Primary ArthroplastyClosed Incision Negative Pressure Wound Therapy vs Conventional Dry Dressings After Primary Knee Arthroplasty: A Randomized Controlled Study
Section snippets
Materials and Methods
Fifty-seven primary knee arthroplasty surgeries in 33 patients performed by 3 surgeons occurring between February and December 2014 in our institution were included in this study. Twenty-three patients underwent bilateral total knee arthroplasty, 9 patients underwent unilateral total knee arthroplasty, and 1 patient underwent bilateral unicompartmental knee arthroplasty. All total knee arthroplasty procedures were using a subvastus approach under computer-assisted navigation specifically using
Results
Thirty-three patients (19 males and 14 females) underwent 57 primary knee arthroplasties. The breakdown of all patient demographics is shown in Table 1. Mean age was 66 (45-80), body mass index 29.79 (23-44), ASA 2 (1-3), and CCI 2.33 (0-5). One patient had a diagnosis of rheumatoid arthritis (n = 1), the rest had osteoarthritis (n = 32). None of the patients included in this study were considered high risk with a mean ASA of 2 (1-3) and CCI of 2.33 (0-5). The average length of stay was 4.1
Discussion
Our study has indicated that routine application of NPWT post knee arthroplasty has no economic benefit. There were benefits in regard to wound leakage and wound protection, but other QoL factors were similar between the groups. We found no clear benefit of wound healing or cost in the utilization of the NPWT for routine knee arthroplasty incision sites.
Surgical site infections post arthroplasty surgery increases the risk of deep wound and prosthesis infections dramatically. Current
Acknowledgments
The authors sincerely thank the rest of the staff at Orthopaedic Research Institute of Queensland for their assistance throughout this study with paperwork and organization. The authors also show their appreciations and thanks to the nursing staff in theater and the orthopedic ward at the Mater Health Services North Queensland Ltd who assisted them with the dressing application and changes. The authors also thank Dr Geoffrey Dobson and Dr Hayley Letson at the James Cook University for their
References (37)
- et al.
Infection burden for hip and knee arthroplasty in the United States
J Arthroplasty
(2008) - et al.
Risk factors for superficial wound complications in hip and knee arthroplasty
Clin Microbiol Infect
(2014) - et al.
Predictors of wound infection in hip and knee joint replacement: results from a 20 year surveillance program
J Orthop Res
(2002) - et al.
Effect of negative pressure wound therapy on wound healing
Curr Probl Surg
(2014) - et al.
Closed incision negative pressure therapy versus antimicrobial dressings following revision hip and knee surgery: a comparative study
J Arthroplasty
(2016) - et al.
Clinical outcome after poststernotomy mediastinitis: vacuum-assisted closure versus conventional treatment
Ann Thorac Surg
(2005) The management of peri-prosthetic infection in total joint arthroplasty
J Bone Jt Surg Br
(2006)- Australian Orthopaedic Association National Joint Replacement Registry. Revision Hip and Knee Arthroplasty....
How-to guide: prevent surgical site infection for hip and knee arthroplasty 2012
(2012)- et al.
Wound infection in hip and knee arthroplasty
J Bone Joint Surg Br
(2000)
Factors associated with prolonged wound
J Bone Jt Surg
Infection after total hip replacement
J Bone Jt Surg
First experience with a new negative pressure incision management system on surgical incisions after cardiac surgery in high risk patients
J Cardiothorac Surg
Use of negative pressure wound therapy over clean, closed surgical incisions
Int Wound J
“Homemade” negative pressure wound therapy: treatment of comples wounds under challenging conditions
Wounds
A prospective, blinded, randomized, controlled clinical trial of topical negative pressure use in skin grafting
Plast Reconstr Surg
Negative-pressure wound therapy over surgically closed wounds in open fractures
J Orthop Surg (Hong Kong)
Simplified negative pressure wound therapy: clinical evaluation of an ultraportable, no-canister system
Int Wound J
Cited by (50)
Negative pressure wound therapy in patients with diabetes undergoing left internal thoracic artery harvest: A randomized control trial
2024, Journal of Thoracic and Cardiovascular SurgeryCitation Excerpt :Potential additional benefits to a regular dressing include apposition of wound edges together and keeping the wound dry.29 There is now a body of evidence to support this type of wound therapy in colorectal, orthopedic, and cardiothoracic surgery.11,12,30 NIRS uses wavelength analysis to measure the relative amounts of oxygenated and deoxygenated hemoglobin in a volume of tissue.
Orthopaedic surgical dressings
2021, Orthoplastic SurgeryEffectiveness of Different Wound Dressings in the Reduction of Blisters and Periprosthetic Joint Infection After Total Joint Arthroplasty: A Systematic Review and Network Meta-Analysis
2021, Journal of ArthroplastyCitation Excerpt :In terms of blind assessment, 3 studies [25,32,41] had blinding of participants and personnel, and 6 studies [22,27,32–34,41] had blinding of all assessors. The bias of incomplete outcome data was found in 4 studies [27,32,33,41], and possible selective reporting existed in 3 studies [34,39,41]. Finally, 8 studies showed some concerns [22,23,25,30,31,33,34,39], and 2 studies had high risk for overall bias [26,29].
Closed Incision Negative Pressure Wound Therapy for Elective Hip and Knee Arthroplasty: A Systematic Review and Meta-Analysis of Randomized Controlled Trials
2021, Journal of ArthroplastyCitation Excerpt :Only 2 studies reported cost data for ciNPWT and standard dry dressings, but the data were not comparable [19,23]. Gillespie et al [19] reported average cost per day in the hospital, whereas Manoharan et al [23] reported average total cost during the entire hospital length of stay. The use of ciNPWT has shown promise in minimizing wound infections across many surgical fields, especially in the field of orthopedic trauma.
Human research ethics approval and trial registration: Ethics committee approval for this trial was obtained through Internal Regulatory Governance Body at the Mater Health Services North Queensland Human Research Ethics Committee, Approval number–MHS20131216-02. The trial was also registered with the Australia New Zealand Clinical Trials Registry, Registration code–ACTRN12615001350516. No changes to methods were made during the trial period.
One or more of the authors of this paper have disclosed potential or pertinent conflicts of interest, which may include receipt of payment, either direct or indirect, institutional support, or association with an entity in the biomedical field which may be perceived to have potential conflict of interest with this work. For full disclosure statements refer to http://dx.doi.org/10.1016/j.arth.2016.04.016