P-1513. <i>In Vitro</i> Activity of Ceftaroline against Bacterial Pathogens from Pediatric Patients Collected During the ATLAS Global Surveillance Program in 2018-2022

Abstract Background The parenteral cephem ceftaroline fosamil is approved for treatment of adults and children with complicated skin and soft tissue infections (SSTI) and community-acquired bacterial pneumonia (CABP) caused by susceptible isolates of Staphylococcus aureus (methicillin-resistant [MRSA; SSTI] and methicillin-susceptible [MSSA; SSTI and CABP]), β-hemolytic streptococci (Streptococcus pyogenes and Streptococcus agalactiae [SSTI]); Streptococcus pneumoniae (CABP, including concurrent bacteremia), Haemophilus influenzae (CABP), and isolates of Escherichia coli, Klebsiella pneumoniae and Klebsiella oxytoca (SSTI and CABP). Several pathogens causing CABP are also frequently associated with bloodstream infections (BSI). This study examined the in vitro susceptibility to ceftaroline and comparator agents among pathogens isolated from pediatric patients with SSTI, respiratory tract infections (RTI), and BSI as part of the Antimicrobial Testing Leadership and Surveillance (ATLAS) surveillance program in 2018-2022. Methods 16,533 non-duplicate, clinically relevant isolates of S. aureus, β-hemolytic streptococci, S. pneumoniae, H. influenzae, M. catarrhalis and Enterobacterales were collected from patients aged 0-17 years old with BSI, RTI and SSTI by 285 medical centres in 60 countries. In vitro susceptibility to ceftaroline was determined by CLSI broth microdilution and results were interpreted using CLSI 2024 breakpoints where available. Extended spectrum β-lactamase (ESBL) screening was performed using the CLSI M100 method. Results The in vitro activity of ceftaroline is summarized in the table. 100% of MSSA and β-hemolytic streptococci isolates, &amp;gt;99% of S. pneumoniae, &amp;gt;99% of H. influenzae, and &amp;gt;92% of ESBL screen-negative E. coli, K. pneumoniae, K. oxytoca and P. mirabilis collected from all pediatric patients combined tested as susceptible to ceftaroline, as did &amp;gt;97% of MRSA. M. catarrhalis ceftaroline MIC values ranged from ≤0.06 - 8 µg/mL, with an MIC90 of 0.25 mg/L. Susceptibility was consistant across each of the age groups. Conclusion Ceftaroline demonstrated potent in vitro activity against a global collection of clinically relevant pathogens collected from pediatric patients. Disclosures Daniel F. Sahm, PhD, Pfizer, Inc.: Advisor/Consultant

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Journal
Open Forum Infectious Diseases
Published
2025-01-29
DOI
https://doi.org/10.1093/ofid/ofae631.1682
Primary Topic
Antibiotics Pharmacokinetics and Efficacy
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article
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article

P-1513. In Vitro Activity of Ceftaroline against Bacterial Pathogens from Pediatric Patients Collected During the ATLAS Global Surveillance Program in 2018-2022

Gregory W. Stone, Meredith Hackel, Daniel F. Sahm
Open Forum Infectious Diseases
Antibiotics Pharmacokinetics and Efficacy
article

P-1513. In Vitro Activity of Ceftaroline against Bacterial Pathogens from Pediatric Patients Collected During the ATLAS Global Surveillance Program in 2018-2022

Gregory W. Stone, Meredith Hackel, Daniel F. Sahm
article en

Abstract

Abstract Background The parenteral cephem ceftaroline fosamil is approved for treatment of adults and children with complicated skin and soft tissue infections (SSTI) and community-acquired bacterial pneumonia (CABP) caused by susceptible isolates of Staphylococcus aureus (methicillin-resistant [MRSA; SSTI] and methicillin-susceptible [MSSA; SSTI and CABP]), β-hemolytic streptococci (Streptococcus pyogenes and Streptococcus agalactiae [SSTI]); Streptococcus pneumoniae (CABP, including concurrent bacteremia), Haemophilus influenzae (CABP), and isolates of Escherichia coli, Klebsiella pneumoniae and Klebsiella oxytoca (SSTI and CABP). Several pathogens causing CABP are also frequently associated with bloodstream infections (BSI). This study examined the in vitro susceptibility to ceftaroline and comparator agents among pathogens isolated from pediatric patients with SSTI, respiratory tract infections (RTI), and BSI as part of the Antimicrobial Testing Leadership and Surveillance (ATLAS) surveillance program in 2018-2022. Methods 16,533 non-duplicate, clinically relevant isolates of S. aureus, β-hemolytic streptococci, S. pneumoniae, H. influenzae, M. catarrhalis and Enterobacterales were collected from patients aged 0-17 years old with BSI, RTI and SSTI by 285 medical centres in 60 countries. In vitro susceptibility to ceftaroline was determined by CLSI broth microdilution and results were interpreted using CLSI 2024 breakpoints where available. Extended spectrum β-lactamase (ESBL) screening was performed using the CLSI M100 method. Results The in vitro activity of ceftaroline is summarized in the table. 100% of MSSA and β-hemolytic streptococci isolates, &amp;gt;99% of S. pneumoniae, &amp;gt;99% of H. influenzae, and &amp;gt;92% of ESBL screen-negative E. coli, K. pneumoniae, K. oxytoca and P. mirabilis collected from all pediatric patients combined tested as susceptible to ceftaroline, as did &amp;gt;97% of MRSA. M. catarrhalis ceftaroline MIC values ranged from ≤0.06 - 8 µg/mL, with an MIC90 of 0.25 mg/L. Susceptibility was consistant across each of the age groups. Conclusion Ceftaroline demonstrated potent in vitro activity against a global collection of clinically relevant pathogens collected from pediatric patients. Disclosures Daniel F. Sahm, PhD, Pfizer, Inc.: Advisor/Consultant

Open Forum Infectious DiseasesVol. 12(Supplement_1)
Pfizer (United States) (US)
Openalex Percentile: Top 98%
Antibiotics Pharmacokinetics and Efficacy
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