A “Hail-Mary” Oral Antimicrobial Strategy for a Complex Case of Persistent MRSA Bacteremia

Persistent bacteremia caused by methicillin-resistant Staphylococcus aureus (MRSA) has a high mortality rate. While combination parenteral antibiotic regimens have shortened duration of bacteremia in some trials, they were also associated with increased nephrotoxicity and did not improve clinical outcomes. We cared for a patient with MRSA bacteremia that persisted for nearly 3 weeks. Due to medical ethical complexities, intravenous therapy could not be administered after day 6, so oral linezolid was started. On day 20 of persistent bacteremia, we attempted a “hail Mary” intensification by adding oral moxifloxacin and rifampin. On day 21, blood cultures cleared. Causality from the intensification cannot be presumed, but the temporal association was intriguing. Nevertheless, an oral regimen successfully cleared persistent S. aureus bacteremia, calling into question the necessity to wait until clearance of bacteremia before initiation of oral therapy. These results support the future study of all-oral therapy for S. aureus bacteremia.

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Publication Details

Journal
Infectious Diseases in Clinical Practice
Published
2026-06-25
DOI
https://doi.org/10.1097/ipc.0000000000001631
Primary Topic
Antimicrobial Resistance in Staphylococcus
Type
article
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article

A “Hail-Mary” Oral Antimicrobial Strategy for a Complex Case of Persistent MRSA Bacteremia

Bassam Ghanem, Kayshaliya Sharma, C. Lynch, Kusha Davar et al.
Infectious Diseases in Clinical Practice
Antimicrobial Resistance in Staphylococcus
article

A “Hail-Mary” Oral Antimicrobial Strategy for a Complex Case of Persistent MRSA Bacteremia

Bassam Ghanem, Kayshaliya Sharma, C. Lynch, Kusha Davar, Todd C Lee, Devin Clark, M. Gabriela Cabanilla, Brad Spellberg
article en

Abstract

Persistent bacteremia caused by methicillin-resistant Staphylococcus aureus (MRSA) has a high mortality rate. While combination parenteral antibiotic regimens have shortened duration of bacteremia in some trials, they were also associated with increased nephrotoxicity and did not improve clinical outcomes. We cared for a patient with MRSA bacteremia that persisted for nearly 3 weeks. Due to medical ethical complexities, intravenous therapy could not be administered after day 6, so oral linezolid was started. On day 20 of persistent bacteremia, we attempted a “hail Mary” intensification by adding oral moxifloxacin and rifampin. On day 21, blood cultures cleared. Causality from the intensification cannot be presumed, but the temporal association was intriguing. Nevertheless, an oral regimen successfully cleared persistent S. aureus bacteremia, calling into question the necessity to wait until clearance of bacteremia before initiation of oral therapy. These results support the future study of all-oral therapy for S. aureus bacteremia.

Infectious Diseases in Clinical PracticeVol. 34(4)
University of Southern California (US), University of New Mexico Hospital (US), University of New Mexico (US), King Abdulaziz Medical City (SA), Los Angeles Medical Center (US), California Hospital Medical Center Foundation (US), McGill University (CA)
Good health and well-being
Openalex Percentile: Top 7%
Antimicrobial Resistance in Staphylococcus
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