Tigecycline in the Treatment of Ventilator-Associated Pneumonia Due to Stenotrophomonas maltophilia: A Multicenter Retrospective Cohort Study

Introduction Tigecycline is a potential alternative to trimethoprim–sulfamethoxazole in treating Stenotrophomonas maltophilia infections due to its potent in vitro antimicrobial activity. Clinical evidence regarding the use of tigecycline in the treatment of S. maltophilia infections is scarce. In t...

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Veröffentlicht in:Infectious diseases and therapy 2021-12, Vol.10 (4), p.2415-2429
Hauptverfasser: Zha, Lei, Zhang, Dayan, Pan, Lingling, Ren, Zhichu, Li, Xiang, Zou, Yi, Li, Shirong, Luo, Shuangqi, Yang, Gang, Tefsen, Boris
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container_end_page 2429
container_issue 4
container_start_page 2415
container_title Infectious diseases and therapy
container_volume 10
creator Zha, Lei
Zhang, Dayan
Pan, Lingling
Ren, Zhichu
Li, Xiang
Zou, Yi
Li, Shirong
Luo, Shuangqi
Yang, Gang
Tefsen, Boris
description Introduction Tigecycline is a potential alternative to trimethoprim–sulfamethoxazole in treating Stenotrophomonas maltophilia infections due to its potent in vitro antimicrobial activity. Clinical evidence regarding the use of tigecycline in the treatment of S. maltophilia infections is scarce. In this study, we assessed the efficacy of tigecycline treating ventilator-associated pneumonia (VAP) due to S. maltophilia in comparison with fluoroquinolones. Methods This is a multicenter retrospective cohort study of patients admitted between January 2017 and December 2020 with the diagnosis of VAP caused by S. maltophilia receiving either tigecycline or fluoroquinolones as the definitive therapy ≥ 48 h. Clinical outcomes including 28-day mortality, clinical cure and microbiological cure were analyzed. Results Of 82 patients with S. maltophilia VAP included, 46 received tigecycline, and 36 received fluoroquinolones; 70.7% of patients had polymicrobial pneumonia, and the appropriate empiric therapy was applied to only 14.6% of patients. The overall 28-day mortality was 39%. Compared with patients receiving fluoroquinolones, tigecycline therapy resulted in worse clinical cure (32.6% vs. 63.9%, p  = 0.009) and microbiological cure (28.6% vs. 59.1%, p  = 0.045), while there was no statistical difference between 28-day mortality (47.8% vs. 27.8%, p  = 0.105) in the two groups. Similar results were also shown in the inverse probability of treatment weighted univariable regression model and multivariable regression model. Conclusions The standard dose of tigecycline therapy was associated with a lower clinical and microbiological cure rate but not associated with an increased 28-day mortality in patients with S. maltophilia VAP compared with fluoroquinolones. Considering the unfavorable clinical outcomes, we therefore recommend against using the standard dose of tigecycline in treating S. maltophilia VAP unless new clinical evidence emerges.
doi_str_mv 10.1007/s40121-021-00516-5
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Clinical evidence regarding the use of tigecycline in the treatment of S. maltophilia infections is scarce. In this study, we assessed the efficacy of tigecycline treating ventilator-associated pneumonia (VAP) due to S. maltophilia in comparison with fluoroquinolones. Methods This is a multicenter retrospective cohort study of patients admitted between January 2017 and December 2020 with the diagnosis of VAP caused by S. maltophilia receiving either tigecycline or fluoroquinolones as the definitive therapy ≥ 48 h. Clinical outcomes including 28-day mortality, clinical cure and microbiological cure were analyzed. Results Of 82 patients with S. maltophilia VAP included, 46 received tigecycline, and 36 received fluoroquinolones; 70.7% of patients had polymicrobial pneumonia, and the appropriate empiric therapy was applied to only 14.6% of patients. The overall 28-day mortality was 39%. Compared with patients receiving fluoroquinolones, tigecycline therapy resulted in worse clinical cure (32.6% vs. 63.9%, p  = 0.009) and microbiological cure (28.6% vs. 59.1%, p  = 0.045), while there was no statistical difference between 28-day mortality (47.8% vs. 27.8%, p  = 0.105) in the two groups. Similar results were also shown in the inverse probability of treatment weighted univariable regression model and multivariable regression model. Conclusions The standard dose of tigecycline therapy was associated with a lower clinical and microbiological cure rate but not associated with an increased 28-day mortality in patients with S. maltophilia VAP compared with fluoroquinolones. Considering the unfavorable clinical outcomes, we therefore recommend against using the standard dose of tigecycline in treating S. maltophilia VAP unless new clinical evidence emerges.</description><identifier>ISSN: 2193-8229</identifier><identifier>EISSN: 2193-6382</identifier><identifier>DOI: 10.1007/s40121-021-00516-5</identifier><identifier>PMID: 34374953</identifier><language>eng</language><publisher>Cheshire: Springer Healthcare</publisher><subject>Analysis ; Antibiotics ; Bacterial pneumonia ; Care and treatment ; China ; Clinical outcomes ; Cohort analysis ; Drug dosages ; Health aspects ; Infectious Diseases ; Internal Medicine ; Medical research ; Medicine ; Medicine &amp; Public Health ; Medicine, Experimental ; Mortality ; Original Research ; Pneumonia ; Ventilators</subject><ispartof>Infectious diseases and therapy, 2021-12, Vol.10 (4), p.2415-2429</ispartof><rights>The Author(s) 2021</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s) 2021. 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Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-7d218cad8ea5f650073025aac803d4594bbdc79da7f0ebce9bffb740db13da093</citedby><cites>FETCH-LOGICAL-c518t-7d218cad8ea5f650073025aac803d4594bbdc79da7f0ebce9bffb740db13da093</cites><orcidid>0000-0003-4897-0703</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354101/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354101/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids></links><search><creatorcontrib>Zha, Lei</creatorcontrib><creatorcontrib>Zhang, Dayan</creatorcontrib><creatorcontrib>Pan, Lingling</creatorcontrib><creatorcontrib>Ren, Zhichu</creatorcontrib><creatorcontrib>Li, Xiang</creatorcontrib><creatorcontrib>Zou, Yi</creatorcontrib><creatorcontrib>Li, Shirong</creatorcontrib><creatorcontrib>Luo, Shuangqi</creatorcontrib><creatorcontrib>Yang, Gang</creatorcontrib><creatorcontrib>Tefsen, Boris</creatorcontrib><title>Tigecycline in the Treatment of Ventilator-Associated Pneumonia Due to Stenotrophomonas maltophilia: A Multicenter Retrospective Cohort Study</title><title>Infectious diseases and therapy</title><addtitle>Infect Dis Ther</addtitle><description>Introduction Tigecycline is a potential alternative to trimethoprim–sulfamethoxazole in treating Stenotrophomonas maltophilia infections due to its potent in vitro antimicrobial activity. Clinical evidence regarding the use of tigecycline in the treatment of S. maltophilia infections is scarce. In this study, we assessed the efficacy of tigecycline treating ventilator-associated pneumonia (VAP) due to S. maltophilia in comparison with fluoroquinolones. Methods This is a multicenter retrospective cohort study of patients admitted between January 2017 and December 2020 with the diagnosis of VAP caused by S. maltophilia receiving either tigecycline or fluoroquinolones as the definitive therapy ≥ 48 h. Clinical outcomes including 28-day mortality, clinical cure and microbiological cure were analyzed. Results Of 82 patients with S. maltophilia VAP included, 46 received tigecycline, and 36 received fluoroquinolones; 70.7% of patients had polymicrobial pneumonia, and the appropriate empiric therapy was applied to only 14.6% of patients. The overall 28-day mortality was 39%. Compared with patients receiving fluoroquinolones, tigecycline therapy resulted in worse clinical cure (32.6% vs. 63.9%, p  = 0.009) and microbiological cure (28.6% vs. 59.1%, p  = 0.045), while there was no statistical difference between 28-day mortality (47.8% vs. 27.8%, p  = 0.105) in the two groups. Similar results were also shown in the inverse probability of treatment weighted univariable regression model and multivariable regression model. Conclusions The standard dose of tigecycline therapy was associated with a lower clinical and microbiological cure rate but not associated with an increased 28-day mortality in patients with S. maltophilia VAP compared with fluoroquinolones. 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Clinical evidence regarding the use of tigecycline in the treatment of S. maltophilia infections is scarce. In this study, we assessed the efficacy of tigecycline treating ventilator-associated pneumonia (VAP) due to S. maltophilia in comparison with fluoroquinolones. Methods This is a multicenter retrospective cohort study of patients admitted between January 2017 and December 2020 with the diagnosis of VAP caused by S. maltophilia receiving either tigecycline or fluoroquinolones as the definitive therapy ≥ 48 h. Clinical outcomes including 28-day mortality, clinical cure and microbiological cure were analyzed. Results Of 82 patients with S. maltophilia VAP included, 46 received tigecycline, and 36 received fluoroquinolones; 70.7% of patients had polymicrobial pneumonia, and the appropriate empiric therapy was applied to only 14.6% of patients. The overall 28-day mortality was 39%. Compared with patients receiving fluoroquinolones, tigecycline therapy resulted in worse clinical cure (32.6% vs. 63.9%, p  = 0.009) and microbiological cure (28.6% vs. 59.1%, p  = 0.045), while there was no statistical difference between 28-day mortality (47.8% vs. 27.8%, p  = 0.105) in the two groups. Similar results were also shown in the inverse probability of treatment weighted univariable regression model and multivariable regression model. Conclusions The standard dose of tigecycline therapy was associated with a lower clinical and microbiological cure rate but not associated with an increased 28-day mortality in patients with S. maltophilia VAP compared with fluoroquinolones. Considering the unfavorable clinical outcomes, we therefore recommend against using the standard dose of tigecycline in treating S. maltophilia VAP unless new clinical evidence emerges.</abstract><cop>Cheshire</cop><pub>Springer Healthcare</pub><pmid>34374953</pmid><doi>10.1007/s40121-021-00516-5</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-4897-0703</orcidid><oa>free_for_read</oa></addata></record>
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subjects Analysis
Antibiotics
Bacterial pneumonia
Care and treatment
China
Clinical outcomes
Cohort analysis
Drug dosages
Health aspects
Infectious Diseases
Internal Medicine
Medical research
Medicine
Medicine & Public Health
Medicine, Experimental
Mortality
Original Research
Pneumonia
Ventilators
title Tigecycline in the Treatment of Ventilator-Associated Pneumonia Due to Stenotrophomonas maltophilia: A Multicenter Retrospective Cohort Study
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