Clinical Characteristics of Rapidly Progressive Fatal Hemorrhagic Pneumonia Caused by Stenotrophomonas maltophilia

Objective Hemorrhagic pneumonia due to Stenotrophomonas maltophilia (SM) in severely immunocompromised patients has a very poor prognosis. However, the risk factors for hemorrhagic pneumonia are not clear. Methods This study assessed the predictive factors of hemorrhagic pneumonia caused by SM. The...

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Veröffentlicht in:Internal Medicine 2020/01/15, Vol.59(2), pp.193-198
Hauptverfasser: Imoto, Waki, Yamada, Koichi, Yamairi, Kazushi, Shibata, Wataru, Namikawa, Hiroki, Yukawa, Satomi, Yoshii, Naoko, Nakaie, Kiyotaka, Hirose, Asao, Koh, Hideo, Watanabe, Tetsuya, Asai, Kazuhisa, Nakamae, Hirohisa, Kaneko, Yukihiro, Kawaguchi, Tomoya, Hino, Masayuki, Kakeya, Hiroshi
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container_end_page 198
container_issue 2
container_start_page 193
container_title Internal Medicine
container_volume 59
creator Imoto, Waki
Yamada, Koichi
Yamairi, Kazushi
Shibata, Wataru
Namikawa, Hiroki
Yukawa, Satomi
Yoshii, Naoko
Nakaie, Kiyotaka
Hirose, Asao
Koh, Hideo
Watanabe, Tetsuya
Asai, Kazuhisa
Nakamae, Hirohisa
Kaneko, Yukihiro
Kawaguchi, Tomoya
Hino, Masayuki
Kakeya, Hiroshi
description Objective Hemorrhagic pneumonia due to Stenotrophomonas maltophilia (SM) in severely immunocompromised patients has a very poor prognosis. However, the risk factors for hemorrhagic pneumonia are not clear. Methods This study assessed the predictive factors of hemorrhagic pneumonia caused by SM. The medical records of patients admitted to Osaka City University Hospital with SM bacteremia between January 2008 and December 2017 were retrospectively reviewed. Patients All patients who had positive blood cultures for SM were included in this study. They were categorized into two groups: the SM bacteremia with hemorrhagic pneumonia group and the SM bacteremia without hemorrhagic pneumonia group. The clinical background characteristics and treatments were compared between these groups. Results The 35 patients with SM bacteremia included 4 with hemorrhagic pneumonia and 31 without hemorrhagic pneumonia. Hematologic malignancy (p=0.03) and thrombocytopenia (p=0.04) as well as the prior use of quinolone within 30 days (p=0.04) were more frequent in the SM bacteremia patients with hemorrhagic pneumonia than in those without hemorrhagic pneumonia. The mortality of the SM bacteremia patients with hemorrhagic pneumonia was higher than that of those without hemorrhagic pneumonia group (p=0.02). Conclusion Patients with SM bacteremia who have hematologic malignancy, thrombocytopenia, and a history of using quinolone within the past 30 days should be treated with deliberation.
doi_str_mv 10.2169/internalmedicine.3358-19
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However, the risk factors for hemorrhagic pneumonia are not clear. Methods This study assessed the predictive factors of hemorrhagic pneumonia caused by SM. The medical records of patients admitted to Osaka City University Hospital with SM bacteremia between January 2008 and December 2017 were retrospectively reviewed. Patients All patients who had positive blood cultures for SM were included in this study. They were categorized into two groups: the SM bacteremia with hemorrhagic pneumonia group and the SM bacteremia without hemorrhagic pneumonia group. The clinical background characteristics and treatments were compared between these groups. Results The 35 patients with SM bacteremia included 4 with hemorrhagic pneumonia and 31 without hemorrhagic pneumonia. Hematologic malignancy (p=0.03) and thrombocytopenia (p=0.04) as well as the prior use of quinolone within 30 days (p=0.04) were more frequent in the SM bacteremia patients with hemorrhagic pneumonia than in those without hemorrhagic pneumonia. The mortality of the SM bacteremia patients with hemorrhagic pneumonia was higher than that of those without hemorrhagic pneumonia group (p=0.02). Conclusion Patients with SM bacteremia who have hematologic malignancy, thrombocytopenia, and a history of using quinolone within the past 30 days should be treated with deliberation.</description><identifier>ISSN: 0918-2918</identifier><identifier>EISSN: 1349-7235</identifier><identifier>DOI: 10.2169/internalmedicine.3358-19</identifier><identifier>PMID: 31941869</identifier><language>eng</language><publisher>Japan: The Japanese Society of Internal Medicine</publisher><subject>Adult ; Bacteremia ; Female ; Gram-Negative Bacterial Infections - complications ; Gram-Negative Bacterial Infections - drug therapy ; Hematologic Neoplasms - complications ; Hemoptysis - microbiology ; Hemorrhage ; Hemorrhage - microbiology ; hemorrhagic pneumonia ; Humans ; Immunocompromised Host ; Immunocompromised hosts ; Internal medicine ; Male ; Malignancy ; Medical records ; Middle Aged ; Original ; Patients ; Pneumonia ; Pneumonia, Bacterial - complications ; Pneumonia, Bacterial - drug therapy ; Prognosis ; quinolone ; Quinolones - therapeutic use ; Retrospective Studies ; Risk Factors ; Stenotrophomonas maltophilia ; Stenotrophomonas maltophilia - immunology ; Thrombocytopenia ; Thrombocytopenia - complications ; Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use</subject><ispartof>Internal Medicine, 2020/01/15, Vol.59(2), pp.193-198</ispartof><rights>2020 by The Japanese Society of Internal Medicine</rights><rights>Copyright Japan Science and Technology Agency 2020</rights><rights>Copyright © 2020 by The Japanese Society of Internal Medicine</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c666t-bfdfadea3583167dac10836a45e2e096a75829b1e59f4c3293d1c6c4398e5f743</citedby><cites>FETCH-LOGICAL-c666t-bfdfadea3583167dac10836a45e2e096a75829b1e59f4c3293d1c6c4398e5f743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008057/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7008057/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1883,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31941869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Imoto, Waki</creatorcontrib><creatorcontrib>Yamada, Koichi</creatorcontrib><creatorcontrib>Yamairi, Kazushi</creatorcontrib><creatorcontrib>Shibata, Wataru</creatorcontrib><creatorcontrib>Namikawa, Hiroki</creatorcontrib><creatorcontrib>Yukawa, Satomi</creatorcontrib><creatorcontrib>Yoshii, Naoko</creatorcontrib><creatorcontrib>Nakaie, Kiyotaka</creatorcontrib><creatorcontrib>Hirose, Asao</creatorcontrib><creatorcontrib>Koh, Hideo</creatorcontrib><creatorcontrib>Watanabe, Tetsuya</creatorcontrib><creatorcontrib>Asai, Kazuhisa</creatorcontrib><creatorcontrib>Nakamae, Hirohisa</creatorcontrib><creatorcontrib>Kaneko, Yukihiro</creatorcontrib><creatorcontrib>Kawaguchi, Tomoya</creatorcontrib><creatorcontrib>Hino, Masayuki</creatorcontrib><creatorcontrib>Kakeya, Hiroshi</creatorcontrib><title>Clinical Characteristics of Rapidly Progressive Fatal Hemorrhagic Pneumonia Caused by Stenotrophomonas maltophilia</title><title>Internal Medicine</title><addtitle>Intern. Med.</addtitle><description>Objective Hemorrhagic pneumonia due to Stenotrophomonas maltophilia (SM) in severely immunocompromised patients has a very poor prognosis. However, the risk factors for hemorrhagic pneumonia are not clear. Methods This study assessed the predictive factors of hemorrhagic pneumonia caused by SM. The medical records of patients admitted to Osaka City University Hospital with SM bacteremia between January 2008 and December 2017 were retrospectively reviewed. Patients All patients who had positive blood cultures for SM were included in this study. They were categorized into two groups: the SM bacteremia with hemorrhagic pneumonia group and the SM bacteremia without hemorrhagic pneumonia group. The clinical background characteristics and treatments were compared between these groups. Results The 35 patients with SM bacteremia included 4 with hemorrhagic pneumonia and 31 without hemorrhagic pneumonia. Hematologic malignancy (p=0.03) and thrombocytopenia (p=0.04) as well as the prior use of quinolone within 30 days (p=0.04) were more frequent in the SM bacteremia patients with hemorrhagic pneumonia than in those without hemorrhagic pneumonia. The mortality of the SM bacteremia patients with hemorrhagic pneumonia was higher than that of those without hemorrhagic pneumonia group (p=0.02). 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Yamada, Koichi ; Yamairi, Kazushi ; Shibata, Wataru ; Namikawa, Hiroki ; Yukawa, Satomi ; Yoshii, Naoko ; Nakaie, Kiyotaka ; Hirose, Asao ; Koh, Hideo ; Watanabe, Tetsuya ; Asai, Kazuhisa ; Nakamae, Hirohisa ; Kaneko, Yukihiro ; Kawaguchi, Tomoya ; Hino, Masayuki ; Kakeya, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c666t-bfdfadea3583167dac10836a45e2e096a75829b1e59f4c3293d1c6c4398e5f743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Bacteremia</topic><topic>Female</topic><topic>Gram-Negative Bacterial Infections - complications</topic><topic>Gram-Negative Bacterial Infections - drug therapy</topic><topic>Hematologic Neoplasms - complications</topic><topic>Hemoptysis - microbiology</topic><topic>Hemorrhage</topic><topic>Hemorrhage - microbiology</topic><topic>hemorrhagic pneumonia</topic><topic>Humans</topic><topic>Immunocompromised Host</topic><topic>Immunocompromised hosts</topic><topic>Internal medicine</topic><topic>Male</topic><topic>Malignancy</topic><topic>Medical records</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Patients</topic><topic>Pneumonia</topic><topic>Pneumonia, Bacterial - complications</topic><topic>Pneumonia, Bacterial - drug therapy</topic><topic>Prognosis</topic><topic>quinolone</topic><topic>Quinolones - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Stenotrophomonas maltophilia</topic><topic>Stenotrophomonas maltophilia - immunology</topic><topic>Thrombocytopenia</topic><topic>Thrombocytopenia - complications</topic><topic>Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Imoto, Waki</creatorcontrib><creatorcontrib>Yamada, Koichi</creatorcontrib><creatorcontrib>Yamairi, Kazushi</creatorcontrib><creatorcontrib>Shibata, Wataru</creatorcontrib><creatorcontrib>Namikawa, Hiroki</creatorcontrib><creatorcontrib>Yukawa, Satomi</creatorcontrib><creatorcontrib>Yoshii, Naoko</creatorcontrib><creatorcontrib>Nakaie, Kiyotaka</creatorcontrib><creatorcontrib>Hirose, Asao</creatorcontrib><creatorcontrib>Koh, Hideo</creatorcontrib><creatorcontrib>Watanabe, Tetsuya</creatorcontrib><creatorcontrib>Asai, Kazuhisa</creatorcontrib><creatorcontrib>Nakamae, Hirohisa</creatorcontrib><creatorcontrib>Kaneko, Yukihiro</creatorcontrib><creatorcontrib>Kawaguchi, Tomoya</creatorcontrib><creatorcontrib>Hino, Masayuki</creatorcontrib><creatorcontrib>Kakeya, Hiroshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Imoto, Waki</au><au>Yamada, Koichi</au><au>Yamairi, Kazushi</au><au>Shibata, Wataru</au><au>Namikawa, Hiroki</au><au>Yukawa, Satomi</au><au>Yoshii, Naoko</au><au>Nakaie, Kiyotaka</au><au>Hirose, Asao</au><au>Koh, Hideo</au><au>Watanabe, Tetsuya</au><au>Asai, Kazuhisa</au><au>Nakamae, Hirohisa</au><au>Kaneko, Yukihiro</au><au>Kawaguchi, Tomoya</au><au>Hino, Masayuki</au><au>Kakeya, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Characteristics of Rapidly Progressive Fatal Hemorrhagic Pneumonia Caused by Stenotrophomonas maltophilia</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. Med.</addtitle><date>2020-01-15</date><risdate>2020</risdate><volume>59</volume><issue>2</issue><spage>193</spage><epage>198</epage><pages>193-198</pages><issn>0918-2918</issn><eissn>1349-7235</eissn><abstract>Objective Hemorrhagic pneumonia due to Stenotrophomonas maltophilia (SM) in severely immunocompromised patients has a very poor prognosis. However, the risk factors for hemorrhagic pneumonia are not clear. Methods This study assessed the predictive factors of hemorrhagic pneumonia caused by SM. The medical records of patients admitted to Osaka City University Hospital with SM bacteremia between January 2008 and December 2017 were retrospectively reviewed. Patients All patients who had positive blood cultures for SM were included in this study. They were categorized into two groups: the SM bacteremia with hemorrhagic pneumonia group and the SM bacteremia without hemorrhagic pneumonia group. The clinical background characteristics and treatments were compared between these groups. Results The 35 patients with SM bacteremia included 4 with hemorrhagic pneumonia and 31 without hemorrhagic pneumonia. Hematologic malignancy (p=0.03) and thrombocytopenia (p=0.04) as well as the prior use of quinolone within 30 days (p=0.04) were more frequent in the SM bacteremia patients with hemorrhagic pneumonia than in those without hemorrhagic pneumonia. The mortality of the SM bacteremia patients with hemorrhagic pneumonia was higher than that of those without hemorrhagic pneumonia group (p=0.02). Conclusion Patients with SM bacteremia who have hematologic malignancy, thrombocytopenia, and a history of using quinolone within the past 30 days should be treated with deliberation.</abstract><cop>Japan</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>31941869</pmid><doi>10.2169/internalmedicine.3358-19</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Bacteremia
Female
Gram-Negative Bacterial Infections - complications
Gram-Negative Bacterial Infections - drug therapy
Hematologic Neoplasms - complications
Hemoptysis - microbiology
Hemorrhage
Hemorrhage - microbiology
hemorrhagic pneumonia
Humans
Immunocompromised Host
Immunocompromised hosts
Internal medicine
Male
Malignancy
Medical records
Middle Aged
Original
Patients
Pneumonia
Pneumonia, Bacterial - complications
Pneumonia, Bacterial - drug therapy
Prognosis
quinolone
Quinolones - therapeutic use
Retrospective Studies
Risk Factors
Stenotrophomonas maltophilia
Stenotrophomonas maltophilia - immunology
Thrombocytopenia
Thrombocytopenia - complications
Trimethoprim, Sulfamethoxazole Drug Combination - therapeutic use
title Clinical Characteristics of Rapidly Progressive Fatal Hemorrhagic Pneumonia Caused by Stenotrophomonas maltophilia
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