TY - JOUR
T1 - Ceftaroline for severe community-acquired pneumonia
T2 - A real-world two-centre experience in Italy and Spain
AU - Bassetti, Matteo
AU - Russo, Alessandro
AU - Cilloniz, Catia
AU - Giacobbe, Daniele Roberto
AU - Vena, Antonio
AU - Amaro, Rosanel
AU - Graziano, Elena
AU - Soriano, Alex
AU - Torres, Antoni
N1 - Funding Information:
Guarantor: Prof. Bassetti is the guarantor of the entire manuscript and is responsible for the content of the manuscript, including the data collected and its analysis. We are indebted to the nursing staff and the attending physicians for their cooperation in this study. Dr Cilloniz is the recipient of a Postdoctoral Grant (Strategic plan for research and innovation in health-PERIS 2016-2020) and SEPAR fellowship 2018. Funding: This study was supported by Ciber de Enfermedades Respiratorias (CibeRes CB06/06/0028), and 2009 Support to Research Groups of Catalonia 911; IDIBAPS. The funding sources had no role in the design or conduct of the study; collection, management, analysis, or interpretation of the data; preparation, review, or approval of the manuscript; or decision to submit the manuscript for publication. Competing interests: The authors declare that they have no conflicts of interest. Outside the submitted work, MB has participated in advisory boards and/or received speaker honoraria from Achaogen, Angelini, Astellas, Bayer, Basilea, BioM?rieux, Cidara, Gilead, Menarini, MSD, Nabriva, Paratek, Pfizer, Roche, Melinta, Shionogi, Tetraphase, VenatoRx and Vifor and has received study grants from Angelini, Basilea, Astellas, Shionogi, Cidara, Melinta, Gilead, Pfizer and MSD. AT has participated in Advisory Boards for Pfizer, Polyphor, Wokard, Paratek and The Medicines CO. Outside the submitted word, DRG has received honoraria from Stepstone Pharma GmbH, and an unconditioned grant from MSD Italia. Ethical approval: The study was approved by the local ethics committees of the Spanish (Register: 2009/5451) and Italian centre. Author contributions: Study Concept and Design: MB, AR, CC and AT. Acquisition, Analysis, or Interpretation of Data: MB, AR, CC, RA, AS, EG, DRG. Drafting of the Manuscript: MB, AR, CC, AT. Critical Revision of the Manuscript for Important Intellectual Content: MB, AR, DRG, CC, EG, AT. Statistical Analysis: MB, AR, DRG. Administrative, Technical, or Material Support: MB, AR, CC, RA, EG, AS, AT. Study Supervision: MB, AR, CC, AS and AT.
Funding Information:
Guarantor: Prof. Bassetti is the guarantor of the entire manuscript and is responsible for the content of the manuscript, including the data collected and its analysis. We are indebted to the nursing staff and the attending physicians for their cooperation in this study. Dr Cilloniz is the recipient of a Postdoctoral Grant (Strategic plan for research and innovation in health-PERIS 2016-2020) and SEPAR fellowship 2018.
Publisher Copyright:
© 2020
PY - 2020/4
Y1 - 2020/4
N2 - Background: Ceftaroline is one of latest additions to the armamentarium for treating community-acquired pneumonia (CAP). This study aimed to describe the outcome of severe CAP (SCAP) in a cohort of hospitalised patients treated with ceftaroline. Methods: A retrospective, observational study of patients with SCAP treated with ceftaroline in two hospitals in Spain and Italy. The primary objective was to explore 30-day mortality after diagnosis of SCAP. Results: During the study period the following were observed: there were 89 cases of SCAP treated with ceftaroline and 53 cases used in combination with other antibiotics (60%). Overall, 30-day mortality and clinical failure were 20% (18 of 89) and 36% (32 of 89), respectively. Independent predictors of 30-day mortality were: increasing age (OR for 1 year increase 1.0, 95% CI 1.0–1.1, P 0.043), presence of solid neoplasm (OR 4.0, 95% CI 1.0–15.1, P 0.044) and concomitant therapy with oseltamivir (OR 8.5, 95% CI 1.2°57.3, P 0.029). The only independent predictor of clinical failure was the time elapsing from SCAP diagnosis to ceftaroline therapy (OR for each passing day 1.5, 95% CI 1.1–1.9, P 0.003). The clinical success rate was 64% (57 of 89). In the subgroups of patients with proven Streptococcus pneumoniae, methicillin-susceptible Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) infection, clinical success was 83% (10 of 12), 75% (three of four) and 56% (five of nine), respectively. Conclusions: Considering its spectrum of activity, ceftaroline could represent an important therapeutic option for SCAP. Further studies are needed to identify the precise clinical success rate against MRSA in a larger cohort of patients with SCAP.
AB - Background: Ceftaroline is one of latest additions to the armamentarium for treating community-acquired pneumonia (CAP). This study aimed to describe the outcome of severe CAP (SCAP) in a cohort of hospitalised patients treated with ceftaroline. Methods: A retrospective, observational study of patients with SCAP treated with ceftaroline in two hospitals in Spain and Italy. The primary objective was to explore 30-day mortality after diagnosis of SCAP. Results: During the study period the following were observed: there were 89 cases of SCAP treated with ceftaroline and 53 cases used in combination with other antibiotics (60%). Overall, 30-day mortality and clinical failure were 20% (18 of 89) and 36% (32 of 89), respectively. Independent predictors of 30-day mortality were: increasing age (OR for 1 year increase 1.0, 95% CI 1.0–1.1, P 0.043), presence of solid neoplasm (OR 4.0, 95% CI 1.0–15.1, P 0.044) and concomitant therapy with oseltamivir (OR 8.5, 95% CI 1.2°57.3, P 0.029). The only independent predictor of clinical failure was the time elapsing from SCAP diagnosis to ceftaroline therapy (OR for each passing day 1.5, 95% CI 1.1–1.9, P 0.003). The clinical success rate was 64% (57 of 89). In the subgroups of patients with proven Streptococcus pneumoniae, methicillin-susceptible Staphylococcus aureus and methicillin-resistant S. aureus (MRSA) infection, clinical success was 83% (10 of 12), 75% (three of four) and 56% (five of nine), respectively. Conclusions: Considering its spectrum of activity, ceftaroline could represent an important therapeutic option for SCAP. Further studies are needed to identify the precise clinical success rate against MRSA in a larger cohort of patients with SCAP.
KW - Ceftaroline
KW - Influenza
KW - Methicillin-resistance Staphylococcus aureus (MRSA)
KW - Severe community-acquired pneumonia
KW - Streptococcus pneumoniae
UR - http://www.scopus.com/inward/record.url?scp=85081921835&partnerID=8YFLogxK
U2 - 10.1016/j.ijantimicag.2020.105921
DO - 10.1016/j.ijantimicag.2020.105921
M3 - Original Article
C2 - 32061999
AN - SCOPUS:85081921835
SN - 0924-8579
VL - 55
JO - International Journal of Antimicrobial Agents
JF - International Journal of Antimicrobial Agents
IS - 4
M1 - 105921
ER -