TY - JOUR
T1 - Effect of Combined β-Lactam/Macrolide Therapy on Mortality According to the Microbial Etiology and Inflammatory Status of Patients With Community-Acquired Pneumonia
AU - Ceccato, Adrian
AU - Cilloniz, Catia
AU - Martin-Loeches, Ignacio
AU - Ranzani, Otavio T.
AU - Gabarrus, Albert
AU - Bueno, Leticia
AU - Garcia-Vidal, Carolina
AU - Ferrer, Miquel
AU - Niederman, Michael S.
AU - Torres, Antoni
N1 - Funding Information:
Author contributions: A. T. had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: A. C., A. T.; data collection: A. C., C. C., L. B., C. G.-V., M. F.; statistical analysis: A. G.; analysis and interpretation of data: A. C., I. M.-L., O. T. R., C. G.-V., M. F., M. S. N., A. T.; drafting of the manuscript: A. C.; critical revision of the manuscript for important intellectual content: I. M.-L., O. T. R., C. G.-V., M. F., M. S. N., and A. T.; and study supervision: A. T., Financial/nonfinancial disclosures: None declared., Other contributions: The authors are indebted to all medical and nursing colleagues for their assistance and cooperation in this study. The authors thank Michael Maudsley, BA (University of Barcelona) for assistance in the language review., Role of sponsors: The funding sources had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication., Additional information: The e-Appendix, e-Figure, and e-Tables can be found in the Supplemental Materials section of the online article., FUNDING/SUPPORT: Dr Ceccato is supported by SEPAR-ALAT. Dr Cilloniz is the recipient of ERS Short-Term Fellowship and Postdoctoral Grant PERIS 2016-2020 (Pla Estratègic de Recerca i Innovació en Salut). Dr Garcia-Vidal has received an Intensificació Grant, a grant supported by the Catalan Health Agency PERIS (Pla Estratègic de Recerca i Innovació en Salut).
Funding Information:
FUNDING/SUPPORT: Dr Ceccato is supported by SEPAR-ALAT. Dr Cilloniz is the recipient of ERS Short-Term Fellowship and Postdoctoral Grant PERIS 2016-2020 (Pla Estratègic de Recerca i Innovació en Salut). Dr Garcia-Vidal has received an Intensificació Grant, a grant supported by the Catalan Health Agency PERIS (Pla Estratègic de Recerca i Innovació en Salut).
Funding Information:
Author contributions: A. T. had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: A. C. A. T.; data collection: A. C. C. C. L. B. C. G.-V. M. F.; statistical analysis: A. G.; analysis and interpretation of data: A. C. I. M.-L. O. T. R. C. G.-V. M. F. M. S. N. A. T.; drafting of the manuscript: A. C.; critical revision of the manuscript for important intellectual content: I. M.-L. O. T. R. C. G.-V. M. F. M. S. N. and A. T.; and study supervision: A. T. Financial/nonfinancial disclosures: None declared. Other contributions: The authors are indebted to all medical and nursing colleagues for their assistance and cooperation in this study. The authors thank Michael Maudsley, BA (University of Barcelona) for assistance in the language review. Role of sponsors: The funding sources had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. Additional information: The e-Appendix, e-Figure, and e-Tables can be found in the Supplemental Materials section of the online article. FUNDING/SUPPORT: Dr Ceccato is supported by SEPAR-ALAT. Dr Cilloniz is the recipient of ERS Short-Term Fellowship and Postdoctoral Grant PERIS 2016-2020 (Pla Estrat?gic de Recerca i Innovaci? en Salut). Dr Garcia-Vidal has received an Intensificaci? Grant, a grant supported by the Catalan Health Agency PERIS (Pla Estrat?gic de Recerca i Innovaci? en Salut).
Publisher Copyright:
© 2018 American College of Chest Physicians
PY - 2019/4
Y1 - 2019/4
N2 - Background: Antibiotic combinations that include macrolides have shown lower mortality rates than β-lactams in monotherapy or combined with fluoroquinolones in patients with community-acquired pneumonia (CAP). However, this effect has not been studied according to the levels of C-reactive protein in CAP with identified microbial cause. In patients with CAP and known microbial cause we aimed to evaluate 30-day mortality of a β-lactam plus macrolide (BL + M) compared with a fluoroquinolone alone or with a β-lactam (FQ ± BL). Methods: We analyzed a prospective observational cohort of patients with CAP admitted to the Hospital Clinic of Barcelona between 1996 and 2016. We included only patients with known microbial cause. Results: Of 1,715 patients (29%) with known etiology, a total of 932 patients (54%) received BL + M. Despite lower crude mortality in the BL + M group in the overall population (BL + M, 5% vs FQ ± BL, 8%; P =.015), after adjustment by a propensity score and baseline characteristics, the combination of BL + M had a protective effect on mortality only in patients with high inflammatory response (C-reactive protein, > 15 mg/dL) and pneumococcal CAP (adjusted OR, 0.28; 95% CI, 0.09-0.93). No benefits on mortality were observed for the population without high inflammatory response and pneumococcal CAP or with other etiologies. Conclusions: The combination of a β-lactam with a macrolide was associated with decreased mortality in patients with pneumococcal CAP and in patients with high systemic inflammatory response. When both factors occurred together, BL + M was protective for mortality in the multivariate analysis.
AB - Background: Antibiotic combinations that include macrolides have shown lower mortality rates than β-lactams in monotherapy or combined with fluoroquinolones in patients with community-acquired pneumonia (CAP). However, this effect has not been studied according to the levels of C-reactive protein in CAP with identified microbial cause. In patients with CAP and known microbial cause we aimed to evaluate 30-day mortality of a β-lactam plus macrolide (BL + M) compared with a fluoroquinolone alone or with a β-lactam (FQ ± BL). Methods: We analyzed a prospective observational cohort of patients with CAP admitted to the Hospital Clinic of Barcelona between 1996 and 2016. We included only patients with known microbial cause. Results: Of 1,715 patients (29%) with known etiology, a total of 932 patients (54%) received BL + M. Despite lower crude mortality in the BL + M group in the overall population (BL + M, 5% vs FQ ± BL, 8%; P =.015), after adjustment by a propensity score and baseline characteristics, the combination of BL + M had a protective effect on mortality only in patients with high inflammatory response (C-reactive protein, > 15 mg/dL) and pneumococcal CAP (adjusted OR, 0.28; 95% CI, 0.09-0.93). No benefits on mortality were observed for the population without high inflammatory response and pneumococcal CAP or with other etiologies. Conclusions: The combination of a β-lactam with a macrolide was associated with decreased mortality in patients with pneumococcal CAP and in patients with high systemic inflammatory response. When both factors occurred together, BL + M was protective for mortality in the multivariate analysis.
KW - Streptococcus pneumoniae
KW - community-acquired pneumonia
KW - inflammatory response
KW - macrolide
KW - sepsis
UR - http://www.scopus.com/inward/record.url?scp=85061941481&partnerID=8YFLogxK
U2 - 10.1016/j.chest.2018.11.006
DO - 10.1016/j.chest.2018.11.006
M3 - Original Article
C2 - 30471269
AN - SCOPUS:85061941481
SN - 0012-3692
VL - 155
SP - 795
EP - 804
JO - Chest
JF - Chest
IS - 4
ER -