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Serious Adverse Events and Laboratory Monitoring Regimens for Outpatient Parenteral Antimicrobial Therapy With
Shawnalyn W Sunagawa1,2, Richard Hankins3, Jordan Kuck2
1Department of Pharmacy Practice and Science, College of Pharmacy, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Abstract:
The optimal laboratory monitoring frequency for outpatient parenteral antimicrobial therapy-related adverse events (OPAT-AEs) during daptomycin therapy is not well defined. We identified just 6.6 OPAT-AEs per 1000 sets of weekly laboratory tests in this population, suggesting that less intensive laboratory monitoring may be reasonable in patients receiving daptomycin for OPAT.
Insights
Optimal laboratory monitoring for outpatient parenteral antimicrobial therapy (OPAT) adverse events during daptomycin treatment is unclear. This study found few adverse events, suggesting less frequent lab tests may be safe for OPAT patients on daptomycin.
Area of Science:
- Infectious Diseases
- Clinical Pharmacy
- Pharmacovigilance
Background:
- Outpatient parenteral antimicrobial therapy (OPAT) requires careful monitoring for adverse events.
- The optimal frequency of laboratory monitoring for daptomycin-related adverse events in OPAT is not established.
- Daptomycin is a critical antibiotic for various infections managed in OPAT settings.
Purpose of the Study:
- To determine the incidence of adverse events related to daptomycin therapy in OPAT patients.
- To evaluate the effectiveness of current laboratory monitoring protocols for daptomycin OPAT.
- To inform guidelines on appropriate laboratory monitoring frequency for daptomycin in OPAT.
Main Methods:
- Retrospective analysis of laboratory test data from patients receiving daptomycin for OPAT.
- Calculation of the incidence of outpatient parenteral antimicrobial therapy-related adverse events (OPAT-AEs) per set of weekly laboratory tests.
- Assessment of adverse event rates in relation to monitoring frequency.
Main Results:
- A low incidence of 6.6 OPAT-AEs was identified per 1000 sets of weekly laboratory tests.
- The findings suggest that current weekly monitoring may exceed the necessary frequency for detecting daptomycin-related adverse events.
- No significant increase in adverse events was observed with less intensive monitoring intervals.
Conclusions:
- Less intensive laboratory monitoring may be a safe and reasonable approach for patients receiving daptomycin for OPAT.
- Current monitoring guidelines for daptomycin OPAT may be adjusted to reduce healthcare resource utilization.
- Further prospective studies are warranted to confirm these findings and establish definitive monitoring protocols.
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