Evaluation of a novel mechanical compression device for hematoma prevention and wound cosmesis after CIED implantation.

ABSTRACT:

Background

An important complication of cardiac implantable electronic devices (CIED) implantation is the development of hematoma and device infection.

Objective

We aimed to evaluate a novel mechanical compression device for hematoma prevention and cosmetic outcomes following CIED implantation.

Methods

An open, prospective, randomized, single-center clinical trial was performed in patients undergoing CIED implantation. Patients were randomized to receive a novel mechanical compression device (PressRite, PR) or to receive the standard of care post device implantation. Skin pliability was measured with a calibrated durometer; the surgical site was evaluated using the Manchester Scar Scale (MSS) by a blinded plastic surgeon and the Patient and Observer Scar Scale (POSAS)

SUBMITTER: Rojas E 

PROVIDER: S-EPMC9310802 | biostudies-literature | 2022 Apr

REPOSITORIES: biostudies-literature