# Real-World Comparison of Intravenous vs. Oral Antimicrobial Therapy for Bone and Joint Infections

**Authors:** Maura Kreiser, Sarah Al Mansi, Ismaeel Yunusa, Caroline Derrick, P. Brandon Bookstaver, Majdi N. Al-Hasan, Yorika Hammett, Morgan Pizzuti

PMC · DOI: 10.3390/pharmacy14020048 · 2026-03-14

## TL;DR

This study compares oral and intravenous antimicrobial treatments for bone and joint infections in real-world settings, finding similar treatment success but underuse of oral therapy.

## Contribution

The study provides real-world evidence supporting the use of oral antimicrobial therapy for bone and joint infections, despite its underutilization.

## Key findings

- Treatment failure rates were similar between intravenous and oral antimicrobial groups.
- Oral antimicrobial therapy was underutilized despite comparable effectiveness.
- Peripheral vascular disease and higher comorbidity scores were risk factors for treatment failure.

## Abstract

Well-designed randomized controlled trials (RCTs) have demonstrated safe and effective use of oral antimicrobial therapy for bone and joint infections. Application of data for implementation into real-world practice, however, has inherent challenges. This retrospective cohort study compared real-world use of intravenous versus oral antimicrobial therapy in bone and joint infections within a large healthcare system comprising both academic and community medical centers. The primary outcome was the proportion of treatment failure. Key secondary outcomes included the proportion of patients with logistical failure and risk factors associated with treatment and logistical failure. Among 166 patients included, 136 (82%) and 30 (18%) received predominantly intravenous and oral antimicrobial therapy, respectively. Treatment failure occurred in (77/121) 64% versus (18/25) 72% of patients in the intravenous and oral antimicrobial groups (p = 0.491; OR, 1.38; 95% CI, 0.56–3.33). Logistical failure occurred in 29% versus 47% of patients in the intravenous and oral antimicrobial groups (p = 0.150; OR, 1.93; 95% CI 0.79–4.70). Risk factors for treatment failure included peripheral vascular disease (OR, 2.61; 95% CI 1.02–7.80) and higher Charlson Comorbidity Index scores (OR, 1.18; 95% CI 1.04–1.36). Similar to previously published RCTs, treatment failure appeared comparable between groups; however, oral antimicrobial therapy was overall underutilized.

## Linked entities

- **Diseases:** peripheral vascular disease (MONDO:0005294)

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** rash (MESH:D005076), infectious disease (MESH:D003141), bone marrow suppression (MESH:D001855), wound dehiscence (MESH:D013529), lymphoma (MESH:D008223), ID (MESH:C537985), AIDS (MESH:D000163), diabetes (MESH:D003920), rhabdomyolysis (MESH:D012206), cytopenia (MESH:D006402), Thrombocytopenia (MESH:D013921), Diabetic foot infections (MESH:D017719), musculoskeletal infections (MESH:D009140), peripheral arterial disease (MESH:D058729), prediabetes (MESH:D011236), Osteomyelitis (MESH:D010019), infection (MESH:D007239), incarcerated (MESH:D060725), PVD (MESH:D016491), injury to (MESH:D014947), bacteremia (MESH:D016470), mycobacterial, fungal, or viral infections (OMIM:614172), Comorbidity (MESH:D004194), epidural abscess (MESH:D020802), tumor (MESH:D009369), leukemia (MESH:D007938), Mortality (MESH:D003643), Bone and Joint Infection (MESH:D001847), bacterial (MESH:D001424)
- **Chemicals:** oritavancin (MESH:C100708), linezolid (MESH:D000069349), tedizolid (MESH:C546016), dalbavancin (MESH:C469289), cephalosporins (MESH:D002511), methicillin (MESH:D008712), aminopenicillins (-), vancomycin (MESH:D014640), rifampicin (MESH:D012293), fluoroquinolones (MESH:D024841)
- **Species:** Homo sapiens (human, species) [taxon 9606], Cutibacterium (genus) [taxon 1912216], Staphylococcus aureus (species) [taxon 1280]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13010755/full.md

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Source: https://tomesphere.com/paper/PMC13010755