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A Retrospective Assessment of Midline Catheter Failures Focusing on
Catheter Composition

Bunch, J

Aug 16, 2024

JIN Manuscript

The Art and Science of Infusion Nursing

OPEN

270 Copyright © 2020 The Author. Published by Wolters Kluwer Health, Inc. Journal of Infusion Nursing

on behalf of the Infusion Nurses Society.

BACKGROUND

In 2016, approximately 95% of all peripherally inserted

central catheters (PICCs) were composed of polyurethane

(PU). 1 PU has been used to manufacture vascular access

devices (VADs) for decades, during which it has been thor-

oughly studied and considered generally well tolerated.

Safety and efficacy issues commonly reported include

catheter dysfunction, phlebitis, and thrombosis. 2 Low

water content of a foreign object introduced into the body

is a significant trigger to systemic reaction. The structural

makeup of PU is hydrophobic, causing the body to react to

the material leading to protein adherence. 3 In addition to

protein adhering to hydrophobic material, the introduction

of such material into the bloodstream increases the likeli-

hood of inflammatory cell adhesion and surface-induced

thrombosis. 4


https://journals.lww.com/journalofinfusionnursing/fulltext/2022/09000/a_retrospective_assessment_of_midline_catheter.6.aspx

The medical device industry has used PU as a base

substance to mitigate some intrinsic issues found in hydro-

phobic materials. Hydrophilic polymers and hydrogels have

been grafted onto medical devices to decrease throm-

bogenicity. 3 , 5 In the vascular access industry, engineers

have added fluoro-oligomer to modify the PU (MPU),

impregnated the catheter with antibiotics, and coated the

devices with antithrombogenic or antimicrobial properties

( Figure 1 ). 6-8 Hydrophobic surfaces create high energy,

which attracts proteins and cells floating by as the body

responds to the apparent foreign object. Lowering the

surface energy of PU by adding fluoro-oligomer can lower

adhesion while the catheter remains hydrophobic. 3 , 5 The

other option is to change the surface energy by using a

different base material that is hydrophilic. 3

One alternative material to PU currently on the mar-

ket in the United States is polyvinyl alcohol (PVA)–based

ABSTRACT

Vascular access specialists are responsible for assessing the patient in their unique situation and determining the

correct vascular access device to complete the therapeutic goal without complication or failure. This retrospective

cohort study compared the failure rates of a variety of polyurethane (PU) midline catheters and a midline catheter

constructed of an emerging hydrophilic biomaterial (HBM). A total of 205 patients received a midline catheter and

were situationally randomized by the facility where they received it. Patients who had received a midline catheter

between March 2021 and May 2021 were assessed for catheter-related failures leading to increased staff time,

delays in treatment, or replacement with a new vascular access device to complete the therapy. There were 101

patients in the PU cohort and 104 patients in the HBM cohort. Comparing overall failure rates between the groups

revealed a 23.8% failure rate in the PU control group and only a 3.8% failure rate in the HBM group. This suggests

that a midline catheter constructed of HBM biomaterial is associated with significantly lower rates of failure, thereby

improving patient experience and health care economics.

Key words: catheter , complication , failure , hydrogel , hydrophilic , hydrophobic , material , midline , polyurethane

Author Affiliation: ProVasc Ltd, Romeoville, Illinois.

Joseph Bunch, RN, is the chief executive officer and principal

owner of ProVasc Ltd, a Chicagoland-based vascular access group.

He is responsible for the strategic direction, vision, and clinical

performance of the group. As a registered nurse for more than 22

years, he has placed more than 50 000 vascular access devices.

Disclosures: Financial support for data mining and statistical anal-

ysis was provided by Access Vascular Inc (Billerica, MA, USA) after

all data for the vascular access devices were recorded. No off-label

or investigative actions were part of this study .

This is an open-access article distributed under the terms of the

Creative Commons Attribution-Non Commercial-No Derivatives

License 4.0 (CCBY-NC-ND), where it is permissible to download

and share the work provided it is properly cited. The work cannot

be changed in any way or used commercially without permission

from the journal.

Corresponding Author: Joseph Bunch, RN, ProVasc Ltd, 1079

Redondo Dr, Romeoville, IL 60446 ( admin@picclines.net ).

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