Wound Complications after 2-Octyl Skin Closure Systems for Total Joint Arthroplasty
- PMID: 32455101
- PMCID: PMC7242402
- DOI: 10.7150/jbji.42079
Wound Complications after 2-Octyl Skin Closure Systems for Total Joint Arthroplasty
Abstract
Introduction: Total joint arthroplasty is projected to expand rapidly by 2030. With large numbers of patients undergoing TJA, the choice of incisional closure has come into question. We compared the 2-Ocyl cyanoacrylate closure system of Dermabond ® Prineo ® with Exofin Fusion ® to compare rates of adverse wound outcomes after total joint arthroplasty. Secondary outcome measures were age, sex, and medical comorbidities between groups. Methods: We retrospectively reviewed adverse wound outcomes with skin closure in TJA in 281 patients (160 Dermabond Prineo and 121 Exofin Fusion). Clinical charts were analyzed out to the 6-week post-op visit. Results: The rate of overall adverse superficial wound outcomes was similar between the two groups with Dermabond Prineo (N=20) and Exofin Fusion (N=19). The rate of cellulitis was significantly higher for Dermabond Prineo when compared to Exofin Fusion (P=0.033). No other significant differences were found for rate of superficial or deep wound complications or for secondary outcomes. Conclusions: The two 2-octyl wound closure systems had similar adverse superficial wound complications. Except for Dermabond Prineo having a higher rate of post-operative cellulitis, there were no statistically significant differences for other superficial or deep adverse wound outcomes or secondary outcomes. A future randomized control trial or prospective cohort study is needed for a more robust analysis.
Keywords: 2-cyanoacrylate; 2-octyl; Dermabond; Exofin; Prineo; dermatitis; superficial infection; total joint arthroplasty.
© The author(s).
Conflict of interest statement
Competing Interests: The authors have declared that no competing interest exists.
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