2018
DOI: 10.1093/jac/dky474
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Intravenous catheter-related adverse events exceed drug-related adverse events in outpatient parenteral antimicrobial therapy

Abstract: BackgroundDrug-related adverse events (AEs) are reported to be common amongst patients receiving outpatient parenteral antimicrobial therapy (OPAT). However, comparative data regarding intravenous (iv) catheter-related AEs are lacking.ObjectivesTo compare drug- and iv catheter-related AEs from a large UK OPAT centre.Patients and methodsWe reviewed 544 OPAT episodes [median (IQR) age: 57 (39–71) years, 60% male, 13% with diabetes] with a median (IQR) duration of 7 (2–18) days. Clinically significant drug- and i… Show more

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Cited by 45 publications
(33 citation statements)
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“…We identified a total of 133 patients treated for BJI through our OPAT service, comprising approximately a quarter of all our OPAT patients (5). Non-vertebral, native osteomyelitis was the most common type of BJI, with a range of other native and prosthetic joint infections also being treated ( Table 1).…”
Section: Resultsmentioning
confidence: 99%
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“…We identified a total of 133 patients treated for BJI through our OPAT service, comprising approximately a quarter of all our OPAT patients (5). Non-vertebral, native osteomyelitis was the most common type of BJI, with a range of other native and prosthetic joint infections also being treated ( Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…OVIVA provided strong evidence that BJI could be treated with appropriate oral antibiotic regimens, but most patients were recruited from two specialist bone and joint infection centres (7). Making use of a welldefined and prospectively recorded cohort of patients receiving OPAT (5,8), we provide the first real-world assessment that implementation of comparable criteria rendered the majority (80%) of our BJI cohort eligible for oral antibiotic treatment. We had elected not to participate in OVIVA as our practice at the time of recruitment was shorter than six weeks of IV therapy, reflected in median IV therapy duration of 29 days (IQR 18-45).…”
Section: Discussionmentioning
confidence: 99%
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