97.9%) of the H. influenzae strains were nontypeable (NTHi). H. influenzae was detected in 26.0% of NR-CAP cases and 51.2% of Rec-CAP cases, whereas Mycoplasma pneumoniae was the predominant pathogen in the NR-CAP group (accounting for 34.9% of cases) but not in the Rec-CAP group (19.3%). Viruses were found in 30.4% of cases, with respiratory syncytial virus, parainfluenzaviruses, and influenzaviruses detected most frequently. Mixed infections were found in 18.9% of NR-CAP cases and 30.1% of Rec-CAP cases. Conclusions. A variety of microorganisms were isolated with frequent mixed infection. NTHi was one of the major pathogens found, especially in association with recurrent CAP, possibly because of improved detection with the FOB with BAL procedure. This suggests that the burden of pediatric CAP could be reduced by addressing NTHi as a major causative pathogen. |
doi_str_mv | 10.1093/cid/cir235 |
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Precise etiologic diagnosis in pediatric community-acquired pneumonia (CAP) remains challenging. Methods. We conducted a retrospective study of CAP etiology in 2 groups of pediatric patients who underwent flexible bronchoscopy (FOB) with bronchoalveolar lavage (BAL); children with acute nonresponsive CAP (NR-CAP; n = 127) or recurrent CAP (Rec-CAP; n = 123). Procedural measures were taken to limit contamination risk and quantitative bacterial culture of BAL fluid (significance cutoff point, ≥10⁴ colony-forming units/mL) was used. Blood culture results, serological test results, nasopharyngeal secretion findings, and pleural fluid culture results were also assessed, where available. Results. An infectious agent was detected in 76.0% of cases. In 51.2% of infections, aerobic bacteria were isolated, of which 75.0%, 28.9%, and 13.3% were Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae, respectively. Most (97.9%) of the H. influenzae strains were nontypeable (NTHi). H. influenzae was detected in 26.0% of NR-CAP cases and 51.2% of Rec-CAP cases, whereas Mycoplasma pneumoniae was the predominant pathogen in the NR-CAP group (accounting for 34.9% of cases) but not in the Rec-CAP group (19.3%). Viruses were found in 30.4% of cases, with respiratory syncytial virus, parainfluenzaviruses, and influenzaviruses detected most frequently. Mixed infections were found in 18.9% of NR-CAP cases and 30.1% of Rec-CAP cases. Conclusions. A variety of microorganisms were isolated with frequent mixed infection. NTHi was one of the major pathogens found, especially in association with recurrent CAP, possibly because of improved detection with the FOB with BAL procedure. This suggests that the burden of pediatric CAP could be reduced by addressing NTHi as a major causative pathogen.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/cir235</identifier><identifier>PMID: 21628484</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; and Commentaries ; Antibiotics ; Antibodies, Bacterial - blood ; Bacteria - classification ; Bacteria - isolation & purification ; Biological and medical sciences ; Blood - microbiology ; Bronchoalveolar Lavage Fluid - microbiology ; Child ; Child, Preschool ; Children ; Coinfection ; Community-Acquired Infections - drug therapy ; Community-Acquired Infections - epidemiology ; Community-Acquired Infections - microbiology ; Etiology ; Female ; Haemophilus influenzae ; Humans ; Infant ; Infections ; Infectious diseases ; Male ; Medical sciences ; Nasopharynx - microbiology ; Pathogens ; Pediatrics ; Pleural Effusion - microbiology ; Pneumology ; Pneumonia ; Pneumonia, Bacterial - drug therapy ; Pneumonia, Bacterial - epidemiology ; Pneumonia, Bacterial - microbiology ; Prevalence ; Recurrence ; Respiratory system : syndromes and miscellaneous diseases ; Retrospective Studies ; Viruses</subject><ispartof>Clinical infectious diseases, 2011-06, Vol.52 (12), p.1437-1444</ispartof><rights>Copyright © 2011 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>The Author 2011. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-144bb5d637ca857e1e36cd4b0e9a1875820adb17f3107e1cc2362ee67ca292fd3</citedby><cites>FETCH-LOGICAL-c487t-144bb5d637ca857e1e36cd4b0e9a1875820adb17f3107e1cc2362ee67ca292fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23024437$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23024437$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,780,784,803,885,1584,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24350310$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21628484$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Schutter, Iris</creatorcontrib><creatorcontrib>De Wachter, Elke</creatorcontrib><creatorcontrib>Crokaert, Françoise</creatorcontrib><creatorcontrib>Verhaegen, Jan</creatorcontrib><creatorcontrib>Soetens, Oriane</creatorcontrib><creatorcontrib>Piérard, Denis</creatorcontrib><creatorcontrib>Malfroot, Anne</creatorcontrib><title>Microbiology of Bronchoalveolar Lavage Fluid in Children With Acute Nonresponding or Recurrent Community-Acquired Pneumonia: Identification of Nontypeable Haemophilus influenzae as a Major Pathogen</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Background. Precise etiologic diagnosis in pediatric community-acquired pneumonia (CAP) remains challenging. Methods. We conducted a retrospective study of CAP etiology in 2 groups of pediatric patients who underwent flexible bronchoscopy (FOB) with bronchoalveolar lavage (BAL); children with acute nonresponsive CAP (NR-CAP; n = 127) or recurrent CAP (Rec-CAP; n = 123). Procedural measures were taken to limit contamination risk and quantitative bacterial culture of BAL fluid (significance cutoff point, ≥10⁴ colony-forming units/mL) was used. Blood culture results, serological test results, nasopharyngeal secretion findings, and pleural fluid culture results were also assessed, where available. Results. An infectious agent was detected in 76.0% of cases. In 51.2% of infections, aerobic bacteria were isolated, of which 75.0%, 28.9%, and 13.3% were Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae, respectively. Most (97.9%) of the H. influenzae strains were nontypeable (NTHi). H. influenzae was detected in 26.0% of NR-CAP cases and 51.2% of Rec-CAP cases, whereas Mycoplasma pneumoniae was the predominant pathogen in the NR-CAP group (accounting for 34.9% of cases) but not in the Rec-CAP group (19.3%). Viruses were found in 30.4% of cases, with respiratory syncytial virus, parainfluenzaviruses, and influenzaviruses detected most frequently. Mixed infections were found in 18.9% of NR-CAP cases and 30.1% of Rec-CAP cases. Conclusions. A variety of microorganisms were isolated with frequent mixed infection. NTHi was one of the major pathogens found, especially in association with recurrent CAP, possibly because of improved detection with the FOB with BAL procedure. This suggests that the burden of pediatric CAP could be reduced by addressing NTHi as a major causative pathogen.</description><subject>Adolescent</subject><subject>and Commentaries</subject><subject>Antibiotics</subject><subject>Antibodies, Bacterial - blood</subject><subject>Bacteria - classification</subject><subject>Bacteria - isolation & purification</subject><subject>Biological and medical sciences</subject><subject>Blood - microbiology</subject><subject>Bronchoalveolar Lavage Fluid - microbiology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Coinfection</subject><subject>Community-Acquired Infections - drug therapy</subject><subject>Community-Acquired Infections - epidemiology</subject><subject>Community-Acquired Infections - microbiology</subject><subject>Etiology</subject><subject>Female</subject><subject>Haemophilus influenzae</subject><subject>Humans</subject><subject>Infant</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nasopharynx - microbiology</subject><subject>Pathogens</subject><subject>Pediatrics</subject><subject>Pleural Effusion - microbiology</subject><subject>Pneumology</subject><subject>Pneumonia</subject><subject>Pneumonia, Bacterial - drug therapy</subject><subject>Pneumonia, Bacterial - epidemiology</subject><subject>Pneumonia, Bacterial - microbiology</subject><subject>Prevalence</subject><subject>Recurrence</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>Retrospective Studies</subject><subject>Viruses</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhhtR3HX14l3JRQShNen0R2YPwji47sKsLqJ4bKqT6pkM6aQ36QyM_8__ZZYZd_TiIVSgHt6n4M2y54y-ZXTG30mt0vMFrx5kp6ziTV5XM_Yw_Wkl8lJwcZI9CWFDKWOCVo-zk4LVhShFeZr9utbSu04741Y74nrywTsr1w7MFp0BT5awhRWSCxO1ItqSxVob5dGSH3pak7mME5LPznoMo7NK2xVxnnxFGX2CJrJwwxCtnnb5XN5G7VGRG4txcFbDOblSidG9ljBpZ-_0KWrajQidQXIJOLgx-WJI5t5EtD8BCQQC5Bo2yXMD09qt0D7NHvVgAj47zLPs-8XHb4vLfPnl09VivsxlKZopZ2XZdZWqeSNBVA0y5LVUZUdxBkw0lSgoqI41PWc0baUseF0g1gkvZkWv-Fn2fp87xm5AJdP1Hkw7ej2A37UOdPvvxup1u3LbtkmBgjYp4PUhwLvbiGFqBx0kGgMWXQytqGeCFrSiiXyzJ1M9IXjs7y2Mtne1t6n2dl97gl_-fdc9-qfnBLw6ABAkmN6DlTocuZInJaNHzsXx_8IXe24TJuePOZwWZckb_htE59Ls</recordid><startdate>20110615</startdate><enddate>20110615</enddate><creator>De Schutter, Iris</creator><creator>De Wachter, Elke</creator><creator>Crokaert, Françoise</creator><creator>Verhaegen, Jan</creator><creator>Soetens, Oriane</creator><creator>Piérard, Denis</creator><creator>Malfroot, Anne</creator><general>Oxford University Press</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><scope>5PM</scope></search><sort><creationdate>20110615</creationdate><title>Microbiology of Bronchoalveolar Lavage Fluid in Children With Acute Nonresponding or Recurrent Community-Acquired Pneumonia: Identification of Nontypeable Haemophilus influenzae as a Major Pathogen</title><author>De Schutter, Iris ; De Wachter, Elke ; Crokaert, Françoise ; Verhaegen, Jan ; Soetens, Oriane ; Piérard, Denis ; Malfroot, Anne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-144bb5d637ca857e1e36cd4b0e9a1875820adb17f3107e1cc2362ee67ca292fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>and Commentaries</topic><topic>Antibiotics</topic><topic>Antibodies, Bacterial - blood</topic><topic>Bacteria - classification</topic><topic>Bacteria - isolation & purification</topic><topic>Biological and medical sciences</topic><topic>Blood - microbiology</topic><topic>Bronchoalveolar Lavage Fluid - microbiology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Coinfection</topic><topic>Community-Acquired Infections - drug therapy</topic><topic>Community-Acquired Infections - epidemiology</topic><topic>Community-Acquired Infections - microbiology</topic><topic>Etiology</topic><topic>Female</topic><topic>Haemophilus influenzae</topic><topic>Humans</topic><topic>Infant</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nasopharynx - microbiology</topic><topic>Pathogens</topic><topic>Pediatrics</topic><topic>Pleural Effusion - microbiology</topic><topic>Pneumology</topic><topic>Pneumonia</topic><topic>Pneumonia, Bacterial - drug therapy</topic><topic>Pneumonia, Bacterial - epidemiology</topic><topic>Pneumonia, Bacterial - microbiology</topic><topic>Prevalence</topic><topic>Recurrence</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>Retrospective Studies</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Schutter, Iris</creatorcontrib><creatorcontrib>De Wachter, Elke</creatorcontrib><creatorcontrib>Crokaert, Françoise</creatorcontrib><creatorcontrib>Verhaegen, Jan</creatorcontrib><creatorcontrib>Soetens, Oriane</creatorcontrib><creatorcontrib>Piérard, Denis</creatorcontrib><creatorcontrib>Malfroot, Anne</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Schutter, Iris</au><au>De Wachter, Elke</au><au>Crokaert, Françoise</au><au>Verhaegen, Jan</au><au>Soetens, Oriane</au><au>Piérard, Denis</au><au>Malfroot, Anne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microbiology of Bronchoalveolar Lavage Fluid in Children With Acute Nonresponding or Recurrent Community-Acquired Pneumonia: Identification of Nontypeable Haemophilus influenzae as a Major Pathogen</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2011-06-15</date><risdate>2011</risdate><volume>52</volume><issue>12</issue><spage>1437</spage><epage>1444</epage><pages>1437-1444</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. Precise etiologic diagnosis in pediatric community-acquired pneumonia (CAP) remains challenging. Methods. We conducted a retrospective study of CAP etiology in 2 groups of pediatric patients who underwent flexible bronchoscopy (FOB) with bronchoalveolar lavage (BAL); children with acute nonresponsive CAP (NR-CAP; n = 127) or recurrent CAP (Rec-CAP; n = 123). Procedural measures were taken to limit contamination risk and quantitative bacterial culture of BAL fluid (significance cutoff point, ≥10⁴ colony-forming units/mL) was used. Blood culture results, serological test results, nasopharyngeal secretion findings, and pleural fluid culture results were also assessed, where available. Results. An infectious agent was detected in 76.0% of cases. In 51.2% of infections, aerobic bacteria were isolated, of which 75.0%, 28.9%, and 13.3% were Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae, respectively. Most (97.9%) of the H. influenzae strains were nontypeable (NTHi). H. influenzae was detected in 26.0% of NR-CAP cases and 51.2% of Rec-CAP cases, whereas Mycoplasma pneumoniae was the predominant pathogen in the NR-CAP group (accounting for 34.9% of cases) but not in the Rec-CAP group (19.3%). Viruses were found in 30.4% of cases, with respiratory syncytial virus, parainfluenzaviruses, and influenzaviruses detected most frequently. Mixed infections were found in 18.9% of NR-CAP cases and 30.1% of Rec-CAP cases. Conclusions. A variety of microorganisms were isolated with frequent mixed infection. NTHi was one of the major pathogens found, especially in association with recurrent CAP, possibly because of improved detection with the FOB with BAL procedure. This suggests that the burden of pediatric CAP could be reduced by addressing NTHi as a major causative pathogen.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>21628484</pmid><doi>10.1093/cid/cir235</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent and Commentaries Antibiotics Antibodies, Bacterial - blood Bacteria - classification Bacteria - isolation & purification Biological and medical sciences Blood - microbiology Bronchoalveolar Lavage Fluid - microbiology Child Child, Preschool Children Coinfection Community-Acquired Infections - drug therapy Community-Acquired Infections - epidemiology Community-Acquired Infections - microbiology Etiology Female Haemophilus influenzae Humans Infant Infections Infectious diseases Male Medical sciences Nasopharynx - microbiology Pathogens Pediatrics Pleural Effusion - microbiology Pneumology Pneumonia Pneumonia, Bacterial - drug therapy Pneumonia, Bacterial - epidemiology Pneumonia, Bacterial - microbiology Prevalence Recurrence Respiratory system : syndromes and miscellaneous diseases Retrospective Studies Viruses |
title | Microbiology of Bronchoalveolar Lavage Fluid in Children With Acute Nonresponding or Recurrent Community-Acquired Pneumonia: Identification of Nontypeable Haemophilus influenzae as a Major Pathogen |
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