Pneumococal community-acquired pneumonia in the intensive care unit: Azithromycin remains protective despite macrolide resistance
Streptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in SP, guidelines recommend the use of macrolides as part of a combination regiment for intensive care unit (ICU) patients with CAP. We sought t...
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Published in | Respiratory medicine Vol. 177; p. 106307 |
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Format | Journal Article |
Language | English |
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01.02.2021
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Abstract | Streptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in SP, guidelines recommend the use of macrolides as part of a combination regiment for intensive care unit (ICU) patients with CAP. We sought to describe if macrolide resistance effects outcomes in SP CAP in the ICU and if macrolides remain associated with a mortality advantage in an era of greater resistance.
We identified all patients with SP CAP admitted to the ICU between January 2012 and December 2016, and hospital mortality represented the primary endpoint. We recorded markers of acute and chronic disease severity (eg, Charlson score, need for mechanical ventilation and/or vasopressors) along with infection-related variables including the presence of macrolide resistance. We compared subjects treated with azithromycin to those not given this agent.
The cohort included 140 subjects (89.2% on mechanical ventilation, 14.3% crude mortality). Macrolide resistance occurred often (60.8%) and, in univariate analyses, was associated with higher mortality while azithromycin use appeared linked to fewer death. In multivariate analysis controlling for multiple confounders including macrolide resistance and the timeliness and appropriateness of antibiotic therapy, treatment with azithromycin resulted in fewer death (Adjusted odds ratio 0.27, 95% confidence interval: 0.09–0.85, p = 0.024). Macrolide resistance, however, was not independently related to mortality.
Macrolide resistance appears frequently in SP ICU CAP. The addition of azithromycin to the antibiotic regimen in this scenario is significantly associated with a reduction in in-hospital mortality independent of multiple co-variates.
•Macrolide resistance is common in Streptococcus pneumoniae causing severe community-acquired pneumonia.•Azithromycin treatment is associated with survival in S. pneumoniae community-acquired pneumonia in critically ill patients.•The benefit related to azithromycin is independent of multiple possible factors to include macrolide resistance. |
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AbstractList | Streptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in SP, guidelines recommend the use of macrolides as part of a combination regiment for intensive care unit (ICU) patients with CAP. We sought to describe if macrolide resistance effects outcomes in SP CAP in the ICU and if macrolides remain associated with a mortality advantage in an era of greater resistance.
We identified all patients with SP CAP admitted to the ICU between January 2012 and December 2016, and hospital mortality represented the primary endpoint. We recorded markers of acute and chronic disease severity (eg, Charlson score, need for mechanical ventilation and/or vasopressors) along with infection-related variables including the presence of macrolide resistance. We compared subjects treated with azithromycin to those not given this agent.
The cohort included 140 subjects (89.2% on mechanical ventilation, 14.3% crude mortality). Macrolide resistance occurred often (60.8%) and, in univariate analyses, was associated with higher mortality while azithromycin use appeared linked to fewer death. In multivariate analysis controlling for multiple confounders including macrolide resistance and the timeliness and appropriateness of antibiotic therapy, treatment with azithromycin resulted in fewer death (Adjusted odds ratio 0.27, 95% confidence interval: 0.09–0.85, p = 0.024). Macrolide resistance, however, was not independently related to mortality.
Macrolide resistance appears frequently in SP ICU CAP. The addition of azithromycin to the antibiotic regimen in this scenario is significantly associated with a reduction in in-hospital mortality independent of multiple co-variates.
•Macrolide resistance is common in Streptococcus pneumoniae causing severe community-acquired pneumonia.•Azithromycin treatment is associated with survival in S. pneumoniae community-acquired pneumonia in critically ill patients.•The benefit related to azithromycin is independent of multiple possible factors to include macrolide resistance. Streptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in SP, guidelines recommend the use of macrolides as part of a combination regiment for intensive care unit (ICU) patients with CAP. We sought to describe if macrolide resistance effects outcomes in SP CAP in the ICU and if macrolides remain associated with a mortality advantage in an era of greater resistance. We identified all patients with SP CAP admitted to the ICU between January 2012 and December 2016, and hospital mortality represented the primary endpoint. We recorded markers of acute and chronic disease severity (eg, Charlson score, need for mechanical ventilation and/or vasopressors) along with infection-related variables including the presence of macrolide resistance. We compared subjects treated with azithromycin to those not given this agent. The cohort included 140 subjects (89.2% on mechanical ventilation, 14.3% crude mortality). Macrolide resistance occurred often (60.8%) and, in univariate analyses, was associated with higher mortality while azithromycin use appeared linked to fewer death. In multivariate analysis controlling for multiple confounders including macrolide resistance and the timeliness and appropriateness of antibiotic therapy, treatment with azithromycin resulted in fewer death (Adjusted odds ratio 0.27, 95% confidence interval: 0.09-0.85, p = 0.024). Macrolide resistance, however, was not independently related to mortality. Macrolide resistance appears frequently in SP ICU CAP. The addition of azithromycin to the antibiotic regimen in this scenario is significantly associated with a reduction in in-hospital mortality independent of multiple co-variates. BackgroundStreptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in SP, guidelines recommend the use of macrolides as part of a combination regiment for intensive care unit (ICU) patients with CAP. We sought to describe if macrolide resistance effects outcomes in SP CAP in the ICU and if macrolides remain associated with a mortality advantage in an era of greater resistance.MethodsWe identified all patients with SP CAP admitted to the ICU between January 2012 and December 2016, and hospital mortality represented the primary endpoint. We recorded markers of acute and chronic disease severity (eg, Charlson score, need for mechanical ventilation and/or vasopressors) along with infection-related variables including the presence of macrolide resistance. We compared subjects treated with azithromycin to those not given this agent.ResultsThe cohort included 140 subjects (89.2% on mechanical ventilation, 14.3% crude mortality). Macrolide resistance occurred often (60.8%) and, in univariate analyses, was associated with higher mortality while azithromycin use appeared linked to fewer death. In multivariate analysis controlling for multiple confounders including macrolide resistance and the timeliness and appropriateness of antibiotic therapy, treatment with azithromycin resulted in fewer death (Adjusted odds ratio 0.27, 95% confidence interval: 0.09–0.85, p = 0.024). Macrolide resistance, however, was not independently related to mortality.ConclusionsMacrolide resistance appears frequently in SP ICU CAP. The addition of azithromycin to the antibiotic regimen in this scenario is significantly associated with a reduction in in-hospital mortality independent of multiple co-variates. Streptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in SP, guidelines recommend the use of macrolides as part of a combination regiment for intensive care unit (ICU) patients with CAP. We sought to describe if macrolide resistance effects outcomes in SP CAP in the ICU and if macrolides remain associated with a mortality advantage in an era of greater resistance.BACKGROUNDStreptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in SP, guidelines recommend the use of macrolides as part of a combination regiment for intensive care unit (ICU) patients with CAP. We sought to describe if macrolide resistance effects outcomes in SP CAP in the ICU and if macrolides remain associated with a mortality advantage in an era of greater resistance.We identified all patients with SP CAP admitted to the ICU between January 2012 and December 2016, and hospital mortality represented the primary endpoint. We recorded markers of acute and chronic disease severity (eg, Charlson score, need for mechanical ventilation and/or vasopressors) along with infection-related variables including the presence of macrolide resistance. We compared subjects treated with azithromycin to those not given this agent.METHODSWe identified all patients with SP CAP admitted to the ICU between January 2012 and December 2016, and hospital mortality represented the primary endpoint. We recorded markers of acute and chronic disease severity (eg, Charlson score, need for mechanical ventilation and/or vasopressors) along with infection-related variables including the presence of macrolide resistance. We compared subjects treated with azithromycin to those not given this agent.The cohort included 140 subjects (89.2% on mechanical ventilation, 14.3% crude mortality). Macrolide resistance occurred often (60.8%) and, in univariate analyses, was associated with higher mortality while azithromycin use appeared linked to fewer death. In multivariate analysis controlling for multiple confounders including macrolide resistance and the timeliness and appropriateness of antibiotic therapy, treatment with azithromycin resulted in fewer death (Adjusted odds ratio 0.27, 95% confidence interval: 0.09-0.85, p = 0.024). Macrolide resistance, however, was not independently related to mortality.RESULTSThe cohort included 140 subjects (89.2% on mechanical ventilation, 14.3% crude mortality). Macrolide resistance occurred often (60.8%) and, in univariate analyses, was associated with higher mortality while azithromycin use appeared linked to fewer death. In multivariate analysis controlling for multiple confounders including macrolide resistance and the timeliness and appropriateness of antibiotic therapy, treatment with azithromycin resulted in fewer death (Adjusted odds ratio 0.27, 95% confidence interval: 0.09-0.85, p = 0.024). Macrolide resistance, however, was not independently related to mortality.Macrolide resistance appears frequently in SP ICU CAP. The addition of azithromycin to the antibiotic regimen in this scenario is significantly associated with a reduction in in-hospital mortality independent of multiple co-variates.CONCLUSIONSMacrolide resistance appears frequently in SP ICU CAP. The addition of azithromycin to the antibiotic regimen in this scenario is significantly associated with a reduction in in-hospital mortality independent of multiple co-variates. |
ArticleNumber | 106307 |
Author | Hampton, Nicolas Micek, Scott T. Simmons, James Shorr, Andrew F. Kollef, Marin H. |
Author_xml | – sequence: 1 givenname: Andrew F. surname: Shorr fullname: Shorr, Andrew F. email: Andrew.shorr@gmail.com organization: Pulmonary & Critical Care Medicine, Washington Hospital Center, Washington, DC, USA – sequence: 2 givenname: James surname: Simmons fullname: Simmons, James organization: Department of Pharmacy Practice, St. Louis College of Pharmacy, St. Louis, MO, USA – sequence: 3 givenname: Nicolas surname: Hampton fullname: Hampton, Nicolas organization: Center for Clinical Excellence, BJC Health, St. Louis, MO, USA – sequence: 4 givenname: Scott T. surname: Micek fullname: Micek, Scott T. organization: Department of Pharmacy Practice, St. Louis College of Pharmacy, St. Louis, MO, USA – sequence: 5 givenname: Marin H. surname: Kollef fullname: Kollef, Marin H. organization: Pulmonary & Critical Care Medicine, Washington University School of Medicine, St. Louis, MO, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33486205$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1093/cid/cis414 10.1097/00003246-198510000-00009 10.1016/j.ccm.2018.07.006 10.1186/1471-2334-14-61 10.1016/0021-9681(87)90171-8 10.1136/bmj.j2471 10.3389/fcimb.2016.00098 10.1001/jamainternmed.2014.4887 10.1164/rccm.201908-1581ST 10.1016/j.jiac.2019.05.027 10.1164/rccm.201502-0212OC 10.1016/j.ijantimicag.2015.04.010 10.1007/s00408-015-9822-7 10.1055/s-0036-1592313 10.1093/jac/dkp088 10.1097/CCM.0b013e3182a66b9b 10.1016/j.rmed.2007.04.018 10.1128/AAC.00006-07 10.1016/j.rmed.2018.05.020 10.1093/jac/46.1.19 |
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References | Tessmer, Welte, Martus (bib8) 2009; 63 Reyes Calzada, Martínez Tomas, Cremades Romero (bib10) 2007; 101 Koch, Esteban, Chin (bib19) 2000; 46 Suzuki, Sasabuchi, Hatakeyama (bib17) 2019; 25 Arnold, Lopardo, Wiemken (bib7) 2018; 140 Schroeder, Stephens (bib13) 2016; 6 Waterer (bib2) 2016; 37 Asadi, Sligl, Eurich (bib5) 2012; 55 Lodise, Kwa, Cosler (bib9) 2007; 51 Charlson, Pompei, Ales (bib14) 1987; 40 Raz-Pasteur, Shasha, Paul (bib6) 2015; 46 Cilloniz, Albert, Liapikou (bib18) 2015; 191 Sligl, Asadi, Eurich (bib4) 2014; 42 Arnold, Bordon, Fernandez-Botran (bib20) 2016; 194 Garin, Genné, Carballo (bib16) 2014; 174 Wunderink (bib1) 2018; 39 Micek, Lang, Fuller (bib12) 2014; 14 Knaus, Draper, Wagner (bib15) 1985; 13 Wunderink, Waterer (bib11) 2017 Jul 10; 358 Metlay, Waterer, Long (bib3) 2019; 200 Raz-Pasteur (10.1016/j.rmed.2021.106307_bib6) 2015; 46 Cilloniz (10.1016/j.rmed.2021.106307_bib18) 2015; 191 Wunderink (10.1016/j.rmed.2021.106307_bib1) 2018; 39 Schroeder (10.1016/j.rmed.2021.106307_bib13) 2016; 6 Arnold (10.1016/j.rmed.2021.106307_bib20) 2016; 194 Koch (10.1016/j.rmed.2021.106307_bib19) 2000; 46 Suzuki (10.1016/j.rmed.2021.106307_bib17) 2019; 25 Tessmer (10.1016/j.rmed.2021.106307_bib8) 2009; 63 Knaus (10.1016/j.rmed.2021.106307_bib15) 1985; 13 Charlson (10.1016/j.rmed.2021.106307_bib14) 1987; 40 Arnold (10.1016/j.rmed.2021.106307_bib7) 2018; 140 Asadi (10.1016/j.rmed.2021.106307_bib5) 2012; 55 Micek (10.1016/j.rmed.2021.106307_bib12) 2014; 14 Sligl (10.1016/j.rmed.2021.106307_bib4) 2014; 42 Lodise (10.1016/j.rmed.2021.106307_bib9) 2007; 51 Wunderink (10.1016/j.rmed.2021.106307_bib11) 2017; 358 Metlay (10.1016/j.rmed.2021.106307_bib3) 2019; 200 Reyes Calzada (10.1016/j.rmed.2021.106307_bib10) 2007; 101 Garin (10.1016/j.rmed.2021.106307_bib16) 2014; 174 Waterer (10.1016/j.rmed.2021.106307_bib2) 2016; 37 |
References_xml | – volume: 46 start-page: 242 year: 2015 end-page: 248 ident: bib6 article-title: Fluoroquinolones or macrolides alone versus combined with β-lactams for adults with community-acquired pneumonia: systematic review and meta-analysis publication-title: Int. J. Antimicrob. Agents – volume: 191 start-page: 1265 year: 2015 end-page: 1272 ident: bib18 article-title: The effect of macrolide resistance on the presentation and outcome of patients hospitalized for Streptococcus pneumoniae pneumonia publication-title: Am. J. Respir. Crit. Care Med. – volume: 174 start-page: 1894 year: 2014 end-page: 1901 ident: bib16 article-title: β-Lactam monotherapy vs β-lactam-macrolide combination treatment in moderately severe community-acquired pneumonia: a randomized noninferiority trial publication-title: JAMA Intern Med – volume: 101 start-page: 1909 year: 2007 end-page: 1915 ident: bib10 article-title: Empiric treatment in hospitalized community-acquired pneumonia. Impact on mortality, length of stay and re- admission publication-title: Respir. Med. – volume: 51 start-page: 3977 year: 2007 end-page: 3982 ident: bib9 article-title: Comparison of beta-lactam and macrolide combination therapy versus fluoroquinolone monotherapy in hospitalized Veterans Affairs patients with community-acquired pneumonia publication-title: Antimicrob. Agents Chemother. – volume: 46 start-page: 19 year: 2000 end-page: 26 ident: bib19 article-title: Apoptosis, oxidative metabolism and interleukin-8 production in human neutrophils exposed to azithromycin: effects of Streptococcus pneumoniae publication-title: J. Antimicrob. Chemother. – volume: 200 start-page: e45 year: 2019 end-page: e67 ident: bib3 article-title: Diagnosis and treatment of adults with community-acquired pneumonia. An official clinical practice guideline of the American thoracic society and infectious diseases society of America publication-title: Am. J. Respir. Crit. Care Med. – volume: 6 start-page: 98 year: 2016 ident: bib13 article-title: Macrolide resistance in Streptococcus pneumoniae publication-title: Front Cell Infect Microbiol – volume: 39 start-page: 723 year: 2018 end-page: 731 ident: bib1 article-title: Guidelines to manage community-acquired pneumonia publication-title: Clin. Chest Med. – volume: 194 start-page: 155 year: 2016 end-page: 162 ident: bib20 article-title: Macrolide use and neutrophil function/cytokine levels in hospitalized patients with community-acquired pneumonia: a pilot study publication-title: Lung – volume: 37 start-page: 799 year: 2016 end-page: 805 ident: bib2 article-title: Community-acquired pneumonia: a global perspective publication-title: Semin. Respir. Crit. Care Med. – volume: 140 start-page: 115 year: 2018 end-page: 121 ident: bib7 article-title: Macrolide therapy is associated with lower mortality in community- acquired bacteraemic pneumonia publication-title: Respir. Med. – volume: 358 start-page: j2471 year: 2017 Jul 10 ident: bib11 article-title: Advances in the causes and management of community acquired pneumonia in adults publication-title: BMJ – volume: 25 start-page: 1012 year: 2019 end-page: 1018 ident: bib17 article-title: Azithromycin plus β-lactam versus levofloxacin plus β-lactam for severe community-acquired pneumonia: a retrospective nationwide database analysis publication-title: J. Infect. Chemother. – volume: 14 start-page: 61 year: 2014 ident: bib12 article-title: Clinical implications for patients treated inappropriately for community-acquired pneumonia in the emergency department publication-title: BMC Infect. Dis. – volume: 42 start-page: 420 year: 2014 end-page: 432 ident: bib4 article-title: Macrolides and mortality in critically ill patients with community-acquired pneumonia: a systematic review and meta-analysis publication-title: Crit. Care Med. – volume: 13 start-page: 818 year: 1985 end-page: 829 ident: bib15 article-title: Apache II: a severity of disease classification system publication-title: Crit. Care Med. – volume: 63 start-page: 1025 year: 2009 end-page: 1033 ident: bib8 article-title: Impact of intravenous {beta}-lactam/macrolide versus {beta}-lactam monotherapy on mortality in hospitalized patients with community-acquired pneumonia publication-title: J. Antimicrob. Chemother. – volume: 55 start-page: 371 year: 2012 end-page: 380 ident: bib5 article-title: Macrolide-based regimens and mortality in hospitalized patients with community- acquired pneumonia: a systematic review and meta-analysis publication-title: Clin. Infect. Dis. – volume: 40 start-page: 373 year: 1987 end-page: 383 ident: bib14 article-title: A new method of classifying prognostic comorbidity in longitudinal studies: development and validation publication-title: J. Chron. Dis. – volume: 55 start-page: 371 year: 2012 ident: 10.1016/j.rmed.2021.106307_bib5 article-title: Macrolide-based regimens and mortality in hospitalized patients with community- acquired pneumonia: a systematic review and meta-analysis publication-title: Clin. Infect. Dis. doi: 10.1093/cid/cis414 – volume: 13 start-page: 818 year: 1985 ident: 10.1016/j.rmed.2021.106307_bib15 article-title: Apache II: a severity of disease classification system publication-title: Crit. Care Med. doi: 10.1097/00003246-198510000-00009 – volume: 39 start-page: 723 year: 2018 ident: 10.1016/j.rmed.2021.106307_bib1 article-title: Guidelines to manage community-acquired pneumonia publication-title: Clin. Chest Med. doi: 10.1016/j.ccm.2018.07.006 – volume: 14 start-page: 61 year: 2014 ident: 10.1016/j.rmed.2021.106307_bib12 article-title: Clinical implications for patients treated inappropriately for community-acquired pneumonia in the emergency department publication-title: BMC Infect. Dis. doi: 10.1186/1471-2334-14-61 – volume: 40 start-page: 373 year: 1987 ident: 10.1016/j.rmed.2021.106307_bib14 article-title: A new method of classifying prognostic comorbidity in longitudinal studies: development and validation publication-title: J. Chron. Dis. doi: 10.1016/0021-9681(87)90171-8 – volume: 358 start-page: j2471 year: 2017 ident: 10.1016/j.rmed.2021.106307_bib11 article-title: Advances in the causes and management of community acquired pneumonia in adults publication-title: BMJ doi: 10.1136/bmj.j2471 – volume: 6 start-page: 98 year: 2016 ident: 10.1016/j.rmed.2021.106307_bib13 article-title: Macrolide resistance in Streptococcus pneumoniae publication-title: Front Cell Infect Microbiol doi: 10.3389/fcimb.2016.00098 – volume: 174 start-page: 1894 year: 2014 ident: 10.1016/j.rmed.2021.106307_bib16 article-title: β-Lactam monotherapy vs β-lactam-macrolide combination treatment in moderately severe community-acquired pneumonia: a randomized noninferiority trial publication-title: JAMA Intern Med doi: 10.1001/jamainternmed.2014.4887 – volume: 200 start-page: e45 year: 2019 ident: 10.1016/j.rmed.2021.106307_bib3 article-title: Diagnosis and treatment of adults with community-acquired pneumonia. An official clinical practice guideline of the American thoracic society and infectious diseases society of America publication-title: Am. J. Respir. Crit. Care Med. doi: 10.1164/rccm.201908-1581ST – volume: 25 start-page: 1012 year: 2019 ident: 10.1016/j.rmed.2021.106307_bib17 article-title: Azithromycin plus β-lactam versus levofloxacin plus β-lactam for severe community-acquired pneumonia: a retrospective nationwide database analysis publication-title: J. Infect. Chemother. doi: 10.1016/j.jiac.2019.05.027 – volume: 191 start-page: 1265 year: 2015 ident: 10.1016/j.rmed.2021.106307_bib18 article-title: The effect of macrolide resistance on the presentation and outcome of patients hospitalized for Streptococcus pneumoniae pneumonia publication-title: Am. J. Respir. Crit. Care Med. doi: 10.1164/rccm.201502-0212OC – volume: 46 start-page: 242 year: 2015 ident: 10.1016/j.rmed.2021.106307_bib6 article-title: Fluoroquinolones or macrolides alone versus combined with β-lactams for adults with community-acquired pneumonia: systematic review and meta-analysis publication-title: Int. J. Antimicrob. Agents doi: 10.1016/j.ijantimicag.2015.04.010 – volume: 194 start-page: 155 year: 2016 ident: 10.1016/j.rmed.2021.106307_bib20 article-title: Macrolide use and neutrophil function/cytokine levels in hospitalized patients with community-acquired pneumonia: a pilot study publication-title: Lung doi: 10.1007/s00408-015-9822-7 – volume: 37 start-page: 799 year: 2016 ident: 10.1016/j.rmed.2021.106307_bib2 article-title: Community-acquired pneumonia: a global perspective publication-title: Semin. Respir. Crit. Care Med. doi: 10.1055/s-0036-1592313 – volume: 63 start-page: 1025 year: 2009 ident: 10.1016/j.rmed.2021.106307_bib8 article-title: Impact of intravenous {beta}-lactam/macrolide versus {beta}-lactam monotherapy on mortality in hospitalized patients with community-acquired pneumonia publication-title: J. Antimicrob. Chemother. doi: 10.1093/jac/dkp088 – volume: 42 start-page: 420 year: 2014 ident: 10.1016/j.rmed.2021.106307_bib4 article-title: Macrolides and mortality in critically ill patients with community-acquired pneumonia: a systematic review and meta-analysis publication-title: Crit. Care Med. doi: 10.1097/CCM.0b013e3182a66b9b – volume: 101 start-page: 1909 year: 2007 ident: 10.1016/j.rmed.2021.106307_bib10 article-title: Empiric treatment in hospitalized community-acquired pneumonia. Impact on mortality, length of stay and re- admission publication-title: Respir. Med. doi: 10.1016/j.rmed.2007.04.018 – volume: 51 start-page: 3977 year: 2007 ident: 10.1016/j.rmed.2021.106307_bib9 article-title: Comparison of beta-lactam and macrolide combination therapy versus fluoroquinolone monotherapy in hospitalized Veterans Affairs patients with community-acquired pneumonia publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.00006-07 – volume: 140 start-page: 115 year: 2018 ident: 10.1016/j.rmed.2021.106307_bib7 article-title: Macrolide therapy is associated with lower mortality in community- acquired bacteraemic pneumonia publication-title: Respir. Med. doi: 10.1016/j.rmed.2018.05.020 – volume: 46 start-page: 19 year: 2000 ident: 10.1016/j.rmed.2021.106307_bib19 article-title: Apoptosis, oxidative metabolism and interleukin-8 production in human neutrophils exposed to azithromycin: effects of Streptococcus pneumoniae publication-title: J. Antimicrob. Chemother. doi: 10.1093/jac/46.1.19 |
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Snippet | Streptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide resistance in... BackgroundStreptococcus pneumoniae (SP) remains the leading pathogen in community-acquired pneumonia (CAP). Despite the increasing prevalence of macrolide... |
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SubjectTerms | Antibiotics Azithromycin Blood Chronic illnesses Chronic obstructive pulmonary disease Comorbidity Disease Hospitals Intensive care Intensive care unit Mechanical ventilation Mortality Multivariate analysis Pathogens Patients Pneumonia Streptococcus infections Variables |
Title | Pneumococal community-acquired pneumonia in the intensive care unit: Azithromycin remains protective despite macrolide resistance |
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