Does longer peripheral intravenous catheter length optimise antimicrobial delivery? Protocol for the LEADER study

Author:

Corley Amanda1,O’Brien Catherine2,Larsen Emily3,Peach Hannah4,Rickard Claire5,Hewer Barbara6,Pearse India2,Fenn Mary7,Cocksedge Ruth8,Marsh Nicole9

Affiliation:

1. Research Fellow (Clinician Researcher), School of Nursing and Midwifery, Griffith University, Nathan, Australia/Nursing and Midwifery Research Centre, Royal Brisbane and Women’s Hospital, Herston, Australia

2. Nurse Researcher, Nursing and Midwifery Research Centre, Royal Brisbane and Women’s Hospital

3. Research Fellow (Vascular Access), School of Nursing and Midwifery, Griffith University/Nursing and Midwifery Research Centre, Royal Brisbane and Women’s Hospital

4. Clinical Research Nurse, Nursing and Midwifery Research Centre, Royal Brisbane and Women’s Hospital

5. Professor of Infection Prevention and Vascular Access, School of Nursing, Midwifery and Social Work, The University of Queensland, Brisbane, Australia/Herston Infectious Diseases Institute, Metro North Health, Herston, Australia

6. Clinical Nurse Consultant, Vascular Access and Surveillance and Education, Royal Brisbane and Women’s Hospital

7. Senior Research Assistant, School of Nursing and Midwifery, Griffith University

8. Senior Research Assistant, School of Medicine and Dentistry, Griffith University

9. Nursing and Midwifery Director, Research, Nursing and Midwifery Research Centre, Royal Brisbane and Women’s Hospital/Professor, School of Nursing and Midwifery, Griffith University

Abstract

Background: Hospitalised patients receiving intravenous antimicrobial therapy require a reliable device through which this is delivered. Short peripheral intravenous catheters (PIVCs) are the default device for antimicrobial therapy but up to half fail before therapy completion, leading to suboptimal drug dosing, patient distress from repeated insertions, and increased healthcare costs. This study will investigate the use of long PIVCs to determine if they are more reliable at delivering antimicrobial therapy. Methods: A two-arm, parallel randomised controlled trial of hospitalised adults requiring at least 3 days of peripherally compatible intravenous antimicrobials. Participants will be randomised to a short (<4 cm) or long (4.5-6.4 cm) PIVC. After interim analysis ( n=70) for feasibility and safety, 192 participants will be recruited. Primary outcome is disruption to antimicrobial administration from all-cause PIVC failure. Secondary outcomes include: number of devices to complete therapy, patient-reported pain and satisfaction, and a cost analysis. Ethical and regulatory approvals have been received.

Publisher

Mark Allen Group

Subject

General Nursing

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