P-1859. A Stewardship Focused Evaluation of Patients Treated with Ceftriaxone for Infections due to Penicillin Susceptible Streptococcus spp. in Outpatient Parenteral Antimicrobial Therapy

Abstract Background In the outpatient parenteral antimicrobial therapy (OPAT) setting there are limited data quantifying the tradeoffs of using broader spectrum, but more convenient, antimicrobial regimens. This is particularly true with respect to adverse drug events, including Clostridioides difficile infection (CDI) and subsequent multidrug resistant (MDR) organism isolation.Table 1.Patient Cohort CharacteristicsTable 2.Primary and Secondary Outcomes Methods We performed a retrospective cohort analysis of adult patients with confirmed penicillin susceptible streptococcal infection, who received ceftriaxone (CRO) or penicillin through the OPAT service at a large academic medical center. The primary outcome was a composite outcome of clinical success rate without a significant OPAT-related adverse event (AE) or superinfection. The two components of this were successful therapy completion (completion of full planned treatment duration without an infection-related admission or ED visit, no change in therapy due to a drug-related AE, and improved or resolved infection at the end of therapy) and lack of CDI or MDR organism isolation within 12 months of therapy completion. Secondary outcomes included the individual components of the primary outcome. Results Patient characteristics reported in Table 1. Outcomes data reported in Table 2. The primary outcome was achieved in 83.1% of patients. Eleven total AEs occurred on therapy; 4 identified as catheter-related and 7 identified as drug-related. There were 1.4 cases of CDI over 1 year per 1000 days of therapy. A total of 9 MDR isolations were identified during the 1-year follow-up period. All CDI and MDR isolations were in CRO treated patients. Conclusion Our data are consistent with similar studies demonstrating high rates of clinical efficacy when utilizing CRO to treat highly penicillin-susceptible Streptococcus spp. infections. CRO was well tolerated and led to fewer line-related AEs than previously reported with more frequently administered regimens for these infections. Despite CRO being a broader-spectrum agent than necessary for highly penicillin-susceptible Streptococcus spp. infections, low adverse event rates, including long-term CDI and MDR isolation, make it an attractive choice for use in the OPAT context. Disclosures Trevor C. Van Schooneveld, MD, FSHEA, FIDSA, BioMerieux: Advisor/Consultant|BioMerieux: Grant/Research Support Mark E. Rupp, MD, Armata: Advisor/Consultant|Citius Pharmaceuticals, Inc.: Advisor/Consultant|Magnolia: Grant/Research Support|Teleflex: Advisor/Consultant Bryan T. Alexander, PharmD, BCIDP, AAHIVP, Astellas Pharma: Advisor/Consultant|Merck: Grant/Research Support

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Journal
Open Forum Infectious Diseases
Published
2026-01-01
DOI
https://doi.org/10.1093/ofid/ofaf695.2028
Primary Topic
Antibiotics Pharmacokinetics and Efficacy
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article
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article

P-1859. A Stewardship Focused Evaluation of Patients Treated with Ceftriaxone for Infections due to Penicillin Susceptible Streptococcus spp. in Outpatient Parenteral Antimicrobial Therapy

M. E. Rupp, Scott Bergman, Richard Hankins, Bryan Alexander et al.
Open Forum Infectious Diseases
Antibiotics Pharmacokinetics and Efficacy
article

P-1859. A Stewardship Focused Evaluation of Patients Treated with Ceftriaxone for Infections due to Penicillin Susceptible Streptococcus spp. in Outpatient Parenteral Antimicrobial Therapy

M. E. Rupp, Scott Bergman, Richard Hankins, Bryan Alexander, Molly M Miller, Trevor C Van Schooneveld, Elizabeth Lyden, Melissa LeMaster, Nicolás Cortés-Penfield, Jillian M Mack, Sara Azimi
article en

Abstract

Abstract Background In the outpatient parenteral antimicrobial therapy (OPAT) setting there are limited data quantifying the tradeoffs of using broader spectrum, but more convenient, antimicrobial regimens. This is particularly true with respect to adverse drug events, including Clostridioides difficile infection (CDI) and subsequent multidrug resistant (MDR) organism isolation.Table 1.Patient Cohort CharacteristicsTable 2.Primary and Secondary Outcomes Methods We performed a retrospective cohort analysis of adult patients with confirmed penicillin susceptible streptococcal infection, who received ceftriaxone (CRO) or penicillin through the OPAT service at a large academic medical center. The primary outcome was a composite outcome of clinical success rate without a significant OPAT-related adverse event (AE) or superinfection. The two components of this were successful therapy completion (completion of full planned treatment duration without an infection-related admission or ED visit, no change in therapy due to a drug-related AE, and improved or resolved infection at the end of therapy) and lack of CDI or MDR organism isolation within 12 months of therapy completion. Secondary outcomes included the individual components of the primary outcome. Results Patient characteristics reported in Table 1. Outcomes data reported in Table 2. The primary outcome was achieved in 83.1% of patients. Eleven total AEs occurred on therapy; 4 identified as catheter-related and 7 identified as drug-related. There were 1.4 cases of CDI over 1 year per 1000 days of therapy. A total of 9 MDR isolations were identified during the 1-year follow-up period. All CDI and MDR isolations were in CRO treated patients. Conclusion Our data are consistent with similar studies demonstrating high rates of clinical efficacy when utilizing CRO to treat highly penicillin-susceptible Streptococcus spp. infections. CRO was well tolerated and led to fewer line-related AEs than previously reported with more frequently administered regimens for these infections. Despite CRO being a broader-spectrum agent than necessary for highly penicillin-susceptible Streptococcus spp. infections, low adverse event rates, including long-term CDI and MDR isolation, make it an attractive choice for use in the OPAT context. Disclosures Trevor C. Van Schooneveld, MD, FSHEA, FIDSA, BioMerieux: Advisor/Consultant|BioMerieux: Grant/Research Support Mark E. Rupp, MD, Armata: Advisor/Consultant|Citius Pharmaceuticals, Inc.: Advisor/Consultant|Magnolia: Grant/Research Support|Teleflex: Advisor/Consultant Bryan T. Alexander, PharmD, BCIDP, AAHIVP, Astellas Pharma: Advisor/Consultant|Merck: Grant/Research Support

Open Forum Infectious DiseasesVol. 13(Supplement_1)
Nebraska Medical Center (US), University of Nebraska Medical Center (US)
Openalex Percentile: Top 90%
Antibiotics Pharmacokinetics and Efficacy
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