Dermabond PRINEO for Total Shoulder Arthroplasty

Inclusion Criteria

• •Subjects will be included if:
• •They are 18 years or older;
• •They are undergoing primary total shoulder arthroplasty by the principal and co-investigator.
• •They are willing and have the capacity to provide informed consent;
• •They expect to continue their post-operative follow up care with their operating surgeons at Medical University of South Carolina (MUSC).
• •Subjects will be excluded if:
• •They have a unique, identifying tattoo or skin marking within 2 inches of intended site of surgical incision
• •They self-report a known hypersensitivity to cyanoacrylate, formaldehyde, benzalkonium chloride, or pressure sensitive adhesive;
• •They self-report or have a documented prior ipsilateral shoulder arthroplasty or other open ipsilateral shoulder surgery utilizing the delto-pectoral approach;
• •Their medical record shows that they are HIV positive or otherwise immunocompromised;
• •Their medical record shows a skin abnormality or dermatological condition which affects skin healing;
• •They report a personal or family history of significant keloid or significant hypertrophic scar formations, or other problems with wound healing.