Effect of Etiology and Timing of Respiratory Tract Infections on Development of Bronchiolitis Obliterans Syndrome
Background Among the many potential risk factors influencing the development of bronchiolitis obliterans syndrome (BOS), acute cellular rejection is the most frequently identified. Despite the unique susceptibility of the lung allograft to pathogens, the association with respiratory tract infections...
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creator | Valentine, Vincent G., MD, FACP Gupta, Meera R., MD Walker, James E., MD Seoane, Leonardo, MD Bonvillain, Ryan W., BS Lombard, Gisele A., RNC, BSN Weill, David, MD Dhillon, Gundeep S., MD |
description | Background Among the many potential risk factors influencing the development of bronchiolitis obliterans syndrome (BOS), acute cellular rejection is the most frequently identified. Despite the unique susceptibility of the lung allograft to pathogens, the association with respiratory tract infections remains unclear. In this study we analyze the role respiratory tract infections have on the development of BOS after lung transplantation. Methods Data from a single center were analyzed from 161 lung recipients transplanted from November 1990 to November 2005, and who survived >180 days. Univariate and multivariate Cox regression analyses were performed using BOS development and the time-scale was reported with hazard ratios (HRs) and confidence intervals (CIs). Results Significant findings by univariate analysis per 100 patient-days prior to BOS onset included acute rejection, cytomegalovirus (CMV) pneumonitis, Gram-negative respiratory tract infections, Gram-positive respiratory tract infections and fungal pneumonias. Multivariate analysis indicated acute rejection, Gram-negative, Gram-positive and fungal pneumonias with HRs (CI) of 84 (23 to 309), 6.6 (1.2 to 37), 6,371 (84 to 485,000) and 314 (53 to 1,856) to be associated with BOS, respectively. Acute rejection, CMV pneumonitis, Gram-positive pneumonia and fungal pneumonitis in the first 100 days had HRs (CI) of 1.8 (1.1 to 3.2), 3.1 (1.3 to 6.9), 3.8 (1.5 to 9.4) and 2.1 (1.1 to 4.0), respectively, and acute rejection and fungal pneumonitis in the late post-operative period with HRs (CI) of 2.3 (1.2 to 4.4) and 1.5 (1.1 to 1.9), respectively. Conclusions In addition to acute rejection, pneumonias with GP, GN and fungal pathogens occurring prior to BOS are independent determinants of chronic allograft dysfunction. Early recognition and treatment of these pathogens in lung transplant recipients may improve long-term outcomes after transplantation. |
doi_str_mv | 10.1016/j.healun.2008.11.907 |
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Despite the unique susceptibility of the lung allograft to pathogens, the association with respiratory tract infections remains unclear. In this study we analyze the role respiratory tract infections have on the development of BOS after lung transplantation. Methods Data from a single center were analyzed from 161 lung recipients transplanted from November 1990 to November 2005, and who survived >180 days. Univariate and multivariate Cox regression analyses were performed using BOS development and the time-scale was reported with hazard ratios (HRs) and confidence intervals (CIs). Results Significant findings by univariate analysis per 100 patient-days prior to BOS onset included acute rejection, cytomegalovirus (CMV) pneumonitis, Gram-negative respiratory tract infections, Gram-positive respiratory tract infections and fungal pneumonias. Multivariate analysis indicated acute rejection, Gram-negative, Gram-positive and fungal pneumonias with HRs (CI) of 84 (23 to 309), 6.6 (1.2 to 37), 6,371 (84 to 485,000) and 314 (53 to 1,856) to be associated with BOS, respectively. Acute rejection, CMV pneumonitis, Gram-positive pneumonia and fungal pneumonitis in the first 100 days had HRs (CI) of 1.8 (1.1 to 3.2), 3.1 (1.3 to 6.9), 3.8 (1.5 to 9.4) and 2.1 (1.1 to 4.0), respectively, and acute rejection and fungal pneumonitis in the late post-operative period with HRs (CI) of 2.3 (1.2 to 4.4) and 1.5 (1.1 to 1.9), respectively. Conclusions In addition to acute rejection, pneumonias with GP, GN and fungal pathogens occurring prior to BOS are independent determinants of chronic allograft dysfunction. Early recognition and treatment of these pathogens in lung transplant recipients may improve long-term outcomes after transplantation.</description><identifier>ISSN: 1053-2498</identifier><identifier>EISSN: 1557-3117</identifier><identifier>DOI: 10.1016/j.healun.2008.11.907</identifier><identifier>PMID: 19201342</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Biological and medical sciences ; Bronchiolitis Obliterans - epidemiology ; Bronchiolitis Obliterans - etiology ; Bronchiolitis Obliterans - physiopathology ; Cardiology. Vascular system ; Child ; Chronic obstructive pulmonary disease, asthma ; Female ; Follow-Up Studies ; Graft Rejection - epidemiology ; Gram-Negative Bacterial Infections - epidemiology ; Gram-Negative Bacterial Infections - etiology ; Gram-Positive Bacterial Infections - epidemiology ; Gram-Positive Bacterial Infections - etiology ; Humans ; Incidence ; Lung Transplantation - adverse effects ; Lung Transplantation - mortality ; Lung Transplantation - pathology ; Male ; Medical sciences ; Middle Aged ; Mycoses - epidemiology ; Mycoses - etiology ; Pneumology ; Pneumonia - epidemiology ; Pneumonia - etiology ; Postoperative Complications - epidemiology ; Respiratory Tract Infections - epidemiology ; Respiratory Tract Infections - etiology ; Respiratory Tract Infections - physiopathology ; Retrospective Studies ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the heart ; Survival Rate ; Time Factors ; Young Adult</subject><ispartof>The Journal of heart and lung transplantation, 2009-02, Vol.28 (2), p.163-169</ispartof><rights>International Society for Heart and Lung Transplantation</rights><rights>2009 International Society for Heart and Lung Transplantation</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-f740f9cae74b131e3d5a5e91f4c92bf1a4ef158828b10e0af9f9116376f96fd73</citedby><cites>FETCH-LOGICAL-c511t-f740f9cae74b131e3d5a5e91f4c92bf1a4ef158828b10e0af9f9116376f96fd73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1053249808017063$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21193475$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19201342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Valentine, Vincent G., MD, FACP</creatorcontrib><creatorcontrib>Gupta, Meera R., MD</creatorcontrib><creatorcontrib>Walker, James E., MD</creatorcontrib><creatorcontrib>Seoane, Leonardo, MD</creatorcontrib><creatorcontrib>Bonvillain, Ryan W., BS</creatorcontrib><creatorcontrib>Lombard, Gisele A., RNC, BSN</creatorcontrib><creatorcontrib>Weill, David, MD</creatorcontrib><creatorcontrib>Dhillon, Gundeep S., MD</creatorcontrib><title>Effect of Etiology and Timing of Respiratory Tract Infections on Development of Bronchiolitis Obliterans Syndrome</title><title>The Journal of heart and lung transplantation</title><addtitle>J Heart Lung Transplant</addtitle><description>Background Among the many potential risk factors influencing the development of bronchiolitis obliterans syndrome (BOS), acute cellular rejection is the most frequently identified. Despite the unique susceptibility of the lung allograft to pathogens, the association with respiratory tract infections remains unclear. In this study we analyze the role respiratory tract infections have on the development of BOS after lung transplantation. Methods Data from a single center were analyzed from 161 lung recipients transplanted from November 1990 to November 2005, and who survived >180 days. Univariate and multivariate Cox regression analyses were performed using BOS development and the time-scale was reported with hazard ratios (HRs) and confidence intervals (CIs). Results Significant findings by univariate analysis per 100 patient-days prior to BOS onset included acute rejection, cytomegalovirus (CMV) pneumonitis, Gram-negative respiratory tract infections, Gram-positive respiratory tract infections and fungal pneumonias. Multivariate analysis indicated acute rejection, Gram-negative, Gram-positive and fungal pneumonias with HRs (CI) of 84 (23 to 309), 6.6 (1.2 to 37), 6,371 (84 to 485,000) and 314 (53 to 1,856) to be associated with BOS, respectively. Acute rejection, CMV pneumonitis, Gram-positive pneumonia and fungal pneumonitis in the first 100 days had HRs (CI) of 1.8 (1.1 to 3.2), 3.1 (1.3 to 6.9), 3.8 (1.5 to 9.4) and 2.1 (1.1 to 4.0), respectively, and acute rejection and fungal pneumonitis in the late post-operative period with HRs (CI) of 2.3 (1.2 to 4.4) and 1.5 (1.1 to 1.9), respectively. Conclusions In addition to acute rejection, pneumonias with GP, GN and fungal pathogens occurring prior to BOS are independent determinants of chronic allograft dysfunction. Early recognition and treatment of these pathogens in lung transplant recipients may improve long-term outcomes after transplantation.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Bronchiolitis Obliterans - epidemiology</subject><subject>Bronchiolitis Obliterans - etiology</subject><subject>Bronchiolitis Obliterans - physiopathology</subject><subject>Cardiology. Vascular system</subject><subject>Child</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Graft Rejection - epidemiology</subject><subject>Gram-Negative Bacterial Infections - epidemiology</subject><subject>Gram-Negative Bacterial Infections - etiology</subject><subject>Gram-Positive Bacterial Infections - epidemiology</subject><subject>Gram-Positive Bacterial Infections - etiology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Lung Transplantation - adverse effects</subject><subject>Lung Transplantation - mortality</subject><subject>Lung Transplantation - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mycoses - epidemiology</subject><subject>Mycoses - etiology</subject><subject>Pneumology</subject><subject>Pneumonia - epidemiology</subject><subject>Pneumonia - etiology</subject><subject>Postoperative Complications - epidemiology</subject><subject>Respiratory Tract Infections - epidemiology</subject><subject>Respiratory Tract Infections - etiology</subject><subject>Respiratory Tract Infections - physiopathology</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the heart</subject><subject>Survival Rate</subject><subject>Time Factors</subject><subject>Young Adult</subject><issn>1053-2498</issn><issn>1557-3117</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFklFr1TAYhosobm7-A5He6F1rvqRpmxtB51EHg8F2vA5p-mXLsU3OknbQf2_qOSjsZldfCM_7Jjx8WfYOSAkE6k-78h7VMLuSEtKWAKUgzYvsFDhvCgbQvExnwllBK9GeZG9i3BFCKOP0dXYCghJgFT3NHjbGoJ5yb_LNZP3g75ZcuT7f2tG6u_X6BuPeBjX5sOTboBJ76daI9S7m3uXf8BEHvx_R_W35GrzT96nJTjbm112aGFRCbxfXBz_iefbKqCHi2-M8y35932wvfhZX1z8uL75cFZoDTIVpKmKEVthUHTBA1nPFUYCptKCdAVWhAd62tO2AIFFGGAFQs6Y2ojZ9w86yj4feffAPM8ZJjjZqHAbl0M9R1rUgwMUKVgdQBx9jQCP3wY4qLBKIXFXLnTyolqtqCSCT6hR7f-yfuxH7_6Gj2wR8OAIqajWYZEHb-I-jAIJVDU_c5wOHycajxSCjtug09jYkz7L39rmfPC3Qg3U2vfkbF4w7PweXTEuQkUoib9e1WLeCtAQaUjP2B_XqtNA</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Valentine, Vincent G., MD, FACP</creator><creator>Gupta, Meera R., MD</creator><creator>Walker, James E., MD</creator><creator>Seoane, Leonardo, MD</creator><creator>Bonvillain, Ryan W., BS</creator><creator>Lombard, Gisele A., RNC, BSN</creator><creator>Weill, David, MD</creator><creator>Dhillon, Gundeep S., MD</creator><general>Elsevier Inc</general><general>Elsevier</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>20090201</creationdate><title>Effect of Etiology and Timing of Respiratory Tract Infections on Development of Bronchiolitis Obliterans Syndrome</title><author>Valentine, Vincent G., MD, FACP ; Gupta, Meera R., MD ; Walker, James E., MD ; Seoane, Leonardo, MD ; Bonvillain, Ryan W., BS ; Lombard, Gisele A., RNC, BSN ; Weill, David, MD ; Dhillon, Gundeep S., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-f740f9cae74b131e3d5a5e91f4c92bf1a4ef158828b10e0af9f9116376f96fd73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Bronchiolitis Obliterans - epidemiology</topic><topic>Bronchiolitis Obliterans - etiology</topic><topic>Bronchiolitis Obliterans - physiopathology</topic><topic>Cardiology. Vascular system</topic><topic>Child</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Graft Rejection - epidemiology</topic><topic>Gram-Negative Bacterial Infections - epidemiology</topic><topic>Gram-Negative Bacterial Infections - etiology</topic><topic>Gram-Positive Bacterial Infections - epidemiology</topic><topic>Gram-Positive Bacterial Infections - etiology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Lung Transplantation - adverse effects</topic><topic>Lung Transplantation - mortality</topic><topic>Lung Transplantation - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mycoses - epidemiology</topic><topic>Mycoses - etiology</topic><topic>Pneumology</topic><topic>Pneumonia - epidemiology</topic><topic>Pneumonia - etiology</topic><topic>Postoperative Complications - epidemiology</topic><topic>Respiratory Tract Infections - epidemiology</topic><topic>Respiratory Tract Infections - etiology</topic><topic>Respiratory Tract Infections - physiopathology</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the heart</topic><topic>Survival Rate</topic><topic>Time Factors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valentine, Vincent G., MD, FACP</creatorcontrib><creatorcontrib>Gupta, Meera R., MD</creatorcontrib><creatorcontrib>Walker, James E., MD</creatorcontrib><creatorcontrib>Seoane, Leonardo, MD</creatorcontrib><creatorcontrib>Bonvillain, Ryan W., BS</creatorcontrib><creatorcontrib>Lombard, Gisele A., RNC, BSN</creatorcontrib><creatorcontrib>Weill, David, MD</creatorcontrib><creatorcontrib>Dhillon, Gundeep S., MD</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>The Journal of heart and lung transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valentine, Vincent G., MD, FACP</au><au>Gupta, Meera R., MD</au><au>Walker, James E., MD</au><au>Seoane, Leonardo, MD</au><au>Bonvillain, Ryan W., BS</au><au>Lombard, Gisele A., RNC, BSN</au><au>Weill, David, MD</au><au>Dhillon, Gundeep S., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Etiology and Timing of Respiratory Tract Infections on Development of Bronchiolitis Obliterans Syndrome</atitle><jtitle>The Journal of heart and lung transplantation</jtitle><addtitle>J Heart Lung Transplant</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>28</volume><issue>2</issue><spage>163</spage><epage>169</epage><pages>163-169</pages><issn>1053-2498</issn><eissn>1557-3117</eissn><abstract>Background Among the many potential risk factors influencing the development of bronchiolitis obliterans syndrome (BOS), acute cellular rejection is the most frequently identified. Despite the unique susceptibility of the lung allograft to pathogens, the association with respiratory tract infections remains unclear. In this study we analyze the role respiratory tract infections have on the development of BOS after lung transplantation. Methods Data from a single center were analyzed from 161 lung recipients transplanted from November 1990 to November 2005, and who survived >180 days. Univariate and multivariate Cox regression analyses were performed using BOS development and the time-scale was reported with hazard ratios (HRs) and confidence intervals (CIs). Results Significant findings by univariate analysis per 100 patient-days prior to BOS onset included acute rejection, cytomegalovirus (CMV) pneumonitis, Gram-negative respiratory tract infections, Gram-positive respiratory tract infections and fungal pneumonias. Multivariate analysis indicated acute rejection, Gram-negative, Gram-positive and fungal pneumonias with HRs (CI) of 84 (23 to 309), 6.6 (1.2 to 37), 6,371 (84 to 485,000) and 314 (53 to 1,856) to be associated with BOS, respectively. Acute rejection, CMV pneumonitis, Gram-positive pneumonia and fungal pneumonitis in the first 100 days had HRs (CI) of 1.8 (1.1 to 3.2), 3.1 (1.3 to 6.9), 3.8 (1.5 to 9.4) and 2.1 (1.1 to 4.0), respectively, and acute rejection and fungal pneumonitis in the late post-operative period with HRs (CI) of 2.3 (1.2 to 4.4) and 1.5 (1.1 to 1.9), respectively. Conclusions In addition to acute rejection, pneumonias with GP, GN and fungal pathogens occurring prior to BOS are independent determinants of chronic allograft dysfunction. Early recognition and treatment of these pathogens in lung transplant recipients may improve long-term outcomes after transplantation.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19201342</pmid><doi>10.1016/j.healun.2008.11.907</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Aged Biological and medical sciences Bronchiolitis Obliterans - epidemiology Bronchiolitis Obliterans - etiology Bronchiolitis Obliterans - physiopathology Cardiology. Vascular system Child Chronic obstructive pulmonary disease, asthma Female Follow-Up Studies Graft Rejection - epidemiology Gram-Negative Bacterial Infections - epidemiology Gram-Negative Bacterial Infections - etiology Gram-Positive Bacterial Infections - epidemiology Gram-Positive Bacterial Infections - etiology Humans Incidence Lung Transplantation - adverse effects Lung Transplantation - mortality Lung Transplantation - pathology Male Medical sciences Middle Aged Mycoses - epidemiology Mycoses - etiology Pneumology Pneumonia - epidemiology Pneumonia - etiology Postoperative Complications - epidemiology Respiratory Tract Infections - epidemiology Respiratory Tract Infections - etiology Respiratory Tract Infections - physiopathology Retrospective Studies Surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the heart Survival Rate Time Factors Young Adult |
title | Effect of Etiology and Timing of Respiratory Tract Infections on Development of Bronchiolitis Obliterans Syndrome |
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