Comparing the use of midline catheters versus peripherally inserted central catheters for patients requiring peripherally compatible therapies: A pilot randomised controlled trial (the compact trial).

Infect Dis Health

Nursing and Midwifery Research Centre, Internal Medicine Services, Infectious Diseases, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia; School of Nursing and Midwifery, Centre for Applied Health Economics, School of Medicine and Dentistry, Patient Centred Health Services, Menzies Health Institute Queensland, Alliance for Vascular Access, Teaching and Research, Griffith University, Brisbane, Queensland, Australia; School of Nursing, Midwifery and Social Work, UQ Centre for Clinical Research, University of Queensland, Herston, Queensland, Australia; Herston Infectious Diseases Institute, Metro North Health, Herston, Queensland, Australia. Electronic address:

Published: November 2023

AI Article Synopsis

Article Abstract

Background: Midline catheter (MC) use has increased in acute-care settings, particularly for patients with difficult venous access or requiring peripherally compatible intravenous therapy for up-to 14 days. Our aim was to assess feasibility and generate clinical data comparing MCs with Peripherally Inserted Central Catheters (PICCs).

Methods: A two-arm parallel group pilot randomised controlled trial (RCT), comparing MCs with PICCs, was conducted in a large tertiary hospital in Queensland between September 2020 and January 2021. The primary outcome was study feasibility, measured against rates of eligibility (>75%), consent (>90%), attrition (<5%); protocol adherence (>90%) and missing data (<5%). The primary clinical outcome was all-cause device failure.

Results: In total, 25 patients were recruited. The median patient age was 59-62 years; most patients were overweight/obese, with ≥2 co-morbidities.

Primary Outcomes: The eligibility and protocol adherence criteria were not met; of 159 screened patients, only 25 (16%) were eligible, and three patients did not receive their allocated intervention post-randomisation (88% adherence). All-cause failure occurred in two patients allocated to MC (20%) and one PICC (8.3%).

Conclusions: Our study found that a fully powered RCT testing MCs compared with PICCs is not currently feasible in our setting. We recommend a robust process evaluation before the introduction of MCs into clinical practice.

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Source
http://dx.doi.org/10.1016/j.idh.2023.03.007DOI Listing

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