New Access Vascular Retrospective Data Review Demonstrates Midline Catheters Composed of Advanced Biomaterials May Improve Dwell Times
Data also finds using materials that mimic the body’s chemistry leads to meaningful reductions in complications such as phlebitis, occlusion, and infections
Billerica, MA – July 12, 2022 – Access Vascular, Inc. (AVI) today shared initial findings from a retrospective review of patient records that demonstrates an increase in dwell times compared to other commercially-available devices and no complications when using AVI’s consistently hydrophilic materials for midline catheters.
As a result of a three-month retrospective evaluation of 29 HydroMID midline catheters at a long-term, acute care U.S. hospital conducted in early 2022, AVI’s biomaterial-based catheters were found to have an average dwell time of 15.8 days. Further, there were no incidences of phlebitis, occlusion, deep vein thrombosis (DVT), or blood stream infections.
Traditional, polyurethane-based midline catheters have a median dwell time of only 61 days and an incidence of phlebitis of up to 35%2, exhibit up to 7% rate of DVT3, a 0.88% incidence of catheter-related bloodstream infection4 and an average occlusion rate of 22%5.
“Midlines are an essential vascular access tool, but clinicians have been hampered for years by polyurethane-based catheters that must continually be replaced or that lead to unnecessary and frequent complications,” said Access Vascular, Inc. CEO James Biggins. “This new data shows that choosing the right catheter can make all the difference, giving clinicians the trust and competence they desire from their vascular access devices. We are confident that new, ongoing studies will demonstrate even longer dwell times for AVI’s biomaterial-based catheters.”
AVI’s patented hydrophilic biomaterial catheters mimic the body’s chemistry to significantly reduce the most common and costly complications associated with vascular access procedures. Given the high utilization and complication rates of standard catheters, the use of AVI devices may meaningfully improve patient outcomes.
To learn more about AVI and its family of biomaterial-based catheters, please visit https://www.accessvascularinc.com/.
About Access Vascular
Access Vascular was founded to address the most common and costly complications of intravenous therapy: infection, thrombosis, and phlebitis. Taking a foundationally different approach to thrombus reduction, the company manufactures intravenous catheters from a hydrophilic material that retains significant amounts of water. Engineered to mimic the body’s natural chemistry, Access Vascular catheters are designed to evade the foreign body response and complications that come with it. Our award-winning, FDA-cleared products are HydroPICC®and HydroMID®. For more information, please visit www.accessvascularinc.com.
Chopra V, Kaatz S, Swaminathan L, et al. Variation in use and outcomes related to midline catheters: results from a multicenter pilot study. BMJ Qual Saf. 2019;28(9):714-720. doi:10.1136/bmjqs-2018-008554
Lee AY, Levine MN, Butler G, Webb C, Costantini L, Gu C, Julian JA. Incidence, risk factors, and outcomes of catheter-related thrombosis in adult patients with cancer. J Clin Oncol. 2006 Mar 20;24(9):1404-8. doi: 10.1200/JCO.2005.03.5600. PMID: 16549834.
Ponec D, Irwin D, Haire WD, Hill PA, Li X, McCluskey ER; COOL Investigators. Recombinant tissue plasminogen activator occluded central venous access devices: a double blind placebo controlled trial—the Cardiovascular Thrombolytic to Open Interv Radiol. 2001 Aug;12(8):9515.
Hogle, N. (2020). Am J. of Inf Ctrl, 48 (9) 1108-1110.
Hawes ML. Assessing and Restoring Patency in Midline Catheters. J Infus Nurs. 2020 Jul/Aug;43(4):213-221. doi: 10.1097/NAN.0000000000000376. PMID: 32618955.
