Novel Central Line Securement Vest to Prevent Mechanical Complications of Tunneled Central Lines: Experience from a Cohort of Pediatric Patients with Intestinal Failure

Author:

St. Pierre-Hetz Ryan1,Ackerman Kimberly2,Dresser Christian P.1,Yaworski Jane Anne2,Cercone Angelica3,Rudolph Jeffrey2,Wisniewski Stephen R.4,Manole Mioara D.1

Affiliation:

1. Department of Pediatrics, Division of Emergency Medicine, Children’s Hospital of Pittsburgh, Pittsburgh, PA

2. Department of Pediatrics, Division of Gastroenterology, Children’s Hospital of Pittsburgh, Pittsburgh, PA

3. Division of Emergency Medical Services, Department of Emergency Medicine, University of Pittsburgh, Pittsburgh, PA

4. Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA

Abstract

Highlights Abstract Background: Tunneled central lines are used to deliver medications, hydration, and total parenteral nutrition. The current modality for their securement is by a transparent sterile adhesive. Mechanical line traumas, including line fissures, breaks and dislodgements, occur frequently in children. A novel device, the Central Line Securement Vest, was created to protect central lines from mechanical trauma. Objective: We present here our experience with the device and report its use in patients with intestinal failure treated at our institution. Methods: All patients who have used the Central Line Securement Vest at our institution during the last decade were identified. We reviewed the patients’ electronic records and compared the rate of line mechanical trauma, line infections, line replacements, Emergency Department (ED) visits, and hospital admissions for a period of 12 months before and after the use of the device. Results: Ten patients were identified. Four patients had purchased the device at the time of line insertion. Six patients had a period of time of line use before beginning use of the device. The rate of line traumas and infections decreased after using the device: 0.19 ± 0.15 vs 0.05 ± 0.04 trauma/month, pre– vs post–device use, P < 0.05. Similarly, the rate of line infections decreased post–device use: 0.18 ± 0.13 vs 0.09 ± 0.06 infections/month, pre– vs post–device use, P < 0.05. The rate of line replacements, ED visits, and hospital admissions were similar pre– and post–device use. Conclusion: We report here our institution’s experience with a novel central line securement device designed to protect the line from mechanical trauma.

Publisher

Association for Vascular Access

Subject

Medicine (miscellaneous)

Reference12 articles.

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2. Characteristics of a cohort of home parenteral nutrition patients at the time of enrollment in the Sustain Registry;DiMaria-Ghalili,;JPEN J Parenter Enteral Nutr,2015

3. Alexander, Mary O’Grady, Naomi B Lillian. Guidelines for the prevention of intravascular catheter-related infections. 2011. https://www.cdc.gov/infectioncontrol/pdf/guidelines/bsi-guidelines-H.pdf. Published online July 2011. Accessed May 12, 2021.

4. A prospective survey on incidence and outcome of Broviac/Hickman catheter-related complications in pediatric patients affected by hematological and oncological diseases;Cesaro;Ann Hematol,2004

5. Complications of central venous access devices: a systematic review;Ullman;Pediatrics,2015

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