A review of evidence, antimicrobial stability, and feasibility considerations for OPAT continuous infusion

Author:

Van Abel Amy L.1ORCID,Childs-Kean Lindsey M.2,Jensen Kelsey L.3,Mynatt Ryan P.4,Ryan Keenan L.5ORCID,Rivera Christina G.6

Affiliation:

1. Department of Pharmacy, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA

2. College of Pharmacy, University of Florida, Gainesville, FL, USA

3. Mayo Clinic Health System – Southeast Minnesota Region, Austin, MN, USA

4. Infectious Diseases, UK HealthCare, Lexington, KY, USA

5. Department of Pharmacy, University of New Mexico, Albuquerque, NM, USA

6. Department of Pharmacy, Mayo Clinic, Rochester, MN, USA

Abstract

Outpatient parenteral antimicrobial therapy (OPAT) has been widely used in clinical practice for many decades because of its associated cost savings, reductions in inpatient hospital days, and decreases in hospital-associated infections. Despite this long history, evolving practice patterns and new drug delivery devices continue to present challenges as well as opportunities for clinicians when designing appropriate outpatient antimicrobial regimens. One such change is the increasing use of extended and continuous infusion (CI) of antimicrobials to optimize the achievement of pharmacokinetic and pharmacodynamic targets. Elastomeric devices are also becoming increasingly popular in OPAT, including for the delivery of CI. In this article, we review the clinical evidence for CI in OPAT, as well as practical considerations of patient preferences, cost, and antimicrobial stability.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Infectious Diseases

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